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Pediatrics
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July 20, 2023
Parent-Reported Clinical Utility of Pediatric Genomic Sequencing
Hadley Stevens Smith, Bart S Ferket, Bruce D Gelb, et al.
Patient Education and Counseling
|
May 10, 2021
Burden or benefit? Effects of providing education about and the option to request additional genomic findings from diagnostic exome sequencing: A randomized controlled trial
Christine Rini, Myra I Roche, Feng-Chang Lin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 15, 2021
US private payers' perspectives on insurance coverage for genome sequencing versus exome sequencing: A study by the Clinical Sequencing Evidence-Generating Research Consortium (CSER)
Kathryn A Phillips, Julia R Trosman, Michael P Douglas, et al.
Plos One
|
December 18, 2018
Increasing the diagnostic yield of exome sequencing by copy number variant analysis
Daniel S Marchuk, Kristy Crooks, Natasha Strande, et al.
The Journal of Heart Valve Disease
|
May 16, 2018
Genetic Complexity of Mitral Valve Prolapse Revealed by Clinical and Genetic Evaluation of a Large Family
Gloria T Haskell, Brian C Jensen, Cecile Skrzynia, et al.
Schizophrenia Bulletin Open
|
October 6, 2025
Obstacles, Opportunities, and Ethical Considerations for Genomic Investigations of Individuals Continuously Hospitalized with Treatment-resistant Schizophrenia
Richard C Josiassen, Rose Mary Xavier, Tyler E Dietterich, et al.
American Journal of Medical Genetics. Part A
|
April 30, 2015
The phenotype of multiple congenital anomalies-hypotonia-seizures syndrome 1: report and review
Natario L Couser, Maheer M Masood, Natasha T Strande, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry
|
August 1, 2025
Delineating lifetime multimorbidity associated with 16p13.11 duplication: A literature review, meta-analysis, and case study
Rose Mary Xavier, Wenxin Bian, Fadhah Alshammari, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
July 21, 2024
Advancing Genetic Testing in Kidney Diseases: Report From a National Kidney Foundation Working Group
Nora Franceschini, David L Feldman, Jonathan S Berg, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 20, 2020
Correction: An approach to integrating exome sequencing for fetal structural anomalies into clinical practice
Neeta L Vora, Kelly Gilmore, Alicia Brandt, et al.
Page
of 17
Search research articles
Search
Showing results (81-90 of 168) with videos related to
Sort By:
Page
of 17
Pediatrics
|
July 20, 2023
Parent-Reported Clinical Utility of Pediatric Genomic Sequencing
Hadley Stevens Smith, Bart S Ferket, Bruce D Gelb, et al.
Patient Education and Counseling
|
May 10, 2021
Burden or benefit? Effects of providing education about and the option to request additional genomic findings from diagnostic exome sequencing: A randomized controlled trial
Christine Rini, Myra I Roche, Feng-Chang Lin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 15, 2021
US private payers' perspectives on insurance coverage for genome sequencing versus exome sequencing: A study by the Clinical Sequencing Evidence-Generating Research Consortium (CSER)
Kathryn A Phillips, Julia R Trosman, Michael P Douglas, et al.
Plos One
|
December 18, 2018
Increasing the diagnostic yield of exome sequencing by copy number variant analysis
Daniel S Marchuk, Kristy Crooks, Natasha Strande, et al.
The Journal of Heart Valve Disease
|
May 16, 2018
Genetic Complexity of Mitral Valve Prolapse Revealed by Clinical and Genetic Evaluation of a Large Family
Gloria T Haskell, Brian C Jensen, Cecile Skrzynia, et al.
Schizophrenia Bulletin Open
|
October 6, 2025
Obstacles, Opportunities, and Ethical Considerations for Genomic Investigations of Individuals Continuously Hospitalized with Treatment-resistant Schizophrenia
Richard C Josiassen, Rose Mary Xavier, Tyler E Dietterich, et al.
American Journal of Medical Genetics. Part A
|
April 30, 2015
The phenotype of multiple congenital anomalies-hypotonia-seizures syndrome 1: report and review
Natario L Couser, Maheer M Masood, Natasha T Strande, et al.
Progress in Neuro-Psychopharmacology & Biological Psychiatry
|
August 1, 2025
Delineating lifetime multimorbidity associated with 16p13.11 duplication: A literature review, meta-analysis, and case study
Rose Mary Xavier, Wenxin Bian, Fadhah Alshammari, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation
|
July 21, 2024
Advancing Genetic Testing in Kidney Diseases: Report From a National Kidney Foundation Working Group
Nora Franceschini, David L Feldman, Jonathan S Berg, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 20, 2020
Correction: An approach to integrating exome sequencing for fetal structural anomalies into clinical practice
Neeta L Vora, Kelly Gilmore, Alicia Brandt, et al.
Page
of 17