Karen S Raraigh

7PUBLICATIONS
28CO-AUTHORS
Psycholinguistics (incl. speech production and comprehension)Counselling, wellbeing and community servicesGene expression (incl. microarray and other genome-wide approaches)Infant and child healthGene and molecular therapy
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Publications (7)

|Dec 28, 2025
Developing a primer for communicating about penetrance, expressivity, and genotype-phenotype correlation of R117H and the poly-T tract in CFTR.

Karen S Raraigh, Jessica R Balcom, Elinor Langfelder-Schwind

|Jan 08, 2024
Two rare variants that affect the same amino acid in CFTR have distinct responses to ivacaftor.

Hongyu Li, Mayuree Rodrat, Majid K Al-Salmani

|Jul 08, 2023
The utilization of genetic counselors by patient support groups.

Sadie Roulston, Karen Raraigh, Amy Malinowski

|Apr 22, 2022
DNA sequencing analysis of cystic fibrosis transmembrane conductance regulator gene identifies cystic fibrosis-associated variants in the Severe Asthma Research Program.

Manuel E Izquierdo, Chad R Marion, Wendy C Moore

|Dec 29, 2021
Genetic counseling access for parents of newborns who screen positive for cystic fibrosis: Consensus guidelines.

Elinor Langfelder-Schwind, Karen S Raraigh, Richard B Parad

|Oct 21, 2020
Evaluation of both exonic and intronic variants for effects on RNA splicing allows for accurate assessment of the effectiveness of precision therapies.

Anya T Joynt, Taylor A Evans, Matthew J Pellicore

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Frequent Collaborators

3 joint publications

Elinor Langfelder-Schwind

2 joint publications

Richard B Parad

2 joint publications

Gary R Cutting

1 joint publications

Sadie Roulston