RTI uses cookies to offer you the best experience online. By clicking “accept” on this website, you opt in and you agree to the use of cookies. If you would like to know more about how RTI uses cookies and how to manage them please view our Privacy Policy here. You can “opt out” or change your mind by visiting: http://optout.aboutads.info/. Click “accept” to agree.

Search Results

Showing results 1 to 20 of 60.

Article

Genetic load is associated with hypothalamic-pituitary-adrenal (HPA) axis dysregulation in macaques

September 21, 2012
Article

Establishing the medical actionability of genomic variants

August 31, 2022
Article

Universal tumor screening for Lynch syndrome: Assessment of the perspectives of patients with colorectal cancer regarding benefits and barriers

September 15, 2015
Article

Universal screening for Lynch syndrome among patients with colorectal cancer: patient perspectives on screening and sharing results with at-risk relatives

July 01, 2017
Article

Evaluation of mailed results versus telephone disclosure of normal cancer genetic test results in a low-risk underserved population

July 01, 2024
Article

A systematic framework for selecting gene-condition pairs for inclusion in newborn sequencing panels: Early check implementation

October 04, 2024
Article

Adaptation and early implementation of the PREdiction model for gene mutations (PREMM5™) for lynch syndrome risk assessment in a diverse population

April 01, 2022
Article

The association between maternal occupation and Down syndrome: A report from the national Down syndrome project

January 01, 2020
Article

Patient and provider perspectives on adherence to and care coordination of Lynch Syndrome surveillance recommendations: Findings from qualitative interviews

May 01, 2018
Article

A BAC transgenic mouse model reveals neuron subtype-specific effects of a Generalized Epilepsy with Febrile Seizures Plus (GEFS+) mutation

July 01, 2009
Article

Evidence-based assessments of clinical actionability in the context of secondary findings: Updates from ClinGen's Actionability Working Group

November 01, 2018
Article

Improving care for marginalized populations at risk for hereditary cancer syndromes: Innovations that expanded reach in the CHARM Study

January 01, 2024
Article

Co-occuring diagnoses among FMR1 premutation allele carriers

April 01, 2010
Article

Expert and lay perspectives on burden, risk, tolerability, and acceptability of clinical interventions for genetic disorders

November 01, 2019
Article

The Healthcare Systems Research Network (HCSRN) as an environment for dissemination and implementation research: A case study of developing a multi-site research study in precision medicine

April 12, 2019
Article

Neuropsychological findings from older premutation carrier males and their noncarrier siblings from families with fragile X syndrome

May 01, 2011
Article

Identifying patients with Lynch syndrome using a universal tumor screening program in an integrated healthcare system

April 18, 2022
Article

Cancer health assessments reaching many (CHARM): A clinical trial assessing a multimodal cancer genetics services delivery program and its impact on diverse populations

July 01, 2021
Article

Barriers to family history knowledge and family communication among LGBTQ+ individuals in the context of hereditary cancer risk assessment

February 01, 2022
Article

Investigation of phenotypes associated with mood and anxiety among male and female fragile X premutation carriers

September 01, 2008