Constrained multivariate association with longitudinal phenotypes

por Melton, Phillip E., Peralta, Juan M., Almasy, Laura
Publicado 2016

A variance component-based gene burden test

por Peralta, Juan M, Almeida, Marcio, Kent, Jack W, Blangero, John
Publicado 2014

Heritability and genetic associations of triglyceride and HDL-C levels using pedigree-based and empirical kinships

por Blackburn, Nicholas B., Porto, Arthur, Peralta, Juan M., Blangero, John
Publicado 2018

Reliability of genomic predictions of complex human phenotypes

por Porto, Arthur, Peralta, Juan M., Blackburn, Nicholas B., Blangero, John
Publicado 2018

Genome-wide linkage scan for loci influencing plasma triglyceride levels

por Peralta, Juan M., Blackburn, Nicholas B., Porto, Arthur, Blangero, John, Charlesworth, Jac
Publicado 2018

Pedigree-based random effect tests to screen gene pathways

por Almeida, Marcio, Peralta, Juan M, Farook, Vidya, Puppala, Sobha, Kent, John W, Duggirala, Ravindranath, Blangero, John
Publicado 2014

Toward the identification of causal genes in complex diseases: a gene-centric joint test of significance combining genomic and transcriptomic data

por Charlesworth, Jac C, Peralta, Juan M, Drigalenko, Eugene, Göring, Harald HH, Almasy, Laura, Dyer, Thomas D, Blangero, John
Publicado 2009

Searching for master regulators of transcription in a human gene expression data set

por Buil, Alfonso, Perera-Lluna, Alexandre, Souto, Ramon, Peralta, Juan M, Almasy, Laura, Vallverdu, Montserrat, Caminal, Pere, Soria, Jose M
Publicado 2007

Genotype-by-socioeconomic status interaction influences heart disease risk scores and carotid artery thickness in Mexican Americans: the predominant role of education in comparison...

por Diego, Vincent P., Manusov, Eron G., Mao, Xi, Curran, Joanne E., Göring, Harald, Almeida, Marcio, Mahaney, Michael C., Peralta, Juan M., Blangero, John, Williams-Blangero, Sarah
Publicado 2023

Genetic Effects on DNA Methylation and Its Potential Relevance for Obesity in Mexican Americans

por Carless, Melanie A., Kulkarni, Hemant, Kos, Mark Z., Charlesworth, Jac, Peralta, Juan M., Göring, Harald H. H., Curran, Joanne E., Almasy, Laura, Dyer, Thomas D., Comuzzie, Anthony G., Mahaney, Michael C., Blangero, John
Publicado 2013

Transcriptomic Profiling of Fibropapillomatosis in Green Sea Turtles (Chelonia mydas) From South Texas

por Blackburn, Nicholas B., Leandro, Ana Cristina, Nahvi, Nina, Devlin, Mariana A., Leandro, Marcelo, Martinez Escobedo, Ignacio, Peralta, Juan M., George, Jeff, Stacy, Brian A., deMaar, Thomas W., Blangero, John, Keniry, Megan, Curran, Joanne E.
Publicado 2021

Evaluation of estimated genetic values and their application to genome-wide investigation of systolic blood pressure

por Quillen, Ellen E, Voruganti, V Saroja, Chittoor, Geetha, Rubicz, Rohina, Peralta, Juan M, Almeida, Marcio AA, Kent, Jack W, Diego, Vincent P, Dyer, Thomas D, Comuzzie, Anthony G, Göring, Harald HH, Duggirala, Ravindranath, Almasy, Laura, Blangero, John
Publicado 2014

Data for Genetic Analysis Workshop 18: human whole genome sequence, blood pressure, and simulated phenotypes in extended pedigrees

por Almasy, Laura, Dyer, Thomas D, Peralta, Juan M, Jun, Goo, Wood, Andrew R, Fuchsberger, Christian, Almeida, Marcio A, Kent, Jack W, Fowler, Sharon, Blackwell, Tom W, Puppala, Sobha, Kumar, Satish, Curran, Joanne E, Lehman, Donna, Abecasis, Goncalo, Duggirala, Ravindranath, Blangero, John
Publicado 2014

