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Patient Education and Counseling
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November 2, 2020
Testing a best practices risk result format to communicate genetic risks
Kyle W Davis, Debra L Roter, Tara Schmidlen, et al.
Plos One
|
October 20, 2023
An integrated framework for examining groundwater vulnerability in the Mekong River Delta region
Kathryn A Powlen, Saira Haider, Kyle W Davis, et al.
Glia
|
October 4, 2016
Differential Kv1.3, KCa3.1, and Kir2.1 expression in "classically" and "alternatively" activated microglia
Hai M Nguyen, Eva M Grössinger, Makoto Horiuchi, et al.
International Journal of Molecular Sciences
|
March 27, 2019
Parent-of-Origin Effects in 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) Syndrome
Kyle W Davis, Moises Serrano, Sara Loddo, et al.
Scientific Reports
|
April 1, 2022
NeuroSCORE is a genome-wide omics-based model that identifies candidate disease genes of the central nervous system
Kyle W Davis, Colleen G Bilancia, Megan Martin, et al.
Neurology. Genetics
|
February 12, 2020
Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disorders
E Robert Wassman, Karen S Ho, Diana Bertrand, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 3, 2023
The landscape of reported VUS in multi-gene panel and genomic testing: Time for a change
Heidi L Rehm, Joseph T Alaimo, Swaroop Aradhya, et al.
American Journal of Human Genetics
|
March 24, 2026
The Electronic Medical Records and Genomics study: Design and analytic framework for assessing the impact of genome-informed risk assessments
Nita Limdi, T Mark Beasley, Josh Cortopassi, et al.
American Journal of Human Genetics
|
March 24, 2026
Return of genome-informed risk-assessment results for common conditions to 23,840 adults and children: An eMERGE network study
Lucinda P Lawson, Cynthia A Prows, Josh Cortopassi, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Patient Education and Counseling
|
November 2, 2020
Testing a best practices risk result format to communicate genetic risks
Kyle W Davis, Debra L Roter, Tara Schmidlen, et al.
Plos One
|
October 20, 2023
An integrated framework for examining groundwater vulnerability in the Mekong River Delta region
Kathryn A Powlen, Saira Haider, Kyle W Davis, et al.
Glia
|
October 4, 2016
Differential Kv1.3, KCa3.1, and Kir2.1 expression in "classically" and "alternatively" activated microglia
Hai M Nguyen, Eva M Grössinger, Makoto Horiuchi, et al.
International Journal of Molecular Sciences
|
March 27, 2019
Parent-of-Origin Effects in 15q11.2 BP1-BP2 Microdeletion (Burnside-Butler) Syndrome
Kyle W Davis, Moises Serrano, Sara Loddo, et al.
Scientific Reports
|
April 1, 2022
NeuroSCORE is a genome-wide omics-based model that identifies candidate disease genes of the central nervous system
Kyle W Davis, Colleen G Bilancia, Megan Martin, et al.
Neurology. Genetics
|
February 12, 2020
Critical exon indexing improves clinical interpretation of copy number variants in neurodevelopmental disorders
E Robert Wassman, Karen S Ho, Diana Bertrand, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 3, 2023
The landscape of reported VUS in multi-gene panel and genomic testing: Time for a change
Heidi L Rehm, Joseph T Alaimo, Swaroop Aradhya, et al.
American Journal of Human Genetics
|
March 24, 2026
The Electronic Medical Records and Genomics study: Design and analytic framework for assessing the impact of genome-informed risk assessments
Nita Limdi, T Mark Beasley, Josh Cortopassi, et al.
American Journal of Human Genetics
|
March 24, 2026
Return of genome-informed risk-assessment results for common conditions to 23,840 adults and children: An eMERGE network study
Lucinda P Lawson, Cynthia A Prows, Josh Cortopassi, et al.
Page
of 1