Jean‐François Deleuze

Commissariat à l'Énergie Atomique et aux Énergies Alternatives

Also affiliated with Université Paris-Saclay, Centre National de Recherche en Génomique Humaine, CEA Paris-Saclay

Immunology and MicrobiologyMedicine

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 2%percentile

3.5Author DataRank

Indexed papers

3in 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 3 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 →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers

Acta Neuropathologica(2022)10.1007/s00401-022-02454-z

Top 10%

2.1DataRank

Top 10%139 citations

Sven J. van der Lee, Duber Gomez‐Fonseca, Itziar de Rojas, Carolina Dalmasso, Benjamin Grenier‐Boley +95 more

Papers

Driven by 38 papers — median percentile 75. Top paper: “Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers”.

Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers

Acta Neuropathologica(2022)10.1007/s00401-022-02454-z

Top 10%

2.1DataRank

Top 10%139 citations

Sven J. van der Lee, Duber Gomez‐Fonseca, Itziar de Rojas, Carolina Dalmasso, Benjamin Grenier‐Boley +95 more

Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers

Movement Disorders(2023)10.1002/mds.29337

Top 25%

0.809DataRank

Top 25%28 citations

Elise A. Lucotte, Cloé Domenighetti, Matthew H. Law, Mark M. Iles, Kevin M. Brown +89 more

Association of Rare APOE Missense Variants V236E and R251G With Risk of Alzheimer Disease

JAMA Neurology(2022)10.1001/jamaneurol.2022.1166

N/A

0.681DataRank · unranked

93 citations

Michaël E. Belloy, Benjamin Grenier‐Boley, Itziar de Rojas, Atahualpa Castillo-Morales, Iris E. Jansen +95 more

A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels

Blood(2024)10.1182/blood.2023021452

N/A

0.601DataRank · unranked

23 citations

Paula Reventún, Michael R. Brown, Adam S. Heath, Jennifer E. Huffman, Ngoc‐Quynh Le +90 more

Genome-wide association study reveals mechanisms underlying dilated cardiomyopathy and myocardial resilience

Nature Genetics(2024)10.1038/s41588-024-01975-5

N/A

0.601DataRank · unranked

54 citations

Joel Rämö, Daria R. Kramarenko, Leonoor F. J. M. Wijdeveld, Jan Haas, Mark Chaffin +55 more

Genome-wide meta-analysis for Alzheimer’s disease cerebrospinal fluid biomarkers

medRxiv(2022)10.1101/2022.03.08.22271043

Top 35%

0.564DataRank

Top 35%12 citations

Sven J. van der Lee, Duber Gomez‐Fonseca, Itziar de Rojas, Carolina Dalmasso, Benjamin Grenier‐Boley +95 more

Sexual dimorphism in cancer: insights from transcriptional signatures in kidney tissue and renal cell carcinoma

Human Molecular Genetics(2021)10.1093/hmg/ddab031

N/A

0.561DataRank · unranked

41 citations

Peng Li, Szilvia Ecsedi, Behnoush Abedi‐Ardekani, Geoffroy Durand, Nivonirina Robinot +20 more

Transcriptome-wide association study and Mendelian randomization in pancreatic cancer identifies susceptibility genes and causal relationships with type 2 diabetes and venous thromboembolism

EBioMedicine(2024)10.1016/j.ebiom.2024.105233

N/A

0.497DataRank · unranked

15 citations

Chelsea A. Isom, Yangzi Liu, David-Alexandre Trégouët, Sara Lindström, Lu Wang +52 more

Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease

Nature Communications(2023)10.1038/s41467-023-36997-w

N/A

0.434DataRank · unranked

17 citations

Jeffrey Haessler, Jan Walter Benjamins, L. Repetto, Jie Yao, Aaron Isaacs +89 more

Whole-genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles

Blood(2024)10.1182/blood.2023022596

N/A

0.416DataRank · unranked

15 citations

Jayna Nicholas, Julie Hahn, Adam S. Heath, Laura M. Raffield, Lisa R. Yanek +95 more

Molecular determinants of thrombosis recurrence risk across venous thromboembolism subtypes

Blood(2025)10.1182/blood.2024027879

N/A

0.373DataRank · unranked

11 citations

Florian Thibord, Ohanna Cavalcanti de Lima Bezerra, Jennifer A. Brody, Astrid van Hylckama Vlieg, Lénaïck Gourhant +29 more

