M. Nie

Yan Qin, Xuemei Li, Hai-yun Wang, 2015, Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists.

Prevalence of Parathyroid Carcinoma and Atypical Parathyroid Neoplasms in 153 Patients With Multiple Endocrine Neoplasia Type 1: Case Series and Literature Review

M. Nie, X. Xing, W. Xia, 2020, Frontiers in Endocrinology.

Association of genetic variants of vit D binding protein (DBP/GC) and of the enzyme catalyzing its 25-hydroxylation (DCYP2R1) and serum vit D in postmenopausal women

M. Nie, X. Xing, W. Xia, 2002, Hormones.

Growth Hormone Is Beneficial for Induction of Spermatogenesis in Adult Patients With Congenital Combined Pituitary Hormone Deficiency

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

Glucose tolerance and insulin responsiveness in Gitelman syndrome patients

Xuemei Li, Xiaoyan Peng, Limeng Chen, 2017, Endocrine connections.

Effects of variation in retinol binding protein 4 gene and adipose specific expression of gestational diabetes in Beijing, China.

Ming Li, M. Nie, H. Xiang, 2012, Diabetes research and clinical practice.

[Association of the extra-gonadal manifestations with different pathogenic gene mutations in male patients with congenital hypogonadotropic hypogonadism].

Rongrong Chen, J. Duan, M. Nie, 2015, Zhonghua yi xue za zhi.

Association of KCNQ1 gene polymorphism with gestational diabetes mellitus in a Chinese population

M. Nie, F. Ping, W. Li, 2009, Diabetologia.

The Body Composition in Early Pregnancy is Associated with the Risk of Development of Gestational Diabetes Mellitus Late During the Second Trimester

M. Nie, Liangkun Ma, Yanping Liu, 2020, Diabetes, metabolic syndrome and obesity : targets and therapy.

Metabolic Effects of Recombinant Human Growth Hormone Replacement Therapy on Juvenile Patients after Craniopharyngioma Resection

M. Nie, Xueyan Wu, J. Mao, 2022, International journal of endocrinology.

Reversal of idiopathic hypogonadotropic hypogonadism: a cohort study in Chinese patients

J. Duan, Li Li, L. Min, 2014, Asian journal of andrology.

Metabolic Effects of Testosterone Replacement Therapy in Patients with Type 2 Diabetes Mellitus or Metabolic Syndrome: A Meta-Analysis

M. Nie, Xueyan Wu, J. Mao, 2020, International journal of endocrinology.

Analysis of genetic and clinical characteristics of a Chinese Kallmann syndrome cohort with ANOS1 mutations.

Hongbing Zhang, Rongrong Chen, M. Nie, 2017, European journal of endocrinology.

A novel long-range deletion spanning CDC73 and upper-stream genes discovered in a kindred of familial primary hyperparathyroidism

M. Nie, X. Xing, W. Xia, 2021, Endocrine.

Familial isolated primary hyperparathyroidism/hyperparathyroidism‐jaw tumour syndrome caused by germline gross deletion or point mutations of CDC73 gene in Chinese

M. Nie, X. Xing, W. Xia, 2014, Clinical endocrinology.

Novel mutations of CYP27B1 gene lead to reduced activity of 1α-hydroxylase in Chinese patients.

Hua Su, T. Yuan, M. Nie, 2012, Bone.

Clinical and Genetic Analysis of Multiple Endocrine Neoplasia Type 1-Related Primary Hyperparathyroidism in Chinese

M. Nie, X. Xing, W. Xia, 2016, PloS one.

Pulsatile GnRH Therapy May Restore Hypothalamus–Pituitary–Testis Axis Function in Patients With Congenital Combined Pituitary Hormone Deficiency: A Prospective, Self-Controlled Trial

U. Kaiser, L. Min, M. Nie, 2017, The Journal of clinical endocrinology and metabolism.

PRIMARY HYPERPARATHYROIDISM DURING PREGNANCY: A CASE SERIES OF EIGHT PATIENTS.

