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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
Intermediate FMR1 CGG repeat sizes (35-54) may also contribute to fertility issues in women with potential premature ovarian insufficiency

Clinical Genomics

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

Conference:
NSGC 2016

Authors:
Amal Yussuf, Tiffiney Carter, Elaine C. Weltmer, Zöe Powis, Jing Wang

Poster Abstract
From a trio to a duo: Non-paternity identified through diagnostic exome sequencing

Clinical Genomics

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

Conference:
NSGC 2016

Authors:
Sha Tang, Taylor Cain, Zöe Powis, Dima El-Khechen

Abstract Poster
EpiGC: A collaborative approach to an emerging professional and clinical need

Clinical Genomics

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

Conference:
NSGC 2016

Authors:
Amanda Bergner, Stephanie Gandomi, Beth Rosen Sheidley, Katherine Helbig

Abstract Poster
Facing the challenge of genetic counselors’ need for education about genomic technologies: Opportunities for improvement in training for genetic counselors

Clinical Genomics

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

Conference:
NSGC 2016

Authors:
Devon Lamb Thrush, Kimerbly Banks, Samantha Freeze, Darnelle L. Dorsainville, JennifertEichmeyer, Kelly Farwell Hagman

Abstract Poster

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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

Intermediate FMR1 CGG repeat sizes (35-54) may also contribute to fertility issues in women with potential premature ovarian insufficiency

From a trio to a duo: Non-paternity identified through diagnostic exome sequencing

EpiGC: A collaborative approach to an emerging professional and clinical need

Facing the challenge of genetic counselors’ need for education about genomic technologies: Opportunities for improvement in training for genetic counselors

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