Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes

Por Hutcheson, Holli B, Olson, Lana M, Bradford, Yuki, Folstein, Susan E, Santangelo, Susan L, Sutcliffe, James S, Haines, Jonathan L
Publicado em 2004

Multiphenotype association study of patients randomized to initiate antiretroviral regimens in AIDS Clinical Trials Group protocol A5202

Por Verma, Anurag, Bradford, Yuki, Verma, Shefali S., Pendergrass, Sarah A., Daar, Eric S., Venuto, Charles, Morse, Gene D., Ritchie, Marylyn D., Haas, David W.
Publicado no Pharmacogenet Genomics (2017)

BIOFILTER AS A FUNCTIONAL ANNOTATION PIPELINE FOR COMMON AND RARE COPY NUMBER BURDEN

Por KIM, DOKYOON, LUCAS, ANASTASIA, GLESSNER, JOSEPH, VERMA, SHEFALI S., BRADFORD, YUKI, LI, RUOWANG, FRASE, ALEX T., HAKONARSON, HAKON, PEISSIG, PEGGY, BRILLIANT, MURRAY, RITCHIE, MARYLYN D.
Publicado no Pac Symp Biocomput (2016)

Phenome-Wide Association Study to Explore Relationships between Immune System Related Genetic Loci and Complex Traits and Diseases

Por Verma, Anurag, Basile, Anna O., Bradford, Yuki, Kuivaniemi, Helena, Tromp, Gerard, Carey, David, Gerhard, Glenn S., Crowe, James E., Ritchie, Marylyn D., Pendergrass, Sarah A.
Publicado no PLoS One (2016)

Genetic Determinants of Response to Warfarin during Initial Anticoagulation

Por Schwarz, Ute I., Ritchie, Marylyn D., Bradford, Yuki, Li, Chun, Dudek, Scott M., Frye-Anderson, Amy, Kim, Richard B., Roden, Dan M., Stein, C. Michael
Publicado em 2008

Identification of genetic interaction networks via an evolutionary algorithm evolved Bayesian network

Por Li, Ruowang, Dudek, Scott M., Kim, Dokyoon, Hall, Molly A., Bradford, Yuki, Peissig, Peggy L., Brilliant, Murray H., Linneman, James G., McCarty, Catherine A., Bao, Le, Ritchie, Marylyn D.
Publicado no BioData Min (2016)

Genetic variants associated with angiotensin-converting enzyme inhibitor-associated angioedema

Por Pare, Guillaume, Kubo, Michiaki, Byrd, James B., McCarty, Catherine A., Woodard-Grice, Alencia, Teo, Koon K., Anand, Sonia S., Zuvich, Rebecca L., Bradford, Yuki, Ross, Stephanie, Nakamura, Yusuke, Ritchie, Marylyn, Brown, Nancy J.
Publicado em 2013

Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis

Por McCauley, Jacob L., Zuvich, Rebecca L., Bradford, Yuki, Kenealy, Shannon J., Schnetz-Boutaud, Nathalie, Gregory, Simon G., Hauser, Stephen L., Oksenberg, Jorge R., Mortlock, Douglas P., Pericak-Vance, Margaret A., Haines, Jonathan L.
Publicado em 2009

KIAA1462, A Coronary Artery Disease Associated Gene, Is a Candidate Gene for Late Onset Alzheimer Disease in APOE Carriers

Por Murdock, Deborah G., Bradford, Yuki, Schnetz-Boutaud, Nathalie, Mayo, Ping, Allen, Melissa J., D’Aoust, Laura N., Liang, Xueying, Mitchell, Sabrina L., Zuchner, Stephan, Small, Gary W., Gilbert, John R., Pericak-Vance, Margaret A., Haines, Jonathan L.
Publicado em 2013

Controlling for population structure and genotyping platform bias in the eMERGE multi-institutional biobank linked to electronic health records

