Jing Wang

发表

On the Origin of Tibetans and Their Genetic Basis in Adapting High-Altitude Environments

Jing Wang, Xu Ma, Jun Yu, 2011, PloS one.

Comprehensive molecular diagnosis of 67 Chinese Usher syndrome probands: high rate of ethnicity specific mutations in Chinese USH patients

Lichun Jiang, Yumei Li, Rui Chen, 2015, Orphanet Journal of Rare Diseases.

FABP4: a novel candidate gene for polycystic ovary syndrome

F. Zhang, Jingjing Liu, Binbin Wang, 2009, Endocrine.

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

Binbin Wang, Jing Wang, Xu Ma, 2010, Pathology.

Spatial pattern and variations in the prevalence of congenital heart disease in children aged 4-18 years in the Qinghai-Tibetan Plateau.

Z. Ren, Zongfu Cao, Binbin Wang, 2018, The Science of the total environment.

Lack of association between interleukin-1a gene (IL-1a) C (-889) T variant and polycystic ovary syndrome in chinese women

Jingjing Liu, Binbin Wang, Jing Wang, 2009, Endocrine.

Mosaic Ring-like Small Supernumerary Marker Chromosome and Gene Mutation in a Male With Intermittent Azoospermia: A Rare Case Report

Binbin Wang, Jing Wang, Qiaoqin Li, 2020, American journal of men's health.

Association Between Alzheimer’s Disease and the NOS3 gene Glu298Asp Polymorphism in Chinese

Binbin Wang, Jing Wang, Xu Ma, 2008, Journal of Molecular Neuroscience.

Exome Sequencing and Gene Prioritization Correct Misdiagnosis in a Chinese Kindred with Familial Amyloid Polyneuropathy

Xuegong Zhang, P. Sham, H. Chen, 2016, Scientific Reports.

Mutation analysis of Connexon43 gene in Chinese patients with congenital heart defects.

Mugen Liu, Shiguo Liu, Binbin Wang, 2010, International journal of cardiology.

Mutations in Hnrnpa1 cause congenital heart defects

P. Sham, P. Kwok, You-Qiang Song, 2018, JCI insight.

Mutations in Hnrnpa 1 cause congenital heart defects

P. Sham, P. Kwok, You-Qiang Song, 2018 .

Title Mutations in Hnrnpa 1 cause congenital heart defects

P. Sham, P. Kwok, You-Qiang Song, 2018 .

A novel variation of GDF3 in Chinese Han children with a broad phenotypic spectrum of non-syndromic CHDs

Binbin Wang, Jing Wang, G. Kang, 2014, Cardiology in the Young.

The HHEX gene is not related to congenital heart disease in 296 Chinese patients

Binbin Wang, Longfei Cheng, Jing Wang, 2013, World Journal of Pediatrics.

Novel mutations of NODAL gene in Chinese patients with congenital heart disease.

Binbin Wang, Longfei Cheng, Jing Wang, 2012, Genetic testing and molecular biomarkers.

Identifying novel mutations of NKX2-5 congenital heart disease patients of Chinese minority groups.

Binbin Wang, Longfei Cheng, Jing Wang, 2011, International journal of cardiology.

Genetic variation of SAL-Like 4 (SALL4) in ventricular septal defect.

Binbin Wang, Jing Wang, Xu Ma, 2010, International journal of cardiology.

Lack of an association between CYP1A1 gene Ile462Val polymorphism and polycystic ovary syndrome in Chinese

Jingjing Liu, Binbin Wang, Jing Wang, 2009, Endocrine.

Absence of association on aldehyde dehydrogenase 2 (ALDH2) polymorphism with Mongolian Alzheimer patients

Binbin Wang, Jing Wang, Xu Ma, 2010, Neuroscience Letters.

Lack of an Association between Alzheimer’s Disease and the Cystatin C (CST3) Gene G73A Polymorphism in Mainland Chinese

D. Peng, Binbin Wang, Jing Wang, 2008, Dementia and Geriatric Cognitive Disorders.

The association of mitochondrial aldehyde dehydrogenase gene (ALDH2) polymorphism with susceptibility to late-onset Alzheimer's disease in Chinese

Binbin Wang, Jing Wang, Xu Ma, 2008, Journal of the Neurological Sciences.

Identification of KANSL1 as a novel pathogenic gene for developmental dysplasia of the hip

Jing Wang, Binbin Wang, Xiaowen Xu, 2022, Journal of Molecular Medicine.

