Search Results - Pulit, Sara L.

Sexual dimorphisms in genetic loci linked to body fat distribution by Pulit, Sara L., Karaderi, Tugce, Lindgren, Cecilia M.

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Genetic and epigenetic studies of adiposity and cardiometabolic disease by Holmes, Michael V., Pulit, Sara L., Lindgren, Cecilia M.

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Multiethnic Genetic Association Studies Improve Power for Locus Discovery by Pulit, Sara L., Voight, Benjamin F., de Bakker, Paul I. W.

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Association Claims in the Sequencing Era by Pulit, Sara L., Leusink, Maarten, Menelaou, Androniki, de Bakker, Paul I. W.

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GWAS identifies 14 loci for device-measured physical activity and sleep duration by Doherty, Aiden, Smith-Byrne, Karl, Ferreira, Teresa, Holmes, Michael V., Holmes, Chris, Pulit, Sara L., Lindgren, Cecilia M.

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SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap by Johnson, Andrew D., Handsaker, Robert E., Pulit, Sara L., Nizzari, Marcia M., O'Donnell, Christopher J., de Bakker, Paul I. W.

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A replication study of genetic risk loci for ischemic stroke in a Dutch population: a case-control study by Hauer, Allard J., Pulit, Sara L., van den Berg, Leonard H., de Bakker, Paul I. W., Veldink, Jan H., Ruigrok, Ynte M.

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Author Correction: A replication study of genetic risk loci for ischemic stroke in a Dutch population: a case-control study by Hauer, Allard J., Pulit, Sara L., van den Berg, Leonard H., de Bakker, Paul I. W., Veldink, Jan H., Ruigrok, Ynte M.

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The project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the public by VAN DER SPEK, RICK A.A., VAN RHEENEN, WOUTER, PULIT, SARA L., KENNA, KEVIN P., VAN DEN BERG, LEONARD H., VELDINK, JAN H.

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Causal relationships between obesity and the leading causes of death in women and men by Censin, Jenny C., Peters, Sanne A. E., Bovijn, Jonas, Ferreira, Teresa, Pulit, Sara L., Mägi, Reedik, Mahajan, Anubha, Holmes, Michael V., Lindgren, Cecilia M.

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Fine-mapping in the MHC region accounts for 18% additional genetic risk for celiac disease by Gutierrez-Achury, Javier, Zhernakova, Alexandra, Pulit, Sara L., Trynka, Gosia, Hunt, Karen A., Romanos, Jihane, Raychaudhuri, Soumya, van Heel, David A., Wijmenga, Cisca, de Bakker, Paul I.W.

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Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke by von Berg, Joanna, van der Laan, Sander W., McArdle, Patrick F., Malik, Rainer, Kittner, Steven J., Mitchell, Braxton D., Worrall, Bradford B., de Ridder, Jeroen, Pulit, Sara L.

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No association between gluten sensitivity and amyotrophic lateral sclerosis by Visser, Anne E., Pazoki, Raha, Pulit, Sara L., van Rheenen, Wouter, Raaphorst, Joost, van der Kooi, Anneke J., Ricaño-Ponce, Isis, Wijmenga, Cisca, Otten, Henny G., Veldink, Jan H., van den Berg, Leonard H.

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Negative selection in humans and fruit flies involves synergistic epistasis by Sohail, Mashaal, Vakhrusheva, Olga A., Sul, Jae Hoon, Pulit, Sara L., Francioli, Laurent C., van den Berg, Leonard H., Veldink, Jan H., de Bakker, Paul I. W., Bazykin, Georgii A., Kondrashov, Alexey S., Sunyaev, Shamil R.

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Deleterious Alleles in the Human Genome Are on Average Younger Than Neutral Alleles of the Same Frequency by Kiezun, Adam, Pulit, Sara L., Francioli, Laurent C., van Dijk, Freerk, Swertz, Morris, Boomsma, Dorret I., van Duijn, Cornelia M., Slagboom, P. Eline, van Ommen, G. J. B., Wijmenga, Cisca, de Bakker, Paul I. W., Sunyaev, Shamil R.

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Using previously genotyped controls in genome-wide association studies (GWAS): application to the Stroke Genetics Network (SiGN) by Mitchell, Braxton D., Fornage, Myriam, McArdle, Patrick F., Cheng, Yu-Ching, Pulit, Sara L., Wong, Quenna, Dave, Tushar, Williams, Stephen R., Corriveau, Roderick, Gwinn, Katrina, Doheny, Kimberly, Laurie, Cathy C., Rich, Stephen S., de Bakker, Paul I. W.

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MicroRNA-196a links human body fat distribution to adipose tissue extracellular matrix composition by Hilton, Catriona, Neville, Matt J., Wittemans, Laura B.L., Todorcevic, Marijana, Pinnick, Katherine E., Pulit, Sara L., Luan, Jian'an, Kulyté, Agné, Dahlman, Ingrid, Wareham, Nicholas J., Lotta, Luca A., Arner, Peter, Lindgren, Cecilia M., Langenberg, Claudia, Karpe, Fredrik

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Atrial fibrillation genetic risk differentiates cardioembolic stroke from other stroke subtypes by Pulit, Sara L., Weng, Lu-Chen, McArdle, Patrick F., Trinquart, Ludovic, Choi, Seung Hoan, Mitchell, Braxton D., Rosand, Jonathan, de Bakker, Paul I. W., Benjamin, Emelia J., Ellinor, Patrick T., Kittner, Steven J., Lubitz, Steven A., Anderson, Christopher D.

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Machine Learning based histology phenotyping to investigate the epidemiologic and genetic basis of adipocyte morphology and cardiometabolic traits by Glastonbury, Craig A., Pulit, Sara L., Honecker, Julius, Censin, Jenny C., Laber, Samantha, Yaghootkar, Hanieh, Rahmioglu, Nilufer, Pastel, Emilie, Kos, Katerina, Pitt, Andrew, Hudson, Michelle, Nellåker, Christoffer, Beer, Nicola L., Hauner, Hans, Becker, Christian M., Zondervan, Krina T., Frayling, Timothy M., Claussnitzer, Melina, Lindgren, Cecilia M.

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Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics by Bovijn, Jonas, Krebs, Kristi, Chen, Chia-Yen, Boxall, Ruth, Censin, Jenny C., Ferreira, Teresa, Pulit, Sara L., Glastonbury, Craig A., Laber, Samantha, Millwood, Iona Y., Lin, Kuang, Li, Liming, Chen, Zhengming, Milani, Lili, Smith, George Davey, Walters, Robin G., Mägi, Reedik, Neale, Benjamin M., Lindgren, Cecilia M., Holmes, Michael V.

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