Search Results - Do, Ron

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

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

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

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

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

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

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

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

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

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

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

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

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

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Searching for missing heritability: Designing rare variant association studies by 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.

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Statin Use in Relation to Intraocular Pressure, Glaucoma, and Ocular Coherence Tomography Parameters in the UK Biobank by 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.

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Variation at the NFATC2 Locus Increases the Risk of Thiazolidinedione-Induced Edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) Study by 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

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Systematic Functional Dissection of Common Genetic Variation Affecting Red Blood Cell Traits by 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.

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Exome sequencing identifies GATA1 mutations resulting in Diamond-Blackfan anemia by 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.

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A Genotype-First Approach to Exploring Mendelian Cardiovascular Traits with Clear External Manifestations by 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.

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Population-Based Penetrance of Deleterious Clinical Variants by 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

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