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Sayantan Das

Showing results (31-40 of 37) with videos related to

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American Journal of Human Genetics|December 3, 2015
Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic ArchitecturePhilip E Stuart, Rajan P Nair, Lam C Tsoi, et al.
Human Molecular Genetics|October 4, 2017
Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signallingNick Dand, Sören Mucha, Lam C Tsoi, et al.
Annals of Neurology|May 3, 2021
Genomewide Association Studies of LRRK2 Modifiers of Parkinson's DiseaseDongbing Lai, Babak Alipanahi, Pierre Fontanillas, et al.
Nature Genetics|August 23, 2016
A reference panel of 64,976 haplotypes for genotype imputationShane McCarthy, Sayantan Das, Warren Kretzschmar, et al.
Nature Communications|December 19, 2020
Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular diseaseJonas B Nielsen, Oren Rom, Ida Surakka, et al.
Hypertension (Dallas, Tex. : 1979)|June 2, 2022
Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and HypertensionTanika N Kelly, Xiao Sun, Karen Y He, et al.
Nature|February 11, 2021
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed ProgramDaniel Taliun, Daniel N Harris, Michael D Kessler, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
American Journal of Human Genetics|December 3, 2015
Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic ArchitecturePhilip E Stuart, Rajan P Nair, Lam C Tsoi, et al.
Human Molecular Genetics|October 4, 2017
Exome-wide association study reveals novel psoriasis susceptibility locus at TNFSF15 and rare protective alleles in genes contributing to type I IFN signallingNick Dand, Sören Mucha, Lam C Tsoi, et al.
Annals of Neurology|May 3, 2021
Genomewide Association Studies of LRRK2 Modifiers of Parkinson's DiseaseDongbing Lai, Babak Alipanahi, Pierre Fontanillas, et al.
Nature Genetics|August 23, 2016
A reference panel of 64,976 haplotypes for genotype imputationShane McCarthy, Sayantan Das, Warren Kretzschmar, et al.
Nature Communications|December 19, 2020
Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular diseaseJonas B Nielsen, Oren Rom, Ida Surakka, et al.
Hypertension (Dallas, Tex. : 1979)|June 2, 2022
Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and HypertensionTanika N Kelly, Xiao Sun, Karen Y He, et al.
Nature|February 11, 2021
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed ProgramDaniel Taliun, Daniel N Harris, Michael D Kessler, et al.
Pageof 4