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Plos Genetics|July 7, 2020
Linking protein to phenotype with Mendelian Randomization detects 38 proteins with causal roles in human diseases and traitsAndrew D Bretherick, Oriol Canela-Xandri, Peter K Joshi, et al.
Plos Genetics|January 13, 2010
Modeling of environmental effects in genome-wide association studies identifies SLC2A2 and HP as novel loci influencing serum cholesterol levelsWilmar Igl, Asa Johansson, James F Wilson, et al.
Croatian Medical Journal|March 5, 2009
Genome-wide association study of biochemical traits in Korcula Island, CroatiaTatijana Zemunik, Mladen Boban, Gordan Lauc, et al.
European Journal of Human Genetics : EJHG|February 16, 2012
Genome-wide analysis of epistasis in body mass index using multiple human populationsWen-Hua Wei, Gib Hemani, Attila Gyenesei, et al.
Nature Communications|June 16, 2026
Disease-associated genetic variants can cause missense effects in tissue-specific protein isoformsGiovanna Weykopf, Mihaly Badonyi, Elias T Friman, et al.
Nature Communications|August 6, 2015
Multicohort analysis of the maternal age effect on recombinationHilary C Martin, Ryan Christ, Julie G Hussin, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 5, 2019
The genetic landscape of Scotland and the IslesEdmund Gilbert, Seamus O'Reilly, Michael Merrigan, et al.
Scientific Reports|January 13, 2022
A multi-omics study of circulating phospholipid markers of blood pressureJun Liu, Paul S de Vries, Fabiola Del Greco M, et al.
Investigative Ophthalmology & Visual Science|May 31, 2018
Family-Based Genome-Wide Association Study of South Indian Pedigrees Supports WNT7B as a Central Corneal Thickness LocusBao Jian Fan, Xueli Chen, Nisha Sondhi, et al.
American Journal of Human Genetics|September 2, 2008
Runs of homozygosity in European populationsRuth McQuillan, Anne-Louise Leutenegger, Rehab Abdel-Rahman, et al.
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