Identification of a novel heterozygous SOX9 variant in a Chinese family with congenital heart disease

Binbin Wang, Jing Wang, Chunyan Wang, 2022, Molecular genetics & genomic medicine.

Association analysis between the tag SNP for sonic hedgehog rs9333613 polymorphism and male sexual orientation.

Binbin Wang, Jing Wang, Xu Ma, 2012, Journal of andrology.

A novel mutation in GJA8 causing congenital cataract–microcornea syndrome in a Chinese pedigree

Binbin Wang, Jing Wang, Xu Ma, 2010, Molecular vision.

A Novel CRYGD Mutation (p.Trp43Arg) Causing Autosomal Dominant Congenital Cataract in a Chinese Family

Binbin Wang, Jing Wang, Sirui Zhou, 2011, Human mutation.

Haplotype analysis of chemokine CXCL12 polymorphisms and susceptibility to premature ovarian failure in Chinese women.

Binbin Wang, Jing Wang, Xu Ma, 2011, Human reproduction.

Two novel mutations of the IRX4 gene in patients with congenital heart disease

Binbin Wang, Jing Wang, Xu Ma, 2011, Human Genetics.

CFC1 mutations in Chinese children with congenital heart disease.

Shiguo Liu, Binbin Wang, Jing Wang, 2011, International journal of cardiology.

A novel mutation in the connexin 46 (GJA3) gene associated with congenital cataract in a Chinese pedigree

Binbin Wang, Jing Wang, Xu Ma, 2011, Molecular vision.

A novel GJA8 mutation (p.I31T) causing autosomal dominant congenital cataract in a Chinese family

Binbin Wang, Jing Wang, Xu Ma, 2009, Molecular vision.

Metagenomic Analysis of Gut Microbiome in Gout Patients with Different Chinese Traditional Medicine Treatments

Binbin Wang, Jing Wang, Jianwei Chen, 2022, Evidence-based complementary and alternative medicine : eCAM.

Positive Correlation Between Beta-3-Adrenergic Receptor (ADRB3) Gene and Gout in a Chinese Male Population

Dongmei Meng, Shiguo Liu, Binbin Wang, 2011, The Journal of Rheumatology.

The PGAM4 gene in non-obstructive azoospermia

Binbin Wang, Jing Wang, Xu Ma, 2013, Systems biology in reproductive medicine.

Mutational analysis of human bone morphogenetic protein 15 in Chinese women with polycystic ovary syndrome.

Jingjing Liu, Binbin Wang, Jing Wang, 2011, Metabolism: clinical and experimental.

Association of polymorphisms in the estrogen receptor β (ESR2) with unexplained recurrent spontaneous abortion (URSA) in Chinese population

Binbin Wang, Jing Wang, Xu Ma, 2012, Journal of Maternal-Fetal & Neonatal Medicine.

The ESR1 gene in unexplained recurrent spontaneous abortion

Binbin Wang, Jing Wang, Xu Ma, 2014, Systems biology in reproductive medicine.

Case Report: Tetralogy of Fallot in a Chinese Family Caused by a Novel Missense Variant of MYOM2

Lei Wei, Binbin Wang, Jing Wang, 2022, Frontiers in Cardiovascular Medicine.

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

Binbin Wang, Jing Wang, Xiaojin He, 2016, Journal of Assisted Reproduction and Genetics.

No association between polymorphisms in PTEN and primary ovarian insufficiency in a Han Chinese population

Binbin Wang, Jing Wang, Xu Ma, 2015, Reproductive Biology and Endocrinology.

Polyalanine repeat expansion mutation of the HOXD13 gene in a Chinese family with unusual clinical manifestations of synpolydactyly.

Binbin Wang, Jing Wang, Xu Ma, 2011, European journal of medical genetics.

Strong Association Between Angiotensin I-Converting Enzyme I/D Polymorphism and Unexplained Recurrent Miscarriage of Chinese Women—A Case–Control Study

Binbin Wang, Jing Wang, Xu Ma, 2011, Reproductive Sciences.

Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) in Chinese patients with congenital bilateral absence of vas deferens.

Xinyu Zhang, Binbin Wang, Longfei Cheng, 2012, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Functional Analysis of Two Novel Mutations in TWIST1 Protein Motifs Found in Ventricular Septal Defect Patients

Binbin Wang, Longfei Cheng, Jing Wang, 2015, Pediatric Cardiology.

