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Neurology. Genetics
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September 22, 2016
Mendelian randomization shows a causal effect of low vitamin D on multiple sclerosis risk
Brooke Rhead, Maria Bäärnhielm, Milena Gianfrancesco, et al.
Arthritis & Rheumatology (Hoboken, N.J.)
|
October 11, 2016
Rheumatoid Arthritis Naive T Cells Share Hypermethylation Sites With Synoviocytes
Brooke Rhead, Calliope Holingue, Michael Cole, et al.
Molecular Psychiatry
|
May 23, 2024
Pharmacogenomic insights in psychiatric care: uncovering novel actionability, allele-specific CYP2D6 copy number variation, and phenoconversion in 15,000 patients
Jai N Patel, Sarah A Morris, Raul Torres, et al.
American Journal of Epidemiology
|
January 12, 2017
Causal Effect of Genetic Variants Associated With Body Mass Index on Multiple Sclerosis Susceptibility
Milena A Gianfrancesco, M Maria Glymour, Stefan Walter, et al.
Nucleic Acids Research
|
November 19, 2009
ENCODE whole-genome data in the UCSC Genome Browser
Kate R Rosenbloom, Timothy R Dreszer, Michael Pheasant, et al.
BMJ Open
|
October 12, 2022
COVID-19 susceptibility and severity risks in a cross-sectional survey of over 500 000 US adults
Spencer C Knight, Shannon R McCurdy, Brooke Rhead, et al.
Breast Cancer Research : BCR
|
May 25, 2023
Molecular profiling of a real-world breast cancer cohort with genetically inferred ancestries reveals actionable tumor biology differences between European ancestry and African ancestry patient populations
Minoru Miyashita, Joshua S K Bell, Stephane Wenric, et al.
Nature Communications
|
December 7, 2021
Proximal and distal effects of genetic susceptibility to multiple sclerosis on the T cell epigenome
Tina Roostaei, Hans-Ulrich Klein, Yiyi Ma, et al.
Plos One
|
November 1, 2018
Increased DNA methylation of SLFN12 in CD4+ and CD8+ T cells from multiple sclerosis patients
Brooke Rhead, Ina S Brorson, Tone Berge, et al.
Nature Genetics
|
April 12, 2022
Expanded COVID-19 phenotype definitions reveal distinct patterns of genetic association and protective effects
Genevieve H L Roberts, Raghavendran Partha, Brooke Rhead, et al.
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of 4
Search research articles
Search
Showing results (11-20 of 31) with videos related to
Sort By:
Page
of 4
Neurology. Genetics
|
September 22, 2016
Mendelian randomization shows a causal effect of low vitamin D on multiple sclerosis risk
Brooke Rhead, Maria Bäärnhielm, Milena Gianfrancesco, et al.
Arthritis & Rheumatology (Hoboken, N.J.)
|
October 11, 2016
Rheumatoid Arthritis Naive T Cells Share Hypermethylation Sites With Synoviocytes
Brooke Rhead, Calliope Holingue, Michael Cole, et al.
Molecular Psychiatry
|
May 23, 2024
Pharmacogenomic insights in psychiatric care: uncovering novel actionability, allele-specific CYP2D6 copy number variation, and phenoconversion in 15,000 patients
Jai N Patel, Sarah A Morris, Raul Torres, et al.
American Journal of Epidemiology
|
January 12, 2017
Causal Effect of Genetic Variants Associated With Body Mass Index on Multiple Sclerosis Susceptibility
Milena A Gianfrancesco, M Maria Glymour, Stefan Walter, et al.
Nucleic Acids Research
|
November 19, 2009
ENCODE whole-genome data in the UCSC Genome Browser
Kate R Rosenbloom, Timothy R Dreszer, Michael Pheasant, et al.
BMJ Open
|
October 12, 2022
COVID-19 susceptibility and severity risks in a cross-sectional survey of over 500 000 US adults
Spencer C Knight, Shannon R McCurdy, Brooke Rhead, et al.
Breast Cancer Research : BCR
|
May 25, 2023
Molecular profiling of a real-world breast cancer cohort with genetically inferred ancestries reveals actionable tumor biology differences between European ancestry and African ancestry patient populations
Minoru Miyashita, Joshua S K Bell, Stephane Wenric, et al.
Nature Communications
|
December 7, 2021
Proximal and distal effects of genetic susceptibility to multiple sclerosis on the T cell epigenome
Tina Roostaei, Hans-Ulrich Klein, Yiyi Ma, et al.
Plos One
|
November 1, 2018
Increased DNA methylation of SLFN12 in CD4+ and CD8+ T cells from multiple sclerosis patients
Brooke Rhead, Ina S Brorson, Tone Berge, et al.
Nature Genetics
|
April 12, 2022
Expanded COVID-19 phenotype definitions reveal distinct patterns of genetic association and protective effects
Genevieve H L Roberts, Raghavendran Partha, Brooke Rhead, et al.
Page
of 4