Personensuche
Personensuche
Es wurde 1 Person gefunden.
Aktuelle Veranstaltungen
-
2023 SS
- Nervensystem und Psyche
- Psychische Störungen im Kindes- und Jugendalter im Spannungsfeld zwischen Biologie und Umwelt
- Doktorandenseminar
- Vorstellung aktueller Studien im Bereich der Kinder- und Jugendpsychiatrie
- Praktikum für Doktoranden des molekulargenetischen Labors
- Doktorandenseminar des molekulargenetischen Labors
Vergangene Veranstaltungen (max. 10)
-
2022 WS
- 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
-
2022 SS
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.
-
Genetic variants in genes involved in creatine biosynthesis in patients with severe obesity or anorexia nervosaIn: Frontiers in Genetics Jg. 14 (2023)ISSN: 1664-8021Online Volltext: dx.doi.org/ (Open Access)
-
Lipocalin 2 - mutation screen and serum levels in patients with anorexia nervosa or obesity and in lean individualsIn: Frontiers in Endocrinology Jg. 14 (2023)ISSN: 1664-2392Online Volltext: dx.doi.org/ (Open Access)
-
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 - 112ISSN: 1573-2517; 0165-0327Online Volltext: dx.doi.org/
-
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)ISSN: 1664-8021Online Volltext: dx.doi.org/ Online Volltext (Open Access)
-
Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severityIn: Human Genetics Jg. 141 (2022) Nr. 1, S. 147 - 173ISSN: 1432-1203; 0018-7348; 0340-6717Online Volltext: dx.doi.org/ (Open Access)
-
Detailed stratified GWAS analysis for severe COVID-19 in four European populationsIn: Human Molecular Genetics Jg. 31 (2022) Nr. 23, S. 3945 - 3966ISSN: 1460-2083; 0964-6906Online Volltext: dx.doi.org/ (Open Access)
-
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 - 185ISSN: 1664-2880; 1422-4917Online Volltext: dx.doi.org/ (Open Access)
-
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 - 226ISSN: 1664-2880; 1422-4917Online Volltext: dx.doi.org/ (Open Access)
-
Evidence for correlations between BMI-associated SNPs and circRNAsIn: Scientific Reports Jg. 12 (2022) Nr. 1,ISSN: 2045-2322Online Volltext: dx.doi.org/ (Open Access)
-
Expression of CXCR4 on CD4⁺ T cells predicts body composition parameters in female adolescents with anorexia nervosaIn: Frontiers in Psychiatry Jg. 13 (2022)ISSN: 1664-0640Online Volltext: dx.doi.org/ (Open Access)
-
PTBP2 – a gene with relevance for both Anorexia nervosa and body weight regulationIn: Translational Psychiatry Jg. 12 (2022) Nr. 1,ISSN: 2158-3188Online Volltext: dx.doi.org/ (Open Access)
-
Prevalence estimates of putatively pathogenic leptin variants in the gnomAD databaseIn: PLoS ONE Jg. 17 (2022) Nr. 9,ISSN: 1932-6203Online Volltext: dx.doi.org/ Online Volltext (Open Access)
-
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)ISSN: 1664-0640Online Volltext: dx.doi.org/ Online Volltext (Open Access)
-
The adrenal steroid profile in adolescent depression : a valuable bio-readout?In: Translational Psychiatry Jg. 12 (2022) Nr. 1,ISSN: 2158-3188Online Volltext: dx.doi.org/ (Open Access)
-
The promise of new anti-obesity therapies arising from knowledge of genetic obesity traitsIn: Nature Reviews Endocrinology Jg. 18 (2022) Nr. 10, S. 623 - 637ISSN: 1759-5029; 1759-5037Online Volltext: dx.doi.org/ (Open Access)
-
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 - 2591ISSN: 1436-6215; 1436-6207; 1435-1293; 0044-264XOnline Volltext: dx.doi.org/ Online Volltext (Open Access)
-
Alterations in B cell subsets correlate with body composition parameters in female adolescents with anorexia nervosaIn: Scientific Reports Jg. 11 (2021) Nr. 1, S. 1125ISSN: 2045-2322Online Volltext: dx.doi.org/ (Open Access)
-
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,ISSN: 2218-1989Online Volltext: dx.doi.org/ (Open Access)
-
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,ISSN: 2045-2322Online Volltext: dx.doi.org/ (Open Access)
-
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 - 5ISSN: 1664-2880; 1422-4917Online Volltext: dx.doi.org/
-
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)ISSN: 1664-2392Online Volltext: dx.doi.org/ Online Volltext (Open Access)
-
Mapping the human genetic architecture of COVID-19In: Nature Jg. 600 (2021) S. 472 - 477ISSN: 0028-0836; 1476-4687Online Volltext: dx.doi.org/ (Open Access)
-
Rapid amelioration of anorexia nervosa in a male adolescent during metreleptin treatment including recovery from hypogonadotropic hypogonadismIn: European Child and Adolescent Psychiatry Jg. 31 (2021) S. 1573 - 1579ISSN: 1018-8827; 1435-165XOnline Volltext: dx.doi.org/ (Open Access)
-
Shared genetic risk between eating disorder‐ and substance‐use‐related phenotypes : Evidence from genome‐wide association studiesIn: Addiction Biology Jg. 26 (2021) Nr. 1,ISSN: 1369-1600; 1355-6215Online Volltext: dx.doi.org/; Online Volltext: dx.doi.org/ (Open Access)
-
Size Matters: The CAG Repeat Length of the Androgen Receptor Gene, Testosterone, and Male Adolescent Depression SeverityIn: Frontiers in Psychiatry Jg. 12 (2021)ISSN: 1664-0640Online Volltext: dx.doi.org/ Online Volltext (Open Access)
