检索结果 - Do, Ron

Exome sequencing and complex disease: practical aspects of rare variant association studies 由 Do, Ron, Kathiresan, Sekar, Abecasis, Gonçalo R.

获取全文 获取全文 获取全文

HOPS: a quantitative score reveals pervasive horizontal pleiotropy in human genetic variation is driven by extreme polygenicity of human traits and diseases 由 Jordan, Daniel M., Verbanck, Marie, Do, Ron

获取全文 获取全文 获取全文

What can we learn about lipoprotein metabolism and coronary heart disease from studying rare variants? 由 Jeff, Janina M., Peloso, Gina M., Do, Ron

获取全文 获取全文 获取全文

Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases 由 Verbanck, Marie, Chen, Chia-Yen, Neale, Benjamin, Do, Ron

获取全文 获取全文 获取全文

Overcoming constraints on the detection of recessive selection in human genes from population frequency data 由 Balick, Daniel J., Jordan, Daniel M., Sunyaev, Shamil, Do, Ron

获取全文 获取全文 获取全文

Probing the aggregated effects of purifying selection per individual on 1,380 medical phenotypes in the UK Biobank 由 Vy, Ha My T., Jordan, Daniel M., Balick, Daniel J., Do, Ron

获取全文 获取全文 获取全文

No evidence that selection has been less effective at removing deleterious mutations in Europeans than in Africans 由 Do, Ron, Balick, Daniel, Li, Heng, Adzhubei, Ivan, Sunyaev, Shamil, Reich, David

获取全文 获取全文 获取全文

Dominance of Deleterious Alleles Controls the Response to a Population Bottleneck 由 Balick, Daniel J., Do, Ron, Cassa, Christopher A., Reich, David, Sunyaev, Shamil R.

获取全文 获取全文 获取全文

Non-invasive ventilation versus mechanical ventilation in hypoxemic patients with COVID-19 由 Forrest, Iain S., Jaladanki, Suraj K., Paranjpe, Ishan, Glicksberg, Benjamin S., Nadkarni, Girish N., Do, Ron

获取全文 获取全文 获取全文

Plasma biomarkers are associated with renal outcomes in individuals with APOL1 risk variants 由 Nadkarni, Girish N, Chauhan, Kinsuk, Verghese, Divya, Parikh, Chirag R., Do, Ron, Horowitz, Carol R., Bottinger, Erwin, Coca, Steven G.

获取全文 获取全文 获取全文

No causal effects of serum urate levels on the risk of chronic kidney disease: A Mendelian randomization study 由 Jordan, Daniel M., Choi, Hyon K., Verbanck, Marie, Topless, Ruth, Won, Hong-Hee, Nadkarni, Girish, Merriman, Tony R., Do, Ron

获取全文 获取全文 获取全文

Coronary Risk Estimation Based on Clinical Data in Electronic Health Records 由 Petrazzini, Ben O., Chaudhary, Kumardeep, Márquez-Luna, Carla, Forrest, Iain S., Rocheleau, Ghislain, Cho, Judy, Narula, Jagat, Nadkarni, Girish, Do, Ron

获取全文 获取全文 获取全文

Intraocular Pressure, Glaucoma, and Dietary Caffeine Consumption: A Gene—Diet Interaction Study from the UK Biobank 由 Kim, Jihye, Aschard, Hugues, Kang, Jae H., Lentjes, Marleen A.H., Do, Ron, Wiggs, Janey L., Khawaja, Anthony P., Pasquale, Louis R.

获取全文 获取全文 获取全文

Searching for missing heritability: Designing rare variant association studies 由 Zuk, Or, Schaffner, Stephen F., Samocha, Kaitlin, Do, Ron, Hechter, Eliana, Kathiresan, Sekar, Daly, Mark J., Neale, Benjamin M., Sunyaev, Shamil R., Lander, Eric S.

获取全文 获取全文 获取全文

Statin Use in Relation to Intraocular Pressure, Glaucoma, and Ocular Coherence Tomography Parameters in the UK Biobank 由 Kim, Jihye, Kennedy Neary, Marianne T., Aschard, Hugues, Palakkamanil, Mathew M., Do, Ron, Wiggs, Janey L., Khawaja, Anthony P., Pasquale, Louis R., Kang, Jae H.

获取全文 获取全文 获取全文

Variation at the NFATC2 Locus Increases the Risk of Thiazolidinedione-Induced Edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) Study 由 Bailey, Swneke D., Xie, Changchun, Do, Ron, Montpetit, Alexandre, Diaz, Rafael, Mohan, Viswanathan, Keavney, Bernard, Yusuf, Salim, Gerstein, Hertzel C., Engert, James C., Anand, Sonia

获取全文 获取全文 获取全文

Systematic Functional Dissection of Common Genetic Variation Affecting Red Blood Cell Traits 由 Ulirsch, Jacob C., Nandakumar, Satish K., Wang, Li, Giani, Felix C., Zhang, Xiaolan, Rogov, Peter, Melnikov, Alexandre, McDonel, Patrick, Do, Ron, Mikkelsen, Tarjei S., Sankaran, Vijay G.

获取全文 获取全文 获取全文

Exome sequencing identifies GATA1 mutations resulting in Diamond-Blackfan anemia 由 Sankaran, Vijay G., Ghazvinian, Roxanne, Do, Ron, Thiru, Prathapan, Vergilio, Jo-Anne, Beggs, Alan H., Sieff, Colin A., Orkin, Stuart H., Nathan, David G., Lander, Eric S., Gazda, Hanna T.

获取全文 获取全文 获取全文

A Genotype-First Approach to Exploring Mendelian Cardiovascular Traits with Clear External Manifestations 由 Wenger, Brittany M., Patel, Nihir, Lui, Madeline, Moscati, Arden, Do, Ron, Stewart, Douglas R., Tartaglia, Marco, Muiño-Mosquera, Laura, De Backer, Julie, Kontorovich, Amy R., Gelb, Bruce D.

获取全文 获取全文 获取全文

Population-Based Penetrance of Deleterious Clinical Variants 由 Forrest, Iain S., Chaudhary, Kumardeep, Vy, Ha My T., Petrazzini, Ben O., Bafna, Shantanu, Jordan, Daniel M., Rocheleau, Ghislain, Loos, Ruth J. F., Nadkarni, Girish N., Cho, Judy H., Do, Ron

获取全文 获取全文 获取全文