Lasse Pihlstrøm
Position: Postdoc, MD, PhD

Author network for Lasse Pihlstrøm by COREMINE medical

Publications 2017

Berge-Seidl V, Pihlstrøm L, Maple-Grødem J, Forsgren L, Linder J, Larsen JP, Tysnes OB, Toft M (2017)
The GBA variant E326K is associated with Parkinson's disease and explains a genome-wide association signal
Neurosci Lett, 658, 48-52 (in press)
PubMed 28830825

Blauwendraat C, Faghri F, Pihlstrom L, Geiger JT, Elbaz A, Lesage S, Corvol JC, May P, Nicolas A, Abramzon Y, Murphy NA, Gibbs JR, Ryten M, Ferrari R, Bras J, Guerreiro R, Williams J, Sims R, Lubbe S, Hernandez DG, Mok KY, Robak L, Campbell RH, Rogaeva E, Traynor BJ et al. (2017)
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases
Neurobiol Aging, 57, 247.e9-247.e13
PubMed 28602509

Ezat B, Pihlstrøm L, Aasly J, Tysnes OB, Egge A, Dietrichs E (2017)
Use of advanced therapies for Parkinson's disease in Norway
Tidsskr Nor Laegeforen, 137 (9), 619-623
PubMed 28468476

Fagan ES, Pihlstrøm L (2017)
Genetic risk factors for cognitive decline in Parkinson's disease: a review of the literature
Eur J Neurol, 24 (4), 561-e20
PubMed 28220571

Faiz KW, Pihlstrøm L (2017)
[No title available]
Tidsskr Nor Laegeforen, 137 (4), 298
PubMed 28225240

Iqbal Z, Rydning SL, Wedding IM, Koht J, Pihlstrøm L, Rengmark AH, Henriksen SP, Tallaksen CM, Toft M (2017)
Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia
PLoS One, 12 (3), e0174667
PubMed 28362824

Pihlstrøm L (2017)
[No title available]
Tidsskr Nor Laegeforen, 137 (5), 388
PubMed 28272576

Publications 2016

Chelban V, Manole A, Pihlstrøm L, Schottlaender L, Efthymiou S, OConnor E, Meissner WG, Holton JL, Houlden H (2016)
Analysis of the prion protein gene in multiple system atrophy
Neurobiol Aging, 49, 216.e15-216.e18
PubMed 27793473

Iqbal Z, Pihlstrøm L, Rengmark A, Henriksen SP, Linder J, Forsgren L, Toft M (2016)
Rare variants in dementia genes and Parkinson's disease
Eur J Hum Genet, 24 (12), 1661-1662
PubMed 27329738

Pihlstrøm L (2016)
[Not Available]
Tidsskr Nor Laegeforen, 136 (10), 944
PubMed 27272377

Pihlstrøm L (2016)
[No title available]
Tidsskr Nor Laegeforen, 136 (18), 1570
PubMed 27731607

Pihlstrøm L, Morset KR, Grimstad E, Vitelli V, Toft M (2016)
A cumulative genetic risk score predicts progression in Parkinson's disease
Mov Disord, 31 (4), 487-90
PubMed 26853697

Rengmark A, Pihlstrøm L, Linder J, Forsgren L, Toft M (2016)
Low frequency of GCH1 and TH mutations in Parkinson's disease
Parkinsonism Relat Disord, 29, 109-11
PubMed 27185167

Publications 2015

Lill CM, Rengmark A, Pihlstrøm L, Fogh I, Shatunov A, Sleiman PM, Wang LS, Liu T, Lassen CF, Meissner E, Alexopoulos P, Calvo A, Chio A, Dizdar N, Faltraco F, Forsgren L, Kirchheiner J, Kurz A, Larsen JP, Liebsch M, Linder J, Morrison KE, Nissbrandt H, Otto M, Pahnke J et al. (2015)
The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease
Alzheimers Dement, 11 (12), 1407-1416
PubMed 25936935

Pihlstrøm L (2015)
[The wonders of practical teaching]
Tidsskr Nor Laegeforen, 135 (20), 1878
PubMed 26534820

Pihlstrøm L, Rengmark A, Bjørnarå KA, Dizdar N, Fardell C, Forsgren L, Holmberg B, Larsen JP, Linder J, Nissbrandt H, