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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jun 8, 2023. (Total: 217765Documents)
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Records 1 - 7 (of 7 Records)

Query Trace: Migraine with Aura and KCNK18[original query]
Functional analysis of missense variants in the TRESK (KCNK18) K channel.
Scientific reports 2012 2 237.
Andres-Enguix Isabelle, Shang Lijun, Stansfeld Phillip J, Morahan Julia M, Sansom Mark S P, Lafrenière Ronald G, Roy Bishakha, Griffiths Lyn R, Rouleau Guy A, Ebers George C, Cader Zameel M, Tucker Stephen
Association analysis of STX1A gene variants in common forms of migraine.
Cephalalgia : an international journal of headache 2012 Feb 32 (3): 203-12.
Tropeano Maria, Wöber-Bingöl Ciçek, Karwautz Andreas, Wagner Gudrun, Vassos Evangelos, Campos-de-Sousa Sara, Graggaber Andrea, Zesch Heidi E, Kienbacher Christian, Natriashvili Sofia, Kanbur Incifer, Wöber Christian, Collier David
KCNK18 (TRESK) genetic variants in Italian patients with migraine.
Headache 2014 Oct 54 (9): 1515-22.
Rainero Innocenzo, Rubino Elisa, Gallone Salvatore, Zavarise Paola, Carli Daniela, Boschi Silvia, Fenoglio Pierpaola, Savi Lidia, Gentile Salvatore, Benna Paolo, Pinessi Lorenzo, Dalla Volta Giorg
Molecular factors in migraine.
Oncotarget 2016 May .
Kowalska Marta, Prendecki MichaÅ, Kozubski Wojciech, Lianeri Margarita, Dorszewska Jolan
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
Analysis of Genetic Variants in SCN1A, SCN2A, KCNK18, TRPA1 and STX1A as a Possible Marker of Migraine.
Current genomics 2020 Apr 21 (3): 224-236.
Kowalska Marta, Prendecki Micha?, Kapelusiak-Pielok Magdalena, Grzelak Teresa, ?agan-J?drzejczyk Urszula, Wiszniewska Ma?gorzata, Kozubski Wojciech, Dorszewska Jolan
Study of variants in genes implicated in rare familial migraine syndromes and their association with migraine in 200,000 exome-sequenced UK Biobank participants.
Annals of human genetics 2022 8 86 (6): 353-360.
Markel Katherine Alexis, Curtis Dav
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