Human Genome Epidemiology Literature Finder
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Records 1 - 9 (of 9 Records) |
| Query Trace: Migraine with Aura and CACNA1A[original query] |
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| Involvement of the CACNA1A gene containing region on 19p13 in migraine with and without aura. Neurology 2001 Apr 56 (8): 1028-32. Terwindt G M, Ophoff R A, van Eijk R, Vergouwe M N, Haan J, Frants R R, Sandkuijl L A, Ferrari M D, |
| Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine. Archives of neurology 2002 Jun 59 (6): 1016-8. Terwindt Gisela, Kors Esther, Haan Joost, Vermeulen Frans, Van den Maagdenberg Arn, Frants Rune, Ferrari Mich |
| [An update on the familial headache syndromes]. Rinsho shinkeigaku = Clinical neurology 2005 1 44 (11): 944-7. Takeshima Takao, Kusumi Masayoshi, Fukuhara Yoko, Kowa Hisanori, Adachi Yoshiki, Nakashima Ken |
| The interplay of two single nucleotide polymorphisms in the CACNA1A gene may contribute to migraine susceptibility. Neuroscience letters 2009 Mar 453 (1): 12-5. D'Onofrio Mara, Ambrosini Anna, Di Mambro Alessandra, Arisi Ivan, Santorelli Filippo M, Grieco Gaetano S, Nicoletti Ferdinando, Nappi Giuseppe, Pierelli Francesco, Schoenen Jean, Buzzi Maria Gabriel |
| Genetic studies of Polish migraine patients: screening for causative mutations in four migraine-associated genes. Human genomics 2016 10 (1): 3. Domitrz Izabela, Kosiorek Michalina, ?ekanowski Cezary, Kami?ska An |
| Possible Involvement of the CACNA1E Gene in Migraine: A Search for Single Nucleotide Polymorphism in Different Clinical Phenotypes. Headache 2017 Jun . Ambrosini Anna, D'Onofrio Mara, Buzzi Maria Gabriella, Arisi Ivan, Grieco Gaetano S, Pierelli Francesco, Santorelli Filippo M, Schoenen Je |
| Higher burden of rare frameshift indels in genes related to synaptic transmission separate familial hemiplegic migraine from common types of migraine. Journal of medical genetics 2020 1 57 (9): 610-616. Rasmussen Andreas Hoiberg, Olofsson Isa, Chalmer Mona Ameri, Olesen Jes, Hansen Thomas Folkma |
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles.
Nature genetics 2022 02 54 (2): 152-160. Hautakangas Heidi, Winsvold Bendik S, Ruotsalainen Sanni E, Bjornsdottir Gyda, Harder Aster V E, Kogelman Lisette J A, Thomas Laurent F, Noordam Raymond, Benner Christian, Gormley Padhraig, Artto Ville, Banasik Karina, Bjornsdottir Anna, Boomsma Dorret I, Brumpton Ben M, Burgdorf Kristoffer Sølvsten, Buring Julie E, Chalmer Mona Ameri, de Boer Irene, Dichgans Martin, Erikstrup Christian, Färkkilä Markus, Garbrielsen Maiken Elvestad, Ghanbari Mohsen, Hagen Knut, Häppölä Paavo, Hottenga Jouke-Jan, Hrafnsdottir Maria G, Hveem Kristian, Johnsen Marianne Bakke, Kähönen Mika, Kristoffersen Espen S, Kurth Tobias, Lehtimäki Terho, Lighart Lannie, Magnusson Sigurdur H, Malik Rainer, Pedersen Ole Birger, Pelzer Nadine, Penninx Brenda W J H, Ran Caroline, Ridker Paul M, Rosendaal Frits R, Sigurdardottir Gudrun R, Skogholt Anne Heidi, Sveinsson Olafur A, Thorgeirsson Thorgeir E, Ullum Henrik, Vijfhuizen Lisanne S, Widén Elisabeth, van Dijk Ko Willems, , , , Aromaa Arpo, Belin Andrea Carmine, Freilinger Tobias, Ikram M Arfan, Järvelin Marjo-Riitta, Raitakari Olli T, Terwindt Gisela M, Kallela Mikko, Wessman Maija, Olesen Jes, Chasman Daniel I, Nyholt Dale R, Stefánsson Hreinn, Stefansson Kari, van den Maagdenberg Arn M J M, Hansen Thomas Folkmann, Ripatti Samuli, Zwart John-Anker, Palotie Aarno, Pirinen Mat |
| Whole Exome Sequencing of Hemiplegic Migraine Patients Shows an Increased Burden of Missense Variants in CACNA1H and CACNA1I Genes. Molecular neurobiology 2023 2 . Maksemous Neven, Harder Aster V E, Ibrahim Omar, Vijfhuizen Lisanne S, Sutherland Heidi, Pelzer Nadine, de Boer Irene, Terwindt Gisela M, Lea Rodney A, van den Maagdenberg Arn M J M, Griffiths Lyn |
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