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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.

    Artikel in Zeitschriften

  • Müller, Wolfgang-Ulrich; Hinney, Anke; Scherbaum, Norbert; Weimar, Christian; Kleinschnitz, Christoph; Peters, Triinu; Hochfeld, Lara; Pechlivanis, Sonali; Stang, Andreas; Jokisch, Martha; Kowall, Bernd
    Klotho KL-VS haplotype does not improve cognition in a population-based sample of adults age 55-87 years
    In: Scientific Reports Jg. 11 (2021) Nr. 1,
    ISSN: 2045-2322
  • Pechlivanis, Sonali; Mahabadi, Amir Abbas; Hoffmann, Per; Nöthen, Markus M.; Bröcker-Preuß, Martina; Erbel, Raimund; Moebus, Susanne; Stang, Andreas; Jöckel, Karl-Heinz
    Association between lipoprotein(a) (Lp(a)) levels and Lp(a) genetic variants with coronary artery calcification
    In: BMC Medical Genetics Jg. 21 (2020) Nr. 1, S. 62
    ISSN: 1471-2350
  • Pechlivanis, Sonali; Moebus, Susanne; Lehmann, Nils; Erbel, Raimund; Mahabadi, Amir Abbas; Hoffmann, Per; Jöckel, Karl-Heinz; Nöthen, Markus M.; Bachmann, Hagen Sjard
    Genetic risk scores for coronary artery disease and its traditional risk factors : Their role in the progression of coronary artery calcification ; Results of the Heinz Nixdorf Recall study
    In: PLoS ONE Jg. 15 (2020) Nr. 5, S. e0232735
    ISSN: 1932-6203
  • Kleszka, Kira; Leu, Tristan; Quinting, Theresa; Jastrow, Holger; Pechlivanis, Sonali; Fandrey, Joachim; Schreiber, Timm
    Hypoxia-inducible factor-2α is crucial for proper brain development
    In: Scientific Reports Jg. 10 (2020) Nr. 1, S. 19146
    ISSN: 2045-2322
  • Pechlivanis, Sonali; Lehmann, Nils; Hoffmann, Per; Nöthen, Markus M.; Jöckel, Karl-Heinz; Erbel, Raimund; Moebus, Susanne
    Risk prediction for coronary heart disease by a genetic risk score : results from the Heinz Nixdorf Recall study
    In: BMC Medical Genetics Jg. 21 (2020) S. 178
    ISSN: 1471-2350
  • Malhotra, Rajeev; Mauer, Andreas C.; Lino Cardenas, Christian L.; Guo, Xiuqing; Yao, Jie; Zhang, Xiaoling; Wunderer, Florian; Smith, Albert V.; Wong, Quenna; Pechlivanis, Sonali; Hwang, Shih-Jen; Wang, Judy; Lu, Lingyi; Nicholson, Christopher J.; Shelton, Georgia; Buswell, Mary D.; Barnes, Hanna J.; Sigurslid, Haakon H.; Slocum, Charles; Rourke, Caitlin O; Rhee, David K.; Bagchi, Aranya; Nigwekar, Sagar U.; Buys, Emmanuel S.; Campbell, Catherine Y.; Harris, Tamara; Budoff, Matthew; Criqui, Michael H.; Rotter, Jerome I.; Johnson, Andrew D.; Song, Ci; Franceschini, Nora; Debette, Stephanie; Hoffmann, Udo; Kälsch, Hagen; Nöthen, Markus M.; Sigurdsson, Sigurdur; Freedman, Barry I.; Bowden, Donald W.; Jöckel, Karl-Heinz; Moebus, Susanne; Erbel, Raimund; Feitosa, Mary F.; Gudnason, Vilmundur; Thanassoulis, George; Zapol, Warren M.; Lindsay, Mark E.; Bloch, Donald B.; Post, Wendy S.; O’Donnell, Christopher J.
