Jia Rao

Also affiliated with XinHua Hospital, Children's Hospital of Fudan University

MedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 3 papers. Top paper: “Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome”.

Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome

Journal of the American Society of Nephrology(2021)10.1681/asn.2020040490

N/A

0.505DataRank · unranked

28 citations

Slim Mzoughi, Ronen Schneider, Susanne J. Kühl, Denny Schanze, Verena Klämbt +38 more

Human and mouse studies establish TBX6 in Mendelian CAKUT and as a potential driver of kidney defects associated with the 16p11.2 microdeletion syndrome

Kidney International(2020)10.1016/j.kint.2020.04.045

N/A

0DataRank · unranked

35 citations

Nan Wu, Shuangshuang Dong, Ling Zhang, Yanxue Zhao, Wei‐Sheng Chen +25 more

Invariant natural killer T cells drive hepatic homeostasis in nonalcoholic fatty liver disease via sustained IL‐10 expression in CD170+ Kupffer cells

European Journal of Immunology(2023)10.1002/eji.202350474

N/A

0DataRank · unranked

10 citations

Jinke Geng, Shuangshuang Zhang, Jia Rao, Yansong Zhu, Shaodong Xu +5 more