-
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)ISSN: 1664-8021Online Volltext: dx.doi.org/ Online Volltext (Open Access)
-
Synaptic processes and immune-related pathways implicated in Tourette syndromeIn: Translational Psychiatry Jg. 11 (2021) Nr. 1, S. 56ISSN: 2158-3188Online Volltext: dx.doi.org/ (Open Access)
-
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 - 3424ISSN: 1436-6215; 1436-6207; 1435-1293; 0044-264XOnline Volltext: dx.doi.org/ (Open Access)
-
Genetic and epigenetic findings in anorexia nervosaIn: Medizinische Genetik Jg. 32 (2020) Nr. 1, S. 25 - 29ISSN: 1863-5490; 0936-5931Online Volltext: dx.doi.org/ (Open Access)
-
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)ISSN: 1664-2392Online Volltext: dx.doi.org/ Online Volltext (Open Access)
-
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, S. 303ISSN: 2158-3188Online Volltext: dx.doi.org/ (Open Access)
-
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)ISSN: 1664-8021Online Volltext: dx.doi.org/ Online Volltext (Open Access)
-
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 - 3338ISSN: 1460-2083; 0964-6906Online Volltext: dx.doi.org/ Online Volltext (Open Access)
-
Assessing Causal links between metabolic traits, inflammation and Schizophrenia : a Univariable and Multivariable Bidirectional Mendelian Randomization StudyIn: European Neuropsychopharmacology Jg. 29 (2019) S. 211ISSN: 1873-7862; 0924-977XOnline Volltext: dx.doi.org/
-
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 - 1514ISSN: 1464-3685Online Volltext: dx.doi.org/ (Open Access)
-
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 - 586ISSN: 1873-2402; 0006-3223Online Volltext: dx.doi.org/ (Open Access)
-
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 - 21ISSN: 1467-7881; 1467-789XOnline Volltext: dx.doi.org/
-
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. 1138ISSN: 1873-7862; 0924-977XOnline Volltext: dx.doi.org/
-
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 - 1214ISSN: 1061-4036; 1546-1718Online Volltext: dx.doi.org/ Online Volltext (Open Access)
-
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms Across Eight Psychiatric DisordersIn: Cell Jg. 179 (2019) Nr. 7, S. 1469 - 1482.e11.ISSN: 0092-8674; 1097-4172Online Volltext: dx.doi.org/ (Open Access)
-
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 - 227ISSN: 1535-7228; 0002-953XOnline Volltext: dx.doi.org/ (Open Access)
-
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. 960ISSN: 2072-6643Online Volltext: dx.doi.org/ (Open Access)
-
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 - 376ISSN: 1552-485X; 1552-4841; 1096-8628; 0148-7299Online Volltext: dx.doi.org/ (Open Access)
-
Vitamin D and the Risk of Depression : A Causal Relationship? Findings from a Mendelian Randomization StudyIn: Nutrients Jg. 11 (2019) Nr. 5, S. 1085ISSN: 2072-6643Online Volltext: dx.doi.org/ Online Volltext (Open Access)
-
Correction: Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosaIn: Molecular Psychiatry Jg. 23 (2018) Nr. 9, S. 1ISSN: 1476-5578; 1359-4184Online Volltext: dx.doi.org/ (Open Access)
-
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. 57ISSN: 1471-244XOnline Volltext: dx.doi.org/ (Open Access)
-
High-throughput DNA methylation analysis in anorexia nervosa confirms TNXB hypermethylationIn: The World Journal of Biological Psychiatry Jg. 19 (2018) Nr. 3, S. 187 - 199ISSN: 1562-2975; 1814-1412Online Volltext: dx.doi.org/; Online Volltext: dx.doi.org/ (Open Access)
-
Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosaIn: Molecular Psychiatry Jg. 23 (2018) Nr. 5, S. 1169 - 1180ISSN: 1476-5578; 1359-4184Online Volltext: dx.doi.org/ (Open Access)
-
Monogene Adipositas : Neue diagnostische und therapeutische MöglichkeitenIn: Monatsschrift Kinderheilkunde Jg. 166 (2018) Nr. 5, S. 388 - 394ISSN: 0026-9298; 1433-0474Online Volltext: dx.doi.org/
-
Relevance of polymorphisms in MC4R and BDNF in short normal stature.In: BMC Pediatrics Jg. 18 (2018) S. 278ISSN: 1471-2431Online Volltext: dx.doi.org/ Online Volltext (Open Access)
-
The Effect of SH2B1 Variants on Expression of Leptin- and Insulin-Induced Pathways in Murine HypothalamusIn: Obesity Facts Jg. 11 (2018) S. 93 - 108ISSN: 1662-4033; 1662-4025Online Volltext: dx.doi.org/ (Open Access)
-
The association of Leptin and Food Addiction in Adolescent Psychiatric PatientsIn: Journal of Behavioral Addictions Jg. 7 (2018) Nr. Suppl. 1, S. 128 - 128ISSN: 2062-5871
-
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 - 628ISSN: 1099-0968; 1072-4133Online Volltext: dx.doi.org/
-
The role of genetic variation of human metabolism for BMI, mental traits and mental disordersIn: Molecular Metabolism Jg. 12 (2018) S. 1 - 11ISSN: 2212-8778Online Volltext: dx.doi.org/ Online Volltext (Open Access)
-
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. 34ISSN: 1743-7075Online Volltext: dx.doi.org/ (Open Access)
