检索结果 - Zawistowski, Matthew

A geometric framework for evaluating rare variant tests of association 由 Liu, Keli, Fast, Shannon, Zawistowski, Matthew, Tintle, Nathan L.

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A Coalescent Model for Genotype Imputation 由 Jewett, Ethan M., Zawistowski, Matthew, Rosenberg, Noah A., Zöllner, Sebastian

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

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Leveraging summary statistics to make inferences about complex phenotypes in large biobanks 由 Gasdaska, Angela, Friend, Derek, Chen, Rachel, Westra, Jason, Zawistowski, Matthew, Lindsey, William, Tintle, Nathan

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Genome-Wide Association Study of Pelvic Organ Prolapse using the Michigan Genomics Initiative 由 Cox, Caroline K., Pandit, Anita, Zawistowski, Matthew, Dutta, Diptavo, Narla, Goutham, Swenson, Carolyn W.

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The Veterans Affairs Cardiac Risk Score: Recalibrating the ASCVD Score for Applied Use 由 Sussman, Jeremy B., Wiitala, Wyndy L., Zawistowski, Matthew, Hofer, Timothy P., Bentley, Douglas, Hayward, Rodney A.

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Analysis of rare variant population structure in Europeans explains differential stratification of gene-based tests 由 Zawistowski, Matthew, Reppell, Mark, Wegmann, Daniel, St Jean, Pamela L, Ehm, Margaret G, Nelson, Matthew R, Novembre, John, Zöllner, Sebastian

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The influence of genomic context on mutation patterns in the human genome inferred from rare variants 由 Schaibley, Valerie M., Zawistowski, Matthew, Wegmann, Daniel, Ehm, Margaret G., Nelson, Matthew R., St. Jean, Pamela L., Abecasis, Gonçalo R., Novembre, John, Zöllner, Sebastian, Li, Jun Z.

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Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans 由 Carlson, Jedidiah, Locke, Adam E., Flickinger, Matthew, Zawistowski, Matthew, Levy, Shawn, Myers, Richard M., Boehnke, Michael, Kang, Hyun Min, Scott, Laura J., Li, Jun Z., Zöllner, Sebastian

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Meta-MultiSKAT: Multiple phenotype meta-analysis for region-based association test 由 Dutta, Diptavo, Taliun, Sarah A. Gagliano, Weinstock, Joshua S., Zawistowski, Matthew, Sidore, Carlo, Fritsche, Lars G., Cucca, Francesco, Schlessinger, David, Abecasis, Gonçalo R., Brummett, Chad M., Lee, Seunggeun

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A rare coding allele in IFIH1 is protective for psoriatic arthritis 由 Budu-Aggrey, Ashley, Bowes, John, Stuart, Philip E, Zawistowski, Matthew, Tsoi, Lam C, Nair, Rajan, Jadon, Deepak Rohit, McHugh, Neil, Korendowych, Eleanor, Elder, James T, Barton, Anne, Raychaudhuri, Soumya

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Association of Polygenic Risk Scores for Multiple Cancers in a Phenome-wide Study: Results from The Michigan Genomics Initiative 由 Fritsche, Lars G., Gruber, Stephen B., Wu, Zhenke, Schmidt, Ellen M., Zawistowski, Matthew, Moser, Stephanie E., Blanc, Victoria M., Brummett, Chad M., Kheterpal, Sachin, Abecasis, Gonçalo R., Mukherjee, Bhramar

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LabWAS: Novel findings and study design recommendations from a meta-analysis of clinical labs in two independent biobanks 由 Goldstein, Jeffery A., Weinstock, Joshua S., Bastarache, Lisa A., Larach, Daniel B., Fritsche, Lars G., Schmidt, Ellen M., Brummett, Chad M., Kheterpal, Sachin, Abecasis, Goncalo R., Denny, Joshua C., Zawistowski, Matthew

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Methods for Association Analysis and Meta-Analysis of Rare Variants in Families 由 Feng, Shuang, Pistis, Giorgio, Zhang, He, Zawistowski, Matthew, Mulas, Antonella, Zoledziewska, Magdalena, Holmen, Oddgeir L., Busonero, Fabio, Sanna, Serena, Hveem, Kristian, Willer, Cristen, Cucca, Francesco, Liu, Dajiang J., Abecasis, Gonçalo R.

