Yuan Yang

发表

Hereditary features, treatment, and prognosis of the lipoprotein glomerulopathy in patients with the APOE Kyoto mutation.

Songming Huang, Yunqiang Liu, P. Fu, 2014, Kidney international.

Identification of target messenger RNA substrates for mouse RBMY.

Huaqin Sun, D. Tao, Yongxin Ma, 2008, Molecular human reproduction.

Clinical and genetic features of patients with sporadic amyotrophic lateral sclerosis in south-west China

Dong Zhou, H. Shang, Yan Zeng, 2009, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

A case of lipoprotein glomerulopathy with thrombotic microangiopathy due to malignant hypertension

P. Fu, Zhangxue Hu, Yu Wu, 2013, BMC Nephrology.

Evidence for the involvement of the proximal copy of the MAGEA9 gene in Xq28-linked CNV67 specific to spermatogenic failure†

Dong Yang, Q. Dong, Yunqiang Liu, 2017, Biology of Reproduction.

Modified tibial tunnel placement for single-bundle posterior cruciate ligament reconstruction reduces the “Killer Turn” in a biomechanical model

Jian Li, Qi Li, Yuan Yang, 2019, Medicine.

Are gene polymorphisms related to treatment outcomes of methotrexate in patients with rheumatoid arthritis? A systematic review and meta-analysis.

Yuehong Chen, K. Zou, Yuan Yang, 2017, Pharmacogenomics.

Identical twins:one with anti-glomerular basement membrane glomerulonephritis,the other with systemic lupus erythematosus

P. Fu, Zhangxue Hu, Yu Wu, 2013, BMC Nephrology.

Expression and localization of the spermatogenesis-related gene, Znf230, in mouse testis and spermatozoa during postnatal development.

Wei Zhang, Yunqiang Liu, Jiyun Yang, 2008, BMB reports.

Expression and localization of the spermatogenesis-related gene , Znf 230 , in mouse testis and spermatozoa during postnatal development

Yunqiang Liu, Jiyun Yang, D. Su, 2008 .

mTOR complex 1 signalling regulates the balance between lipid synthesis and oxidation in hypoxia lymphocytes

Min Yang, Yuan Yang, Yan Liang, 2017, Bioscience reports.

A novel HNF1B mutation p.R177Q in autosomal dominant tubulointerstitial kidney disease and maturity-onset diabetes of the young type 5

Zhangxue Hu, Yuan Yang, T. Tao, 2020, Medicine.

Putative mutation of PKD1 gene responsible for autosomal dominant polycystic kidney disease in a Chinese family

Zhangxue Hu, Si-zhong Zhang, Yuan Yang, 2011, International journal of urology : official journal of the Japanese Urological Association.

Treatment for lupus nephritis: an overview of systematic reviews and meta-analyses

Yuehong Chen, K. Zou, Yuan Yang, 2017, Rheumatology International.

Serum Interleukin-18 Level is Associated With Disease Activity and Interstitial Lung Disease in Patients With Dermatomyositis.

Yuan Yang, Yi Liu, G. Yin, 2017, Archives of rheumatology.

Risk factors for early mortality in patients with primary central nervous system lymphoma: A large-cohort retrospective study.

Yanhui Liu, Q. Mao, Yuan Yang, 2020, World neurosurgery.

The significance of preoperative hematological inflammatory markers in patients with meningiomas

Yanhui Liu, Yuan Yang, Mao Li, 2019, Clinical Neurology and Neurosurgery.

Significance of Pretreatment Red Blood Cell Distribution Width in Patients with Newly Diagnosed Glioblastoma

Yanhui Liu, Q. Mao, Yuan Yang, 2017, Medical science monitor : international medical journal of experimental and clinical research.

Association Between Osteoprotegerin Gene Polymorphisms and Rheumatoid Arthritis Susceptibility: A Meta-analysis.

Yuehong Chen, Yuan Yang, Gang Liu, 2016, Archives of medical research.

Meta-analysis of peritumoural rCBV values derived from dynamic susceptibility contrast imaging in differentiating high-grade gliomas from intracranial metastases.

Yanhui Liu, Xiang Wang, Q. Mao, 2014, International journal of clinical and experimental medicine.

