Gabriel Capellá

Department of Natural and Environmental Resources

Also affiliated with Institut d'Investigació Biomédica de Bellvitge, Institut Català d'Oncologia, Centro de Investigación Biomédica en Red de Cáncer

MedicineBiochemistry, 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 2%percentile

2.7Author 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.

Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database

EClinicalMedicine(2023)10.1016/j.eclinm.2023.101909

Top 12%

1.7DataRank

Top 12%115 citations

Saskia Haupt, Toni T. Seppälä, Julian R. Sampson, Lone Sunde, Inge Bernstein +95 more

Papers

Driven by 12 papers — median percentile 84. Top paper: “Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database”.

Mortality by age, gene and gender in carriers of pathogenic mismatch repair gene variants receiving surveillance for early cancer diagnosis and treatment: a report from the prospective Lynch syndrome database

EClinicalMedicine(2023)10.1016/j.eclinm.2023.101909

Top 12%

1.7DataRank

Top 12%115 citations

Saskia Haupt, Toni T. Seppälä, Julian R. Sampson, Lone Sunde, Inge Bernstein +95 more

Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

European Journal of Cancer(2021)10.1016/j.ejca.2021.02.022

Top 21%

0.978DataRank

Top 21%23 citations

Mev Dominguez–Valentin, Emma J. Crosbie, Christoph Engel, Stefan Aretz, Finlay Macrae +81 more

Cancer risk and overall survival in APC I1307K carriers.

Journal of Clinical Oncology(2020)10.1200/jco.2020.38.15_suppl.1592

N/A

0DataRank · unranked

1 citations

Joseph D. Bonner, Flavio Lejbkowicz, Stephanie L. Schmit, Hedy S. Rennert, Joel K. Greenson +11 more

Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study

The Lancet Oncology(2021)10.1016/s1470-2045(21)00189-3

N/A

0DataRank · unranked

121 citations

James G. Dowty, Jeanette C. Reece, Grant Lee, Allyson Templeton, John‐Paul Plazzer +95 more

First international workshop of the ATM and cancer risk group (4-5 December 2019)

Familial Cancer(2021)10.1007/s10689-021-00248-y

N/A

0DataRank · unranked

19 citations

Douglas F. Easton, Anne‐Laure Renault, Sean V. Tavtigian, Jonine L. Bernstein, Zsofia Kote‐Jarai +51 more

Gene-specific ACMG/AMP classification criteria for germline APC variants: Recommendations from the ClinGen InSiGHT Hereditary Colorectal Cancer/Polyposis Variant Curation Expert Panel

Genetics in Medicine(2023)10.1016/j.gim.2023.100992

N/A

0DataRank · unranked

33 citations

Xiaoyu Yin, Marcy E. Richardson, Marta Pineda, Andreas Laner, Deborah Ritter +27 more

Constitutional MLH1 Methylation Is a Major Contributor to Mismatch Repair–Deficient, MLH1-Methylated Colorectal Cancer in Patients Aged 55 Years and Younger

Journal of the National Comprehensive Cancer Network(2023)10.6004/jnccn.2023.7020

N/A

0DataRank · unranked

30 citations

Estela Dámaso, Rocio Alvarez, Lisa Zhou, Yajing Hu, Márcio A. Diniz +5 more

MLH1-methylated endometrial cancer under 60 years of age as the “sentinel” cancer in female carriers of high-risk constitutional MLH1 epimutation

Gynecologic Oncology(2023)10.1016/j.ygyno.2023.02.017

N/A

0DataRank · unranked

20 citations

Rocio Alvarez, Lisa Zhou, Francesca Paola Aguirre, Estela Dámaso, Marta Pineda +13 more

Large-scale application of ClinGen-InSiGHT APC-specific ACMG/AMP variant classification criteria leads to substantial reduction in VUS

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.09.002

N/A

0DataRank · unranked

15 citations

Marcy E. Richardson, Andreas Laner, Xuemei Shi, Elisabet Ognedal, Valeria Vasta +27 more

Issue Information

Human Mutation(2018)10.1002/humu.23568

N/A

0DataRank · unranked

0 citations

R. Donald Harvey, Tracy Dudding‐Byth, Liliana Catherine Patiño, Isabelle Beau, Adrien Morel +135 more

Phenotype Correlations With Pathogenic DNA Variants in the MUTYH Gene: A Review of Over 2000 Cases

Human Mutation(2024)10.1155/2024/8520275

N/A

0DataRank · unranked

10 citations

John‐Paul Plazzer, Gabriel Capellá, Andrew Latchford, Emily A.W. Nadeau, Marc S. Greenblatt +2 more

Risk-reducing hysterectomy and bilateral salpingo-oophorectomy in female heterozygotes of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database report

Genetics in Medicine(2020)10.1038/s41436-020-01029-1

N/A

0DataRank · unranked

43 citations

Emma J. Crosbie, Christoph Engel, Stefan Aretz, Finlay Macrae, Ingrid Winship +83 more

Gabriel Capellá

Indexed papers

Top data-sharing exemplar

Papers