Posters Archive

Conference

Authors

Collaborators

Clear

Showing 10 of 560 Results

Multiple molecular diagnoses identified through diagnostic exome sequencing

Clinical Genomics

Date:
Tuesday, Mar 24, 2015 12:00am – 12:00pm

Conference:
ACMG 2015

Authors:
Kelly Radtke, Vruti Mehta, Marilyn Tsang, Deepali Shinde, Wendy Alcaraz, Brigette Tippin Davis, Elizabeth Chao, Sha Tang, Kelly Farwell, Layla Shahmirzadi, Dima El-Khechen, Zöe Powis, Christina L. Alamillo, Christian Gund, Cameron Mroske, Katherine Helbig, Jianbo James Song

Collaborators:

University of California, Irvine

Poster
The likelihood of positive results from diagnostic exome sequencing is not predicted by ordering physician specialty

Clinical Genomics

Date:
Tuesday, Mar 24, 2015 12:00am – 12:00pm

Conference:
ACMG 2015

Authors:
Wendy Alcaraz, Elena Rosenberg, Vruti Mehta, Marilyn Tsang, Deepali Shinde, Kelly Radtke, Shuwei Li, Brigette Tippin Davis, Elizabeth Chao, Sha Tang, Zöe Powis, Kelly Farwell Hagman, Layla Shahmirzadi, Dima El-Khechen, Christina L. Alamillo, Katherine Helbig, Christian Gund, Cameron Mroske, Jianbo James Song

Collaborators:

University of California, Irvine

Poster
A retrospective analysis of multigene panel testing for Marfan syndrome, aneurysm, and related disorders: Diagnostic yield and cardiac phenotypic spectrum

Cardiology

Date:
Tuesday, Mar 24, 2015 12:00am – 12:00pm

Conference:
ACMG 2015

Authors:
Tami Johnston, Jill Dolinsky, Jade Tinker, Melissa Dempsey, Brigette Tippin Davis, Jennifer Thompson, Tricia Zion, Rachel McFarland, Ira Lu

Poster Abstract
A novel gene not so novel anymore: Personalized in vitro model and further evidence for association of DNM1 with early infantile epileptic encephalopathy through clinical exome sequencing

Clinical Genomics

Date:
Tuesday, Mar 24, 2015 12:00am – 12:00pm

Conference:
ACMG 2015

Authors:
Deepali Shinde, Sha Tang, Dima El-Khechen, Katherine Helbig, Mark E. Nunes

Poster
Exome sequencing covers >99% of mutations identified on targeted next-generation sequencing panels

Clinical Genomics

Date:
Tuesday, Mar 24, 2015 12:00am – 12:00pm

Conference:
ACMG 2015

Authors:
Elizabeth Chao, Wenbo Mu, Holly Laduca, Sha Tang, Jefferey Chen, Hsiao-Mei Lu, Huy Vuong, Kelly Farwell, Layla Shahmirzadi

Collaborators:

University of California, Irvine

Poster Abstract
Diagnostic whole exome sequencing identifies alterations in the novel gene, WARS2, in a patient with severe infantile-onset leukoencephalopathy

Clinical Genomics

Date:
Tuesday, Mar 24, 2015 12:00am – 12:00pm

Conference:
ACMG 2015

Authors:
Wendy Alcaraz, Deepali Shinde, Sha Tang, Julie Cohen, Ali Fatemi

Collaborators:

Kennedy Krieger Institute

Poster
Diagnostic exome sequencing positively identified relevant alterations in half of prenatal samples tested

Clinical Genomics

Date:
Tuesday, Mar 24, 2015 12:00am – 12:00pm

Conference:
ACMG 2015

Authors:
Vruti Mehta, Marilyn Tsang, Brigette Tippin Davis, Sha Tang, Elizabeth Chao, Christina L. Alamillo, Kelly Farwell, Layla Shahmirzadi, Dima El-Khechen, Zöe Powis, Katherine Helbig, Christian Gund

Collaborators:

University of California, Irvine

Poster Abstract
Yield of multi-gene testing in affected and unaffected patients meeting NCCN BRCA1/2 testing criteria

Oncology

Date:
Saturday, Mar 14, 2015 12:00am – 12:00pm

Conference:
NCoBC 2015

Authors:
Elizabeth Chao, Leslie Bucheit, Kimerbly Banks, Rachel McFarland

Abstract
Transitioning from single to multi-gene testing for hereditary cancer predisposition: An advanced practice nurse’s experience

Oncology

Date:
Saturday, Mar 14, 2015 12:00am – 12:00pm

Conference:
NCoBC 2015

Authors:
Kelly Fulk, Virginia Speare, Holly Laduca, Laura Panos, Elizabeth Chao, Phyllis Everett

Abstract Poster
Characterizing the mutation spectrum in BRCA1/2-negative early-onset breast cancer patients undergoing multigene panel testing

Oncology

Date:
Thursday, Feb 26, 2015 12:00am – 12:00pm

Conference:
Miami Breast Cancer Conference 2015

Authors:
Selvi Palaniappan, Holly Laduca, Shuwei Li, Elizabeth Chao, Rachel McFarland

Poster Abstract

… …

Scientific Posters

Filter By

Multiple molecular diagnoses identified through diagnostic exome sequencing

The likelihood of positive results from diagnostic exome sequencing is not predicted by ordering physician specialty

A retrospective analysis of multigene panel testing for Marfan syndrome, aneurysm, and related disorders: Diagnostic yield and cardiac phenotypic spectrum

A novel gene not so novel anymore: Personalized in vitro model and further evidence for association of DNM1 with early infantile epileptic encephalopathy through clinical exome sequencing

Exome sequencing covers >99% of mutations identified on targeted next-generation sequencing panels

Diagnostic whole exome sequencing identifies alterations in the novel gene, WARS2, in a patient with severe infantile-onset leukoencephalopathy

Diagnostic exome sequencing positively identified relevant alterations in half of prenatal samples tested

Yield of multi-gene testing in affected and unaffected patients meeting NCCN BRCA1/2 testing criteria

Transitioning from single to multi-gene testing for hereditary cancer predisposition: An advanced practice nurse’s experience

Characterizing the mutation spectrum in BRCA1/2-negative early-onset breast cancer patients undergoing multigene panel testing

Patients

PROVIDERS

Solutions

Resources

Company

NOTICES

Scientific Posters

Filter By

Get in Touch