Monika Oláhová

Also affiliated with Wellcome Centre for Mitochondrial Research, Newcastle University

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 8 papers. Top paper: “NovelDNM1Lvariants impair mitochondrial dynamics through divergent mechanisms”.

NovelDNM1Lvariants impair mitochondrial dynamics through divergent mechanisms

Life Science Alliance(2022)10.26508/lsa.202101284

N/A

0.871DataRank · unranked

25 citations

John M. Egner, Jack J. Collier, Oliver M. Russell, Charlotte L. Alston, Megan Cleland Harwig +19 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

Biallelic variants in MRPL49 cause variable clinical presentations, including sensorineural hearing loss, leukodystrophy, and ovarian insufficiency

medRxiv(2024)10.1101/2024.10.10.24315152

N/A

0DataRank · unranked

2 citations

Leigh Demain, Alfredo Cabrera‐Orefice, Isabelle Schrauwen, Hanan E. Shamseldin, Alessandro Rea +26 more

RTN4IP1 is essential for the final stages of mitochondrial complex I assembly and coenzyme Q biosynthesis

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.09.04.610987

N/A

0DataRank · unranked

0 citations

Rachel M. Guerra, Jack J. Collier, Juliana Heidler, Kyle Thompson, Chelsea R. White +8 more

Bi-allelic variants in MRPL49 cause variable clinical presentations, including sensorineural hearing loss, leukodystrophy, and ovarian insufficiency

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.02.005

N/A

0DataRank · unranked

7 citations

Leigh Demain, Alfredo Cabrera‐Orefice, Isabelle Schrauwen, Hanan E. Shamseldin, Alessandro Rea +41 more

POLRMT mutations impair mitochondrial transcription causing neurological disease

Nature Communications(2021)10.1038/s41467-021-21279-0

N/A

0DataRank · unranked

60 citations

Bradley Peter, Zsolt Szilágyi, Héctor Díaz-Maldonado, Meenakshi Singh, Ewen W. Sommerville +34 more

RTN4IP1 is required for the final stages of mitochondrial complex I assembly and CoQ biosynthesis

The EMBO Journal(2025)10.1038/s44318-025-00533-x

N/A

0DataRank · unranked

1 citations

Rachel M. Guerra, Jack J. Collier, Juliana Heidler, Kyle Thompson, Chelsea R. White +9 more