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2024 SS
- Doktorandenseminar
- Psychische Störungen im Kindes- und Jugendalter im Spannungsfeld zwischen Biologie und Umwelt
- Nervensystem und Psyche
- Doktorandenseminar des molekulargenetischen Labors
- Praktikum für Doktoranden des molekulargenetischen Labors
- Vorstellung aktueller Studien im Bereich der Kinder- und Jugendpsychiatrie
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2023 WS
Die folgenden Publikationen sind in der Online-Universitätsbibliographie der Universität Duisburg-Essen verzeichnet. Weitere Informationen finden Sie gegebenenfalls auch auf den persönlichen Webseiten der Person.
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Does hypoleptinemia trigger entrapment in anorexia nervosa? : Etiological and clinical considerationsIn: European Eating Disorders Review Jg. 32 (2024) Nr. 3, S. 557 - 574Online Volltext: dx.doi.org/ (Open Access)
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Early versus late response to PD-1-based immunotherapy in metastatic melanomaIn: European Journal of Cancer (EJC) Jg. 210 (2024) 114295Online Volltext: dx.doi.org/ (Open Access)
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Epigenetic alterations in patients with anorexia nervosa : A systematic reviewIn: Molecular Psychiatry (2024) in pressOnline Volltext: dx.doi.org/ (Open Access)
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Genetic and functional analyses of CTBP2 in anorexia nervosa and body weight regulationIn: Molecular Psychiatry (2024) in pressOnline Volltext: dx.doi.org/ (Open Access)
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Genetische Ursachen der Adipositas und ihre therapeutischen Implikationen : Erkenntnisse der ForschungIn: Diabetes Aktuell für die Hausarztpraxis Jg. 22 (2024) Nr. 4, S. 152 - 161Online Volltext: dx.doi.org/
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No evidence for a causal contribution of bioavailable testosterone to ADHD in sex-combined and sex-specific two-sample Mendelian randomization studiesIn: European Child and Adolescent Psychiatry Jg. 33 (2024) Nr. 10, S. 3613 - 3623Online Volltext: dx.doi.org/ (Open Access)
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No relationship between male pubertal timing and depression : new insights from epidemiology and Mendelian randomizationIn: Psychological Medicine Jg. 54 (2024) Nr. 9, S. 1975 - 1984Online Volltext: dx.doi.org/ (Open Access)
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Unexpected identification of obesity-associated mutations in LEP and MC4R genes in patients with anorexia nervosaIn: Scientific Reports Jg. 14 (2024) 7067Online Volltext: dx.doi.org/ (Open Access)
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What Amount of Weight Loss Can Entail Anorexia Nervosa or Atypical Anorexia Nervosa After Bariatric Surgery?In: International Journal of Eating Disorders (2024) in pressOnline Volltext: dx.doi.org/ (Open Access)
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A second update on mapping the human genetic architecture of COVID-19In: Nature Jg. 621 (2023) S. E7 - E26Online Volltext: dx.doi.org/ (Open Access)
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Could leptin substitution therapy potentially terminate entrapment in anorexia nervosa?In: Nature Reviews Endocrinology Jg. 19 (2023) Nr. 8, S. 435 - 436Online Volltext: dx.doi.org/
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Evaluation of the MC3R gene pertaining to body weight and height regulation and puberty developmentIn: Scientific Reports Jg. 13 (2023) Nr. 1, 10419Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Genetic variants in genes involved in creatine biosynthesis in patients with severe obesity or anorexia nervosaIn: Frontiers in Genetics Jg. 14 (2023) 1128133Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Lipocalin 2 - mutation screen and serum levels in patients with anorexia nervosa or obesity and in lean individualsIn: Frontiers in Endocrinology Jg. 14 (2023) 1137308Online Volltext: dx.doi.org/ (Open Access)
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Age at menarche relates to depression in adolescent girls : Comparing a clinical sample to the general pediatric populationIn: Journal of Affective Disorders Jg. 318 (2022) S. 103 - 112Online Volltext: dx.doi.org/
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Causal Effect of Age at Menarche on the Risk for Depression : Results From a Two-Sample Multivariable Mendelian Randomization StudyIn: Frontiers in Genetics Jg. 13 (2022) 918584Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severityIn: Human Genetics Jg. 141 (2022) Nr. 1, S. 147 - 173Online Volltext: dx.doi.org/ (Open Access)
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Detailed stratified GWAS analysis for severe COVID-19 in four European populationsIn: Human Molecular Genetics Jg. 31 (2022) Nr. 23, S. 3945 - 3966Online Volltext: dx.doi.org/ (Open Access)
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Ebenen der genetischen Analyse komplexer Phänotypen am Beispiel der Anorexia nervosa und der Varianz des KörpergewichtsIn: Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie Jg. 50 (2022) Nr. 3, S. 175 - 185Online Volltext: dx.doi.org/ (Open Access)
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Ernährungseffekten auf der Spur : Wie die Genetik helfen kann, Zusammenhänge zwischen Ernährung und seelischer Gesundheit aufzudeckenIn: Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie Jg. 50 (2022) Nr. 3, S. 217 - 226Online Volltext: dx.doi.org/ (Open Access)
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Evidence for correlations between BMI-associated SNPs and circRNAsIn: Scientific Reports Jg. 12 (2022) Nr. 1, 12643Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Expression of CXCR4 on CD4⁺ T cells predicts body composition parameters in female adolescents with anorexia nervosaIn: Frontiers in Psychiatry Jg. 13 (2022) 960905Online Volltext: dx.doi.org/ (Open Access)
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PTBP2 – a gene with relevance for both Anorexia nervosa and body weight regulationIn: Translational Psychiatry Jg. 12 (2022) Nr. 1, 241Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Prevalence estimates of putatively pathogenic leptin variants in the gnomAD databaseIn: PLoS ONE Jg. 17 (2022) Nr. 9, e0266642Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Rapid amelioration of anorexia nervosa in a male adolescent during metreleptin treatment including recovery from hypogonadotropic hypogonadismIn: European Child and Adolescent Psychiatry Jg. 31 (2022) S. 1573 - 1579Online Volltext: dx.doi.org/ (Open Access)
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Subjective reward processing and catechol-O- methyltransferase Val158Met polymorphism as potential research domain criteria in addiction : A pilot studyIn: Frontiers in Psychiatry Jg. 13 (2022) 992657Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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The adrenal steroid profile in adolescent depression : a valuable bio-readout?In: Translational Psychiatry Jg. 12 (2022) Nr. 1, 255Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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The promise of new anti-obesity therapies arising from knowledge of genetic obesity traitsIn: Nature Reviews Endocrinology Jg. 18 (2022) Nr. 10, S. 623 - 637Online Volltext: dx.doi.org/ (Open Access)
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A mendelian randomization study on causal effects of 25(OH)vitamin D levels on attention deficit/hyperactivity disorderIn: European Journal of Nutrition Jg. 60 (2021) Nr. 5, S. 2581 - 2591Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Alterations in B cell subsets correlate with body composition parameters in female adolescents with anorexia nervosaIn: Scientific Reports Jg. 11 (2021) Nr. 1, S. 1125Online Volltext: dx.doi.org/ (Open Access)
