Agnès Rötig

Also affiliated with Inserm, Université Paris Cité, Institut Necker Enfants Malades, Assistance Publique – Hôpitaux de Paris, Institut des Maladies Génétiques Imagine

Biochemistry, Genetics and Molecular BiologyNeuroscience

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

2in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 2 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 8 papers. Top paper: “Inborn errors of complex II – Unusual human mitochondrial diseases”.

Inborn errors of complex II – Unusual human mitochondrial diseases

Biochimica et Biophysica Acta (BBA) - Bioenergetics(2002)10.1016/s0005-2728(01)00228-6

N/A

0.736DataRank · unranked

134 citations

Agnès Rötig, Pierre Rustin

Modeling of Antigenomic Therapy of Mitochondrial Diseases by Mitochondrially Addressed RNA Targeting a Pathogenic Point Mutation in Mitochondrial DNA

Journal of Biological Chemistry(2014)10.1074/jbc.m113.528968

N/A

0.590DataRank · unranked

50 citations

Anne-Marie Heckel, Mikhail Vysokikh, Ilya Dovydenko, Mariya Meschaninova, Agnès Rötig +5 more

Systematic analysis of NDUFAF6 in complex I assembly and mitochondrial disease

Nature Metabolism(2024)10.1038/s42255-024-01039-2

N/A

0.470DataRank · unranked

22 citations

Rachel M. Guerra, Laura Steenberge, Charlotte L. Alston, Kei Murayama, Yasushi Okazaki +10 more

Biallelic variants in TAMM41 are associated with low muscle cardiolipin levels, leading to neonatal mitochondrial disease

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100097

N/A

0DataRank · unranked

15 citations

L Bianchi, Francesca Rastelli, Florence Piron‐Prunier, Sophie Ayciriex, Claude Besmond +21 more

Loss of MTX2 causes mandibuloacral dysplasia and links mitochondrial dysfunction to altered nuclear morphology

Nature Communications(2020)10.1038/s41467-020-18146-9

N/A

0DataRank · unranked

64 citations

Karim Harhouri, Morgane Le Mao, Geneviève Baujat, Sheela Nampoothiri, Hülya Kayserili +25 more

Systematic analysis of NDUFAF6 in complex I assembly and mitochondrial disease

Research Square(2023)10.21203/rs.3.rs-3332602/v1

N/A

0DataRank · unranked

0 citations

Andrew Y. Sung, Rachel M. Guerra, Laura Steenberge, Charlotte L. Alston, Kei Murayama +10 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

Genotypic and phenotypic spectrum of infantile liver failure due to pathogenic TRMU variants

Genetics in Medicine(2022)10.1016/j.gim.2022.09.015

N/A

0DataRank · unranked

17 citations

Yael Mozer‐Glassberg, Yuval E. Landau, Lea D. Schlieben, Holger Prokisch, René G. Feichtinger +56 more