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Journal of Genetic Counseling
|
October 19, 2021
Do research participants share genomic screening results with family members?
Julia Wynn, Hila Milo Rasouly, Tania Vasquez-Loarte, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 2, 2019
Correction: Evaluation of the cost and effectiveness of diverse recruitment methods for a genetic screening study
Hila Milo Rasouly, Julia Wynn, Maddalena Marasa, et al.
JAMA Oncology
|
April 21, 2022
Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple Diseases
Chenjie Zeng, Lisa A Bastarache, Ran Tao, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 2, 2019
Evaluation of the cost and effectiveness of diverse recruitment methods for a genetic screening study
Hila Milo Rasouly, Julia Wynn, Maddalena Marasa, et al.
Human Molecular Genetics
|
December 4, 2020
Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice
Ella M M A Martin, Annabelle Enriquez, Duncan B Sparrow, et al.
NPJ Digital Medicine
|
April 14, 2021
Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies
Ning Shang, Atlas Khan, Fernanda Polubriaginof, et al.
American Journal of Human Genetics
|
August 4, 2015
Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development
Asaf Vivante, Marc-Jens Kleppa, Julian Schulz, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
November 14, 2018
CureGN Study Rationale, Design, and Methods: Establishing a Large Prospective Observational Study of Glomerular Disease
Laura H Mariani, Andrew S Bomback, Pietro A Canetta, et al.
Nature Medicine
|
June 17, 2022
Genome-wide polygenic score to predict chronic kidney disease across ancestries
Atlas Khan, Michael C Turchin, Amit Patki, et al.
Cerebellum (London, England)
|
November 11, 2025
Correction: The Natural History Study and Biomarker Collection of the Clinical Research Consortium for the Study of Cerebellar Ataxia (CRC-SCA)
Yicheng Lin, Nadia Amokrane, Sandie Worley, et al.
Page
of 58
Search research articles
Search
Showing results (521-530 of 574) with videos related to
Sort By:
Page
of 58
Journal of Genetic Counseling
|
October 19, 2021
Do research participants share genomic screening results with family members?
Julia Wynn, Hila Milo Rasouly, Tania Vasquez-Loarte, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 2, 2019
Correction: Evaluation of the cost and effectiveness of diverse recruitment methods for a genetic screening study
Hila Milo Rasouly, Julia Wynn, Maddalena Marasa, et al.
JAMA Oncology
|
April 21, 2022
Association of Pathogenic Variants in Hereditary Cancer Genes With Multiple Diseases
Chenjie Zeng, Lisa A Bastarache, Ran Tao, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 2, 2019
Evaluation of the cost and effectiveness of diverse recruitment methods for a genetic screening study
Hila Milo Rasouly, Julia Wynn, Maddalena Marasa, et al.
Human Molecular Genetics
|
December 4, 2020
Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice
Ella M M A Martin, Annabelle Enriquez, Duncan B Sparrow, et al.
NPJ Digital Medicine
|
April 14, 2021
Medical records-based chronic kidney disease phenotype for clinical care and "big data" observational and genetic studies
Ning Shang, Atlas Khan, Fernanda Polubriaginof, et al.
American Journal of Human Genetics
|
August 4, 2015
Mutations in TBX18 Cause Dominant Urinary Tract Malformations via Transcriptional Dysregulation of Ureter Development
Asaf Vivante, Marc-Jens Kleppa, Julian Schulz, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
November 14, 2018
CureGN Study Rationale, Design, and Methods: Establishing a Large Prospective Observational Study of Glomerular Disease
Laura H Mariani, Andrew S Bomback, Pietro A Canetta, et al.
Nature Medicine
|
June 17, 2022
Genome-wide polygenic score to predict chronic kidney disease across ancestries
Atlas Khan, Michael C Turchin, Amit Patki, et al.
Cerebellum (London, England)
|
November 11, 2025
Correction: The Natural History Study and Biomarker Collection of the Clinical Research Consortium for the Study of Cerebellar Ataxia (CRC-SCA)
Yicheng Lin, Nadia Amokrane, Sandie Worley, et al.
Page
of 58