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Evaluation of metabolic profiles of patients with anorexia nervosa at inpatient admission, short-and long-term weight regain : Descriptive and pattern analysisIn: Metabolites Jg. 11 (2021) Nr. 1, 7Online Volltext: dx.doi.org/ (Open Access)
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Klotho KL-VS haplotype does not improve cognition in a population-based sample of adults age 55-87 yearsIn: Scientific Reports Jg. 11 (2021) Nr. 1, 13852Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Kurzzeitige Behandlung von Patient_innen mit Anorexia nervosa mit rekombinant hergestelltem Human-Leptin (Metreleptin) : Rasch einsetzende positive Effekte auf Stimmung, Kognition und VerhaltenIn: Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie Jg. 49 (2021) Nr. 1, S. 1 - 5Online Volltext: dx.doi.org/
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Lack of Evidence for a Relationship Between the Hypothalamus-Pituitary-Adrenal and the Hypothalamus-Pituitary-Thyroid Axis in Adolescent DepressionIn: Frontiers in Endocrinology Jg. 12 (2021) 662243Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Mapping the human genetic architecture of COVID-19In: Nature Jg. 600 (2021) S. 472 - 477Online Volltext: dx.doi.org/ (Open Access)
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Shared genetic risk between eating disorder‐ and substance‐use‐related phenotypes : Evidence from genome‐wide association studiesIn: Addiction Biology Jg. 26 (2021) Nr. 1, e12880Online Volltext: dx.doi.org/; Online Volltext: dx.doi.org/ (Open Access)
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Size Matters: The CAG Repeat Length of the Androgen Receptor Gene, Testosterone, and Male Adolescent Depression SeverityIn: Frontiers in Psychiatry Jg. 12 (2021) 732759Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Suggestive Evidence for Causal Effect of Leptin Levels on Risk for Anorexia Nervosa : Results of a Mendelian Randomization StudyIn: Frontiers in Genetics Jg. 12 (2021) 733606Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Synaptic processes and immune-related pathways implicated in Tourette syndromeIn: Translational Psychiatry Jg. 11 (2021) Nr. 1, S. 56Online Volltext: dx.doi.org/ (Open Access)
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Effect of vitamin D deficiency on depressive symptoms in child and adolescent psychiatric patients : results of a randomized controlled trialIn: European Journal of Nutrition Jg. 59 (2020) Nr. 8, S. 3415 - 3424Online Volltext: dx.doi.org/ (Open Access)
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Genetic and epigenetic findings in anorexia nervosaIn: Medizinische Genetik Jg. 32 (2020) Nr. 1, S. 25 - 29Online Volltext: dx.doi.org/ (Open Access)
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No Effect of Thyroid Dysfunction and Autoimmunity on Health-Related Quality of Life and Mental Health in Children and Adolescents : Results From a Nationwide Cross-Sectional StudyIn: Frontiers in Endocrinology Jg. 11 (2020) 454Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Short-term metreleptin treatment of patients with anorexia nervosa : rapid on-set of beneficial cognitive, emotional, and behavioral effectsIn: Translational Psychiatry Jg. 10 (2020) Nr. 1, 303Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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The Role of Genetic Variation of BMI, Body Composition, and Fat Distribution for Mental Traits and Disorders : A Look-Up and Mendelian Randomization StudyIn: Frontiers in Genetics Jg. 11 (2020) 373Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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A trans-ancestral meta-analysis of genome-wide association studies reveals loci associated with childhood obesityIn: Human Molecular Genetics Jg. 28 (2019) Nr. 19, S. 3327 - 3338Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Assessing Causal links between metabolic traits, inflammation and Schizophrenia : a Univariable and Multivariable Bidirectional Mendelian Randomization StudyIn: European Neuropsychopharmacology Jg. 29 (2019) S. 211Online Volltext: dx.doi.org/
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Assessing causal links between metabolic traits, inflammation and schizophrenia : a univariable and multivariable, bidirectional Mendelian-randomization studyIn: International Journal of Epidemiology Jg. 48 (2019) Nr. 5, S. 1505 - 1514Online Volltext: dx.doi.org/ (Open Access)
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Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders : A Swedish Nationwide Population Study Using Multiple Genetically Informative ApproachesIn: Biological Psychiatry Jg. 86 (2019) Nr. 8, S. 577 - 586Online Volltext: dx.doi.org/ (Open Access)
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Gain-of-function variants in the melanocortin 4 receptor gene confer susceptibility to binge eating disorder in subjects with obesity : a systematic review and meta-analysisIn: Obesity Reviews Jg. 20 (2019) Nr. 1, S. 13 - 21Online Volltext: dx.doi.org/
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Genetic and gene expression analysis in CTBP2 : A gene derived from genome-wide data in anorexia nervosa and body weight regulationIn: European Neuropsychopharmacology Jg. 29 (2019) Nr. Supplement 4, S. 1138Online Volltext: dx.doi.org/
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Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosaIn: Nature Genetics Jg. 51 (2019) Nr. 8, S. 1207 - 1214Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms Across Eight Psychiatric DisordersIn: Cell Jg. 179 (2019) Nr. 7, S. 1469 - 1482.e11.Online Volltext: dx.doi.org/ (Open Access)
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Interrogating the genetic determinants of Tourette's syndrome and other tiC disorders through genome-wide association studiesIn: The American Journal of Psychiatry Jg. 176 (2019) Nr. 3, S. 217 - 227Online Volltext: dx.doi.org/ (Open Access)
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Melanocortin-4 Receptor and Lipocalin 2 Gene Variants in Spanish Children with Abdominal Obesity : Effects on BMI-SDS After a Lifestyle InterventionIn: Nutrients Jg. 11 (2019) Nr. 5, S. 960Online Volltext: dx.doi.org/ (Open Access)
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The involvement of the canonical Wnt-signaling receptor LRP5 and LRP6 gene variants with ADHD and sexual dimorphism : Association study and meta-analysisIn: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics Jg. 180 (2019) Nr. 6, S. 365 - 376Online Volltext: dx.doi.org/ (Open Access)
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Vitamin D and the Risk of Depression : A Causal Relationship? Findings from a Mendelian Randomization StudyIn: Nutrients Jg. 11 (2019) Nr. 5, S. 1085Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Correction: Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosaIn: Molecular Psychiatry Jg. 23 (2018) Nr. 9, S. 1Online Volltext: dx.doi.org/ (Open Access)
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Effect of an vitamin D deficiency on depressive symptoms in child and adolescent psychiatric patients - a randomized controlled trial : study protocolIn: BMC Psychiatry Jg. 18 (2018) Nr. 1, S. 57Online Volltext: dx.doi.org/ (Open Access)
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High-throughput DNA methylation analysis in anorexia nervosa confirms TNXB hypermethylationIn: The World Journal of Biological Psychiatry Jg. 19 (2018) Nr. 3, S. 187 - 199Online Volltext: dx.doi.org/; Online Volltext: dx.doi.org/ (Open Access)
