NCOR2 is a novel candidate gene for migraine-epilepsy phenotype

Marjo Eveliina Nuottamo; Paavo Häppölä; Ville Artto; Heidi Hautakangas; Matti Pirinen; Tero Hiekkalinna; Pekka Ellonen; Maija Lepistö; Eija Hämäläinen; Auli Siren; Anna-Elina Lehesjoki; Mikko Kallela; Aarno Palotie; Mari Anneli Kaunisto; Maija Wessman

doi:10.1177/03331024211068065

NCOR2 is a novel candidate gene for migraine-epilepsy phenotype

Marjo Eveliina Nuottamo, Paavo Häppölä, Ville Artto, Heidi Hautakangas, Matti Pirinen, Tero Hiekkalinna, Pekka Ellonen, Maija Lepistö, Eija Hämäläinen, Auli Siren, Anna-Elina Lehesjoki, Mikko Kallela, Aarno Palotie, Mari Anneli Kaunisto, Maija Wessman

Research output: Contribution to journal › Article › Scientific › peer-review

Original language	English
Article number	03331024211068065
Journal	Cephalalgia
Volume	42
Issue number	7
Pages (from-to)	631-644
Number of pages	14
ISSN	0333-1024
DOIs	https://doi.org/10.1177/03331024211068065
Publication status	Published - Jun 2022
MoE publication type	A1 Journal article-refereed

Fields of Science

Neurological disorder
12q24
31
linkage analysis
next-generation sequencing (NGS) technologies
comorbidity
pathophysiology
FAMILIAL HEMIPLEGIC MIGRAINE
RETT-SYNDROME
LINKAGE
IDENTIFICATION
MUTATIONS
RESOURCE
PROGRAM
MECP2
3112 Neurosciences

Access to Document

10.1177/03331024211068065

Nuottamo_et_al_2022_Revised_manuscriptAccepted author manuscript, 719 KBLicence: Unspecified

Cite this

Nuottamo, M. E., Häppölä, P., Artto, V., Hautakangas, H., Pirinen, M., Hiekkalinna, T., Ellonen, P., Lepistö, M., Hämäläinen, E., Siren, A., Lehesjoki, A.-E., Kallela, M., Palotie, A., Kaunisto, M. A., & Wessman, M. (2022). NCOR2 is a novel candidate gene for migraine-epilepsy phenotype. Cephalalgia, 42(7), 631-644. Article 03331024211068065. https://doi.org/10.1177/03331024211068065

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title = "NCOR2 is a novel candidate gene for migraine-epilepsy phenotype",

keywords = "Neurological disorder, 12q24, 31, linkage analysis, next-generation sequencing (NGS) technologies, comorbidity, pathophysiology, FAMILIAL HEMIPLEGIC MIGRAINE, RETT-SYNDROME, LINKAGE, IDENTIFICATION, MUTATIONS, RESOURCE, PROGRAM, MECP2, 3112 Neurosciences",

author = "Nuottamo, {Marjo Eveliina} and Paavo H{\"a}pp{\"o}l{\"a} and Ville Artto and Heidi Hautakangas and Matti Pirinen and Tero Hiekkalinna and Pekka Ellonen and Maija Lepist{\"o} and Eija H{\"a}m{\"a}l{\"a}inen and Auli Siren and Anna-Elina Lehesjoki and Mikko Kallela and Aarno Palotie and Kaunisto, {Mari Anneli} and Maija Wessman",

year = "2022",

month = jun,

doi = "10.1177/03331024211068065",

language = "English",

volume = "42",

pages = "631--644",

journal = "Cephalalgia",

issn = "0333-1024",

publisher = "SAGE Publications Ltd STM",

number = "7",

}

Nuottamo, ME, Häppölä, P , Artto, V , Hautakangas, H , Pirinen, M , Hiekkalinna, T, Ellonen, P, Lepistö, M, Hämäläinen, E, Siren, A, Lehesjoki, A-E , Kallela, M , Palotie, A , Kaunisto, MA & Wessman, M 2022, 'NCOR2 is a novel candidate gene for migraine-epilepsy phenotype', Cephalalgia, vol. 42, no. 7, 03331024211068065, pp. 631-644. https://doi.org/10.1177/03331024211068065

TY - JOUR

T1 - NCOR2 is a novel candidate gene for migraine-epilepsy phenotype

AU - Nuottamo, Marjo Eveliina

AU - Häppölä, Paavo

AU - Artto, Ville

AU - Hautakangas, Heidi

AU - Pirinen, Matti

AU - Hiekkalinna, Tero

AU - Ellonen, Pekka

AU - Lepistö, Maija

AU - Hämäläinen, Eija

AU - Siren, Auli

AU - Lehesjoki, Anna-Elina

AU - Kallela, Mikko

AU - Palotie, Aarno

AU - Kaunisto, Mari Anneli

AU - Wessman, Maija

PY - 2022/6

Y1 - 2022/6

KW - Neurological disorder

KW - 12q24

KW - 31

KW - linkage analysis

KW - next-generation sequencing (NGS) technologies

KW - comorbidity

KW - pathophysiology

KW - FAMILIAL HEMIPLEGIC MIGRAINE

KW - RETT-SYNDROME

KW - LINKAGE

KW - IDENTIFICATION

KW - MUTATIONS

KW - RESOURCE

KW - PROGRAM

KW - MECP2

KW - 3112 Neurosciences

U2 - 10.1177/03331024211068065

DO - 10.1177/03331024211068065

M3 - Article

SN - 0333-1024

VL - 42

SP - 631

EP - 644

JO - Cephalalgia

JF - Cephalalgia

IS - 7

M1 - 03331024211068065

ER -