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Dr. Sonali Pechlivanis

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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

  • Tannemann, Nico; Erbel, Raimund; Nöthen, Markus M.; Jöckel, Karl-Heinz; Pechlivanis, Sonali
    Genetic polymorphisms affecting telomere length and their association with cardiovascular disease in the Heinz-Nixdorf-Recall study
    In: PLoS ONE, Jg. 19, 2024, Nr. 5, e0303357
    DOI (Open Access)
  • Mohren, Lars; Erdlenbruch, Friedrich; Leitão, Elsa; Kilpert, Fabian; Hönes, G. Sebastian; Kaya, Sabine; Schröder, Christopher; Thieme, Andreas; Sturm, Marc; Park, Joohyun; Schlüter, Agatha; Ruiz, Montserrat; Morales de la Prida, Moisés; Casasnovas, Carlos; Becker, Kerstin; Roggenbuck, Ulla; Pechlivanis, Sonali; Kaiser, Frank J.; Synofzik, Matthis; Wirth, Thomas; Anheim, Mathieu; Haack, Tobias B.; Lockhart, Paul J.; Jöckel, Karl-Heinz; Pujol, Aurora; Klebe, Stephan; Timmann, Dagmar; Depienne, Christel
    Identification and characterisation of pathogenic and non-pathogenic FGF14 repeat expansions
    In: Nature Communications, Jg. 15, 2024, Nr. 1, 7665
    DOI, Online Volltext (Open Access)
  • van de Vegte, Yordi J.; Pechlivanis, Sonali; Moebus, Susanne; van der Harst, Pim
    Genetic insights into resting heart rate and its role in cardiovascular disease
    In: Nature Communications, Jg. 14, 2023, Nr. 1, 4646
    DOI (Open Access)
  • Müller, Bernhard W.; 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, 13852
    DOI, Online Volltext (Open Access)
  • Pechlivanis, Sonali; Jung, Dominik; Moebus, Susanne; Lehmann, Nils; Mahabadi, Amir A.; Hoffmann, Per; Erbel, Raimund; Nöthen, Markus M.; Bachmann, Hagen S.
    Pharmacogenetic association of diabetes-associated genetic risk score with rapid progression of coronary artery calcification following treatment with HMG-CoA-reductase inhibitors : Results of the Heinz Nixdorf Recall Study
    In: Naunyn-Schmiedeberg's Archives of Pharmacology, Jg. 394, 2021, Nr. 8, S. 1713 – 1725
    DOI (Open Access)
  • 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
    DOI, Online Volltext (Open Access)
  • 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
    DOI, Online Volltext (Open Access)
  • 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, 19146
    DOI, Online Volltext (Open Access)
  • 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
    DOI, Online Volltext (Open Access)
  • 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
    DOI, Online Volltext (Open Access)
  • 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, 225521
    DOI, Online Volltext (Open Access)
  • 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, 30
    DOI (Open Access)
  • 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
    DOI, Online Volltext (Open Access)
  • 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
  • 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
    DOI (Open Access)
  • 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
    DOI
  • 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: Genomic and Precision Medicine, Jg. 10, 2017, Nr. 2
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • Gaulton, Kyle J.; Ferreira, Teresa; Lee, Yeji; Raimondo, Anne; Mägi, Reedik; Reschen, Michael E.; Mahajan, Anubha; Locke, Adam; Rayner, N. William; Robertson, Neil; Scott, Robert A.; Prokopenko, Inga; Scott, Laura J.; Green, Todd; Sparso, Thomas; Thuillier, Dorothee; Yengo, Loic; Grallert, Harald; Wahl, Simone; Frånberg, Mattias; Strawbridge, Rona J.; Kestler, Hans; Chheda, Himanshu; Eisele, Lewin; Gustafsson, Stefan; Steinthorsdottir, Valgerdur; Thorleifsson, Gudmar; Qi, Lu; Karssen, Lennart C.; Van Leeuwen, Elisabeth M.; Willems, Sara M.; Li, Man; Chen, Han; Fuchsberger, Christian; Kwan, Phoenix; Ma, Clement; Linderman, Michael; Lu, Yingchang; Thomsen, Soren K.; Rundle, Jana K.; Beer, Nicola L.; Van De Bunt, Martijn; Chalisey, Anil; Kang, Hyun Min; Voight, Benjamin F.; Abecasis, Gonçalo R.; Almgren, Peter; Baldassarre, Damiano; Balkau, Beverley; Benediktsson, Rafn; Blüher, Matthias; Boeing, Heiner; Bonnycastle, Lori L.; Bottinger, Erwin P.; Burtt, Noël P.; Carey, Jason; Charpentier, Guillaume; Chines, Peter S.; Cornelis, Marilyn C.; Couper, David J.; Crenshaw, Andrew T.; Van Dam, Rob M.; Doney, Alex S. F.; Dorkhan, Mozhgan; Edkins, Sarah; Eriksson, Johan G.; Esko, Tonu; Eury, Elodie; Fadista, João; Flannick, Jason; Fontanillas, Pierre; Fox, Caroline; Franks, Paul W.; Gertow, Karl; Gieger, Christian; Gigante, Bruna; Gottesman, Omri; Grant, George B.; Grarup, Niels; Groves, Christopher J.; Hassinen, Maija; Have, Christian T.; Herder, Christian; Holmen, Oddgeir L.; Hreidarsson, Astradur B.; Humphries, Steve E.; Hunter, David J.; Jackson, Anne U.; Jonsson, Anna; Jørgensen, Marit E.; Jørgensen, Torben; Kao, Wen-Hong L.; Kerrison, Nicola D.; Kinnunen, Leena; Klopp, Norman; Kong, Augustine; Kovacs, Peter; Kraft, Peter; Kravic, Jasmina; Langford, Cordelia; Leander, Karin; Liang, Liming; Lichtner, Peter; Lindgren, Cecilia M.; Lindholm, Eero; Linneberg, Allan; Liu, Ching-Ti; Lobbens, Stéphane; Luan, Jian'fan; Lyssenko, Valeriya; Männistö, Satu; McLeod, Olga; Meyer, Julia; Mihailov, Evelin; Mirza, Ghazala; Mühleisen, Thomas W.; Müller-Nurasyid, Martina; Navarro, Carmen; Nöthen, Markus M.; Oskolkov, Nikolay N.; Owen, Katharine R.; Palli, Domenico; Pechlivanis, Sonali; Peltonen, Leena; Perry, John R. B.; Platou, Carl G. P.; Roden, Michael; Ruderfer, Douglas; Rybin, Denis; Van Der Schouw, Yvonne T.; Sennblad, Bengt; Sigurosson, Gunnar; Stančáková, Alena; Steinbach, Gerald; Storm, Petter; Strauch, Konstantin; Stringham, Heather M.; Sun, Qi; Thorand, Barbara; Tikkanen, Emmi; Tonjes, Anke; Trakalo, Joseph; Tremoli, Elena; Tuomi, Tiinamaija; Wennauer, Roman; Wiltshire, Steven; Wood, Andrew R.; Zeggini, Eleftheria; Dunham, Ian; Birney, Ewan; Pasquali, Lorenzo; Ferrer, Jorge; Loos, Ruth J. F.; Dupuis, Josée; Florez, Jose C.; Boerwinkle, Eric; Pankow, James S.; Van Duijn, Cornelia; Sijbrands, Eric; Meigs, James B.; Hu, Frank B.; Thorsteinsdottir, Unnur; Stefansson, Kari; Lakka, Timo A.; Rauramaa, Rainer; Stumvoll, Michael; Pedersen, Nancy L.; Lind, Lars; Keinanen-Kiukaanniemi, Sirkka M.; Korpi-Hyövälti, Eeva; Saaristo, Timo E.; Saltevo, Juha; Kuusisto, Johanna; Laakso, Markku; Metspalu, Andres; Erbel, Raimund; Jöckel, Karl-Heinz; Moebus, Susanne; Ripatti, Samuli; Salomaa, Veikko; Ingelsson, Erik; Boehm, Bernhard O.; Bergman, Richard N.; Collins, Francis S.; Mohlke, Karen L.; Koistinen, Heikki; Tuomilehto, Jaakko; Hveem, Kristian; Njølstad, Inger; Deloukas, Panagiotis; Donnelly, Peter J.; Frayling, Timothy M.; Hattersley, Andrew T.; De Faire, Ulf; Hamsten, Anders; Illig, Thomas; Peters, Annette; Cauchi, Stephane; Sladek, Rob; Froguel, Philippe; Hansen, Torben; Pedersen, Oluf; Morris, Andrew D.; Palmer, Collin N. A.; Kathiresan, Sekar; Melander, Olle; Nilsson, Peter M.; Groop, Leif C.; Barroso, Inês; Langenberg, Claudia; Wareham, Nicholas J.; O'Callaghan, Christopher A.; Gloyn, Anna L.; Altshuler, David; Boehnke, Michael; Teslovich, Tanya M.; McCarthy, Mark I.; Morris, Andrew P.
    Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci
    In: Nature Genetics, Jg. 47, 2015, Nr. 12, S. 1415 – 1425
    DOI, Online Volltext (Open Access)
  • 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
    DOI, Online Volltext (Open Access)
  • 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
    DOI, Online Volltext (Open Access)
  • 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
    DOI
  • 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
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI, Online Volltext (Open Access)
  • 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
    DOI
  • 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
    DOI
  • 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
    DOI
  • 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
    DOI
  • 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
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • 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
    DOI (Open Access)
  • Randall, Joshua; Winkler, Thomas M.; Kutalik, Zoltan; Scherag, Andre; Erbel, Raimund; Moebus, Susanne; Pechlivanis, Sonali; Loos, Ruth J. F.; Lindgren, Cecilia M.; North, Kari E.; Heid, Iris M.; et al.
    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, e1003500
    DOI (Open Access)
  • 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
    DOI
  • 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
    DOI
  • 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
    DOI
  • 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
    DOI
  • 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
    DOI
  • 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
    DOI
  • 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
    DOI
  • 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
    DOI (Open Access)

    • 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. Basingstoke: Nature Publishing Group, Jg. 26, 2019, Nr. Suppl., S. 761 – 762
    DOI (Open Access)
  • 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
    In: Journal of Investigative Dermatology. Amsterdam: Elsevier, Jg. 137, 2017, Nr. 10 Suppl. 2, S. S239
    DOI (Open Access)
  • Pechlivanis, Sonali; Scherag, Andre; Miihleisen, T. W.; Möhlenkamp, Stefan; Erbel, Raimund; Jöckel, Karl-Heinz; Nothen, M. M.; Moebus, Susanne
    Association of Diabetes-Mellitus-Related genetic variants with coronary artery calcification
    In: Atherosclerosis Supplements: Elsevier, Jg. 12, 2011, Nr. 1, S. 128
    DOI