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Author Details

Jingjing Li
2013
18
11
PMIDPaper TitleJournal TitlePublished Year
35716026Exome sequencing identifies genetic variants in anophthalmia and microphthalmia.Am J Med Genet A2022
36167075Systems analysis of de novo mutations in congenital heart diseases identified a protein network in the hypoplastic left heart syndrome.Cell Syst2022
34430814A panoramic view of proteomics and multiomics in precision health.iScience2021
34189540Common and rare variant analyses combined with single-cell multiomics reveal cell-type-specific molecular mechanisms of COVID-19 severity.medRxiv2021
32907840A Deep Learning Framework Identifies Pathogenic Noncoding Somatic Mutations from Personal Prostate Cancer Genomes.Cancer Research2020
30674050A Genome-Wide Analysis of Clinical Chorioamnionitis among Preterm Infants.American Journal of Perinatology2019
30644444The contributions of genetics to premature birth.Pediatric Research2019
30560947Understanding health disparities.J Perinatol2019
30901546Gene-Environment Interaction in the Era of Precision Medicine.Cell2019
29937092Natural Selection Has Differentiated the Progesterone Receptor among Human Populations.Am J Hum Genet2018
30193110Decoding the Genomics of Abdominal Aortic Aneurysm.Cell2018
28388617Fetal de novo mutations and preterm birth.PLoS Genet2017
26963946The genetic predisposition to bronchopulmonary dysplasia.Curr Opin Pediatr2016
26030808Exome Sequencing of Neonatal Blood Spots and the Identification of Genes Implicated in Bronchopulmonary Dysplasia.Am J Respir Crit Care Med2015
26949739Identification of Human Neuronal Protein Complexes Reveals Biochemical Activities and Convergent Mechanisms of Action in Autism Spectrum Disorders.Cell Syst2015
25409826Principles of regulatory information conservation between mouse and human.Nature2014
25549968Integrated systems analysis reveals a molecular network underlying autism spectrum disorders.Mol Syst Biol2014
24136358Extensive variation in chromatin states across humans.Science2013
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