Canlyniadau Chwilio - Do, Ron

Exome sequencing and complex disease: practical aspects of rare variant association studies gan 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 gan 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? gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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 gan 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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