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Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosaIn: Molecular Psychiatry Jg. 23 (2018) Nr. 5, S. 1169 - 1180Online Volltext: dx.doi.org/ (Open Access)
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Monogene Adipositas : Neue diagnostische und therapeutische MöglichkeitenIn: Monatsschrift Kinderheilkunde Jg. 166 (2018) Nr. 5, S. 388 - 394Online Volltext: dx.doi.org/
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Relevance of polymorphisms in MC4R and BDNF in short normal stature.In: BMC Pediatrics Jg. 18 (2018) S. 278Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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The Effect of SH2B1 Variants on Expression of Leptin- and Insulin-Induced Pathways in Murine HypothalamusIn: Obesity Facts Jg. 11 (2018) S. 93 - 108Online Volltext: dx.doi.org/ (Open Access)
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The association of Leptin and Food Addiction in Adolescent Psychiatric PatientsIn: Journal of Behavioral Addictions Jg. 7 (2018) Nr. Suppl. 1, S. 128 - 128
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The association of serum leptin levels with food addiction is moderated by weight status in adolescent psychiatric inpatientsIn: European Eating Disorders Review Jg. 26 (2018) Nr. 6, S. 618 - 628Online Volltext: dx.doi.org/
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The role of genetic variation of human metabolism for BMI, mental traits and mental disordersIn: Molecular Metabolism Jg. 12 (2018) S. 1 - 11Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Waist-hip ratio related genetic loci are associated with risk of impaired fasting glucose in Chinese children : A case control studyIn: Nutrition and Metabolism Jg. 15 (2018) S. 34Online Volltext: dx.doi.org/ (Open Access)
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A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signalingIn: Scientific Reports Jg. 7 (2017) Nr. 1,Online Volltext: dx.doi.org/ (Open Access)
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Anorexia nervosa and body mass index : combined GWAS and functional ex-vivo studiesIn: European Neuropsychopharmacology Jg. 27 (2017) Nr. Supplement 4, Abstracts of the 30th ECNP Congress, S. 525 - S525Online Volltext: dx.doi.org/
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Estimated prevalence of potentially damaging variants in the leptin gene.In: Molecular and Cellular Pediatrics Jg. 4 (2017) Nr. 1, S. 10Online Volltext: dx.doi.org/ (Open Access)
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Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass indexIn: Molecular Psychiatry Jg. 22 (2017) S. 192 - 201Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Exploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosaIn: Psychiatric Genetics Jg. 27 (2017) Nr. 4, S. 152 - 158Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Food addiction in gambling disorder: Frequency and clinical outcomesIn: Frontiers in Psychology Jg. 8 (2017) S. 473Online Volltext: dx.doi.org/ (Open Access)
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Genetische Ursachen der AdipositasIn: Der Gastroenterologe Jg. 12 (2017) Nr. 1, S. 60 - 65Online Volltext: dx.doi.org/
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Polygene Varianten und Epigenetik bei AdipositasIn: Medizinische Genetik Jg. 29 (2017) Nr. 4, S. 365 - 373Online Volltext: dx.doi.org/ (Open Access)
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Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood ObesityIn: Scientific Reports Jg. 7 (2017) Nr. 1, S. 4394Online Volltext: dx.doi.org/ (Open Access)
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Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia NervosaIn: The American Journal of Psychiatry Jg. 174 (2017) Nr. 9, S. 850 - 858Online Volltext: dx.doi.org/ (Open Access)
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Analysis of genes involved in body weight regulation by targeted re-sequencingIn: PLoS ONE Jg. 11 (2016) Nr. 2, S. e0147904Online Volltext: dx.doi.org/ (Open Access)
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Association of common variants identified by recent genome-wide association studies with obesity in Chinese children : A case-control studyIn: BMC Medical Genetics Jg. 17 (2016) S. 7Online Volltext: dx.doi.org/ (Open Access)
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Cover Image, Volume 171B, Number 6, September 2016In: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics Jg. 171 (2016) Nr. 6, S. IOnline Volltext: dx.doi.org/
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Decreased melanocortin-4 receptor function conferred by an infrequent variant at the human melanocortin receptor accessory protein 2 geneIn: Obesity Jg. 24 (2016) Nr. 9, S. 1976 - 1982Online Volltext: dx.doi.org/
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Interindividual Variation in DNA Methylation at a Putative POMC Metastable Epiallele Is Associated with ObesityIn: Cell Metabolism Jg. 24 (2016) Nr. 3, S. 502 - 509Online Volltext: dx.doi.org/ (Open Access)
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Pathway analysis in attention deficit hyperactivity disorder : An ensemble approachIn: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics Jg. 171 (2016) Nr. 6, S. 815 - 826Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Case–Control Genome-Wide Association Study of Persistent Attention-Deficit Hyperactivity Disorder Identifies FBXO33 as a Novel Susceptibility Gene for the DisorderIn: Neuropsychopharmacology Jg. 40 (2015) Nr. 4, S. 915 - 926Online Volltext: dx.doi.org/
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Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity : a systematic review and meta-analysis with evidence from up to 331 175 individualsIn: Human Molecular Genetics Jg. 24 (2015) Nr. 12, S. 3582 - 3594Online Volltext: dx.doi.org/ (Open Access)
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Fine mapping of a GWAS-derived obesity candidate region on chromosome 16p11.2In: PLoS ONE Jg. 10 (2015) Nr. 5, S. e0125660Online Volltext: dx.doi.org/ (Open Access)
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Genetik und Epigenetik der AdipositasIn: Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz Jg. 58 (2015) Nr. 2, S. 154 - 158Online Volltext: dx.doi.org/
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Indications for potential parent-of-origin effects within the FTO geneIn: PLoS ONE Jg. 10 (2015) Nr. 3, S. e0119206Online Volltext: dx.doi.org/ (Open Access)
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Perspektiven der genetischen Forschung bei Essstörungen am Beispiel der Anorexia nervosaIn: Psychotherapie, Psychosomatik, Medizinische Psychologie (PPmP) Jg. 65 (2015) Nr. 1, S. 8 - 10Online Volltext: dx.doi.org/
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A genome-wide association study of anorexia nervosaIn: Molecular Psychiatry Jg. 19 (2014) Nr. 10, S. 1085 - 1094Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Catechol-O-Methyltransferase Val158Met Polymorphism Is Associated with Somatosensory Amplification and Nocebo ResponsesIn: PLoS ONE Jg. 9 (2014) Nr. 9, S. 0107665Online Volltext: dx.doi.org/ (Open Access)
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FTO Gene : Association to Weight Regain after Lifestyle Intervention in Overweight ChildrenIn: Hormone Research in Paediatrics Jg. 81 (2014) Nr. 6, S. 391 - 396Online Volltext: dx.doi.org/
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Genes and the hypothalamic control of metabolism in humansIn: Best Practice and Research Clinical Endocrinology and Metabolism Jg. 28 (2014) Nr. 5, S. 635 - 647Online Volltext: dx.doi.org/
