Xu Ma

Xu Ma, Ming-wei Zhu, Jun Luo, 2006, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

A Meta-Analysis of the Association between ESR 1 Genetic Variants and the Risk of Breast Cancer

Xu Ma, Hao Huang, Jiaying Yang, 2016 .

A Meta-Analysis of the Association between ESR1 Genetic Variants and the Risk of Breast Cancer

Xu Ma, Hao Huang, Jiaying Yang, 2016, PloS one.

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.

Haplotype‐based association of two SNPs in miR‐423 with unexplained recurrent pregnancy loss in a Chinese Han population

Jing Gao, Xu Ma, Yong-Yong Wang, 2019, Experimental cell research.

The roles of two novel FBN1 gene mutations in the genotype-phenotype correlations of Marfan syndrome and ectopia lentis patients with marfanoid habitus.

Feng Gu, Xu Ma, Dan Li, 2008, Genetic testing.

Abnormal Expression of MST1 and YAP1 in Fetal Heart Tissue in a Hyperglycemic Environment and Their Roles in Mediating Apoptosis

Yanhua Li, Xu Ma, C. Shi, 2020 .

Role of GAB1/PI3K/AKT signaling high glucose-induced cardiomyocyte apoptosis.

Yingyu Chen, Xu Ma, Shanshan Hu, 2017, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

ROCK1/p53/NOXA signaling mediates cardiomyocyte apoptosis in response to high glucose in vitro and vivo.

J. Zhao, Lei Sun, Xu Ma, 2017, Biochimica et biophysica acta. Molecular basis of disease.

Cited2 participates in cardiomyocyte apoptosis and maternal diabetes-induced congenital heart abnormality.

Xu Ma, C. Shi, D. Su, 2016, Biochemical and biophysical research communications.

Peroxisome proliferator-activated receptor γ2 Pro12Ala (rs1801282) polymorphism and breast cancer susceptibility: a meta-analysis.

Hongwei Wang, Xu Ma, Linggen Gao, 2013, Molecular Medicine Reports.

The Subjective Quality of Life in Young People With Tourette Syndrome in China

Shiguo Liu, Xu Ma, Xinhua Zhang, 2017, Journal of attention disorders.

Identification of two novel mutations of the HOMEZ gene in Chinese patients with isolated ventricular septal defect.

Xu Ma, Xiao-cheng Liu, Qin Yang, 2013, Genetic testing and molecular biomarkers.

A novel variation of PLAGL1 in Chinese patients with isolated ventricular septal defect.

Xu Ma, Xiao-cheng Liu, Qin Yang, 2012, Genetic testing and molecular biomarkers.

Association of catechol‐O‐methyl transferase (COMT) gene −287A/G polymorphism with susceptibility to obsessive–compulsive disorder in Chinese Han population

Shiguo Liu, Xu Ma, Changgui Li, 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Do obsessive–compulsive disorder and Tourette syndrome share a common susceptibility gene? An association study of the BDNF Val66Met polymorphism in the Chinese Han population

Shiguo Liu, Xu Ma, Xinhua Zhang, 2015, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

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

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

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

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

TAQIB and I405V polymorphisms of CETP are moderately associated with obesity risk in the Chinese adult population

Li-sheng Liu, K. Lindpaintner, Xingyu Wang, 2010, Acta Diabetologica.

Variations of CITED2 Are Associated with Congenital Heart Disease (CHD) in Chinese Population

Xu Ma, Congmin Li, Yuan Wu, 2014, PloS one.

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.

Two novel HAND1 mutations in Chinese patients with ventricular septal defect.

Mugen Liu, Binbin Wang, Xu Ma, 2012, Clinica chimica acta; international journal of clinical chemistry.

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.

Compound heterozygous variants of the FBXO7 gene resulting in infantile‐onset Parkinsonian‐pyramidal syndrome in siblings of a Chinese family

Xu Ma, Qian Liu, Yousheng Yan, 2020, Journal of clinical laboratory analysis.

Identification of Two Missense Mutations in DUOX1 (p.R1307Q) and DUOXA1 (p.R56W) That Can Cause Congenital Hypothyroidism Through Impairing H2O2 Generation

Shiguo Liu, Xu Ma, Hongwei Zang, 2019, Front. Endocrinol..

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

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

Novel homozygous mutation in TUBB8 associated with oocyte maturation defect-2 in a consanguineous marriage family

Binbin Wang, Xu Ma, Yunxia Cao, 2020 .

