Advertisement

Browse Subject Areas

?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

Genetic testing

Open Window: When Easily Identifiable Genomes and Traits Are in the Public Domain

Misha Angrist

openSNP–A Crowdsourced Web Resource for Personal Genomics

Bastian Greshake, Philipp E. Bayer, Helge Rausch, Julia Reda

Serum Bilirubin Concentration in Healthy Adult North-Europeans Is Strictly Controlled by the UGT1A1 TA-Repeat Variants

Marianne K. Kringen, Armin P. Piehler, [ ... ], Petter Urdal

In Their Own Words: Treating Very Young BRCA1/2 Mutation-Positive Women with Care and Caution

Lindsey M. Hoskins, Allison Werner-Lin, Mark H. Greene

Identification of Candidate Children for Maturity-Onset Diabetes of the Young Type 2 (MODY2) Gene Testing: A Seven-Item Clinical Flowchart (7-iF)

Michele Pinelli, Fabio Acquaviva, [ ... ], Italian Study Group on Diabetes of the Italian Society of Pediatric Endocrinology and Diabetology (ISPED)

Use of HbA1c in the Identification of Patients with Hyperglycaemia Caused by a Glucokinase Mutation: Observational Case Control Studies

Anna M. Steele, Kirsty J. Wensley, [ ... ], Beverley M. Shields

Genetic Testing for TMEM154 Mutations Associated with Lentivirus Susceptibility in Sheep

Michael P. Heaton, Theodore S. Kalbfleisch, [ ... ], the International Sheep Genomics Consortium

Comparing Alternative Methods for Holding Virgin Honey Bee Queens for One Week in Mailing Cages before Mating

Gianluigi Bigio, Christoph Grüter, Francis L. W. Ratnieks

Impact of Genetic Notification on Smoking Cessation: Systematic Review and Pooled-Analysis

Sylviane de Viron, Johan Van der Heyden, [ ... ], Herman Van Oyen

Exome Sequencing and Genetic Testing for MODY

Stefan Johansson, Henrik Irgens, [ ... ], Pål R. Njølstad

The p.V37I Exclusive Genotype Of GJB2: A Genetic Risk-Indicator of Postnatal Permanent Childhood Hearing Impairment

Lei Li, Jingrong Lu, [ ... ], Hao Wu

Myocardial Structural Alteration and Systolic Dysfunction in Preclinical Hypertrophic Cardiomyopathy Mutation Carriers

Kai Hang Yiu, Douwe E. Atsma, [ ... ], Nina Ajmone Marsan

Characterization of a Large Group of Individuals with Huntington Disease and Their Relatives Enrolled in the COHORT Study

E. Ray Dorsey, the Huntington Study Group COHORT Investigators

Advertisement

Create a weekly email alert for: Genetic testing

You can change these options by clicking profile then "Alerts and Notifications"