List of works by Binbin Wang

A novel mutation of Hyaluronan synthase 2 gene in Chinese children with ventricular septal defect

scientific article

A rare frameshift variant in trans with the IVS9-5T allele of CFTR in a Chinese pedigree with congenital aplasia of vas deferens

scientific article published on 10 November 2019

A study of TNF-alpha-238 and -308 polymorphisms with different outcomes of persistent hepatitis B virus infection in China ⬇️

scientific article published on December 1, 2010

Analysis of CNVs of CFTR gene in Chinese Han population with CBAVD

scientific article published on 19 September 2020

Association between -238 but not -308 polymorphism of Tumor necrosis factor alpha (TNF-alpha)v and unexplained recurrent spontaneous abortion (URSA) in Chinese population ⬇️

scientific article published on September 28, 2010

Association between thrombophilia gene polymorphisms and preeclampsia: a meta-analysis

scientific article

Association of ARNTL and PER1 genes with Parkinson's disease: a case-control study of Han Chinese.

scientific article

CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdens

scientific article published on 03 June 2016

CYP46A1 functional promoter haplotypes decipher genetic susceptibility to Alzheimer's disease

scientific article published on January 2010

Clinical and molecular analysis of a Chinese family with autosomal dominant neurohypophyseal diabetes insipidus associated with a novel missense mutation in the vasopressin-neurophysin II gene.

scientific article published on 4 February 2012

Compound heterozygous mutations in CFTR causing CBAVD in Chinese pedigrees

scientific article published on 18 November 2018

FABP4: a novel candidate gene for polycystic ovary syndrome

scientific article published on 21 October 2009

Genetic analysis of tumor necrosis factor-alpha (TNF-alpha) G-308A and Saitohin Q7R polymorphisms with Alzheimer's disease

scientific article published on 8 April 2008

Genetic association between PAX2 and mullerian duct anomalies in Han Chinese females

scientific article

Genetic association of polymorphism rs1333049 with gout.

scientific article published on 9 May 2011

Genetic variations in GJA3, GJA8, LIM2, and age-related cataract in the Chinese population: a mutation screening study.

scientific article

HOXA10, EMX2 and TENM1 expression in the mid-secretory endometrium of infertile women with a Müllerian duct anomaly

scientific article published on 29 January 2016

Identification and functional analysis of a novel LHX1 mutation associated with congenital absence of the uterus and vagina

scientific article published on 02 January 2017

Identified OAS3 gene variants associated with coexistence of HBsAg and anti-HBs in chronic HBV infection.

scientific article published on 27 March 2018

Indicators of Male Gout Patients' Comorbidities with the Theory on Traditional Chinese Medicine

article

MYH9-related disease: description of a large Chinese pedigree and a survey of reported mutations

scientific article

New Gene Variants Associated with the Risk of Chronic HBV Infection

scientific article published on 15 April 2020

New candidate gene POU5F1 associated with premature ovarian failure in Chinese patients

scientific article published on 20 November 2010

Novel mutation in SP2 in a Chinese pedigree with Neural tube defects

scientific article published on 31 May 2018

Novel risk loci for rheumatoid arthritis in Han Chinese and congruence with risk variants in Europeans

scientific article

On the origin of Tibetans and their genetic basis in adapting high-altitude environments

scientific article

Pathogenic role of ADGRG2 in CBAVD patients replicated in Chinese population

scientific article published on 14 August 2017

Polymorphisms in the presumptive promoter region of the SLC2A9 gene are associated with gout in a Chinese male population

scientific article

Serum Metabolic Profiling Analysis of Gout Patients Treated with Traditional Chinese Medicine Tongfengtai Granules Based on Gas Chromatography-Mass Spectrometry

scientific article published on 26 April 2020

Short read mapping for exome sequencing

scientific article published on 01 January 2013

The Arg233Lys AQP0 mutation disturbs aquaporin0-calmodulin interaction causing polymorphic congenital cataract

scientific article

The DNA methylation profile of PLA2G4C gene promoter in schizophrenia

scientific article published on 09 August 2012

Two novel HAND1 mutations in Chinese patients with ventricular septal defect

scientific article published on 18 October 2011

Two single nucleotide polymorphisms in the GDF5 gene are associated with development dysplasia of the hip in Chinese female population

scientific article

[Research progress on molecular genetics of male homosexuality].

scientific article published in August 2016

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