Developmental mechanisms of arsenite toxicity in zebrafish (Danio rerio) embryos.

Zongfu Cao, Xu Ma, Hong-Fei Xia, 2009, Aquatic toxicology.

Association of IL8 −251A/T, IL12B −1188A/C and TNF-α −238A/G polymorphisms with Tourette syndrome in a family-based association study in a Chinese Han population

Shiguo Liu, Xu Ma, F. Che, 2011, Neuroscience Letters.

Role of EBAF/Nodal/p27 signaling pathway in development of placenta in normal and diabetic rats.

Xu Ma, Yining Jin, C. Shi, 2021, Developmental biology.

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.

The identification of a novel mutation of nicotinic acetylcholine receptor gene CHRNB2 in a Chinese patient: Its possible implication in non-familial nocturnal frontal lobe epilepsy

Xu Ma, Liwen Wu, Q. Lu, 2011, Epilepsy Research.

A R54L Mutation of CRYAA Associated with Autosomal Dominant Nuclear Cataracts in a Chinese Family

Xu Ma, Siquan Zhu, Fan Yang, 2013, Current eye research.

Novel alanyl-tRNA synthetase 2 (AARS2) homozygous mutation in a consanguineous Chinese family with premature ovarian insufficiency.

Binbin Wang, Xu Ma, Yunxia Cao, 2019, Fertility and sterility.

A single nucleotide polymorphism in the MTOR gene is associated with recurrent spontaneous abortion in the Chinese female population

Xu Ma, Yunxia Cao, Chenzhi Zong, 2015, Systems biology in reproductive 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.

Mutation analysis of congenital cataract in a Chinese family identified a novel missense mutation in the connexin 46 gene (GJA3)

Binbin Wang, Xu Ma, Shanshan Hu, 2010, Molecular vision.

MicroRNA expression and regulation in the uterus during embryo implantation in rat

Zongfu Cao, Xu Ma, Hong-Fei Xia, 2014, The FEBS journal.

A novel mutation in AlphaA‐crystallin (CRYAA) caused autosomal dominant congenital cataract in a large Chinese family

Feng Gu, Yong-Bin Yan, Xu Ma, 2008, Human mutation.

Rare homozygous mutation in TUBB8 associated with oocyte maturation defect-2 in a consanguineous mating family

Binbin Wang, Xu Ma, Yunxia Cao, 2020, Journal of Ovarian Research.

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

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

An association study of HFE gene mutation with idiopathic male infertility in the Chinese Han population.

T. Liu, Binbin Wang, Xu Ma, 2012, Asian journal of andrology.

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

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

A case-control association study between Obsessive-Compulsive Disorder (OCD) and the MCP-1 -2518G/A polymorphism in a Chinese sample.

Shiguo Liu, Xu Ma, Xinhua Zhang, 2012, Revista brasileira de psiquiatria.

The association between glucose-6-phosphate dehydrogenase deficiency and abnormal blood pressure among prepregnant reproductive-age Chinese females

Xingyu Wang, Xu Ma, T. Guan, 2018, Hypertension Research.

No significant association between Catechol-O-methyl transferase (COMT) −287A/G gene polymorphism and Tourette’s syndrome in family-based association study in Chinese Han population

Shiguo Liu, Xu Ma, F. Che, 2011, European Child & Adolescent Psychiatry.

Clinical and genetic study of SPG6 mutation in a Chinese family with hereditary spastic paraplegia

Xu Ma, Ji-jun Teng, Fei-feng Li, 2008, Journal of the Neurological Sciences.

Mutations in EPAS1 in congenital heart disease in Tibetans

Binbin Wang, Xu Ma, Qiu-hong Chen, 2018, Bioscience reports.

CFC1 mutations in Chinese children with congenital heart disease.

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

Association between CRP gene polymorphisms and the risk of preeclampsia in Han Chinese women.

Qidi Wang, Xingyu Wang, Xu Ma, 2014, Genetic testing and molecular biomarkers.

Research progress on cell signal transduction pathway mediating age-related cataract

Xu Ma, Shanshan Hu, Zhongying Wang, 2021 .

Mutation screening of crystallin genes in Chinese families with congenital cataracts

Zongfu Cao, Juhua Yang, Lijuan Liu, 2019, Molecular vision.

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.

A new mutation in BFSP2 (G1091A) causes autosomal dominant congenital lamellar cataracts

Meng Zhang, Xu Ma, Si-quan Zhu, 2008, Molecular vision.

