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Yanning Song
Observed names:
Y N Song,
Y Song,
Yan‐Ning Song,
Yongjian Song
Institutions:
Shanghai Polytechnic University,
Capital Medical University,
Beijing Children’s Hospital
Observed institutions:
Shanghai Polytechnic University,
Capital Medical University,
Ruijin Hospital,
Chinese PLA General Hospital,
Beijing Anzhen Hospital,
Beijing Children’s Hospital
show all 6
ORCID:
0000-0002-2320-1724
Observed ORCID:
0000-0002-2320-1724
OpenAlex ID:
A5101943393
Effect of human umbilical cord-derived mesenchymal stem cells on lung damage in severe COVID-19 patients: a randomized, double-blind, placebo-controlled phase 2 trial
2021
·
Lei Shi
, Hai Huang
, et al.
·
Signal Transduction and Targeted Therapy
·
286
PDF
Altered gut microbiota and its metabolites correlate with plasma cytokines in schizophrenia inpatients with aggression
2022
·
Hongxin Deng
, Lei He
, et al.
·
BMC Psychiatry
·
43
PDF
Exome sequencing reveals genetic architecture in patients with isolated or syndromic short stature
2021
·
Xin Fan
, Sen Zhao
, et al.
·
Journal of genetics and genomics/Journal of Genetics and Genomics
·
40
Clinical characteristics and genotype‐phenotype correlations of 130 Chinese children in a high‐homogeneity single‐center cohort with 5α‐reductase 2 deficiency
2020
·
Lijun Fan
, Yanning Song
, et al.
·
Molecular Genetics & Genomic Medicine
·
31
PDF
New insights into 5α-reductase type 2 deficiency based on a multi-centre study: regional distribution and genotype–phenotype profiling of SRD5A2 in 190 Chinese patients
2019
·
Baoheng Gui
, Yanning Song
, et al.
·
Journal of Medical Genetics
·
28
Phenotype and Molecular Characterizations of 30 Children From China With NR5A1 Mutations
2018
·
Yanning Song
, Lijun Fan
, et al.
·
Frontiers in Pharmacology
·
28
PDF
Novel phenotypes and genotypes in Antley-Bixler syndrome caused by cytochrome P450 oxidoreductase deficiency: based on the first cohort of Chinese children
2019
·
Lijun Fan
, Xiaoya Ren
, et al.
·
Orphanet Journal of Rare Diseases
·
24
PDF
A Gender-, Age-, and Weight Status-Specific Analysis of the High Prevalence of Hyperuricemia Among Chinese Children and Adolescents with Obesity
2024
·
Meijuan Liu
, Bingyan Cao
, et al.
·
Diabetes Metabolic Syndrome and Obesity
·
21
PDF
Prenatal and early diagnosis of Chinese 3-M syndrome patients with novel pathogenic variants
2017
·
Xuyun Hu
, Hongdou Li
, et al.
·
Clinica Chimica Acta
·
17
Association between serum uric acid-to-high-density lipoprotein cholesterol ratio and metabolic dysfunction-associated steatotic liver disease among Chinese children with obesity
2025
·
Meijuan Liu
, Bingyan Cao
, et al.
·
Frontiers in Endocrinology
·
12
PDF
Whole Exome Sequencing Uncovered the Genetic Architecture of Growth Hormone Deficiency Patients
2021
·
Chenxi Yu
, Bobo Xie
, et al.
·
Frontiers in Endocrinology
·
12
PDF
Analysis of genetic and clinical characteristics of androgen insensitivity syndrome: a cohort study including 12 families
2024
·
Zheng Yuan
, Lijun Fan
, et al.
·
European Journal of Endocrinology
·
11
Growth Pattern in Chinese Children With 5α-Reductase Type 2 Deficiency: A Retrospective Multicenter Study
2019
·
Xiu Zhao
, Yanning Song
, et al.
·
Frontiers in Pharmacology
·
8
PDF
Novel pathogenic RECQL4 variants in Chinese patients with Rothmund-Thomson syndrome
2018
·
Baoheng Gui
, Yanning Song
, et al.
·
Gene
·
8
Effect of Antithyroid Drugs Treatment Duration on The Remission Rates of Graves' Disease in Children and Adolescents: A Single‐Arm Meta‐Analysis and Systematic Review
2024
·
Yang Li
, Xin‐Meng Wang
, et al.
·
Clinical Endocrinology
·
6
PDF
Heterozygous Recurrent Mutations Inducing Dysfunction of ROR2 Gene in Patients With Short Stature
2021
·
Baoheng Gui
, Chenxi Yu
, et al.
·
Frontiers in Cell and Developmental Biology
·
5
PDF
[Clinical phenotype and gene analysis of 86 cases of 5 alpha reductase deficiency].
2019
·
Y N Song
, L J Fan
, et al.
·
PubMed
·
5
SOX2 heterozygous mutations cause multiple extraocular phenotypes in boys
2021
·
Yi Wang
, Lijun Fan
, et al.
·
Chinese Medical Journal
·
3
Variant analysis of the chromodomain helicase DNA ‐binding protein 7 in pediatric disorders of sex development
2019
·
Beibei Zhang
, Yanning Song
, et al.
·
Pediatric Investigation
·
3
PDF
Non‐surgical Treatment May be Appropriate for Most Chinese Children With Monogenic Congenital Hyperinsulinism Based on a Retrospective Study of 121 Patients
2024
·
Ming Cheng
, Chang Su
, et al.
·
Pediatric Diabetes
·
1
PDF
[A case of ultrasound-guided microwave ablation for Graves disease].
2022
·
Y N Song
, W Y Shi
, et al.
·
PubMed
·
1
Growth Curves of Chinese Children with Androgen Insensitivity Syndrome: A Multicenter Registry Study
2022
·
Xiu Zhao
, Zhe Su
, et al.
·
Journal of Personalized Medicine
·
1
PDF
Treatment with Human Umbilical Cord-Derived Mesenchymal Stem Cells for Severe COVID-19 Patients with Lung Damage: A Randomised, Double-Blind, Placebo‑Controlled Phase 2 Trial
2020
·
Lei Shi
, Hai Huang
, et al.
·
SSRN Electronic Journal
·
1
[Gender selection and postoperative follow-up analysis in 85 children with 46, XY disorders of sex development].
2019
·
M Zhao
, C X Gong
, et al.
·
PubMed
·
1
The wide clinical expression spectrum presented in two families with NR5A1 mutation
2018
·
Yanning Song
, LijunFan
, et al.
·
Clinical Practice
·
1
PDF
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Works count:
32
Citation count:
598
H-index:
11
I10-index:
12
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