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Lyn R Griffiths

Showing results (101-110 of 261) with videos related to

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Scientific Reports|December 16, 2015
The Influence of OLR1 and PCSK9 Gene Polymorphisms on Ischemic Stroke: Evidence from a Meta-AnalysisAnthony Au, Lyn R Griffiths, Kian-Kai Cheng, et al.
Headache|April 9, 2014
Investigation of brain-derived neurotrophic factor (BDNF) gene variants in migraineHeidi G Sutherland, Bridget H Maher, Astrid J Rodriguez-Acevedo, et al.
Meta Gene|January 22, 2015
Genetic polymorphisms in miRNAs targeting the estrogen receptor and their effect on breast cancer riskGiang T Nguyen-Dien, Robert A Smith, Larisa M Haupt, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 25, 2003
Prospects for whole genome linkage disequilibrium mapping in domestic dog breedsChangbaig Hyun, Lucio J Filippich, Rod A Lea, et al.
Genomics|April 8, 2026
Identification of case-specific copy number variants reveals novel genetic insights into familial hemiplegic migraine pathogenesisMohammed M Alfayyadh, Thais Zielke, Neven Maksemous, et al.
BMC Genomics|June 3, 2014
In silico analyses reveal common cellular pathways affected by loss of heterozygosity (LOH) events in the lymphomagenesis of Non-Hodgkin's lymphoma (NHL)Carlos Aya-Bonilla, Emily Camilleri, Larisa M Haupt, et al.
Neurobiology of Stress|February 3, 2025
Shared genetic risk and causal associations between Post-traumatic stress disorder and migraine with antithrombotic agents and other medicationsCharlotte K Bainomugisa, , Dagmar Bruenig, et al.
The Journal of Headache and Pain|October 28, 2011
Variants in the human potassium channel gene (KCNN3) are associated with migraine in a high risk genetic isolateHannah C Cox, Rod A Lea, Claire Bellis, et al.
Clinical & Experimental Ophthalmology|June 3, 2011
Prevalence and predictors of refractive error in a genetically isolated population: the Norfolk Island Eye StudyJustin C Sherwin, John Kelly, Alex W Hewitt, et al.
BMC Cancer|May 14, 2010
A new method to detect loss of heterozygosity using cohort heterozygosity comparisonsMichael R Green, Paul Jardine, Peter Wood, et al.
Pageof 27

Showing results (101-110 of 261) with videos related to

Sort By:
Pageof 27
Scientific Reports|December 16, 2015
The Influence of OLR1 and PCSK9 Gene Polymorphisms on Ischemic Stroke: Evidence from a Meta-AnalysisAnthony Au, Lyn R Griffiths, Kian-Kai Cheng, et al.
Headache|April 9, 2014
Investigation of brain-derived neurotrophic factor (BDNF) gene variants in migraineHeidi G Sutherland, Bridget H Maher, Astrid J Rodriguez-Acevedo, et al.
Meta Gene|January 22, 2015
Genetic polymorphisms in miRNAs targeting the estrogen receptor and their effect on breast cancer riskGiang T Nguyen-Dien, Robert A Smith, Larisa M Haupt, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 25, 2003
Prospects for whole genome linkage disequilibrium mapping in domestic dog breedsChangbaig Hyun, Lucio J Filippich, Rod A Lea, et al.
Genomics|April 8, 2026
Identification of case-specific copy number variants reveals novel genetic insights into familial hemiplegic migraine pathogenesisMohammed M Alfayyadh, Thais Zielke, Neven Maksemous, et al.
BMC Genomics|June 3, 2014
In silico analyses reveal common cellular pathways affected by loss of heterozygosity (LOH) events in the lymphomagenesis of Non-Hodgkin's lymphoma (NHL)Carlos Aya-Bonilla, Emily Camilleri, Larisa M Haupt, et al.
Neurobiology of Stress|February 3, 2025
Shared genetic risk and causal associations between Post-traumatic stress disorder and migraine with antithrombotic agents and other medicationsCharlotte K Bainomugisa, , Dagmar Bruenig, et al.
The Journal of Headache and Pain|October 28, 2011
Variants in the human potassium channel gene (KCNN3) are associated with migraine in a high risk genetic isolateHannah C Cox, Rod A Lea, Claire Bellis, et al.
Clinical & Experimental Ophthalmology|June 3, 2011
Prevalence and predictors of refractive error in a genetically isolated population: the Norfolk Island Eye StudyJustin C Sherwin, John Kelly, Alex W Hewitt, et al.
BMC Cancer|May 14, 2010
A new method to detect loss of heterozygosity using cohort heterozygosity comparisonsMichael R Green, Paul Jardine, Peter Wood, et al.
Pageof 27