Tina Pesaran

12PUBLICATIONS
88CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Predictive and prognostic markersCancer geneticsEpigenetics (incl. genome methylation and epigenomics)Molecular targets
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Publications (12)

|Apr 09, 2026
Combining multiplexed assays of variant effect for enhanced BRCA2 variant classification.

Chunling Hu, Sounak Sahu, Wenan Chen

|Nov 08, 2024
Pathogenic Variants in Cancer Susceptibility Genes Predispose to Ductal Carcinoma In Situ of the Breast.

Huaizhi Huang, Ronan E Couch, Rachid Karam

|Nov 03, 2024
Reduced penetrance BRCA1 and BRCA2 pathogenic variants in clinical germline genetic testing.

Tuya Pal, Erin Mundt, Marcy E Richardson

|May 30, 2023
Functional and Clinical Characterization of Variants of Uncertain Significance Identifies a Hotspot for Inactivating Missense Variants in RAD51C.

Chunling Hu, Anil Belur Nagaraj, Hermela Shimelis

|Jun 06, 2022
An integrative model for the comprehensive classification of BRCA1 and BRCA2 variants of uncertain clinical significance.

Edwin S Iversen, Gary Lipton, Steven N Hart

|Oct 30, 2021
Classification of the canonical splice alteration <i>MUTYH</i> c.934-2A > G is likely benign based on RNA and clinical data.

Felicia Hernandez, Blair R Conner, Marcy E Richardson

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Frequent Collaborators

8 joint publications

Rachid Karam

6 joint publications

Susan M Domchek

6 joint publications

Fergus J Couch

6 joint publications

Siddhartha Yadav