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Kyriacos Markianos

Showing results (21-30 of 41) with videos related to

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Scientific Reports|August 22, 2020
Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorderKlaus Schmitz-Abe, Guzman Sanchez-Schmitz, Ryan N Doan, et al.
Research Square|May 19, 2023
Multi-ancestry GWAS of Fuchs corneal dystrophy highlights roles of laminins, collagen, and endothelial cell regulationNeal Peachey, Bryan Gorman, Michael Francis, et al.
BMC Genomics|October 15, 2015
Association mapping by pooled sequencing identifies TOLL 11 as a protective factor against Plasmodium falciparum in Anopheles gambiaeSeth N Redmond, Karin Eiglmeier, Christian Mitri, et al.
Nature Communications|July 4, 2026
A large-scale multi-ancestry mitochondrial variant association analysis for cardiometabolic traitsJin J Zhou, Aubrey Jensen, David C Samuels, et al.
Neurology|August 27, 2013
Recessive truncating titin gene, TTN, mutations presenting as centronuclear myopathyOzge Ceyhan-Birsoy, Pankaj B Agrawal, Carlos Hidalgo, et al.
Blood|August 5, 2016
A recurring mutation in the respiratory complex 1 protein NDUFB11 is responsible for a novel form of X-linked sideroblastic anemiaDaniel A Lichtenstein, Andrew W Crispin, Anoop K Sendamarai, et al.
American Journal of Hematology|October 22, 2021
Congenital X-linked neutropenia with myelodysplasia and somatic tetraploidy due to a germline mutation in SEPT6Raffaele Renella, Katelyn Gagne, Ellen Beauchamp, et al.
Communications Biology|April 6, 2024
A multi-ancestry GWAS of Fuchs corneal dystrophy highlights the contributions of laminins, collagen, and endothelial cell regulationBryan R Gorman, Michael Francis, Cari L Nealon, et al.
Neurology|April 3, 2015
Loss of PCLO function underlies pontocerebellar hypoplasia type IIIMustafa Y Ahmed, Barry A Chioza, Anna Rajab, et al.
American Journal of Human Genetics|June 20, 2023
Autoimmune alleles at the major histocompatibility locus modify melanoma susceptibilityJames V Talwar, David Laub, Meghana S Pagadala, et al.
Pageof 5

Showing results (21-30 of 41) with videos related to

Sort By:
Pageof 5
Scientific Reports|August 22, 2020
Homozygous deletions implicate non-coding epigenetic marks in Autism spectrum disorderKlaus Schmitz-Abe, Guzman Sanchez-Schmitz, Ryan N Doan, et al.
Research Square|May 19, 2023
Multi-ancestry GWAS of Fuchs corneal dystrophy highlights roles of laminins, collagen, and endothelial cell regulationNeal Peachey, Bryan Gorman, Michael Francis, et al.
BMC Genomics|October 15, 2015
Association mapping by pooled sequencing identifies TOLL 11 as a protective factor against Plasmodium falciparum in Anopheles gambiaeSeth N Redmond, Karin Eiglmeier, Christian Mitri, et al.
Nature Communications|July 4, 2026
A large-scale multi-ancestry mitochondrial variant association analysis for cardiometabolic traitsJin J Zhou, Aubrey Jensen, David C Samuels, et al.
Neurology|August 27, 2013
Recessive truncating titin gene, TTN, mutations presenting as centronuclear myopathyOzge Ceyhan-Birsoy, Pankaj B Agrawal, Carlos Hidalgo, et al.
Blood|August 5, 2016
A recurring mutation in the respiratory complex 1 protein NDUFB11 is responsible for a novel form of X-linked sideroblastic anemiaDaniel A Lichtenstein, Andrew W Crispin, Anoop K Sendamarai, et al.
American Journal of Hematology|October 22, 2021
Congenital X-linked neutropenia with myelodysplasia and somatic tetraploidy due to a germline mutation in SEPT6Raffaele Renella, Katelyn Gagne, Ellen Beauchamp, et al.
Communications Biology|April 6, 2024
A multi-ancestry GWAS of Fuchs corneal dystrophy highlights the contributions of laminins, collagen, and endothelial cell regulationBryan R Gorman, Michael Francis, Cari L Nealon, et al.
Neurology|April 3, 2015
Loss of PCLO function underlies pontocerebellar hypoplasia type IIIMustafa Y Ahmed, Barry A Chioza, Anna Rajab, et al.
American Journal of Human Genetics|June 20, 2023
Autoimmune alleles at the major histocompatibility locus modify melanoma susceptibilityJames V Talwar, David Laub, Meghana S Pagadala, et al.
Pageof 5