Up-regulation of miR-98 and unraveling regulatory mechanisms in gestational diabetes mellitus

Y. Hu, Y. Li, Xu Ma, 2016, Scientific Reports.

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.

Screening of PAH Common Mutations in Chinese Phenylketonuria Patients Using iPLEX MALDI-TOF MS

Xu Ma, Yousheng Yan, Chuan Zhang, 2020, ACS omega.

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, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

The ESR1 gene in unexplained recurrent spontaneous abortion

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

GSK3β and MCL-1 mediate cardiomyocyte apoptosis in response to high glucose

J. Zhao, Xu Ma, Shanshan Hu, 2019, Histochemistry and Cell Biology.

Association study between MAO-A gene promoter VNTR polymorphisms and obsessive-compulsive disorder.

Shiguo Liu, Xu Ma, Xinhua Zhang, 2013, Journal of anxiety disorders.

A Novel Mutation in the Connexin 50 Gene (GJA8) Associated with Autosomal Dominant Congenital Nuclear Cataract in a Chinese Family

Meng Zhang, Xu Ma, Siquan Zhu, 2010, Current eye research.

Therapeutic effect of human umbilical cord-derived mesenchymal stem cells on injured rat endometrium during its chronic phase

Y. Li, Xu Ma, Hong-Fei Xia, 2018, Stem Cell Research & Therapy.

The miRNA-29b Is Downregulated in Placenta During Gestational Diabetes Mellitus and May Alter Placenta Development by Regulating Trophoblast Migration and Invasion Through a HIF3A-Dependent Mechanism

Y. Hu, Xu Ma, Hong-Fei Xia, 2020, Frontiers in Endocrinology.

The implication of p66shc in oxidative stress induced by deltamethrin.

Zongfu Cao, Xu Ma, Hongyu Jin, 2017, Chemico-biological interactions.

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.

Progesterone production requires activation of caspase-3 in preovulatory granulosa cells in a serum starvation model

Wei Han, Xu Ma, Ying Hu, 2012, Steroids.

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.

Apolipoprotein E Gene Variants and Risk of Coronary Heart Disease: A Meta-Analysis

Xu Ma, Lina Wang, H. Zhi, 2016, BioMed research international.

Incorrect Institutional Affiliations of Authors in the Article by Jiang et al (Arthritis Rheumatol, May 2014)

P. Visscher, M. Brown, D. Willner, 2014 .

The connexin 46 mutant (V44M) impairs gap junction function causing congenital cataract

Xu Ma, Shanshan Hu, C. Shi, 2017, Journal of Genetics.

The DNA methylation profile of PLA2G4C gene promoter in schizophrenia

Xu Ma, Qiong Yu, C. Kou, 2012, Psychiatry Research.

The dynamics of polycomb group proteins in early embryonic nervous system in mouse and human

Xu Ma, Hong-Fei Xia, Yuan Ji, 2013, International Journal of Developmental Neuroscience.

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.

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

Binbin Wang, Xu Ma, J. Xie, 2018, Evidence-based complementary and alternative medicine : eCAM.

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.

Lack of genetic association of 5‐HTR2A 102 T/C and ‐1438A/G polymorphisms with Tourette syndrome in a family‐based association study in a Chinese Han population

Shiguo Liu, Xu Ma, Xinhua Zhang, 2016, Asia-Pacific psychiatry : official journal of the Pacific Rim College of Psychiatrists.

No Association of Pri-miR-143 rs41291957 Polymorphism with the Risk of Congenital Heart Disease in a Chinese Population

Juhua Yang, Xu Ma, Guican Zhang, 2014, Pediatric Cardiology.

A novel mutation in FRMD7 causing X-linked idiopathic congenital nystagmus in a large family

Meng Zhang, Feng Gu, Xu Ma, 2008, Molecular vision.

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.

A Rare Rs139365823 Polymorphism in Pre-miR-138 Is Associated with Risk of Congenital Heart Disease in a Chinese Population.

F. Tan, Xu Ma, Cailing Lu, 2018, DNA and Cell Biology.

Evaluation of droplet digital PCR for non-invasive prenatal diagnosis of phenylketonuria

Xu Ma, F. Wang, Yousheng Yan, 2019, Analytical and Bioanalytical Chemistry.

