Emmanuelle Génin

Also affiliated with Université de Bretagne Occidentale, École nationale d'ingénieurs de Brest, Centre Hospitalier Régional Universitaire de Brest

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

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 10 papers. Top paper: “Missing heritability of complex diseases: case solved?”.

Missing heritability of complex diseases: case solved?

Human Genetics(2020)10.1007/s00439-019-02034-4

N/A

0.810DataRank · unranked

220 citations

Emmanuelle Génin

Benchmark of computational methods to detect digenism in sequencing data

European Journal of Human Genetics(2025)10.1038/s41431-025-01834-9

N/A

0.165DataRank · unranked

2 citations

Donald F. Conrad, Anaı̈s Baudot, Elisabeth Tournier‐Lasserve, Principal investigators, Emmanuelle Génin +30 more

Role of the Common PRSS1-PRSS2 Haplotype in Alcoholic and Non-Alcoholic Chronic Pancreatitis: Meta- and Re-Analyses

Genes(2020)10.3390/genes11111349

N/A

0DataRank · unranked

17 citations

Emmanuelle Génin, D.N. Cooper, Emmanuelle Masson, Claude Férec, Jian‐Min Chen +1 more

A BBS1 SVA F retrotransposon insertion is a frequent cause of Bardet‐Biedl syndrome

Clinical Genetics(2020)10.1111/cge.13878

N/A

0DataRank · unranked

26 citations

Samuel Nicaise, Manuela Antin, Anne‐Sophie Leuvrey, Elsa Nourisson, Carmen C. Leitch +22 more

Role of the common PRSS1-PRSS2 haplotype in alcoholic and non-alcoholic chronic pancreatitis: meta- and re-analyses

medRxiv(2020)10.1101/2020.10.13.20212365

N/A

0DataRank · unranked

1 citations

Emmanuelle Génin, D.N. Cooper, Emmanuelle Masson, Claude Férec, Jian‐Min Chen +1 more

Title Page / Table of Contents

Human Heredity(2015)10.1159/000448082

N/A

0DataRank · unranked

0 citations

Paul J. Newcombe, John P. A. Ioannidis, Emmanuelle Génin, Françoise Clerget‐Darpoux, Claire Dandine‐Roulland +10 more

PSAP‐Genomic‐Regions: A Method Leveraging Population Data to Prioritize Coding and Non‐Coding Variants in Whole Genome Sequencing for Rare Disease Diagnosis

Genetic Epidemiology(2024)10.1002/gepi.22593

N/A

0DataRank · unranked

2 citations

Ozvan Bocher, Chaker Aloui, Anne‐Louise Leutenegger, Ozan Özışık, Anaı̈s Baudot +7 more

Easy-PSAP: An Integrated Workflow to Prioritize Pathogenic Variants in Sequence Data from a Single Individual

Human Heredity(2025)10.1159/000543671

N/A

0DataRank · unranked

0 citations

Marc B. Gros-La-Faige, Daniel P. Lewinsohn, Mathilde Nguyen, Lourdes Velo‐Suárez, Anthony F. Herzig +6 more

SLITRK2, an X-linked modifier of the age at onset in C9orf72 frontotemporal lobar degeneration

Brain(2021)10.1093/brain/awab171

N/A

0DataRank · unranked

26 citations

Agnès Camuzat, Khalid El Hachimi, Justine Guégan, Daisy Rinaldi, Serena Lattante +40 more

Author and Subject Index

Human Heredity(2015)10.1159/000443902

N/A

0DataRank · unranked

0 citations

Paul J. Newcombe, John P. A. Ioannidis, Emmanuelle Génin, Françoise Clerget‐Darpoux, Claire Dandine‐Roulland +10 more