Dayna Morel Swols

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 4 papers. Top paper: “Genome sequencing reveals novel variants in a diverse population with congenital anterior segment anomalies”.

Genome sequencing reveals novel variants in a diverse population with congenital anterior segment anomalies

Scientific Reports(2025)10.1038/s41598-024-84205-6

N/A

0.241DataRank · unranked

4 citations

Maria Fernanda Villalba, Dayna Morel Swols, Rayan Abou Khzam, Brittney Keira Johnson, LéShon Peart +6 more

Dispersed DNA variants underlie hearing loss in South Florida’s minority population

Human Genomics(2023)10.1186/s40246-023-00556-7

N/A

0DataRank · unranked

11 citations

Joanna Gonzalez, Dayna Morel Swols, Duygu Duman, Turçin Saridogan, Memoona Ramzan +11 more

A Novel Missense Variant in LMX1A Leads to Autosomal Dominant Nonsyndromic Hearing Loss

American Journal of Medical Genetics Part A(2025)10.1002/ajmg.a.64281

N/A

0DataRank · unranked

1 citations

Dayna Morel Swols, Güney Bademci, Mustafa Tekin, Ryan Chen

A clinical and genotype-phenotype analysis of MACF1 variants

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.08.010

N/A

0DataRank · unranked

1 citations

Rachel Schot, Kimberly A. Aldinger, David B. Everman, Camerun Washington, Julie R. Jones +85 more