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Jonathan L Haines

Showing results (41-50 of 537) with videos related to

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Neuroscience Letters|November 1, 2005
Mutations in GABRA1, GABRA5, GABRG2 and GABRD receptor genes are not a major factor in the pathogenesis of familial focal epilepsy preceded by febrile seizuresShaochun Ma, Bassel Abou-Khalil, Marcia A Blair, et al.
Neuroscience Letters|April 17, 2009
Resolving the relationship between ApolipoproteinE and depressionMichael A Slifer, Eden R Martin, John R Gilbert, et al.
Plos One|February 14, 2013
Enabling genomic-phenomic association discovery without sacrificing anonymityRaymond D Heatherly, Grigorios Loukides, Joshua C Denny, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|September 25, 2025
Spatial distribution of Intra-retinal Hyper-reflective foci and impact on progression in eyes with intermediate Age-related macular degenerationAditya Verma, Muneeswar G Nittala, Jonathan L Haines, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Opposing effects of SARS-CoV-2/COVID-19 infection and recombinant zoster vaccination on the risk of late-onset Alzheimer diseaseCarly M Rose, Shiying Liu, William S Bush, et al.
Epilepsia|March 11, 2004
Autosomal dominant lateral temporal epilepsy: two families with novel mutations in the LGI1 genePeter Hedera, Bassel Abou-Khalil, Amy E Crunk, et al.
Plos One|July 5, 2013
Correction: Enabling Genomic-Phenomic Association Discovery without Sacrificing AnonymityRaymond D Heatherly, Grigorios Loukides, Joshua C Denny, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|June 24, 2003
Exploratory subsetting of autism families based on savant skills improves evidence of genetic linkage to 15q11-q13Erika L Nurmi, Michael Dowd, Ovsanna Tadevosyan-Leyfer, et al.
Genetic Epidemiology|December 14, 2007
Confronting complexity in late-onset Alzheimer disease: application of two-stage analysis approach addressing heterogeneity and epistasisTricia A Thornton-Wells, Jason H Moore, Eden R Martin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 25, 2006
Familial essential tremor with apparent autosomal dominant inheritance: should we also consider other inheritance modes?Shaochun Ma, Thomas L Davis, Marcia A Blair, et al.
Pageof 54

Showing results (41-50 of 537) with videos related to

Sort By:
Pageof 54
Neuroscience Letters|November 1, 2005
Mutations in GABRA1, GABRA5, GABRG2 and GABRD receptor genes are not a major factor in the pathogenesis of familial focal epilepsy preceded by febrile seizuresShaochun Ma, Bassel Abou-Khalil, Marcia A Blair, et al.
Neuroscience Letters|April 17, 2009
Resolving the relationship between ApolipoproteinE and depressionMichael A Slifer, Eden R Martin, John R Gilbert, et al.
Plos One|February 14, 2013
Enabling genomic-phenomic association discovery without sacrificing anonymityRaymond D Heatherly, Grigorios Loukides, Joshua C Denny, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|September 25, 2025
Spatial distribution of Intra-retinal Hyper-reflective foci and impact on progression in eyes with intermediate Age-related macular degenerationAditya Verma, Muneeswar G Nittala, Jonathan L Haines, et al.
Medrxiv : the Preprint Server for Health Sciences|February 6, 2026
Opposing effects of SARS-CoV-2/COVID-19 infection and recombinant zoster vaccination on the risk of late-onset Alzheimer diseaseCarly M Rose, Shiying Liu, William S Bush, et al.
Epilepsia|March 11, 2004
Autosomal dominant lateral temporal epilepsy: two families with novel mutations in the LGI1 genePeter Hedera, Bassel Abou-Khalil, Amy E Crunk, et al.
Plos One|July 5, 2013
Correction: Enabling Genomic-Phenomic Association Discovery without Sacrificing AnonymityRaymond D Heatherly, Grigorios Loukides, Joshua C Denny, et al.
Journal of the American Academy of Child and Adolescent Psychiatry|June 24, 2003
Exploratory subsetting of autism families based on savant skills improves evidence of genetic linkage to 15q11-q13Erika L Nurmi, Michael Dowd, Ovsanna Tadevosyan-Leyfer, et al.
Genetic Epidemiology|December 14, 2007
Confronting complexity in late-onset Alzheimer disease: application of two-stage analysis approach addressing heterogeneity and epistasisTricia A Thornton-Wells, Jason H Moore, Eden R Martin, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 25, 2006
Familial essential tremor with apparent autosomal dominant inheritance: should we also consider other inheritance modes?Shaochun Ma, Thomas L Davis, Marcia A Blair, et al.
Pageof 54