Volume 17 Issue 10, October 2015

On the cover | Jenifer Padilla

“Jazz”

“Jazz”was created on very large hotpress paper, approximately 8 ft long by 5 ft tall. Using very large oil pastels I was able to use my entire body to make the fluid marks. The lines were part from life and part improvisation while listening to my favorite music. You can see more of my work at www.PEARONAWIRE.com.

In This Issue

In this Issue

In This Issue 05 Oct 2015

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News Briefs

News Briefs

News Briefs 05 Oct 2015

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Original Research Article

Economic evaluation of genetic screening for Lynch syndrome in Germany

Franziska Severin
Björn Stollenwerk
Wolf Rogowski
Original Research Article 08 Jan 2015
Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios

Xiaolin Zhu
Slavé Petrovski
David B. Goldstein
Original Research Article Open Access 15 Jan 2015
Assessment of incidental findings in 232 whole-exome sequences from the Baylor–Hopkins Center for Mendelian Genomics

Julie Jurgens
Hua Ling
Nara Sobreira
Original Research Article 08 Jan 2015
Implications of polygenic risk-stratified screening for prostate cancer on overdiagnosis

Nora Pashayan
Stephen W. Duffy
Paul D. Pharoah
Original Research Article Open Access 08 Jan 2015
Small-scale high-throughput sequencing–based identification of new therapeutic tools in cystic fibrosis

Jennifer Bonini
Jessica Varilh
Magali Taulan-Cadars
Original Research Article 08 Jan 2015
An effective strategy to prevent allopurinol-induced hypersensitivity by HLA typing

Jae-Woo Jung
Dong-Ki Kim
Hye-Ryun Kang
Original Research Article 29 Jan 2015
Racial variation in frequency and phenotypes of APC and MUTYH mutations in 6,169 individuals undergoing genetic testing

Jennifer A. Inra
Ewout W. Steyerberg
Fay Kastrinos

Focus:

Focus on Gastrointestinal Diseases
Original Research Article 15 Jan 2015
Acceptability and feasibility of a virtual counselor (VICKY) to collect family health histories

Catharine Wang
Timothy Bickmore
Michael Paasche-Orlow
Original Research Article 15 Jan 2015

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Brief Report

Identifying gene disruptions in novel balanced de novo constitutional translocations in childhood cancer patients by whole-genome sequencing

Deborah I. Ritter
Katherine Haines
Sharon E. Plon
Brief Report 08 Jan 2015
Maternal cell-free DNA–based screening for fetal microdeletion and the importance of careful diagnostic follow-up

Svetlana A. Yatsenko
David G. Peters
Aleksandar Rajkovic
Brief Report 08 Jan 2015

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Corrigendum

Correction: Corrigendum: Whole-exome sequencing reveals diverse modes of inheritance in sporadic mild to moderate sensorineural hearing loss in a pediatric population

Corrigendum 05 Oct 2015

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Volume 17 Issue 10, October 2015

In This Issue

In this Issue

News Briefs

News Briefs

Original Research Article

Economic evaluation of genetic screening for Lynch syndrome in Germany

Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios

Assessment of incidental findings in 232 whole-exome sequences from the Baylor–Hopkins Center for Mendelian Genomics

Implications of polygenic risk-stratified screening for prostate cancer on overdiagnosis

Small-scale high-throughput sequencing–based identification of new therapeutic tools in cystic fibrosis

An effective strategy to prevent allopurinol-induced hypersensitivity by HLA typing

Racial variation in frequency and phenotypes of APC and MUTYH mutations in 6,169 individuals undergoing genetic testing

Acceptability and feasibility of a virtual counselor (VICKY) to collect family health histories

Brief Report

Identifying gene disruptions in novel balanced de novo constitutional translocations in childhood cancer patients by whole-genome sequencing

Maternal cell-free DNA–based screening for fetal microdeletion and the importance of careful diagnostic follow-up

Corrigendum

Correction: Corrigendum: Whole-exome sequencing reveals diverse modes of inheritance in sporadic mild to moderate sensorineural hearing loss in a pediatric population

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