Search Results - Sebastian Zöllner
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Mouse segmental duplication and copy number variation by Xinwei She, Ze Cheng, Sebastian Zöllner, Deanna M. Church, Evan E. Eichler
Published 2008Artigo -
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The influence of genomic context on mutation patterns in the human genome inferred from rare variants by Valerie M. Schaibley, Matthew Zawistowski, Daniel Wegmann, Margaret G. Ehm, Matthew R. Nelson, Pamela L. St. Jean, Gonçalo R. Abecasis, John Novembre, Sebastian Zöllner, Jun Z. Li
Published 2013Artigo -
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Metabolic syndrome in bipolar disorder and schizophrenia: dietary and lifestyle factors compared to the general population by Michael J. Bly, Stephan F. Taylor, Gregory W. Dalack, Rodica Pop‐Busui, Kyle J. Burghardt, Simon J. Evans, Melvin I McInnis, Tyler Grove, Robert D. Brook, Sebastian Zöllner, Vicki L. Ellingrod
Published 2013Artigo -
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The Michigan Genomics Initiative: A biobank linking genotypes and electronic clinical records in Michigan Medicine patients by Matthew Zawistowski, Lars G. Fritsche, Anita Pandit, Brett Vanderwerff, Snehal Patil, Ellen M. Schmidt, Peter VandeHaar, Cristen J. Willer, Chad M. Brummett, Sachin Kheterpal, Xiang Zhou, Michael Boehnke, Gonçalo R. Abecasis, Sebastian Zöllner
Published 2023Artigo -
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Ancestry estimation and control of population stratification for sequence-based association studies by Chaolong Wang, Xiaowei Zhan, Jennifer L. Bragg‐Gresham, Hyun Min Kang, Dwight Stambolian, Emily Y. Chew, Kari Branham, John R. Heckenlively, Robert S. Fulton, Richard K. Wilson, Elaine R. Mardis, Xihong Lin, Anand Swaroop, Sebastian Zöllner, Gonçalo R. Abecasis
Published 2014Artigo -
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Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries by Ida Surakka, Kuan-Han Wu, Whitney Hornsby, Brooke N. Wolford, Fred Y. Shen, Wei Zhou, Jennifer E. Huffman, Anita Pandit, Yao Hu, Ben Brumpton, Anne Heidi Skogholt, Maiken E. Gabrielsen, Robin Walters, Kristian Hveem, Charles Kooperberg, Sebastian Zöllner, Peter W.F. Wilson, Nadia R. Sutton, Mark J. Daly, Benjamin M. Neale, Cristen J. Willer
Published 2023Artigo -
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Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans by Jedidiah Carlson, Adam E. Locke, Matthew Flickinger, Matthew Zawistowski, Shawn Levy, R Myers, Michael Boehnke, Hyun Min Kang, Laura J. Scott, Jun Z. Li, Sebastian Zöllner, Devin Absher, Huda Akil, Gerome Breen, Margit Burmeister, Sarah Cohen‐Woods, William G. Iacono, James A. Knowles, Lisa N. Legrand, Qing Lu, Matthew McGue, Melvin G. McInnis, Carlos N. Pato, Michele T. Pato, Margarita Rivera, Janet L. Sobell, John B. Vincent, Stanley J. Watson
Published 2018Artigo
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