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Vesna Lukic

Showing results (1-10 of 9) with videos related to

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Human Genetics|August 18, 2014
Using familial information for variant filtering in high-throughput sequencing studiesMelanie Bahlo, Rick Tankard, Vesna Lukic, et al.
Neurology. Genetics|April 12, 2016
In silico prioritization based on coexpression can aid epileptic encephalopathy gene discoveryKaren L Oliver, Vesna Lukic, Saskia Freytag, et al.
Plos One|July 12, 2014
Harnessing gene expression networks to prioritize candidate epileptic encephalopathy genesKaren L Oliver, Vesna Lukic, Natalie P Thorne, et al.
Anesthesiology|July 24, 2019
Genetic Analysis of Patients Who Experienced Awareness with Recall while under General AnesthesiaJamie W Sleigh, Kate Leslie, Andrew J Davidson, et al.
International Journal of Ophthalmology|September 19, 2018
Miroslav Stamenkovic, Vesna Lukic, Sonja Suvakov, et al.
American Journal of Medical Genetics. Part A|June 5, 2021
Expanding the clinical and radiological phenotypes of leukoencephalopathy due to biallelic HMBS mutationsChloe A Stutterd, Alexa Kidd, Chris Florkowski, et al.
Neurology. Genetics|April 12, 2016
Complete callosal agenesis, pontocerebellar hypoplasia, and axonal neuropathy due to AMPD2 lossAshley P L Marsh, Vesna Lukic, Kate Pope, et al.
Human Mutation|October 11, 2021
A family study implicates GBE1 in the etiology of autism spectrum disorderMiriam Fanjul-Fernández, Natasha J Brown, Peter Hickey, et al.
Nature Genetics|March 3, 2017
Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetranceAshley P L Marsh, Delphine Heron, Timothy J Edwards, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Human Genetics|August 18, 2014
Using familial information for variant filtering in high-throughput sequencing studiesMelanie Bahlo, Rick Tankard, Vesna Lukic, et al.
Neurology. Genetics|April 12, 2016
In silico prioritization based on coexpression can aid epileptic encephalopathy gene discoveryKaren L Oliver, Vesna Lukic, Saskia Freytag, et al.
Plos One|July 12, 2014
Harnessing gene expression networks to prioritize candidate epileptic encephalopathy genesKaren L Oliver, Vesna Lukic, Natalie P Thorne, et al.
Anesthesiology|July 24, 2019
Genetic Analysis of Patients Who Experienced Awareness with Recall while under General AnesthesiaJamie W Sleigh, Kate Leslie, Andrew J Davidson, et al.
International Journal of Ophthalmology|September 19, 2018
Miroslav Stamenkovic, Vesna Lukic, Sonja Suvakov, et al.
American Journal of Medical Genetics. Part A|June 5, 2021
Expanding the clinical and radiological phenotypes of leukoencephalopathy due to biallelic HMBS mutationsChloe A Stutterd, Alexa Kidd, Chris Florkowski, et al.
Neurology. Genetics|April 12, 2016
Complete callosal agenesis, pontocerebellar hypoplasia, and axonal neuropathy due to AMPD2 lossAshley P L Marsh, Vesna Lukic, Kate Pope, et al.
Human Mutation|October 11, 2021
A family study implicates GBE1 in the etiology of autism spectrum disorderMiriam Fanjul-Fernández, Natasha J Brown, Peter Hickey, et al.
Nature Genetics|March 3, 2017
Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetranceAshley P L Marsh, Delphine Heron, Timothy J Edwards, et al.
Pageof 1