🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Bru Cormand

Instituto de Salud Carlos III

ORCID: 0000-0001-5318-4382

Also affiliated with Centre for Biomedical Network Research on Rare Diseases, Centro de Investigación Biomédica en Red, Sant Joan de Déu Research Foundation, Institut de Biomedicina de la Universitat de Barcelona, Universitat de Barcelona

MedicineBiochemistry, 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 7%percentile

0.104Author 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 →

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

Multi-ancestry genome-wide association study of endometriosis and its clinical manifestations in ~1.4 million women: translating gene discovery into pathogenic mechanisms and therapeutic targets

medRxiv(2025)10.1101/2025.09.03.25335012

Top 78%

0.104DataRank

Top 78%1 citations

Jun He, Solveig Løkhammer, Selena Aranda, Dan Qiu, David Davtian +12 more

Papers

Driven by 15 papers — median percentile 22. Top paper: “Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains”.

Genome-wide analyses of ADHD identify 27 risk loci, refine the genetic architecture and implicate several cognitive domains

Nature Genetics(2023)10.1038/s41588-022-01285-8

N/A

6.1DataRank · unranked

775 citations

G. Bragi Walters, Georgios Athanasiadis, Raymond K. Walters, Karen Therrien, Trine Tollerup Nielsen +81 more

Shared genetic background between children and adults with attention deficit/hyperactivity disorder

Neuropsychopharmacology(2020)10.1038/s41386-020-0664-5

N/A

1.9DataRank · unranked

108 citations

Ditte Demontis, Cristina Sánchez‐Mora, Tetyana Zayats, Marieke Klein, Nina Roth Mota +49 more

Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups

Nature Genetics(2022)10.1038/s41588-022-01171-3

N/A

1.7DataRank · unranked

76 citations

Jakob Grove, Thomas D. Als, Joanna Martin, Georgios Voloudakis, Sandra Meier +29 more

Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p

Nature Genetics(2022)10.1038/s41588-022-01203-y

N/A

1.3DataRank · unranked

55 citations

Emi Ling, Serkan Erdin, Derek J.C. Tai, Rachita Yadav, Jakob Grove +94 more

Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache

International Journal of Epidemiology(2020)10.1093/ije/dyaa050

N/A

0.665DataRank · unranked

83 citations

Derek Klarin, Scott M. Damrauer, Kyong-Mi Chang, Philip S. Tsao, Themistocles L. Assimes +93 more

DIRAS2 is Associated with Adult ADHD, Related Traits, and Co-Morbid Disorders

Neuropsychopharmacology(2011)10.1038/npp.2011.120

N/A

0.574DataRank · unranked

45 citations

T Trang Nguyen, Lena Weißflog, Christian P Jacob, Marcel Romanos, Tobias J Renner +39 more

Genetic architecture of ADHD and overlap with other psychiatric disorders and cognition-related phenotypes

Neuroscience & Biobehavioral Reviews(2023)10.1016/j.neubiorev.2023.105313

N/A

0.561DataRank · unranked

41 citations

Marina Mitjans, C.A. Hartman, María Soler Artigas, Ditte Demontis, Henrik Larsson +8 more

Polygenic association between attention-deficit/hyperactivity disorder liability and cognitive impairments

Psychological Medicine(2021)10.1017/s0033291720005218

N/A

0.385DataRank · unranked

12 citations

Joanna Martin, Anna‐Sophie Rommel, Philip Asherson, Tobias Banaschewski, Jan K. Buitelaar +20 more

Diagnosing migraine from genome-wide genotype data: a machine learning analysis

Brain(2025)10.1093/brain/awaf172

N/A

0.269DataRank · unranked

5 citations

Tjaša Kumelj, Bendik S Winsvold, Marte‐Helene Bjørk, Parashkev Nachev, Manjit Matharu +70 more

Multi-ancestry genome-wide association study of endometriosis and its clinical manifestations in ~1.4 million women: translating gene discovery into pathogenic mechanisms and therapeutic targets

medRxiv(2025)10.1101/2025.09.03.25335012

Top 78%

0.104DataRank

Top 78%1 citations

Jun He, Solveig Løkhammer, Selena Aranda, Dan Qiu, David Davtian +12 more

Genetic contribution to the comorbidity between attention-deficit/hyperactivity disorder and substance use disorders

Psychiatry Research(2024)10.1016/j.psychres.2024.115758

N/A

0DataRank · unranked

17 citations

Marina Mitjans, Manuela R. Kouakou, Eleni Friligkou, Brenda Cabrera‐Mendoza, Joseph D. Deak +19 more

rbfox1 LoF mutants show disrupted bdnf/trkb2 and crhb/nr3c2 expression and increased cortisol levels during development coupled with signs of allostatic overload in adulthood

Translational Psychiatry(2025)10.1038/s41398-025-03703-x

N/A

0DataRank · unranked

1 citations

Judit García‐González, Saeedeh Hosseinian, Peter Ashdown, Sofia Anagianni, Xian Wang +5 more

Pleiotropic contribution of rbfox1 to psychiatric and neurodevelopmental phenotypes in a zebrafish model

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.02.23.529711

N/A

0DataRank · unranked

3 citations

Maja R. Adel, Judit García‐González, Adele Leggieri, Laura López-Blanch, Manuel Irimia +5 more

SLK is mutated in individuals with a neurodevelopmental disorder

EBioMedicine(2025)10.1016/j.ebiom.2025.105725

N/A

0DataRank · unranked

2 citations

Norah Altuwaijri, Jun‐yi Zhu, Stéphanie Efthymiou, Hangnoh Lee, Jianli Duan +94 more

Pleiotropic contribution of rbfox1 to psychiatric and neurodevelopmental phenotypes in two zebrafish models

Translational Psychiatry(2024)10.1038/s41398-024-02801-6

N/A

0DataRank · unranked

6 citations

Maja R. Adel, Judit García‐González, Adele Leggieri, Laura López-Blanch, Manuel Irimia +5 more