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American Journal of Human Genetics|November 27, 2010
A homozygous mutation in the tight-junction protein JAM3 causes hemorrhagic destruction of the brain, subependymal calcification, and congenital cataractsGaneshwaran H Mochida, Vijay S Ganesh, Jillian M Felie, et al.Frontiers in Immunology|November 16, 2018
Early Induction of Human Regulatory Dermal Antigen Presenting Cells by Skin-Penetrating Schistosoma Mansoni CercariaeBéatrice M F Winkel, Mirjam R Dalenberg, Clarize M de Korne, et al.Annals of Clinical and Translational Neurology|August 3, 2024
Protein-extending ACTN2 frameshift variants cause variable myopathy phenotypes by protein aggregationJohanna Ranta-Aho, Kevin J Felice, Per Harald Jonson, et al.Plos Pathogens|September 8, 2020
Plasmodium sporozoites induce regulatory macrophagesBéatrice M F Winkel, Leonard R Pelgrom, Roos van Schuijlenburg, et al.Nature Genetics|February 2, 2010
Mutations in PNKP cause microcephaly, seizures and defects in DNA repairJun Shen, Edward C Gilmore, Christine A Marshall, et al.Emerging Infectious Diseases|December 2, 2020
Fatal Case of Chronic Jamestown Canyon Virus Encephalitis Diagnosed by Metagenomic Sequencing in Patient Receiving RituximabIsaac H Solomon, Vijay S Ganesh, Guixia Yu, et al.Journal of Urban Health : Bulletin of the New York Academy of Medicine|March 27, 2026
A Multicenter Qualitative Stakeholder Evaluation of the Hospital-Based Violence Intervention Programs in the Los Angeles County Safety-Net Healthcare SystemZachary E Thompson, Barbara Turner, Jennifer Laughter, et al.Nature Materials|February 7, 2018
Quantitative self-assembly prediction yields targeted nanomedicinesYosi Shamay, Janki Shah, Mehtap Işık, et al.Muscle & Nerve|July 29, 2024
Dominant stop-loss HNRNPA1 variants in juvenile-onset myopathyJohnnie Turner, Christine C Bruels, Audrey L Daugherty, et al.Nature Genetics|October 2, 2012
CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar developmentGaneshwaran H Mochida, Vijay S Ganesh, Maria I de Michelena, et al.Pageof 29