Marc Abramowicz

Also affiliated with Hôpital Beau-Séjour

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

1in 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 1 indexed paper 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 6 papers. Top paper: “Dementia prevention in memory clinics: recommendations from the European task force for brain health services”.

Dementia prevention in memory clinics: recommendations from the European task force for brain health services

The Lancet Regional Health - Europe(2023)10.1016/j.lanepe.2022.100576

N/A

0.781DataRank · unranked

182 citations

Daniele Altomare, Federica Ribaldi, Nicolas Villain, Carol Brayne, Naaheed Mukadam +38 more

Modifiable risk factors for dementia and dementia risk profiling. A user manual for Brain Health Services—part 2 of 6

Alzheimer s Research & Therapy(2021)10.1186/s13195-021-00895-4

N/A

0.706DataRank · unranked

110 citations

Timothy Rittman, Shabina Hayat, Carol Brayne, Frank Jessen, Kaj Blennow +38 more

Collagen IV deficiency causes hypertrophic remodeling and endothelium-dependent hyperpolarization in small vessel disease with intracerebral hemorrhage

EBioMedicine(2024)10.1016/j.ebiom.2024.105315

N/A

0.489DataRank · unranked

25 citations

Cameron R Thomson, Laura Gonzalez-Trueba, Yuan Yan Sin, Alessandra Granata, Graham Hamilton +24 more

A Familial Heterozygous Null Mutation of MET in Autism Spectrum Disorder

Autism Research(2014)10.1002/aur.1396

N/A

0.406DataRank · unranked

14 citations

Vanessa Wermenbol, Bruno Pichon, Sandra Acosta, Jelle van den Ameele, Camille Perazzolo +7 more

The clinical utility of polygenic risk scores in genomic medicine practices: a systematic review

Human Genetics(2022)10.1007/s00439-022-02452-x

N/A

0DataRank · unranked

85 citations

Brittany Zick, Angeliki Balasopoulou, Constantina Chalikiopoulou, Collet Dandara, Ghada El‐Kamah +15 more

Recurrent de novo variants in the spliceosomal factor CRNKL1 are associated with severe microcephaly and pontocerebellar hypoplasia with seizures

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.05.013

N/A

0DataRank · unranked

1 citations

Rosie Sullivan, Mischa S. G. Ruegg, Julia A. Horsfield, Jordan Doran, Gemma Poke +30 more