-
A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signalingIn: Scientific Reports Jg. 7 (2017) Nr. 1,ISSN: 2045-2322Online Volltext: dx.doi.org/ (Open Access)
-
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 - S525ISSN: 1873-7862; 0924-977XOnline Volltext: dx.doi.org/
-
Estimated prevalence of potentially damaging variants in the leptin gene.In: Molecular and Cellular Pediatrics Jg. 4 (2017) Nr. 1, S. 10ISSN: 2194-7791Online Volltext: dx.doi.org/ (Open Access)
-
Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass indexIn: Molecular Psychiatry Jg. 22 (2017) S. 192 - 201ISSN: 1476-5578; 1359-4184Online Volltext: dx.doi.org/ Online Volltext (Open Access)
-
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 - 158ISSN: 1473-5873; 0955-8829Online Volltext: dx.doi.org/ Online Volltext (Open Access)
-
Food addiction in gambling disorder: Frequency and clinical outcomesIn: Frontiers in Psychology Jg. 8 (2017) S. 473ISSN: 1664-1078Online Volltext: dx.doi.org/ (Open Access)
-
Genetische Ursachen der AdipositasIn: Der Gastroenterologe Jg. 12 (2017) Nr. 1, S. 60 - 65ISSN: 1861-9681; 1861-969XOnline Volltext: dx.doi.org/
-
Polygene Varianten und Epigenetik bei AdipositasIn: Medizinische Genetik Jg. 29 (2017) Nr. 4, S. 365 - 373ISSN: 1863-5490; 0936-5931Online Volltext: dx.doi.org/ (Open Access)
-
Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood ObesityIn: Scientific Reports Jg. 7 (2017) Nr. 1, S. 4394ISSN: 2045-2322Online Volltext: dx.doi.org/ (Open Access)
-
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 - 858ISSN: 0002-953X; 1535-7228Online Volltext: dx.doi.org/ (Open Access)
-
Analysis of genes involved in body weight regulation by targeted re-sequencingIn: PLoS ONE Jg. 11 (2016) Nr. 2, S. e0147904ISSN: 1932-6203Online Volltext: dx.doi.org/ (Open Access)
-
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. 7ISSN: 1471-2350Online Volltext: dx.doi.org/ (Open Access)
-
Cover Image, Volume 171B, Number 6, September 2016In: American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics Jg. 171 (2016) Nr. 6, S. IISSN: 1552-485X; 1552-4841; 1096-8628; 0148-7299Online Volltext: dx.doi.org/
-
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 - 1982ISSN: 1930-7381Online Volltext: dx.doi.org/
-
Interindividual Variation in DNA Methylation at a Putative POMC Metastable Epiallele Is Associated with ObesityIn: Cell Metabolism Jg. 24 (2016) Nr. 3, S. 502 - 509ISSN: 1550-4131Online Volltext: dx.doi.org/ (Open Access)
-
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 - 826ISSN: 1552-485X; 1552-4841; 1096-8628; 0148-7299Online Volltext: dx.doi.org/ Online Volltext (Open Access)
-
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 - 926ISSN: 1740-634X; 0893-133XOnline Volltext: dx.doi.org/
-
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 - 3594ISSN: 0964-6906Online Volltext: dx.doi.org/ (Open Access)
-
Fine mapping of a GWAS-derived obesity candidate region on chromosome 16p11.2In: PLoS ONE Jg. 10 (2015) Nr. 5, S. e0125660ISSN: 1932-6203Online Volltext: dx.doi.org/ (Open Access)
-
Genetik und Epigenetik der AdipositasIn: Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz Jg. 58 (2015) Nr. 2, S. 154 - 158ISSN: 1436-9990; 1437-1588Online Volltext: dx.doi.org/
-
Indications for potential parent-of-origin effects within the FTO geneIn: PLoS ONE Jg. 10 (2015) Nr. 3, S. e0119206ISSN: 1932-6203Online Volltext: dx.doi.org/ (Open Access)
-
Perspektiven der genetischen Forschung bei Essstörungen am Beispiel der Anorexia nervosaIn: Psychotherapie, Psychosomatik, Medizinische Psychologie (PPmP) Jg. 65 (2015) Nr. 1, S. 8 - 10ISSN: 0937-2032; 1439-1058Online Volltext: dx.doi.org/
-
A genome-wide association study of anorexia nervosaIn: Molecular Psychiatry Jg. 19 (2014) Nr. 10, S. 1085 - 1094ISSN: 1476-5578; 1359-4184Online Volltext: dx.doi.org/ Online Volltext (Open Access)
-
Catechol-O-Methyltransferase Val158Met Polymorphism Is Associated with Somatosensory Amplification and Nocebo ResponsesIn: PLoS ONE Jg. 9 (2014) Nr. 9, S. 0107665ISSN: 1932-6203Online Volltext: dx.doi.org/ (Open Access)
-
FTO Gene : Association to Weight Regain after Lifestyle Intervention in Overweight ChildrenIn: Hormone Research in Paediatrics Jg. 81 (2014) Nr. 6, S. 391 - 396ISSN: 0018-5051; 1663-2818Online Volltext: dx.doi.org/
-
Genes and the hypothalamic control of metabolism in humansIn: Best Practice and Research Clinical Endocrinology and Metabolism Jg. 28 (2014) Nr. 5, S. 635 - 647ISSN: 1521-690X; 1532-1908Online Volltext: dx.doi.org/
-
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 - 293ISSN: 1552-485X; 1552-4841; 1096-8628; 0148-7299Online Volltext: dx.doi.org/
-
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 - 121ISSN: 1476-5578; 1359-4184Online Volltext: dx.doi.org/ (Open Access)
-
Mitochondrial DNA Variants in ObesityIn: PLoS ONE Jg. 9 (2014) Nr. 5, S. e94882ISSN: 1932-6203Online Volltext: dx.doi.org/ (Open Access)
-
