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Human Molecular Genetics|April 10, 2010
In silico replication of the genome-wide association results of the Type 1 Diabetes Genetics ConsortiumHui-Qi Qu, Jonathan P Bradfield, Quan Li, et al.Frontiers in Endocrinology|May 20, 2025
Investigating TSHR gene variants in consanguineous families: novel insights into variable expression in familial congenital hypothyroidismZakiye Nadeali, Zohreh Mohammadi-Zaniani, Sajjad Biglari, et al.Human Mutation|June 3, 2010
Unexpected allelic heterogeneity and spectrum of mutations in Fowler syndrome revealed by next-generation exome sequencingEmilie Lalonde, Steffen Albrecht, Kevin C H Ha, et al.Frontiers in Immunology|March 3, 2023
Clinical application of immune repertoire sequencing in solid organ transplantPaaksum Wong, Davide P Cina, Karen R Sherwood, et al.Ebiomedicine|June 25, 2025
Metabolome-wide Mendelian randomisation reveals causal links between circulating metabolites and type 1 diabetesBasile Jumentier, Isabel Gamache, Dominika A Michalek, et al.Pediatrics in Review|December 31, 2023
Cushing Syndrome in ChildhoodAnthony Parish, Clement Cheung, Anna Ryabets-Lienhard, et al.Epigenetics|December 23, 2009
Cell culture-induced aberrant methylation of the imprinted IG DMR in human lymphoblastoid cell linesAabida Saferali, Elin Grundberg, Soizik Berlivet, et al.Diabetes Research and Clinical Practice|July 5, 2025
Non-syndromic WFS1 mutations are not a rare cause of diabetes in PakistanIbrar Rafique, Asif Mir, Natalija Popovic, et al.World Journal of Diabetes|December 10, 2021
Comprehensive genetic screening reveals wide spectrum of genetic variants in monogenic forms of diabetes among Pakistani populationIbrar Rafique, Asif Mir, Shajee Siddiqui, et al.Journal of the Endocrine Society|January 25, 2023
A Novel Somatic Mutation Implicates ATP6V0D1 in Proinsulin ProcessingParizad Avari, Pei Chia Eng, Ming Hu, et al.Pageof 16