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Genetic variation at the CELF1 (CUGBP, elav-like family member 1 gene) locus is genome-wide associated with Alzheimer's disease and obesityIn: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics Jg. 165 (2014) Nr. 4, S. 283 - 293Online Volltext: dx.doi.org/
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Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorderIn: Molecular Psychiatry Jg. 19 (2014) Nr. 1, S. 115 - 121Online Volltext: dx.doi.org/ (Open Access)
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Mitochondrial DNA Variants in ObesityIn: PLoS ONE Jg. 9 (2014) Nr. 5, S. e94882Online Volltext: dx.doi.org/ (Open Access)
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The Origin of the Obesity Associated Pomc DNA Hypermethylation VariantIn: Endocrine Reviews Jg. 35 (2014) Nr. Suppl. 3,
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A novel SP1/SP3 dependent intronic enhancer governing transcription of the UCP3 gene in brown adipocytesIn: PLoS ONE Jg. 8 (2013) Nr. 12, S. e83426Online Volltext: dx.doi.org/ (Open Access)
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Analyses of Non-Synonymous Obesity Risk Alleles in SH2B1 (rs7498665) and APOB48R (rs180743) in Obese Children and Adolescents Undergoing a 1-year Lifestyle InterventionIn: Experimental and Clinical Endocrinology & Diabetes Jg. 121 (2013) Nr. 6, S. 334 - 337Online Volltext: dx.doi.org/
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Association analyses for dopamine receptor gene polymorphisms and weight status in a longitudinal analysis in obese children before and after lifestyle interventionIn: BMC Pediatrics Jg. 13 (2013) Nr. 1,Online Volltext: dx.doi.org/ (Open Access)
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Bipolar disorder risk alleles in children with ADHDIn: Journal of Neural Transmission Jg. 120 (2013) Nr. 11, S. 1611 - 1617Online Volltext: dx.doi.org/
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Common obesity risk alleles in childhood attention-deficit/hyperactivity disorderIn: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics Jg. 162 (2013) Nr. 4, S. 295 - 305Online Volltext: dx.doi.org/
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Gene Set of Nuclear-Encoded Mitochondrial Regulators Is Enriched for Common Inherited Variation in ObesityIn: PLoS ONE Jg. 8 (2013) Nr. 2, S. e55884Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Genetics of Eating DisordersIn: Current Psychiatry Reports Jg. 15 (2013) Nr. 12, S. 423Online Volltext: dx.doi.org/
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Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architectureIn: Nature Genetics Jg. 45 (2013) Nr. 5, S. 501 - 512Online Volltext: dx.doi.org/
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Meta-analysis of genome-wide association studies on ADHD : A dimensional approachIn: Behavior Genetics Jg. 43 (2013) Nr. 6, S. 520 - 521
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Molecular Genetic Aspects of Weight RegulationIn: Deutsches Ärzteblatt international Jg. 110 (2013) Nr. 19, S. 338 - 344Online Volltext: dx.doi.org/
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No impact of obesity susceptibility loci on weight regain after a lifestyle intervention in overweight childrenIn: Journal of Pediatric Endocrinology and Metabolism (JPEM) Jg. 26 (2013) Nr. 11-12, S. 1209 - 1213Online Volltext: dx.doi.org/
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Successful treatment with atomoxetine of an adolescent boy with attention deficit/hyperactivity disorder, extreme obesity, and reduced melanocortin 4 receptor functionIn: Obesity Facts Jg. 6 (2013) Nr. 1, S. 109 - 115Online Volltext: dx.doi.org/
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A genome-wide association meta-analysis identifies new childhood obesity lociIn: Nature Genetics Jg. 44 (2012) Nr. 5, S. 526 - 531Online Volltext: dx.doi.org/
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Addendum: Genome-wide association study in German patients with attention deficit/hyperactivity disorderIn: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics Jg. 159B (2012) Nr. 4, S. 476Online Volltext: dx.doi.org/
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Changes of peripheral alpha LPHA-Melanocortin stimulating hormone (alpha-MSH) in childhood craniopharyngioma patients in comparison with other forms of childhood obesityIn: Neuro-Oncology Jg. 14 (2012) Nr. Suppl. 1, S. 23
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Common variants at 12q15 and 12q24 are associated with infant head circumferenceIn: Nature Genetics Jg. 44 (2012) Nr. 5, S. 532 - 538Online Volltext: dx.doi.org/
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Common variants at 6q22 and 17q21 are associated with intracranial volumeIn: Nature Genetics Jg. 44 (2012) Nr. 5, S. 539 - 544Online Volltext: dx.doi.org/
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Comparison of metabolic profiles of acutely ill and short-term weight recovered patients with anorexia nervosa reveals alterations of 33 out of 163 metabolitesIn: Journal of Psychiatric Research Jg. 46 (2012) Nr. 12, S. 1600 - 1609Online Volltext: dx.doi.org/
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DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorderIn: PLoS ONE Jg. 7 (2012) Nr. 4, Art. Nr. e35424Online Volltext: dx.doi.org/ (Open Access)
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Do Common Variants Separate between Obese Melanocortin-4 Receptor Gene Mutation Carriers and Non-Carriers? : The Impact of Cryptic RelatednessIn: Hormone Research in Paediatrics Jg. 77 (2012) Nr. 6, S. 358 - 368Online Volltext: dx.doi.org/
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Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and humanIn: Nature Jg. 483 (2012) Nr. 7389, S. 350 - 354Online Volltext: dx.doi.org/
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Erratum to: Impact of FTO genotypes on BMI and weight in polycystic ovary syndrome : a systematic review and meta-analysisIn: Diabetologia Jg. 55 (2012) Nr. 10, S. 2858 - 2859Online Volltext: dx.doi.org/
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Evaluating The Role Of Reference Models In Copy Number Variation AnalysesIn: Genetic Epidemiology Jg. 36 (2012) Nr. 2, S. 133
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Fat mass and obesity-associated gene (FTO) in eating disorders : Evidence for association of the rs9939609 obesity risk allele with Bulimia nervosa and anorexia nervosaIn: Obesity Facts Jg. 5 (2012) Nr. 3, S. 408 - 419Online Volltext: dx.doi.org/
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Impact of FTO Genotypes on Weight and Body Mass Index in Polycystic Ovary Syndrome : A Systematic Review and Meta-AnalysisIn: Diabetes Jg. 61 (2012) Nr. Suppl. 1, S. A507 - A507
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Impact of FTO genotypes on BMI and weight in polycystic ovary syndrome : A systematic review and meta-analysisIn: Diabetologia Jg. 55 (2012) Nr. 10, S. 2636 - 2645Online Volltext: dx.doi.org/ (Open Access)
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Mutation screen in the GWAS derived obesity gene SH2B1 including functional analyses of detected variantsIn: BMC Medical Genomics Jg. 5 (2012) S. 65Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Rescue of melanocortin 4 receptor (MC4R) nonsense mutations by aminoglycoside-mediated read-throughIn: Obesity Jg. 20 (2012) Nr. 5, S. 1074 - 1081Online Volltext: dx.doi.org/
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SDCCAG8 obesity alleles and reduced weight loss after a lifestyle intervention in overweight children and adolescentsIn: Obesity Jg. 20 (2012) Nr. 2, S. 466 - 470Online Volltext: dx.doi.org/