Molecular characteristics of varicocele: integration of whole-exome and transcriptome sequencing.

Luchen Yang, Zhu-feng Peng, Q. Dong, 2020, Fertility and sterility.

DEPTOR-mTOR Signaling Is Critical for Lipid Metabolism and Inflammation Homeostasis of Lymphocytes in Human PBMC Culture

Yuan Yang, Yan Liang, G. Yin, 2017, Journal of immunology research.

Mutation scanning of the COQ2 gene in ethnic Chinese patients with multiple-system atrophy

Wei Song, H. Shang, Yuan Yang, 2015, Neurobiology of Aging.

GCH1 mutation and clinical study of Chinese patients with dopa‐responsive dystonia

H. Shang, Yuan Yang, Xiaoyan Guo, 2010, Movement disorders : official journal of the Movement Disorder Society.

A novel mutation of the ε‐sarcoglycan gene in a Chinese family with myoclonus‐dystonia syndrome

J. Burgunder, H. Shang, S. Wu, 2008, Movement disorders : official journal of the Movement Disorder Society.

Unmethylated state of 5′ upstream CpG islands may be necessary but not sufficient for the testis-enriched expression of ZNF230/Znf230

D. Tao, Yongxin Ma, Yunqiang Liu, 2013, Genes & Genomics.

Genetic variants of ADAM17 are implicated in the pathological process of Kawasaki disease and secondary coronary artery lesions via the TGF-β/SMAD3 signaling pathway

Q. Peng, Hanmin Liu, Yuan Yang, 2016, European Journal of Pediatrics.

Spastin mutation screening in Chinese patients with pure hereditary spastic paraplegia.

J. Burgunder, Rui Huang, H. Shang, 2014, Parkinsonism & related disorders.

A novel fibrillin-1 gene missense mutation associated with neonatal Marfan syndrome: a case report and review of the mutation spectrum

Q. Peng, Hanmin Liu, Yuan Yang, 2016, BMC Pediatrics.

A novel missense variant c.71G > T (p.Gly24Val) of the CRYBA4 gene contributes to autosomal-dominant congenital cataract in a Chinese family

Yunqiang Liu, Yuan Yang, Chen Liang, 2022, International Ophthalmology.

Identification of Palmitoleic Acid Controlled by mTOR Signaling as a Biomarker of Polymyositis

Yuan Yang, G. Yin, Ying Wang, 2017, Journal of immunology research.

Metachronous Basal Cell Carcinoma and Primary Plasmacytic Leukemia Associated With Dermatomyositis

Yuan Yang, G. Yin, Q. Xie, 2014 .

The common variant N372H in BRCA2 gene may be associated with idiopathic male infertility with azoospermia or severe oligozoospermia.

Yongxin Ma, Si-zhong Zhang, Yuan Yang, 2006, European journal of obstetrics, gynecology, and reproductive biology.

Demethylation of CpG islands in the 5' upstream regions mediates the expression of the human testis-specific gene MAGEB16 and its mouse homolog Mageb16

D. Tao, Yongxin Ma, Yunqiang Liu, 2014, BMB reports.

[Genetic and clinical study of three Chinese pedigrees with Fabry disease].

Xiao-xia Liu, Yuan Yang, Zhang-Xue Hu, 2013, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Common AZFc structure may possess the optimal spermatogenesis efficiency relative to the rearranged structures mediated by non-allele homologous recombination

Q. Dong, Yunqiang Liu, Yuan Yang, 2015, Scientific Reports.

A new mutant transcript generated in Znf230 exon 2 knockout mice reveals a potential exon structure in the targeting vector sequence.

D. Tao, Yongxin Ma, Yunqiang Liu, 2013, Acta biochimica et biophysica Sinica.

A conformal hydrogel nanocomposite for local delivery of paclitaxel

M. Gou, Jiumeng Zhang, Ting Du, 2017, Journal of biomaterials science. Polymer edition.

Is the primary AZFc duplication a potential risk for male infertility?: A systematic review and meta‐analysis

Yuan Yang, Shengyu Xie, Yangwei Zhang, 2020, Andrology.

