Juan Li

发表

Molecular and phenotypic spectrum of Noonan syndrome in Chinese patients

Jian Wang, Niu Li, Xiumin Wang, 2019, Clinical genetics.

Urine concentrations of perfluoroalkyl acids in children and contributions of dietary factors: a cross-sectional study from Shanghai, China

Zhemin Shen, Tao Yuan, Yuning Ma, 2021, Environmental Science and Pollution Research.

Clinical and molecular genetic characterization of two patients with mutations in the phosphoglucomutase 1 (PGM1) gene

Yiping Shen, Jian Wang, Niu Li, 2018, Journal of pediatric endocrinology & metabolism : JPEM.

Effects of circulating vitamin D concentrations on emotion, behavior and attention: A cross-sectional study in preschool children with follow-up behavior experiments in juvenile mice.

Bin Wang, Mingqing Xu, Xiaodan Yu, 2020, Journal of affective disorders.

Development of a sensitive HPLC‐MS/MS method for 25‐hydroxyvitamin D2 and D3 measurement in capillary blood

B. Liu, Tao Yuan, Xiaodan Yu, 2020, Journal of clinical laboratory analysis.

Associations between maternal vitamin D status during three trimesters and cord blood 25(OH)D concentrations in newborns: a prospective Shanghai birth cohort study

Jun Zhang, Mingqing Xu, Ying Tian, 2021, European Journal of Nutrition.

Novel pathogenic ACAN variants in non-syndromic short stature patients.

Yiping Shen, Tingting Yu, Jian Wang, 2017, Clinica chimica acta; international journal of clinical chemistry.

Novel compound heterozygous variants in the LHCGR gene identified in a subject with Leydig cell hypoplasia type 1

Yiping Shen, Jian Wang, Niu Li, 2018, Journal of pediatric endocrinology & metabolism : JPEM.

De Novo Mutation of KAT6B Gene Causing Atypical Say–Barber–Biesecker–Young–Simpson Syndrome or Genitopatellar Syndrome

Tingting Yu, Jian Wang, Niu Li, 2017, Fetal and pediatric pathology.

Evaluating the variety of GNAS inactivation disorders and their clinical manifestations in 11 Chinese children

Jian Wang, Niu Li, Yu Ding, 2022, BMC Endocrine Disorders.

Clinical and molecular analysis in a cohort of Chinese children with Cornelia de Lange syndrome

Jian Wang, Yufei Xu, Xiumin Wang, 2020, Scientific Reports.

Molecular and phenotypic spectrum of Noonan syndrome in Chinese patients

Jian Wang, Niu Li, Xiumin Wang, 2019, Clinical genetics.

The impact of the COVID‐19 pandemic on the care of pulmonary hypertension patients outside the Hubei province in China

Zhe Zhang, Chunli Liu, Q. Jiang, 2022, Pulmonary circulation.

Increased transactivation and impaired repression of β-catenin-mediated transcription associated with a novel SOX3 missense mutation in an X-linked hypopituitarism pedigree with modest growth failure

Yiping Shen, Tingting Yu, Jian Wang, 2018, Molecular and Cellular Endocrinology.

Turner syndrome caused by rare complex structural abnormalities involving chromosome X.

Jian Wang, Niu Li, Xiumin Wang, 2017, Experimental and therapeutic medicine.

Causal variants screened by whole exome sequencing in a patient with maternal uniparental isodisomy of chromosome 10 and a complicated phenotype

Yiping Shen, Tingting Yu, Jian Wang, 2016, Experimental and therapeutic medicine.

Molecular characterization of 25 Chinese pedigrees with 21-hydroxylase deficiency.

Peirong Yang, Jian Wang, Ying Wang, 2011, Genetic testing and molecular biomarkers.

Clinical Profiles and Genetic Spectra of 814 Chinese Children With Short Stature

Jian Wang, Niu Li, Xiumin Wang, 2021, The Journal of clinical endocrinology and metabolism.

Screening for Coding Variants in FTO and SH2B1 Genes in Chinese Patients with Obesity

Yiping Shen, Yongguo Yu, R. Yao, 2013, PloS one.

Novel mutations in the CYP11B2 gene causing aldosterone synthase deficiency.

Yiping Shen, Tingting Yu, Jian Wang, 2016, Molecular medicine reports.

SOPH Syndrome with Growth Hormone Deficiency, Normal Bone Age, and Novel Compound Heterozygous Mutations in NBAS

Yiping Shen, Jian Wang, Niu Li, 2018, Fetal and pediatric pathology.

Clinical and genetic analysis in a Chinese cohort of children and adolescents with diabetes/persistent hyperglycemia

Jian Wang, Niu Li, F. Jiang, 2020, Journal of diabetes investigation.

New Insights from Unbiased Panel and Whole-Exome Sequencing in a Large Chinese Cohort with Disorders of Sex Development.

Yiping Shen, Tingting Yu, Jian Wang, 2019, European journal of endocrinology.

Evaluation of Immunogenicity by Pseudovirus Neutralization Assays for SARS‐CoV‐2 Variants after Primary and Booster Immunization

Shanshan Zhou, Xiaojing Wen, Juan Li, 2022, International Journal of Infectious Diseases.

Complex clinical manifestations and new insights in RNA sequencing of children with diabetes and WFS1 variants

Xin Li, Niu Li, Xiumin Wang, 2023, Frontiers in Endocrinology.

Evaluation of basal sex hormone levels for activation of the hypothalamic–pituitary–gonadal axis

Peirong Yang, Shijian Liu, Yongguo Yu, 2018, Journal of pediatric endocrinology & metabolism : JPEM.

[Endocrine and metabolic features of female children with Prader-Willi syndrome: an analysis of 4 cases].

Jian Wang, Yu Ding, Juan Li, 2017, Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics.

Multibioinspired Design of Durable Janus Copper Foam with Asymmetric and Cooperative Alternating Wettability for Efficient Fog Harvesting

J. Wang, Bo-Sheng Bai, Zhen Guo, 2023, SSRN Electronic Journal.

Clinical characteristics and follow-up of 5 young Chinese males with gonadotropin-releasing hormone deficiency caused by mutations in the KAL1 gene

Jian Wang, Niu Li, Xiumin Wang, 2015, Meta gene.

Biallelic mutations in GPD1 gene in a Chinese boy mainly presented with obesity, insulin resistance, fatty liver, and short stature

Yiping Shen, Tingting Yu, Jian Wang, 2017, American journal of medical genetics. Part A.