The Origin of the Obesity Associated Pomc DNA Hypermethylation VariantIn: Endocrine Reviews Jg. 35 (2014) Nr. Suppl. 3,ISSN: 0163-769X
-
A novel SP1/SP3 dependent intronic enhancer governing transcription of the UCP3 gene in brown adipocytesIn: PLoS ONE Jg. 8 (2013) Nr. 12, S. e83426ISSN: 1932-6203Online Volltext: dx.doi.org/ (Open Access)
-
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 - 337ISSN: 0947-7349; 1439-3646Online Volltext: dx.doi.org/
-
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,ISSN: 1471-2431Online Volltext: dx.doi.org/ (Open Access)
-
Bipolar disorder risk alleles in children with ADHDIn: Journal of Neural Transmission Jg. 120 (2013) Nr. 11, S. 1611 - 1617ISSN: 1435-1463; 0300-9564Online Volltext: dx.doi.org/
-
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 - 305ISSN: 1552-485X; 1552-4841; 1096-8628; 0148-7299Online Volltext: dx.doi.org/
-
Gene Set of Nuclear-Encoded Mitochondrial Regulators Is Enriched for Common Inherited Variation in ObesityIn: PLoS ONE Jg. 8 (2013) Nr. 2, S. e55884ISSN: 1932-6203Online Volltext: dx.doi.org/ Online Volltext (Open Access)
-
Genetics of Eating DisordersIn: Current Psychiatry Reports Jg. 15 (2013) Nr. 12, S. 423ISSN: 1535-1645; 1523-3812Online Volltext: dx.doi.org/
-
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 - 512ISSN: 1061-4036; 1546-1718Online Volltext: dx.doi.org/
-
Meta-analysis of genome-wide association studies on ADHD : A dimensional approachIn: Behavior Genetics Jg. 43 (2013) Nr. 6, S. 520 - 521ISSN: 0001-8244; 1573-3297
-
Molecular Genetic Aspects of Weight RegulationIn: Deutsches Ärzteblatt international Jg. 110 (2013) Nr. 19, S. 338 - 344ISSN: 1866-0452Online Volltext: dx.doi.org/
-
No impact of obesity susceptibility loci on weight regain after a lifestyle intervention in overweight childrenIn: The Journal of Pediatric Endocrinology and Metabolism Jg. 26 (2013) Nr. 11-12, S. 1209 - 1213ISSN: 0334-018X; 2191-0251Online Volltext: dx.doi.org/
-
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 - 115ISSN: 1662-4033; 1662-4025Online Volltext: dx.doi.org/
-
A genome-wide association meta-analysis identifies new childhood obesity lociIn: Nature Genetics Jg. 44 (2012) Nr. 5, S. 526 - 531ISSN: 1061-4036; 1546-1718Online Volltext: dx.doi.org/
-
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. 476ISSN: 1552-485X; 1552-4841; 1096-8628; 0148-7299Online Volltext: dx.doi.org/
-
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. 23ISSN: 1522-8517; 1523-5866
-
Common variants at 12q15 and 12q24 are associated with infant head circumferenceIn: Nature Genetics Jg. 44 (2012) Nr. 5, S. 532 - 538ISSN: 1061-4036; 1546-1718Online Volltext: dx.doi.org/
-
Common variants at 6q22 and 17q21 are associated with intracranial volumeIn: Nature Genetics Jg. 44 (2012) Nr. 5, S. 539 - 544ISSN: 1061-4036; 1546-1718Online Volltext: dx.doi.org/
-
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 - 1609ISSN: 1879-1379; 0022-3956Online Volltext: dx.doi.org/
-
DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorderIn: PLoS ONE Jg. 7 (2012) Nr. 4, Art. Nr. e35424ISSN: 1932-6203Online Volltext: dx.doi.org/ (Open Access)
-
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 - 368ISSN: 0018-5051; 1663-2818Online Volltext: dx.doi.org/
-
Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and humanIn: Nature Jg. 483 (2012) Nr. 7389, S. 350 - 354ISSN: 0028-0836; 1476-4687Online Volltext: dx.doi.org/
-
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 - 2859ISSN: 0012-186X; 1432-0428Online Volltext: dx.doi.org/
-
Evaluating The Role Of Reference Models In Copy Number Variation AnalysesIn: Genetic Epidemiology Jg. 36 (2012) Nr. 2, S. 133ISSN: 0741-0395
-
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 - 419ISSN: 1662-4033; 1662-4025Online Volltext: dx.doi.org/
-
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 - A507ISSN: 1939-327X; 0012-1797
-
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 - 2645ISSN: 0012-186X; 1432-0428Online Volltext: dx.doi.org/ (Open Access)
-
Mutation screen in the GWAS derived obesity gene SH2B1 including functional analyses of detected variantsIn: BMC Medical Genomics Jg. 5 (2012) S. 65ISSN: 1755-8794Online Volltext: dx.doi.org/ Online Volltext (Open Access)
-
Rescue of melanocortin 4 receptor (MC4R) nonsense mutations by aminoglycoside-mediated read-throughIn: Obesity Jg. 20 (2012) Nr. 5, S. 1074 - 1081ISSN: 1930-7381; 1930-739X; 1071-7323Online Volltext: dx.doi.org/
-
SDCCAG8 obesity alleles and reduced weight loss after a lifestyle intervention in overweight children and adolescentsIn: Obesity Jg. 20 (2012) Nr. 2, S. 466 - 470ISSN: 1930-7381; 1930-739X; 1071-7323Online Volltext: dx.doi.org/
-
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 - 77ISSN: 1439-4286Online Volltext: dx.doi.org/
-
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 - 203ISSN: 1662-4033Online Volltext: dx.doi.org/
-
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 - 243ISSN: 1601-1848; 1601-183XOnline Volltext: dx.doi.org/
-