Pentachloronitrobenzene alters progesterone production and primordial follicle recruitment in cultured granulosa cells and rat ovary†

Haiying Yu, Xu Ma, Huixia Yang, 2019, Biology of Reproduction.

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.

Autosomal Dominant Congenital Nuclear Cataracts Caused by a CRYAA Gene Mutation

Meng Zhang, Xu Ma, Si-quan Zhu, 2010, Current eye research.

Mutation G61C in the CRYGD gene causing autosomal dominant congenital coralliform cataracts

Meng Zhang, Shiguo Liu, Xu Ma, 2008, Molecular vision.

Effects of congenital cataract mutation R116H on alphaA-crystallin structure, function and stability.

Feng Gu, Yong-Bin Yan, Xu Ma, 2010, Biochimica et biophysica acta.

Copy Number Variation of Multiple Genes in SAPHO Syndrome

X. Tian, Xu Ma, Changlong Guo, 2019, The Journal of Rheumatology.

Therapeutic effect of human umbilical cord-derived mesenchymal stem cells on injured rat endometrium during its chronic phase

Y. Li, Xu Ma, Hong-Fei Xia, 2018, Stem Cell Research & Therapy.

Mutation Analysis of 63 Northwest Chinese Probands with Oculocutaneous Albinism

Zongfu Cao, Xu Ma, Z. Chuan, 2020, Current eye research.

Reactivation of methylation-silenced tumor suppressor gene p16INK4a by nordihydroguaiaretic acid and its implication in G1 cell cycle arrest.

Xu Ma, Nan Yao, S. Bai, 2008, Life sciences.

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.

MiR-101 Is Involved in Human Breast Carcinogenesis by Targeting Stathmin1

Y. Hu, Xu Ma, Hong-Fei Xia, 2012, PloS one.

Seroepidemiological survey of hepatitis B virus infection among 764,460 women of childbearing age in rural China: A cross-sectional study.

Xu Ma, Jun Cheng, Yuan He, 2016, Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology.

Comparison of three surgical models of bone tissue defects in cleft palate in rabbits.

Xu Ma, Xue-Cheng Sun, Hu Wang, 2019, International journal of pediatric otorhinolaryngology.

A G57W Mutation of CRYGS Associated with Autosomal Dominant Pulverulent Cataracts in a Chinese Family

Xu Ma, Siquan Zhu, Zhenfei Yang, 2015, Ophthalmic genetics.

Embryonic ectoderm development protein is regulated by microRNAs in human neural tube defects.

Y. Hu, Xu Ma, Ge Song, 2011, American journal of obstetrics and gynecology.

Anti-PABPC1 Co-Immunoprecipitation for Examining the miRNAs Directly Targeting the 3′-UTR of EED mRNA

Y. Hu, Xu Ma, Kun Yin, 2014, PloS one.

Haplotype‐based association of two SNPs in miR‐323b with unexplained recurrent spontaneous abortion in a Chinese Han population

Xu Ma, Lu Zhang, Xue-qin Wang, 2018, Journal of cellular physiology.

MicroRNA biogenesis pathway genes polymorphisms and cancer risk: a systematic review and meta-analysis

Xu Ma, Jieyu He, Lina Wang, 2016, PeerJ.

Clinical and Genetic Analysis of a Compound Heterozygous Mutation in the Thyroglobulin Gene in a Chinese Twin Family With Congenital Goiter and Hypothyroidism

Shiguo Liu, Xu Ma, Shengli Yan, 2012, Twin Research and Human Genetics.

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

Chunmei Zhang, Binbin Wang, Xu Ma, 2011, Molecular vision.

The TOMM40 gene rs2075650 polymorphism contributes to Alzheimer’s disease in Caucasian, and Asian populations

Xu Ma, Biyun Xu, Bingwei Chen, 2016, Neuroscience Letters.

Evaluation of next-generation sequencing software in mapping and assembly

Rui Jiang, You-Qiang Song, Xu Ma, 2011, Journal of Human Genetics.

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.

Novel Risk Loci for Rheumatoid Arthritis in Han Chinese and Congruence With Risk Variants in Europeans

Yi Wang, Tao Yue, Mengtao Li, 2014, Arthritis & rheumatology.

Mutation spectrum of PAH gene in phenylketonuria patients in Northwest China: identification of twenty novel variants

Xu Ma, Yousheng Yan, Chuan Zhang, 2019, Metabolic Brain Disease.