Combined analysis of genome-wide-linked susceptibility loci to Kawasaki disease in Han Chinese

Q. Peng, D. Tao, Yongxin Ma, 2013, Human Genetics.

The prognostic role of controlling nutritional status scores in patients with solid tumors.

Yanhui Liu, Yuan Yang, Mao Li, 2017, Clinica chimica acta; international journal of clinical chemistry.

An Integrative Survival Analysis with Identification of Prognostic Factors in the Patients with Coexisting Glioma and Intracranial Aneurysm.

Yanhui Liu, Xiang Wang, Q. Mao, 2017, World neurosurgery.

Genome-Wide Loci Linked to Non-Obstructive Azoospermia Susceptibility May Be Independent of Reduced Sperm Production in Males with Normozoospermia1

D. Tao, Yongxin Ma, Yunqiang Liu, 2015, Biology of reproduction.

Circulating miR-128 as a potential diagnostic biomarker for glioma

Yanhui Liu, Xiang Wang, Q. Mao, 2017, Clinical Neurology and Neurosurgery.

Malignancy risk of anti-tumor necrosis factor alpha blockers: an overview of systematic reviews and meta-analyses

Yuehong Chen, Yuan Yang, Jianhong Sun, 2015, Clinical Rheumatology.

Mosaic isodicentric Y chromosome harboring intact AZF region in a cryptozoospermic male with normal hormone levels

D. Tao, Yuan Yang, Shengyu Xie, 2020, Asian journal of andrology.

Phenotypic expression of partial AZFc deletions is independent of the variations in DAZL and BOULE in a Han population.

D. Tao, Yongxin Ma, Yunqiang Liu, 2010, Journal of andrology.

Y chromosome haplogroups may confer susceptibility to partial AZFc deletions and deletion effect on spermatogenesis impairment.

D. Tao, Yongxin Ma, Yunqiang Liu, 2008, Human reproduction.

Absence of the H2AX Mutations in Idiopathic Infertile Men with Spermatogenic Impairment

Yongxin Ma, D. Su, Si-zhong Zhang, 2008, Systems biology in reproductive medicine.

DAZ1/DAZ2 cluster deletion mediated by gr/gr recombination per se may not be sufficient for spermatogenesis impairment: a study of Chinese normozoospermic men.

Si-zhong Zhang, Yuan Yang, Z. A, 2006, Asian journal of andrology.

Chromosomal abnormality and Y chromosome microdeletion in Chinese patients with azoospermia or severe oligozoospermia.

Si-zhong Zhang, Yuan Yang, Wei Zhang, 2006, Yi chuan xue bao = Acta genetica Sinica.

Pineal Region Glioblastomas: Clinical Characteristics, Treatment and Survival Outcome.

Yanhui Liu, Q. Mao, Yuan Yang, 2020, World neurosurgery.

Single nucleotide polymorphism C677T in the methylenetetrahydrofolate reductase gene might be a genetic risk factor for infertility for Chinese men with azoospermia or severe oligozoospermia.

Wei Zhang, Si-zhong Zhang, Yuan Yang, 2007, Asian journal of andrology.

Mutations of the Cyclin A1 Gene are Not a Common Cause of Male Infertility

Si-zhong Zhang, Yuan Yang, A. Zhoucun, 2009, Systems biology in reproductive medicine.

Single nucleotide polymorphisms of the gonadotrophin-regulated testicular helicase (GRTH) gene may be associated with the human spermatogenesis impairment.

Si-zhong Zhang, Yuan Yang, Z. A, 2006, Human reproduction.

A significant effect of the TSPY1 copy number on spermatogenesis efficiency and the phenotypic expression of the gr/gr deletion.

D. Tao, Yongxin Ma, Yunqiang Liu, 2013, Human molecular genetics.

Microarray profiling of microRNAs expressed in testis tissues of developing primates

Yuan Yang, Yongxin Ma, Huaqin Sun, 2009, Journal of Assisted Reproduction and Genetics.

DNA demethylation facilitates the specific transcription of the mouse X-linked Tsga8 gene in round spermatids†.

Yi-lu Lu, D. Tao, Yongxin Ma, 2018, Biology of reproduction.