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 - 75ISSN: 1662-4033Online Volltext: dx.doi.org/
-
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 - 296ISSN: 1662-4033Online Volltext: dx.doi.org/
-
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 - 6ISSN: 0021-972X; 1945-7197Online Volltext: dx.doi.org/ (Open Access)
-
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 - 711ISSN: 1879-1379; 0022-3956Online Volltext: dx.doi.org/
-
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 - 897ISSN: 1552-485X; 1552-4841; 1096-8628; 0148-7299Online Volltext: dx.doi.org/
-
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 - 839ISSN: 1930-7381; 1930-739XOnline Volltext: dx.doi.org/
-
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 - 852ISSN: 0964-6906; 1460-2083Online Volltext: dx.doi.org/
-
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 - 441ISSN: 1399-5448; 1399-543XOnline Volltext: dx.doi.org/
-
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 - 170ISSN: 0014-2999Online Volltext: dx.doi.org/
-
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 - 512ISSN: 1536-2310; 1557-8100Online Volltext: dx.doi.org/
-
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass indexIn: Nature Genetics Jg. 42 (2010) Nr. 11, S. 937 - 948ISSN: 1061-4036; 1546-1718Online Volltext: dx.doi.org/
-
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass indexIn: Nature Genetics Jg. 42 (2010) Nr. 11, S. 937 - 948ISSN: 1061-4036; 1546-1718Online Volltext: dx.doi.org/ (Open Access)
-
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 - 579ISSN: 1930-739X; 1930-7381; 1550-8528; 1071-7323Online Volltext: dx.doi.org/ (Open Access)
-
Association of variants in gastric inhibitory polypeptide receptor gene with impaired glucose homeostasis in obese children and adolescents from BerlinIn: European Journal of Endocrinology Jg. 163 (2010) Nr. 2, S. 259 - 264ISSN: 1479-683X; 0804-4643Online Volltext: dx.doi.org/
-
Changes of peripheral alpha-melanocyte-stimulating hormone in childhood obesityIn: Metabolism Jg. 59 (2010) Nr. 2, S. 186 - 194ISSN: 1532-8600; 0026-0495Online Volltext: dx.doi.org/
-
Child and adolescent psychiatric geneticsIn: European Child & Adolescent Psychiatry Jg. 19 (2010) Nr. 3, S. 259 - 279ISSN: 1435-165X; 1018-8827Online Volltext: dx.doi.org/
-
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 - 303ISSN: 1662-4033; 1662-4025Online Volltext: dx.doi.org/ (Open Access)
-
Eating disorders: the current status of molecular genetic researchIn: European Child & Adolescent Psychiatry Jg. 19 (2010) Nr. 3, S. 211 - 226ISSN: 1435-165X; 1018-8827Online Volltext: dx.doi.org/ (Open Access)
-
Estrogen receptor 1 gene (ESR1) is associated with restrictive anorexia nervosaIn: Neuropsychopharmacology Jg. 35 (2010) Nr. 8, S. 1818 - 1825ISSN: 1740-634X; 0893-133XOnline Volltext: dx.doi.org/ Online Volltext (Open Access)
-
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 - 158ISSN: 1552-485X; 1552-4841; 1096-8628; 0148-7299Online Volltext: dx.doi.org/
-
From monogenic to polygenic obesity : Recent advancesIn: European Child & Adolescent Psychiatry Jg. 19 (2010) Nr. 3, S. 297 - 310ISSN: 1435-165X; 1018-8827Online Volltext: dx.doi.org/ (Open Access)
-
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 - 1545ISSN: 0307-0565; 1476-5497Online Volltext: dx.doi.org/ (Open Access)
-
Genetic findings in anorexia and bulimia nervosaIn: Progress in Molecular Biology and Translational Science Jg. 94 (2010) S. 241 - 270ISSN: 1878-0814; 1877-1173Online Volltext: dx.doi.org/
-
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 - 189ISSN: 0021-9150; 1567-5688; 1879-1484Online Volltext: dx.doi.org/
-
Genetische Ursachen der Adipositas : Zum Stand der ForschungIn: Bundesgesundheitsblatt - Gesundheitsforschung - Gesundheitsschutz Jg. 53 (2010) Nr. 7, S. 674 - 680ISSN: 1437-1588; 1436-9990Online Volltext: dx.doi.org/
-
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. e13967ISSN: 1932-6203Online Volltext: dx.doi.org/ Online Volltext (Open Access)
-
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) S. 12ISSN: 1471-2350Online Volltext: dx.doi.org/ (Open Access)
-
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. 2ISSN: 1471-2350Online Volltext: dx.doi.org/ (Open Access)
-
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 - 840ISSN: 1879-1379; 0022-3956Online Volltext: dx.doi.org/
-
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 - 2002ISSN: 0021-972X; 1945-7197Online Volltext: dx.doi.org/
-
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,ISSN: 1553-7404Online Volltext: dx.doi.org/ (Open Access)
-
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 - 295ISSN: 1879-1360; 0022-3999Online Volltext: dx.doi.org/
-
Adipositas/ÜbergewichtIn: Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie Jg. 37 (2009) Nr. 4, S. 237 - 244ISSN: 1422-4917Online Volltext: dx.doi.org/
-
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 - 967ISSN: 1468-2044; 0003-9888Online Volltext: dx.doi.org/
-
