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Academic Journal

Functional polymorphisms of the 5-HT1A and 5-HT1B receptor are associated with clinical symptoms in migraineurs.

  • Authors : Marziniak M; Department of Neurology, University of Würzburg, Würzburg, Germany. ; Mössner R

Subjects: Alleles*; Migraine Disorders/Migraine Disorders/Migraine Disorders/*genetics ; Migraine Disorders/Migraine Disorders/Migraine Disorders/*physiopathology

  • Source: Journal of neural transmission (Vienna, Austria : 1996) [J Neural Transm (Vienna)] 2007 Sep; Vol. 114 (9), pp. 1227-32. Date of Electronic Publication: 2007 Apr 10.Publisher: Springer-Verlag Country of Publication: Austria NLM ID: 9702341 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

High anxiety and migraine are associated with the s allele of the 5HTTLPR gene polymorphism.

  • Authors : Gonda X; Laboratory of Neurochemistry and Experimental Medicine, National Institute of Psychiatry and Neurology, Huvosvolgyi ut 116, H-1021 Budapest, Hungary.; Rihmer Z

Subjects: Alleles*; Anxiety Disorders/Anxiety Disorders/Anxiety Disorders/*epidemiology ; Anxiety Disorders/Anxiety Disorders/Anxiety Disorders/*genetics

  • Source: Psychiatry research [Psychiatry Res] 2007 Jan 15; Vol. 149 (1-3), pp. 261-6. Date of Electronic Publication: 2006 Nov 17.Publisher: Elsevier/North-Holland Biomedical Press Country of Publication: Ireland NLM ID: 7911385 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Clinical susceptibility to migraine with aura is modified by dopamine D2 receptor (DRD2) NcoI alleles.

Subjects: Alleles*; Migraine Disorders/Migraine Disorders/Migraine Disorders/*physiopathology ; Receptors, Dopamine D2/Receptors, Dopamine D2/Receptors, Dopamine D2/*genetics

  • Source: Neurology [Neurology] 1997 Jul; Vol. 49 (1), pp. 201-6.Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 0401060 Publication Model: Print Cited Medium: Print ISSN:

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Academic Journal

Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection.

Subjects: Alleles* ; Polymorphism, Single Nucleotide*; Carotid Artery, Internal, Dissection/Carotid Artery, Internal, Dissection/Carotid Artery, Internal, Dissection/*genetics

  • Source: Nature genetics [Nat Genet] 2015 Jan; Vol. 47 (1), pp. 78-83. Date of Electronic Publication: 2014 Nov 24.Publisher: Nature Pub. Co Country of Publication: United States NLM ID: 9216904 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Altered allelic distributions of the serotonin transporter gene in migraine without aura and migraine with aura.

  • Authors : Ogilvie AD; Department of Psychiatry, University of Cambridge, Addenbrooke's Hospital, UK. ; Russell MB

Subjects: Alleles* ; Membrane Transport Proteins* ; Nerve Tissue Proteins*

  • Source: Cephalalgia : an international journal of headache [Cephalalgia] 1998 Jan; Vol. 18 (1), pp. 23-6.Publisher: Country of Publication: England NLM ID: 8200710 Publication Model: Print Cited Medium: Print ISSN: 0333-1024 (Print) Linking ISSN:

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Academic Journal

Prevalence of HLA DQB1*0602 allele in patients with migraine.

Subjects: Alleles*; HLA-DQ Antigens/HLA-DQ Antigens/HLA-DQ Antigens/*genetics ; Membrane Glycoproteins/Membrane Glycoproteins/Membrane Glycoproteins/*genetics

  • Source: Arquivos de neuro-psiquiatria [Arq Neuropsiquiatr] 2007 Dec; Vol. 65 (4B), pp. 1123-5.Publisher: Thieme Country of Publication: Germany NLM ID: 0125444 Publication Model: Print Cited Medium: Print ISSN: 0004-282X (Print) Linking

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Academic Journal

Common CX3CR1 alleles are associated with a reduced risk of headaches.

  • Authors : Combadière C; INSERM U543, Laboratoire d'Immunologie Cellulaire, Faculté de Médecine Pitié-Salpêtrière, 91 Boulevard de l'Hôpital, 75634 Paris, France.; Godin O

Subjects: Alleles*; Headache/Headache/Headache/*genetics ; Receptors, Chemokine/Receptors, Chemokine/Receptors, Chemokine/*genetics

  • Source: Headache [Headache] 2008 Jul; Vol. 48 (7), pp. 1061-6. Date of Electronic Publication: 2008 Jan 08.Publisher: Wiley Country of Publication: United States NLM ID: 2985091R Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura.

Subjects: Alleles*; Calcium Channels/Calcium Channels/Calcium Channels/*genetics ; Chromosomes, Human, Pair 19/Chromosomes, Human, Pair 19/Chromosomes, Human, Pair 19/*genetics

  • Source: Neurology [Neurology] 2001 Apr 24; Vol. 56 (8), pp. 1028-32.Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 0401060 Publication Model: Print Cited Medium: Print ISSN:

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Academic Journal

A dopamine D4 receptor exon 3 VNTR allele protecting against migraine without aura.

  • Authors : de Sousa SC; Social, Genetic and Developmental Centre, Institute of Psychiatry, University of London, London, United Kingdom.; Karwautz A

Subjects: Alleles* ; Genetic Predisposition to Disease*; Migraine without Aura/Migraine without Aura/Migraine without Aura/*genetics

  • Source: Annals of neurology [Ann Neurol] 2007 Jun; Vol. 61 (6), pp. 574-8.Publisher: Wiley-Liss Country of Publication: United States NLM ID: 7707449 Publication Model: Print Cited Medium: Print ISSN: 0364-5134 (Print)

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Periodical

Second gene identified for familial hemiplegic migraine.

Subjects: Alleles*; Migraine with Aura/Migraine with Aura/Migraine with Aura/*genetics ; Mutation, Missense/Mutation, Missense/Mutation, Missense/*genetics

  • Source: The Lancet. Neurology [Lancet Neurol] 2003 Mar; Vol. 2 (3), pp. 137.Publisher: Lancet Pub. Group Country of Publication: England NLM ID: 101139309 Publication Model: Print Cited Medium: Print ISSN: 1474-4422

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