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The last 5 uploaded publications
A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies
Xihao Li, Han Chen, Margaret Sunitha Selvaraj, Eric Van Buren, Hufeng Zhou, Yuxuan Wang, Ryan Sun, Zachary R. McCaw, Zhi Yu, Min-Zhi Jiang, Daniel DiCorpo, Sheila M. Gaynor, Rounak Dey, Donna K. Arnett, Emelia Benjamin, Joshua C. Bis, John Blangero, Eric Boerwinkle, Donald W. Bowden, Jennifer A. Brody, Brian E. Cade, April P. Carson, Jenna C. Carlson, Nathalie Chami, Yii‐Der Ida Chen, Joanne E. Curran, Paul S. de Vries, Myriam Fornage, Nora Franceschini, Barry I. Freedman, C. Charles Gu, Nancy L. Heard‐Costa, Jiang He, Lifang Hou, Yi-Jen Hung, Marguerite R. Irvin, Robert C. Kaplan, Sharon L.R. Kardia, Tanika N. Kelly, Iain R. Konigsberg, Charles Kooperberg, Brian G. Kral, Changwei Li, Yun Li, Honghuang Lin, Yongmei Liu, Ruth J. F. Loos, Michael C. Mahaney, Lisa W. Martin, Rasika A. Mathias, Braxton D. Mitchell, May E. Montasser, Alanna C. Morrison, Take Naseri, Kari E. North, Patricia A. Peyser, Bruce M. Psaty, Susan Redline, Alexander P. Reiner, Stephen S. Rich, Colleen M. Sitlani, Albert V. Smith, Kent D. Taylor, Hemant K. Tiwari, Ramachandran S. Vasan, Satupaitea Viali, Zhe Wang, Jennifer Wessel, Lisa R. Yanek, Bing Yu, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Christine M. Albert, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan E. Arking, Allison E. Ashley‐Koch, Stella Aslibekyan, Tim Assimes, Dimitrios Avramopoulos, Najib Ayas, Adithya Balasubramanian, J. A. Barnard, Kathleen C. Barnes, R. Graham Barr, Emily Barron‐Casella, Lucas Barwick, Terri H. Beaty, Gerald J. Beck, Diane M. Becker, Lewis C. Becker, Rebecca Beer, Amber L. Beitelshees (2025). A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies. , 5(2), DOI: https://doi.org/10.1038/s43588-024-00764-8.
Article44 days agoWhole genome sequencing based analysis of inflammation biomarkers in the Trans-Omics for Precision Medicine (TOPMed) consortium.
Min-Zhi Jiang, Sheila M. Gaynor, Xihao Li, Eric Van Buren, A.M. Stilp, Erin Buth, Fei Fei Wang, Regina Manansala, Stephanie M. Gogarten, Zilin Li, Linda M. Polfus, Shabnam Salimi, Joshua C. Bis, Nathan Pankratz, Lisa R. Yanek, Peter Durda, Russell P. Tracy, Stephen S. Rich, Jerome I. Rotter, Braxton D. Mitchell, Joshua P. Lewis, Bruce M. Psaty, Katherine Pratte, Edwin K. Silverman, Robert C. Kaplan, Christy L. Avery, Kari E. North, Rasika A. Mathias, Nauder Faraday, Honghuang Lin, Biqi Wang, April P. Carson, Arnita F. Norwood, Richard A. Gibbs, Charles Kooperberg, Jessica I. Lundin, Annette Peters, Josée Dupuis, Lifang Hou, Myriam Fornage, Emelia Benjamin, Alexander P. Reiner, Russell P. Bowler, Xihong Lin, Paul L. Auer, Laura M. Raffield (2024). Whole genome sequencing based analysis of inflammation biomarkers in the Trans-Omics for Precision Medicine (TOPMed) consortium.. , 33(16), DOI: https://doi.org/10.1093/hmg/ddae050.
Article44 days agoWhole Genome Sequencing Based Analysis of Inflammation Biomarkers in the Trans-Omics for Precision Medicine (TOPMed) Consortium
Min-Zhi Jiang, Sheila M. Gaynor, Xihao Li, Eric Van Buren, Adrienne M. Stilp, Erin Buth, Fei Fei Wang, Regina Manansala, Stephanie M. Gogarten, Zilin Li, Linda M. Polfus, Shabnam Salimi, Joshua C. Bis, Nathan Pankratz, Lisa R. Yanek, Peter Durda, Russell P. Tracy, Stephen S. Rich, Jerome I. Rotter, Braxton D. Mitchell, Joshua P. Lewis, Bruce M. Psaty, Katherine Pratte, Edwin K. Silverman, Robert C. Kaplan, Christy L. Avery, Kari North, Rasika A. Mathias, Nauder Faraday, Honghuang Lin, Biqi Wang, April P. Carson, Arnita F. Norwood, Richard A. Gibbs, Charles Kooperberg, Jessica Lundin, Ulrike Peters, Josée Dupuis, Lifang Hou, Myriam Fornage, Emelia Benjamin, Alexander P. Reiner, Russell P. Bowler, Xihong Lin, Paul L. Auer, Laura M. Raffield (2023). Whole Genome Sequencing Based Analysis of Inflammation Biomarkers in the Trans-Omics for Precision Medicine (TOPMed) Consortium. , DOI: https://doi.org/10.1101/2023.09.10.555215.