Por Crosslin, David R., Tromp, Gerard, Burt, Amber, Kim, Daniel S., Verma, Shefali S., Lucas, Anastasia M., Bradford, Yuki, Crawford, Dana C., Armasu, Sebastian M., Heit, John A., Hayes, M. Geoffrey, Kuivaniemi, Helena, Ritchie, Marylyn D., Jarvik, Gail P., de Andrade, Mariza
Publicado no Front Genet (2014)

eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants

Por Verma, Anurag, Verma, Shefali S., Pendergrass, Sarah A., Crawford, Dana C., Crosslin, David R., Kuivaniemi, Helena, Bush, William S., Bradford, Yuki, Kullo, Iftikhar, Bielinski, Suzette J., Li, Rongling, Denny, Joshua C., Peissig, Peggy, Hebbring, Scott, De Andrade, Mariza, Ritchie, Marylyn D., Tromp, Gerard
Publicado no BMC Med Genomics (2016)

Imputation and quality control steps for combining multiple genome-wide datasets

Por Verma, Shefali S., de Andrade, Mariza, Tromp, Gerard, Kuivaniemi, Helena, Pugh, Elizabeth, Namjou-Khales, Bahram, Mukherjee, Shubhabrata, Jarvik, Gail P., Kottyan, Leah C., Burt, Amber, Bradford, Yuki, Armstrong, Gretta D., Derr, Kimberly, Crawford, Dana C., Haines, Jonathan L., Li, Rongling, Crosslin, David, Ritchie, Marylyn D.
Publicado no Front Genet (2014)

Epistatic Gene-Based Interaction Analyses for Glaucoma in eMERGE and NEIGHBOR Consortium

Por Verma, Shefali Setia, Cooke Bailey, Jessica N., Lucas, Anastasia, Bradford, Yuki, Linneman, James G., Hauser, Michael A., Pasquale, Louis R., Peissig, Peggy L., Brilliant, Murray H., McCarty, Catherine A., Haines, Jonathan L., Wiggs, Janey L., Vrabec, Tamara R., Tromp, Gerard, Ritchie, Marylyn D.
Publicado no PLoS Genet (2016)

Quality Control Procedures for Genome Wide Association Studies

Por Turner, Stephen, Armstrong, Loren L., Bradford, Yuki, Carlson, Christopher S., Crawford, Dana C., Crenshaw, Andrew T., de Andrade, Mariza, Doheny, Kimberly F., Haines, Jonathan L., Hayes, Geoffrey, Jarvik, Gail, Jiang, Lan, Kullo, Iftikhar J., Li, Rongling, Ling, Hua, Manolio, Teri A., Matsumoto, Martha, McCarty, Catherine A., McDavid, Andrew N., Mirel, Daniel B., Paschall, Justin E., Pugh, Elizabeth W., Rasmussen, Luke V., Wilke, Russell A., Zuvich, Rebecca L., Ritchie, Marylyn D.
Publicado em 2011

Genetic Variants Associated with Serum Thyroid Stimulating Hormone (TSH) Levels in European Americans and African Americans from the eMERGE Network

Por Malinowski, Jennifer R., Denny, Joshua C., Bielinski, Suzette J., Basford, Melissa A., Bradford, Yuki, Peissig, Peggy L., Carrell, David, Crosslin, David R., Pathak, Jyotishman, Rasmussen, Luke, Pacheco, Jennifer, Kho, Abel, Newton, Katherine M., Li, Rongling, Kullo, Iftikhar J., Chute, Christopher G., Chisholm, Rex L., Jarvik, Gail P., Larson, Eric B., McCarty, Catherine A., Masys, Daniel R., Roden, Dan M., de Andrade, Mariza, Ritchie, Marylyn D., Crawford, Dana C.
Publicado no PLoS One (2014)

Genome- and Phenome-Wide Analysis of Cardiac Conduction Identifies Markers of Arrhythmia Risk

Por Ritchie, Marylyn D., Denny, Joshua C., Zuvich, Rebecca L., Crawford, Dana C., Schildcrout, Jonathan S., Bastarache, Lisa, Ramirez, Andrea H., Mosley, Jonathan D., Pulley, Jill M., Basford, Melissa A., Bradford, Yuki, Rasmussen, Luke V., Pathak, Jyotishman, Chute, Christopher G., Kullo, Iftikhar J., McCarty, Catherine A., Chisholm, Rex L., Kho, Abel N., Carlson, Christopher S., Larson, Eric B., Jarvik, Gail P., Sotoodehnia, Nona, Manolio, Teri A., Li, Rongling, Masys, Daniel R., Haines, Jonathan L., Roden, Dan M.
Publicado em 2013

