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

Shenzhao Lu

Baylor College of Medicine

ORCID: 0000-0003-3117-3900
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 20 papers — median percentile 60. Top paper: “Sphingolipids in neurodegenerative diseases”.

Sphingolipids in neurodegenerative diseases

Frontiers in Neuroscience(2023)10.3389/fnins.2023.1137893
N/A
0.574DataRank · unranked
45 citations

Debdeep Dutta, Shenzhao Lu, Hugo J. Bellen, Xueyang Pan

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

'Fly-ing' from rare to common neurodegenerative disease mechanisms

Trends in Genetics(2022)10.1016/j.tig.2022.03.018
N/A
0DataRank · unranked
35 citations

Matthew J. Moulton, Shenzhao Lu, Hugo J. Bellen, Mengqi Ma

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
0DataRank · unranked
29 citations

Mengqi Ma, Xiao Mao, Carlos A. Bacino, Joseph Jankovic, V. Reid Sutton +15 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
0DataRank · unranked
27 citations

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

Very-long-chain fatty acids induce glial-derived sphingosine-1-phosphate synthesis, secretion, and neuroinflammation

Cell Metabolism(2023)10.1016/j.cmet.2023.03.022
N/A
0DataRank · unranked
73 citations

Qi Ye, Ye-Jin Park, Zhongyuan Zuo, Jung-Wan Mok, Oguz Kanca +6 more

Allelic strengths of encephalopathy-associated UBA5 variants correlate between in vivo and in vitro assays

eLife(2023)10.7554/elife.89891
N/A
0DataRank · unranked
8 citations

Albert N. Alvarez, Mengqi Ma, Shenzhao Lu, Michael Crawford, Lauren C. Briere +8 more

Allelic strengths of encephalopathy-associated UBA5 variants correlate between in vivo and in vitro assays

(2023)10.7554/elife.89891.1
N/A
0DataRank · unranked
3 citations

Albert N. Alvarez, Mengqi Ma, Shenzhao Lu, Michael Crawford, Lauren C. Briere +8 more

Allelic strengths of encephalopathy-associated UBA5 variants correlate between in vivo and in vitro assays

(2023)10.7554/elife.89891.2
N/A
0DataRank · unranked
2 citations

Albert N. Alvarez, Mengqi Ma, Shenzhao Lu, Michael Crawford, Lauren C. Briere +8 more

Allelic strengths of encephalopathy-associated UBA5 variants correlate between in vivo and in vitro assays

medRxiv(2023)10.1101/2023.07.17.23292782
N/A
0DataRank · unranked
0 citations

Albert N. Alvarez, Mengqi Ma, Shenzhao Lu, Michael Crawford, Lauren C. Briere +8 more

Reviewer #3 (Public Review): Allelic strengths of encephalopathy-associated UBA5 variants correlate between in vivo and in vitro assays

(2023)10.7554/elife.89891.2.sa0
N/A
0DataRank · unranked
0 citations

Albert N. Alvarez, Mengqi Ma, Shenzhao Lu, Michael W. Crawford, Lauren C. Briere +8 more

Tau is required for glial lipid droplet formation and resistance to neuronal oxidative stress

Nature Neuroscience(2024)10.1038/s41593-024-01740-1
N/A
0DataRank · unranked
53 citations

Isha Ralhan, Xin Li, Shenzhao Lu, Matthew J. Moulton, Ye-Jin Park +10 more

De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.02.007
N/A
0DataRank · unranked
10 citations

Alice M. Tao, Shenzhao Lu, Mengqi Ma, Shabab B. Hannan, Rachel Slaugh +43 more

Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for hepatocellular carcinoma

Genetics in Medicine(2024)10.1016/j.gim.2024.101125
N/A
0DataRank · unranked
3 citations

Mythily Ganapathi, Yiming Zheng, Kai-Li Tan, Oguz Kanca, Kevin E. Bove +21 more

Heterozygous variants in PLCG1 affect hearing, vision, cardiac, and immune function

eLife(2024)10.7554/elife.95887
N/A
0DataRank · unranked
2 citations

Yiming Zheng, Mingxi Deng, Shenzhao Lu, Xueyang Pan, Xi Luo +25 more

TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.06.019
N/A
0DataRank · unranked
47 citations

Heidi Cope, Zelha Nil, Thomas A. Ravenscroft, Wu‐Lin Charng, Shenzhao Lu +42 more

Heterozygous variants in PLCG1 affect hearing, vision, cardiac, and immune function

medRxiv(2024)10.1101/2024.01.08.23300523
N/A
0DataRank · unranked
0 citations

Yiming Zheng, Mingxi Deng, Shenzhao Lu, Xueyang Pan, Xi Luo +25 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