Volume 17 Issue 1, January 2015

News Briefs

A systematic review and critical assessment of 11 discordant meta-analyses on reduced-function CYP2C19 genotype and risk of adverse clinical outcomes in clopidogrel users

• Ruben L. Osnabrugge
• Stuart J. Head
• A. Cecile J.W. Janssens

The translational potential of research on the ethical, legal, and social implications of genomics

• Wylie Burke
• Paul Appelbaum
• Eric Juengst

Agalsidase alfa and agalsidase beta in the treatment of Fabry disease: does the dose really matter?

• Antonio Pisani
• Eleonora Riccio
• Massimo Sabbatini

Is it time for BRCA1/2 mutation screening in the general adult population?: impact of population characteristics

• Glenn E. Palomaki

Reporting genomic secondary findings: ACMG members weigh in

• Maren T. Scheuner
• Jane Peredo
• James Evans

Neurofibromatosis type 1 and chronic neurological conditions in the United States: an administrative claims analysis

• Chinwe C. Madubata
• Margaret A. Olsen
• Kimberly J. Johnson

Characteristics associated with genetic counseling referral and BRCA1/2 testing among women in a large integrated health system

• Cecelia A. Bellcross
• Lucy A. Peipins
• Steven Leadbetter

Differences in BRCA counseling and testing practices based on ordering provider type

• Deborah Cragun
• Lucia Camperlengo
• Tuya Pal

Molecular testing for the BRCA1 and BRCA2 Ashkenazi Jewish founder mutations: a report on the College of American Pathologists proficiency testing surveys

• Laura J. Tafe
• Michael B. Datto
• Felicitas L. Lacbawan

Evidence synthesis and guideline development in genomic medicine: current status and future prospects

• Sheri D. Schully
• Tram Kim Lam
• Muin J. Khoury

ACMG policy statement: updated recommendations regarding analysis and reporting of secondary findings in clinical genome-scale sequencing

A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic Counselors: referral indications for cancer predisposition assessment

• Heather Hampel
• Robin L. Bennett
• Georgia L. Wiesner

Prenatal diagnosis in India is not limited to sex selection

• Ashwin B. Dalal
• Prajnya Ranganath
• Meenal Agarwal

Response to Dalal et al.

• Kamlesh Madan
• Martijn H. Breuning

Judith G. Hall: a genetic journey

• Judith G. Hall

Erratum: Comprehensive CFTR gene analysis of the French cystic fibrosis screened newborn cohort: implications for diagnosis, genetic counseling, and mutation-specific therapy

Correction: Corrigendum: A clinical appraisal of different Z-score equations for aortic root assessment in the diagnostic evaluation of Marfan syndrome