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Research Square
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April 27, 2026
Precision Medicine in Rural Settings: Patient Perspectives on Clinician-Ordered Genetic Testing
Anne C Madeo, Kimberly A Kaphingst, Melissa Yack, et al.
Research Square
|
July 3, 2026
Precision Medicine in Rural Settings: Clinician Perspectives on Clinician-Ordered Genetic Testing
Anne C Madeo, Kimberly A Kaphingst, Melissa Yack, et al.
Human Molecular Genetics
|
October 24, 2002
Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28
Linda M Peters, David W Anderson, Andrew J Griffith, et al.
Archives of Otolaryngology--Head & Neck Surgery
|
May 18, 2005
Investigation of the role of congenital cytomegalovirus infection in the etiology of enlarged vestibular aqueducts
Shannon P Pryor, Gail J Demmler, Anne C Madeo, et al.
American Journal of Medical Genetics. Part A
|
June 15, 2007
Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain
Tomoko Makishima, Anne C Madeo, Carmen C Brewer, et al.
The New England Journal of Medicine
|
April 15, 2005
Modification of human hearing loss by plasma-membrane calcium pump PMCA2
Julie M Schultz, Yandan Yang, Ariel J Caride, et al.
The Laryngoscope
|
December 10, 2009
SLC26A4 genotype, but not cochlear radiologic structure, is correlated with hearing loss in ears with an enlarged vestibular aqueduct
Kelly A King, Byung Yoon Choi, Christopher Zalewski, et al.
JAMA Otolaryngology-- Head & Neck Surgery
|
September 21, 2013
Use of SLC26A4 mutation testing for unilateral enlargement of the vestibular aqueduct
Parna Chattaraj, Fabian R Reimold, Julie A Muskett, et al.
JCO Clinical Cancer Informatics
|
March 9, 2026
Cascade Chatbot: A Scalable Approach to Family-Based Genetic Testing for Hereditary Cancer Syndromes
Lauren B Davis Rivera, Lauren Mitchell, Muhammad Danyal Ahsan, et al.
JCO Oncology Practice
|
March 17, 2026
Economic Evaluation of GARDE: A Digital Health Platform for Population-Level Hereditary Cancer Risk Assessment
Muhammad Danyal Ahsan, Kimberly A Kaphingst, Wendy K Kohlmann, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 24) with videos related to
Sort By:
Page
of 3
Research Square
|
April 27, 2026
Precision Medicine in Rural Settings: Patient Perspectives on Clinician-Ordered Genetic Testing
Anne C Madeo, Kimberly A Kaphingst, Melissa Yack, et al.
Research Square
|
July 3, 2026
Precision Medicine in Rural Settings: Clinician Perspectives on Clinician-Ordered Genetic Testing
Anne C Madeo, Kimberly A Kaphingst, Melissa Yack, et al.
Human Molecular Genetics
|
October 24, 2002
Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28
Linda M Peters, David W Anderson, Andrew J Griffith, et al.
Archives of Otolaryngology--Head & Neck Surgery
|
May 18, 2005
Investigation of the role of congenital cytomegalovirus infection in the etiology of enlarged vestibular aqueducts
Shannon P Pryor, Gail J Demmler, Anne C Madeo, et al.
American Journal of Medical Genetics. Part A
|
June 15, 2007
Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain
Tomoko Makishima, Anne C Madeo, Carmen C Brewer, et al.
The New England Journal of Medicine
|
April 15, 2005
Modification of human hearing loss by plasma-membrane calcium pump PMCA2
Julie M Schultz, Yandan Yang, Ariel J Caride, et al.
The Laryngoscope
|
December 10, 2009
SLC26A4 genotype, but not cochlear radiologic structure, is correlated with hearing loss in ears with an enlarged vestibular aqueduct
Kelly A King, Byung Yoon Choi, Christopher Zalewski, et al.
JAMA Otolaryngology-- Head & Neck Surgery
|
September 21, 2013
Use of SLC26A4 mutation testing for unilateral enlargement of the vestibular aqueduct
Parna Chattaraj, Fabian R Reimold, Julie A Muskett, et al.
JCO Clinical Cancer Informatics
|
March 9, 2026
Cascade Chatbot: A Scalable Approach to Family-Based Genetic Testing for Hereditary Cancer Syndromes
Lauren B Davis Rivera, Lauren Mitchell, Muhammad Danyal Ahsan, et al.
JCO Oncology Practice
|
March 17, 2026
Economic Evaluation of GARDE: A Digital Health Platform for Population-Level Hereditary Cancer Risk Assessment
Muhammad Danyal Ahsan, Kimberly A Kaphingst, Wendy K Kohlmann, et al.
Page
of 3