A single nucleotide polymorphism in a miR-1302 binding site in CGA increases the risk of idiopathic male infertility.

D. Tao, Yongxin Ma, Yunqiang Liu, 2011, Fertility and sterility.

CGCG clinical practice guidelines for the management of adult diffuse gliomas.

Yu Wang, Lei Han, Pei Yang, 2016, Cancer letters.

Epigenetic modification‐dependent androgen receptor occupancy facilitates the ectopic TSPY1 expression in prostate cancer cells

D. Tao, Yunqiang Liu, Mohan Liu, 2020, Cancer science.

Testis‐specific protein, Y‐linked 1 activates PI3K/AKT and RAS signaling pathways through suppressing IGFBP3 expression during tumor progression

Q. Dong, D. Tao, Yunqiang Liu, 2019, Cancer science.

Spermatogenic phenotype of testis-specific protein, Y-encoded, 1 (TSPY1) dosage deficiency is independent of variations in TSPY-like 1 (TSPYL1) and TSPY-like 5 (TSPYL5): a case-control study in a Han Chinese population.

Yunqiang Liu, Yuan Yang, Jinyan Xu, 2018, Reproduction, fertility, and development.

GLIS1 rs797906: An Increased Risk Factor for Late-Onset Parkinson’s Disease in the Han Chinese Population

Wei Song, Rui Huang, H. Shang, 2012, European Neurology.

Clinical practice guidelines for the management of adult diffuse gliomas.

Shuai Liu, D. Nam, Z. Ram, 2020, Cancer letters.

Identification of novel mutations in Chinese Hans with autosomal dominant polycystic kidney disease

Lin Zou, Yongxin Ma, Yunqiang Liu, 2011, BMC Medical Genetics.

Epigenetic modifications promote the expression of the orphan nuclear receptor NR0B1 in human lung adenocarcinoma cells

Yi-lu Lu, D. Tao, Yongxin Ma, 2016, Oncotarget.

Single-nucleotide Polymorphism rs2290692 in the 3′UTR of ITPKC Associated With Susceptibility to Kawasaki Disease in a Han Chinese Population

Qing Wu, Yuan Yang, Bo Li, 2012, Pediatric Cardiology.

Complex role of connexin 43 in astrocytic tumors and possible promotion of glioma‑associated epileptic discharge (Review).

Yanhui Liu, Xiang Wang, Q. Mao, 2017, Molecular medicine reports.

Combined analysis of genome-wide-linked susceptibility loci to Kawasaki disease in Han Chinese

Q. Peng, D. Tao, Yongxin Ma, 2013, Human Genetics.

Weighted correlation network analysis identifies multiple susceptibility loci for low‐grade glioma

Yanhui Liu, Xiang Wang, Q. Mao, 2022, Cancer medicine.

Endoscopic papillectomy of benign papillary tumors

F. Liu, MinMin Zhang, Zhendong Jin, 2020, Medicine.

Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum

J. Burgunder, H. Shang, Xueping Chen, 2008, Movement disorders : official journal of the Movement Disorder Society.

Identification of novel single-nucleotide variants altering RNA splicing of PKD1 and PKD2

D. Tao, Yunqiang Liu, Yuan Yang, 2021, Journal of Human Genetics.

Identification of novel single-nucleotide variants altering RNA splicing of PKD1 and PKD2

D. Tao, Yunqiang Liu, Yuan Yang, 2021, Journal of human genetics.

A novel missense variant c.71G > T (p.Gly24Val) of the CRYBA4 gene contributes to autosomal-dominant congenital cataract in a Chinese family

Yunqiang Liu, Yuan Yang, Chen Liang, 2022, International Ophthalmology.

Is BRD7 associated with spermatogenesis impairment and male infertility in humans? A case-control study in a Han Chinese population

D. Tao, Yunqiang Liu, Mohan Liu, 2021, Basic and Clinical Andrology.

A rare mutant of OFD1 gene responsible for Joubert syndrome with significant phenotype variation

Yunqiang Liu, Yuan Yang, Hai-bo Qu, 2020, Molecular genetics and genomics : MGG.

