🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Nan Wu

Chinese Academy of Medical Sciences & Peking Union Medical College

ORCID: 0000-0002-9429-2889

Also affiliated with Peking Union Medical College Hospital

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 9 papers. Top paper: “Functional biology of the Steel syndrome founder allele and evidence for clan genomics derivation of COL27A1 pathogenic alleles worldwide”.

Functional biology of the Steel syndrome founder allele and evidence for clan genomics derivation of COL27A1 pathogenic alleles worldwide

European Journal of Human Genetics(2020)10.1038/s41431-020-0632-x
N/A
0DataRank · unranked
40 citations

Gözde Yeşil, Harikiran Nistala, Alper Gezdirici, Yavuz Bayram, Kalyan C. Nannuru +32 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

Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndrome

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2020.12.014
N/A
0DataRank · unranked
90 citations

Sen Zhao, Angad Jolly, Lianlei Wang, Hongxin Pan, Jian Yuan +72 more

Exome sequencing reveals genetic architecture in patients with isolated or syndromic short stature

Journal of genetics and genomics/Journal of Genetics and Genomics(2021)10.1016/j.jgg.2021.02.008
N/A
0DataRank · unranked
41 citations

Sen Zhao, Chenxi Yu, Di Wu, Zihui Yan, Lijun Fan +25 more

Expanding the mutation and phenotype spectrum of MYH3-associated skeletal disorders

npj Genomic Medicine(2022)10.1038/s41525-021-00273-x
N/A
0DataRank · unranked
26 citations

Shuyang Zhang, Sigrún Hallgrímsdóttir, Yuzhi Zuo, Xiaoxin Li, Dominyka Batkovskyte +31 more

Impaired glycine neurotransmission causes adolescent idiopathic scoliosis

Journal of Clinical Investigation(2023)10.1172/jci168783
N/A
0DataRank · unranked
32 citations

Ming Yue, Jason Pui Yin Cheung, Prudence Wing Hang Cheung, Yanhui Fan, Meicheng Wu +21 more

COL11A2 as a candidate gene for vertebral malformations and congenital scoliosis

Human Molecular Genetics(2023)10.1093/hmg/ddad117
N/A
0DataRank · unranked
22 citations

Elizabeth Wohler, Vida Erfani, Guozhuang Li, Alexya N. Aguilera, Alberto Santiago-Cornier +11 more

Variants in the SOX9 transactivation middle domain induce axial skeleton dysplasia and scoliosis

medRxiv(2023)10.1101/2023.05.29.23290174
N/A
0DataRank · unranked
1 citations

Zhaoyang Liu, Sen Zhao, Kexin Xu, Valeria Aceves, Cheng Qiu +14 more

Planar cell polarity zebrafish models of congenital scoliosis reveal underlying defects in notochord morphogenesis

Development(2024)10.1242/dev.202829
N/A
0DataRank · unranked
4 citations

Sen Zhao, Chenjun Shi, Marie-Claude Guyot, Meijiang Liao, Josephine T. Tauer +9 more