Interleukin 1 beta (IL-1β) promoter C [−511] T polymorphism but not C [+3953] T polymorphism is associated with polycystic ovary syndrome

Jingjing Liu, Binbin Wang, Jing Wang, 2010, Endocrine.

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

Binbin Wang, Jing Wang, Yanqiong Song, 2018, CNS neuroscience & therapeutics.

Assessment of Transcatheter or Surgical Closure of Atrial Septal Defect using Interpretable Deep Keypoint Stadiometry

Jing Wang, Fangyun Wang, Bonai Fan, 2022, Research.

Research_9790653 1..10

Jing Wang, Fangyun Wang, Bonai Fan, 2022 .

Identification of novel missense mutations of GDF9 in Chinese women with polycystic ovary syndrome.

Jingjing Liu, Binbin Wang, Jing Wang, 2010, Reproductive biomedicine online.

TNFRSF21 mutations cause high myopia

Binbin Wang, Jing Wang, Xu Ma, 2019, Journal of Medical Genetics.

Application of a deep convolutional neural network in the diagnosis of neonatal ocular fundus hemorrhage

Binbin Wang, Jing Wang, Xu Ma, 2018, Bioscience reports.

Analysis of FOXO3 mutation in 114 Chinese women with premature ovarian failure.

Binbin Wang, Jing Wang, Xu Ma, 2010, Reproductive biomedicine online.

A draft genome of the medicinal plant Cremastra appendiculata (D. Don) provides insights into the colchicine biosynthetic pathway

Sunil Kumar Sahu, Huan Liu, Binbin Wang, 2022, Communications Biology.

Fertility outcome of patients with CBAVD: a single-institution experience

Binbin Wang, Jing Wang, Chengquan Ma, 2021, Journal of Men’s Health.

Association between TP53 gene Arg72Pro polymorphism and idiopathic infertility in southeast Chinese Han males

Binbin Wang, Jing Wang, Xu Ma, 2013, Systems biology in reproductive medicine.

New Gene Variants Associated with the Risk of Chronic HBV Infection

Jianguo Zhang, D. Zhernakova, Jing Wang, 2020, Virologica Sinica.

New Gene Variants Associated with the Risk of Chronic HBV Infection

S. O’Brien, Jianguo Zhang, D. Zhernakova, 2020, Virologica Sinica.

Identification of LBX2 as a novel causal gene of atrial septal defect.

Zhan Yin, Binbin Wang, Jing Wang, 2018, International journal of cardiology.

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

Xuegong Zhang, P. Sham, Xueya Zhou, 2016, Scientific Reports.

Consanguineous familial study revealed biallelic FIGLA mutation associated with premature ovarian insufficiency

Binbin Wang, Jing Wang, Yunxia Cao, 2018, Journal of Ovarian Research.

A novel homozygous mutation of bone morphogenetic protein 15 identified in a consanguineous marriage family with primary ovarian insufficiency.

Binbin Wang, Jing Wang, Yunxia Cao, 2017, Reproductive biomedicine online.

A homozygous NOBOX truncating variant causes defective transcriptional activation and leads to primary ovarian insufficiency

Binbin Wang, Jing Wang, Kehkooi Kee, 2016, Human reproduction.

A dominant negative mutation at the ATP binding domain of AMHR2 is associated with a defective anti-Müllerian hormone signaling pathway.

Wei Zhang, Xueya Zhou, Binbin Wang, 2016, Molecular human reproduction.

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

Binbin Wang, Jing Wang, Xu Ma, 2010, Reproductive biology and endocrinology : RB&E.

Association analysis between polymorphism rs2373115 of gene GRB-associated binding protein 2 and Mongolian Alzheimer patients

Binbin Wang, Jing Wang, Xu Ma, 2010, Neuroscience Letters.

CAPS Mutations Are Potentially Associated with Unexplained Recurrent Pregnancy Loss.

Binbin Wang, Jing Wang, Xu Ma, 2019, The American journal of pathology.

Analyses of growth differentiation factor 9 (GDF9) and bone morphogenetic protein 15 (BMP15) mutation in Chinese women with premature ovarian failure

Binbin Wang, Jing Wang, Xu Ma, 2010, Clinical endocrinology.

Sequence variants of KHDRBS1 as high penetrance susceptibility risks for primary ovarian insufficiency by mis-regulating mRNA alternative splicing

Binbin Wang, Jing Wang, Kehkooi Kee, 2017, Human reproduction.

