Volume 17 Issue 6, June 2015

On the cover | Anita Wolfenden

“Vessel”

Vessel. “I have worked with thick watercolor paper for several years, and I like the stark clean lines and the soft, slightly fuzzy surface of the paper that reflects light so beautifully. I like working with holes and shadows, and in this piece I have added a cut piece of black Tyvek as a contrast to the softer white shapes.” More of the artist’s work can be seen at http://awolfenden.com.

In This Issue

In this Issue

In This Issue 02 Jun 2015

Advertisement

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News Briefs

News Briefs

News Briefs 02 Jun 2015

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Systematic Review

An overview of recommendations and translational milestones for genomic tests in cancer

Christine Q. Chang
Sharna R. Tingle
John P.A. Ioannidis
Systematic Review 23 Oct 2014

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Commentary

Genomic screening of the general adult population: key concepts for assessing net benefit with systematic evidence reviews

Anya E.R. Prince
Jonathan S. Berg
Gail Henderson
Commentary 18 Sept 2014

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Review

Solving the molecular diagnostic testing conundrum for Mendelian disorders in the era of next-generation sequencing: single-gene, gene panel, or exome/genome sequencing

Yuan Xue
Arunkanth Ankala
Madhuri R. Hegde
Review 18 Sept 2014

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Original Research Article

Mortality of New York children with sickle cell disease identified through newborn screening

Ying Wang
Gang Liu
Scott D. Grosse
Original Research Article 25 Sept 2014
Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity

Nina De Rocker
Sarah Vergult
Björn Menten
Original Research Article 18 Sept 2014
Disparities in uptake of BRCA1/2 genetic testing in a randomized trial of telephone counseling

Morgan Butrick
Scott Kelly
Marc D. Schwartz
Original Research Article Open Access 18 Sept 2014
Is it all Lynch syndrome?: An assessment of family history in individuals with mismatch repair–deficient tumors

Katherine M. Dempsey
Russell Broaddus
Karen Lu

Focus:

Focus on Gastrointestinal Diseases
Original Research Article 23 Oct 2014
Development of a tiered and binned genetic counseling model for informed consent in the era of multiplex testing for cancer susceptibility

Angela R. Bradbury
Linda Patrick-Miller
Susan M. Domchek
Original Research Article 09 Oct 2014
Clinically relevant lessons from Family HealthLink: a cancer and coronary heart disease familial risk assessment tool

Kevin Sweet
Amy C. Sturm
Doreen Agnese
Original Research Article 30 Oct 2014

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Brief Report

Parents are interested in newborn genomic testing during the early postpartum period

Susan E. Waisbren
Danielle K. Bäck
Robert C. Green
Brief Report 04 Dec 2014

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ACMG Policy Statement

Clinical utility of genetic and genomic services: a position statement of the American College of Medical Genetics and Genomics

Collection:

ACMG Statements and Guidelines
ACMG Policy Statement 12 Mar 2015

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Letter to the Editor

The challenge of defining pathogenicity: the example of AHI1

Raoul Heller
Hanno J. Bolz
Letter to the Editor 02 Jun 2015
Response to Heller and Bolz

Zi-Bing Jin
Xiu-Feng Huang
Letter to the Editor 02 Jun 2015
The cost-effectiveness of routine testing for Lynch syndrome in newly diagnosed patients with colorectal cancer in the United States: corrected estimates

Scott D. Grosse
Glenn E. Palomaki
Heather Hampel
Letter to the Editor 02 Jun 2015

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Genetic Legacy

Reproducing Genetics

Joe Leigh Simpson
Genetic Legacy 02 Jun 2015

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Erratum

Erratum: A genome sequencing program for novel undiagnosed diseases

Erratum 02 Jun 2015

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Corrigendum

Correction: Corrigendum: Too much, too soon?: Commercial provision of noninvasive prenatal screening for subchromosomal abnormalities and beyond

Corrigendum 02 Jun 2015

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Volume 17 Issue 6, June 2015

In This Issue

In this Issue

News Briefs

News Briefs

Systematic Review

An overview of recommendations and translational milestones for genomic tests in cancer

Commentary

Genomic screening of the general adult population: key concepts for assessing net benefit with systematic evidence reviews

Review

Solving the molecular diagnostic testing conundrum for Mendelian disorders in the era of next-generation sequencing: single-gene, gene panel, or exome/genome sequencing

Original Research Article

Mortality of New York children with sickle cell disease identified through newborn screening

Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity

Disparities in uptake of BRCA1/2 genetic testing in a randomized trial of telephone counseling

Is it all Lynch syndrome?: An assessment of family history in individuals with mismatch repair–deficient tumors

Development of a tiered and binned genetic counseling model for informed consent in the era of multiplex testing for cancer susceptibility

Clinically relevant lessons from Family HealthLink: a cancer and coronary heart disease familial risk assessment tool

Brief Report

Parents are interested in newborn genomic testing during the early postpartum period

ACMG Policy Statement

Clinical utility of genetic and genomic services: a position statement of the American College of Medical Genetics and Genomics

Letter to the Editor

The challenge of defining pathogenicity: the example of AHI1

Response to Heller and Bolz

The cost-effectiveness of routine testing for Lynch syndrome in newly diagnosed patients with colorectal cancer in the United States: corrected estimates

Genetic Legacy

Reproducing Genetics

Erratum

Erratum: A genome sequencing program for novel undiagnosed diseases

Corrigendum

Correction: Corrigendum: Too much, too soon?: Commercial provision of noninvasive prenatal screening for subchromosomal abnormalities and beyond

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