Evidence for a predisposing background for CAG expansion leading to HTT mutation in a Chinese population

H. Shang, D. Tao, Yongxin Ma, 2010, Journal of the Neurological Sciences.

TSPY1 suppresses USP7-mediated p53 function and promotes spermatogonial proliferation

Q. Dong, Yunqiang Liu, Mohan Liu, 2018, Cell Death & Disease.

A 3D‐Engineered Conformal Implant Releases DNA Nanocomplexs for Eradicating the Postsurgery Residual Glioblastoma

Jiankang He, Tianyi Kang, Yuan Yang, 2017, Advanced science.

Surgical treatment and survival outcome of patients with adult thalamic glioma: a single institution experience of 8 years

Q. Yue, Yanhui Liu, Xiang Wang, 2020, Journal of Neuro-Oncology.

Prognostic Factors for the Survival Outcome of Bilateral Thalamic Glioma: An Integrated Survival Analysis.

Yanhui Liu, Q. Mao, Yuan Yang, 2017, World neurosurgery.

Promoter demethylation mediates the expression of ZNF645, a novel cancer/testis gene.

D. Tao, Yongxin Ma, Yunqiang Liu, 2010, BMB reports.

Deep brain stimulation of the thalamic ventral intermediate nucleus for Benedikt’s syndrome mainly present as tremor: a long-term case observation

Yuelong Wang, Yuan Yang, Shizhen Zhang, 2018, Acta Neurochirurgica.

ALK-positive anaplastic large cell lymphoma with multifocal bone involvements : a case report and review of the literature

Yuehong Chen, Yuan Yang, Yi Liu, 2018 .

Mutation screening of the FKBP6 gene and its association study with spermatogenic impairment in idiopathic infertile men.

Si-zhong Zhang, Yuan Yang, Wei Zhang, 2007, Reproduction.

Clinical and Pathologic Features and Prognostic Factors for Recurrent Gliomas.

Yanhui Liu, Q. Mao, Yuan Yang, 2019, World neurosurgery.

An analysis of 170 glioma patients and systematic review to investigate the association between IDH-1 mutations and preoperative glioma-related epilepsy

Yanhui Liu, Xiang Wang, Q. Mao, 2016, Journal of Clinical Neuroscience.

The potential risk factors for atypical and anaplastic meningiomas: clinical series of 1,239 cases.

Yanhui Liu, Xiang Wang, Q. Mao, 2014, International journal of clinical and experimental medicine.

Huihui Dong, Yanhui Liu, Xiang Wang, 2016, Clinical Neurology and Neurosurgery.

[Analysis of HINT1 gene variant in a case with neuromyotonia and axonal neuropathy].

Yunqiang Liu, Yuan Yang, Jinyan Xu, 2019, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Clinical Characteristics and Prognostic Analysis of Glioma in Human Immunodeficiency Virus-Infected Patients.

Yanhui Liu, Q. Mao, Yuan Yang, 2018, World neurosurgery.

Targeted disruption of the mouse testis-enriched gene Znf230 does not affect spermatogenesis or fertility

D. Tao, Yongxin Ma, Yunqiang Liu, 2014, Genetics and molecular biology.

Human RING finger protein ZNF645 is a novel testis-specific E3 ubiquitin ligase.

D. Tao, Yunqiang Liu, D. Su, 2010, Asian journal of andrology.

Giant Prolactinomas: Outcomes of Multimodal Treatments for 42 Cases with Long-Term Follow-Up

S. Yin, Yuan Yang, Yu Hu, 2018, Experimental and Clinical Endocrinology & Diabetes.

A rare case of unilateral adrenal hyperplasia accompanied by hypokalaemic periodic paralysis caused by a novel dominant mutation in CACNA1S: features and prognosis after adrenalectomy

Q. Dong, Yuan Yang, Ying Shen, 2014, BMC Urology.

A novel ADCK4 mutation in a Chinese family with ADCK4-Associated glomerulopathy.

Zhangxue Hu, Yuan Yang, Jing Yang, 2018, Biochemical and biophysical research communications.

Mutation screening and association study of the TSSK4 Gene in Chinese infertile men with impaired spermatogenesis.

Yongxin Ma, D. Su, Si-zhong Zhang, 2008, Journal of andrology.

