Author

Rui-Meng Yang

Observed name: R.‐f. Yang

Institutions: Shanghai Jiao Tong University, Fudan University Shanghai Cancer Center, Shanghai Ninth People's Hospital, State Key Laboratory of Medical Genomics

Observed institutions: Shanghai Jiao Tong University, Fudan University Shanghai Cancer Center, Shanghai Ninth People's Hospital, Tongji Hospital, State Key Laboratory of Medical Genomics

ORCID: 0009-0008-1890-0409

Observed ORCID: 0009-0008-1890-0409

OpenAlex ID: A5101538804

Identification of Eukaryotic Translation Initiation Factor 4B as a Novel Candidate Gene for Congenital Hypothyroidism

2024 · Feng Sun, Rui-Jia Zhang, et al. · The Journal of Clinical Endocrinology & Metabolism · 9

The rs5934505 single nucleotide polymorphism ( SNP ) is associated with low testosterone and late‐onset hypogonadism, but the rs10822184 SNP is associated with overweight and obesity in a Chinese Han population: a case–control study

2015 · Y.‐p. Chen, L.‐L. Nie, et al. · Andrology · 9

TSHR Variant Screening and Phenotype Analysis in 367 Chinese Patients With Congenital Hypothyroidism

2024 · Hai-Yang Zhang, Feng-Yao Wu, et al. · Annals of Laboratory Medicine · 4

First large-scale screening of Notch biallelic variants implicates novel candidate genes in congenital hypothyroidism

2026 · Feng-Yao Wu, Chen-Yang Wu, et al. · The Journal of Clinical Endocrinology & Metabolism · 2

Works count: 5

Citation count: 26

H-index: 3

I10-index: