Resultados da busca - Sebastian Zöllner

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  1. 1
    Coalescent-Based Association Mapping and Fine Mapping of Complex Trait Loci

    Coalescent-Based Association Mapping and Fine Mapping of Complex Trait Loci por Sebastian Zöllner, Jonathan K. Pritchard

    Publicado em 2004
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  2. 2
    Overcoming the Winner’s Curse: Estimating Penetrance Parameters from Case-Control Data

    Overcoming the Winner’s Curse: Estimating Penetrance Parameters from Case-Control Data por Sebastian Zöllner, Jonathan K. Pritchard

    Publicado em 2007
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  3. 3
    A Quantitative Comparison of the Similarity between Genes and Geography in Worldwide Human Populations

    A Quantitative Comparison of the Similarity between Genes and Geography in Worldwide Human Populations por Chaolong Wang, Sebastian Zöllner, Noah A. Rosenberg

    Publicado em 2012
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  4. 4
    Mapping Genes through the Use of Linkage Disequilibrium Generated by Genetic Drift: ‘Drift Mapping’ in Small Populations with No Demographic Expansion

    Mapping Genes through the Use of Linkage Disequilibrium Generated by Genetic Drift: ‘Drift Mapping’ in Small Populations with No Demographic Expansion por Joseph D. Terwilliger, Sebastian Zöllner, Maris Laan, Svante Pääbo

    Publicado em 1998
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  5. 5
    Signatures of Domain Shuffling in the Human Genome

    Signatures of Domain Shuffling in the Human Genome por Henrik Kaessmann, Sebastian Zöllner, Anton Nekrutenko, Wen‐Hsiung Li

    Publicado em 2002
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  6. 6
    Mouse segmental duplication and copy number variation

    Mouse segmental duplication and copy number variation por Xinwei She, Ze Cheng, Sebastian Zöllner, Deanna M. Church, Evan E. Eichler

    Publicado em 2008
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  7. 7
    Selection on Human Genes as Revealed by Comparisons to Chimpanzee cDNA

    Selection on Human Genes as Revealed by Comparisons to Chimpanzee cDNA por Ines Hellmann, Sebastian Zöllner, Wolfgang Enard, Ingo Ebersberger, Birgit Nickel, Svante Pääbo

    Publicado em 2003
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  8. 8
    Extending Rare-Variant Testing Strategies: Analysis of Noncoding Sequence and Imputed Genotypes

    Extending Rare-Variant Testing Strategies: Analysis of Noncoding Sequence and Imputed Genotypes por Matthew Zawistowski, Shyam Gopalakrishnan, Jun Ding, Yun Li, Sara A. Grimm, Sebastian Zöllner

    Publicado em 2010
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  9. 9
    Evidence for Extensive Transmission Distortion in the Human Genome

    Evidence for Extensive Transmission Distortion in the Human Genome por Sebastian Zöllner, Xiaoquan Wen, Neil A. Hanchard, Mark Herbert, Carole Ober, Jonathan K. Pritchard

    Publicado em 2004
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  10. 10
    Extensive Linkage Disequilibrium in Small Human Populations in Eurasia

    Extensive Linkage Disequilibrium in Small Human Populations in Eurasia por Henrik Kaessmann, Sebastian Zöllner, Anna Gustafsson, Victor Wiebe, Maris Laan, Joakim Lundeberg, Mathias Uhlén, Svante Pääbo

    Publicado em 2002
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  11. 11
    Long Runs of Homozygosity Are Enriched for Deleterious Variation

    Long Runs of Homozygosity Are Enriched for Deleterious Variation por Zachary A. Szpiech, Jishu Xu, Trevor J. Pemberton, Weiping Peng, Sebastian Zöllner, Noah A. Rosenberg, Jun Z. Li

    Publicado em 2013
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  12. 12
    Genome-wide significance testing of variation from single case exomes

    Genome-wide significance testing of variation from single case exomes por Amy B. Wilfert, Katherine R. Chao, Madhurima Kaushal, Sanjay Jain, Sebastian Zöllner, David R. Adams, Donald F. Conrad

    Publicado em 2016
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  13. 13
    PNPLA3 Risk Allele Association With ALT Response to Semaglutide Treatment

    PNPLA3 Risk Allele Association With ALT Response to Semaglutide Treatment por Esteban Urias, Nicholas R. Tedesco, Antonino Oliveri, Chinmay Raut, Matthew Zawistowski, Sebastian Zöllner, Elizabeth K. Speliotes, Vincent Chen

    Publicado em 2023
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  14. 14
    Risk Factors Associated With Metabolic Syndrome in Bipolar and Schizophrenia Subjects Treated With Antipsychotics

    Risk Factors Associated With Metabolic Syndrome in Bipolar and Schizophrenia Subjects Treated With Antipsychotics por Vicki L. Ellingrod, Stephan F. Taylor, Gregory W. Dalack, Tyler Grove, Michael J. Bly, Robert D. Brook, Sebastian Zöllner, Rodica Pop‐Busui

    Publicado em 2012
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  15. 15
    The influence of genomic context on mutation patterns in the human genome inferred from rare variants

    The influence of genomic context on mutation patterns in the human genome inferred from rare variants por 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

    Publicado em 2013
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  16. 16
    Metabolic syndrome in bipolar disorder and schizophrenia: dietary and lifestyle factors compared to the general population

    Metabolic syndrome in bipolar disorder and schizophrenia: dietary and lifestyle factors compared to the general population por 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

    Publicado em 2013
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  17. 17
    The Michigan Genomics Initiative: A biobank linking genotypes and electronic clinical records in Michigan Medicine patients

    The Michigan Genomics Initiative: A biobank linking genotypes and electronic clinical records in Michigan Medicine patients por 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

    Publicado em 2023
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  18. 18
    Ancestry estimation and control of population stratification for sequence-based association studies

    Ancestry estimation and control of population stratification for sequence-based association studies por 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

    Publicado em 2014
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  19. 19
    Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries

    Multi-ancestry meta-analysis identifies 5 novel loci for ischemic stroke and reveals heterogeneity of effects between sexes and ancestries por 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

    Publicado em 2023
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  20. 20
    Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans

    Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans por 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

    Publicado em 2018
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