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Proceedings of the National Academy of Sciences of the United States of America|March 24, 2025
Genomic analysis of 11,555 probands identifies 60 dominant congenital heart disease genesMichael C Sierant, Sheng Chih Jin, Kaya Bilguvar, et al.
European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology|February 16, 2025
Methylation profile scores of environmental exposures and risk of relapse after a first episode of schizophreniaAlex-González Segura, Llucia Prohens, Laura Julià, et al.
American Journal of Human Genetics|July 14, 2015
The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and OpportunitiesJessica X Chong, Kati J Buckingham, Shalini N Jhangiani, et al.
Science (New York, N.Y.)|November 25, 2017
Molecular and cellular reorganization of neural circuits in the human lineageAndré M M Sousa, Ying Zhu, Mary Ann Raghanti, et al.
American Journal of Human Genetics|July 25, 2020
Bi-allelic HPDL Variants Cause a Neurodegenerative Disease Ranging from Neonatal Encephalopathy to Adolescent-Onset Spastic ParaplegiaRalf A Husain, Mona Grimmel, Matias Wagner, et al.
Science Translational Medicine|February 15, 2023
Age-dependent impairment in antibody responses elicited by a homologous CoronaVac booster doseBruno Andraus Filardi, Valter Silva Monteiro, Pedro Vellosa Schwartzmann, et al.
Nature Genetics|March 15, 2011
Genome-wide association study identifies susceptibility loci for IgA nephropathyAli G Gharavi, Krzysztof Kiryluk, Murim Choi, et al.
Neuron|December 23, 2018
Mutations in Chromatin Modifier and Ephrin Signaling Genes in Vein of Galen MalformationDaniel Duran, Xue Zeng, Sheng Chih Jin, et al.
Neuron|July 10, 2018
De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital HydrocephalusCharuta Gavankar Furey, Jungmin Choi, Sheng Chih Jin, et al.
Iscience|October 21, 2020
Exome Sequencing Implicates Impaired GABA Signaling and Neuronal Ion Transport in Trigeminal NeuralgiaWeilai Dong, Sheng Chih Jin, August Allocco, et al.
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