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American Journal of Human Genetics|June 5, 2018
Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic SpectrumAndrea Ganna, F Kyle Satterstrom, Seyedeh M Zekavat, et al.
Medrxiv : the Preprint Server for Health Sciences|March 24, 2021
Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortalityTomoko Nakanishi, Sara Pigazzini, Frauke Degenhardt, et al.
The Journal of Clinical Investigation|October 1, 2021
Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortalityTomoko Nakanishi, Sara Pigazzini, Frauke Degenhardt, et al.
Plos Genetics|August 13, 2013
Gene × physical activity interactions in obesity: combined analysis of 111,421 individuals of European ancestryShafqat Ahmad, Gull Rukh, Tibor V Varga, et al.
Scientific Data|January 20, 2023
Deep phenotyping and genomic data from a nationally representative study on dementia in IndiaJinkook Lee, Sarah Petrosyan, Pranali Khobragade, et al.
Plos Genetics|May 31, 2019
Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish populationManuel A Rivas, Brandon E Avila, Jukka Koskela, et al.
Plos Genetics|May 26, 2018
Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish populationManuel A Rivas, Brandon E Avila, Jukka Koskela, et al.
Nature Medicine|February 23, 2026
Genetic regulation across germline and somatic variation on the Y chromosome contributes to type 2 diabetesGo Sato, Yuji Yamamoto, Kyuto Sonehara, et al.
Nature|May 29, 2020
The mutational constraint spectrum quantified from variation in 141,456 humansKonrad J Karczewski, Laurent C Francioli, Grace Tiao, et al.
American Journal of Epidemiology|December 21, 2012
Meta-analysis investigating associations between healthy diet and fasting glucose and insulin levels and modification by loci associated with glucose homeostasis in data from 15 cohortsJennifer A Nettleton, Marie-France Hivert, Rozenn N Lemaitre, et al.
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