Exome-Sequencing Identifies Novel Genes Associated with Recurrent Pregnancy Loss in a Chinese Cohort

Binbin Wang, Xu Ma, Yunxia Cao, 2021, Frontiers in Genetics.

Aberrant promoter methylation of the TPEF gene in esophageal squamous cell carcinoma.

Xu Ma, Y. Cui, S-N Tan, 2008, Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus.

Genome-Wide Association Identifies Risk Pathways for SAPHO Syndrome

Ruikun Cai, Xu Ma, Yichao Dong, 2021, Frontiers in Cell and Developmental Biology.

Association analysis of interleukin‐23 receptor SNPs and SAPHO syndrome in Chinese people

Xu Ma, Changlong Guo, Chen Li, 2019, International journal of rheumatic diseases.

Arsenic impairs embryo development via down-regulating Dvr1 expression in zebrafish.

Peng Li, Xu Ma, Xinyu Tan, 2012, Toxicology letters.

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.

Genome-wide microRNA profiling in human fetal nervous tissues by oligonucleotide microarray

Xu Ma, H. Xiao, Jian-Jun Zhao, 2006, Child's Nervous System.

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.

Identification of a Novel Mutation in a Pseudohypoparathyroidism Family

Binbin Wang, Xu Ma, Zhi-min Miao, 2011, International journal of endocrinology.

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.

Developing ABEmax-NG with Precise Targeting and Expanded Editing Scope to Model Pathogenic Splice Site Mutations In Vivo

Qiang Sun, Xu Ma, Xingxu Huang, 2019, iScience.

Downregulation of SOX11 in fetal heart tissue, under hyperglycemic environment, mediates cardiomyocytes apoptosis

Xu Ma, C. Shi, D. Su, 2020, Journal of biochemical and molecular toxicology.

Retinoic acid downregulates microRNAs to induce abnormal development of spinal cord in spina bifida rat model

Xu Ma, Jian-Jun Zhao, Daguang Sun, 2008, Child's Nervous System.

an association study between DLGAP 1 rs 11081062 and EFNA 5 rs 26728 polymorphisms with obsessive – compulsive disorder in a chinese han population

Shiguo Liu, Xu Ma, Haitao Niu, 2015 .

NOTCH2 variant D1853H is mutated in two non-syndromic premature ovarian insufficiency patients from a Chinese pedigree

C. Yin, Binbin Wang, Xu Ma, 2020, Journal of Ovarian Research.

The Same Chromosome 9p21.3 Locus Is Associated With Type 2 Diabetes and Coronary Artery Disease in a Chinese Han Population

Baofeng Yang, Fan Wang, X. Tu, 2011, Diabetes.

Whole exome sequencing reveals novel CEP104 mutations in a Chinese patient with Joubert syndrome

Zongfu Cao, Ruikun Cai, Yufei Yu, 2019, Molecular genetics & genomic medicine.

A nonsense mutation of CRYGC associated with autosomal dominant congenital nuclear cataracts and microcornea in a Chinese pedigree

Xu Ma, Siquan Zhu, Zhenfei Yang, 2012, Molecular vision.

Erectile dysfunction in Fragile X patients.

Feng Gu, Xu Ma, Hai-yin Zhang, 2006, Asian journal of andrology.

Erectile dysfunction in Fragile X men

Feng Gu, Xu Ma, H. Y. Zhang, 2006 .

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.

Identification of novel deep intronic PAH gene variants in patients diagnosed with phenylketonuria

C. Yin, Xu Ma, Linlin Zhang, 2021, Human mutation.

High-Throughput Sequencing Reveals Immunological Characteristics of the TRB-/IgH-CDR3 Region of Umbilical Cord Blood.

Ruikun Cai, Xuerui Tan, Qidi Wang, 2016, The Journal of pediatrics.

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

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

Mutation analysis of TCOF1 gene in Chinese Treacher Collins syndrome patients

Zongfu Cao, Cuixia Chen, Xu Ma, 2020, Journal of clinical laboratory analysis.

Novel mutations in HSF4 cause congenital cataracts in Chinese families

Zongfu Cao, Juhua Yang, Lijuan Liu, 2018, BMC Medical Genetics.

A novel COL1A1 nonsense mutation causing osteogenesis imperfecta in a Chinese family

Feng Gu, Xu Ma, Xiaorong Li, 2007, Molecular vision.

Identification of two novel pathogenic variants of PIBF1 by whole exome sequencing in a 2-year-old boy with Joubert syndrome

Yun Peng, Zongfu Cao, Ruikun Cai, 2020, BMC medical genetics.