M. Nie, X. Xing, Sixing Chen, 2019, Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists.

Genotype–Phenotype Correlation Analysis and Identification of a Novel SRD5A2 Mutation in Four Unrelated Chinese Patients with 5α-Reductase Deficiency

Ting Gui, M. Nie, Xueyan Wu, 2022, International journal of general medicine.

Five novel mutations of SRD5A2 found in eight Chinese patients with 46,XY disorders of sex development.

M. Nie, Xueyan Wu, J. Mao, 2011, Molecular human reproduction.

The diagnostic value of the olfactory evaluation for congenital hypogonadotropic hypogonadism

Kepu Chen, H. You, F. Feng, 2022, Frontiers in Endocrinology.

Novel HRPT2/CDC73 Gene Mutations and Loss of Expression of Parafibromin in Chinese Patients with Clinically Sporadic Parathyroid Carcinomas

M. Nie, X. Xing, W. Xia, 2012, PloS one.

Impaired geometry, volumetric density, and microstructure of cortical and trabecular bone assessed by HR-pQCT in both sporadic and MEN1-related primary hyperparathyroidism

Y. Jiang, M. Nie, X. Xing, 2019, Osteoporosis International.

Clinical phenotypes of Chinese primary hyperparathyroidism patients are associated with the calcium-sensing receptor gene R990G polymorphism.

M. Nie, X. Xing, O. Wang, 2013, European journal of endocrinology.

The Clinical Phenotypes in Chinese Primary Hyperparathyroidism Patients was Associated with Calcium-sensing Receptor Gene R 990 G Polymorphisms

M. Nie, X. Xing, O. Wang, 2013 .

The Bioinformatics Analysis of Aldosterone-Producing Adenoma and Verification of Differentially Expressed Genes

M. Nie, Yinjie Gao, Yushi Zhang, 2021, International journal of endocrinology.

High prevalence of hypertension and target organ damage in patients with 11β‐hydroxylase deficiency

M. Nie, J. Mao, Xi Wang, 2022, Clinical endocrinology.

Novel FSHβ mutation in a male patient with isolated FSH deficiency and infertility.

M. Nie, Mingxuan Cui, Xueyan Wu, 2017, European journal of medical genetics.

The prevalence of heterozygous CYP21A2 deficiency in patients with idiopathic acne, hirsutism, or both

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

Clinical Severity of Gitelman Syndrome Determined by Serum Magnesium

C. Chen, Yan Qin, Xuemei Li, 2014, American Journal of Nephrology.

Relationship between growth hormone deficiency and nonalcoholic fatty liver disease in patients with pituitary stalk interruption syndrome

M. Nie, Xueyan Wu, J. Mao, 2022, Clinical endocrinology.

Heteroplasmy level of the mitochondrial tRNaLeu(UUR) A3243G mutation in a Chinese family is positively associated with earlier age-of-onset and increasing severity of diabetes.

Heng Wang, M. Nie, Yun Zhang, 2009, Chinese medical sciences journal = Chung-kuo i hsueh k'o hsueh tsa chih.

Fumarate hydratase gene germline variants and mosaicism associated with pheochromocytoma and paraganglioma

M. Nie, Yinjie Gao, A. Tong, 2022, Annals of the New York Academy of Sciences.

Novel Mutations in FKBP10 and PLOD2 Cause Rare Bruck Syndrome in Chinese Patients

M. Nie, X. Xing, W. Xia, 2014, PloS one.

Increased urinary prostaglandin E2 metabolite: A potential therapeutic target of Gitelman syndrome

C. Chen, Yan Qin, Xuemei Li, 2017, PloS one.

High incidence of hypertension-mediated organ damage in a series of Chinese patients with 17α-hydroxylase deficiency

M. Nie, Xueyan Wu, J. Mao, 2021, Endocrine.

Genetic Screening in a Large Chinese Cohort of Childhood Onset Hypoparathyroidism by Next‐Generation Sequencing Combined with TBX1‐MLPA