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 - 317ISSN: 1476-5578; 1359-4184Online Volltext: dx.doi.org/ (Open Access)
-
Association studies on ghrelin and ghrelin receptor gene polymorphisms with obesityIn: Obesity Jg. 17 (2009) Nr. 4, S. 745 - 754ISSN: 1930-7381; 1930-739XOnline Volltext: dx.doi.org/ (Open Access)
-
Causal attributions of obese men and women in genetic testing: Implications of genetic/biological attributionsIn: Psychology & Health Jg. 24 (2009) Nr. 7, S. 749 - 761ISSN: 1476-8321; 0887-0446Online Volltext: dx.doi.org/
-
Environmental and Genetic Risk Factors in ObesityIn: Child and Adolescent Psychiatric Clinics of North America Jg. 18 (2009) Nr. 1, S. 83 - 94ISSN: 1056-4993Online Volltext: dx.doi.org/
-
Exploring the genetic link between RLS and ADHDIn: Journal of Psychiatric Research Jg. 43 (2009) Nr. 10, S. 941 - 945ISSN: 1879-1379; 0022-3956Online Volltext: dx.doi.org/
-
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 - 799ISSN: 1744-6872; 1744-6880Online Volltext: dx.doi.org/
-
Gastric inhibitory polypeptide receptor : Association analyses for obesity of several polymorphisms in large study groupsIn: BMC Medical Genetics Jg. 10 (2009)ISSN: 1471-2350Online Volltext: dx.doi.org/ (Open Access)
-
Increased constraints on MC4R during primate and human evolutionIn: Human Genetics Jg. 124 (2009) Nr. 6, S. 633 - 647ISSN: 0340-6717Online Volltext: dx.doi.org/
-
Lifestyle intervention in obese children with variations in the melanocortin 4 receptor geneIn: Obesity Jg. 17 (2009) Nr. 2, S. 382 - 389ISSN: 1930-7381; 1930-739XOnline Volltext: dx.doi.org/
-
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. e1000694ISSN: 1553-7404; 1553-7390Online Volltext: dx.doi.org/ (Open Access)
-
Non-replication of an association of CTNNBL1 polymorphisms and obesity in a population of Central European ancestryIn: BMC Medical Genetics Jg. 10 (2009)ISSN: 1471-2350Online Volltext: dx.doi.org/ (Open Access)
-
Procolipase gene : no association with early-onset obesity or fat intakeIn: Obesity Facts Jg. 2 (2009) Nr. 1, S. 40 - 44ISSN: 1662-4033; 1662-4025Online Volltext: dx.doi.org/ (Open Access)
-
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 - 512ISSN: 1435-1463; 0300-9564Online Volltext: dx.doi.org/
-
'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. 85ISSN: 1471-2350Online Volltext: dx.doi.org/ (Open Access)
-
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 - 1244ISSN: 0964-6906; 1460-2083Online Volltext: dx.doi.org/ (Open Access)
-
Association of the MC4R V103I polymorphism with the metabolic syndrome: The KORA studyIn: Obesity Jg. 16 (2008) Nr. 2, S. 369 - 376ISSN: 1930-739X; 1930-7381Online Volltext: dx.doi.org/
-
Common variants near MC4R are associated with fat mass, weight and risk of obesityIn: Nature Genetics Jg. 40 (2008) Nr. 6, S. 768 - 775ISSN: 1061-4036; 1546-1718Online Volltext: dx.doi.org/
-
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 - 1524ISSN: 0307-0565; 1476-5497Online Volltext: dx.doi.org/ (Open Access)
-
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 - 626ISSN: 1939-327X; 0012-1797Online Volltext: dx.doi.org/ (Open Access)
-
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)ISSN: 1753-2000Online Volltext: dx.doi.org/ Online Volltext (Open Access)
-
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 - 1398ISSN: 1552-485X; 1552-4841; 1096-8628; 0148-7299Online Volltext: dx.doi.org/ Online Volltext
-
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 - 1134ISSN: 1018-4813; 1476-5438Online Volltext: dx.doi.org/ (Open Access)
-
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 - 1078ISSN: 1435-1463; 0300-9564Online Volltext: dx.doi.org/
-
Val103Ile polymorphism of the melanocortin-4 receptor gene (MC4R) in cancer cachexiaIn: BMC Cancer Jg. 8 (2008)ISSN: 1471-2407Online Volltext: dx.doi.org/ (Open Access)
-
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 - 658ISSN: 1365-2265; 0300-0664Online Volltext: dx.doi.org/ Online Volltext (Open Access)
-
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)ISSN: 1471-2350Online Volltext: dx.doi.org/ (Open Access)
-
Association and linkage of allelic variants of the dopamine transporter gene in ADHDIn: Molecular Psychiatry Jg. 12 (2007) Nr. 10, S. 923 - 933ISSN: 1359-4184; 1476-5578Online Volltext: dx.doi.org/ (Open Access)
-
Definable Somatic Disorders in Overweight Children and AdolescentsIn: Journal of Pediatrics Jg. 150 (2007) Nr. 6, S. 618 - 622.e5ISSN: 0022-3476Online Volltext: dx.doi.org/
-
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 - 521ISSN: 1435-1463; 0300-9564Online Volltext: dx.doi.org/
-
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,ISSN: 1932-6203Online Volltext: dx.doi.org/ (Open Access)
-
Is information on genetic determinants of obesity helpful or harmful for obese people? : A randomized clinical trialIn: Journal of General Internal Medicine Jg. 22 (2007) Nr. 11, S. 1553 - 1559ISSN: 0884-8734; 1525-1497Online Volltext: dx.doi.org/
-
