Ryan H. Peretz

Biochemistry, Genetics and Molecular BiologyMedicine

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 3 papers. Top paper: “Prospective diagnosis of MT-ATP6-related mitochondrial disease by newborn screening”.

Prospective diagnosis of MT-ATP6-related mitochondrial disease by newborn screening

Molecular Genetics and Metabolism(2021)10.1016/j.ymgme.2021.06.007

N/A

0DataRank · unranked

20 citations

Nicholas Ah Mew, Hilary J. Vernon, Rebecca Ganetzky, Ryan H. Peretz

A de novo hexokinase 1 (HK1) variant presenting as Boucher–Neuhäuser syndrome

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.63045

N/A

0DataRank · unranked

6 citations

Wadih M. Zein, Robert B. Hufnagel, Christine W. Ku, Rena A. Godfrey, Lynne A. Wolfe +4 more

The remarkable journey of one female individual with ornithine transcarbamylase deficiency diagnosed post‐mortem

JIMD Reports(2023)10.1002/jmd2.12361

N/A

0DataRank · unranked

1 citations

Ryan H. Peretz, Angela Pipitone Dempsey, Jacquelyn Britton, Lisa E. Kratz, Ada Hamosh +4 more