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

Michael J. Gambello

Emory University

ORCID: 0000-0001-6501-4962
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 5%percentile
0.463Author DataRank

Indexed papers

2in 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 2 indexed papers 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.

Comprehensive phenotyping of 3q29 deletion syndrome: recommendations for clinical care

medRxiv(2020)10.1101/2020.07.25.20162149
Top 56%
0.290DataRank
Top 56%4 citations

Michael J. Gambello, Melissa M. Murphy, Katrina Aberizk, Emily Black, T. Lindsey Burrell +19 more

Papers

Driven by 8 papers — median percentile 38. Top paper: “Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum–associated degradation pathway”.

Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum–associated degradation pathway

Genetics in Medicine(2014)10.1038/gim.2014.22
N/A
0.821DataRank · unranked
238 citations

Vandana Shashi, Matthew Bainbridge, Michael J. Gambello, Thomas Bast, Rebecca Crimian +29 more

Comprehensive phenotyping of 3q29 deletion syndrome: recommendations for clinical care

medRxiv(2020)10.1101/2020.07.25.20162149
Top 56%
0.290DataRank
Top 56%4 citations

Michael J. Gambello, Melissa M. Murphy, Katrina Aberizk, Emily Black, T. Lindsey Burrell +19 more

Musculoskeletal phenotypes in 3q29 deletion syndrome

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63384
Top 67%
0.173DataRank
Top 67%2 citations

Jacob C. Tilmon, Melissa M. Murphy, Michael J. Gambello, Rossana Sanchez Russo, John P. Dormans +2 more

Correction: Corrigendum: Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum–associated degradation pathway

Genetics in Medicine(2014)10.1038/gim.2014.61
N/A
0.136DataRank · unranked
1 citations

Vandana Shashi, Matthew N. Bainbridge, Michael J. Gambello, Farah Zahir, Thomas Bast +28 more

Longitudinal multi-omics reveals pathogenic TSC2 variants disrupt developmental trajectories of human cortical organoids derived from Tuberous Sclerosis Complex

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.10.07.617121
N/A
0DataRank · unranked
5 citations

Shaojun Yu, Xiangru Li, Zhen Wang, Rui Chen, Christina Michalski +13 more

Ornithine decarboxylase, the rate-limiting enzyme of polyamine synthesis, modifies brain pathology in a mouse model of tuberous sclerosis complex

Human Molecular Genetics(2020)10.1093/hmg/ddaa121
N/A
0DataRank · unranked
9 citations

James T Mckenna, Caroline Yoon, Tracy Murray Stewart, Robert A. Casero, Michael J. Gambello +1 more

Convergent and distributed effects of the 3q29 deletion on the human neural transcriptome

Translational Psychiatry(2021)10.1038/s41398-021-01435-2
N/A
0DataRank · unranked
18 citations

Ryan H. Purcell, the Emory 3q29 Project, Katrina Aberizk, Hallie Averbach, Emily Black +37 more

Musculoskeletal phenotypes in 3q29 deletion syndrome

medRxiv(2023)10.1101/2023.04.03.23288084
N/A
0DataRank · unranked
1 citations

Jacob C. Tilmon, Melissa M. Murphy, Michael J. Gambello, Rossana Sanchez Russo, John P. Dormans +2 more