Migraine headache: a review of the molecular genetics of a common disorder

Genome-wide association analysis identifies susceptibility loci for migraine without aura

(2012) Tobias Freilinger et al.   NATURE GENETICS

Pharmacogenomics in neurology: Current state and future steps

(2011) Andrew Chan et al.   ANNALS OF NEUROLOGY

New directions in migraine

(2011) Greg A Weir et al.   BMC Medicine

A new Italian FHM2 family: Clinical aspects and functional analysis of the disease-associated mutation

(2011) Lucio Santoro et al.   CEPHALALGIA

Cortical Excitability in Chronic Migraine

(2011) Gianluca Coppola et al.   Current Pain and Headache Reports

Heritability and genome-wide linkage analysis of migraine in the genetic isolate of Norfolk Island

(2011) Hannah C. Cox et al.   GENE

Genetics of migraine in the age of genome-wide association studies

(2011) Markus Schürks   JOURNAL OF HEADACHE AND PAIN

Identification of molecular genetic factors that influence migraine

(2011) Bridget H. Maher et al.   MOLECULAR GENETICS AND GENOMICS

Natural history of MELAS associated with mitochondrial DNA m.3243A>G genotype

(2011) P. Kaufmann et al.   NEUROLOGY

Prophylaxis of migraine: general principles and patient acceptance

(2011) Domenico D'Amico et al.   Neuropsychiatric Disease and Treatment

Association of a Notch 3 gene polymorphism with migraine susceptibility

(2010) S Menon et al.   CEPHALALGIA

Gene polymorphisms involved in triptans pharmacokinetics and pharmacodynamics in migraine therapy

(2010) Giovanna Gentile et al.   Expert Opinion on Drug Metabolism & Toxicology

Role of 2 Common Variants of 5HT2A Gene in Medication Overuse Headache

(2010) Salvatore Terrazzino et al.   HEADACHE

Genetic polymorphisms related to efficacy and overuse of triptans in chronic migraine

(2010) Giovanna Gentile et al.   JOURNAL OF HEADACHE AND PAIN

A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura

(2010) Ronald G Lafrenière et al.   NATURE MEDICINE

Mitochondrial Encephalopathy, Lactic Acidosis, and Strokelike Episodes

(2009) Douglas M. Sproule et al.   Annals of the New York Academy of Sciences

Molecular genetics of migraine

(2009) Boukje de Vries et al.   HUMAN GENETICS

Lack of association between five serotonin metabolism-related genes and medication overuse headache

(2009) Sabina Cevoli et al.   JOURNAL OF HEADACHE AND PAIN

Drug consumption in medication overuse headache is influenced by brain-derived neurotrophic factor Val66Met polymorphism

(2009) Cherubino Di Lorenzo et al.   JOURNAL OF HEADACHE AND PAIN

Energetics, epigenetics, mitochondrial genetics

(2009) Douglas C. Wallace et al.   MITOCHONDRION

The Epidemiology, Burden, and Comorbidities of Migraine

(2009) Marcelo E. Bigal et al.   NEUROLOGIC CLINICS

Elicited repetitive daily blindness: A new phenotype associated with hemiplegic migraine and SCN1A mutations

(2009) K. Vahedi et al.   NEUROLOGY

Mitochondrial DNA haplogroups influence the therapeutic response to riboflavin in migraineurs

(2009) C. Di Lorenzo et al.   NEUROLOGY

Human Genome Sequencing Using Unchained Base Reads on Self-Assembling DNA Nanoarrays

(2009) R. Drmanac et al.   SCIENCE

Angiotensin-converting enzyme gene insertion/deletion polymorphism in migraine patients

(2008) Erling Tronvik et al.   BMC Neurology

First Mutation in the Voltage-Gated Nav1.1 Subunit Gene SCN1A with Co-Occurring Familial Hemiplegic Migraine and Epilepsy

(2008) M-J Castro et al.   CEPHALALGIA

Animal models of migraine headache and aura

(2008) Katharina Eikermann-Haerter et al.   CURRENT OPINION IN NEUROLOGY

A high-density association screen of 155 ion transport genes for involvement with common migraine

(2008) Dale R. Nyholt et al.   HUMAN MOLECULAR GENETICS

Diverse Functional Consequences of Mutations in the Na+/K+-ATPase α2-Subunit Causing Familial Hemiplegic Migraine Type 2

(2008) Neslihan N. Tavraz et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Self-Limited Hyperexcitability: Functional Effect of a Familial Hemiplegic Migraine Mutation of the Nav1.1 (SCN1A) Na+ Channel

(2008) S. Cestele et al.   JOURNAL OF NEUROSCIENCE

Stepwise Developmental Regression Associated With Novel CACNA1A Mutation

(2008) Andrea A. Guerin et al.   PEDIATRIC NEUROLOGY

Epilepsy as part of the phenotype associated withATP1A2mutations

(2007) Liesbet Deprez et al.   EPILEPSIA