Elicia Estrella

Also affiliated with Harvard University, Boston Children's Museum

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

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 8 papers. Top paper: “POLRMT mutations impair mitochondrial transcription causing neurological disease”.

POLRMT mutations impair mitochondrial transcription causing neurological disease

Nature Communications(2021)10.1038/s41467-021-21279-0

N/A

0DataRank · unranked

60 citations

Bradley Peter, Zsolt Szilágyi, Héctor Díaz-Maldonado, Meenakshi Singh, Ewen W. Sommerville +34 more

Diagnostic capabilities of nanopore long‐read sequencing in muscular dystrophy

Annals of Clinical and Translational Neurology(2022)10.1002/acn3.51612

N/A

0DataRank · unranked

40 citations

Hannah R. Littel, Audrey L. Daugherty, Seth A. Stafki, Elicia Estrella, Emily S. McGaughy +19 more

Mendelian Disorders in an Interstitial Cystitis/Bladder Pain Syndrome Cohort

Advanced Genetics(2022)10.1002/ggn2.202200013

N/A

0DataRank · unranked

4 citations

Shira Rockowitz, Marielle Thorne, Pressley Smith, Jeanette Petit, Veronica Zehnder +9 more

Bi-allelic variants in HMGCR cause an autosomal-recessive progressive limb-girdle muscular dystrophy

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.04.006

N/A

0DataRank · unranked

37 citations

Tanya L. Schwab, Sarah K. Macklin‐Mantia, A. Reghan Foley, Filippo Pinto e Vairo, Davut Pehli̇van +25 more

Variants in DTNA cause a mild, dominantly inherited muscular dystrophy

Acta Neuropathologica(2023)10.1007/s00401-023-02551-7

N/A

0DataRank · unranked

12 citations

Christine C. Bruels, Sandra Donkervoort, A. Reghan Foley, Anna Codina, José C. Milisenda +29 more

Dominant stop‐loss HNRNPA1 variants in juvenile‐onset myopathy

Muscle & Nerve(2024)10.1002/mus.28214

N/A

0DataRank · unranked

0 citations

Christine C. Bruels, Audrey L. Daugherty, Elicia Estrella, Seth A. Stafki, Safoora B. Syeda +15 more

Effects of HMG CoA reductase ( HMGCR ) deficiency on skeletal muscle development

FEBS Journal(2025)10.1111/febs.17406

N/A

0DataRank · unranked

6 citations

Hannah R. Littel, Natalya M. Wells, Johnnie Turner, Gloriana Campos, Sree Venigalla +16 more

Interstitial Cystitis: a phenotype and rare variant exome sequencing study

medRxiv(2025)10.1101/2025.02.16.25322147

N/A

0DataRank · unranked

0 citations

Ayan Malakar, Sarath Babu Krishna Murthy, Miguel Verbitsky, Atlas Kahn, Elicia Estrella +10 more