Prevention and Control of Pathogens Based on Big-Data Mining and Visualization Analysis

Hao Lin, Zongfu Cao, Ruikun Cai, 2021, Frontiers in Molecular Biosciences.

Lack of association between polymorphism -592A/C in the promoter region of the IL10 gene and Tourette's syndrome in a family-based association study in the Chinese Han population.

Shiguo Liu, Xu Ma, F. Che, 2011, Genetic testing and molecular biomarkers.

Variant analysis of 92 Chinese Han families with hearing loss

Xu Ma, Shasha Huang, P. Dai, 2022, BMC medical genomics.

BRG1 variant rs1122608 on chromosome 19p13.2 confers protection against stroke and regulates expression of pre-mRNA-splicing factor SFRS3

Y. Zhang, Tangchun Wu, Fan Wang, 2014, Human Genetics.

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

You-Qiang Song, L. Chu, Binbin Wang, 2010, Journal of Alzheimer's disease : JAD.

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.

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 .

The polymorphism of rs6505162 in the MIR423 coding region and recurrent pregnancy loss.

Y. Hu, Y. Li, Xu Ma, 2015, Reproduction.

Functional Study of One Nucleotide Mutation in Pri-MiR-125a Coding Region which Related to Recurrent Pregnancy Loss

Y. Hu, Shiguo Liu, Xu Ma, 2014, PloS one.

Two common SNPs in pri-miR-125a alter the mature miRNA expression and associate with recurrent pregnancy loss in a Han-Chinese population

Xu Ma, T. He, Yi Cui, 2011, RNA biology.

Tea consumption and risk of type 2 diabetes mellitus: a systematic review and meta-analysis update

Xu Ma, Jian Yang, Qun-xia Mao, 2014, BMJ Open.

A SNP in pri-miR-10a is associated with recurrent spontaneous abortion in a Han-Chinese population

Y. Li, Xu Ma, Lu Zhang, 2016, OncoTarget.

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.

A case-control study of interleukin-12 1188A/C polymorphism in obsessive-compulsive disorder in Chinese population

Shiguo Liu, Xu Ma, Xinhua Zhang, 2012, Acta Neuropsychiatrica.

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.

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

Binbin Wang, Xu Ma, Yakun Zhao, 2012, Endocrine.

Mutation analysis, treatment and prenatal diagnosis of Chinese cases of methylmalonic acidemia

Zongfu Cao, Cuixia Chen, Xu Ma, 2020, Scientific Reports.

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.

No association of functional variant in pri-miR-218 and risk of congenital heart disease in a Chinese population.

Xiaozhong Peng, Juhua Yang, Xu Ma, 2013, Gene.

Profiling the pattern of human TRB/IGH‐CDR3 repertoire in liver transplantation patients via high‐throughput sequencing analysis

Xu Ma, Chunlin Wang, Qiang He, 2020, Scandinavian journal of immunology.

High throughput sequencing reveals the diversity of TRB-CDR3 repertoire in patients with psoriasis vulgaris.

Ruikun Cai, Qidi Wang, Xingyu Wang, 2016, International immunopharmacology.

A preliminary study on the associations between Ureaplasma, Mycoplasma and the vaginal microbiome

Xu Ma, Bei Wang, X. Hong, 2021, Medicine in Microecology.

Genetic variants in the MicroRNA biosynthetic pathway Gemin3 and Gemin4 are associated with a risk of cancer: a meta-analysis

Xu Ma, Jieyu He, Lina Wang, 2016, PeerJ.

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.

A novel frameshift mutation in FRMD7 causing X-linked idiopathic congenital nystagmus.

Feng Gu, Juhua Yang, Xu Ma, 2008, Genetic testing.

Variable number tandem repeats in dopamine receptor D4 in Tourette's syndrome

Shiguo Liu, Xu Ma, Haitao Niu, 2014, Movement disorders : official journal of the Movement Disorder Society.

Decreased mRNA and protein expression of TWIST1 in myocardial tissue of fetuses with ventricular septal defects.

Qidi Wang, Xu Ma, Yuting Wang, 2015, Molecular medicine reports.

Significant Association between OPG/TNFRSF11B Variant and Common Complex Ischemic Stroke.

X. Tu, Qiuyun Chen, Chengqi Xu, 2018, Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association.

Identification of a novel RPGR exon ORF15 mutation in a family with X-linked retinitis pigmentosa.

