Alyssa Blesson

Biochemistry, 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

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 3 papers. Top paper: “Expansion of the Genotypic and Phenotypic Spectrum of ASH1L-Related Syndromic Neurodevelopmental Disorder”.

Expansion of the Genotypic and Phenotypic Spectrum of ASH1L-Related Syndromic Neurodevelopmental Disorder

Genes(2024)10.3390/genes15040423

N/A

0.545DataRank · unranked

10 citations

Alyssa Blesson, Juliann M. Savatt, Abigail Sveden, Sonal Mahida, Heather C. Hazlett +3 more

Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.08.003

N/A

0DataRank · unranked

42 citations

Somayeh Bakhtiari, Ashley P.L. Marsh, Rauan Kaiyrzhanov, Matias Wagner, Sheetal Shetty +95 more

LARP1 haploinsufficiency is associated with an autosomal dominant neurodevelopmental disorder

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100345

N/A

0DataRank · unranked

6 citations

Raymond J. Louie, Olivia Larner, Robert G. Best, Kevin Chen, Josephine Morris +27 more