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

Xiao Mao

Changsha Hospital for Maternal and Child Health Care

ORCID: 0000-0003-1455-0858

Also affiliated with Education Department of Hunan Province, Hunan Provincial Maternal and Child Health Hospital, University of South China

NeuroscienceBiochemistry, Genetics and Molecular BiologyMedicine

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 8 papers. Top paper: “De Novo Variants in CDK19 Are Associated with a Syndrome Involving Intellectual Disability and Epileptic Encephalopathy”.

De Novo Variants in CDK19 Are Associated with a Syndrome Involving Intellectual Disability and Epileptic Encephalopathy

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.04.001
N/A
0.574DataRank · unranked
45 citations

Xiao Mao, Hua Wang, Ye-Jin Park, Paul C. Marcogliese, Jill A. Rosenfeld +12 more

Variants in CAPZA2, a member of an F-actin capping complex, cause intellectual disability and developmental delay

Human Molecular Genetics(2020)10.1093/hmg/ddaa078
N/A
0.515DataRank · unranked
30 citations

Xiao Mao, Richard H. van Jaarsveld, Li Shu, Paulien A. Terhal, Zhengjun Jia +8 more

De novo variants in FRMD5 are associated with developmental delay, intellectual disability, ataxia, and abnormalities of eye movement

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.09.005
N/A
0.510DataRank · unranked
29 citations

Mengqi Ma, Xiao Mao, Carlos A. Bacino, Joseph Jankovic, V. Reid Sutton +15 more

MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignature

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.05.001
N/A
0.406DataRank · unranked
14 citations

Maria Carla Borroto, Sadegheh Haghshenas, A Namasivayam, Jack Reilly, Michael A. Levy +61 more

Rare de novo gain-of-function missense variants in DOT1L are associated with developmental delay and congenital anomalies

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.09.009
N/A
0.396DataRank · unranked
13 citations

Ashish R. Deshwar, Yan Huang, Scott Barish, Xi Zhang, Sanaa Choufani +30 more

Biallelic MED16 variants disrupt neural development and lead to an intellectual disability syndrome

Journal of genetics and genomics/Journal of Genetics and Genomics(2025)10.1016/j.jgg.2025.04.004
N/A
0DataRank · unranked
1 citations

Zhenglong Xiang, Yaqin Xiang, Pan Hu, Mei He, Zhenming Guo +11 more

The fly homolog ofSUPT16H, a gene associated with neurodevelopmental disorders, is required in a cell-autonomous fashion for cell survival

Human Molecular Genetics(2022)10.1093/hmg/ddac259
N/A
0DataRank · unranked
21 citations

Xi Zhang, Yiming Zheng, Shenzhao Lu, Xueyang Pan, Xiao Mao +6 more

Novel dominant and recessive variants in human ROBO1 cause distinct neurodevelopmental defects through different mechanisms

Human Molecular Genetics(2022)10.1093/hmg/ddac070
N/A
0DataRank · unranked
17 citations

Mengqi Ma, Xiao Mao, Davut Pehli̇van, Oguz Kanca, Feride Un-Candan +10 more