Genome-Wide Association Study of Serum Creatinine Levels during Vancomycin Therapy

Por Van Driest, Sara L., McGregor, Tracy L., Velez Edwards, Digna R., Saville, Ben R., Kitchner, Terrie E., Hebbring, Scott J., Brilliant, Murray, Jouni, Hayan, Kullo, Iftikhar J., Creech, C. Buddy, Kannankeril, Prince J., Vear, Susan I., Brothers, Kyle B., Bowton, Erica A., Shaffer, Christian M., Patel, Neelam, Delaney, Jessica T., Bradford, Yuki, Wilson, Sarah, Olson, Lana M., Crawford, Dana C., Potts, Amy L., Ho, Richard H., Roden, Dan M., Denny, Josh C.
Publicado no PLoS One (2015)

Pitfalls of Merging GWAS Data: Lessons Learned in the eMERGE Network and Quality Control Procedures to Maintain High Data Quality

Por Zuvich, Rebecca L., Armstrong, Loren L., Bielinski, Suzette J., Bradford, Yuki, Carlson, Christopher S., Crawford, Dana C., Crenshaw, Andrew T., de Andrade, Mariza, Doheny, Kimberly F., Haines, Jonathan L., Hayes, M. Geoffrey, Jarvik, Gail P., Jiang, Lan, Kullo, Iftikhar J., Li, Rongling, Ling, Hua, Manolio, Teri A., Matsumoto, Martha E., McCarty, Catherine A., McDavid, Andrew N., Mirel, Daniel B., Olson, Lana M., Paschall, Justin E., Pugh, Elizabeth W., Rasmussen, Luke V., Rasmussen-Torvik, Laura J., Turner, Stephen D., Wilke, Russell A., Ritchie, Marylyn D.
Publicado em 2011

Variants Near FOXE1 Are Associated with Hypothyroidism and Other Thyroid Conditions: Using Electronic Medical Records for Genome- and Phenome-wide Studies

Por Denny, Joshua C., Crawford, Dana C., Ritchie, Marylyn D., Bielinski, Suzette J., Basford, Melissa A., Bradford, Yuki, Chai, High Seng, Bastarache, Lisa, Zuvich, Rebecca, Peissig, Peggy, Carrell, David, Ramirez, Andrea H., Pathak, Jyotishman, Wilke, Russell A., Rasmussen, Luke, Wang, Xiaoming, Pacheco, Jennifer A., Kho, Abel N., Hayes, M. Geoffrey, Weston, Noah, Matsumoto, Martha, Kopp, Peter A., Newton, Katherine M., Jarvik, Gail P., Li, Rongling, Manolio, Teri A., Kullo, Iftikhar J., Chute, Christopher G., Chisholm, Rex L., Larson, Eric B., McCarty, Catherine A., Masys, Daniel R., Roden, Dan M., de Andrade, Mariza
Publicado em 2011

A Large Candidate Gene Survey Identifies the KCNE1 D85N Polymorphism as a Possible Modulator of Drug-Induced Torsades de Pointes

Por Kääb, Stefan, Crawford, Dana C., Sinner, Moritz F., Behr, Elijah R., Kannankeril, Prince J., Wilde, Arthur A. M., Bezzina, Connie R., Schulze-Bahr, Eric, Guicheney, Pascale, Bishopric, Nanette H., Myerburg, Robert J., Schott, Jean-Jacques, Pfeufer, Arne, Beckmann, Britt-Maria, Martens, Eimo, Zhang, Taifang, Stallmeyer, Birgit, Zumhagen, Sven, Denjoy, Isabelle, Bardai, Abdennasser, Van Gelder, Isabelle C., Jamshidi, Yalda, Dalageorgou, Chrysoula, Marshall, Vanessa, Jeffery, Steve, Shakir, Saad, Camm, A. John, Steinbeck, Gerhard, Perz, Siegfried, Lichtner, Peter, Meitinger, Thomas, Peters, Annette, Wichmann, H.-Erich, Ingram, Christiana, Bradford, Yuki, Carter, Shannon, Norris, Kris, Ritchie, Marylyn D., George, Alfred L., Roden, Dan M.
Publicado em 2011