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Familial typical migraine: linkage to chromosome 19p13 and evidence for genetic heterogeneity

Neurology, 1998-05, Vol.50 (5), p.1428-1432

1998

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Methylation differences at the HLA-DRB1 locus in CD4+ T-Cells are associated with multiple sclerosis

Multiple sclerosis, 2014-07, Vol.20 (8), p.1033-1041

2014

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DNA Methylation Signatures of Multiple Sclerosis Occur Independently of Known Genetic Risk and Are Primarily Attributed to B Cells and Monocytes

International journal of molecular sciences, 2023-08, Vol.24 (16), p.12576

2023

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CD4+ T-cell DNA methylation changes during pregnancy significantly correlate with disease-associated methylation changes in autoimmune diseases

Epigenetics, 2022, Vol.17 (9), p.1040-1055

2022

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β-Actin—an unsuitable internal control for RT-PCR

Molecular and cellular probes, 2001-10, Vol.15 (5), p.307-311

2001

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Association of a Notch 3 gene polymorphism with migraine susceptibility

Cephalalgia, 2011-02, Vol.31 (3), p.264-270

2011

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EHMTI-0047. Genetic association and gene expression studies suggest that genetic variants in the SYNE1 and TNF genes are related to menstrual migraine: Doc 766

Journal of headache and pain, 2014-09, Vol.15, p.1

2014

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The estrogen receptor 1 G594A polymorphism is associated with migraine susceptibility in two independent case/control groups

Neurogenetics, 2004-06, Vol.5 (2), p.129-133

2004

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EHMTI-0047. Genetic association and gene expression studies suggest that genetic variants in the SYNE1 and TNF genes are related to menstrual migraine

Journal of headache and pain, 2014-09, Vol.15 (Suppl 1), p.B11-B11, Article B11

2014

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Investigation of hormone receptor genes in migraine

Neurogenetics, 2005-02, Vol.6 (1), p.17-23

2005

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The Methylentetrahydrofolate Reductase Gene Variant (C677T) as a Risk Factor for Essential Hypertension in Caucasians

Hypertension Research, 2004, Vol.27(9), pp.663-667

2004

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Review: Nicotinic receptors and stages of nicotine dependence

Journal of Psychopharmacology, 2010-06, Vol.24 (6), p.793-808

2010

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Association of estrogen receptor and glucocorticoid receptor gene polymorphisms with sporadic breast cancer

International journal of cancer, 2001-07, Vol.95 (4), p.271-275

2001

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No role for estrogen receptor 1 gene intron 1 Pvu II and exon 4 C325G polymorphisms in migraine susceptibility

BMC medical genetics, 2006-02, Vol.7 (1), p.12-12, Article 12

2006

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Genetic investigation of methylenetetrahydrofolate reductase (MTHFR) and catechol- O-methyl transferase (COMT) in multiple sclerosis

Brain research bulletin, 2006-04, Vol.69 (3), p.327-331

2006

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A Large-Scale Study of the Relationship Between Blood and Breath Alcohol Concentrations in New Zealand Drinking Drivers

Journal of forensic sciences, 2006-01, Vol.51 (1), p.173-178

2006

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CARD15 allele frequency differences in New Zealand Maori: ancestry specific susceptibility to Crohn’s disease in New Zealand?

Gut, 2006-04, Vol.55 (4), p.580-580

2006

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Genetic variants of angiotensin converting enzyme and methylenetetrahydrofolate reductase may act in combination to increase migraine susceptibility

Brain research. Molecular brain research., 2005-05, Vol.136 (1), p.112-117

2005

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A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine

Neurogenetics, 2005-05, Vol.6 (2), p.67-72

2005

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Evidence for allelic association of the dopamine β-hydroxylase gene (DBH) with susceptibility to typical migraine

Neurogenetics, 2000-09, Vol.3 (1), p.35-40

2000

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Phenotypical Characterisation of the Isolated Norfolk Island Population Focusing on Epidemiological Indicators of Cardiovascular Disease

Human heredity, 2005-01, Vol.60 (4), p.211-219

2005

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Investigation of the CACNA1A gene as a candidate for typical migraine susceptibility

American journal of medical genetics, 2001-12, Vol.105 (8), p.707-712

2001

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Investigation of the low-density lipoprotein receptor gene and cholesterol as a risk factor for migraine

Journal of the neurological sciences, 2004-12, Vol.227 (1), p.95-100

2004

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A typical migraine susceptibility region localizes to chromosome 1q31

Neurogenetics, 2002-03, Vol.4 (1), p.17-22

2002

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Expression of glucocorticoid and progesterone nuclear receptor genes in archival breast cancer tissue

Breast cancer research : BCR, 2003-01, Vol.5 (1), p.R9-12, Article R9

2003

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Familial typical migraine: linkage to chromosome 19p13 and evidence for genetic heterogeneity

Methylation differences at the HLA-DRB1 locus in CD4+ T-Cells are associated with multiple sclerosis

DNA Methylation Signatures of Multiple Sclerosis Occur Independently of Known Genetic Risk and Are Primarily Attributed to B Cells and Monocytes

CD4+ T-cell DNA methylation changes during pregnancy significantly correlate with disease-associated methylation changes in autoimmune diseases

β-Actin—an unsuitable internal control for RT-PCR

Association of a Notch 3 gene polymorphism with migraine susceptibility

EHMTI-0047. Genetic association and gene expression studies suggest that genetic variants in the SYNE1 and TNF genes are related to menstrual migraine: Doc 766

The estrogen receptor 1 G594A polymorphism is associated with migraine susceptibility in two independent case/control groups

EHMTI-0047. Genetic association and gene expression studies suggest that genetic variants in the SYNE1 and TNF genes are related to menstrual migraine

Investigation of hormone receptor genes in migraine

The Methylentetrahydrofolate Reductase Gene Variant (C677T) as a Risk Factor for Essential Hypertension in Caucasians

Review: Nicotinic receptors and stages of nicotine dependence

Association of estrogen receptor and glucocorticoid receptor gene polymorphisms with sporadic breast cancer

No role for estrogen receptor 1 gene intron 1 Pvu II and exon 4 C325G polymorphisms in migraine susceptibility

Genetic investigation of methylenetetrahydrofolate reductase (MTHFR) and catechol- O-methyl transferase (COMT) in multiple sclerosis

A Large-Scale Study of the Relationship Between Blood and Breath Alcohol Concentrations in New Zealand Drinking Drivers

CARD15 allele frequency differences in New Zealand Maori: ancestry specific susceptibility to Crohn’s disease in New Zealand?

Genetic variants of angiotensin converting enzyme and methylenetetrahydrofolate reductase may act in combination to increase migraine susceptibility

A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine

Evidence for allelic association of the dopamine β-hydroxylase gene (DBH) with susceptibility to typical migraine

Phenotypical Characterisation of the Isolated Norfolk Island Population Focusing on Epidemiological Indicators of Cardiovascular Disease

Investigation of the CACNA1A gene as a candidate for typical migraine susceptibility

Investigation of the low-density lipoprotein receptor gene and cholesterol as a risk factor for migraine

A typical migraine susceptibility region localizes to chromosome 1q31

Expression of glucocorticoid and progesterone nuclear receptor genes in archival breast cancer tissue

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