    Letter: HDAC9 is implicated in atherosclerotic aortic calcification and affects vascular smooth muscle cell phenotype
    In: Nature Genetics Jg. 51 (2019) Nr. 11, S. 1580 - 1587
    ISSN: 1061-4036; 1546-1718
  • Pechlivanis, Sonali; Heilmann-Heimbach, Stefanie; Erbel, Raimund; Mahabadi, Amir A.; Hochfeld, Lara M.; Jöckel, Karl-Heinz; Nöthen, Markus M.; Moebus, Susanne
    Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall Study
    In: PLoS ONE Jg. 14 (2019) Nr. 11, S. 225521
    ISSN: 1932-6203
  • Chattopadhyay, Subhayan; Thomsen, Hauke; da Silva Filho, Miguel Inacio; Weinhold, Niels; Hoffmann, Per; Nöthen, Markus M.; Marina, Arendt; Jöckel, Karl-Heinz; Schmidt, Börge; Pechlivanis, Sonali; Langer, Christian; Goldschmidt, Hartmut; Hemminki, Kari; Försti, Asta
    Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance : a genome-wide genetic interaction study
    In: Molecular Medicine Jg. 24 (2018) Nr. 1, S. 30
    ISSN: 1076-1551; 1528-3658
  • Scott, Robert A.; Scott, Laura J.; Mägi, Reedik; Marullo, Letizia; Gaulton, Kyle J.; Kaakinen, Marika; Pervjakova, Natalia; Pers, Tune H.; Johnson, Andrew D.; Eicher, John D.; Jackson, Anne U.; Ferreira, Teresa; Lee, Yeji; Ma, Clement; Steinthorsdottir, Valgerdur; Thorleifsson, Gudmar; Qi, Lu; Van Zuydam, Natalie R.; Mahajan, Anubha; Chen, Han; Almgren, Peter; Voight, Ben F.; Grallert, Harald; Müller-Nurasyid, Martina; Ried, Janina S.; Rayner, Nigel W.; Robertson, Neil; Karssen, Lennart C.; van Leeuwen, Elisabeth M.; Willems, Sara M.; Fuchsberger, Christian; Kwan, Phoenix; Teslovich, Tanya M.; Chanda, Pritam; Li, Man; Lu, Yingchang; Dina, Christian; Thuillier, Dorothee; Yengo, Loic; Jiang, Longda; Sparso, Thomas; Kestler, Hans A.; Chheda, Himanshu; Eisele, Lewin; Gustafsson, Stefan; Frånberg, Mattias; Strawbridge, Rona J.; Benediktsson, Rafn; Hreidarsson, Astradur B.; Kong, Augustine; Sigurðsson, Gunnar; Kerrison, Nicola D.; Luan, Jian'an; Liang, Liming; Meitinger, Thomas; Roden, Michael; Thorand, Barbara; Esko, Tõnu; Mihailov, Evelin; Fox, Caroline; Liu, Ching-Ti; Rybin, Denis; Isomaa, Bo; Lyssenko, Valeriya; Tuomi, Tiinamaija; Couper, David J.; Pankow, James S.; Grarup, Niels; Have, Christian T.; Jørgensen, Marit E.; Jørgensen, Torben; Linneberg, Allan; Cornelis, Marilyn C.; van Dam, Rob M.; Hunter, David J.; Kraft, Peter; Sun, Qi; Edkins, Sarah; Owen, Katharine R.; Perry, John R B; Wood, Andrew R.; Zeggini, Eleftheria; Tajes-Fernandes, Juan; Abecasis, Goncalo R.; Bonnycastle, Lori L.; Chines, Peter S.; Stringham, Heather M.; Koistinen, Heikki A.; Kinnunen, Leena; Sennblad, Bengt; Mühleisen, Thomas W.; Nöthen, Markus M.; Pechlivanis, Sonali; Baldassarre, Damiano; Gertow, Karl; Humphries, Steve E.; Tremoli, Elena; Klopp, Norman; Meyer, Julia; Steinbach, Gerald; Wennauer, Roman; Eriksson, Johan G.; Mӓnnistö, Satu; Peltonen, Leena; Tikkanen, Emmi; Charpentier, Guillaume; Eury, Elodie; Lobbens, Stéphane; Gigante, Bruna; Leander, Karin; McLeod, Olga; Bottinger, Erwin