Independent test assessment using the extreme value distribution theory

por Almeida, Marcio, Blondell, Lucy, Peralta, Juan M., Kent, Jack W., Jun, Goo, Teslovich, Tanya M., Fuchsberger, Christian, Wood, Andrew R., Manning, Alisa K., Frayling, Timothy M., Cingolani, Pablo E., Sladek, Robert, Dyer, Thomas D., Abecasis, Goncalo, Duggirala, Ravindranath, Blangero, John
Publicado 2016

Cocktail-party listening and cognitive abilities show strong pleiotropy

por Mathias, Samuel R., Knowles, Emma E. M., Mollon, Josephine, Rodrigue, Amanda L., Woolsey, Mary K., Hernandez, Alyssa M., Garret, Amy S., Fox, Peter T., Olvera, Rene L., Peralta, Juan M., Kumar, Satish, Göring, Harald H. H., Duggirala, Ravi, Curran, Joanne E., Blangero, John, Glahn, David C.
Publicado 2023

The Genetic contribution to solving the cocktail-party problem

por Mathias, Samuel R., Knowles, Emma E.M., Mollon, Josephine, Rodrigue, Amanda L., Woolsey, Mary K., Hernandez, Alyssa M., Garrett, Amy S., Fox, Peter T., Olvera, Rene L., Peralta, Juan M., Kumar, Satish, Göring, Harald H.H., Duggirala, Ravi, Curran, Joanne E., Blangero, John, Glahn, David C.
Publicado 2022

Omics-squared: human genomic, transcriptomic and phenotypic data for genetic analysis workshop 19

por Blangero, John, Teslovich, Tanya M., Sim, Xueling, Almeida, Marcio A., Jun, Goo, Dyer, Thomas D., Johnson, Matthew, Peralta, Juan M., Manning, Alisa, Wood, Andrew R., Fuchsberger, Christian, Kent, Jack W., Aguilar, David A., Below, Jennifer E., Farook, Vidya S., Arya, Rector, Fowler, Sharon, Blackwell, Tom W., Puppala, Sobha, Kumar, Satish, Glahn, David C., Moses, Eric K., Curran, Joanne E., Thameem, Farook, Jenkinson, Christopher P., DeFronzo, Ralph A., Lehman, Donna M., Hanis, Craig, Abecasis, Goncalo, Boehnke, Michael, Göring, Harald, Duggirala, Ravindranath, Almasy, Laura
Publicado 2016

Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole genome sequencing studies at scale

por Li, Xihao, Li, Zilin, Zhou, Hufeng, Gaynor, Sheila M., Liu, Yaowu, Chen, Han, Sun, Ryan, Dey, Rounak, Arnett, Donna K., Aslibekyan, Stella, Ballantyne, Christie M., Bielak, Lawrence F., Blangero, John, Boerwinkle, Eric, Bowden, Donald W., Broome, Jai G., Conomos, Matthew P., Correa, Adolfo, Cupples, L. Adrienne, Curran, Joanne E., Freedman, Barry I., Guo, Xiuqing, Hindy, George, Irvin, Marguerite R., Kardia, Sharon L. R., Kathiresan, Sekar, Khan, Alyna T., Kooperberg, Charles L., Laurie, Cathy C., Liu, X. Shirley, Mahaney, Michael C., Manichaikul, Ani W., Martin, Lisa W., Mathias, Rasika A., McGarvey, Stephen T., Mitchell, Braxton D., Montasser, May E., Moore, Jill E., Morrison, Alanna C., O’Connell, Jeffrey R., Palmer, Nicholette D., Pampana, Akhil, Peralta, Juan M., Peyser, Patricia A., Psaty, Bruce M., Redline, Susan, Rice, Kenneth M., Rich, Stephen S., Smith, Jennifer A., Tiwari, Hemant K., Tsai, Michael Y., Vasan, Ramachandran S., Wang, Fei Fei, Weeks, Daniel E., Weng, Zhiping, Wilson, James G., Yanek, Lisa R., Neale, Benjamin M., Sunyaev, Shamil R., Abecasis, Gonçalo R., Rotter, Jerome I., Willer, Cristen J., Peloso, Gina M., Natarajan, Pradeep, Lin, Xihong
Publicado 2020

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixe...

por Kowalski, Madeline H., Qian, Huijun, Hou, Ziyi, Rosen, Jonathan D., Tapia, Amanda L., Shan, Yue, Jain, Deepti, Argos, Maria, Arnett, Donna K., Avery, Christy, Barnes, Kathleen C., Becker, Lewis C., Bien, Stephanie A., Bis, Joshua C., Blangero, John, Boerwinkle, Eric, Bowden, Donald W., Buyske, Steve, Cai, Jianwen, Cho, Michael H., Choi, Seung Hoan, Choquet, Hélène, Cupples, L. Adrienne, Cushman, Mary, Daya, Michelle, de Vries, Paul S., Ellinor, Patrick T., Faraday, Nauder, Fornage, Myriam, Gabriel, Stacey, Ganesh, Santhi K., Graff, Misa, Gupta, Namrata, He, Jiang, Heckbert, Susan R., Hidalgo, Bertha, Hodonsky, Chani J., Irvin, Marguerite R., Johnson, Andrew D., Jorgenson, Eric, Kaplan, Robert, Kardia, Sharon L. R., Kelly, Tanika N., Kooperberg, Charles, Lasky-Su, Jessica A., Loos, Ruth J. F., Lubitz, Steven A., Mathias, Rasika A., McHugh, Caitlin P., Montgomery, Courtney, Moon, Jee-Young, Morrison, Alanna C., Palmer, Nicholette D., Pankratz, Nathan, Papanicolaou, George J., Peralta, Juan M., Peyser, Patricia A., Rich, Stephen S., Rotter, Jerome I., Silverman, Edwin K., Smith, Jennifer A., Smith, Nicholas L., Taylor, Kent D., Thornton, Timothy A., Tiwari, Hemant K., Tracy, Russell P., Wang, Tao, Weiss, Scott T., Weng, Lu-Chen, Wiggins, Kerri L., Wilson, James G., Yanek, Lisa R., Zöllner, Sebastian, North, Kari E., Auer, Paul L., Raffield, Laura M., Reiner, Alexander P., Li, Yun
Publicado 2019

Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program

por DiCorpo, Daniel, Gaynor, Sheila M., Russell, Emily M., Westerman, Kenneth E., Raffield, Laura M., Majarian, Timothy D., Wu, Peitao, Sarnowski, Chloé, Highland, Heather M., Jackson, Anne, Hasbani, Natalie R., de Vries, Paul S., Brody, Jennifer A., Hidalgo, Bertha, Guo, Xiuqing, Perry, James A., O’Connell, Jeffrey R., Lent, Samantha, Montasser, May E., Cade, Brian E., Jain, Deepti, Wang, Heming, D’Oliveira Albanus, Ricardo, Varshney, Arushi, Yanek, Lisa R., Lange, Leslie, Palmer, Nicholette D., Almeida, Marcio, Peralta, Juan M., Aslibekyan, Stella, Baldridge, Abigail S., Bertoni, Alain G., Bielak, Lawrence F., Chen, Chung-Shiuan, Chen, Yii-Der Ida, Choi, Won Jung, Goodarzi, Mark O., Floyd, James S., Irvin, Marguerite R., Kalyani, Rita R., Kelly, Tanika N., Lee, Seonwook, Liu, Ching-Ti, Loesch, Douglas, Manson, JoAnn E., Minster, Ryan L., Naseri, Take, Pankow, James S., Rasmussen-Torvik, Laura J., Reiner, Alexander P., Reupena, Muagututi’a Sefuiva, Selvin, Elizabeth, Smith, Jennifer A., Weeks, Daniel E., Xu, Huichun, Yao, Jie, Zhao, Wei, Parker, Stephen, Alonso, Alvaro, Arnett, Donna K., Blangero, John, Boerwinkle, Eric, Correa, Adolfo, Cupples, L. Adrienne, Curran, Joanne E., Duggirala, Ravindranath, He, Jiang, Heckbert, Susan R., Kardia, Sharon L. R., Kim, Ryan W., Kooperberg, Charles, Liu, Simin, Mathias, Rasika A., McGarvey, Stephen T., Mitchell, Braxton D., Morrison, Alanna C., Peyser, Patricia A., Psaty, Bruce M., Redline, Susan, Shuldiner, Alan R., Taylor, Kent D., Vasan, Ramachandran S., Viaud-Martinez, Karine A., Florez, Jose C., Wilson, James G., Sladek, Robert, Rich, Stephen S., Rotter, Jerome I., Lin, Xihong, Dupuis, Josée, Meigs, James B., Wessel, Jennifer, Manning, Alisa K.
Publicado 2022