Identifying intragenic functional modules of genomic variations associated with cancer phenotypes by learning representation of association networks

por Kim, Minsu, Huffman, Jennifer E., Justice, Amy, Goethert, Ian, Agasthya, Greeshma, Danciu, Ioana
Publicado 2022

The total burden of rare, non-synonymous exome genetic variants is not associated with childhood or late-life cognitive ability

por Marioni, Riccardo E., Penke, Lars, Davies, Gail, Huffman, Jennifer E., Hayward, Caroline, Deary, Ian J.
Publicado 2014

Recent genomic heritage in Scotland

por Amador, Carmen, Huffman, Jennifer, Trochet, Holly, Campbell, Archie, Porteous, David, Wilson, James F, Hastie, Nick, Vitart, Veronique, Hayward, Caroline, Navarro, Pau, Haley, Chris S
Publicado 2015

Pedigree- and SNP-Associated Genetics and Recent Environment are the Major Contributors to Anthropometric and Cardiometabolic Trait Variation

por Xia, Charley, Amador, Carmen, Huffman, Jennifer, Trochet, Holly, Campbell, Archie, Porteous, David, Hastie, Nicholas D., Hayward, Caroline, Vitart, Veronique, Navarro, Pau, Haley, Chris S.
Publicado 2016

Alternative splicing of OAS1 alters the risk for severe COVID-19

por Huffman, Jennifer, Butler-Laporte, Guillaume, Khan, Atlas, Drivas, Theodore G., Peloso, Gina M., Nakanishi, Tomoko, Verma, Anurag, Kiryluk, Krzysztof, Richards, J. Brent, Zeberg, Hugo
Publicado 2021

Correction: Pedigree- and SNP-Associated Genetics and Recent Environment are the Major Contributors to Anthropometric and Cardiometabolic Trait Variation

por Xia, Charley, Amador, Carmen, Huffman, Jennifer, Trochet, Holly, Campbell, Archie, Porteous, David, Scotland, Generation, Hastie, Nicholas D., Hayward, Caroline, Vitart, Veronique, Navarro, Pau, Haley, Chris S.
Publicado 2017

Uncovering Networks from Genome-Wide Association Studies via Circular Genomic Permutation

por Cabrera, Claudia P., Navarro, Pau, Huffman, Jennifer E., Wright, Alan F., Hayward, Caroline, Campbell, Harry, Wilson, James F., Rudan, Igor, Hastie, Nicholas D., Vitart, Veronique, Haley, Chris S.
Publicado 2012

Ferric citrate controls serum phosphorus in dialysis patients: retrospective data

por Hain, Debra J., Marinaro, Meredith, Koeper, David W., Rosenthal, Melissa A., Chillemi, Salvatore, Huffman, Jennifer M., Gerbeling, Teresa, Pritsiolas, James M., Loram, Lisa C., Pergola, Pablo E.
Publicado 2017

Rare coding variants pinpoint genes that control human hematological traits

por Mousas, Abdou, Ntritsos, Georgios, Chen, Ming-Huei, Song, Ci, Huffman, Jennifer E., Tzoulaki, Ioanna, Elliott, Paul, Psaty, Bruce M., Auer, Paul L., Johnson, Andrew D., Evangelou, Evangelos, Lettre, Guillaume, Reiner, Alexander P.
Publicado 2017

Genomic prediction of complex human traits: relatedness, trait architecture and predictive meta-models

por Spiliopoulou, Athina, Nagy, Reka, Bermingham, Mairead L., Huffman, Jennifer E., Hayward, Caroline, Vitart, Veronique, Rudan, Igor, Campbell, Harry, Wright, Alan F., Wilson, James F., Pong-Wong, Ricardo, Agakov, Felix, Navarro, Pau, Haley, Chris S.
Publicado 2015

Platelet Reactivity in Individuals Over 65 Years Old Is Not Modulated by Age

por Chan, Melissa V., Chen, Ming-Huei, Barwari, Temo, Huffman, Jennifer E., Armstrong, Paul C., Hwang, Shih-Jen, Santer, Peter, Wierer, Brigitte, Mayr, Manuel, Kiechl, Stefan, Johnson, Andrew D., Willeit, Johann, Warner, Timothy D.
Publicado 2020

Multi-ancestry fine mapping implicates OAS1 splicing in risk of severe COVID-19

por Huffman, Jennifer E., Butler-Laporte, Guillaume, Khan, Atlas, Pairo-Castineira, Erola, Drivas, Theodore G., Peloso, Gina M., Nakanishi, Tomoko, Ganna, Andrea, Verma, Anurag, Baillie, J. Kenneth, Kiryluk, Krzysztof, Richards, J. Brent, Zeberg, Hugo
Publicado 2022

