Ana Rivera‐Barahona

Also affiliated with Instituto de Investigaciones Biomédicas Sols-Morreale, Centre for Biomedical Network Research on Rare Diseases, Centro de Investigación Biomédica en Red, Instituto de Investigación de Enfermedades Raras, Universidad Autónoma de Madrid

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 2 papers. Top paper: “Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome”.

Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.09.005

N/A

0DataRank · unranked

54 citations

Phillip C. Aoto, Erik M.F. Machal, Ana Rivera‐Barahona, Patricia Soto‐Bielicka, Daniela Bertinetti +37 more

Mutations in SCNM1 cause orofaciodigital syndrome due to minor intron splicing defects affecting primary cilia

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.08.009

N/A

0DataRank · unranked

16 citations

Ana Rivera‐Barahona, Carmen‐Lisset Flores, Ghada A. Otaify, Rasha M. Elhossini, Marina Leonor Pérez-Sanz +14 more