Risk factor studies of age-at-onset in a sample ascertained for Parkinson disease affected sibling pairs: a cautionary tale

por Wilk, Jemma B, Lash, Timothy L
Publicado 2007

Genome-wide association of sleep and circadian phenotypes

por Gottlieb, Daniel J, O'Connor, George T, Wilk, Jemma B
Publicado 2007

A case-only analysis of the interaction between N-acetyltransferase 2 haplotypes and tobacco smoke in breast cancer etiology

por Lash, Timothy L, Bradbury, Brian D, Wilk, Jemma B, Aschengrau, Ann
Publicado 2005

Departure from multiplicative interaction for catechol-O-methyltransferase genotype and active/passive exposure to tobacco smoke among women with breast cancer

por Bradbury, Brian D, Wilk, Jemma B, Aschengrau, Ann, Lash, Timothy L
Publicado 2006

Framingham Heart Study genome-wide association: results for pulmonary function measures

por Wilk, Jemma B, Walter, Robert E, Laramie, Jason M, Gottlieb, Daniel J, O'Connor, George T
Publicado 2007

Association between adiponectin and heart failure risk in the Physicians' Health Study

por Djoussé, Luc, Wilk, Jemma B., Hanson, Naomi Q., Glynn, Robert, Tsai, Michael Y., Gaziano, J. Michael
Publicado 2013

Evidence for a gene influencing heart rate on chromosome 5p13-14 in a meta-analysis of genome-wide scans from the NHLBI Family Blood Pressure Program

por Laramie, Jason M, Wilk, Jemma B, Hunt, Steven C, Ellison, R Curtis, Chakravarti, Aravinda, Boerwinkle, Eric, Myers, Richard H
Publicado 2006

Self-report data as a tool for subtype identification in genetically-defined Parkinson’s Disease

por Winslow, Ashley R., Hyde, Craig L., Wilk, Jemma B., Eriksson, Nicholas, Cannon, Paul, Miller, Melissa R., Hirst, Warren D.
Publicado 2018

On the Analysis of Genome-Wide Association Studies in Family-Based Designs: A Universal, Robust Analysis Approach and an Application to Four Genome-Wide Association Studies

por Won, Sungho, Wilk, Jemma B., Mathias, Rasika A., O'Donnell, Christopher J., Silverman, Edwin K., Barnes, Kathleen, O'Connor, George T., Weiss, Scott T., Lange, Christoph
Publicado 2009

Polymorphisms near EXOC4 and LRGUK on chromosome 7q32 are associated with Type 2 Diabetes and fasting glucose; The NHLBI Family Heart Study

por Laramie, Jason M, Wilk, Jemma B, Williamson, Sally L, Nagle, Michael W, Latourelle, Jeanne C, Tobin, Jennifer E, Province, Michael A, Borecki, Ingrid B, Myers, Richard H
Publicado 2008

Postmortem Interval Influences α-Synuclein Expression in Parkinson Disease Brain

por Dumitriu, Alexandra, Moser, Carlee, Hadzi, Tiffany C., Williamson, Sally L., Pacheco, Christopher D., Hendricks, Audrey E., Latourelle, Jeanne C., Wilk, Jemma B., DeStefano, Anita L., Myers, Richard H.
Publicado 2012

A Genome-Wide Association Study of Pulmonary Function Measures in the Framingham Heart Study

por Wilk, Jemma B., Chen, Ting-hsu, Gottlieb, Daniel J., Walter, Robert E., Nagle, Michael W., Brandler, Brian J., Myers, Richard H., Borecki, Ingrid B., Silverman, Edwin K., Weiss, Scott T., O'Connor, George T.
Publicado 2009

Genetic associations of protein-coding variants in human disease

por Sun, Benjamin B., Kurki, Mitja I., Foley, Christopher N., Mechakra, Asma, Chen, Chia-Yen, Marshall, Eric, Wilk, Jemma B., Chahine, Mohamed, Chevalier, Philippe, Christé, Georges, Palotie, Aarno, Daly, Mark J., Runz, Heiko
Publicado 2022

Genomewide association study for onset age in Parkinson disease

por Latourelle, Jeanne C, Pankratz, Nathan, Dumitriu, Alexandra, Wilk, Jemma B, Goldwurm, Stefano, Pezzoli, Gianni, Mariani, Claudio B, DeStefano, Anita L, Halter, Cheryl, Gusella, James F, Nichols, William C, Myers, Richard H, Foroud, Tatiana
Publicado 2009

Vitamin D-responsive SGPP2 variants associated with lung cell expression and lung function

por Reardon, Brian J, Hansen, Joyanna G, Crystal, Ronald G, Houston, Denise K, Kritchevsky, Stephen B, Harris, Tamara, Lohman, Kurt, Liu, Yongmei, O’Connor, George T, Wilk, Jemma B, Mezey, Jason, Gao, Chuan, Cassano, Patricia A
Publicado 2013

Thymic stromal lymphopoietin (TSLP) is associated with allergic rhinitis in children with asthma

por Bunyavanich, Supinda, Melen, Erik, Wilk, Jemma B, Granada, Mark, Soto-Quiros, Manuel E, Avila, Lydiana, Lasky-Su, Jessica, Hunninghake, Gary M, Wickman, Magnus, Pershagen, Göran, O'Connor, George T, Weiss, Scott T, Celedόn, Juan C
Publicado 2011

Copy Number Variation in Familial Parkinson Disease

por Pankratz, Nathan, Dumitriu, Alexandra, Hetrick, Kurt N., Sun, Mei, Latourelle, Jeanne C., Wilk, Jemma B., Halter, Cheryl, Doheny, Kimberly F., Gusella, James F., Nichols, William C., Myers, Richard H., Foroud, Tatiana, DeStefano, Anita L.
Publicado 2011

Genome-Wide Detection of Allele Specific Copy Number Variation Associated with Insulin Resistance in African Americans from the HyperGEN Study

por Irvin, Marguerite R., Wineinger, Nathan E., Rice, Treva K., Pajewski, Nicholas M., Kabagambe, Edmond K., Gu, Charles C., Pankow, Jim, North, Kari E., Wilk, Jemma B., Freedman, Barry I., Franceschini, Nora, Broeckel, Uli, Tiwari, Hemant K., Arnett, Donna K.
Publicado 2011

Genetic Signatures of Exceptional Longevity in Humans

por Sebastiani, Paola, Solovieff, Nadia, DeWan, Andrew T., Walsh, Kyle M., Puca, Annibale, Hartley, Stephen W., Melista, Efthymia, Andersen, Stacy, Dworkis, Daniel A., Wilk, Jemma B., Myers, Richard H., Steinberg, Martin H., Montano, Monty, Baldwin, Clinton T., Hoh, Josephine, Perls, Thomas T.
Publicado 2012

Asthma-susceptibility variants identified using probands in case-control and family-based analyses

por Himes, Blanca E, Lasky-Su, Jessica, Wu, Ann C, Wilk, Jemma B, Hunninghake, Gary M, Klanderman, Barbara, Murphy, Amy J, Lazarus, Ross, Soto-Quiros, Manuel E, Avila, Lydiana, Celedón, Juan C, Lange, Christoph, O'Connor, George T, Raby, Benjamin A, Silverman, Edwin K, Weiss, Scott T
Publicado 2010