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The fatty acid amide hydrolase (FAAH) gene variant rs324420 AA/AC is not associated with weight loss in a 1-year lifestyle intervention for obese children and adolescentsIn: Hormone and Metabolic Research Jg. 44 (2012) Nr. 1, S. 75 - 77Online Volltext: dx.doi.org/
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Association of the rs10830963 Polymorphism in MTNR1B with Fasting Glucose Levels in Chinese Children and AdolescentsIn: Obesity Facts Jg. 4 (2011) Nr. 3, S. 197 - 203Online Volltext: dx.doi.org/
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Association study in eating disorders : TPH2 associates with anorexia nervosa and self-induced vomitingIn: Genes, Brain and Behavior Jg. 10 (2011) Nr. 2, S. 236 - 243Online Volltext: dx.doi.org/
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Common Variants Near MC4R : Exploring Gender Effects in Overweight and Obese Children and Adolescents Participating in a Lifestyle InterventionIn: Obesity Facts Jg. 4 (2011) Nr. 1, S. 67 - 75Online Volltext: dx.doi.org/
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Evaluation of the obesity genes FTO and MC4R and the type 2 diabetes mellitus gene TCF7L2 for contribution to stroke risk : The Mannheim-Heidelberg Stroke StudyIn: Obesity Facts Jg. 4 (2011) Nr. 4, S. 290 - 296Online Volltext: dx.doi.org/
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Genetic association and gene expression analysis identify FGFR1 as a new susceptibility gene for human obesityIn: The Journal of Clinical Endocrinology & Metabolism (JCEM) Jg. 96 (2011) Nr. 6, S. E962 - 6Online Volltext: dx.doi.org/ (Open Access)
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Genetic variation of the ghrelin activator gene ghrelin O-acyltransferase (GOAT) is associated with anorexia nervosa.In: Journal of Psychiatric Research Jg. 45 (2011) Nr. 5, S. 706 - 711Online Volltext: dx.doi.org/
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Genome-wide association study in German patients with attention deficit/hyperactivity disorderIn: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics Jg. 156B (2011) Nr. 8, S. 888 - 897Online Volltext: dx.doi.org/
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Lack of association of cd36 snps with early onset obesity : A meta-analysis in 9,973 european subjectsIn: Obesity Jg. 19 (2011) Nr. 4, S. 833 - 839Online Volltext: dx.doi.org/
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Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysisIn: Human Molecular Genetics Jg. 20 (2011) Nr. 4, S. 840 - 852Online Volltext: dx.doi.org/
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Relationship between MTNR1B (melatonin receptor 1B gene) polymorphism rs10830963 and glucose levels in overweight children and adolescentsIn: Pediatric Diabetes Jg. 12 (2011) Nr. 4 Part 2, S. 435 - 441Online Volltext: dx.doi.org/
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Successful methylphenidate treatment of early onset extreme obesity in a child with a melanocortin-4 receptor gene mutation and attention deficit/hyperactivity disorderIn: European Journal of Pharmacology Jg. 660 (2011) Nr. 1, S. 165 - 170Online Volltext: dx.doi.org/
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Where in the Genome Are Significant Single Nucleotide Polymorphisms from Genome-Wide Association Studies Located?In: OMICS: A Journal of Integrative Biology Jg. 15 (2011) Nr. 7/8, S. 507 - 512Online Volltext: dx.doi.org/
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Association analyses of 249,796 individuals reveal 18 new loci associated with body mass indexIn: Nature Genetics Jg. 42 (2010) Nr. 11, S. 937 - 948Online Volltext: dx.doi.org/ (Open Access)
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Association analyses of 249,796 individuals reveal 18 new loci associated with body mass indexIn: Nature Genetics Jg. 42 (2010) Nr. 11, S. 937 - 948Online Volltext: dx.doi.org/
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Association of the MC4R V103I polymorphism with obesity : A chinese case-control study and meta-analysis in 55,195 individualsIn: Obesity Jg. 18 (2010) Nr. 3, S. 573 - 579Online Volltext: dx.doi.org/ (Open Access)
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Association of variants in gastric inhibitory polypeptide receptor gene with impaired glucose homeostasis in obese children and adolescents from BerlinIn: European Journal of Endocrinology (EJE) Jg. 163 (2010) Nr. 2, S. 259 - 264Online Volltext: dx.doi.org/
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Changes of peripheral alpha-melanocyte-stimulating hormone in childhood obesityIn: Metabolism Jg. 59 (2010) Nr. 2, S. 186 - 194Online Volltext: dx.doi.org/
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Child and adolescent psychiatric geneticsIn: European Child & Adolescent Psychiatry Jg. 19 (2010) Nr. 3, S. 259 - 279Online Volltext: dx.doi.org/
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Chipping away the 'missing heritability': GIANT steps forward in the molecular elucidation of obesity - But still lots to goIn: Obesity Facts Jg. 3 (2010) Nr. 5, S. 294 - 303Online Volltext: dx.doi.org/ (Open Access)
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Eating disorders: the current status of molecular genetic researchIn: European Child & Adolescent Psychiatry Jg. 19 (2010) Nr. 3, S. 211 - 226Online Volltext: dx.doi.org/ (Open Access)
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Estrogen receptor 1 gene (ESR1) is associated with restrictive anorexia nervosaIn: Neuropsychopharmacology Jg. 35 (2010) Nr. 8, S. 1818 - 1825Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Familiality and molecular genetics of attention networks in ADHDIn: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics Jg. 153B (2010) Nr. 1, S. 148 - 158Online Volltext: dx.doi.org/
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From monogenic to polygenic obesity : Recent advancesIn: European Child & Adolescent Psychiatry Jg. 19 (2010) Nr. 3, S. 297 - 310Online Volltext: dx.doi.org/ (Open Access)
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Genes and lifestyle factors in obesity : Results from 12 462 subjects from MONICA/KORAIn: International Journal of Obesity Jg. 34 (2010) Nr. 10, S. 1538 - 1545Online Volltext: dx.doi.org/ (Open Access)
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Genetic findings in anorexia and bulimia nervosaIn: Progress in Molecular Biology and Translational Science Jg. 94 (2010) S. 241 - 270Online Volltext: dx.doi.org/
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Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery diseaseIn: Atherosclerosis Jg. 208 (2010) Nr. 1, S. 183 - 189Online Volltext: dx.doi.org/
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Genetische Ursachen der Adipositas : Zum Stand der ForschungIn: Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz Jg. 53 (2010) Nr. 7, S. 674 - 680Online Volltext: dx.doi.org/
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Investigation of a Genome Wide Association Signal for Obesity : Synthetic Association and Haplotype Analyses at the Melanocortin 4 Receptor Gene LocusIn: PLoS ONE Jg. 5 (2010) Nr. 11, S. e13967Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Large effects on body mass index and insulin resistance of fat mass and obesity associated gene (FTO) variants in patients with polycystic ovary syndrome (PCOS)In: BMC Medical Genetics Jg. 11 (2010) 12Online Volltext: dx.doi.org/ (Open Access)
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Mutation screen and association studies for the fatty acid amide hydrolase (FAAH) gene and early onset and adult obesityIn: BMC Medical Genetics Jg. 11 (2010) S. 2Online Volltext: dx.doi.org/ (Open Access)
