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Germline testing in Asian American and Pacific Islander women with breast cancer

Oncology

Date:
Monday, Jun 1, 2026 1:30pm – 4:30pm

Conference:
ASCO 2026

Authors:
Jennifer Tseng, John Michael O Ranola, Kristin Kohler, Magan Trottier

Collaborators:

City of Hope

Abstract Poster
Actionable germline findings in endometrial cancer from a large multigene panel tested cohort

Oncology

Session:
#572

Date:
Monday, Jun 1, 2026 1:30pm – 4:30pm

Conference:
ASCO 2026

Authors:
Adela Rodriguez-Hernandez, Brittany L. Bychkovsky, Carolyn Horton, Huma Rana, Jessica D. St. Laurent, Judy E. Garber, Linda M. Polfus, Magan Trottier, Miki Horiguchi

Collaborators:

Dana Farber Cancer Institute
Harvard Medical School
Massachusetts General Hospital

Abstract Poster
Germline Pathogenic/Likely Pathogenic (P/LP) Variants in Epithelial Neuroendocrine Neoplasms: The Case for Universal Germline Genetic Testing

Oncology

Session:
#165

Date:
Saturday, May 30, 2026 9:00am – 12:00pm

Conference:
ASCO 2026

Authors:
Andrew Bellizzi, Brittany Sears, Cassidy Carraway, Chandrikha Chandrasekharan, Daniel M. Halperin, Jennifer A. Chan, Matthew Gao, Olatunji B. Alese, Po HEar, Renuka Iyer, Seth Jason Concors, Simron Singh, Udhayvir Singh Grewal

Collaborators:

Dana Farber Cancer Institute
Emory University
Harvard Medical School
Roswell Park Comprehensive Cancer Center
The University of Texas MD Anderson Cancer Center
University of Iowa
University of Toronto

Abstract
Clinical impact of integrating BRCA2 MAVE data for variant reclassification: A real‑world evaluation

Oncology

Session:
#96

Date:
Tuesday, May 26, 2026 12:00am – 12:00am

Conference:
MSS 2026

Authors:
Kristin Kohler, Ashley P.L. Marsh, Colin Young, PhD, Jamie Weyandt, PhD, Sarah Dugger, Daniel Zimmerman, Magan Trottier, Steven Harrison, Marcy E. Richardson

Abstract Poster
Germline Pathogenic Variants in Individuals with Renal Cell Carcinoma

Oncology

Session:
#IP71-05

Date:
Sunday, May 17, 2026 3:30pm – 5:30pm

Conference:
AUA 2026

Authors:
Carolyn Horton, Cassidy Carraway, Huma Rana, Magan Trottier, Michael Serzan, Miki Horiguchi

Collaborators:

Dana Farber Cancer Institute

Abstract Poster
Candidate eQTL detection for risk refinement using paired DNA-RNA panel data

General

Session:
#PO.PR01.02

Date:
Tuesday, Apr 21, 2026 9:00am – 12:00pm

Conference:
AACR 2026

Authors:
Adam Chamberlin, Bojan Losic, David Burks, Donavan Cheng, Esther Hsiao, Hoda Mirsafian, John Watterson, Linda M. Polfus, Matthew Schultz, Tina Pesaran, MA, MS, CGC

Abstract Poster
Long read genome sequencing for cerebellar ataxia

General
Neurology

Session:
#16-009

Date:
Monday, Apr 20, 2026 8:00am – 9:00am

Conference:
AAN 2026

Authors:
Changrui Xiao, Christopher M. Gomez, Emmanuèle C Délot, Erica Smith, Eric Vilain, Greta Pitsava, Ivan De Dios, Kirsten Blanco, Krista Bluske, Niki Maki, Rebekah Barrick, Seth Berger, Soma Das

Collaborators:

University of California, Irvine
University of Chicago

Abstract Poster
HiFi long‑read WGS: sequencing performance of buccal and saliva samples and estimation of non‑human DNA contamination from unaligned HiFi reads

Research

Date:
Friday, Mar 13, 2026 12:00am – 12:00am

Conference:
ACMG 2026

Authors:
Stuti Joshi, Kenny Chen, Tiantian Geier, Erica Smith, Sami Belhadj, John Harting, Yun-Hua Hsiao, Bojan Losic, Seth Berger, David Brohawn, Emmanuele C. Delot

Collaborators:

University of California, Irvine

Poster
Never stop looking: Dual diagnoses due to updated gene–disease relationships in exome patients

Clinical Genomics

Date:
Friday, Mar 13, 2026 10:30am – 11:30am

Conference:
ACMG 2026

Authors:
Wendy Alcaraz, Victoria Ellis, Stephany Tandy, Erica D Smith

Poster Abstract
Use of Pangenome reference improves variant calling in clinical genome sequencing

Clinical Genomics
Research

Date:
Friday, Mar 13, 2026 10:30am – 11:30am

Conference:
ACMG 2026

Authors:
Erica Smith, Julian Stone-Farhat, Matthew Schultz, Ali Alhafidh, David Brohawn, Marcus Mahar, Ermanno Florio

Poster Abstract

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Germline testing in Asian American and Pacific Islander women with breast cancer

Actionable germline findings in endometrial cancer from a large multigene panel tested cohort

Germline Pathogenic/Likely Pathogenic (P/LP) Variants in Epithelial Neuroendocrine Neoplasms: The Case for Universal Germline Genetic Testing

Clinical impact of integrating BRCA2 MAVE data for variant reclassification: A real‑world evaluation

Germline Pathogenic Variants in Individuals with Renal Cell Carcinoma

Candidate eQTL detection for risk refinement using paired DNA-RNA panel data

Long read genome sequencing for cerebellar ataxia

HiFi long‑read WGS: sequencing performance of buccal and saliva samples and estimation of non‑human DNA contamination from unaligned HiFi reads

Never stop looking: Dual diagnoses due to updated gene–disease relationships in exome patients

Use of Pangenome reference improves variant calling in clinical genome sequencing

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