Feng Gu, Xu Ma, Zi-Bing Jin, 2007, Archives of ophthalmology.

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

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

[CAG repeats of DNA polymerase gamma in Chinese males and relationship of idiopathic male infertility to CAG repeats].

Xu Ma, Nan Yao, Xiaohua Jin, 2006, Zhonghua nan ke xue = National journal of andrology.

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 .

Chinese weight‐correction model for maternal serum markers in Down syndrome prenatal screening

Xu Ma, Zuoqi Peng, Yuanyuan Wang, 2007, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

RNA sequencing and bioinformatics analysis of human lens epithelial cells in age-related cataract

Xu Ma, Shanshan Hu, D. Su, 2021, BMC Ophthalmology.

Clinical and genetic study of a novel mutation in the REEP1 gene

Qianqian Wang, Xu Ma, Fei-feng Li, 2009, Synapse.

A novel method to prepare water-dispersible magnetic nanoparticles and their biomedical applications: magnetic capture probe and specific cellular uptake.

Xu Ma, Z. Gu, Changjiang Yu, 2008, Journal of biomedical materials research. Part A.

CITED2 mutation links congenital heart defects to dysregulation of the cardiac gene VEGF and PITX2C expression.

Xu Ma, D. Su, Qian Li, 2012, Biochemical and biophysical research communications.

[Standardization for sharing and utilization of Chinese genetic resources].

Zongfu Cao, Xu Ma, Zuoqi Peng, 2008, Yi chuan = Hereditas.

Embryonic developmental toxicity of selenite in zebrafish (Danio rerio) and prevention with folic acid.

Xu Ma, Jun Zhao, Caisheng Lu, 2012, Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association.

Novel Compound Heterozygous Variants in MKS1 Leading to Joubert Syndrome

Zongfu Cao, Xu Ma, Guangyu Zhang, 2020, Frontiers in Genetics.

Exome sequencing reveals novel IRXI mutation in congenital heart disease.

Qidi Wang, Xiaodong Cao, Xu Ma, 2017, Molecular medicine reports.

Novel A14841G mutation is associated with high penetrance of LHON/C4171A family.

Juhua Yang, Xu Ma, Yihua Zhu, 2009, Biochemical and biophysical research communications.

Minor Allele C of Chromosome 1p32 Single Nucleotide Polymorphism rs11206510 Confers Risk of Ischemic Stroke in the Chinese Han Population

Cong Li, Fan Wang, X. Tu, 2010, Stroke.

Confirmation of the mitochondrial ND1 gene mutation G3635A as a primary LHON mutation.

Juhua Yang, Lijuan Liu, Xu Ma, 2009, Biochemical and biophysical research communications.

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.

Fundus examination of 199 851 newborns by digital imaging in China: a multicentre cross-sectional study

Hong Wang, Wei Guo, Binbin Wang, 2018, British Journal of Ophthalmology.

The connexin 46 mutant (V44M) impairs gap junction function causing congenital cataract

Xu Ma, Shanshan Hu, C. Shi, 2017, Journal of Genetics.

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.

Deep targeted sequencing reveals the diversity of TRB-CDR3 repertoire in patients with preeclampsia.

Ruikun Cai, Xuerui Tan, Qidi Wang, 2019, Human immunology.

A novel nonsense mutation in CRYBB1 associated with autosomal dominant congenital cataract

Zongfu Cao, Feng Gu, Juhua Yang, 2008, Molecular vision.

Lack of association of -251T/A polymorphism in interleukin 8 gene with susceptibility to obsessive-compulsive disorder in Chinese Han population.

Shiguo Liu, Xu Ma, Xinhua Zhang, 2012, Cytokine.

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.

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.

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

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

An association study between DLGAP1 rs11081062 and EFNA5 rs26728 polymorphisms with obsessive–compulsive disorder in a Chinese Han population

Shiguo Liu, Xu Ma, Haitao Niu, 2015, Neuropsychiatric disease and treatment.

Regulation of CARD8 Expression by ANRIL and Association of CARD8 Single Nucleotide Polymorphism rs2043211 (p.C10X) With Ischemic Stroke

Fan Wang, T. Ke, X. Tu, 2014, Stroke.

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.

Identification and Functional Analysis of GJA8 Mutation in a Chinese Family with Autosomal Dominant Perinuclear Cataracts

Lei Zhang, Xu Ma, Zhenfei Yang, 2013, PloS one.

