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Showing results (931-940 of 1,126) with videos related to

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Nature Reviews. Drug Discovery|June 2, 2010
Voluntary exploratory data submissions to the US FDA and the EMA: experience and impactFederico M Goodsaid, Shashi Amur, Jiri Aubrecht, et al.
Journal of the National Cancer Institute|October 15, 2010
Cancer pharmacogenomics and pharmacoepidemiology: setting a research agenda to accelerate translationAndrew N Freedman, Leah B Sansbury, William D Figg, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|November 19, 2024
Lung allograft dysbiosis associates with immune response and primary graft dysfunctionNathaniel C Nelson, Kendrew K Wong, Ian J Mahoney, et al.
American Journal of Epidemiology|April 9, 2025
Defining methodologic and other core competencies for PhD-level training in epidemiologyHailey R Banack, Laura C Rosella, Stephanie Shiau, et al.
American Journal of Respiratory and Critical Care Medicine|February 15, 2024
Longitudinal Lower Airway Microbial Signatures of Acute Cellular Rejection in Lung TransplantationJake G Natalini, Kendrew K Wong, Nathaniel C Nelson, et al.
American Journal of Human Genetics|July 13, 2022
Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcificationsErik Rosenhahn, Thomas J O'Brien, Maha S Zaki, et al.
Genome Medicine|March 17, 2021
Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patientsHenrik Stranneheim, Kristina Lagerstedt-Robinson, Måns Magnusson, et al.
Nature Genetics|March 30, 2026
Biallelic variants in RNU2-2 cause a remarkably frequent developmental and epileptic encephalopathyAdam Jackson, Alexander J M Blakes, Bader Alhaddad, et al.
Clinical Pharmacology and Therapeutics|April 17, 2013
The Pharmacogenomics Research Network Translational Pharmacogenetics Program: overcoming challenges of real-world implementationA R Shuldiner, M V Relling, J F Peterson, et al.
Genome Medicine|March 31, 2026
The genomic medicine center Karolinska 10-year report on genome sequencing for rare diseases and a strategy for stepwise clinical implementationAnna Lindstrand, Kristina Lagerstedt-Robinson, Anders Jemt, et al.
Pageof 113

Showing results (931-940 of 1,126) with videos related to

Sort By:
Pageof 113
Nature Reviews. Drug Discovery|June 2, 2010
Voluntary exploratory data submissions to the US FDA and the EMA: experience and impactFederico M Goodsaid, Shashi Amur, Jiri Aubrecht, et al.
Journal of the National Cancer Institute|October 15, 2010
Cancer pharmacogenomics and pharmacoepidemiology: setting a research agenda to accelerate translationAndrew N Freedman, Leah B Sansbury, William D Figg, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|November 19, 2024
Lung allograft dysbiosis associates with immune response and primary graft dysfunctionNathaniel C Nelson, Kendrew K Wong, Ian J Mahoney, et al.
American Journal of Epidemiology|April 9, 2025
Defining methodologic and other core competencies for PhD-level training in epidemiologyHailey R Banack, Laura C Rosella, Stephanie Shiau, et al.
American Journal of Respiratory and Critical Care Medicine|February 15, 2024
Longitudinal Lower Airway Microbial Signatures of Acute Cellular Rejection in Lung TransplantationJake G Natalini, Kendrew K Wong, Nathaniel C Nelson, et al.
American Journal of Human Genetics|July 13, 2022
Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcificationsErik Rosenhahn, Thomas J O'Brien, Maha S Zaki, et al.
Genome Medicine|March 17, 2021
Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patientsHenrik Stranneheim, Kristina Lagerstedt-Robinson, Måns Magnusson, et al.
Nature Genetics|March 30, 2026
Biallelic variants in RNU2-2 cause a remarkably frequent developmental and epileptic encephalopathyAdam Jackson, Alexander J M Blakes, Bader Alhaddad, et al.
Clinical Pharmacology and Therapeutics|April 17, 2013
The Pharmacogenomics Research Network Translational Pharmacogenetics Program: overcoming challenges of real-world implementationA R Shuldiner, M V Relling, J F Peterson, et al.
Genome Medicine|March 31, 2026
The genomic medicine center Karolinska 10-year report on genome sequencing for rare diseases and a strategy for stepwise clinical implementationAnna Lindstrand, Kristina Lagerstedt-Robinson, Anders Jemt, et al.
Pageof 113