Identification of the p. R116H mutation in a Chinese Family with Novel Variable Cataract Phenotype: Evidence for a Mutational Hot Spot in αA-Crystallin Gene

Binbin Wang, Jing Wang, Xu Ma, 2012, Ophthalmic genetics.

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

Binbin Wang, Jing Wang, Xu Ma, 2011, Reproductive Biomedicine Online.

The study of copy number variations in the regions of NOTCH1 among Chinese VSD and TOF patients.

Binbin Wang, Jing Wang, Xu Ma, 2011, International journal of cardiology.

Analysis of the Association between Catechol-O-Methyltransferase Val158Met and Male Sexual Orientation.

Jing Wang, Feng Wang, T. Feng, 2015, The journal of sexual medicine.

Mutation analysis of the WNT4 gene in Han Chinese women with premature ovarian failure

Binbin Wang, Jing Wang, Xu Ma, 2011, Reproductive biology and endocrinology : RB&E.

Mutation analysis of the WNT 4 gene in Han Chinese women with premature ovarian failure

Binbin Wang, Jing Wang, Xu Ma, 2011 .

Novel missense mutation in PTPN22 in a Chinese pedigree with Hashimoto’s thyroiditis

Ping Yang, Binbin Wang, Jing Wang, 2018, BMC Endocrine Disorders.

Variations of the COL1A1 gene promoter and the relation to developmental dysplasia of the hip.

W. Tian, Binbin Wang, Longfei Cheng, 2013, Genetic testing and molecular biomarkers.

Analysis of cyclin-dependent kinase inhibitor 1B mutation in Han Chinese women with premature ovarian failure.

Binbin Wang, Jing Wang, Xu Ma, 2010, Reproductive biomedicine online.

GPR3 may not be a potential candidate gene for premature ovarian failure.

Binbin Wang, Jing Wang, Xu Ma, 2010, Reproductive biomedicine online.

Mutational analysis of SAL-Like 4 (SALL4) in Han Chinese women with premature ovarian failure.

Binbin Wang, Jing Wang, Xu Ma, 2009, Molecular human reproduction.

Teratocarcinoma-derived growth factor 1 (TDGF1) sequence variants in patients with congenital heart defect.

Shiguo Liu, Binbin Wang, Jing Wang, 2011, International journal of cardiology.

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

Binbin Wang, Longfei Cheng, Jing Wang, 2013, Science China Life Sciences.

Association analysis between HOXD9 genes and the development of developmental dysplasia of the hip in Chinese female Han population

W. Tian, Binbin Wang, Longfei Cheng, 2012, BMC Musculoskeletal Disorders.

Two single-nucleotide polymorphisms in the DKK1 gene are associated with developmental dysplasia of the hip in the Chinese Han female population.

W. Tian, Longfei Cheng, Jing Wang, 2014, Genetic testing and molecular biomarkers.

Binbin Wang, Jing Wang, Xu Ma, 2011, International journal of cardiology.

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

Binbin Wang, Jing Wang, Xu Ma, 2008, Journal of the Neurological Sciences.

Forkhead box H1 (FOXH1) sequence variants in ventricular septal defect.

Binbin Wang, Jing Wang, Xu Ma, 2010, International journal of cardiology.

A novel mutation of HOXA11 in a patient with septate uterus

Binbin Wang, Longfei Cheng, Jing Wang, 2017, Orphanet Journal of Rare Diseases.

A novel mutation of HOXA10 in a Chinese woman with a Mullerian duct anomaly.

Binbin Wang, Longfei Cheng, Jing Wang, 2011, Human reproduction.

Reproductive genetics A novel mutation of HOXA 10 in a Chinese woman with a Müllerian duct anomaly

Binbin Wang, Longfei Cheng, Jing Wang, 2011 .

Genetic analysis of DACT1 in 100 Chinese Han women with Müllerian duct anomalies.

Binbin Wang, Jing Wang, Yunxia Cao, 2016, Reproductive biomedicine online.

Homeobox C9 is not potentially related to congenital heart disease in Chinese patients.

Binbin Wang, Longfei Cheng, Jing Wang, 2012, Genetic testing and molecular biomarkers.

Association between gout and polymorphisms in GCKR in male Han Chinese

Dongmei Meng, Shiguo Liu, Binbin Wang, 2012, Human Genetics.

Genetic association of polymorphism rs1333049 with gout.