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)ISSN: 1471-2156Online Volltext: dx.doi.org/ (Open Access)
-
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 - 844ISSN: 0018-5043Online Volltext: dx.doi.org/
-
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 - 434ISSN: 1096-7206; 1096-7192Online Volltext: dx.doi.org/
-
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 - 526ISSN: 1435-1463; 0300-9564Online Volltext: dx.doi.org/
-
Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolutionIn: Nature Genetics Jg. 39 (2007) Nr. 2, S. 218 - 225ISSN: 1061-4036; 1546-1718Online Volltext: dx.doi.org/
-
Response to Comments on "A Common Genetic Variant Is Associated with Adult and Childhood Obesity"In: Science Jg. 315 (2007) Nr. 5809, S. 187.5 - 187ISSN: 0036-8075; 1095-9203Online Volltext: dx.doi.org/
-
Restoration of signalling capabilities in total loss of function MC4R mutationsIn: Experimental and Clinical Endocrinology & Diabetes Jg. 115 (2007) Nr. S 1, P02_065ISSN: 0947-7349; 1439-3646Online Volltext: dx.doi.org/
-
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 - 1441ISSN: 0307-0565; 1476-5497Online Volltext: dx.doi.org/ (Open Access)
-
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 - 0633ISSN: 1553-7390; 1553-7404Online Volltext: dx.doi.org/ (Open Access)
-
A common genetic variant is associated with adult and childhood obesityIn: Science Jg. 312 (2006) Nr. 5771, S. 279 - 283ISSN: 0036-8075; 1095-9203Online Volltext: dx.doi.org/
-
A genome-wide scan for attention-deficit/hyperactivity disorder in 155 German sib-pairsIn: Molecular Psychiatry Jg. 11 (2006) Nr. 2, S. 196 - 205ISSN: 1359-4184; 1476-5578Online Volltext: dx.doi.org/ (Open Access)
-
A role for β-melanocyte-stimulating hormone in human body-weight regulationIn: Cell Metabolism Jg. 3 (2006) Nr. 2, S. 141 - 146ISSN: 1550-4131Online Volltext: dx.doi.org/ (Open Access)
-
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 - 247ISSN: 0268-9146; 1365-2052Online Volltext: dx.doi.org/
-
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 - 52ISSN: 0955-8829Online Volltext: dx.doi.org/
-
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 - 2783ISSN: 0964-6906; 1460-2083Online Volltext: dx.doi.org/
-
Genetische Aspekte in der Adipositas-Beratung – Auswirkungen auf Körperakzeptanz und subjektives WohlbefindenIn: Verhaltenstherapie: Praxis, Forschung, Perspektiven Jg. 16 (2006) Nr. 3, S. 193 - 200ISSN: 1423-0402; 1016-6262Online Volltext: dx.doi.org/
-
Genetische Befunde bei der Aufmerksamkeitsdefizit- und Hyperaktivitätsstörung (ADHS)In: Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie Jg. 34 (2006) Nr. 6, S. 425 - 433ISSN: 1422-4917Online Volltext: dx.doi.org/
-
Meta-analysis on the effect of the N363S polymorphism of the glucocorticoid receptor gene (GRL) on human obesityIn: BMC Medical Genetics Jg. 7 (2006)ISSN: 1471-2350; 1471-2350Online Volltext: dx.doi.org/ (Open Access)
-
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 - 1769ISSN: 0021-972X; 1945-7197Online Volltext: dx.doi.org/ (Open Access)
-
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 - 538ISSN: 0021-972X; 1945-7197Online Volltext: dx.doi.org/
-
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 - 898ISSN: 0391-4097Online Volltext: dx.doi.org/
-
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 - 442ISSN: 1469-5111; 1461-1457Online Volltext: dx.doi.org/ (Open Access)
-
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 - 434ISSN: 1018-4813Online Volltext: dx.doi.org/ (Open Access)
-
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. e21ISSN: 1468-6244Online Volltext: dx.doi.org/ (Open Access)
-
Brain-derived neurotrophic factor V66M polymorphism in childhood-onset obsessive-compulsive disorderIn: The International Journal of Neuropsychopharmacology Jg. 8 (2005) Nr. 1, S. 133 - 136ISSN: 1469-5111; 1461-1457Online Volltext: dx.doi.org/ (Open Access)
-
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 - 1392ISSN: 0022-3166Online Volltext: dx.doi.org/ (Open Access)
-
Lack of support for the association between GAD2 polymorphisms and severe human obesityIn: PLoS Biology Jg. 3 (2005) Nr. 9,ISSN: 1545-7885; 1544-9173Online Volltext: dx.doi.org/ (Open Access)
-
Mutation analysis of the MCHR1 gene in human obesityIn: European Journal of Endocrinology Jg. 152 (2005) Nr. 6, S. 851 - 862ISSN: 0804-4643Online Volltext: dx.doi.org/ (Open Access)
-
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 - 99ISSN: 1552-485X; 1552-4841; 1096-8628; 0148-7299Online Volltext: dx.doi.org/
-
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 - 249ISSN: 0300-8630Online Volltext: dx.doi.org/
-
Adipositas : Genetik und Gen-Umwelt-InteraktionenIn: Monatsschrift für Kinderheilkunde Jg. 152 (2004) Nr. 8, S. 870 - 878ISSN: 0026-9298Online Volltext: dx.doi.org/
-
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 - 1212ISSN: 0964-6906Online Volltext: dx.doi.org/ (Open Access)
-
