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Dan M Roden

Showing results (471-480 of 593) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|April 8, 2024
Interoperability of phenome-wide multimorbidity patterns: a comparative study of two large-scale EHR systemsNick Strayer, Tess Vessels, Karmel Choi, et al.
Blood|August 13, 2015
Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemiaSeth E Karol, Wenjian Yang, Sara L Van Driest, et al.
Journal of Pathology Informatics|November 26, 2015
Practical considerations in genomic decision support: The eMERGE experienceTimothy M Herr, Suzette J Bielinski, Erwin Bottinger, et al.
Plos One|December 2, 2014
Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE NetworkJennifer R Malinowski, Joshua C Denny, Suzette J Bielinski, et al.
Pharmacogenetics and Genomics|May 26, 2017
Genome-wide association and pathway analysis of left ventricular function after anthracycline exposure in adultsQuinn S Wells, Olivia J Veatch, Joshua P Fessel, et al.
Bioinformatics (Oxford, England)|November 6, 2023
Next-generation phenotyping: introducing phecodeX for enhanced discovery research in medical phenomicsMegan M Shuey, William W Stead, Ida Aka, et al.
Science (New York, N.Y.)|March 29, 2018
Phenotype risk scores identify patients with unrecognized Mendelian disease patternsLisa Bastarache, Jacob J Hughey, Scott Hebbring, et al.
Circulation. Genomic and Precision Medicine|April 18, 2023
Familial Hypercholesterolemia in the Electronic Medical Records and Genomics Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes After Return of ResultsOzan Dikilitas, Alborz Sherafati, Seyedmohammad Saadatagah, et al.
Circulation. Genomic and Precision Medicine|July 26, 2021
Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare <i>KCNH2</i> VariantsKrystian Kozek, Yuko Wada, Luca Sala, et al.
Circulation. Arrhythmia and Electrophysiology|July 9, 2021
Management of Congenital Long-QT Syndrome: Commentary From the ExpertsElizabeth S Kaufman, Lee L Eckhardt, Michael J Ackerman, et al.
Pageof 60

Showing results (471-480 of 593) with videos related to

Sort By:
Pageof 60
Medrxiv : the Preprint Server for Health Sciences|April 8, 2024
Interoperability of phenome-wide multimorbidity patterns: a comparative study of two large-scale EHR systemsNick Strayer, Tess Vessels, Karmel Choi, et al.
Blood|August 13, 2015
Genetics of glucocorticoid-associated osteonecrosis in children with acute lymphoblastic leukemiaSeth E Karol, Wenjian Yang, Sara L Van Driest, et al.
Journal of Pathology Informatics|November 26, 2015
Practical considerations in genomic decision support: The eMERGE experienceTimothy M Herr, Suzette J Bielinski, Erwin Bottinger, et al.
Plos One|December 2, 2014
Genetic variants associated with serum thyroid stimulating hormone (TSH) levels in European Americans and African Americans from the eMERGE NetworkJennifer R Malinowski, Joshua C Denny, Suzette J Bielinski, et al.
Pharmacogenetics and Genomics|May 26, 2017
Genome-wide association and pathway analysis of left ventricular function after anthracycline exposure in adultsQuinn S Wells, Olivia J Veatch, Joshua P Fessel, et al.
Bioinformatics (Oxford, England)|November 6, 2023
Next-generation phenotyping: introducing phecodeX for enhanced discovery research in medical phenomicsMegan M Shuey, William W Stead, Ida Aka, et al.
Science (New York, N.Y.)|March 29, 2018
Phenotype risk scores identify patients with unrecognized Mendelian disease patternsLisa Bastarache, Jacob J Hughey, Scott Hebbring, et al.
Circulation. Genomic and Precision Medicine|April 18, 2023
Familial Hypercholesterolemia in the Electronic Medical Records and Genomics Network: Prevalence, Penetrance, Cardiovascular Risk, and Outcomes After Return of ResultsOzan Dikilitas, Alborz Sherafati, Seyedmohammad Saadatagah, et al.
Circulation. Genomic and Precision Medicine|July 26, 2021
Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare <i>KCNH2</i> VariantsKrystian Kozek, Yuko Wada, Luca Sala, et al.
Circulation. Arrhythmia and Electrophysiology|July 9, 2021
Management of Congenital Long-QT Syndrome: Commentary From the ExpertsElizabeth S Kaufman, Lee L Eckhardt, Michael J Ackerman, et al.
Pageof 60