P.; Gottesman, Omri; Ruderfer, Douglas; Blüher, Matthias; Kovacs, Peter; Tonjes, Anke; Maruthur, Nisa M.; Scapoli, Chiara; Erbel, Raimund; Jöckel, Karl-Heinz; Moebus, Susanne; de Faire, Ulf; Hamsten, Anders; Stumvoll, Michael; Deloukas, Panagiotis; Donnelly, Peter J.; Frayling, Timothy M.; Hattersley, Andrew T.; Ripatti, Samuli; Salomaa, Veikko; Pedersen, Nancy L.; Boehm, Bernhard O.; Bergman, Richard N.; Collins, Francis S.; Mohlke, Karen L.; Tuomilehto, Jaakko; Hansen, Torben; Pedersen, Oluf; Barroso, Inês; Lannfelt, Lars; Ingelsson, Erik; Lind, Lars; Lindgren, Cecilia M.; Cauchi, Stephane; Froguel, Philippe; Loos, Ruth J F; Balkau, Beverley; Boeing, Heiner; Franks, Paul W.; Barricarte Gurrea, Aurelio; Palli, Domenico; van der Schouw, Yvonne T.; Altshuler, David; Groop, Leif C.; Langenberg, Claudia; Wareham, Nicholas J.; Sijbrands, Eric; van Duijn, Cornelia M.; Florez, Jose C.; Meigs, James B.; Boerwinkle, Eric; Gieger, Christian; Strauch, Konstantin; Metspalu, Andres; Morris, Andrew D.; Palmer, Colin N A; Hu, Frank B.; Thorsteinsdottir, Unnur; Stefansson, Kari; Dupuis, Josée; Boehnke, Michael; McCarthy, Mark I.; Prokopenko, Inga
    An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans
    In: Diabetes Jg. 66 (2017) Nr. 11, S. 2888 - 2902
    ISSN: 1939-327X; 0012-1797
  • Kleszka, K.; Pechlivanis, Sonali; Fandrey, Joachim; Schreiber, T.
    Defective brain development in mice lacking hypoxia-inducible factor-2a in neural stem cells
    In: Acta Physiologica Jg. 219 S711 (2017) S. 54 - 54
    ISSN: 1748-1708; 1748-1716
  • Heilmann-Heimbach, Stefanie; Herold, Christine; Hochfeld, Lara M.; Hillmer, Axel M.; Nyholt, Dale R.; Hecker, Julian; Javed, Asif; Chew, Elaine G. Y.; Pechlivanis, Sonali; Drichel, Dmitriy; Heng, Xiu Ting; Del Rosario, Ricardo C.-H.; Fier, Heide L.; Paus, Ralf; Rueedi, Rico; Galesloot, Tessel E.; Moebus, Susanne; Anhalt, Thomas; Prabhakar, Shyam; Li, Rui; Kanoni, Stavroula; Papanikolaou, George; Kutalik, Zoltán; Deloukas, Panos; Philpott, Michael P.; Waeber, Gérard; Spector, Tim D.; Vollenweider, Peter; Kiemeney, Lambertus A. L. M.; Dedoussis, George; Richards, J. Brent; Nothnagel, Michael; Martin, Nicholas G.; Becker, Tim; Hinds, David A.; Nöthen, Markus M.
    Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
    In: Nature Communications Jg. 8 (2017) S. 14694
    ISSN: 2041-1723
  • Dykun, Iryna; Erbel, Raimund; Pechlivanis, Sonali; Nöthen, Markus M.; Lehmann, Nils; Jöckel, Karl-Heinz; Bachmann, Hagen Sjard; Mahabadi, Amir Abbas; Moebus, Susanne
    Pharmacogenetic association of blood-lipid related genetic variants with 5-year progression of coronary artery calcification following the treatment with statin in the Heinz Nixdorf Recall study
    In: Atherosclerosis Jg. 263 (2017) S. e278
    ISSN: 0021-9150
  • Schmidt, Börge; Frölich, Stefanie; Dragano, Nico; Frank, Mirjam; Eisele, Lewin; Pechlivanis, Sonali; Forstner, Andreas J.; Nothen, M. M.; Mahabadi, Amir Abbas; Erbel, Raimund; Moebus, Susanne; Jockel, Karl-Heinz