[Possible association between 278C/A single nucleotide polymorphism of FKBP6 and idiopathic azoospermia].

Si-zhong Zhang, Yuan Yang, Z. A, 2005, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Clinical significance of pre-surgical serum lipid levels in patients with glioblastoma

Yanhui Liu, Xiang Wang, Q. Mao, 2017, Oncotarget.

[Study on the distribution of Y chromosome haplogroups in Sichuan Han population].

Si-zhong Zhang, Yuan Yang, M. Ma, 2007, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Association analysis of LRP8 SNP rs3820198 and rs5174 with Parkinson’s disease in Han Chinese population

Wei Song, Rui Huang, H. Shang, 2012, Neurological research.

GAK rs1564282 and DGKQ rs11248060 increase the risk for Parkinson’s disease in a Chinese population

Wei Song, Rui Huang, H. Shang, 2013, Journal of Clinical Neuroscience.

Neutrophil/Lymphocyte Ratio Is an Independent Prognostic Factor in Elderly Patients with High-Grade Gliomas.

Yanhui Liu, Q. Mao, Yuan Yang, 2019, World neurosurgery.

Genetic Variants of SNCA Are Associated with Susceptibility to Parkinson’s Disease but Not Amyotrophic Lateral Sclerosis or Multiple System Atrophy in a Chinese Population

Wei Song, H. Shang, Ke Chen, 2015, PloS one.

Ataxin-2 intermediate-length polyglutamine: a possible risk factor for Chinese patients with amyotrophic lateral sclerosis

P. Pan, Wei Song, Rui Huang, 2011, Neurobiology of Aging.

The Novel Apolipoprotein E Mutation ApoE Chengdu (c.518T > C, p.L173P) in a Chinese Patient with Lipoprotein Glomerulopathy

Hongyan Wu, Zhangxue Hu, Yuan Yang, 2018, Journal of atherosclerosis and thrombosis.

Copy number variation of functional RBMY1 is associated with sperm motility: an azoospermia factor-linked candidate for asthenozoospermia

Dong Yang, Q. Dong, Yunqiang Liu, 2017, Human reproduction.

No association of five candidate genetic variants with amyotrophic lateral sclerosis in a Chinese population

Rui Huang, H. Shang, Yan Zeng, 2012, Neurobiology of Aging.

[Association of new functional SNP rs72689236 of CASP3 with Kawasaki disease: a meta-analysis].

Q. Peng, Yuan Yang, Chang-hui Chen, 2013, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

An association analysis of the R1628P and G2385R polymorphisms of the LRRK2 gene in multiple system atrophy in a Chinese population.

H. Shang, Yuan Yang, Xiaoyan Guo, 2015, Parkinsonism & related disorders.

SNCA variants rs2736990 and rs356220 as risk factors for Parkinson’s disease but not for amyotrophic lateral sclerosis and multiple system atrophy in a Chinese population

Wei Song, H. Shang, R. Ou, 2014, Neurobiology of Aging.

Association analysis of four candidate genetic variants with sporadic amyotrophic lateral sclerosis in a Chinese population

Wei Song, Rui Huang, H. Shang, 2014, Neurological Sciences.

Significance of the prognostic nutritional index in patients with glioblastoma: A retrospective study

Yanhui Liu, Xiang Wang, Q. Mao, 2016, Clinical Neurology and Neurosurgery.

Association Analysis of Single-Nucleotide Polymorphisms of USP24 and USP40 with Parkinson’s Disease in the Han Chinese Population

Wei Song, Rui Huang, H. Shang, 2012, European Neurology.

Role of rCBV values derived from dynamic susceptibility contrast-enhanced magnetic resonance imaging in differentiating CNS lymphoma from high grade glioma: a meta-analysis.

Yanhui Liu, Xiang Wang, Q. Mao, 2014, International journal of clinical and experimental medicine.

Three adolescents with Lhermitte-Duclos disease

C. You, Yuan Yang, Xuhui Hui, 2009, Journal of Clinical Neuroscience.

A prognostic nomogram for patients with newly diagnosed adult thalamic glioma in a surgical cohort.

Yanhui Liu, Yuan Yang, Mao Qing, 2020, Neuro-oncology.

