Ryan J. Taft

Also affiliated with Illumina (United States)

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 12 papers. Top paper: “De novo mutations in TOMM70, a receptor of the mitochondrial import translocase, cause neurological impairment”.

De novo mutations in TOMM70, a receptor of the mitochondrial import translocase, cause neurological impairment

Human Molecular Genetics(2020)10.1093/hmg/ddaa081

N/A

1.1DataRank · unranked

41 citations

Lauren C. Briere, Oguz Kanca, Paul C. Marcogliese, Melissa Walker, Frances A. High +13 more

Phenotypic and Imaging Spectrum Associated With WDR45

Pediatric Neurology(2020)10.1016/j.pediatrneurol.2020.03.005

N/A

0.571DataRank · unranked

44 citations

Amy Pizzino, Alka Malhotra, Holly Dubbs, Catherine Williams, Omar Sherbini +17 more

Germline mutations in a G protein identify signaling cross-talk in T cells

Science(2024)10.1126/science.add8947

N/A

0.489DataRank · unranked

25 citations

Huie Jing, Ian T. Lamborn, M. Kober, Alexey Koval, Yamina A. Berchiche +95 more

Multi-omics analysis of a pig-to-human decedent kidney xenotransplant

Nature(2025)10.1038/s41586-025-09846-7

N/A

0.437DataRank · unranked

16 citations

Brian D. Piening, Alexa K. Dowdell, Maedeh Mohebnasab, Simon H. Williams, Alexey Stukalov +71 more

A Novel Variant in SQSTM1 Gene Causing Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy in a Peruvian Family

Movement Disorders Clinical Practice(2024)10.1002/mdc3.14025

N/A

0.241DataRank · unranked

4 citations

Patricia Ramirez‐Pajares, Alid Manrique‐Palomino, Amanda Clause, Aditi Chawla, Erin Thorpe +6 more

Further Delineation of the Clinical and Pathologic Features of HIKESHI-Related Hypomyelinating Leukodystrophy

Pediatric Neurology(2021)10.1016/j.pediatrneurol.2021.04.014

N/A

0DataRank · unranked

10 citations

Ayelet Zerem, Akshata Almad, Julia Hacker, Sarah Woidill, Sunetra Sase +15 more

Spinal muscular atrophy diagnosis and carrier screening from genome sequencing data

Genetics in Medicine(2020)10.1038/s41436-020-0754-0

N/A

0DataRank · unranked

148 citations

Alba Sanchis‐Juan, Courtney E. French, Andrew J. Connell, Isabelle Delon, Zoya Kingsbury +8 more

Clinical genome sequencing in patients with suspected rare genetic disease in Peru

npj Genomic Medicine(2024)10.1038/s41525-024-00434-8

N/A

0DataRank · unranked

4 citations

Mario Cornejo‐Olivas, Milagros Dueñas, Nelson Purizaca‐Rosillo, Richard Rodríguez, Karina Milla‐Neyra +45 more

Development of a comprehensive genome-wide cardiovascular disease genetic risk assessment test

medRxiv(2024)10.1101/2024.05.06.24306379

N/A

0DataRank · unranked

1 citations

Alison J. Coffey, Josh Lowry, James Avecilla, Alka Malhotra, Aditi Chawla +23 more

Bi-allelic variants in BCAT1 impair mitochondrial function and are associated with a candidate neurometabolic disorder

Human Genetics and Genomics Advances(2025)10.1016/j.xhgg.2025.100525

N/A

0DataRank · unranked

1 citations

Giulia S. Porcari, Lívia Sertori Finoti, Leonardo Ramos-Rodriguez, Devin M Burris, Justin A. McDonough +15 more

Fatal Perinatal Mitochondrial Cardiac Failure Caused by Recurrent De Novo Duplications in the ATAD3 Locus

Med(2020)10.1016/j.medj.2020.06.004

N/A

0DataRank · unranked

72 citations

Alison G. Compton, Yoshihito Kishita, Daniella H. Hock, AnneMarie E. Welch, Sumudu S. C. Amarasekera +40 more

BLOC1S1 variants cause lysosomal and autophagic defects resulting in a hypomyelinating leukodystrophy with epileptic encephalopathy

medRxiv(2025)10.1101/2025.07.17.25331211

N/A

0DataRank · unranked

0 citations

Carlos González, Chad D. Williamson, Guy Helman, Leslie E. Sanderson, Brianna Disanza +34 more