Lili Wang

1665 Kongjiang Road
Shanghai, 200092, China

Last Updated: 09/26/2026

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Found 15 publications

Genetic analysis of a child with Meier-Gorlin syndrome due to a variant of ORC6 gene

Genetic analysis of a child with Meier-Gorlin syndrome due to a variant of ORC6 gene

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: September 20, 2023

A 25 Mainland Chinese cohort of patients with PURA-related neurodevelopmental disorders: clinical delineation and genotype-phenotype correlations.

A 25 Mainland Chinese cohort of patients with PURA-related neurodevelopmental disorders: clinical delineation and genotype-phenotype correlations.

Journal: European journal of human genetics : EJHG

Published: May 09, 2022

Human breast milk-derived exosomes protect against intestinal ischemia and reperfusion injury in neonatal rats.

Human breast milk-derived exosomes protect against intestinal ischemia and reperfusion injury in neonatal rats.

Journal: Journal of pediatric surgery

Published: February 02, 2022

Chromosomal microarray analysis in fetuses with high-risk prenatal indications: A retrospective study in China.

Chromosomal microarray analysis in fetuses with high-risk prenatal indications: A retrospective study in China.

Journal: Taiwanese journal of obstetrics & gynecology

Published: November 30, 2020

A 29 Mainland Chinese cohort of patients with Phelan-McDermid syndrome: genotype-phenotype correlations and the role of SHANK3 haploinsufficiency in the important phenotypes.

A 29 Mainland Chinese cohort of patients with Phelan-McDermid syndrome: genotype-phenotype correlations and the role of SHANK3 haploinsufficiency in the important phenotypes.

Journal: Orphanet journal of rare diseases

Published: June 28, 2020

High Detection Rate of Copy Number Variations Using Capture Sequencing Data: A Retrospective Study.

High Detection Rate of Copy Number Variations Using Capture Sequencing Data: A Retrospective Study.

Journal: Clinical chemistry

Published: August 18, 2019

Identification of RUNX2 variants associated with cleidocranial dysplasia.

Identification of RUNX2 variants associated with cleidocranial dysplasia.

Journal: Hereditas

Published: March 04, 2019

Circulating tumor cells as an independent prognostic factor in advanced colorectal cancer: a retrospective study in 121 patients.

Circulating tumor cells as an independent prognostic factor in advanced colorectal cancer: a retrospective study in 121 patients.

Journal: International journal of colorectal disease

Published: December 14, 2018

Genetic Evaluation of 114 Chinese Short Stature Children in the Next Generation Era: a Single Center Study.

Genetic Evaluation of 114 Chinese Short Stature Children in the Next Generation Era: a Single Center Study.

Journal: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology

Published: January 15, 2018

Mutation spectrum of hyperphenylalaninemia candidate genes and the genotype-phenotype correlation in the Chinese population.

Mutation spectrum of hyperphenylalaninemia candidate genes and the genotype-phenotype correlation in the Chinese population.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: November 16, 2017

Chromosomal microarray analysis in developmental delay and intellectual disability with comorbid conditions.

Chromosomal microarray analysis in developmental delay and intellectual disability with comorbid conditions.

Journal: BMC medical genomics

Published: July 25, 2017

Targeted/exome sequencing identified mutations in ten Chinese patients diagnosed with Noonan syndrome and related disorders.

Targeted/exome sequencing identified mutations in ten Chinese patients diagnosed with Noonan syndrome and related disorders.

Journal: BMC medical genomics

Published: June 15, 2017

Showing 1-12 of 15

Last Updated: 09/26/2026