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Role of the neurotrophin network in eating disorders' subphenotypes : Body mass index and age at onset of the diseaseIn: Journal of Psychiatric Research Jg. 44 (2010) Nr. 13, S. 834 - 840Online Volltext: dx.doi.org/
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Sympathetic function in human carriers of melanocortin-4 receptor gene mutationsIn: The Journal of Clinical Endocrinology & Metabolism (JCEM) Jg. 95 (2010) Nr. 4, S. 1998 - 2002Online Volltext: dx.doi.org/
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Two New Loci for Body-Weight Regulation Identified in a Joint Analysis of Genome-Wide Association Studies for Early-Onset Extreme Obesity in French and German Study GroupsIn: PLoS Genetics Jg. 6 (2010) Nr. 4,Online Volltext: dx.doi.org/ (Open Access)
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A consultation with genetic information about obesity decreases self-blame about eating and leads to realistic weight loss goals in obese individualsIn: Journal of Psychosomatic Research Jg. 66 (2009) Nr. 4, S. 287 - 295Online Volltext: dx.doi.org/
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Adipositas/ÜbergewichtIn: Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie Jg. 37 (2009) Nr. 4, S. 237 - 244Online Volltext: dx.doi.org/
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Aggravating effect of INSIG2 and FTO on overweight reduction in a one-year lifestyle interventionIn: Archives of Disease in Childhood Jg. 94 (2009) Nr. 12, S. 965 - 967Online Volltext: dx.doi.org/
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Association between the insulin-induced gene 2 (INSIG2) and weight gain in a German sample of antipsychotic-treated schizophrenic patients : Perturbation of SREBP-controlled lipogenesis in drug-related metabolic adverse effects?In: Molecular Psychiatry Jg. 14 (2009) Nr. 3, S. 308 - 317Online Volltext: dx.doi.org/ (Open Access)
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Association studies on ghrelin and ghrelin receptor gene polymorphisms with obesityIn: Obesity Jg. 17 (2009) Nr. 4, S. 745 - 754Online Volltext: dx.doi.org/ (Open Access)
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Causal attributions of obese men and women in genetic testing: Implications of genetic/biological attributionsIn: Psychology & Health Jg. 24 (2009) Nr. 7, S. 749 - 761Online Volltext: dx.doi.org/
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Exploring the genetic link between RLS and ADHDIn: Journal of Psychiatric Research Jg. 43 (2009) Nr. 10, S. 941 - 945Online Volltext: dx.doi.org/
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Functional variants of the serotonin receptor type 3A and B gene are associated with eating disordersIn: Pharmacogenetics and Genomics Jg. 19 (2009) Nr. 10, S. 790 - 799Online Volltext: dx.doi.org/
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Gastric inhibitory polypeptide receptor : Association analyses for obesity of several polymorphisms in large study groupsIn: BMC Medical Genetics Jg. 10 (2009)Online Volltext: dx.doi.org/ (Open Access)
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Increased constraints on MC4R during primate and human evolutionIn: Human Genetics Jg. 124 (2009) Nr. 6, S. 633 - 647Online Volltext: dx.doi.org/
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Lifestyle intervention in obese children with variations in the melanocortin 4 receptor geneIn: Obesity Jg. 17 (2009) Nr. 2, S. 382 - 389Online Volltext: dx.doi.org/
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Meta-analysis of the INSIG2 association with obesity including 74,345 individuals : Does heterogeneity of estimates relate to study design?In: PLoS Genetics Jg. 5 (2009) Nr. 10, S. e1000694Online Volltext: dx.doi.org/ (Open Access)
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Non-replication of an association of CTNNBL1 polymorphisms and obesity in a population of Central European ancestryIn: BMC Medical Genetics Jg. 10 (2009)Online Volltext: dx.doi.org/ (Open Access)
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Procolipase gene : no association with early-onset obesity or fat intakeIn: Obesity Facts Jg. 2 (2009) Nr. 1, S. 40 - 44Online Volltext: dx.doi.org/ (Open Access)
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Serotonin transporter gene polymorphism (5-HTTLPR), environmental conditions, and developing negative emotionality and fear in early childhoodIn: Journal of Neural Transmission Jg. 116 (2009) Nr. 4, S. 503 - 512Online Volltext: dx.doi.org/
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'Fat mass and obesity associated' gene (FTO): No significant association of variant rs9939609 with weight loss in a lifestyle intervention and lipid metabolism markers in German obese children and adolescentsIn: BMC Medical Genetics Jg. 9 (2008) S. 85Online Volltext: dx.doi.org/ (Open Access)
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Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disordersIn: Human Molecular Genetics Jg. 17 (2008) Nr. 9, S. 1234 - 1244Online Volltext: dx.doi.org/ (Open Access)
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Association of the MC4R V103I polymorphism with the metabolic syndrome: The KORA studyIn: Obesity Jg. 16 (2008) Nr. 2, S. 369 - 376Online Volltext: dx.doi.org/
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Common variants near MC4R are associated with fat mass, weight and risk of obesityIn: Nature Genetics Jg. 40 (2008) Nr. 6, S. 768 - 775Online Volltext: dx.doi.org/
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Evidence for an influence of TCF7L2 polymorphism rs7903146 on insulin resistance and sensitivity indices in overweight children and adolescents during a lifestyle interventionIn: International Journal of Obesity Jg. 32 (2008) Nr. 10, S. 1521 - 1524Online Volltext: dx.doi.org/ (Open Access)
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Evidence of an influence of a polymorphism near the INSIG2 on weight loss during a lifestyle intervention in obese children and adolescentsIn: Diabetes Jg. 57 (2008) Nr. 3, S. 623 - 626Online Volltext: dx.doi.org/ (Open Access)
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Lack of association of genetic variants in genes of the endocannabinoid system with anorexia nervosaIn: Child and Adolescent Psychiatry and Mental Health Jg. 2 (2008)Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Meta-analysis of Genome-Wide Linkage Scans of Attention Deficit Hyperactivity DisorderIn: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics Jg. 147B (2008) Nr. 8, S. 1392 - 1398Online Volltext: dx.doi.org/ Online Volltext
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Preferential reciprocal transfer of paternal/maternal DLK1 alleles to obese children : First evidence of polar overdominance in humansIn: European Journal of Human Genetics Jg. 16 (2008) Nr. 9, S. 1126 - 1134Online Volltext: dx.doi.org/ (Open Access)
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Transmission disequilibrium studies in early onset of obsessive-compulsive disorder for polymorphisms in genes of the dopaminergic systemIn: Journal of Neural Transmission Jg. 115 (2008) Nr. 7, S. 1071 - 1078Online Volltext: dx.doi.org/
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Val103Ile polymorphism of the melanocortin-4 receptor gene (MC4R) in cancer cachexiaIn: BMC Cancer Jg. 8 (2008) 85Online Volltext: dx.doi.org/ (Open Access)
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A novel mutation Thr162Arg of the melanocortin 4 receptor gene in a Spanish children and adolescent populationIn: Clinical Endocrinology Jg. 66 (2007) Nr. 5, S. 652 - 658Online Volltext: dx.doi.org/ Online Volltext (Open Access)
