Robert Kopajtich

Also affiliated with Technical University of Munich

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: “Suleiman-El-Hattab syndrome: a histone modification disorder caused by TASP1 deficiency”.

Suleiman-El-Hattab syndrome: a histone modification disorder caused by TASP1 deficiency

Human Molecular Genetics(2022)10.1093/hmg/ddac098

N/A

0.345DataRank · unranked

9 citations

Anna Lena Burgemeister, Vincent Cantagrel, Jeanne Amiel, Karine Siquier-Pernet, Nathalie Boddaert +16 more

Clinical implementation of RNA sequencing for Mendelian disease diagnostics

medRxiv(2021)10.1101/2021.04.01.21254633

N/A

0DataRank · unranked

33 citations

Mirjana Gušić, Robert Kopajtich, Christian Mertes, Nicholas H. Smith, Charlotte L. Alston +48 more

Protonation-Dependent Sequencing of 5-Formylcytidine in RNA

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.11.23.469744

N/A

0DataRank · unranked

1 citations

Supuni Thalalla Gamage, Diamond A. Gallimore, Robert Kopajtich, Christine N. Evans, Samantha R. Nance +7 more

Protonation-Dependent Sequencing of 5-Formylcytidine in RNA

Biochemistry(2022)10.1021/acs.biochem.1c00761

N/A

0DataRank · unranked

21 citations

Supuni Thalalla Gamage, Diamond Gallimore, Robert Kopajtich, Christine N. Evans, Samantha Nance +7 more

Protonation‐Dependent Sequencing of 5‐Formylcytidine in RNA

The FASEB Journal(2022)10.1096/fasebj.2022.36.s1.r5310

N/A

0DataRank · unranked

1 citations

Supuni Thalalla Gamage, Diamond A. Gallimore, Robert Kopajtich, Christine N. Evans, Samantha R. Nance +7 more

Bi-allelic variants in DAP3 result in reduced assembly of the mitoribosomal small subunit with altered apoptosis and a Perrault-syndrome-spectrum phenotype

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.11.007

N/A

0DataRank · unranked

7 citations

Robert Kopajtich, Leigh Demain, Alessandro Rea, Huw B. Thomas, Manuel Schiff +34 more

Biallelic variants in DAP3 result in reduced assembly of the mitoribosomal small subunit with altered intrinsic and extrinsic apoptosis and a Perrault syndrome-spectrum phenotype

medRxiv(2024)10.1101/2024.08.19.24312079

N/A

0DataRank · unranked

2 citations

Robert Kopajtich, Leigh Demain, Alessandro Rea, Huw B. Thomas, Manuel Schiff +35 more

Genotypic diversity and phenotypic spectrum of infantile liver failure syndrome type 1 due to variants in LARS1

Genetics in Medicine(2020)10.1038/s41436-020-0904-4

N/A

0DataRank · unranked

50 citations

Desirée E.C. Smith, Ellen Crushell, Ralf A. Husain, Gajja S. Salomons, Bader Alhaddad +35 more

Bi-allelic mutations in FASTKD5 are associated with cytochrome c oxidase deficiency and early- to late-onset Leigh syndrome

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.05.007

N/A

0DataRank · unranked

2 citations

Woranontee Weraarpachai, Katherine M. Szigety, Robert Kopajtich, James B. Gibson, Johan L.K. Van Hove +13 more