Xueyan Wu

Xueyan Wu, J. Mao, Xi Wang, 2021, Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists.

Novel NR5A1 mutations found in Chinese patients with 46, XY disorders of sex development

M. Nie, Xueyan Wu, J. Mao, 2018, Clinical endocrinology.

Congenital combined pituitary hormone deficiency patients have better responses to gonadotrophin-induced spermatogenesis than idiopathic hypogonadotropic hypogonadism patients.

L. Min, M. Nie, Xueyan Wu, 2015, Human reproduction.

Efficacy of Pulsatile Gonadotropin-Releasing Hormone Therapy in Male Patients: Comparison between Pituitary Stalk Interruption Syndrome and Congenital Hypogonadotropic Hypogonadism.

M. Nie, Xueyan Wu, J. Mao, 2022, Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists.

Assisted reproductive techniques with congenital hypogonadotropic hypogonadism patients: a systematic review and meta-analysis

M. Nie, Xueyan Wu, J. Mao, 2018, BMC Endocrine Disorders.

[Efficacy and safety of letrozole in treatment of male children with disorders of sex development].

M. Nie, Xueyan Wu, J. Mao, 2020, Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences.

Gonadotropin treatment for male partial congenital hypogonadotropic hypogonadism in Chinese patients

M. Nie, Xueyan Wu, J. Mao, 2019, Asian journal of andrology.

Mutation of c.244G>T in NR5A1 gene causing 46, XY DSD by affecting RNA splicing

M. Nie, Xueyan Wu, J. Mao, 2021, Orphanet Journal of Rare Diseases.

Novel rare variants in FGFR1 and clinical characteristics analysis in a series of congenital hypogonadotropic hypogonadism patients

Rongrong Chen, M. Nie, Xueyan Wu, 2021, Clinical endocrinology.

Classification of CHD7 Rare Variants in Chinese Congenital Hypogonadotropic Hypogonadism Patients and Analysis of Their Clinical Characteristics

M. Nie, Xueyan Wu, J. Mao, 2022, Frontiers in Genetics.

The underlying cause of the simple virilizing phenotype in patients with 21-hydroxylase deficiency harboring P31L variant

M. Nie, Xueyan Wu, J. Mao, 2023, Frontiers in Endocrinology.

Bone mineral density and trabecular bone score in patients with 21‐hydroxylase deficiency after glucocorticoid treatment

M. Nie, Xueyan Wu, J. Mao, 2020, Clinical endocrinology.

Optimal treatment for spermatogenesis in male patients with hypogonadotropic hypogonadism

Xueyan Wu, J. Mao, Xi Wang, 2019, Medicine.

Two cases of immunoglobulin G4 (IgG4)-related hypophysitis diagnosed without pituitary biopsy

M. Nie, Xueyan Wu, J. Mao, 2020, Therapeutic advances in endocrinology and metabolism.

Micro‐ribonucleic acid‐binding site variants of type 2 diabetes candidate loci predispose to gestational diabetes mellitus in Chinese Han women

M. Nie, Xueyan Wu, J. Mao, 2018, Journal of diabetes investigation.

Acute Intermittent Porphyria: A Diagnostic Challenge for Endocrinologist

F. Gong, Xueyan Wu, Xi Wang, 2015, Chinese Medical Journal.

Chimeric CYP11B2/CYP11B1 causing 11β-hydroxylase deficiency in Chinese patients with congenital adrenal hyperplasia

M. Nie, Xueyan Wu, W. Xia, 2015, Steroids.

Efficacy and safety of pulsatile gonadotropin-releasing hormone therapy in patients with congenital hypogonadotropic hypogonadism: a multicentre clinical study

M. Nie, Xueyan Wu, J. Mao, 2021, Annals of translational medicine.

The prevalence of chimeric TNXA/TNXB gene and clinical symptoms of Ehlers-Danlos syndrome with 21-hydroxylase deficiency.

M. Nie, Xueyan Wu, J. Mao, 2020, The Journal of clinical endocrinology and metabolism.

Adult-onset idiopathic hypogonadotropic hypogonadism: possible aetiology, clinical manifestations and management.

M. Nie, Xueyan Wu, J. Mao, 2010, Asian journal of andrology.

Bone Mineral Density in Pituitary Stalk Interruption Syndrome: The role of IGF-1 and Testosterone at Different Skeletal Sites.

