Li Jin

Shanghai, 200438, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 18 publications

Ancient genomes illuminate the demographic history of Shandong over the past two millennia.

Ancient genomes illuminate the demographic history of Shandong over the past two millennia.

Journal: Journal of genetics and genomics = Yi chuan xue bao

Published: January 29, 2024

Paternal gene pool of Malays in Southeast Asia and its applications for the early expansion of Austronesians.

Paternal gene pool of Malays in Southeast Asia and its applications for the early expansion of Austronesians.

Journal: American journal of human biology : the official journal of the Human Biology Council

Published: December 12, 2019

Human and mouse studies establish TBX6 in Mendelian CAKUT and as a potential driver of kidney defects associated with the 16p11.2 microdeletion syndrome.

Human and mouse studies establish TBX6 in Mendelian CAKUT and as a potential driver of kidney defects associated with the 16p11.2 microdeletion syndrome.

Journal: Kidney international

Published: August 22, 2019

Increased TBX6 gene dosages induce congenital cervical vertebral malformations in humans and mice.

Increased TBX6 gene dosages induce congenital cervical vertebral malformations in humans and mice.

Journal: Journal of medical genetics

Published: June 01, 2019

Chromosomal microarray analysis in fetuses with congenital anomalies of the kidney and urinary tract: A prospective cohort study and meta-analysis.

Chromosomal microarray analysis in fetuses with congenital anomalies of the kidney and urinary tract: A prospective cohort study and meta-analysis.

Journal: Prenatal diagnosis

Published: August 10, 2018

TBX6 compound inheritance leads to congenital vertebral malformations in humans and mice.

TBX6 compound inheritance leads to congenital vertebral malformations in humans and mice.

Journal: Human molecular genetics

Published: August 06, 2018

Noncoding rare variants of TBX6 in congenital anomalies of the kidney and urinary tract.

Noncoding rare variants of TBX6 in congenital anomalies of the kidney and urinary tract.

Journal: Molecular genetics and genomics : MGG

Published: July 11, 2018

TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model.

TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: July 05, 2018

Reconstruction of Y-chromosome phylogeny reveals two neolithic expansions of Tibeto-Burman populations.

Reconstruction of Y-chromosome phylogeny reveals two neolithic expansions of Tibeto-Burman populations.

Journal: Molecular genetics and genomics : MGG

Published: April 24, 2018

Paternal origin of Paleo-Indians in Siberia: insights from Y-chromosome sequences.

Paternal origin of Paleo-Indians in Siberia: insights from Y-chromosome sequences.

Journal: European journal of human genetics : EJHG

Published: August 29, 2017

An RNA‑sequencing study identifies candidate genes for angiotensin II‑induced cardiac remodeling.

An RNA‑sequencing study identifies candidate genes for angiotensin II‑induced cardiac remodeling.

Journal: Molecular medicine reports

Published: March 13, 2017

Assessing genome-wide copy number variation in the Han Chinese population.

Assessing genome-wide copy number variation in the Han Chinese population.

Journal: Journal of medical genetics

Published: February 21, 2017

Showing 1-12 of 18

Last Updated: 09/26/2026