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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
Clinical Validity scoring of Gene-Disease Associations in Diagnostic Exome Sequencing: Effects on Reporting and Reanalysis

Clinical Genomics

Date:
Wednesday, Jun 22, 2016 11:00am – 12:00am

Conference:
Curating the Clinical Genome 2016

Authors:
Erica Smith, Kelly Radtke, Mari Rossi, Deepali Shinde, Kelly Hagman, MS, CGC, LGC, Sha Tang, Layla Shahmirzadi

Abstract Poster
AmbryShare: A new model to fostering a global effort for sharing genomic data to better understand human disease

AmbryShare

Date:
Wednesday, Jun 22, 2016 11:00am – 12:00pm

Conference:
Curating the Clinical Genome 2016

Authors:
Aaron Elliott, Shuwei Li, Jill Dolinsky, Carin Espenschied, Layla Shahmirzadi, Hsiao-Mei Lu, Charles Dunlop

Poster Abstract
Exploring trends in mutation distribution of multi-gene panel testing based on ethnicity

Clinical Genomics

Date:
Wednesday, Jun 22, 2016 11:00am – 12:00pm

Conference:
Curating the Clinical Genome 2016

Authors:
Laura Panos, Jill Dolinsky, Shuwei Li, Patrick Reineke, Rachel McFarland, Melissa Pronold

Poster Abstract
Impact of hereditary multigene panel testing for cancer survivors.

Oncology

Session:
#156826

Date:
Wednesday, Jun 15, 2016 2:00pm – 6:30pm

Conference:
Cancer Survivorship Symposium 2016

Authors:
Nimmi S. Kapoor, Jennifer Swisher, Rachel McFarland, Mychael Patrick, Lisa D. Curcio

Poster Abstract
Structural quantification, discrimination, and reclassification (SURF) of pathogenic variants

Clinical Genomics

Date:
Sunday, Jun 12, 2016 11:00am – 12:00pm

Conference:
—

Authors:
Adam Chamberlin, Tina Pesaran, MA, MS, CGC, Robert Huether, Hsiao-Mei Lu

Poster Abstract
Prospective Registry of Multiplex Testing (PROMPT): a web-based platform to assess cancer risk of genetic variants.

Oncology

Date:
Friday, Jun 3, 2016 3:00pm – 6:00pm

Conference:
ASCO 2016

Authors:
Jill Dolinsky, Fergus Couch, Michael Francis Walsh, Pragna Gaddam, Laura Digiovanni, Judith Balmaña, Taylor Sittler, Rachel Klein, Stephen E Lincoln, Brian Allen, Justin Leighton, Charles Strom, Vanessa Ranger-Miller, Kyle Brown, Judy Ellen Garber, Susan M. Domchek, Mark E. Robson, Kenneth Offit

Abstract

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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

Clinical Validity scoring of Gene-Disease Associations in Diagnostic Exome Sequencing: Effects on Reporting and Reanalysis

AmbryShare: A new model to fostering a global effort for sharing genomic data to better understand human disease

Exploring trends in mutation distribution of multi-gene panel testing based on ethnicity

Impact of hereditary multigene panel testing for cancer survivors.

Structural quantification, discrimination, and reclassification (SURF) of pathogenic variants

Prospective Registry of Multiplex Testing (PROMPT): a web-based platform to assess cancer risk of genetic variants.

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