Author details

Full Name

Jin Li

Affiliation

ORCID

Career Start Year

2013

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37035746	Identification of copy number variants contributing to hallux valgus.	Front Genet	2023
36316489	ParseCNV2: efficient sequencing tool for copy number variation genome-wide association studies.	Eur J Hum Genet	2023
37120522	Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders.	J Neurodev Disord	2023
35347896	Identification of Novel Loci Shared by Juvenile Idiopathic Arthritis Subtypes Through Integrative Genetic Analysis.	Arthritis Rheumatol	2022
35171267	Genetic analysis for type 1 diabetes genes in juvenile dermatomyositis unveils genetic disease overlap.	Rheumatology (Oxford)	2022
34997821	Improved genetic risk scoring algorithm for type 1 diabetes prediction.	Pediatr Diabetes	2022
34302048	Genetic architecture of type 1 diabetes with low genetic risk score informed by 41 unreported loci.	Commun Biol	2021
33479212	Integrative analysis of genome-wide association studies identifies novel loci associated with neuropsychiatric disorders.	Transl Psychiatry	2021
33677556	Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23.	Eur Heart J	2021
33627065	MONTAGE: a new tool for high-throughput detection of mosaic copy number variation.	BMC Genomics	2021
33926255	New insights into hallux valgus by whole exome sequencing study.	Exp Biol Med (Maywood)	2021
33713608	Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry.	Am J Hum Genet	2021
31447229	CNV Association of Diverse Clinical Phenotypes from eMERGE reveals novel disease biology underlying cardiovascular disease.	Int J Cardiol	2020
32059048	Correction: Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy.	PLoS One	2020
31937769	Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations.	Nat Commun	2020
33076506	The Multi-Omics Architecture of Juvenile Idiopathic Arthritis.	Cells	2020
30878790	Microduplications at the 15q11.2 BP1-BP2 locus are enriched in patients with anorexia nervosa.	J Psychiatr Res	2019
29855607	Genome-wide meta-analysis of SNP-by9-ACEI/ARB and SNP-by-thiazide diuretic and effect on serum potassium in cohorts of European and African ancestry.	Pharmacogenomics J	2019
30760877	Candidate gene analyses for acute pain and morphine analgesia after pediatric day surgery: African American versus European Caucasian ancestry and dose prediction limits.	Pharmacogenomics J	2019
31491410	Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology.	Am J Hum Genet	2019
30972099	Identification of Target Genes at Juvenile Idiopathic Arthritis GWAS Loci in Human Neutrophils.	Front Genet	2019
31447881	Target Genes of Autism Risk Loci in Brain Frontal Cortex.	Front Genet	2019
31160809	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2019
27958378	Large-scale pharmacogenomic study of sulfonylureas and the QT, JT and QRS intervals: CHARGE Pharmacogenomics Working Group.	Pharmacogenomics J	2018
30175238	Meta-analysis of exome array data identifies six novel genetic loci for lung function.	Wellcome Open Res	2018
30266756	Common variants at 5q33.1 predispose to migraine in African-American children.	J Med Genet	2018
30323833	Common and Rare Genetic Risk Factors Converge in Protein Interaction Networks Underlying Schizophrenia.	Front Genet	2018
29549330	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29549329	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29321517	Genome-wide association study of homocysteine in African Americans from the Jackson Heart Study, the Multi-Ethnic Study of Atherosclerosis, and the Coronary Artery Risk in Young Adults study.	J Hum Genet	2018
29632382	Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.	Nat Genet	2018
29540468	Genetic Reduction in Left Ventricular Protein Kinase C-Î± and Adverse Ventricular Remodeling in Human Subjects.	Circ Genom Precis Med	2018
29273807	Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
28146470	Rare and low-frequency coding variants alter human adult height.	Nature	2017
28430825	Discovery and fine-mapping of adiposity loci using high density imputation of genome-wide association studies in individuals of African ancestry: African Ancestry Anthropometry Genetics Consortium.	PLoS Genet	2017
28630421	A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling.	Sci Rep	2017
28715357	Pain versus analgesia: TAOK3 as a pharmacogene.	Pain	2017
28924153	Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma risk.	Nat Commun	2017
28828242	Genome-wide association study identifies novel type II diabetes risk loci in Jordan subpopulations.	PeerJ	2017
28827695	Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling.	Sci Rep	2017
29191242	Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders.	Genome Med	2017
28017375	Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis.	Am J Hum Genet	2017
28296976	Exome-wide association study reveals novel susceptibility genes to sporadic dilated cardiomyopathy.	PLoS One	2017
28039329	A genome-wide interaction analysis of tricyclic/tetracyclic antidepressants and RR and QT intervals: a pharmacogenomics study from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium.	J Med Genet	2017
27769252	Genomic copy number variation association study in Caucasian patients with nonsyndromic cryptorchidism.	BMC Urol	2016
27346689	Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases.	Am J Hum Genet	2016
27346686	Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals.	Am J Hum Genet	2016
27346685	Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits.	Am J Hum Genet	2016
27104816	Pathway-based Genome-wide Association Studies Reveal the Association Between Growth Factor Activity and Inflammatory Bowel Disease.	Inflamm Bowel Dis	2016
27005825	Variants in CXCR4 associate with juvenile idiopathic arthritis susceptibility.	BMC Med Genet	2016