Dongmei Meng, Shiguo Liu, Binbin Wang, 2011, Rheumatology.

Genetic association between BDNF gene polymorphisms and phobic disorders: a case-control study among mainland Han Chinese.

Binbin Wang, Longfei Cheng, Jing Wang, 2011, Journal of affective disorders.

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

Binbin Wang, Longfei Cheng, Jing Wang, 2013, Science China Life Sciences.

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

Xuegong Zhang, Xueya Zhou, Binbin Wang, 2017, Oncotarget.

A SNP site in pri-miR-124 changes mature miR-124 expression but no contribution to Alzheimer's disease in a Mongolian population

Jing Wang, Xu Ma, Bing-Bing Wang, 2012, Neuroscience Letters.

Glutathione S-transferase A1 polymorphism and the risk of recurrent spontaneous abortion in Chinese Han population

Juan Liu, Binbin Wang, Jing Wang, 2014, Journal of Assisted Reproduction and Genetics.

Genetic analysis of ABCG2 gene C421A polymorphism with gout disease in Chinese Han male population

Dongmei Meng, Shiguo Liu, Binbin Wang, 2010, Human Genetics.

A rare variant in MLKL confers susceptibility to ApoE ɛ4-negative Alzheimer's disease in Hong Kong Chinese population

You-Qiang Song, Jiang-Man Li, H. Mak, 2018, Neurobiology of Aging.

Genetic analysis of the FOXL2 gene using quantitative real-time PCR in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome

Binbin Wang, Jing Wang, Xu Ma, 2011, Molecular vision.

Mutation analysis of FOXL2 gene in Chinese patients with premature ovarian failure

Binbin Wang, Jing Wang, Xu Ma, 2010, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

Whole-exome sequencing identified a homozygous BRDT mutation in a patient with acephalic spermatozoa

Binbin Wang, Jing Wang, Kehkooi Kee, 2017, Oncotarget.

A Novel Mutation of Hyaluronan Synthase 2 Gene in Chinese Children with Ventricular Septal Defect

Binbin Wang, Jing Wang, Xu Ma, 2014, PLoS ONE.

HOXA1 Gene Is Not Potentially Related to Ventricular Septal Defect in Chinese Children

Binbin Wang, Longfei Cheng, Jing Wang, 2013, Pediatric Cardiology.

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

Binbin Wang, Jing Wang, Xu Ma, 2010 .

Polymorphisms in the Presumptive Promoter Region of the SLC2A9 Gene Are Associated with Gout in a Chinese Male Population

Dongmei Meng, Shiguo Liu, Binbin Wang, 2012, PloS one.

APOE ε4 is a high-risk factor for Alzheimer's disease in the Mongolian population

Binbin Wang, Jing Wang, Xu Ma, 2010, Journal of the Neurological Sciences.

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

Binbin Wang, Jing Wang, Xu Ma, 2008, Journal of the Neurological Sciences.

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

Binbin Wang, Jing Wang, Xu Ma, 2010, Reproductive biology and endocrinology : RB&E.

A novel non-synonymous mutation in the homeodomain of HOXD13 causes synpolydactyly in a Chinese family.

Xueya Zhou, Binbin Wang, Longfei Cheng, 2012, Clinica chimica acta; international journal of clinical chemistry.

Prevalence of refractive errors in Tibetan adolescents

Binbin Wang, Jing Wang, Xu Ma, 2018, BMC Ophthalmology.

Association between gout and polymorphisms in GCKR in male Han Chinese

Dongmei Meng, Shiguo Liu, Binbin Wang, 2012, Human Genetics.

Pathogenic role of ADGRG2 in CBAVD patients replicated in Chinese population

Tao Li, Binbin Wang, Jing Wang, 2017, Andrology.

The miR-449b polymorphism, rs10061133 A>G, is associated with premature ovarian insufficiency

Binbin Wang, Jing Wang, Yunxia Cao, 2016, Menopause.

Haplotype analysis of chemokine CXCL12 polymorphisms and susceptibility to premature ovarian failure in Chinese women.

Binbin Wang, Jing Wang, Xu Ma, 2011, Human Reproduction.

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

Binbin Wang, Jing Wang, Xu Ma, 2011, Reproductive biomedicine online.

Analyses of growth differentiation factor 9 (GDF9) and bone morphogenetic protein 15 (BMP15) mutation in Chinese women with premature ovarian failure

Binbin Wang, Jing Wang, Xu Ma, 2010, Clinical endocrinology.