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Nature Communications|February 24, 2023
Multitrait genome-wide analyses identify new susceptibility loci and candidate drugs to primary sclerosing cholangitisYounghun Han, Jinyoung Byun, Catherine Zhu, et al.Nature Communications|September 23, 2015
International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathwaysHeather J Cordell, Younghun Han, George F Mells, et al.Genome Research|May 3, 2003
Haplotype structure, LD blocks, and uneven recombination within the LRP5 geneRebecca C J Twells, Charles A Mein, Michael S Phillips, et al.Nature Communications|August 19, 2015
Association analysis identifies new risk loci for congenital heart disease in Chinese populationsYuan Lin, Xuejiang Guo, Bijun Zhao, et al.Plos Genetics|April 28, 2020
Mutations in SPATA13/ASEF2 cause primary angle closure glaucomaNaushin H Waseem, Sancy Low, Amna Z Shah, et al.The American Journal of Gastroenterology|September 2, 2020
Obesity, Diabetes, Coffee, Tea, and Cannabis Use Alter Risk for Alcohol-Related Cirrhosis in 2 Large Cohorts of High-Risk DrinkersJohn B Whitfield, Steven Masson, Suthat Liangpunsakul, et al.Science Translational Medicine|December 3, 2020
Transcriptomic profiling across the nonalcoholic fatty liver disease spectrum reveals gene signatures for steatohepatitis and fibrosisOlivier Govaere, Simon Cockell, Dina Tiniakos, et al.Gastroenterology|March 6, 2021
X Chromosome Contribution to the Genetic Architecture of Primary Biliary CholangitisRosanna Asselta, Elvezia M Paraboschi, Alessio Gerussi, et al.The Journal of Allergy and Clinical Immunology|March 8, 2011
Loss-of-function variants in the filaggrin gene are a significant risk factor for peanut allergySara J Brown, Yuka Asai, Heather J Cordell, et al.Human Molecular Genetics|December 27, 2011
Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controlsRachel Soemedi, Ana Topf, Ian J Wilson, et al.Pageof 27