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Lisa F Barcellos

Showing results (111-120 of 150) with videos related to

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Multiple Sclerosis (Houndmills, Basingstoke, England)|January 10, 2022
Gene-environment interactions increase the risk of pediatric-onset multiple sclerosis associated with ozone pollutionAmin Ziaei, Amy M Lavery, Xiaorong Ma Shao, et al.
Human Molecular Genetics|August 15, 2006
Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosisLisa F Barcellos, Stephen Sawcer, Patricia P Ramsay, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|May 14, 2019
Vitamin D genes influence MS relapses in childrenJennifer S Graves, Lisa F Barcellos, Lauren Krupp, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 11, 2017
Contribution of dietary intake to relapse rate in early paediatric multiple sclerosisSaeedeh Azary, Teri Schreiner, Jennifer Graves, et al.
International Journal of Cancer|June 21, 2018
BMI1 enhancer polymorphism underlies chromosome 10p12.31 association with childhood acute lymphoblastic leukemiaAdam J de Smith, Kyle M Walsh, Stephen S Francis, et al.
Human Molecular Genetics|August 12, 2010
Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12,566 individualsFarren B S Briggs, Selena E Bartlett, Benjamin A Goldstein, et al.
Nature Genetics|July 31, 2007
Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosisSimon G Gregory, Silke Schmidt, Puneet Seth, et al.
Plos Genetics|October 24, 2009
High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regionsLisa F Barcellos, Suzanne L May, Patricia P Ramsay, et al.
Plos One|April 13, 2011
Genome-wide association study identifies genetic loci associated with iron deficiencyChristine E McLaren, Chad P Garner, Clare C Constantine, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|February 9, 2023
Rare and low-frequency coding genetic variants contribute to pediatric-onset multiple sclerosisMary K Horton, Joan E Shim, Amelia Wallace, et al.
Pageof 15

Showing results (111-120 of 150) with videos related to

Sort By:
Pageof 15
Multiple Sclerosis (Houndmills, Basingstoke, England)|January 10, 2022
Gene-environment interactions increase the risk of pediatric-onset multiple sclerosis associated with ozone pollutionAmin Ziaei, Amy M Lavery, Xiaorong Ma Shao, et al.
Human Molecular Genetics|August 15, 2006
Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosisLisa F Barcellos, Stephen Sawcer, Patricia P Ramsay, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|May 14, 2019
Vitamin D genes influence MS relapses in childrenJennifer S Graves, Lisa F Barcellos, Lauren Krupp, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 11, 2017
Contribution of dietary intake to relapse rate in early paediatric multiple sclerosisSaeedeh Azary, Teri Schreiner, Jennifer Graves, et al.
International Journal of Cancer|June 21, 2018
BMI1 enhancer polymorphism underlies chromosome 10p12.31 association with childhood acute lymphoblastic leukemiaAdam J de Smith, Kyle M Walsh, Stephen S Francis, et al.
Human Molecular Genetics|August 12, 2010
Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12,566 individualsFarren B S Briggs, Selena E Bartlett, Benjamin A Goldstein, et al.
Nature Genetics|July 31, 2007
Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosisSimon G Gregory, Silke Schmidt, Puneet Seth, et al.
Plos Genetics|October 24, 2009
High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regionsLisa F Barcellos, Suzanne L May, Patricia P Ramsay, et al.
Plos One|April 13, 2011
Genome-wide association study identifies genetic loci associated with iron deficiencyChristine E McLaren, Chad P Garner, Clare C Constantine, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|February 9, 2023
Rare and low-frequency coding genetic variants contribute to pediatric-onset multiple sclerosisMary K Horton, Joan E Shim, Amelia Wallace, et al.
Pageof 15