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

Thomas J. Nicholas

University of Utah

ORCID: 0000-0002-4198-6414

Also affiliated with Star Center

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 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 9 papers. Top paper: “Outcomes of a single-arm implementation trial of extended-release subcutaneous buprenorphine depot injections in people with opioid dependence”.

Outcomes of a single-arm implementation trial of extended-release subcutaneous buprenorphine depot injections in people with opioid dependence

International Journal of Drug Policy(2021)10.1016/j.drugpo.2021.103492

N/A

2.1DataRank · unranked

52 citations

Jeyran Shahbazi, Marianne Byrne, Jason Grebely, Nicholas Lintzeris, Mark S. Chambers +13 more

Comprehensive variant calling from whole‐genome sequencing identifies a complex inversion that disrupts ZFPM2 in familial congenital diaphragmatic hernia

Molecular Genetics & Genomic Medicine(2022)10.1002/mgg3.1888

N/A

0DataRank · unranked

8 citations

Najla Al‐Sweel, Andrew Farrell, Rong Mao, Pınar Bayrak‐Toydemir, Christine E. Miller +22 more

Rapid genome sequencing identifies a novel de novoSNAP25variant for neonatal congenital myasthenic syndrome

Molecular Case Studies(2022)10.1101/mcs.a006242

N/A

0DataRank · unranked

15 citations

Ting Wen, Andrew Farrell, Rong Mao, Barry Moore, Steven E. Boyden +14 more

Genome sequencing of Pakistani families with male infertility identifies deleterious genotypes in SPAG6, CCDC9, TKTL1, TUBA3C, and M1AP

Andrology(2023)10.1111/andr.13570

N/A

0DataRank · unranked

20 citations

Arvand Akbari, Thomas J. Nicholas, Helen Castillo‐Madeen, Muhammad Ajmal, Taqweem Ul Haq +6 more

Novel molecular mechanism in Malan syndrome uncovered through genome sequencing reanalysis, exon‐level Array, and RNA sequencing

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63516

N/A

0DataRank · unranked

2 citations

Nicola Longo, Robert G. Lewis, Thomas J. Nicholas, Steven E. Boyden, Ashley Andrews +6 more

RNA sequencing provides functional insights and diagnostic resolution in previously unsolved rare disease cases

BMC Medical Genomics(2025)10.1186/s12920-025-02227-z

N/A

0DataRank · unranked

4 citations

John M. O’Shea, Lucilla Pizzo, Ting Wen, Makenzie Fulmer, Jian Zhao +20 more

Identification of 2 novel noncoding variants in patients with Diamond-Blackfan anemia syndrome by whole genome sequencing

Blood Advances(2025)10.1182/bloodadvances.2024015347

N/A

0DataRank · unranked

3 citations

Steven E. Boyden, Caleb M. Hocutt, Robert G. Lewis, Erin E. Baldwin, Jennie Vagher +9 more

De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 families

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.02.012

N/A

0DataRank · unranked

122 citations

Harrison Brand, Harold Wang, Xuefang Zhao, Brent S. Pedersen, Julie Feusier +10 more

Intragenic deletions from whole genome sequencing of 1054 suicide deaths

medRxiv(2025)10.1101/2025.02.28.25323104

N/A

0DataRank · unranked

1 citations

Andrey A. Shabalin, Thomas J. Nicholas, Eric T. Monson, Elliott Ferris, Logan Yefimov +8 more