Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

I Jones

Showing results (701-710 of 752) with videos related to

Pageof 76
Sort By:
Psychological Medicine|November 22, 2016
The impact of education, country, race and ethnicity on the self-report of postpartum depression using the Edinburgh Postnatal Depression ScaleA Di Florio, K Putnam, M Altemus, et al.
European Heart Journal|October 24, 2023
Outcomes of transcatheter pulmonary SAPIEN 3 valve implantation: an international registrySebastien Hascoët, James R Bentham, Luca Giugno, et al.
Nature Communications|May 11, 2026
Endocrine therapy reprogramming of breast cancer facilitates metastatic escape via upregulation of P-Rex1/Rac1 signallingKristine J Fernandez, Ghazal Sultani, Max Nobis, et al.
Molecular Psychiatry|November 13, 2013
Evidence that duplications of 22q11.2 protect against schizophreniaE Rees, G Kirov, A Sanders, et al.
Translational Psychiatry|January 11, 2017
Evidence for genetic heterogeneity between clinical subtypes of bipolar disorderA W Charney, D M Ruderfer, E A Stahl, et al.
Molecular Psychiatry|October 28, 2015
Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorderJ Song, S E Bergen, A Di Florio, et al.
Revista Espanola De Cardiologia (English Ed.)|October 2, 2025
Outcomes of transcatheter patent ductus arteriosus closure in infants weighing 2 to 6 kgSophie Malekzadeh-Milani, Paul Padovani, Kothandam Sivakumar, et al.
Molecular Genetics and Metabolism Reports|March 10, 2017
Dietary practices in isovaleric acidemia: A European surveyA Pinto, A Daly, S Evans, et al.
Molecular Genetics and Metabolism Reports|October 13, 2017
Dietary practices in propionic acidemia: A European surveyA Daly, A Pinto, S Evans, et al.
Nature Genetics|May 27, 2017
Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndromeNatalie D Shaw, Harrison Brand, Zachary A Kupchinsky, et al.
Pageof 76

Showing results (701-710 of 752) with videos related to

Sort By:
Pageof 76
Psychological Medicine|November 22, 2016
The impact of education, country, race and ethnicity on the self-report of postpartum depression using the Edinburgh Postnatal Depression ScaleA Di Florio, K Putnam, M Altemus, et al.
European Heart Journal|October 24, 2023
Outcomes of transcatheter pulmonary SAPIEN 3 valve implantation: an international registrySebastien Hascoët, James R Bentham, Luca Giugno, et al.
Nature Communications|May 11, 2026
Endocrine therapy reprogramming of breast cancer facilitates metastatic escape via upregulation of P-Rex1/Rac1 signallingKristine J Fernandez, Ghazal Sultani, Max Nobis, et al.
Molecular Psychiatry|November 13, 2013
Evidence that duplications of 22q11.2 protect against schizophreniaE Rees, G Kirov, A Sanders, et al.
Translational Psychiatry|January 11, 2017
Evidence for genetic heterogeneity between clinical subtypes of bipolar disorderA W Charney, D M Ruderfer, E A Stahl, et al.
Molecular Psychiatry|October 28, 2015
Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorderJ Song, S E Bergen, A Di Florio, et al.
Revista Espanola De Cardiologia (English Ed.)|October 2, 2025
Outcomes of transcatheter patent ductus arteriosus closure in infants weighing 2 to 6 kgSophie Malekzadeh-Milani, Paul Padovani, Kothandam Sivakumar, et al.
Molecular Genetics and Metabolism Reports|March 10, 2017
Dietary practices in isovaleric acidemia: A European surveyA Pinto, A Daly, S Evans, et al.
Molecular Genetics and Metabolism Reports|October 13, 2017
Dietary practices in propionic acidemia: A European surveyA Daly, A Pinto, S Evans, et al.
Nature Genetics|May 27, 2017
Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndromeNatalie D Shaw, Harrison Brand, Zachary A Kupchinsky, et al.
Pageof 76