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Carl A Anderson

Showing results (81-90 of 140) with videos related to

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Journal of Crohn'S & Colitis|September 30, 2023
Baseline Expression of Immune Gene Modules in Blood is Associated With Primary Response to Anti-TNF Therapy in Crohn's Disease PatientsBenjamin Y H Bai, Mark Reppell, Nizar Smaoui, et al.
Plos Genetics|December 4, 2018
Amino acid residues in five separate HLA genes can explain most of the known associations between the MHC and primary biliary cholangitisRebecca Darlay, Kristin L Ayers, George F Mells, et al.
Nature Genetics|March 15, 2022
Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for 12 immune-mediated diseasesKousik Kundu, Manuel Tardaguila, Alice L Mann, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 24, 2007
A genome-wide linkage study in families with major depression and co-morbid unexplained swellingCarl A Anderson, Alan Maclean, Matthew G Dunnigan, et al.
Nature Genetics|February 24, 2023
Network expansion of genetic associations defines a pleiotropy map of human cell biologyInigo Barrio-Hernandez, Jeremy Schwartzentruber, Anjali Shrivastava, et al.
Nature Communications|August 27, 2025
Splicing QTL mapping in stimulated macrophages associates low-usage splice junctions with immune-mediated disease riskOmar El Garwany, Nikolaos I Panousis, Andrew Knights, et al.
Science Immunology|November 2, 2019
Incomplete genetic reconstitution of B cell pools contributes to prolonged immunosuppression after measlesVelislava N Petrova, Bevan Sawatsky, Alvin X Han, et al.
Nature Genetics|January 10, 2017
Genome-wide association study identifies distinct genetic contributions to prognosis and susceptibility in Crohn's diseaseJames C Lee, Daniele Biasci, Rebecca Roberts, et al.
American Journal of Human Genetics|January 28, 2014
Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defectsKathleen A Williamson, Joe Rainger, James A B Floyd, et al.
Cell|July 23, 2020
Somatic Evolution in Non-neoplastic IBD-Affected ColonSigurgeir Olafsson, Rebecca E McIntyre, Tim Coorens, et al.
Pageof 14

Showing results (81-90 of 140) with videos related to

Sort By:
Pageof 14
Journal of Crohn'S & Colitis|September 30, 2023
Baseline Expression of Immune Gene Modules in Blood is Associated With Primary Response to Anti-TNF Therapy in Crohn's Disease PatientsBenjamin Y H Bai, Mark Reppell, Nizar Smaoui, et al.
Plos Genetics|December 4, 2018
Amino acid residues in five separate HLA genes can explain most of the known associations between the MHC and primary biliary cholangitisRebecca Darlay, Kristin L Ayers, George F Mells, et al.
Nature Genetics|March 15, 2022
Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for 12 immune-mediated diseasesKousik Kundu, Manuel Tardaguila, Alice L Mann, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 24, 2007
A genome-wide linkage study in families with major depression and co-morbid unexplained swellingCarl A Anderson, Alan Maclean, Matthew G Dunnigan, et al.
Nature Genetics|February 24, 2023
Network expansion of genetic associations defines a pleiotropy map of human cell biologyInigo Barrio-Hernandez, Jeremy Schwartzentruber, Anjali Shrivastava, et al.
Nature Communications|August 27, 2025
Splicing QTL mapping in stimulated macrophages associates low-usage splice junctions with immune-mediated disease riskOmar El Garwany, Nikolaos I Panousis, Andrew Knights, et al.
Science Immunology|November 2, 2019
Incomplete genetic reconstitution of B cell pools contributes to prolonged immunosuppression after measlesVelislava N Petrova, Bevan Sawatsky, Alvin X Han, et al.
Nature Genetics|January 10, 2017
Genome-wide association study identifies distinct genetic contributions to prognosis and susceptibility in Crohn's diseaseJames C Lee, Daniele Biasci, Rebecca Roberts, et al.
American Journal of Human Genetics|January 28, 2014
Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defectsKathleen A Williamson, Joe Rainger, James A B Floyd, et al.
Cell|July 23, 2020
Somatic Evolution in Non-neoplastic IBD-Affected ColonSigurgeir Olafsson, Rebecca E McIntyre, Tim Coorens, et al.
Pageof 14