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Keren J Carss

Showing results (1-10 of 35) with videos related to

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BMC Genomics|August 23, 2012
Genomic variation in the vomeronasal receptor gene repertoires of inbred miceElizabeth H Wynn, Gabriela Sánchez-Andrade, Keren J Carss, et al.
Journal of Clinical Medicine|August 4, 2015
Exome Sequencing in Fetuses with Structural MalformationsFiona L Mackie, Keren J Carss, Sarah C Hillman, et al.
Human Molecular Genetics|January 31, 2014
Exome sequencing improves genetic diagnosis of structural fetal abnormalities revealed by ultrasoundKeren J Carss, Sarah C Hillman, Vijaya Parthiban, et al.
Ophthalmic Genetics|November 20, 2018
Whole genome sequencing reveals novel mutations causing autosomal dominant inherited macular degenerationShyamanga Borooah, Chloe M Stanton, Joseph Marsh, et al.
Frontiers in Genetics|July 19, 2019
Rare Genetic Variation in 135 Families With Family History Suggestive of X-Linked Intellectual DisabilityAlba Sanchis-Juan, Christina Bitsara, Kay Yi Low, et al.
Molecular Genetics & Genomic Medicine|April 30, 2020
Structural analysis of pathogenic missense mutations in GABRA2 and identification of a novel de novo variant in the desensitization gateAlba Sanchis-Juan, Marcia A Hasenahuer, James A Baker, et al.
JAMA Cardiology|December 16, 2020
Assessing the Role of Rare Genetic Variation in Patients With Heart FailureGundula Povysil, Olympe Chazara, Keren J Carss, et al.
Molecular Vision|September 14, 2018
Novel homozygous splicing mutations in Alessia Fiorentino, Jing Yu, Gavin Arno, et al.
Nature Reviews. Drug Discovery|October 19, 2022
Using human genetics to improve safety assessment of therapeuticsKeren J Carss, Aimee M Deaton, Alberto Del Rio-Espinola, et al.
Retina (Philadelphia, Pa.)|February 25, 2017
DETAILED RETINAL IMAGING IN CARRIERS OF OCULAR ALBINISMKamron N Khan, Emma C Lord, Gavin Arno, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
BMC Genomics|August 23, 2012
Genomic variation in the vomeronasal receptor gene repertoires of inbred miceElizabeth H Wynn, Gabriela Sánchez-Andrade, Keren J Carss, et al.
Journal of Clinical Medicine|August 4, 2015
Exome Sequencing in Fetuses with Structural MalformationsFiona L Mackie, Keren J Carss, Sarah C Hillman, et al.
Human Molecular Genetics|January 31, 2014
Exome sequencing improves genetic diagnosis of structural fetal abnormalities revealed by ultrasoundKeren J Carss, Sarah C Hillman, Vijaya Parthiban, et al.
Ophthalmic Genetics|November 20, 2018
Whole genome sequencing reveals novel mutations causing autosomal dominant inherited macular degenerationShyamanga Borooah, Chloe M Stanton, Joseph Marsh, et al.
Frontiers in Genetics|July 19, 2019
Rare Genetic Variation in 135 Families With Family History Suggestive of X-Linked Intellectual DisabilityAlba Sanchis-Juan, Christina Bitsara, Kay Yi Low, et al.
Molecular Genetics & Genomic Medicine|April 30, 2020
Structural analysis of pathogenic missense mutations in GABRA2 and identification of a novel de novo variant in the desensitization gateAlba Sanchis-Juan, Marcia A Hasenahuer, James A Baker, et al.
JAMA Cardiology|December 16, 2020
Assessing the Role of Rare Genetic Variation in Patients With Heart FailureGundula Povysil, Olympe Chazara, Keren J Carss, et al.
Molecular Vision|September 14, 2018
Novel homozygous splicing mutations in Alessia Fiorentino, Jing Yu, Gavin Arno, et al.
Nature Reviews. Drug Discovery|October 19, 2022
Using human genetics to improve safety assessment of therapeuticsKeren J Carss, Aimee M Deaton, Alberto Del Rio-Espinola, et al.
Retina (Philadelphia, Pa.)|February 25, 2017
DETAILED RETINAL IMAGING IN CARRIERS OF OCULAR ALBINISMKamron N Khan, Emma C Lord, Gavin Arno, et al.
Pageof 4