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A person-centered approach to characterizing longitudinal ambulatory impairment in Parkinson's disease

Scientific reports, 2024-05, Vol.14 (1), p.11509-11509, Article 11509

2024

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Seroprevalence of aquaporin-4-IgG in a northern California population representative cohort of multiple sclerosis

JAMA neurology, 2014-11, Vol.71 (11), p.1433

2014

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The RNA helicase DDX39B activates FOXP3 RNA splicing to control T regulatory cell fate

eLife, 2023-06, Vol.12

2023

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118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects

BMC medical genetics, 2009-06, Vol.10 (49), p.49-49, Article 49

2009

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Male sexual and reproductive health in multiple sclerosis: a scoping review

Journal of neurology, 2024-05, Vol.271 (5), p.2169-2181

2024

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A higher burden of multiple sclerosis genetic risk confers an earlier onset

Multiple sclerosis, 2022-07, Vol.28 (8), p.1189-1197

2022

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Estimating the prevalence of multiple sclerosis using 56.6 million electronic health records from the United States

Multiple sclerosis, 2020-12, Vol.26 (14), p.1948-1952

2020

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Mind the gap: resources required to receive, process and interpret research-returned whole genome data

Human genetics, 2019-07, Vol.138 (7), p.691-701

2019

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Random Forests for Genetic Association Studies

Statistical applications in genetics and molecular biology, 2011-07, Vol.10 (1), p.1-34

2011

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Experiences of Adversity and Validity of Baseline Concussion Testing

Journal of athletic training, 2024-04, Vol.59 (4), p.373-380

2024

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Prevalence of neuromyelitis optica spectrum disorder in the United States

Multiple sclerosis, 2024-03, Vol.30 (3), p.316-324

2024

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Variation Within DNA Repair Pathway Genes and Risk of Multiple Sclerosis

American journal of epidemiology, 2010-07, Vol.172 (2), p.217-224

2010

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Genome-wide association study of severity in multiple sclerosis

Genes and immunity, 2011-12, Vol.12 (8), p.615-625

2011

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Smoking and Risk of Multiple Sclerosis: Evidence of Modification by NAT1 Variants

Epidemiology (Cambridge, Mass.), 2014-07, Vol.25 (4), p.605-614

2014

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Mobility trajectories in multiple sclerosis: A comparative study of timed 25-foot walk and a patient-reported outcome measure

Multiple sclerosis, 2024-10, Vol.30 (11-12), p.1479-1489

2024

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Age of hypertension onset in multiple sclerosis patients

Multiple sclerosis, 2021-11, Vol.27 (13), p.2108-2111

2021

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Physical Health Burden Among Older Men and Women With Bipolar Disorder: Results From the Gage-Bd Collaboration

The American journal of geriatric psychiatry, 2022-06, Vol.30 (6), p.727-732

2022

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Hypomethylation within gene promoter regions and type 1 diabetes in discordant monozygotic twins

Journal of autoimmunity, 2016-04, Vol.68, p.23-29

2016

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Adverse socioeconomic position during the life course is associated with multiple sclerosis

Journal of epidemiology and community health (1979), 2014-07, Vol.68 (7), p.622-629

2014

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Long-term trajectories of ambulatory impairment in multiple sclerosis

Multiple sclerosis, 2023-09, Vol.29 (10), p.1282-1295

2023

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The Managing Epilepsy Well (MEW) network database: Lessons learned in refining and implementing an integrated data tool in service of a national U.S. Research Collaborative

Epilepsy & behavior, 2021-02, Vol.115, p.107650-107650, Article 107650

2021

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Predicting self-reported depression after the onset of multiple sclerosis using genetic and non-genetic factors

Multiple sclerosis, 2021-04, Vol.27 (4), p.603-612

2021

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The impact of cigarette smoking on cognitive processing speed and brain atrophy in multiple sclerosis

Multiple sclerosis, 2023-06, Vol.29 (7), p.846-855

2023

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Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12 566 individuals

Human molecular genetics, 2010-11, Vol.19 (21), p.4286-4295

2010

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Association of genetic variation in IKZF1, ARID5B, and CEBPE and surrogates for early-life infections with the risk of acute lymphoblastic leukemia in Hispanic children

Cancer causes & control, 2015-04, Vol.26 (4), p.609-619

2015

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A person-centered approach to characterizing longitudinal ambulatory impairment in Parkinson's disease

Seroprevalence of aquaporin-4-IgG in a northern California population representative cohort of multiple sclerosis

The RNA helicase DDX39B activates FOXP3 RNA splicing to control T regulatory cell fate

118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects

Male sexual and reproductive health in multiple sclerosis: a scoping review

A higher burden of multiple sclerosis genetic risk confers an earlier onset

Estimating the prevalence of multiple sclerosis using 56.6 million electronic health records from the United States

Mind the gap: resources required to receive, process and interpret research-returned whole genome data

Random Forests for Genetic Association Studies

Experiences of Adversity and Validity of Baseline Concussion Testing

Prevalence of neuromyelitis optica spectrum disorder in the United States

Variation Within DNA Repair Pathway Genes and Risk of Multiple Sclerosis

Genome-wide association study of severity in multiple sclerosis

Smoking and Risk of Multiple Sclerosis: Evidence of Modification by NAT1 Variants

Mobility trajectories in multiple sclerosis: A comparative study of timed 25-foot walk and a patient-reported outcome measure

Age of hypertension onset in multiple sclerosis patients

Physical Health Burden Among Older Men and Women With Bipolar Disorder: Results From the Gage-Bd Collaboration

Hypomethylation within gene promoter regions and type 1 diabetes in discordant monozygotic twins

Adverse socioeconomic position during the life course is associated with multiple sclerosis

Long-term trajectories of ambulatory impairment in multiple sclerosis

The Managing Epilepsy Well (MEW) network database: Lessons learned in refining and implementing an integrated data tool in service of a national U.S. Research Collaborative

Predicting self-reported depression after the onset of multiple sclerosis using genetic and non-genetic factors

The impact of cigarette smoking on cognitive processing speed and brain atrophy in multiple sclerosis

Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12 566 individuals

Association of genetic variation in IKZF1, ARID5B, and CEBPE and surrogates for early-life infections with the risk of acute lymphoblastic leukemia in Hispanic children

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