Potential role of fractional anisotropy derived from diffusion tensor imaging in differentiating high-grade gliomas from low-grade gliomas: a meta-analysis.

Yanhui Liu, Xiang Wang, Q. Mao, 2014, International journal of clinical and experimental medicine.

A rare mutant of OFD1 gene responsible for Joubert syndrome with significant phenotype variation

Yun-qiang Liu, Yuan Yang, Hai-bo Qu, 2020, Molecular Genetics and Genomics.

Associations between gene polymorphisms and treatment outcomes of methotrexate in patients with juvenile idiopathic arthritis.

Yuehong Chen, K. Zou, Yuan Yang, 2018, Pharmacogenomics.

Some single-nucleotide polymorphisms of the TSSK2 gene may be associated with human spermatogenesis impairment.

Yongxin Ma, Yunqiang Liu, D. Su, 2010, Journal of andrology.

Unmethylated state of 5′ upstream CpG islands may be necessary but not sufficient for the testis-enriched expression of ZNF230/Znf230

D. Tao, Yongxin Ma, Yunqiang Liu, 2014, Genes & Genomics.

[The Clinical Significance of Tumor-associated Antigens in Dermatomyositis Patients with Interstitial Lung Disease].

Yuan Yang, Yi Liu, G. Yin, 2018, Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition.

TSPY1 suppresses USP7-mediated p53 function and promotes spermatogonial proliferation

Q. Dong, Yunqiang Liu, Mohan Liu, 2018, Cell Death & Disease.

Single nucleotide polymorphism C 677 T in the methylenete-trahydrofolate reductase gene might be a genetic risk factor for infertility for Chinese men with azoospermia or severe oligo-zoospermia

Si-zhong Zhang, Yuan Yang, Wei Zhang, 2006 .

Patient-Specific or Conventional Instrumentations: A Meta-analysis of Randomized Controlled Trials

Yipeng Lin, Xuelin Pan, Jian Li, 2020, BioMed research international.

Genetic features and postoperative outcomes of patients with glioblastoma involving the corpus callosum

Yanhui Liu, Xiang Wang, Q. Mao, 2017 .

c.822+126T>G/C: a novel triallelic polymorphism of the TSSK6 gene associated with spermatogenic impairment in a Chinese population.

Yan Peng, Yunqiang Liu, D. Su, 2010, Asian journal of andrology.

Preliminary study of the relationship between DAZ gene copy deletions and spermatogenic impairment in Chinese men.

Si-zhong Zhang, Yuan Yang, C. Xiao, 2006, Fertility and sterility.

Risk Factors for Early Mortality Among Patients with Glioma: A Population-Based Study.

Yanhui Liu, Xiang Wang, Q. Mao, 2020, World neurosurgery.

GAK rs1564282 and DGKQ rs11248060 increase the risk for Parkinson’s disease in a Chinese population

Rui Huang, H. Shang, Jianpeng Li, 2013, Journal of Clinical Neuroscience.

Identification of target messenger RNA substrates for mouse RBMY.

Huaqin Sun, D. Tao, Yongxin Ma, 2008, Molecular human reproduction.

A significant effect of the TSPY1 copy number on spermatogenesis efficiency and the phenotypic expression of the gr/gr deletion.

D. Tao, Yongxin Ma, Yunqiang Liu, 2013, Human molecular genetics.

GCH1 mutation and clinical study of Chinese patients with dopa‐responsive dystonia

H. Shang, Yuan Yang, Xiaoyan Guo, 2010, Movement disorders : official journal of the Movement Disorder Society.

Some single-nucleotide polymorphisms of the TSSK2 gene may be associated with human spermatogenesis impairment.

Yongxin Ma, Yunqiang Liu, D. Su, 2010, Journal of andrology.

Clinical and genetic features of patients with sporadic amyotrophic lateral sclerosis in south-west China

Dong Zhou, H. Shang, Yan Zeng, 2009, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

Some single nucleotide polymorphisms of MSY2 gene might contribute to susceptibility to spermatogenic impairment in idiopathic infertile men.

Ying Deng, D. Su, Si-zhong Zhang, 2008, Urology.