    Socioeconomic Status Interacts with the Genetic Effect of a Chromosome 9p21.3 Common Variant to Influence Coronary Artery Calcification and Incident Coronary Events in the Heinz Nixdorf Recall Study (Risk Factors, Evaluation of Coronary Calcium, and Lifes
    In: Circulation : Cardiovascular Genetics Jg. 10 (2017) Nr. 2,
    ISSN: 1942-325X
  • Schmidt, Börge; Frölich, Stefanie; Dragano, Nico; Frank, Mirjam; Eisele, Lewin; Pechlivanis, Sonali; Forstner, Andreas J.; Nöthen, Markus M.; Mahabadi, Amir Abbas; Erbel, Raimund; Moebus, Susanne; Jöckel, Karl-Heinz
    Socioeconomic Status Interacts with the Genetic Effect of a Chromosome 9p21.3 Common Variant to Influence Coronary Artery Calcification and Incident Coronary Events in the Heinz Nixdorf Recall Study (Risk Factors, Evaluation of Coronary Calcium, and Lifestyle)
    In: Circulation: Genomic and Precision Medicine Jg. 10 (2017) Nr. 2,
    ISSN: 1942-325X
  • Weinhold, Leonie; Wahl, Simone; Pechlivanis, Sonali; Hoffmann, Per; Schmid, Matthias
    A statistical model for the analysis of beta values in DNA methylation studies
    In: BMC Bioinformatics Jg. 17 (2016) Nr. 1, S. 480
    ISSN: 1471-2105
  • Hartwig, Saskia; Kluttig, Alexander; Tiller, Daniel; Fricke, Julia; Müller, Grit; Schipf, Sabine; Völzke, Henry; Schunk, Michaela; Meisinger, Christa; Schienkiewitz, Anja; Heidemann, Christin; Moebus, Susanne; Pechlivanis, Sonali; Werdan, Karl; Kuss, Oliver; Tamayo, Teresa; Haerting, Johannes; Greiser, Karin Halina
    Anthropometric markers and their association with incident type 2 diabetes mellitus : which marker is best for prediction? Pooled analysis of four German population-based cohort studies and comparison with a nationwide cohort study
    In: BMJ Open Jg. 6 (2016) Nr. 1, S. e009266
    ISSN: 2044-6055
  • Locke, Adam E.; Kahali, Bratati; Berndt, Sonja I.; Pechlivanis, Sonali; Erbel, Raimund; Jöckel, Karl-Heinz; Moebus, Susanne; Scherag, Andre; Hirschhorn, Joel N.; Loos, Ruth J. F.; Speliotes, Elizabeth K.; et al.
    Genetic studies of body mass index yield new insights for obesity biology
    In: Nature Jg. 518 (2015) Nr. 7538, S. 197 - 206
    ISSN: 0028-0836; 1476-4687
  • Shungin, Dmitry; Winkler, Thomas W.; Scherag, Andre; Pechlivanis, Sonali; Jöckel, Karl-Heinz; Erbel, Raimund; Möhlenkamp, Stefan; Mohlke, Karen L.
    New genetic loci link adipose and insulin biology to body fat distribution
    In: Nature Jg. 518 (2015) Nr. 7538, S. 187 - 196
    ISSN: 0028-0836; 1476-4687
  • van Setten, Jessica; Isgum, Ivana; Pechlivanis, Sonali; Tragante, Vinicius; de Jong, Pim A; Smolonska, Joanna; Platteel, Mathieu; Hoffmann, Per; Oudkerk, Matthijs; de Koning, Harry J; Nöthen, Markus M; Moebus, Susanne; Erbel, Raimund; Jöckel, Karl-Heinz; Viergever, Max A; Mali, Willem P Th M; de Bakker, Paul I W
    Serum lipid levels, body mass index, and their role in coronary artery calcification : a polygenic analysis
    In: Circulation Jg. 8 (2015) Nr. 2, S. 327 - 333
    ISSN: 1942-325X