The 1425G/A SNP in PRKCH Is Associated With Ischemic Stroke and Cerebral Hemorrhage in a Chinese Population

K. Lindpaintner, J. Mi, Xuerui Tan, 2009, Stroke.

Lack of an association between obsessive-compulsive disorder and polymorphisms in the 3′ untranslated region of GRIN2B in a Chinese Han population

Shiguo Liu, Xu Ma, Xinhua Zhang, 2012, Psychiatry Research.

The novel G10680A mutation is associated with complete penetrance of the LHON/T14484C family.

Zongfu Cao, Juhua Yang, Xu Ma, 2009, Mitochondrion.

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.

An epidemiological study of Alzheimer’s disease in elderly Mongolian and Han populations living in rural areas of Inner Mongolia

Binbin Wang, Xu Ma, Guang-ming Niu, 2011, Aging clinical and experimental research.

Sequencing Analysis of mRNA Profile in Endothelial Cells in Response to ox-LDL

Xu Ma, C. Shi, D. Su, 2021, Biochemical Genetics.

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

Binbin Wang, Jing Wang, Xu Ma, 2014, PloS one.

ALOX5 is associated with tuberculosis in a subset of the pediatric population of North China.

Lin Sun, Binbin Wang, Xu Ma, 2013, Genetic testing and molecular biomarkers.

Mutation Analysis of PAX6 in a Chinese Family and a Patient with a Presumed Sporadic Case of Congenital Aniridia

Xu Ma, Jing Liu, Y. Jie, 2011, Ophthalmic Research.

[A novel PAX6 mutation (c.1286delC) in the patients with hereditary congenital aniridia.].

Juhua Yang, Xu Ma, Y. Tong, 2008, Yi chuan = Hereditas.

Major intrinsic protein (MIP) polymorphism is associated with age-related cataract in Chinese

Binbin Wang, Xu Ma, Shanshan Hu, 2011, Molecular vision.

Retraction: Evaluation of next-generation sequencing software in mapping and assembly.

You-Qiang Song, Binbin Wang, Xu Ma, 2011, Journal of Human Genetics.

Contribution of TIMP3 polymorphisms to the development of preeclampsia in Han Chinese women

Qidi Wang, Xingyu Wang, Xu Ma, 2015, Journal of Assisted Reproduction and Genetics.

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.

Support of positive association in family-based genetic analysis between COL27A1 and Tourette syndrome

Shiguo Liu, Xu Ma, Xinhua Zhang, 2015, Scientific Reports.

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.

The dynamics of polycomb group proteins in early embryonic nervous system in mouse and human

Xu Ma, Yuan Ji, Ji-gao Yang, 2013, International Journal of Developmental Neuroscience.

Novel Risk Loci for Rheumatoid Arthritis in Han Chinese and Congruence With Risk Variants in Europeans

P. Visscher, M. Brown, Liangdan Sun, 2014, Arthritis & rheumatology.

Effects of congenital cataract mutation R116H on alphaA-crystallin structure, function and stability.

Feng Gu, Xu Ma, Zhi Tang, 2010, Biochimica et Biophysica Acta.

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.

High-expression of ROCK1 modulates the apoptosis of lens epithelial cells in age-related cataracts by targeting p53 gene

Lei Sun, Xu Ma, Shanshan Hu, 2020, Molecular Medicine.

The Subjective Quality of Life in Young People With Tourette Syndrome in China

Shiguo Liu, Xu Ma, Xinhua Zhang, 2017, Journal of attention disorders.

Embryonic ectoderm development protein is regulated by microRNAs in human neural tube defects.

Y. Hu, Xu Ma, Ge Song, 2011, American journal of obstetrics and gynecology.

Association of functional variant in GDF1 promoter with risk of congenital heart disease and its regulation by Nkx2.5.

Xu Ma, Cailing Lu, Wei Sheng, 2019, Clinical science.

Association between gout and polymorphisms in GCKR in male Han Chinese

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

Evaluation of next-generation sequencing software in mapping and assembly

You-Qiang Song, Binbin Wang, Xu Ma, 2011, Journal of Human Genetics.

An Association Analysis between 5‐HTTLPR Polymorphism and Obsessive–Compulsive Disorder, Tourette Syndrome in a Chinese Han Population

Shiguo Liu, Xu Ma, Xinhua Zhang, 2011, CNS neuroscience & therapeutics.

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.