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Discrepancies between payer coverage and consensus guidelines for personalizing hereditary cancer risk

Oncology

Date:
Friday, May 3, 2019 6:00pm – 7:30pm

Conference:
—

Authors:
Jill Dolinsky, Patrick Reineke, Nancy Niguidula, Emily Dalton, Jessica Profato, Greg Nogle, Holly Laduca, Lily Hoang, Victoria Ellis

Poster
An analysis of clinical documentation submitted with diagnostic exome sequencing orders and the added burden or benefit of insurance billing

Clinical Genomics

Date:
Friday, Apr 5, 2019 10:30am – 12:00pm

Conference:
—

Authors:
Meghan Towne, Kirsten Blanco, Kelly Radtke, Nancy Kramer, Sheila Saliganan, Stephanie Brooks, Zöe Powis, Kelly Farwell

Poster
By the way: The incidental benefit of exome sequencing to enable life-saving intervention via secondary findings

Clinical Genomics

Date:
Friday, Apr 5, 2019 10:30am – 12:00pm

Conference:
—

Authors:
Sha Tang, Jennifer Huang, Christina L. Alamillo, Zöe Powis, Kelly Farwell Hagman

Poster
Lifetime risk of breast cancer from polygenic risk scores combined with clinical assessment in women referred for genetic testing

Oncology

Date:
Friday, Apr 5, 2019 10:30am – 12:00pm

Conference:
—

Authors:
Mary Helen Black, Stephanie Gutierrez, Shuwei Li, Jill Dolinsky, Jessica Profato, Holly Laduca

Poster
CSNK2B: A novel cause of neurodevelopmental disease and

Clinical Genomics

Session:
#305

Date:
Thursday, Apr 4, 2019 10:00am – 11:30am

Conference:
—

Authors:
Michelle Ernst, C. Working Group, Zöe Powis

Collaborators:

Columbia University
“N of one” is the loneliest number: How a lack of corroborating case reports is hindering the classification of genes

Clinical Genomics

Date:
Thursday, Apr 4, 2019 10:00am – 11:30am

Conference:
—

Authors:
Meghan Towne, Brian Schoenfeld, Kirsten Blanco, Sha Tang, Kelly Radtke, Deepali Shinde, Kelly Farwell Hagman

Poster
Has anything changed? Reclassification of epilepsy genetic variants

Clinical Genomics

Date:
Thursday, Apr 4, 2019 10:00am – 11:30am

Conference:
—

Authors:
Catherine Schultz, Kirsten Blanco, Zöe Powis, Shoji Ichikawa

Poster
VHL Information Sharing International Consortium (VISION): A ClinGen Expert Panel to Evaluate VHL Gene-Specific Criteria for Variant Interpretation

Oncology

Date:
Thursday, Apr 4, 2019 10:00am – 11:30am

Conference:
—

Authors:
Carrie Horton, Kelly McGoldrick, Tina Pesaran, MA, MS, CGC, Deborah I. Ritter

Collaborators:

Baylor College of Medicine
Clinical diagnostic exome sequencing in patients with neuromuscular disorders: Genetic testing challenges for complex conditions

Clinical Genomics

Date:
Thursday, Apr 4, 2019 10:00am – 11:30am

Conference:
—

Authors:
Kirsten Blanco, Julie Stefka, Sha Tang, Zöe Powis, Kelly Farwell Hagman

Poster
Discrepancies in payer coverage and practice guidelines for genetic testing of ACMG cardiovascular genes

Cardiology

Date:
Thursday, Apr 4, 2019 10:00am – 11:30am

Conference:
—

Authors:
Nancy Niguidula, Jill Dolinsky, Greg Nogle, Carrie Horton, Tami Johnston, Heather Zimmermann, Benjamin Feldmann, Illa Hadzimehmedagic, Zöe Powis

… …

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Discrepancies between payer coverage and consensus guidelines for personalizing hereditary cancer risk

An analysis of clinical documentation submitted with diagnostic exome sequencing orders and the added burden or benefit of insurance billing

By the way: The incidental benefit of exome sequencing to enable life-saving intervention via secondary findings

Lifetime risk of breast cancer from polygenic risk scores combined with clinical assessment in women referred for genetic testing

CSNK2B: A novel cause of neurodevelopmental disease and

“N of one” is the loneliest number: How a lack of corroborating case reports is hindering the classification of genes

Has anything changed? Reclassification of epilepsy genetic variants

VHL Information Sharing International Consortium (VISION): A ClinGen Expert Panel to Evaluate VHL Gene-Specific Criteria for Variant Interpretation

Clinical diagnostic exome sequencing in patients with neuromuscular disorders: Genetic testing challenges for complex conditions

Discrepancies in payer coverage and practice guidelines for genetic testing of ACMG cardiovascular genes

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