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Analysis of sequence variations in the suppressor of cytokine signaling (SOCS)-3 gene in extremely obese children and adolescentsIn: BMC Medical Genetics Jg. 8 (2007)Online Volltext: dx.doi.org/ (Open Access)
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Association and linkage of allelic variants of the dopamine transporter gene in ADHDIn: Molecular Psychiatry Jg. 12 (2007) Nr. 10, S. 923 - 933Online Volltext: dx.doi.org/ (Open Access)
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Definable Somatic Disorders in Overweight Children and AdolescentsIn: Journal of Pediatrics Jg. 150 (2007) Nr. 6, S. 618 - 622.e5Online Volltext: dx.doi.org/
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Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sampleIn: Journal of Neural Transmission Jg. 114 (2007) Nr. 4, S. 513 - 521Online Volltext: dx.doi.org/
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Genome Wide Association (GWA) study for early onset extreme obesity supports the role of fat mass and obesity associated gene (FTO) variantsIn: PLoS ONE Jg. 2 (2007) Nr. 12,Online Volltext: dx.doi.org/ (Open Access)
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Is information on genetic determinants of obesity helpful or harmful for obese people? : A randomized clinical trialIn: Journal of General Internal Medicine (JGIM) Jg. 22 (2007) Nr. 11, S. 1553 - 1559Online Volltext: dx.doi.org/
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Mutation screen and association studies in the Diacylglycerol O-acyltransferase homolog 2 gene (DGAT2), a positional candidate gene for early onset obesity on chromosome 11q13In: BMC Genetics Jg. 8 (2007)Online Volltext: dx.doi.org/ (Open Access)
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No association of sequence variants in the neuropeptide Y2 receptor (NPY2R) gene with early onset obesity in GermansIn: Hormone and Metabolic Research Jg. 39 (2007) Nr. 11, S. 840 - 844Online Volltext: dx.doi.org/
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No evidence for an involvement of variants in the cannabinoid receptor gene (CNR1) in obesity in German children and adolescentsIn: Molecular Genetics and Metabolism Jg. 90 (2007) Nr. 4, S. 429 - 434Online Volltext: dx.doi.org/
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No evidence for preferential transmission of common valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor gene (BDNF) in ADHDIn: Journal of Neural Transmission Jg. 114 (2007) Nr. 4, S. 523 - 526Online Volltext: dx.doi.org/
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Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolutionIn: Nature Genetics Jg. 39 (2007) Nr. 2, S. 218 - 225Online Volltext: dx.doi.org/
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Response to Comments on "A Common Genetic Variant Is Associated with Adult and Childhood Obesity"In: Science Jg. 315 (2007) Nr. 5809, S. 187eOnline Volltext: dx.doi.org/
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Restoration of signalling capabilities in total loss of function MC4R mutationsIn: Experimental and Clinical Endocrinology & Diabetes Jg. 115 (2007) Nr. S 1, P02_065Online Volltext: dx.doi.org/
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The V103I polymorphism of the MC4R gene and obesity: Population based studies and meta-analysis of 29 563 individualsIn: International Journal of Obesity Jg. 31 (2007) Nr. 9, S. 1437 - 1441Online Volltext: dx.doi.org/ (Open Access)
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The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohortsIn: PLoS Genetics Jg. 3 (2007) Nr. 4, S. 0627 - 0633Online Volltext: dx.doi.org/ (Open Access)
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A common genetic variant is associated with adult and childhood obesityIn: Science Jg. 312 (2006) Nr. 5771, S. 279 - 283Online Volltext: dx.doi.org/
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A genome-wide scan for attention-deficit/hyperactivity disorder in 155 German sib-pairsIn: Molecular Psychiatry Jg. 11 (2006) Nr. 2, S. 196 - 205Online Volltext: dx.doi.org/ (Open Access)
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A role for β-melanocyte-stimulating hormone in human body-weight regulationIn: Cell Metabolism Jg. 3 (2006) Nr. 2, S. 141 - 146Online Volltext: dx.doi.org/ (Open Access)
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Association of the melanocortin 4 receptor with feed intake and daily gain in F2 Mangalitsa x Piétrain pigsIn: Animal Genetics Jg. 37 (2006) Nr. 3, S. 245 - 247Online Volltext: dx.doi.org/
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Case-control and combined family trios analysis of three polymorphisms in the ghrelin gene in European patients with anorexia and bulimia nervosaIn: Psychiatric Genetics Jg. 16 (2006) Nr. 2, S. 51 - 52Online Volltext: dx.doi.org/
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Evidence for involvement of the vitamin D receptor gene in idiopathic short stature via a genome-wide linkage study and subsequent association studiesIn: Human Molecular Genetics Jg. 15 (2006) Nr. 18, S. 2772 - 2783Online Volltext: dx.doi.org/
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Genetische Aspekte in der Adipositas-Beratung – Auswirkungen auf Körperakzeptanz und subjektives WohlbefindenIn: Verhaltenstherapie: Praxis, Forschung, Perspektiven Jg. 16 (2006) Nr. 3, S. 193 - 200Online Volltext: dx.doi.org/
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Genetische Befunde bei der Aufmerksamkeitsdefizit- und Hyperaktivitätsstörung (ADHS)In: Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie Jg. 34 (2006) Nr. 6, S. 425 - 433Online Volltext: dx.doi.org/
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Meta-analysis on the effect of the N363S polymorphism of the glucocorticoid receptor gene (GRL) on human obesityIn: BMC Medical Genetics Jg. 7 (2006)Online Volltext: dx.doi.org/ (Open Access)
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Prevalence, spectrum, and functional characterization of melanocortin-4 receptor gene mutations in a representative population-based sample and obese adults from GermanyIn: The Journal of Clinical Endocrinology & Metabolism (JCEM) Jg. 91 (2006) Nr. 5, S. 1761 - 1769Online Volltext: dx.doi.org/ (Open Access)
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Rapid communication : The 103I variant of the melanocortin 4 receptor is associated with low serum triglyceride levelsIn: The Journal of Clinical Endocrinology & Metabolism (JCEM) Jg. 91 (2006) Nr. 2, S. 535 - 538Online Volltext: dx.doi.org/
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Several mutations in the melanocortin 4 receptor gene are associated with obesity in Chinese children and adolescentsIn: Journal of Endocrinological Investigation Jg. 29 (2006) Nr. 10, S. 894 - 898Online Volltext: dx.doi.org/
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Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in children and adolescents with obsessive-compulsive disorderIn: The International Journal of Neuropsychopharmacology Jg. 9 (2006) Nr. 4, S. 437 - 442Online Volltext: dx.doi.org/ (Open Access)
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Association of BDNF with restricting anorexia nervosa and minimum body mass index : A family-based association study of eight European populationsIn: European Journal of Human Genetics Jg. 13 (2005) Nr. 4, S. 428 - 434Online Volltext: dx.doi.org/ (Open Access)
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Association of the 103I MC4R allele with decreased body mass in 7937 participants of two population based surveysIn: Journal of medical genetics Jg. 42 (2005) Nr. 4, S. e21Online Volltext: dx.doi.org/ (Open Access)
