Brianna Disanza

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 6 papers. Top paper: “SMARCB1 deletion in atypical teratoid rhabdoid tumors results in human endogenous retrovirus K (HML-2) expression”.

SMARCB1 deletion in atypical teratoid rhabdoid tumors results in human endogenous retrovirus K (HML-2) expression

Scientific Reports(2021)10.1038/s41598-021-92223-x

N/A

0DataRank · unranked

54 citations

Brianna Disanza, Catherine DeMarino, Abigail L. Atkinson, Jared S. Rosenblum, Lisa Henderson +14 more

High density SNP array and reanalysis of genome sequencing uncovers CNVs associated with neurodevelopmental disorders in KOLF2.1J iPSCs

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.06.26.546614

N/A

0DataRank · unranked

4 citations

Jonathan E. Perdomo, Munir E. Khan, Brianna Disanza, Gregory G. Cajka, Sunyimeng Lei +12 more

TDP-43 proteinopathy in ALS is triggered by loss of ASRGL1 and associated with HML-2 expression

Nature Communications(2024)10.1038/s41467-024-48488-7

N/A

0DataRank · unranked

29 citations

Saeed Fathi, Cyrus Rastegar, Elena Rita Simula, Tara T. Doucet-O’Hare, Yong-Han Hank Cheng +22 more

KOLF2.1J iPSCs carry CNVs associated with neurodevelopmental disorders

Cell stem cell(2024)10.1016/j.stem.2024.02.007

N/A

0DataRank · unranked

18 citations

Jonathan E. Perdomo, Munir E. Khan, Thomas Roulé, Brianna Disanza, Gregory G. Cajka +12 more

Bi-allelic variants in BCAT1 impair mitochondrial function and are associated with a candidate neurometabolic disorder

Human Genetics and Genomics Advances(2025)10.1016/j.xhgg.2025.100525

N/A

0DataRank · unranked

1 citations

Giulia S. Porcari, Lívia Sertori Finoti, Leonardo Ramos-Rodriguez, Devin M Burris, Justin A. McDonough +15 more

BLOC1S1 variants cause lysosomal and autophagic defects resulting in a hypomyelinating leukodystrophy with epileptic encephalopathy

medRxiv(2025)10.1101/2025.07.17.25331211

N/A

0DataRank · unranked

0 citations

Carlos González, Chad D. Williamson, Guy Helman, Leslie E. Sanderson, Brianna Disanza +34 more