Preprint44 days agoPowerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies
Xihao Li, Corbin Quick, Hufeng Zhou, Sheila M. Gaynor, Yaowu Liu, Han Chen, Margaret Sunitha Selvaraj, Ryan Sun, Rounak Dey, Donna K. Arnett, Lawrence F. Bielak, Joshua C. Bis, John Blangero, Eric Boerwinkle, Donald W. Bowden, Jennifer A. Brody, Brian E. Cade, Adolfo Correa, L. Adrienne Cupples, Joanne E. Curran, Paul S. de Vries, Ravindranath Duggirala, Barry I. Freedman, Harald H.H. Göring, Xiuqing Guo, Jeffrey Haessler, Rita R. Kalyani, Charles Kooperberg, Brian G. Kral, Leslie A. Lange, Ani Manichaikul, Lisa W. Martin, Stephen T. McGarvey, Braxton D. Mitchell, May E. Montasser, Alanna C. Morrison, Take Naseri, Jeffrey R. O’Connell, Patricia A. Peyser, Bruce M. Psaty, Laura M. Raffield, Susan Redline, Alexander P. Reiner, Muagututi‘a Sefuiva Reupena, Kenneth Rice, Stephen S. Rich, Colleen M. Sitlani, Jennifer A. Smith, Kent D. Taylor, Ramachandran S. Vasan, Cristen J. Willer, James G. Wilson, Lisa R. Yanek, Wei Zhao, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Christine M. Albert, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan E. Arking, Allison E. Ashley‐Koch, Stella Aslibekyan, Tim Assimes, Paul L. Auer, Dimitrios Avramopoulos, Najib Ayas, Adithya Balasubramanian, John Barnard, Kathleen C. Barnes, R. Graham Barr, Emily Barron‐Casella, Lucas Barwick, Terri H. Beaty, Gerald J. Beck, Diane M. Becker, Lewis C. Becker, Rebecca Beer, Amber L. Beitelshees, Emelia Benjamin, Takis Benos, Marcos Bezerra, Thomas W. Blackwell, Nathan R. Blue, Russell P. Bowler, Ulrich Broeckel, Jai Broome, Deborah Brown, Karen Bunting, Esteban G. Burchard, Carlos D. Bustamante, Erin Buth, Jonathan Cardwell, Vincent J. Carey (2022). Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies. , 55(1), DOI: https://doi.org/10.1038/s41588-022-01225-6.
Article44 days agoA framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies
Zilin Li, Xihao Li, Hufeng Zhou, Sheila M. Gaynor, Margaret Sunitha Selvaraj, Theodore Arapoglou, Corbin Quick, Yaowu Liu, Han Chen, Ryan Sun, Rounak Dey, Donna K. Arnett, Paul L. Auer, Lawrence F. Bielak, Joshua C. Bis, Thomas W. Blackwell, John Blangero, Eric Boerwinkle, Donald W. Bowden, Jennifer A. Brody, Brian E. Cade, Matthew P. Conomos, Adolfo Correa, L. Adrienne Cupples, Joanne E. Curran, Paul S. de Vries, Ravindranath Duggirala, Nora Franceschini, Barry I. Freedman, Harald H.H. Göring, Xiuqing Guo, Rita R. Kalyani, Charles Kooperberg, Brian G. Kral, Leslie A. Lange, Bridget M. Lin, Ani Manichaikul, Alisa K. Manning, Lisa W. Martin, Rasika A. Mathias, James B. Meigs, Braxton D. Mitchell, May E. Montasser, Alanna C. Morrison, Take Naseri, Jeffrey R. O’Connell, Patricia A. Peyser, Bruce M. Psaty, Laura M. Raffield, Susan Redline, Alexander P. Reiner, Muagututi‘a Sefuiva Reupena, Kenneth Rice, Stephen S. Rich, Jennifer A. Smith, Kent D. Taylor, Margaret A. Taub, Ramachandran S. Vasan, Daniel E. Weeks, James G. Wilson, Lisa R. Yanek, Wei Zhao, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Christine M. Albert, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan E. Arking, Allison E. Ashley‐Koch, Stella Aslibekyan, Tim Assimes, Dimitrios Avramopoulos, Najib Ayas, Adithya Balasubramanian, John Barnard, Kathleen C. Barnes, R. Graham Barr, Emily Barron‐Casella, Lucas Barwick, Terri H. Beaty, Gerald J. Beck, Diane M. Becker, Lewis C. Becker, Rebecca Beer, Amber L. Beitelshees, Emelia Benjamin, Takis Benos, Marcos Bezerra, Nathan R. Blue, Russell P. Bowler, Ulrich Broeckel, Jai Broome, Deborah Brown (2022). A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies. , 19(12), DOI: https://doi.org/10.1038/s41592-022-01640-x.
Article44 days ago