Luis A. Pérez‐Jurado

ORCID: 0000-0002-1988-3005

Also affiliated with Instituto de Salud Carlos III, Spanish National Centre for Cardiovascular Research, Centre for Biomedical Network Research on Rare Diseases, Centro de Investigación Biomédica en Red, Hospital Del Mar, Instituto Murciano de Investigación Biosanitaria, Barcelona Institute for Global Health, Centro de Investigación Biomédica en Red de Fragilidad y Envejecimiento Saludable, Hospital del Mar Research Institute, Instituto de Investigación de Enfermedades Raras

Biochemistry, 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 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 5 papers. Top paper: “Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders”.

Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

Nature Communications(2020)10.1038/s41467-020-18723-y

N/A

0.808DataRank · unranked

218 citations

Kendra Hoekzema, Davide Vecchio, Huidan Wu, Arvis Sulovari, Bradley P. Coe +95 more

A six-attribute classification of geneticmosaicism

Genetics in Medicine(2020)10.1038/s41436-020-0877-3

N/A

0.668DataRank · unranked

85 citations

Jair Tenorio, Julián Nevado, Gema Gordo, Lara Rodríguez‐Laguna, Marta Feito +9 more

Spliceosome malfunction causes neurodevelopmental disorders with overlapping features

Journal of Clinical Investigation(2023)10.1172/jci171235

N/A

0.578DataRank · unranked

46 citations

Qin Wang, Allan Bayat, Mark R. Battig, Yijing Zhou, Daniëlle G.M. Bosch +95 more

Mutations in the small nuclear RNA gene RNU2-2 cause a severe neurodevelopmental disorder with prominent epilepsy

Nature Genetics(2025)10.1038/s41588-025-02159-5

N/A

0.571DataRank · unranked

44 citations

Koenraad De Wispelaere, Jonathan Lees, Marta Codina‐Solà, Brynjar Ö. Jensson, Emma Hales +47 more

Polymorphic Inversions Underlie the Shared Genetic Susceptibility of Obesity-Related Diseases

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.04.017

N/A

0DataRank · unranked

26 citations

Carlos Ruiz-Arenas, Alejandro Cáceres, Ignasi Morán, Marcos López‐Sánchez, Lorena Alonso +8 more