Binge-eating episodes are not characteristic of carriers of melanocortin-4 receptor gene mutationsIn: Molecular Psychiatry Jg. 9 (2004) Nr. 8, S. 796 - 800ISSN: 1359-4184Online Volltext: dx.doi.org/ (Open Access)
-
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 - 72ISSN: 1552-485X; 1552-4841; 1096-8628; 0148-7299Online Volltext: dx.doi.org/
-
Genetic risk factors in eating disordersIn: American Journal of PharmacoGenomics Jg. 4 (2004) Nr. 4, S. 209 - 223ISSN: 1175-2203Online Volltext: dx.doi.org/
-
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 - 162ISSN: 0021-972X; 1945-7197Online Volltext: dx.doi.org/ (Open Access)
-
Large quantitative effect of melanocortin-4 receptor gene mutations on body mass indexIn: Journal of Medical Genetics (eJMG) Jg. 41 (2004) Nr. 10, S. 795 - 800ISSN: 1468-6244; 0022-2593Online Volltext: dx.doi.org/ (Open Access)
-
Melanocortin-4 Receptor Gene Variant I103 Is Negatively Associated with ObesityIn: American Journal of Human Genetics Jg. 74 (2004) Nr. 3, S. 572 - 581ISSN: 0002-9297Online Volltext: dx.doi.org/ (Open Access)
-
Transmission disequilibrium studies in children and adolescents with obsessive-compulsive disorders pertaining to polymorphisms of genes of the serotonergic pathwayIn: Journal of Neural Transmission Jg. 111 (2004) Nr. 7, S. 817 - 825ISSN: 1435-1463; 0300-9564Online Volltext: dx.doi.org/
-
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 - 455ISSN: 1462-8902Online Volltext: dx.doi.org/
-
Genetik in der Kinder- und JugendpsychiatrieIn: Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie Jg. 50 (2022) Nr. 3, S. 171 - 173ISSN: 1664-2880; 1422-4917Online Volltext: dx.doi.org/
-
Three at one swoop!In: Obesity Facts Jg. 2 (2009) Nr. 1, S. 3 - 6ISSN: 1662-4025; 1662-4033Online Volltext: dx.doi.org/ (Open Access)
-
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 - 346ISSN: 0018-5051; 1663-2818
-
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. 364ISSN: 0018-5051; 1663-2818
-
Genetic variation at three genetic loci involved in anorexia nervosa are associated with body weight regulation
16th International Congress of ESCAP European Society for Child and Adolescent Psychiatry 20–24 June 2015, Madrid, Spain,In: European Child and Adolescent Psychiatry Jg. 24 (2015) Nr. Suppl. 1, S. 64ISSN: 1018-8827Online Volltext: dx.doi.org/ -
The complexity of eating disorders : insight into recent research venues in molecular genetics, neuropsychology, neuroimaging, and social sciences
16th International Congress of ESCAP European Society for Child and Adolescent Psychiatry 20–24 June 2015, Madrid, Spain,In: European Child and Adolescent Psychiatry Jg. 24 (2015) Nr. Suppl. 1, S. S63 - S64ISSN: 1018-8827Online Volltext: dx.doi.org/ -
Addressing Genomic Imprinting in a Family-based Genome-wide Association Study
nineteenth annual meeting of the International Genetic Epidemiology Society,In: Genetic Epidemiology Jg. 34 (2010) Nr. 8, S. 943 - 943ISSN: 0741-0395; 1098-2272Online Volltext: dx.doi.org/ -
Changes of Peripheral Alpha-Melanocyte-Stimulating Hormone in Childhood Craniopharyngioma
42nd Congress of the International Society of Pediatric Oncology (SIOP), October 21-24, 2010, Boston, USA,In: Pediatric Blood and Cancer Jg. 55 (2010) Nr. 5, S. 791 - 791ISSN: 1545-5009; 1545-5017Online Volltext: dx.doi.org/ -
Consultation including Genetic information in People with increades risk for Obesity and MC4R-Mutations
11th International Congress of Behavioral Medicine,In: International Journal of Behavioral Medicine Jg. 17 (2010) Nr. Suppl. 1, S. 118ISSN: 1070-5503; 1532-7558Online Volltext: dx.doi.org/ -
Genetics of obesityIn: European Neuropsychopharmacology Jg. 20 (2010) Nr. Suppl. 3, S. S190ISSN: 1873-7862; 0924-977XOnline Volltext: dx.doi.org/
-
Bias-Corrected Effect Estimators for Genome-Wide Association StudiesIn: Genetic Epidemiology Jg. 32 (2008) Nr. 7, S. 676ISSN: 0741-0395; 1098-2272Online Volltext: dx.doi.org/
-
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 - 513ISSN: 0741-0395; 1098-2272Online Volltext: dx.doi.org/
-
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. 475ISSN: 0741-0395; 1098-2272Online Volltext: dx.doi.org/
-
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. S155ISSN: 0307-0565; 1476-5497Online Volltext: dx.doi.org/
-
Genetics of eating and weight disordersIn: Eating Disorders and Obesity in Children and Adolescents / Hebebrand, Johannes; Herpertz-Dahlmann, Beate (Hrsg.) 2018, S. 67 - 71ISBN: 9780323548526; 9780323548533Online Volltext: dx.doi.org/
-
Polygenic obesityIn: Pediatric Obesity: Etiology, Pathogenesis and Treatment / Freemark, Michael S. (Hrsg.) 2018, S. 183 - 202ISBN: 978-3-319-68191-7; 978-3-319-68192-4Online Volltext: dx.doi.org/
-
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 - 191ISSN: 1877-1173; 1878-0814Online Volltext: dx.doi.org/
-
Association and linkage studies in caucasiansIn: Obesity: Genomics and Postgenomics 2008, S. 255 - 263ISBN: 9781420020137; 978-0-8493-8089-1
-
Genetische Mechanismen der GewichtsregulationDuisburg, Essen (2008) CD