  • Schmidt, Börge; Dragano, Nico; Scherag, Andre; Pechlivanis, Sonali; Hoffmann, Per; Nöthen, Markus; Erbel, Raimund; Jöckel, Karl-Heinz; Moebus, Susanne
    Exploring genetic variants predisposing to diabetes mellitus and their association with indicators of socioeconomic status
    In: BMC Public Health Jg. 14 (2014) Nr. 1, S. 609
    ISSN: 1471-2458
  • Jarick, I.; Volckmar, A.-L.; Pütter, Carolin; Pechlivanis, Sonali; Nguyen. T. T.; Dauvermann, R.; Beck, S.; Albayrak, Özgür; Scherag, S.; Gilsbach, S.; Cichon, S.; Hoffmann, P.; Degenhardt, F.; Nöthen, M. M.; Schreiber, S.; Wichmann, H.-E.; Jöckel, Karl-Heinz; Heinrich, J.; Tiesler, C. M. T.; Faraone, S. V.; Walitza, S.; Sinzig, J.; Freitag, C.; Meyer, J.; Herpertz-Dahlmann, B.; Lehmkuhl, G.; Renner, J.; Warnke, A.; Romanos, M.; Lesch, K.-P.; Reif, A.; Schimmelmann, G.; Hebebrand, Johannes; Scherag, Andre; Hinney, Anke
    Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder
    In: Molecular Psychiatry Jg. 19 (2014) Nr. 1, S. 115 - 121
    ISSN: 1359-4184; 1476-5578
  • Erbel, Raimund; Pechlivanis, Sonali; Moebus, Susanne; Jöckel, Karl-Heinz
    Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
    In: Nature Genetics Jg. 46 (2014) Nr. 3, S. 234 - 244
    ISSN: 1061-4036; 1546-1718
  • Schimmelmann, B.G.; Hinney, Anke; Scherag, Andre; Pütter, Carolin; Pechlivanis, Sonali; Cichon, S.; Jöckel, Karl-Heinz; Schreiber, S.; Wichmann, H.E.; Albayrak, Özgür; Dauvermann, M.; Konrad, K.; Wilhelm, C.; Herpertz-Dahlmann, B.; Lehmkuhl, G.; Sinzig, J.; Renner, T.J.; Romanos, M.; Warnke, A.; Lesch, K.P.; Reif, A.; Hebebrand, Johannes
    Bipolar disorder risk alleles in children with ADHD
    In: Journal of Neural Transmission Jg. 120 (2013) Nr. 11, S. 1611 - 1617
    ISSN: 0300-9564; 1435-1463
  • Icks, Andrea; Albers, Bernhard; Haastert, Burkhard; Pechlivanis, Sonali; Bokhof, Beate; Slomiany, Uta; Erbel, Raimund; Jöckel, Karl-Heinz; Kruse, Johannes; Nowotny, Bettina; Herder, Christian; Giani, Guido; Moebus, Susanne
    Diabetes incidence does not differ between subjects with and without high depressive symptoms - 5-year follow-up results of the Heinz Nixdorf Recall Study
    In: Diabetic medicine Jg. 30 (2013) Nr. 1, S. 65 - 69
    ISSN: 1464-5491; 0742-3071; 1466-5468
  • Thanassoulis, George; Campbell, Catherine Y.; Owens, David S.; Smith, J. Gustav; Smith, Albert V.; Peloso, Gina M.; Kerr, Kathleen F.; Pechlivanis, Sonali; Budoff, Matthew J.; Harris, Tamara B.; Malhotra, Rajeev; O'Brien, Kevin D.; Kamstrup, Pia R.; Nordestgaard, Børge G.; Tybjaerg-Hansen, Anne; Allison, Matthew A.; Aspelund, Thor; Criqui, Michael H.; Heckbert, Susan R.; Hwang, Shih-Jen; Liu, Yongmei; Sjogren, Marketa; Van Der Pals, Jesper; Kälsch, Hagen; Mühleisen, Thomas W.; Nöthen, Markus M.; Cupples, L. Adrienne; Caslake, Muriel; Di Angelantonio, Emanuele; Danesh, John; Rotter, Jerome I.; Sigurdsson, Sigurdur; Wong, Quenna; Erbel, Raimund; Kathiresan, Sekar; Melander, Olle; Gudnason, Vilmundur; O'Donnell, Christopher J.; Post, Wendy S.
