A splice variant in the ACSL5 gene relates migraine with fatty acid activation in mitochondria

Gene co-expression analysis identifies brain regions and cell types involved in migraine pathophysiology: a GWAS-based study using the Allen Human Brain Atlas

(2016) Else Eising et al.   HUMAN GENETICS

A comparison of genomic profiles of complex diseases under different models

(2015) Víctor Potenciano et al.   BMC Medical Genomics

Ebola, Dynamin, and the Cordon Sanitaire of Dr. Adrien Proust

(2015) Gerald Weissmann   FASEB JOURNAL

A functional variant that affects exon-skipping and protein expression ofSP140as genetic mechanism predisposing to multiple sclerosis

(2015) Fuencisla Matesanz et al.   HUMAN MOLECULAR GENETICS

Genome-wide significant association with seven novel multiple sclerosis risk loci

(2015) Christina M Lill et al.   JOURNAL OF MEDICAL GENETICS

Haplotype-based approach to known MS-associated regions increases the amount of explained risk

(2015) Pouya Khankhanian et al.   JOURNAL OF MEDICAL GENETICS

Migraine pathophysiology: lessons from mouse models and human genetics

(2015) Michel D Ferrari et al.   LANCET NEUROLOGY

Interictal, circulating sphingolipids in women with episodic migraine

(2015) B. Lee Peterlin et al.   NEUROLOGY

From migraine genes to mechanisms

(2015) Else A. Tolner et al.   PAIN

Long-chain acyl-CoA synthetase in fatty acid metabolism involved in liver and other diseases: An update

(2015) Sheng Yan   WORLD JOURNAL OF GASTROENTEROLOGY

Riboflavin and migraine: the bridge over troubled mitochondria

(2014) Bruno Colombo et al.   NEUROLOGICAL SCIENCES

Modulating effects of acyl-CoA synthetase 5-derived mitochondrial Wnt2B palmitoylation on intestinal Wnt activity

(2014) Christina Klaus   WORLD JOURNAL OF GASTROENTEROLOGY

Selectivity in Genetic Association with Sub-classified Migraine in Women

(2014) Daniel I. Chasman et al.   PLoS Genetics

Pearls and pitfalls in genetic studies of migraine

(2013) Else Eising et al.   CEPHALALGIA

Biomarkers Associated With Migraine and Their Potential Role in Migraine Management

(2013) Paul Durham et al.   HEADACHE

Genetic risk score analysis indicates migraine with and without comorbid depression are genetically different disorders

(2013) Lannie Ligthart et al.   HUMAN GENETICS

Transcriptome and genome sequencing uncovers functional variation in humans

(2013) Tuuli Lappalainen et al.   NATURE

Genome-wide meta-analysis identifies new susceptibility loci for migraine

(2013) Verneri Anttila et al.   NATURE GENETICS

Mitochondrial Dysfunction in Migraine

(2013) William R. Yorns et al.   Seminars in Pediatric Neurology

Magnetic resonance spectroscopy in migraine: What have we learned so far?

(2012) Harmen Reyngoudt et al.   CEPHALALGIA

CoEnzyme Q10 and Riboflavin: The Mitochondrial Connection

(2012) Herbert G. Markley   HEADACHE

An integrated map of genetic variation from 1,092 human genomes

(2012)   NATURE

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

(2012) Tobias Freilinger et al.   NATURE GENETICS

Interleukin-1 and Stroke: Biomarker, Harbinger of Damage, and Therapeutic Target

(2011) Adam Denes et al.   CEREBROVASCULAR DISEASES

Genome-wide association study reveals three susceptibility loci for common migraine in the general population

(2011) Daniel I Chasman et al.   NATURE GENETICS

High ACSL5 Transcript Levels Associate with Systemic Lupus Erythematosus and Apoptosis in Jurkat T Lymphocytes and Peripheral Blood Cells

(2011) Antonio Catalá-Rabasa et al.   PLoS One

Human intestinal acyl-CoA synthetase 5 is sensitive to the inhibitor triacsin C

(2011) Elke Kaemmerer   WORLD JOURNAL OF GASTROENTEROLOGY

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1

(2010) Verneri Anttila et al.   NATURE GENETICS

Pathogenesis of migraine: from neurotransmitters to neuromodulators and beyond

(2010) G. D’Andrea et al.   NEUROLOGICAL SCIENCES