Local Exome Sequences Facilitate Imputation of Less Common Variants and Increase Power of Genome Wide Association Studies

por Joshi, Peter K., Prendergast, James, Fraser, Ross M., Huffman, Jennifer E., Vitart, Veronique, Hayward, Caroline, McQuillan, Ruth, Glodzik, Dominik, Polašek, Ozren, Hastie, Nicholas D., Rudan, Igor, Campbell, Harry, Wright, Alan F., Haley, Chris S., Wilson, James F., Navarro, Pau
Publicado 2013

Characterisation of Genome-Wide Association Epistasis Signals for Serum Uric Acid in Human Population Isolates

por Wei, Wenhua, Hemani, Gibran, Hicks, Andrew A., Vitart, Veronique, Cabrera-Cardenas, Claudia, Navarro, Pau, Huffman, Jennifer, Hayward, Caroline, Knott, Sara A., Rudan, Igor, Pramstaller, Peter P., Wild, Sarah H., Wilson, James F., Campbell, Harry, Dunlop, Malcolm G., Hastie, Nicholas, Wright, Alan F., Haley, Chris S.
Publicado 2011

Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program

por Peloso, Gina M., Tcheandjieu, Catherine, McGeary, John E., Posner, Daniel C., Ho, Yuk-Lam, Zhou, Jin J., Hilliard, Austin T., Joseph, Jacob, O’Donnell, Christopher J., Efird, Jimmy T., Crawford, Dana C., Wu, Wen-Chih, Arjomandi, Mehrdad, Sun, Yan V., Assimes, Themistocles L, Huffman, Jennifer E.
Publicado 2022

Genome-wide analysis of epistasis in body mass index using multiple human populations

por Wei, Wen-Hua, Hemani, Gib, Gyenesei, Attila, Vitart, Veronique, Navarro, Pau, Hayward, Caroline, Cabrera, Claudia P, Huffman, Jennifer E, Knott, Sara A, Hicks, Andrew A, Rudan, Igor, Pramstaller, Peter P, Wild, Sarah H, Wilson, James F, Campbell, Harry, Hastie, Nicholas D, Wright, Alan F, Haley, Chris S
Publicado 2012

Genetic architecture of heart failure with preserved versus reduced ejection fraction

por Joseph, Jacob, Liu, Chang, Hui, Qin, Aragam, Krishna, Wang, Zeyuan, Charest, Brian, Huffman, Jennifer E., Keaton, Jacob M., Edwards, Todd L., Demissie, Serkalem, Djousse, Luc, Casas, Juan P., Gaziano, J. Michael, Cho, Kelly, Wilson, Peter W. F., Phillips, Lawrence S., O’Donnell, Christopher J., Sun, Yan V.
Publicado 2022

PCSK9 loss of function is protective against extra-coronary atherosclerotic cardiovascular disease in a large multi-ethnic cohort

por Small, Aeron M., Huffman, Jennifer E., Klarin, Derek, Lynch, Julie A., Assimes, Themistocles, DuVall, Scott, Sun, Yan V., Shere, Labiba, Natarajan, Pradeep, Gaziano, Michael, Rader, Daniel J., Wilson, Peter W. F., Tsao, Philip S., Chang, Kyong-Mi, Cho, Kelly, O’Donnell, Christopher J., Casas, Juan P., Damrauer, Scott M.
Publicado 2020

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

por Surakka, Ida, Wu, Kuan-Han, Hornsby, Whitney, Wolford, Brooke N., Shen, Fred, Zhou, Wei, Huffman, Jennifer E., Pandit, Anita, Hu, Yao, Brumpton, Ben, Skogholt, Anne Heidi, Gabrielsen, Maiken E., Walters, Robin G., Hveem, Kristian, Kooperberg, Charles, Zöllner, Sebastian, Wilson, Peter W.F., Sutton, Nadia R., Daly, Mark J., Neale, Benjamin M., Willer, Cristen J.
Publicado 2023

General Framework for Meta‐Analysis of Haplotype Association Tests

por Wang, Shuai, Zhao, Jing Hua, An, Ping, Guo, Xiuqing, Jensen, Richard A., Marten, Jonathan, Huffman, Jennifer E., Meidtner, Karina, Boeing, Heiner, Campbell, Archie, Rice, Kenneth M., Scott, Robert A., Yao, Jie, Schulze, Matthias B., Wareham, Nicholas J., Borecki, Ingrid B., Province, Michael A., Rotter, Jerome I., Hayward, Caroline, Goodarzi, Mark O., Meigs, James B., Dupuis, Josée
Publicado 2016