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2016
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis.van Rheenen, W., Shatunov A., Dekker AM, McLaughlin RL, Diekstra FP, Pulit SL, van der Spek RA, Võsa U., de Jong S., Robinson MR, Yang J., Fogh I., van Doormaal PT, Tazelaar GH, Koppers M., Blokhuis AM, Sproviero W., Jones AR, Kenna KP, van Eijk KR, et al. Nature genetics, 2016/07/25, (2016) Read More / View Supplemental Materials
Abstract
2015
Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension Risk.Yu, B., Pulit SL, Hwang SJ, Brody JA, Amin N., Auer PL, Bis JC, Boerwinkle E., Burke GL, Chakravarti A., Correa A., Dreisbach AW, Franco OH, Ehret GB, Franceschini N., Hofman A., Lin DY, Metcalf GA, Musani SK, Muzny D., et al. Circulation. Cardiovascular genetics, 2015/12/11, (2015) Read More / View Supplemental Materials
Abstract
Fine mapping in the MHC region accounts for 18% additional genetic risk for celiac disease.Gutierrez-Achury, J., Zhernakova A., Pulit SL, Trynka G., Hunt KA, Romanos J., Raychaudhuri S., van Heel DA, Wijmenga C., and de Bakker PI Nature genetics, 2015/04/20, (2015) Read More / View Supplemental Materials
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2014
Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.Arking, DE, Pulit SL, Crotti L., van der Harst P., Munroe PB, Koopmann TT, Sotoodehnia N., Rossin EJ, Morley M., Wang X., Johnson AD, Lundby A., Gudbjartsson DF, Noseworthy PA, Eijgelsheim M., Bradford Y., Tarasov KV, Dörr M., Müller-Nurasyid M., Lahtinen AM, et al. Nature genetics, 2014/06/22, (2014) Read More / View Supplemental Materials
Abstract
A genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathy.Kuiper, JJ, van Setten J., Ripke S., Van't Slot R., Mulder F., Missotten T., Baarsma GS, Francioli LC, Pulit SL, de Kovel CG, Ten Dam-van Loon N., den Hollander AI, Huis In Het Veld P., Hoyng CB, Cordero-Coma M., Martín J., Llorenç V., Arya B., Thomas D., Bakker SC, et al. Human molecular genetics, 2014/06/22, (2014) Read More / View Supplemental Materials
Abstract
Common Variation in Fatty Acid Metabolic Genes and Risk of Incident Sudden Cardiac Arrest.Lemaitre, RN, Johnson CO, Hesselson S., Sotoodhenia N., McKnight B., Sitlani CM, Rea TD, King IB, Kwok PY, Mak A., Li G., Brody J., Larson E., Mozaffarian D., Psaty BM, Huertas-Vazquez A., Tardif JC, Albert CM, Lyytikäinen LP, Arking DE, et al. Heart rhythm : the official journal of the Heart Rhythm Society, 2014/01/10, (2014) Read More / View Supplemental Materials
Abstract
2013
Deleterious alleles in the human genome are on average younger than neutral alleles of the same frequency.Kiezun, A., Pulit SL, Francioli LC, van Dijk F., Swertz M., Boomsma DI, van Duijn CM, Slagboom PE, van Ommen GJ, Wijmenga C., Genome of the Netherlands Consortium, de Bakker PI, and Sunyaev SR PLoS genetics, 2013/02/01, Volume 9, Issue 2, p.e1003301, (2013) Read More / View Supplemental Materials
Abstract
  • Showing 1-7 of 7 Results