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

Yan Huang

Zhejiang Hospital

ORCID: 0000-0003-3833-9248

Also affiliated with Chongqing Medical University

Biochemistry, 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 5%percentile
0.475Author DataRank

Indexed papers

1in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology
Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Top data-sharing exemplar

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

A comprehensive Drosophila resource to identify key functional interactions between SARS-CoV-2 factors and host proteins

Cell Reports(2023)10.1016/j.celrep.2023.112842
Top 40%
0.475DataRank
Top 40%12 citations

Shenzhao Lu, Oguz Kanca, Daniel Bressan, Yan Huang, Mengqi Ma +22 more

Papers

Driven by 12 papers — median percentile 60. Top paper: “Expression of interferon-regulated genes in juvenile dermatomyositis versus Mendelian autoinflammatory interferonopathies”.

Expression of interferon-regulated genes in juvenile dermatomyositis versus Mendelian autoinflammatory interferonopathies

Arthritis Research & Therapy(2020)10.1186/s13075-020-02160-9
N/A
2.8DataRank · unranked
66 citations

Fatima Gunter‐Rahman, John A. McGrath, Esther Lee, Adriana A. de Jesus, Ira N. Targoff +8 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

The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.08.011
N/A
0.500DataRank · unranked
27 citations

Gabrielle Lemire, Lauren C. Briere, Fang Liu, Marja W. Wessels, Xueqi Wang +13 more

A comprehensive Drosophila resource to identify key functional interactions between SARS-CoV-2 factors and host proteins

Cell Reports(2023)10.1016/j.celrep.2023.112842
Top 40%
0.475DataRank
Top 40%12 citations

Shenzhao Lu, Oguz Kanca, Daniel Bressan, Yan Huang, Mengqi Ma +22 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

yippee like 3 (ypel3) is a novel gene required for myelinating and perineurial glia development

PLoS Genetics(2020)10.1371/journal.pgen.1008841
N/A
0DataRank · unranked
22 citations

Aurélie Clément, Sarah J. Stednitz, Jennifer Kyle, Judy Peirce, Marcie McFadden +18 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

MYH2-associated myopathy caused by a novel splice-site variant

Neuromuscular Disorders(2022)10.1016/j.nmd.2022.12.014
N/A
0DataRank · unranked
8 citations

May Christine V. Malicdan, Ellen F. Macnamara, Tanya Lehky, Iren Horkayne‐Szakaly, Yan Huang +6 more

Clinical, genetic, and structural characterization of a novel TUBB4B tubulinopathy

Molecular Genetics and Metabolism Reports(2023)10.1016/j.ymgmr.2023.100990
N/A
0DataRank · unranked
16 citations

Christina Deanne P. Tolete, Yan Huang, Ellen F. Macnamara, David Sept, Galina Nesterova +4 more

Bi-allelic SNAPC4 variants dysregulate global alternative splicing and lead to neuroregression and progressive spastic paraparesis

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.03.001
N/A
0DataRank · unranked
13 citations

Marie Morimoto, Prashant Sharma, Lyse Ruaud, Newell Belnap, Daniel G. Calame +33 more

Loss-of-function variants in TIAM1 are associated with developmental delay, intellectual disability, and seizures

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.01.020
N/A
0DataRank · unranked
39 citations

Rebecca Hernan, Paul C. Marcogliese, Yan Huang, Tracy S. Gertler, Meltem Akçaboy +13 more

Biallelic variants in two complex I genes cause abnormal splicing defects in probands with mild Leigh syndrome

Molecular Genetics and Metabolism(2020)10.1016/j.ymgme.2020.09.008
N/A
0DataRank · unranked
12 citations

Jennifer Wang, Daron L. Ross, Nicholas Balanda, Yan Huang, Rena A. Godfrey +6 more