    Genetic associations with valvular calcification and aortic stenosis
    In: The New England Journal of Medicine Jg. 368 (2013) Nr. 6, S. 503 - 512
    ISSN: 1533-4406; 0028-4793
  • Berndt, Sonja; Gustafsson, Stefan; Magi, Reedik; Ganna, Andrea; Wheeler, Eleanor; Feitosa, Mary; Justice, Anne; Monda, Keri; Croteau-Chonka, Damien; Day, Felix; Pechlivanis, Sonali; Hebebrand, Johannes; Pütter, Carolin; Hinney, Anke; Jöckel, Karl-Heinz; Scherag, Andre
    Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture
    In: Nature Genetics Jg. 45 (2013) Nr. 5, S. 501 - 512
    ISSN: 1061-4036; 1546-1718
  • di Giuseppe, Romina; Pechlivanis, Sonali; Fisher, Eva; Arregui, Maria; Weikert, Beate; Knüppel, Sven; Buijsse, Brian; Fritsche, Andreas; Willich, Stefan N.; Joost, Hans-Georg; Boeing, Heiner; Moebus, Susanne; Weikert, Cornelia
    Microsomal triglyceride transfer protein -164 T > C gene polymorphism and risk of cardiovascular disease : results from the EPIC-Potsdam case-cohort study
    In: BMC Medical Genetics Jg. 14 (2013) Nr. 1, S. 19
    ISSN: 1471-2350
  • Icks, Andrea; Albers, Bernd; Haastert, Burkhard; Pechlivanis, Sonali; Pundt, Noreen; Slomiany, Uta; Erbel, Raimund; Jöckel, Karl-Heinz; Kruse, Johannes; Kulzer, Bernd; Nowotny, Bettina; Herder, Christian; Giani, Guido; Moebus, Susanne
    Risk for High depressive symptoms in diagnosed and previously undetected diabetes : 5-year follow-up results of the Heinz Nixdorf recall study
    In: PLoS ONE Jg. 8 (2013) Nr. 2, S. e56300
    ISSN: 1932-6203
  • Pechlivanis, Sonali; Mühleisen, Thomas W.; Möhlenkamp, Stefan; Schadendorf, Dirk; Erbel, Raimund; Jöckel, Karl-Heinz; Hoffmann, Per; Nöthen, Markus M.; Scherag, Andre; Moebus, Susanne
    Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study
    In: BMC Medical Genetics Jg. 14 (2013) Nr. 1, S. 23
    ISSN: 1471-2350
  • Randall, Joshua; Winkler, Thomas M.; Kutalik, Zoltan; Berndt, Sonja I.; Jackson, Anne U.; Monda, Keri L.; Kilpeläinen, Tuomas O.; Esko, Tuno; Mägi, Reedik; Li, Shengxu; et al.; Scherag, Andre; Erbel, Raimund; Moebus, Susanne; Pechlivanis, Sonali
    Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits
    In: PLoS Genetics Jg. 9 (2013) Nr. 6, S. e1003500
    ISSN: 1553-7404; 1553-7390
  • Hinney, Anke; Scherag, Andre; Jarick, I.; Albayrak, Özgür; Putter, C.; Pechlivanis, Sonali; Dauvermann, M. R.; Beck, S.; Weber, H.; Scherag, S.; Nguyen, T. T.; Volckmar, A. L.; Knoll, N.; Faraone, S. V.; Neale, B. M.; Franke, B.; Cichon, S.; Hoffmann, P.; Nothen, M. M.; Schreiber, S.; Jöckel, Karl-Heinz; Wichmann, H. E.; Freitag, C.; Lempp, T.; Meyer, J.; Gilsbach, S.; Herpertz-Dahlmann, B.; Sinzig, J.; Lehmkuhl, G.; Renner, T. J.; Warnke, A.; Romanos, M.; Lesch, K. P.; Reif, A.; von Schimmelmann, Benno; Hebebrand, Johannes; Psychiat GWAS Consortium, xxx
    Addendum: Genome-wide association study in German patients with attention deficit/hyperactivity disorder
    In: American Journal of Medical Genetics: Part B : Neuropsychiatric Genetics Jg. 159B (2012) Nr. 4, S. 476
    ISSN: 1552-4841; 1552-485X
  • Pechlivanis, Sonali; Erbel, Raimund; Jöckel, Karl-Heinz; Moebus, Susanne; u.a.
    Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
    In: Nature Genetics Jg. 44 (2012) Nr. 9, S. 981 - 990
    ISSN: 1061-4036; 1546-1718
  • Schimming, Tobias T.; Grabellus, Florian; Roßner, Mathias; Pechlivanis, Sonali; Sucker, Antje; Bielefeld, Nicola; Moll, Iris; Schadendorf, Dirk; Hillen, Uwe
    PHH3 immunostaining improves interobserver agreement of mitotic index in thin melanomas
    In: American Journal of Dermatopathology Jg. 34 (2012) Nr. 3, S. 266 - 269
    ISSN: 1533-0311; 0193-1091
  • Heinemann, Anja; Zhao, Fang; Pechlivanis, Sonali; Eberle, Jürgen; Steinle, Alexander; Diederichs, Sven; Schadendorf, Dirk; Paschen, Annette
    Tumor Suppressive MicroRNAs miR-34a/c Control Cancer Cell Expression of ULBP2, a Stress-Induced Ligand of the Natural Killer Cell Receptor NKG2D
    In: Cancer Research Jg. 72 (2012) Nr. 2, S. 460 - 471
    ISSN: 0008-5472; 1538-7445
  • Moebus, Susanne; Möhlenkamp, Stefan; Dragano, N.; Slomiany, U.; Pechlivanis, Sonali; Erbel, Raimund; Mann, Klaus; Jöckel, Karl-Heinz
    Coronary artery calcification and diabetes mellitus : sex-specific impact on incidence of cardiovascular disease – results of the Heinz Nixdorf Recall-Study
    In: Atherosclerosis Supplements Jg. 12 (2011) Nr. 1, S. 63
    ISSN: 1567-5688
  • Hinney, Anke; Scherag, Andre; Jarick, I.; Albayrak, Özgür; Putter, C.; Pechlivanis, Sonali; Dauvermann, M. R.; Beck, S.; Weber, H.; Scherag, S.; Nguyen, T. T.; Volckmar, A. L.; Knoll, N.; Faraone, S. V.; Neale, B. M.; Franke, B.; Cichon, S.; Hoffmann, P.; Nothen, M. M.; Schreiber, S.; Jöckel, Karl-Heinz; Wichmann, H. E.; Freitag, C.; Lempp, T.; Meyer, J.; Gilsbach, S.; Herpertz-Dahlmann, B.; Sinzig, J.; Lehmkuhl, G.; Renner, T. J.; Warnke, A.; Romanos, M.; Lesch, K. P.; Reif, A.; von Schimmelmann, Benno; Hebebrand, Johannes; Psychiat GWAS Consortium, xxx
    Genome-wide association study in German patients with attention deficit/hyperactivity disorder
    In: American Journal of Medical Genetics: Part B : Neuropsychiatric Genetics Jg. 156B (2011) Nr. 8, S. 888 - 897
    ISSN: 1552-4841; 1552-485X
  • Pütter, Carolin; Pechlivanis, Sonali; Nöthen, Markus M.; Jöckel, Karl-Heinz; Wichmann, Heinz-Erich; Scherag, Andre
    Missing Heritability in the Tails of Quantitative Traits? : A Simulation Study on the Impact of Slightly Altered True Genetic Models
    In: Human Heredity Jg. 72 (2011) Nr. 3, S. 173 - 181
    ISSN: 0001-5652; 1423-0062
  • Pechlivanis, Sonali; Scherag, Andre; Mühleisen, Thomas W.; Möhlenkamp, Stefan; Horsthemke, Bernhard; Boes, Tanja; Bröcker-Preuß, Martina; Mann, Klaus; Erbel, Raimund; Jöckel, Karl-Heinz; Nöthen, Markus M.; Moebus, Susanne
    Coronary artery calcification and its relationship to validated genetic variants for diabetes mellitus assessed in the heinz nixdorf recall cohort
    In: Arteriosclerosis, Thrombosis, and Vascular Biology Jg. 30 (2010) Nr. 9, S. 1867 - 1872
    ISSN: 1079-5642; 1524-4636
  • Abstracts

  • Pechlivanis, Sonali; Moebus, Susanne; et.al.
    GWAS meta-analysis yields novel insights into the biology of male-pattern baldness
    In: European Journal of Human Genetics Jg. 26 (2019) Nr. Suppl., S. 761 - 762
    ISSN: 1018-4813
  • Pechlivanis, Sonali; Erbel, Raimund; Nöthen, M.M.; Heilmann-Heimbach, S.; Moebus, Susanne; Hochfeld, L.M.; Mahabadi, Amir Abbas; Jöckel, Karl-Heinz
    Male-pattern baldness and its association with coronary heart disease
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