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Tina Pesaran | Researchclopedia

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Tina Pesaran

Ambry Genetics (United States)ORCID

132

Works

6,153

Citations

33

h-index

55

i10-index

Research Topics

Genomics and Rare Diseases BRCA gene mutations in cancer Cancer Genomics and Diagnostics

Affiliations

University of Maryland, Baltimore2023–2023

Mayo Clinic2018–2018

Baylor College of Medicine2025–2025

QIMR Berghofer Medical Research Institute2021–2021

University of Utah2018–2018

Top Works

Recommendations for interpreting the loss of function PVS1 ACMG/AMP variant criterion

Ahmad Abou Tayoun,Tina Pesaran,et al.

2018846 citations

Genetic factors in colorectal cancer

Genomic variations and chromosomal abnormalities

Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer

Fergus J. Couch,Hermela Shimelis,et al.

2017621 citations

Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria

Vikas Pejaver,Alicia B. Byrne,et al.

2022489 citations

Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients

Holly LaDuca,Aaron J. Stuenkel,et al.

2014336 citations

Triple-Negative Breast Cancer Risk Genes Identified by Multigene Hereditary Cancer Panel Testing

Hermela Shimelis,Holly LaDuca,et al.

2018318 citations

Using the ACMG/AMP framework to capture evidence related to predicted and observed impact on splicing: Recommendations from the ClinGen SVI Splicing Subgroup

Logan C. Walker,Miguel de la Hoya,et al.

2023267 citations

Clinical laboratories collaborate to resolve differences in variant interpretations submitted to ClinVar

Steven M. Harrison,Jill S. Dolinsky,et al.

2017245 citations

A clinical guide to hereditary cancer panel testing: evaluation of gene-specific cancer associations and sensitivity of genetic testing criteria in a cohort of 165,000 high-risk patients

Holly LaDuca,Eric C. Polley,et al.

2019219 citations

Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline <i>CDH1</i> sequence variants

Kristy Lee,Kate Krempely,et al.

2018171 citations