Antithrombin, Protein C, and Protein S: Genome and Transcriptome-Wide Association Studies Identify 7 Novel Loci Regulating Plasma Levels

Arteriosclerosis Thrombosis and Vascular Biology(2023)10.1161/atvbaha.122.318213

N/A

0.312DataRank · unranked

7 citations

Gerard Temprano‐Sagrera, Lori A. Holle, Allison Bebo, Jennifer A. Brody, Ngoc‐Quynh Le +36 more

Genetic analysis of lung cancer reveals novel susceptibility loci and germline impact on somatic mutation burden

medRxiv(2021)10.1101/2021.04.26.21254132

N/A

0.194DataRank · unranked

2 citations

Joshua Atkins, Ricardo Cortez Cardoso Penha, Karl Smith-Byrne, Valérie Gaborieau, Catherine Voegele +28 more

Antithrombin, protein C and protein S: Genome and transcriptome wide association studies identify 7 novel loci regulating plasma levels

medRxiv(2022)10.1101/2022.11.01.22281689

N/A

0.183DataRank · unranked

2 citations

Gerard Temprano‐Sagrera, Lori A. Holle, Allison Bebo, Jennifer A. Brody, Ngoc‐Quynh Le +35 more

Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles

medRxiv(2023)10.1101/2023.06.07.23291095

N/A

0.104DataRank · unranked

1 citations

Jayna Nicolas, Julie Hahn, Adam S. Heath, Laura M. Raffield, Lisa R. Yanek +95 more

Biallelic NAA60 variants with impaired N-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications

Nature Communications(2024)10.1038/s41467-024-46354-0

N/A

0DataRank · unranked

43 citations

Henriette Aksnes, Reza Maroofian, Lauren C. LaMonica, Luís Seabra, Anette Siggervåg +55 more

TAD boundary deletion causes PITX2-related cardiac electrical and structural defects

Nature Communications(2024)10.1038/s41467-024-47739-x

N/A

0DataRank · unranked

24 citations

Hiroshige Murata, Fernanda M. Bosada, Uirá Souto Melo, Takanori Aizawa, Pierre Lindenbaum +39 more

Multi-ancestry polygenic risk scores for venous thromboembolism

Human Molecular Genetics(2024)10.1093/hmg/ddae097

N/A

0DataRank · unranked

6 citations

Florian Thibord, Alicia Domínguez Estirado, Corriene Sept, Kristin Boulier, Vidhya Venkateswaran +42 more

Multi-ancestry polygenic risk scores for venous thromboembolism

medRxiv(2024)10.1101/2024.01.09.24300914

N/A

0DataRank · unranked

2 citations

Florian Thibord, Alicia Domínguez Estirado, Corriene Sept, Kristin Boulier, Vidhya Venkateswaran +31 more

Genetic architecture of spatial electrical biomarkers for cardiac arrhythmia and relationship with cardiovascular disease

UNC Libraries(2024)10.17615/ds6y-7f02

N/A

0DataRank · unranked

0 citations

Jacob A. Brody, Pim van der Harst, Ulrich Schotten, B. Mifsud, Maria Pina Concas +89 more

Genomic Landscape of Thrombosis Recurrence Risk Across Venous Thromboembolism Subtypes

medRxiv(2024)10.1101/2024.12.02.24317788

N/A

0DataRank · unranked

0 citations

Florian Thibord, Ohanna C Bezerra, Jennifer A. Brody, Astrid van Hylckama Vlieg, Lénaïck Gourhant +27 more

Neoantigenic properties of TP53 variants influence cancer risk in individuals with Li-Fraumeni syndrome

EBioMedicine(2025)10.1016/j.ebiom.2025.106065

N/A

0DataRank · unranked

2 citations

Olivier Manches, Jonathan Gaucher, Claire Freyçon, D B Collantes Hoyos, Sandrine Blanchet +14 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

GWAS meta-analysis of CSF Alzheimer's disease biomarkers 18,948 individuals reveal novel loci and genes regulating lipid metabolism, brain volume and autophagy

Research Square(2025)10.21203/rs.3.rs-6597595/v1

N/A

0DataRank · unranked

1 citations

Jigyasha Timsina, Chenyang Jiang, Daniel L. McCartney, Feifei Tao, Carolina Dalmasso +95 more

A transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration

Scientific Reports(2020)10.1038/s41598-020-58510-9

N/A

0DataRank · unranked

63 citations

Susette Lauwen, Christina Kiel, Lars G. Fritsche, Wilmar Igl, Jessica N. Cooke Bailey +95 more

Association between ABO haplotypes and the risk of venous thrombosis: impact on disease risk estimation

Blood(2020)10.1182/blood.2020008997

N/A

0DataRank · unranked

48 citations

Florian Thibord, Kerri L. Wiggins, Ruifang Li‐Gao, Mickael R. Brown, Astrid van Hylckama Vlieg +23 more

Prediction of Breast Cancer Treatment–Induced Fatigue by Machine Learning Using Genome-Wide Association Data

JNCI Cancer Spectrum(2020)10.1093/jncics/pkaa039

N/A

0DataRank · unranked

21 citations

Joseph O. Deasy, Jung Hun Oh, Antonio Di Meglio, Agnès Dumas, Gwenn Menvielle +18 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

Genetic association studies of fibromuscular dysplasia identify new risk loci and shared genetic basis with more common vascular diseases

medRxiv(2020)10.1101/2020.09.16.20195701

N/A

0DataRank · unranked

0 citations

Min‐Lee Yang, Takiy-Eddine Berrandou, Mark K. Bakker, Ozan Dikilitas, Soto Romuald Kiando +47 more

Mutations and variants of ONECUT1 in diabetes

Nature Medicine(2021)10.1038/s41591-021-01502-7

N/A

0DataRank · unranked

58 citations

Sandra Heller, Ivan G. Costa, Valérie Senée, Markus Breunig, Zhijian Li +35 more

A form of muscular dystrophy associated with pathogenic variants in JAG2

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.03.020

N/A

0DataRank · unranked

41 citations

Alison M. Barnard, Sanna Puusepp, Sander Pajusalu, Katrin Õunap, Dorianmarie Vargas‐Franco +53 more

Exome-Wide Association Study Identifies FN3KRP and PGP as New Candidate Longevity Genes

The Journals of Gerontology Series A(2021)10.1093/gerona/glab023

N/A

0DataRank · unranked

22 citations

Marianne Nygaard, Amke Caliebe, Hélène Blanché, Sophie Chantalat, Pilar Galán +16 more

Genetic Analysis of Lung Cancer and the Germline Impact on Somatic Mutation Burden

JNCI Journal of the National Cancer Institute(2022)10.1093/jnci/djac087

N/A

0DataRank · unranked

26 citations

Joshua Atkins, Ricardo Cortez Cardoso Penha, Karl Smith-Byrne, Valérie Gaborieau, Catherine Voegele +28 more

Whole Exome/Genome Sequencing Joint Analysis of a Family with Oligogenic Familial Hypercholesterolemia

Metabolites(2022)10.3390/metabo12030262

N/A

0DataRank · unranked

5 citations

Sandy Elbitar, Anne Philippi, Petra El Khoury, Yara Azar, Miangaly Andrianirina +26 more

Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

medRxiv(2022)10.1101/2022.10.22.22281221

N/A

0DataRank · unranked

10 citations

Estelle Talouarn, Astrid Marchal, Jérémy Manry, Yoann Seeleuthner, Yu Zhang +95 more

Elevated plasma complement factor H related 5 protein is associated with venous thromboembolism

Nature Communications(2023)10.1038/s41467-023-38383-y

N/A

0DataRank · unranked

37 citations

Laura Sánchez‐Rivera, Manal Ibrahim‐Kosta, Clément Naudin, Gaëlle Munsch, Louisa Goumidi +38 more

Investigation of common genetic risk factors between thyroid traits and breast cancer

Human Molecular Genetics(2023)10.1093/hmg/ddad159

N/A

0DataRank · unranked

5 citations

Yazdan Asgari, Pierre‐Emmanuel Sugier, Mojgan Karimi, Cloé Domenighetti, Fabienne Lesueur +11 more

Corrigendum to “Dissecting the genetic heterogeneity of gastric cancer”

EBioMedicine(2023)10.1016/j.ebiom.2023.104709

N/A

0DataRank · unranked

1 citations

Carlo Maj, Jan Gehlen, Oleg Borisov, Stephan Haas, Ines Gockel +95 more

Jean‐François Deleuze

Indexed papers

Top data-sharing exemplar

Papers