Posters Archive

Conference

Authors

Collaborators

Clear

Showing 10 of 560 Results

Discrepant tumor test results in individuals with Lynch syndrome identified by Next-Generation sequencing panels

Oncology

Date:
Monday, Sep 15, 2014 12:00am – 12:00pm

Conference:
14th Annual Epilepsy Awareness Day

Authors:
Tina Pesaran, MA, MS, CGC, Carin Espenschied, Holly Laduca, Roland Dunbrack, Carolyn Horton, Carla Mason, Pia Summerour

Collaborators:

Fox Chase Cancer Center

Abstract
Patients with multiple pathogenic mutations detected by multi-gene panel testing in a Lynch syndrome cohort

Oncology

Date:
Monday, Sep 15, 2014 12:00am – 12:00pm

Conference:
CGA-IGC 2014

Authors:
Holly Laduca, Tina Pesaran, MA, MS, CGC, Carin Espenschied, Pia Summerour, Carla Mason, Carolyn Horton

Abstract
The relationship between renal cell carcinoma and Lynch syndrome – more investigation is needed

Oncology

Date:
Monday, Sep 15, 2014 12:00am – 12:00pm

Conference:
CGA-IGC 2014

Authors:
Elizabeth Chao, Laura Panos, Mary Pritlzaff

Abstract
Further defining the polyposis phenotype associated with PTEN mutations

Oncology

Date:
Monday, Sep 15, 2014 12:00am – 12:00pm

Conference:
CGA-IGC 2014

Authors:
Laura Panos, Holly Laduca, Elizabeth Chao, Elaine Chen Weltmer, Rachel McFarland

Collaborators:

University of California, Irvine

Abstract
Hereditary pancreatic cancer multi-gene test: Preliminary results

Oncology

Date:
Monday, Sep 15, 2014 12:00am – 12:00pm

Conference:
CGA-IGC 2014

Authors:
Jill Dolinsky, Holly Laduca, Emily K. Dalton

Abstract
Individuals with Lynch syndrome and colon polyps identified by multi-gene panels

Oncology

Date:
Monday, Sep 15, 2014 12:00am – 12:00pm

Conference:
CGA-IGC 2014

Authors:
Tina Pesaran, MA, MS, CGC, Holly Laduca, Carin R. Espenschied, Carolyn Horton, Pia Summerour, Carla Mason

Abstract
Unexpected CDH1 mutations identified on multigene panels

General

Date:
Monday, Sep 15, 2014 12:00am – 12:00pm

Conference:
CGA-IGC 2014

Authors:
Sturgeon D, Espenschied C, Lowstuter K, Ricker C, Dolinsky J, Culver JO, Chao E, Moline J, Idos G, McDonnell K, Gruber SB

Collaborators:

Cleveland Clinic
University of Southern California Norris Comprehensive Cancer Center

Abstract
Reclassification of historical mutations in the CFTR gene for cystic fibrosis reveals that 37% of previously-classified “mutations” are variants of unknown significance or benign alterations

General

Date:
Tuesday, Mar 25, 2014 12:00am – 12:00pm

Conference:
ACMG 2014

Authors:
Jade Tinker, Tami Johnston, Melissa Parra, MS, CGC, Kendra Walker, Elaine Chen, Ira Lu, Tim Vo, Chia-Ling Gau, PhD, DABMG

Poster
Mutations in newly discovered Mendelian disease genes represent a significant portion of positive findings in diagnostic exome sequencing (DES)

Clinical Genomics

Date:
Tuesday, Mar 25, 2014 12:00am – 12:00pm

Conference:
ACMG 2014

Authors:
Sha Tang, Stephanie Gandomi, Elizabeth Chao, Kelly Farwell, Layla Shahmirzadi, Dima El-Khechen, Zöe Powis, Ira Lu, Cameron Mroske, Ruth Baxter, Xiang Li, Brigette Tippin, Wenqi Zeng

Collaborators:

University of California, Irvine

Poster
The ever-expanding clinical phenotype associated with PTEN gene mutations: Two remarkably different cases involving the PTEN mutation p.D24G detected by Sanger sequencing and exome sequencing analyses

Clinical Genomics

Date:
Tuesday, Mar 25, 2014 12:00am – 12:00pm

Conference:
ACMG 2014

Authors:
Tina Pesaran, MA, MS, CGC, Sha Tang, Stephany Tandy, Kelly Gonzalez, Layla Shahmirzadi, Wendy K. Chung, Rebecca Sisson, Jessica Mester, Charis Eng, Amie Blanco, Jonathan Terdiman, Frances Oh, Timothy Vo, Chia-Ling Gau, PhD, DABMG

Collaborators:

Cleveland Clinic
Columbia University
University of California, San Francisco

Poster

…

Scientific Posters

Filter By

Discrepant tumor test results in individuals with Lynch syndrome identified by Next-Generation sequencing panels

Patients with multiple pathogenic mutations detected by multi-gene panel testing in a Lynch syndrome cohort

The relationship between renal cell carcinoma and Lynch syndrome – more investigation is needed

Further defining the polyposis phenotype associated with PTEN mutations

Hereditary pancreatic cancer multi-gene test: Preliminary results

Individuals with Lynch syndrome and colon polyps identified by multi-gene panels

Unexpected CDH1 mutations identified on multigene panels

Reclassification of historical mutations in the CFTR gene for cystic fibrosis reveals that 37% of previously-classified “mutations” are variants of unknown significance or benign alterations

Mutations in newly discovered Mendelian disease genes represent a significant portion of positive findings in diagnostic exome sequencing (DES)

The ever-expanding clinical phenotype associated with PTEN gene mutations: Two remarkably different cases involving the PTEN mutation p.D24G detected by Sanger sequencing and exome sequencing analyses

Patients

PROVIDERS

Solutions

Resources

Company

NOTICES

Scientific Posters

Filter By

Get in Touch