Catalina Betancur

Centre National de la Recherche Scientifique

Also affiliated with Inserm, Sorbonne Université, Institut de Biologie Paris-Seine

NeuroscienceBiochemistry, 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 100%percentile

0Author DataRank

Indexed papers

1in 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 1 indexed paper 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 →

Papers

Driven by 9 papers. Top paper: “Functional impact of global rare copy number variation in autism spectrum disorders”.

Functional impact of global rare copy number variation in autism spectrum disorders

Nature(2010)10.1038/nature09146

N/A

1.1DataRank · unranked

2044 citations

Alistair T. Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan +204 more

Patterns and rates of exonic de novo mutations in autism spectrum disorders

Nature(2012)10.1038/nature11011

N/A

1.1DataRank · unranked

1794 citations

Yan Kou, Li Liu, Avi Ma’ayan, Kaitlin E. Samocha, Aniko Sabo +60 more

Strong evidence for genotype–phenotype correlations in Phelan-McDermid syndrome: results from the developmental synaptopathies consortium

Human Molecular Genetics(2021)10.1093/hmg/ddab280

N/A

0.637DataRank · unranked

69 citations

Jennifer H. Foss‐Feig, Catalina Betancur, Paige M. Siper, María del Pilar Trelles-Thorne, Danielle Halpern +14 more

Analysis of X chromosome inactivation in autism spectrum disorders

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics(2008)10.1002/ajmg.b.30688

N/A

0.612DataRank · unranked

58 citations

Elena Bacchelli, Francesca Blasi, Claudio Toma, Catalina Betancur, Pauline Chaste +20 more

Clinical validity assessment of genes frequently tested on intellectual disability/autism sequencing panels

Genetics in Medicine(2022)10.1016/j.gim.2022.05.001

N/A

0DataRank · unranked

25 citations

Taylor I. Bingaman, Carrie-Ann Barry, Andrea Behlmann, Krista Bluske, Bret L. Bostwick +36 more

Updated consensus guidelines on the management of Phelan–McDermid syndrome

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63312

N/A

0DataRank · unranked

49 citations

Mustafa Sahin, Joseph D. Buxbaum, Elizabeth Berry‐Kravis, Latha Soorya, Audrey Thurm +40 more

Phenome-wide profiling identifies genotype-phenotype associations in Phelan-McDermid syndrome using family-sourced data from an international registry

Molecular Autism(2024)10.1186/s13229-024-00619-z

N/A

0DataRank · unranked

5 citations

Maxime Wack, Claire Hassen‐Khodja, Michael McDuffie, Geraldine Bliss, Elizabeth J. Horn +8 more

Deleterious coding variation associated with autism is consistent across populations, as exemplified by admixed Latin American populations

medRxiv(2025)10.1101/2024.12.27.24319460

N/A

0DataRank · unranked

3 citations

Seulgi Jung, F. Kyle Satterstrom, Jack Fu, Tess Levy, Laura G Sloofman +49 more

Psychiatric illness and regression in individuals with Phelan-McDermid syndrome

Journal of Neurodevelopmental Disorders(2020)10.1186/s11689-020-9309-6

N/A

0DataRank · unranked

90 citations

M. Pilar Trelles, Brittany McLarney, Catalina Betancur, Audrey Thurm, A lexander Kolevzon +1 more