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Fine-mapping inflammatory bowel disease loci to single-variant resolution

Nature (London), 2017-07, Vol.547 (7662), p.173-178

2017

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Genetic variants in the region harbouring IL2/IL21 associated with ulcerative colitis

Gut, 2009-06, Vol.58 (6), p.799-804

2009

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Molecular pathogenesis of inflammatory bowel disease: Genotypes, phenotypes and personalized medicine

Annals of medicine (Helsinki), 2007, Vol.39 (3), p.177-199

2007

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A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

Nature genetics, 1995-05, Vol.10 (1), p.111-113

1995

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Gene-centric association mapping of chromosome 3p implicates MST1 in IBD pathogenesis

Mucosal immunology, 2008-03, Vol.1 (2), p.131-138

2008

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A targeted association study in systemic lupus erythematosus identifies multiple susceptibility alleles

Genes and immunity, 2011-01, Vol.12 (1), p.51-58

2011

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Human Methionine Synthase: cDNA Cloning and Identification of Mutations in Patients of the cblG Complementation Group of Folate/Cobalamin Disorders

Human molecular genetics, 1996-12, Vol.5 (12), p.1867-1874

1996

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Severe and mild mutations in cis for the methylenetetrahydrofolate reductase (MTHFR) gene, and description of five novel mutations in MTHFR

American journal of human genetics, 1996-12, Vol.59 (6), p.1268-1275

1996

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MAST3: a novel IBD risk factor that modulates TLR4 signaling

Genes and immunity, 2008-10, Vol.9 (7), p.602-612

2008

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A Remote Sensing and GIS Based Investigation of a Boreal Forest Coal Fire

International journal of coal geology, 2011-04, Vol.86 (1), p.79-86

2011

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Regulation of Gli activity by all-trans retinoic acid in mouse keratinocytes

Cancer research (Chicago, Ill.), 2000-10, Vol.60 (19), p.5386-5389

2000

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Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR)

Mammalian genome, 1998-08, Vol.9 (8), p.652-656

1998

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Seven novel mutations in the methylenetetrahydrofolate reductase gene and genotype/phenotype correlations in severe methylenetetrahydrofolate reductase deficiency

American journal of human genetics, 1995-05, Vol.56 (5), p.1052-1059

1995

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Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification

Nature genetics, 1994-06, Vol.7 (2), p.195-200

1994

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RARγ acts as a tumor suppressor in mouse keratinocytes

Oncogene, 2004-07, Vol.23 (31), p.5350-5359

2004

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Homocystinuria (methylenetetrahydrofolate reductase deficiency) and mutation of factor V gene

Journal of inherited metabolic disease, 1998-08, Vol.21 (6), p.690-691

1998

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Correlation of a common mutation in the methylenetetrahydrofolate reductase gene with plasma homocysteine in patients with premature coronary artery disease

Arteriosclerosis, thrombosis, and vascular biology, 1997-03, Vol.17 (3), p.569-573

1997

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The thermolabile variant 677C→T can further reduce activity when expressed in CIS with severe mutations for human methylenetetrahydrofolate reductase

Human mutation, 2000-08, Vol.16 (2), p.132-138

2000

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A Major Histocompatibility Class I Locus Contributes to Multiple Sclerosis Susceptibility Independently from HLA - DRB1 15 : 01

PloS one, 2010, Vol.5 (6), p.e11296

2010

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In-line microwave blood warming of in-date human packed red blood cells

Critical care medicine, 1995-07, Vol.23 (7), p.1243-1250

1995

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The IMAGEN Consortium: A High-density SNP Map of the MHC in Lupus Identifies Multiple Independent Disease-associated Variants

Clinical immunology (Orlando, Fla.), 2009-01, Vol.131, p.S102-S103

2009

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Multiple transcription start sites and alternative splicing in the methylenetetrahydrofolate reductase gene result in two enzyme isoforms

Mammalian genome, 2002-09, Vol.13 (9), p.483-492

2002

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Fine-mapping inflammatory bowel disease loci to single-variant resolution

Genetic variants in the region harbouring IL2/IL21 associated with ulcerative colitis

Molecular pathogenesis of inflammatory bowel disease: Genotypes, phenotypes and personalized medicine

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

Gene-centric association mapping of chromosome 3p implicates MST1 in IBD pathogenesis

A targeted association study in systemic lupus erythematosus identifies multiple susceptibility alleles

Human Methionine Synthase: cDNA Cloning and Identification of Mutations in Patients of the cblG Complementation Group of Folate/Cobalamin Disorders

Deep resequencing of GWAS loci identifies independent rare variants associated with inflammatory bowel disease

Deep resequencing of GWAS loci identifies rare variants in CARD9, IL23R and RNF186 that are associated with ulcerative colitis

Severe and mild mutations in cis for the methylenetetrahydrofolate reductase (MTHFR) gene, and description of five novel mutations in MTHFR

MAST3: a novel IBD risk factor that modulates TLR4 signaling

A Remote Sensing and GIS Based Investigation of a Boreal Forest Coal Fire

Regulation of Gli activity by all-trans retinoic acid in mouse keratinocytes

High-density mapping of the MHC identifies a shared role for HLA-DRB101:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis

Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR)

Seven novel mutations in the methylenetetrahydrofolate reductase gene and genotype/phenotype correlations in severe methylenetetrahydrofolate reductase deficiency

Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification

RARγ acts as a tumor suppressor in mouse keratinocytes

Homocystinuria (methylenetetrahydrofolate reductase deficiency) and mutation of factor V gene

Correlation of a common mutation in the methylenetetrahydrofolate reductase gene with plasma homocysteine in patients with premature coronary artery disease

The thermolabile variant 677C→T can further reduce activity when expressed in CIS with severe mutations for human methylenetetrahydrofolate reductase

A Major Histocompatibility Class I Locus Contributes to Multiple Sclerosis Susceptibility Independently from HLA - DRB1 15 : 01

In-line microwave blood warming of in-date human packed red blood cells

The IMAGEN Consortium: A High-density SNP Map of the MHC in Lupus Identifies Multiple Independent Disease-associated Variants

Multiple transcription start sites and alternative splicing in the methylenetetrahydrofolate reductase gene result in two enzyme isoforms

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