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Brain-derived neurotrophic factor V66M polymorphism in childhood-onset obsessive-compulsive disorderIn: The International Journal of Neuropsychopharmacology Jg. 8 (2005) Nr. 1, S. 133 - 136Online Volltext: dx.doi.org/ (Open Access)
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Human galanin (GAL) and galanin 1 receptor (GALR1) variations are not involved in fat intake and early onset obesityIn: Journal of Nutrition Jg. 135 (2005) Nr. 6, S. 1387 - 1392Online Volltext: dx.doi.org/ (Open Access)
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Lack of support for the association between GAD2 polymorphisms and severe human obesityIn: PLoS Biology Jg. 3 (2005) Nr. 9, e315Online Volltext: dx.doi.org/ (Open Access)
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Mutation analysis of the MCHR1 gene in human obesityIn: European Journal of Endocrinology Jg. 152 (2005) Nr. 6, S. 851 - 862Online Volltext: dx.doi.org/ (Open Access)
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Mutation screen of the brain derived neurotrophic factor gene (BDNF) : Identification of several genetic variants and association studies in patients with obesity, eating disorders, and attention-deficit/hyperactivity disorderIn: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics Jg. 132B (2005) Nr. 1, S. 96 - 99Online Volltext: dx.doi.org/
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Prävalenz von Melanocortin-4-Rezeptor(MC4R)-Mutationen und Polymorphismen bei adipösen Kindern und Jugendlichen in einer konsekutiven pädiatrischen InanspruchnahmepopulationIn: Klinische Pädiatrie Jg. 217 (2005) Nr. 4, S. 244 - 249Online Volltext: dx.doi.org/
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Adipositas : Genetik und Gen-Umwelt-InteraktionenIn: Monatsschrift Kinderheilkunde Jg. 152 (2004) Nr. 8, S. 870 - 878Online Volltext: dx.doi.org/
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Association of BDNF with anorexia, bulimia and age of onset of weight loss in six European populationsIn: Human Molecular Genetics Jg. 13 (2004) Nr. 12, S. 1205 - 1212Online Volltext: dx.doi.org/ (Open Access)
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Binge-eating episodes are not characteristic of carriers of melanocortin-4 receptor gene mutationsIn: Molecular Psychiatry Jg. 9 (2004) Nr. 8, S. 796 - 800Online Volltext: dx.doi.org/ (Open Access)
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Combined Family Trio and Case-Control Analysis of the COMT Val158Met Polymorphism in European Patients with Anorexia NervosaIn: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics Jg. 124 B (2004) Nr. 1, S. 68 - 72Online Volltext: dx.doi.org/
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Genetic risk factors in eating disordersIn: American Journal of PharmacoGenomics Jg. 4 (2004) Nr. 4, S. 209 - 223Online Volltext: dx.doi.org/
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Ghrelin Receptor Gene : Identification of Several Sequence Variants in Extremely Obese Children and Adolescents, Healthy Normal-Weight and Underweight Students, and Children with Short Normal StatureIn: The Journal of Clinical Endocrinology & Metabolism (JCEM) Jg. 89 (2004) Nr. 1, S. 157 - 162Online Volltext: dx.doi.org/ (Open Access)
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Melanocortin-4 Receptor Gene Variant I103 Is Negatively Associated with ObesityIn: American Journal of Human Genetics Jg. 74 (2004) Nr. 3, S. 572 - 581Online Volltext: dx.doi.org/ (Open Access)
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Variants in the human β₁-, β₂- and β ₃-adrenergic receptor genes are not associated with morbid obesity in children and adolescentsIn: Diabetes, Obesity and Metabolism Jg. 6 (2004) Nr. 6, S. 452 - 455Online Volltext: dx.doi.org/
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Genetik in der Kinder- und JugendpsychiatrieIn: Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie Jg. 50 (2022) Nr. 3, S. 171 - 173Online Volltext: dx.doi.org/
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No Relationship Between Thyroid Function and ADHD : Results From a Nationwide Prospective Epidemiological Study and Mendelian RandomizationIn: Hormone Research in Paediatrics Jg. 96 (2023) Nr. Suppl. 4, S. 121 - 122
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Causal Effect of Age at Menarche on the Risk for Depression: Results from a Two-Sample Multivariable Mendelian Randomization StudyIn: Hormone Research in Paediatrics Jg. 95 (2022) Nr. Suppl. 2, S. 346 - 346
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Size Matters: CAG Repeat Length of the Androgen Receptor Gene, Testosterone, and Male Adolescent Depression SeverityIn: Hormone Research in Paediatrics Jg. 94 (2021) Nr. Suppl. 1, S. 364
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The complexity of eating disorders : insight into recent research venues in molecular genetics, neuropsychology, neuroimaging, and social sciences
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Addressing Genomic Imprinting in a Family-based Genome-wide Association Study
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Changes of Peripheral Alpha-Melanocyte-Stimulating Hormone in Childhood Craniopharyngioma
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Consultation including Genetic information in People with increades risk for Obesity and MC4R-Mutations
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Genetics of obesityIn: European Neuropsychopharmacology Jg. 20 (2010) Nr. Suppl. 3, S. S190Online Volltext: dx.doi.org/
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Bias-Corrected Effect Estimators for Genome-Wide Association StudiesIn: Genetic Epidemiology Jg. 32 (2008) Nr. 7, S. 676Online Volltext: dx.doi.org/
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Linkage genome scan and subsequent association studies show involvement of the vitamin D receptor gene in idiopathic short statureIn: Genetic Epidemiology Jg. 31 (2007) Nr. 5, S. 450 - 513Online Volltext: dx.doi.org/
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The MC4R 1031 allele is associated with features of the metabolic syndrome in the population-based KORA studyIn: Genetic Epidemiology Jg. 31 (2007) Nr. 5, S. 475Online Volltext: dx.doi.org/
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A novel missense mutation in the melanocortin-4 receptor gene (MC4R) in an Austrian 2-year-old girl with extreme obesity and an asymmetry of the amygdaloid nucleiIn: International Journal of Obesity Jg. 29 (2005) Nr. S2, S. S155Online Volltext: dx.doi.org/
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Genetic aspects of obesityIn: Handbook of Eating Disorders and Obesity / Herpertz, Stephan; de Zwaan, Martina; Zipfel, Stephan (Hrsg.) 2024, S. 445 - 450Online Volltext: dx.doi.org/
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Genetics of eating and weight disordersIn: Eating Disorders and Obesity in Children and Adolescents / Hebebrand, Johannes; Herpertz-Dahlmann, Beate (Hrsg.) 2018, S. 67 - 71Online Volltext: dx.doi.org/
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Polygenic obesityIn: Pediatric Obesity: Etiology, Pathogenesis and Treatment / Freemark, Michael S. (Hrsg.) 2018, S. 183 - 202Online Volltext: dx.doi.org/
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Melanocortin-4 Receptor in Energy Homeostasis and Obesity PathogenesisIn: G Protein-Coupled Receptors in Energy Homeostasis and Obesity Pathogenesis / Tao, Ya-Xiong (Hrsg.) 2013, S. 147 - 191Online Volltext: dx.doi.org/
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Association and linkage studies in caucasiansIn: Obesity: Genomics and Postgenomics 2008, S. 255 - 263
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Genetische Mechanismen der GewichtsregulationDuisburg, Essen (2008) CD