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JIMD Reports|August 18, 2018
DPAGT1 Deficiency with Encephalopathy (DPAGT1-CDG): Clinical and Genetic Description of 11 New PatientsBobby G Ng, Hunter R Underhill, Lars Palm, et al.Science Advances|October 12, 2023
A single-cell multi-omic atlas spanning the adult rhesus macaque brainKenneth L Chiou, Xingfan Huang, Martin O Bohlen, et al.Cell|August 7, 2018
A Single-Cell Atlas of In Vivo Mammalian Chromatin AccessibilityDarren A Cusanovich, Andrew J Hill, Delasa Aghamirzaie, et al.Biorxiv : the Preprint Server for Biology|October 17, 2024
Linking candidate causal autoimmune variants to T cell networks using genetic and epigenetic screens in primary human T cellsChing-Huang Ho, Maxwell A Dippel, Meghan S McQuade, et al.Plos One|September 6, 2014
Genome sequencing of idiopathic pulmonary fibrosis in conjunction with a medical school human anatomy courseAkash Kumar, Max Dougherty, Gregory M Findlay, et al.Brain : a Journal of Neurology|February 28, 2015
PI3K/AKT pathway mutations cause a spectrum of brain malformations from megalencephaly to focal cortical dysplasiaLaura A Jansen, Ghayda M Mirzaa, Gisele E Ishak, et al.Proceedings of the National Academy of Sciences of the United States of America|November 4, 2020
Systematic integrated analysis of genetic and epigenetic variation in diabetic kidney diseaseXin Sheng, Chengxiang Qiu, Hongbo Liu, et al.The Journal of Clinical Investigation|May 17, 2021
Transcriptome-wide association analysis identifies DACH1 as a kidney disease risk gene that contributes to fibrosisTomohito Doke, Shizheng Huang, Chengxiang Qiu, et al.Proceedings of the National Academy of Sciences of the United States of America|September 28, 2011
Exome sequencing identifies a spectrum of mutation frequencies in advanced and lethal prostate cancersAkash Kumar, Thomas A White, Alexandra P MacKenzie, et al.Science (New York, N.Y.)|November 13, 2020
A human cell atlas of fetal chromatin accessibilitySilvia Domcke, Andrew J Hill, Riza M Daza, et al.Pageof 47