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Characterization of ADME gene variation in 21 populations by exome sequencing 由 Hovelson, Daniel H., Xue, Zhengyu, Zawistowski, Matthew, Ehm, Margaret G., Harris, Elizabeth C., Stocker, Sophie L., Gross, Annette S., Jang, In-Jin, Ieiri, Ichiro, Lee, Jong-Eun, Cardon, Lon R., Chissoe, Stephanie L., Abecasis, Gonçalo, Nelson, Matthew R.

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Exploring various polygenic risk scores for skin cancer in the phenomes of the Michigan genomics initiative and the UK Biobank with a visual catalog: PRSWeb 由 Fritsche, Lars G., Beesley, Lauren J., VandeHaar, Peter, Peng, Robert B., Salvatore, Maxwell, Zawistowski, Matthew, Gagliano Taliun, Sarah A., Das, Sayantan, LeFaive, Jonathon, Kaleba, Erin O., Klumpner, Thomas T., Moser, Stephanie E., Blanc, Victoria M., Brummett, Chad M., Kheterpal, Sachin, Abecasis, Gonçalo R., Gruber, Stephen B., Mukherjee, Bhramar

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Meta-Analysis of Gene Level Tests for Rare Variant Association 由 Liu, Dajiang J., Peloso, Gina M., Zhan, Xiaowei, Holmen, Oddgeir L., Zawistowski, Matthew, Feng, Shuang, Nikpay, Majid, Auer, Paul L., Goel, Anuj, Zhang, He, Peters, Ulrike, Farrall, Martin, Orho-Melander, Marju, Kooperberg, Charles, McPherson, Ruth, Watkins, Hugh, Willer, Cristen J., Hveem, Kristian, Melander, Olle, Kathiresan, Sekar, Abecasis, Gonçalo R.

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Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis 由 Graham, Sarah E., Nielsen, Jonas B., Zawistowski, Matthew, Zhou, Wei, Fritsche, Lars G., Gabrielsen, Maiken E., Skogholt, Anne Heidi, Surakka, Ida, Hornsby, Whitney E., Fermin, Damian, Larach, Daniel B., Kheterpal, Sachin, Brummett, Chad M., Lee, Seunggeun, Kang, Hyun Min, Abecasis, Goncalo R., Romundstad, Solfrid, Hallan, Stein, Sampson, Matthew G., Hveem, Kristian, Willer, Cristen J.

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Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction 由 Saw, Jacqueline, Yang, Min-Lee, Trinder, Mark, Tcheandjieu, Catherine, Xu, Chang, Starovoytov, Andrew, Birt, Isabelle, Mathis, Michael R., Hunker, Kristina L., Schmidt, Ellen M., Jackson, Linda, Fendrikova-Mahlay, Natalia, Zawistowski, Matthew, Brummett, Chad M., Zoellner, Sebastian, Katz, Alexander, Coleman, Dawn M., Swan, Kirby, O’Donnell, Christopher J., Zhou, Xiang, Li, Jun Z., Gornik, Heather L., Assimes, Themistocles L., Stanley, James C., Brunham, Liam R., Ganesh, Santhi K.

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Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders 由 Eijsbouts, Chris, Zheng, Tenghao, Kennedy, Nicholas A., Bonfiglio, Ferdinando, Anderson, Carl A., Moutsianas, Loukas, Holliday, Joanne, Shi, Jingchunzi, Shringarpure, Suyash, Voda, Alexandru-Ioan, Farrugia, Gianrico, Franke, Andre, Hübenthal, Matthias, Abecasis, Gonçalo, Zawistowski, Matthew, Skogholt, Anne Heidi, Ness-Jensen, Eivind, Hveem, Kristian, Esko, Tõnu, Teder-Laving, Maris, Zhernakova, Alexandra, Camilleri, Michael, Boeckxstaens, Guy, Whorwell, Peter J., Spiller, Robin, McVean, Gil, D’Amato, Mauro, Jostins, Luke, Parkes, Miles

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