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Author Details
Full Name
Jingjing Li
Affiliation
ORCID
Career Start Year
2013
Papers
18
H Index
11
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35716026
Exome sequencing identifies genetic variants in anophthalmia and microphthalmia.
Am J Med Genet A
2022
36167075
Systems analysis of de novo mutations in congenital heart diseases identified a protein network in the hypoplastic left heart syndrome.
Cell Syst
2022
34430814
A panoramic view of proteomics and multiomics in precision health.
iScience
2021
34189540
Common and rare variant analyses combined with single-cell multiomics reveal cell-type-specific molecular mechanisms of COVID-19 severity.
medRxiv
2021
32907840
A Deep Learning Framework Identifies Pathogenic Noncoding Somatic Mutations from Personal Prostate Cancer Genomes.
Cancer Research
2020
30674050
A Genome-Wide Analysis of Clinical Chorioamnionitis among Preterm Infants.
American Journal of Perinatology
2019
30644444
The contributions of genetics to premature birth.
Pediatric Research
2019
30560947
Understanding health disparities.
J Perinatol
2019
30901546
Gene-Environment Interaction in the Era of Precision Medicine.
Cell
2019
29937092
Natural Selection Has Differentiated the Progesterone Receptor among Human Populations.
Am J Hum Genet
2018
30193110
Decoding the Genomics of Abdominal Aortic Aneurysm.
Cell
2018
28388617
Fetal de novo mutations and preterm birth.
PLoS Genet
2017
26963946
The genetic predisposition to bronchopulmonary dysplasia.
Curr Opin Pediatr
2016
26030808
Exome Sequencing of Neonatal Blood Spots and the Identification of Genes Implicated in Bronchopulmonary Dysplasia.
Am J Respir Crit Care Med
2015
26949739
Identification of Human Neuronal Protein Complexes Reveals Biochemical Activities and Convergent Mechanisms of Action in Autism Spectrum Disorders.
Cell Syst
2015
25409826
Principles of regulatory information conservation between mouse and human.
Nature
2014
25549968
Integrated systems analysis reveals a molecular network underlying autism spectrum disorders.
Mol Syst Biol
2014
24136358
Extensive variation in chromatin states across humans.
Science
2013
1 - 18 of 18
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