Author details

Full Name

Robin R Lincoln

Affiliation

ORCID

Career Start Year

1990

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36585249	Remote Observational Research for Multiple Sclerosis: A Natural Experiment.		2023
29310490	Harnessing electronic medical records to advance research on multiple sclerosis.	Mult Scler	2019
30429274	Body mass index, but not vitamin D status, is associated with brain volume change in MS.	Neurology	2018
27464262	Long-term evolution of multiple sclerosis disability in the treatment era.	Ann Neurol	2016
22926855	Vitamin D status predicts new brain magnetic resonance imaging activity in multiple sclerosis.	Ann Neurol	2012
21833088	Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.	Nature	2011
19010793	Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.	Hum Mol Genet	2009
19451531	Quality of life in multiple sclerosis is associated with lesion burden and brain volume measures.	Neurology	2009
19022862	Genotype-Phenotype correlations in multiple sclerosis: HLA genes influence disease severity inferred by 1HMR spectroscopy and MRI measures.	Brain	2009
17660817	Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis.	Nat Genet	2007
17052659	Clustering of autoimmune diseases in families with a high-risk for multiple sclerosis: a descriptive study.	Lancet Neurol	2006
16864824	Men transmit MS more often to their children vs women: the Carter effect.	Neurology	2006
16905561	Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosis.	Hum Mol Genet	2006
16738668	Allelic association of sequence variants in the herpes virus entry mediator-B gene (PVRL2) with the severity of multiple sclerosis.	Genes Immun	2006
16186815	A whole-genome admixture scan finds a candidate locus for multiple sclerosis susceptibility.	Nat Genet	2005
16080120	A high-density screen for linkage in multiple sclerosis.	Am J Hum Genet	2005
14595552	Investigation of seven proposed regions of linkage in multiple sclerosis: an American and French collaborative study.	Neurogenetics	2004
15494893	A second-generation genomic screen for multiple sclerosis.	Am J Hum Genet	2004
15174013	Linkage and association with the NOS2A locus on chromosome 17q11 in multiple sclerosis.	Ann Neurol	2004
14669136	Mapping multiple sclerosis susceptibility to the HLA-DR locus in African Americans.	Am J Hum Genet	2004
12761568	Osteopontin polymorphisms and disease course in multiple sclerosis.	Genes Immun	2003
12557126	HLA-DR2 dose effect on susceptibility to multiple sclerosis and influence on disease course.	Am J Hum Genet	2003
12217953	Multiple susceptibility loci for multiple sclerosis.	Hum Mol Genet	2002
11836653	Association of polymorphisms in the apolipoprotein E region with susceptibility to and progression of multiple sclerosis.	Am J Hum Genet	2002
11834600	Genetic basis for clinical expression in multiple sclerosis.	Brain	2002
11311337	Sequence variation in the transforming growth factor-beta1 (TGFB1) gene and multiple sclerosis susceptibility.	J Neuroimmunol	2001
11714099	Linkage and association analysis of chromosome 19q13 in multiple sclerosis.	Neurogenetics	2001
11528386	PTPRC (CD45) is not associated with the development of multiple sclerosis in U.S. patients.	Nat Genet	2001
10802800	Interaction between HLA-DR2 and abnormal brain MRI in optic neuritis and early MS. Optic Neuritis Study Group.	Neurology	2000
11078868	Interaction between HLA-DR2 and abnormal brain MRI in optic neuritis and early MS	American Journal of Ophthalmology	2000
10803840	CC-chemokine receptor 5 polymorphism and age of onset in familial multiple sclerosis. Multiple Sclerosis Genetics Group.	Immunogenetics	2000
10541588	Linkage analysis of candidate myelin genes in familial multiple sclerosis.	Neurogenetics	1999
9668163	Linkage of the MHC to familial multiple sclerosis suggests genetic heterogeneity. The Multiple Sclerosis Genetics Group.	Hum Mol Genet	1998
8696344	A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group.	Nat Genet	1996
8872171	Tumor necrosis factor (TNF) microsatellite haplotypes in relation to extended haplotypes, susceptibility to diseases associated with the major histocompatibility complex and TNF secretion.	Human Immunology	1996
7818259	Elevated mast cell tryptase in cerebrospinal fluid of multiple sclerosis patients.	Annals of Neurology	1995
8423203	Segregation of immunoglobulin heavy chain constant region genes in multiple sclerosis sibling pairs.	Journal of Neuroimmunology	1993
8099448	Unusual organization of the human T-cell receptor beta-chain gene complex is linked to recombination hotspots.	Proceedings of the National Academy of Sciences of the United States of America	1993
2234430	Cytokine accumulations in CSF of multiple sclerosis patients: frequent detection of interleukin-1 and tumor necrosis factor but not interleukin-6.	Neurology	1990