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Showing results (411-420 of 449) with videos related to

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JAMA Network Open|October 18, 2024
Diet and Survival in Black Women With Epithelial Ovarian CancerTsion A Armidie, Elisa V Bandera, Courtney E Johnson, et al.
Molecular Vision|June 19, 2014
Novel compound heterozygous NMNAT1 variants associated with Leber congenital amaurosisAnna M Siemiatkowska, L Ingeborgh van den Born, Maria M van Genderen, et al.
Human Mutation|August 19, 2021
PRPH2 mutation update: In silico assessment of 245 reported and 7 novel variants in patients with retinal diseaseManon H C A Peeters, Mubeen Khan, Anoek A M B Rooijakkers, et al.
American Journal of Epidemiology|July 30, 2025
Neighborhood disorder and ovarian cancer survival in black womenChristopher Pierson, Stephen J Mooney, Andrew Lawson, et al.
American Journal of Human Genetics|June 3, 2017
Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVREvangelia S Panagiotou, Carla Sanjurjo Soriano, James A Poulter, et al.
Ophthalmology|March 19, 2013
Maternal uniparental isodisomy of chromosome 6 reveals a TULP1 mutation as a novel cause of cone dysfunctionSusanne Roosing, L Ingeborgh van den Born, Carel B Hoyng, et al.
American Journal of Human Genetics|February 18, 2010
Next-generation sequencing of a 40 Mb linkage interval reveals TSPAN12 mutations in patients with familial exudative vitreoretinopathyKonstantinos Nikopoulos, Christian Gilissen, Alexander Hoischen, et al.
American Journal of Human Genetics|August 13, 2011
Exome sequencing and cis-regulatory mapping identify mutations in MAK, a gene encoding a regulator of ciliary length, as a cause of retinitis pigmentosaRıza Köksal Ozgül, Anna M Siemiatkowska, Didem Yücel, et al.
Cancer|January 3, 2025
Comorbid conditions and survival among Black women with ovarian cancerAlicia R Richards, Courtney E Johnson, Nachalie Ramos Montalvo, et al.
JAMA|July 17, 2024
Endometriosis Typology and Ovarian Cancer RiskMollie E Barnard, Leslie V Farland, Bin Yan, et al.
Pageof 45

Showing results (411-420 of 449) with videos related to

Sort By:
Pageof 45
JAMA Network Open|October 18, 2024
Diet and Survival in Black Women With Epithelial Ovarian CancerTsion A Armidie, Elisa V Bandera, Courtney E Johnson, et al.
Molecular Vision|June 19, 2014
Novel compound heterozygous NMNAT1 variants associated with Leber congenital amaurosisAnna M Siemiatkowska, L Ingeborgh van den Born, Maria M van Genderen, et al.
Human Mutation|August 19, 2021
PRPH2 mutation update: In silico assessment of 245 reported and 7 novel variants in patients with retinal diseaseManon H C A Peeters, Mubeen Khan, Anoek A M B Rooijakkers, et al.
American Journal of Epidemiology|July 30, 2025
Neighborhood disorder and ovarian cancer survival in black womenChristopher Pierson, Stephen J Mooney, Andrew Lawson, et al.
American Journal of Human Genetics|June 3, 2017
Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVREvangelia S Panagiotou, Carla Sanjurjo Soriano, James A Poulter, et al.
Ophthalmology|March 19, 2013
Maternal uniparental isodisomy of chromosome 6 reveals a TULP1 mutation as a novel cause of cone dysfunctionSusanne Roosing, L Ingeborgh van den Born, Carel B Hoyng, et al.
American Journal of Human Genetics|February 18, 2010
Next-generation sequencing of a 40 Mb linkage interval reveals TSPAN12 mutations in patients with familial exudative vitreoretinopathyKonstantinos Nikopoulos, Christian Gilissen, Alexander Hoischen, et al.
American Journal of Human Genetics|August 13, 2011
Exome sequencing and cis-regulatory mapping identify mutations in MAK, a gene encoding a regulator of ciliary length, as a cause of retinitis pigmentosaRıza Köksal Ozgül, Anna M Siemiatkowska, Didem Yücel, et al.
Cancer|January 3, 2025
Comorbid conditions and survival among Black women with ovarian cancerAlicia R Richards, Courtney E Johnson, Nachalie Ramos Montalvo, et al.
JAMA|July 17, 2024
Endometriosis Typology and Ovarian Cancer RiskMollie E Barnard, Leslie V Farland, Bin Yan, et al.
Pageof 45