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European Journal of Human Genetics : EJHG|February 20, 2014
A compound heterozygous mutation in GPD1 causes hepatomegaly, steatohepatitis, and hypertriglyceridemiaMugdha Joshi, Jacqueline Eagan, Nirav K Desai, et al.Cancer Research Communications|August 11, 2023
MHC Class II is Induced by IFNγ and Follows Three Distinct Patterns of Expression in Colorectal Cancer OrganoidsOliver J Pickles, Kasun Wanigasooriya, Anetta Ptasinska, et al.Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|June 29, 2026
The Food and Microbiome Longitudinal Investigation (FAMiLI) Study: an Asian American (AsA) Enriched Multi-ethnic Environmental CohortJiyoung Ahn, Zelle Halloran, Dia B Beggs, et al.Scientific Reports|July 15, 2026
Use of organ transplant solution to preserve skeletal muscle for cellular and spatial transcriptomic analysesPrech Uapinyoying, Young Jae Moon, Aiping Zhang, et al.Plos Biology|October 26, 2018
Disruption of CTCF-YY1-dependent looping of the human papillomavirus genome activates differentiation-induced viral oncogene transcriptionIeisha Pentland, Karen Campos-León, Marius Cotic, et al.Journal of Crohn'S & Colitis|February 5, 2020
A Pilot Integrative Analysis of Colonic Gene Expression, Gut Microbiota, and Immune Infiltration in Primary Sclerosing Cholangitis-Inflammatory Bowel Disease: Association of Disease With Bile Acid PathwaysMohammed Nabil Quraishi, Animesh Acharjee, Andrew D Beggs, et al.Brain : a Journal of Neurology|July 15, 2005
Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutationsKumaraswamy Sivakumar, Theodoros Kyriakides, Imke Puls, et al.Journal of the Royal Society of Medicine|June 22, 2023
Trends in SARS-CoV-2 infection and vaccination in school staff, students and their household members from 2020 to 2022 in Wales, UK: an electronic cohort studyEmily Lowthian, Hoda Abbasizanjani, Stuart Bedston, et al.Disease Models & Mechanisms|May 31, 2012
Myotubular myopathy and the neuromuscular junction: a novel therapeutic approach from mouse modelsJames J Dowling, Romain Joubert, Sean E Low, et al.BMC Medical Genetics|November 15, 2018
De novo variant of TRRAP in a patient with very early onset psychosis in the context of non-verbal learning disability and obsessive-compulsive disorder: a case reportChrystal F Mavros, Catherine A Brownstein, Roshni Thyagrajan, et al.Pageof 148