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Geir Bråthen
Geir Bråthen
Adjunct Associate Professor of Neurology
Verified email at ntnu.no - Homepage
Title
Cited by
Cited by
Year
Genome-wide meta-analysis identifies new loci and functional pathways influencing Alzheimer’s disease risk
IE Jansen, JE Savage, K Watanabe, J Bryois, DM Williams, S Steinberg, ...
Nature genetics 51 (3), 404-413, 2019
13532019
EFNS guidelines for diagnosis, therapy and prevention of Wernicke encephalopathy
R Galvin, G Bråthen, A Ivashynka, M Hillbom, R Tanasescu, MA Leone
European Journal of Neurology 17 (12), 1408-1418, 2010
7172010
A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease
DP Wightman, IE Jansen, JE Savage, AA Shadrin, S Bahrami, D Holland, ...
Nature genetics 53 (9), 1276-1282, 2021
2132021
Alcohol withdrawal syndrome: mechanisms, manifestations, and management
S Jesse, G Bråthen, M Ferrara, M Keindl, E Ben‐Menachem, ...
Acta Neurologica Scandinavica 135 (1), 4-16, 2017
1942017
New insights into the genetic etiology of Alzheimer’s disease and related dementias
C Bellenguez, F Küçükali, IE Jansen, L Kleineidam, S Moreno-Grau, ...
Nature genetics 54 (4), 412-436, 2022
1932022
Genetic epidemiology of Charcot–Marie–Tooth in the general population
GJ Braathen, JC Sand, A Lobato, H Høyer, MB Russell
European journal of neurology 18 (1), 39-48, 2011
1872011
Headache prevalence related to smoking and alcohol use. The Head‐HUNT Study
AH Aamodt, LJ Stovner, K Hagen, G Bråthen, J Zwart
European Journal of Neurology 13 (11), 1233-1238, 2006
1672006
A structured, nurse-led intervention program improves quality of life in patients with epilepsy: a randomized, controlled trial
G Helde, G Bovim, G Bråthen, E Brodtkorb
Epilepsy & Behavior 7 (3), 451-457, 2005
1302005
Late onset myasthenia gravis is associated with HLA DRB1* 15: 01 in the Norwegian population
AH Maniaol, A Elsais, ÅR Lorentzen, JF Owe, MK Viken, H Sæther, ...
PloS one 7 (5), e36603, 2012
1282012
De novo mutations in protein kinase genes CAMK2A and CAMK2B cause intellectual disability
S Küry, GM van Woerden, T Besnard, MP Onori, X Latypova, MC Towne, ...
The American Journal of Human Genetics 101 (5), 768-788, 2017
1232017
EFNS guideline on the diagnosis and management of alcohol‐related seizures: report of an EFNS task force
G Bråthen, E Ben‐Menachem, E Brodtkorb, R Galvin, JC Garcia‐Monco, ...
European journal of neurology 12 (8), 575-581, 2005
122*2005
Genetic epidemiology of C harcot–M arie–T ooth disease
GJ Braathen
Acta Neurologica Scandinavica 126, iv-22, 2012
1192012
The validity of questionnaire-based diagnoses: The third Nord-Trøndelag Health Study 2006–2008
K Hagen, JA Zwart, AH Aamodt, KB Nilsen, G Bråthen, G Helde, M Stjern, ...
The journal of headache and pain 11 (1), 67-73, 2010
922010
Nonadherence to treatment causing acute hospitalizations in people with epilepsy: an observational, prospective study
C Samsonsen, A Reimers, G Bråthen, G Helde, E Brodtkorb
Epilepsia 55 (11), e125-e128, 2014
882014
The diversity of seizures related to alcohol use. A study of consecutive patients
G Bråthen, E Brodtkorb, G Helde, T Sand, G Bovim
European Journal of Neurology 6 (6), 697-703, 1999
771999
Registration of Down syndrome in the Medical Birth Registry of Norway: validity and time trends
KK Melve, RT Lie, R Skjaerven, CB Van Der Hagen, GA Gradek, ...
Acta obstetricia et gynecologica Scandinavica 87 (8), 824-830, 2008
762008
Genetic diagnosis of Charcot-Marie-Tooth disease in a population by next-generation sequencing
H Høyer, GJ Braathen, ØL Busk, ØL Holla, M Svendsen, HT Hilmarsen, ...
BioMed research international 2014, 2014
752014
New insights on the genetic etiology of Alzheimer’s and related dementia
C Bellenguez, F Küçükali, I Jansen, V Andrade, S Moreno-Grau, N Amin, ...
MedRxiv, 2020.10. 01.20200659, 2020
602020
MFN2point mutations occur in 3.4% of Charcot-Marie-Tooth families. An investigation of 232 Norwegian CMT families
GJ Braathen, JC Sand, A Lobato, H Høyer, MB Russell
BMC Medical Genetics 11 (1), 1-8, 2010
602010
GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study
A Rongve, A Witoelar, A Ruiz, L Athanasiu, C Abdelnour, J Clarimon, ...
Scientific reports 9 (1), 7013, 2019
542019
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