M. Nie, Xueyan Wu, J. Mao, 2022, Endocrine Practice.

A Rare Case of Coexistence of Pituitary Stalk Interruption Syndrome and Mayer-Rokitansky-Küster-Hauser Syndrome

M. Nie, Xueyan Wu, J. Mao, 2020 .

Novel mutations of HSD17B3 in three Chinese patients with 46,XY Disorders of Sex Development

M. Nie, Mingxuan Cui, Xueyan Wu, 2017, Steroids.

[Clinical values of single or repeated triptorelin stimulating test in the differential diagnosis between idiopathic hypogonadotropic hypogonadism and constitutional delayed puberty].

M. Nie, Xueyan Wu, J. Mao, 2011, Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae.

Novel Microdeletion in the X Chromosome Leads to Kallmann Syndrome, Ichthyosis, Obesity, and Strabismus

M. Nie, Xueyan Wu, J. Mao, 2020, Frontiers in Genetics.

Aromatase Inhibitor Increases the Height of Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.

M. Nie, Xueyan Wu, Bingqing Yu, 2020, Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists.

Investigation of miRNA-binding site variants and risk of gestational diabetes mellitus in Chinese pregnant women

M. Nie, Xueyan Wu, J. Mao, 2017, Acta Diabetologica.

HDL-cholesterol concentration in pregnant Chinese Han women of late second trimester associated with genetic variants in CETP, ABCA1, APOC3, and GALNT2

M. Nie, Mingxuan Cui, Xueyan Wu, 2017, Oncotarget.

First Report of a Novel Missense CLDN19 Mutations Causing Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis in a Chinese Family

Jingjun Li, T. Yuan, X. Xing, 2015, Calcified Tissue International.

The association between six genetic variants and blood lipid levels in pregnant Chinese Han women.

Ying Wang, M. Nie, Xueyan Wu, 2017, Journal of clinical lipidology.

The association between six genetic variants and blood lipid levels of m in pregnant Chinese Han women Short title : SNPs and plasma lipid levels in Han pregnancy

Ying Wang, M. Nie, Xueyan Wu, 2017 .

Combined therapy with GnRH analogue and growth hormone increases adult height in children with short stature and normal pubertal onset

M. Nie, Xueyan Wu, J. Mao, 2020, Endocrine.

Seminal plasma metabolomics signatures of normosmic congenital hypogonadotropic hypogonadism.

Haolong Li, Xueyan Wu, J. Mao, 2023, Heliyon.

[Effect of bodyweight on the onset of puberty of female children and adolescents].

Hui-juan Zhu, H. Pan, Dian-xi Zhang, 2010, Zhongguo yi xue ke xue yuan xue bao. Acta Academiae Medicinae Sinicae.

Osteonecrosis of Femoral Head is Associated with Congenital Multiple Pituitary Hormone Deficiency: Report of Three Cases and Literature Review

M. Nie, Xueyan Wu, J. Mao, 2019, Endocrine research.

Increased bone mineral density in male patients with idiopathic hypogonadotropic hypogonadism who undergo sex hormone therapy: Findings from cross-sectional and longitudinal studies.

M. Nie, Xueyan Wu, J. Mao, 2021, Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists.

Mutational analysis of androgen receptor gene in four Chinese patients with male pseudohermaphroditism.

M. Nie, Xueyan Wu, J. Mao, 2010, Fertility and sterility.

Molecular analysis of 12 Chinese patients with 11β‐hydroxylase deficiency and in vitro functional study of 20 CYP11B1 missense variants

L. Qiu, M. Nie, Xueyan Wu, 2023, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Diabetes insipidus as the first symptom caused by lung cancer metastasis to the pituitary glands: clinical presentations, diagnosis, and management.

M. Nie, Xueyan Wu, J. Mao, 2011, Journal of postgraduate medicine.

Testosterone replacement therapy improves insulin sensitivity and decreases high sensitivity C-reactive protein levels in hypogonadotropic hypogonadal young male patients.

Xueyan Wu, J. Mao, Qian Zhang, 2009, Chinese medical journal.

Seminal plasma metabolomics signatures of normosmic congenital hypogonadotropic hypogonadism.

Haolong Li, Xueyan Wu, J. Mao, 2023, Heliyon.