Associated Papers
Discriminating activating, deactivating and resistance variants in protein kinases.
Singh G et al.
Genome Medicine, 2025
Migraine in monogenic disorders: Shedding light on new therapeutic targets.
Mascarella D et al.
Cephalalgia : an International Journal of Headache, 2025
Frequency enrichment of coding variants in a French-Canadian founder population and its implication for inflammatory bowel diseases.
Bhérer C et al.
Medrxiv : the Preprint Server for Health Sciences, 2025
Circadian clock gene variants in two Japanese families with familial advanced sleep phase.
Ukai M et al.
Sleep, 2025
Variants in the circadian clock genes PER2 and PER3 associate with familial sleep phase disorders.
Plavc L et al.
Chronobiology International, 2024
Genetics of migraine: complexity, implications, and potential clinical applications.
Sutherland HG et al.
The Lancet. Neurology, 2024
Increased presynaptic excitability in a migraine with aura mutation.
Suryavanshi P et al.
Brain : a Journal of Neurology, 2024
Genetic Mechanisms of Migraine: Insights from Monogenic Migraine Mutations.
Gosalia H et al.
International Journal of Molecular Sciences, 2023
Genetics of migraine: where are we now?
Grangeon L et al.
The Journal of Headache and Pain, 2023
Genetics of migraine: Delineation of contemporary understanding of the genetic underpinning of migraine.
de Boer I et al.
Handbook of Clinical Neurology, 2023
The impact of Mendelian sleep and circadian genetic variants in a population setting.
Weedon MN et al.
Plos Genetics, 2022
Kinase domain autophosphorylation rewires the activity and substrate specificity of CK1 enzymes.
Cullati SN et al.
Molecular Cell, 2022
Toward a Molecular Approach to Chronotype Assessment.
Biscontin A et al.
Journal of Biological Rhythms, 2022
Genetics of migraine aura: an update.
de Boer I et al.
The Journal of Headache and Pain, 2020
Structure, regulation, and (patho-)physiological functions of the stress-induced protein kinase CK1 delta (CSNK1D).
Xu P et al.
Gene, 2019
Advances in genetics of migraine.
Sutherland HG et al.
The Journal of Headache and Pain, 2019
Genetics of Migraine: Insights into the Molecular Basis of Migraine Disorders.
Sutherland HG et al.
Headache, 2017
Animal models of monogenic migraine.
Chen SP et al.
Cephalalgia : an International Journal of Headache, 2016
Migraine pathophysiology: lessons from mouse models and human genetics.
Ferrari MD et al.
The Lancet. Neurology, 2015
Genetics of human sleep behavioral phenotypes.
Hsu PK et al.
Methods in Enzymology, 2015
Tef polymorphism is associated with sleep disturbances in patients with Parkinson's disease.
Hua P et al.
Sleep Medicine, 2012
[Functional polymorphisms in clock genes and circadian rhythm sleep disorders].
Ebisawa T
Nihon Shinkei Seishin Yakurigaku Zasshi = Japanese Journal of Psychopharmacology, 2007
Circadian rhythms in the CNS and peripheral clock disorders: human sleep disorders and clock genes.
Ebisawa T
Journal of Pharmacological Sciences, 2007
Functional consequences of a CKIdelta mutation causing familial advanced sleep phase syndrome.
Xu Y et al.
Nature, 2005
Solving the mystery of human sleep schedules one mutation at a time.
Hallows WC et al.
Critical Reviews in Biochemistry and Molecular Biology, 0