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American Journal of Human Genetics|September 3, 2019
Germline 16p11.2 Microdeletion Predisposes to NeuroblastomaLaura E Egolf, Zalman Vaksman, Gonzalo Lopez, et al.Frontiers in Cellular and Infection Microbiology|August 1, 2024
Methylome-wide analysis in systemic microbial-induced experimental periodontal disease in mice with different susceptibilityCristhiam de Jesus Hernandez Martinez, Joseph Glessner, Livia Sertori Finoti, et al.BMC Medical Genetics|September 23, 2010
Population-based study of genetic variation in individuals with autism spectrum disorders from CroatiaLi-San Wang, Dubravka Hranilovic, Kai Wang, et al.Frontiers in Genetics|August 27, 2019
Target Genes of Autism Risk Loci in Brain Frontal CortexYan Sun, Xueming Yao, Michael E March, et al.Molecular Cancer|August 5, 2023
Genomic variants exclusively identified in children with birth defects and concurrent malignant tumors predispose to cancer developmentYichuan Liu, Hui-Qi Qu, Xiao Chang, et al.Nature Communications|October 13, 2015
Bayesian integration of genetics and epigenetics detects causal regulatory SNPs underlying expression variabilityAvinash Das, Michael Morley, Christine S Moravec, et al.Human Mutation|February 3, 2017
Loss-of-Function Mutations in KIF15 Underlying a Braddock-Carey GenocopyPatrick M A Sleiman, Michael March, Kenny Nguyen, et al.International Journal of Pediatric Endocrinology|February 1, 2017
Short stature and hypoparathyroidism in a child with Kenny-Caffey syndrome type 2 due to a novel mutation in <i>FAM111A</i> geneMary B Abraham, Dong Li, Dave Tang, et al.Journal of the National Cancer Institute|February 8, 2022
Identification of Mitochondrial DNA Variants Associated With Risk of NeuroblastomaXiao Chang, Yichuan Liu, Joseph Glessner, et al.Plos One|September 19, 2018
CLEC16A regulates splenocyte and NK cell function in part through MEK signalingRahul Pandey, Marina Bakay, Heather S Hain, et al.Pageof 91