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Phenotypes of patients with APC gene mutations identified via multi-gene cancer panel testing

Oncology

Date:
Sunday, Oct 2, 2016 11:00am – 12:00pm

Conference:
CGA-IGC 2016

Authors:
Tara Namey, Emily Dalton, Carin Espenschied, Amal Yussuf

Abstract Poster
Revisiting the role of CHEK2 mutations in hereditary breast-colorectal cancer probands

Oncology

Date:
Sunday, Oct 2, 2016 11:00am – 12:00pm

Conference:
CGA-IGC 2016

Authors:
Holly Laduca, Ora Gordon, Kimberly Childers, Rachel McFarland

Collaborators:

Providence Health

Abstract
Types and frequencies of Lynch syndrome mutations identified through multigene panel testing

Oncology

Date:
Sunday, Oct 2, 2016 11:00am – 12:00pm

Conference:
CGA-IGC 2016

Authors:
Carin Espenschied, Holly Laduca, Shuwei Li, Heather Hampel, Rachel McFarland, Chia-Ling Gau, PhD, DABMG

Poster Abstract
Types and frequencies of Lynch syndrome mutations identified through multigene panel testing

Oncology

Date:
Friday, Sep 30, 2016 11:30am – 12:45pm

Conference:
NSGC 2016

Authors:
Carin Espenschied, Holly Laduca, Shuwei Li, Heather Hampel, Rachel McFarland, Chia-Ling Gau, PhD, DABMG

Collaborators:

Ohio State University (OSU)

Poster
Secondary findings in trio family members of probands undergoing diagnostic exome sequencing

Clinical Genomics

Date:
Wednesday, Sep 28, 2016 11:00am – 12:00pm

Conference:
NSGC 2016

Authors:
Kelly Hagman, MS, CGC, LGC, Sha Tang, Zöe Powis, Taylor Cain, Christina L. Alamillo, Layla Shahmirzadi
Continued coverage and reimbursement challenges for diagnostic exome sequencing after 5 years, genetic counselors can help to overturn denied cases

Clinical Genomics

Date:
Wednesday, Sep 28, 2016 11:00am – 12:00pm

Conference:
NSGC 2016

Authors:
Kelly Hagman, MS, CGC, LGC, Sha Tang, Zöe Powis, Taylor Cain, Layla Shahmirzadi

Abstract
All in the family: A first look at outcomes when multiple relatives undergo multi-gene panel testing

Clinical Genomics

Date:
Wednesday, Sep 28, 2016 11:00am – 12:00pm

Conference:
NSGC 2016

Authors:
Amal Yussuf, Holly Laduca, Monalyn Umali, Kush Panchani

Poster Abstract
X-linked Mohr-Tranebjaerg syndrome: Variable phenotype in females

Oncology

Date:
Wednesday, Sep 28, 2016 11:00am – 12:00pm

Conference:
NSGC 2016

Authors:
Heather Newman, Zöe Powis, Shelley Towner, William Wilson

Abstract Poster
A retrospective review of family studies in reclassifying variants of unknown significance detected in cardiomyopathy multigene panels

Cardiology

Date:
Wednesday, Sep 28, 2016 11:00am – 12:00pm

Conference:
NSGC 2016

Authors:
Tami Johnston, Melissa Dempsey, Jill Dolinsky, Brigette Tippin Davis, Ira Lu, Alizabeth Berg, Andrea Nagl, Heather Workman, Kendra Walller, Sara Calicchia

Poster Abstract
Breast and colorectal cancer risk in monoallelic MUTYH carriers ascertained via multigene panel testing

Oncology

Date:
Wednesday, Sep 28, 2016 11:00am – 12:00pm

Conference:
NSGC 2016

Authors:
Kelly Fulk, Holly Laduca, Carin Espenschied, Amal Yussuf, Kory Jasperson, Dajun Qian, Yuan Tian

Abstract Poster

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Phenotypes of patients with APC gene mutations identified via multi-gene cancer panel testing

Revisiting the role of CHEK2 mutations in hereditary breast-colorectal cancer probands

Types and frequencies of Lynch syndrome mutations identified through multigene panel testing

Types and frequencies of Lynch syndrome mutations identified through multigene panel testing

Secondary findings in trio family members of probands undergoing diagnostic exome sequencing

Continued coverage and reimbursement challenges for diagnostic exome sequencing after 5 years, genetic counselors can help to overturn denied cases

All in the family: A first look at outcomes when multiple relatives undergo multi-gene panel testing

X-linked Mohr-Tranebjaerg syndrome: Variable phenotype in females

A retrospective review of family studies in reclassifying variants of unknown significance detected in cardiomyopathy multigene panels

Breast and colorectal cancer risk in monoallelic MUTYH carriers ascertained via multigene panel testing

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