M. Nie, X. Xing, W. Xia, 2019, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Growth hormone cocktail improves hepatopulmonary syndrome secondary to hypopituitarism: A case report

M. Nie, Xueyan Wu, J. Mao, 2021, World journal of clinical cases.

A case report of pedigree of a homozygous mutation of the steroidogenic acute regulatory protein causing lipoid congenital adrenal hyperplasia

M. Nie, Lin Lu, Xiaojing Wang, 2017, Medicine.

Gonadotropin-Induced Spermatogenesis in CHH Patients with Cryptorchidism

M. Nie, Xueyan Wu, J. Mao, 2019, International journal of endocrinology.

Pulsatile gonadotropin-releasing hormone therapy is associated with earlier spermatogenesis compared to combined gonadotropin therapy in patients with congenital hypogonadotropic hypogonadism

U. Kaiser, L. Min, M. Nie, 2016, Asian journal of andrology.

Efficacy and Outcome Predictors of Gonadotropin Treatment for Male Congenital Hypogonadotropic Hypogonadism

M. Nie, Xueyan Wu, Xi Wang, 2016, Medicine.

Clinical Characteristics and Spermatogenesis in Patients with Congenital Hypogonadotropic Hypogonadism Caused by FGFR1 Mutations

M. Nie, Xueyan Wu, J. Mao, 2020, International journal of endocrinology.

Comparison of Clinical Characteristics and Spermatogenesis in CHH Patients Caused by PROKR2 and FGFR1 Mutations

M. Nie, Xueyan Wu, J. Mao, 2021, Reproductive Sciences.

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 and Recurrent Mutations of WISP3 in Two Chinese Families with Progressive Pseudorheumatoid Dysplasia

M. Nie, X. Xing, W. Xia, 2012, PloS one.

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.

Recurrent Germline Mutations of CHEK2 as a New Susceptibility Gene in Patients with Pheochromocytomas and Paragangliomas

C. Ling, M. Nie, Yinjie Gao, 2021, International journal of 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.

A novel long-range deletion spanning STX16 and NPEPL1 causing imprinting defects of the GNAS locus discovered in a patient with autosomal-dominant pseudohypoparathyroidism type 1B

M. Nie, X. Xing, W. Xia, 2020, Endocrine.

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.

Bone turnover markers are associated with the PTH levels in different subtypes of pseudohypoparathyroidism type 1 patients

M. Nie, X. Xing, W. Xia, 2021, Clinical endocrinology.

Bone Mineral Density and Its Serial Changes Are Associated With PTH Levels in Pseudohypoparathyroidism Type 1B Patients

M. Nie, X. Xing, W. Xia, 2018, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Clinical and genetic characteristics of Pseudohypoparathyroidism in the Chinese population

M. Nie, X. Xing, W. Xia, 2018, Clinical endocrinology.

The First Mutation Identified in a Chinese Acrodysostosis Patient Confirms a p.G289E Variation of PRKAR1A Causes Acrodysostosis

Chunlin Li, M. Nie, X. Xing, 2014, International journal of molecular sciences.

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

M. Nie, J. Mao, S. Lu, 2011, Journal of postgraduate 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.

Clinical and genetic analysis of atypical parathyroid adenoma compared with parathyroid carcinoma and benign lesions in a Chinese cohort

M. Nie, X. Xing, W. Xia, 2023, Frontiers in Endocrinology.

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.

Association of ESR1 and C6orf97 gene polymorphism with osteoporosis in postmenopausal women

J. Zhao, Jing Zhao, M. Nie, 2014, Molecular Biology Reports.

Expression of Ki-67, galectin-3, fragile histidine triad, and parafibromin in malignant and benign parathyroid tumors.

M. Nie, X. Xing, W. Xia, 2012, Chinese medical journal.

A haplotype of MATN3 is associated with vertebral fracture in Chinese postmenopausal women: Peking Vertebral Fracture (PK-VF) study.

J. Zhao, Qian Chen, M. Nie, 2012, Bone.

Identification of five novel arginine vasopressin gene mutations in patients with familial neurohypophyseal diabetes insipidus.

M. Nie, F. Gu, J. Cen, 2016, International journal of molecular medicine.

Identification of seven novel CYP11B1 gene mutations in Chinese patients with 11β-hydroxylase deficiency

M. Nie, Shi Chen, Lin Lu, 2015, Steroids.

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.

Frequent SLC12A3 mutations in Chinese Gitelman syndrome patients: structure and function disorder

Xuemei Li, Xiaoyan Peng, Lubin Xu, 2021, Endocrine connections.

Primary hyperparathyroidism in Chinese children and adolescents: A single‐centre experience at Peking Union Medical College Hospital

M. Nie, X. Xing, W. Xia, 2017, Clinical endocrinology.

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 .

Post-genome wide association studies and functional analyses identify association of MPP7 gene variants with site-specific bone mineral density.

Johnny S. H. Kwan, P. Sham, Zhi-Jie Dai, 2012, Human molecular genetics.

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

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

GERMLINE GCM2 MUTATION SCREENING IN CHINESE PRIMARY HYPERPARATHYROIDISM PATIENTS.

M. Nie, X. Xing, W. Xia, 2020, Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists.

Association of ESR1 and C6orf97 gene polymorphism with osteoporosis in postmenopausal women

J. Zhao, M. Nie, W. Xia, 2014, Molecular Biology Reports.

[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.

Association study of the miRNA-binding site polymorphisms of CDKN2A/B genes with gestational diabetes mellitus susceptibility

Wei Li, Juntao Liu, Fan Ping, 2015, 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.

Aromatase deficiency in a Chinese adult man caused by novel compound heterozygous CYP19A1 mutations: Effects of estrogen replacement therapy on the bone, lipid, liver and glucose metabolism

Shiuan Chen, Zhike Chen, M. Nie, 2015, Molecular and Cellular Endocrinology.

Novel autosomal recessive gene mutations in aquaporin-2 in two Chinese congenital nephrogenic diabetes insipidus pedigrees.

M. Nie, F. Gu, L. Duan, 2015, International journal of clinical and experimental medicine.

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 .

Association of Six Single Nucleotide Polymorphisms with Gestational Diabetes Mellitus in a Chinese Population

Ying Wang, Jinsong Gao, M. Nie, 2011, PloS one.

The levels of bone turnover markers in Chinese postmenopausal women: Peking Vertebral Fracture study

J. Zhao, M. Nie, X. Xing, 2011, Menopause.

Association of GALNT3 gene polymorphisms with bone mineral density in Chinese postmenopausal women: the Peking Vertebral Fracture study

Chunlin Li, M. Nie, X. Xing, 2014, Menopause.

Bone microstructure of adult patients with non-surgical hypoparathyroidism assessed by high-resolution peripheral quantitative computed tomography

Y. Jiang, M. Nie, X. Xing, 2020, Osteoporosis International.

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.

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.

A Novel De novo GATA-binding Protein 3 Mutation in a Patient with Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome

M. Nie, X. Xing, W. Xia, 2017, Chinese Medical Journal.

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.

Genetic and clinical screening for hereditary primary hyperparathyroidism in a large Chinese cohort: a single‐center study

M. Nie, X. Xing, W. Xia, 2023, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Clinical phenotypes of Chinese primary hyperparathyroidism patients are associated with the calcium-sensing receptor gene R990G polymorphism.

M. Nie, X. Xing, O. Wang, 2013, European journal of endocrinology.

Familial isolated primary hyperparathyroidism/hyperparathyroidism‐jaw tumour syndrome caused by germline gross deletion or point mutations of CDC73 gene in Chinese

M. Nie, X. Xing, W. Xia, 2014, Clinical endocrinology.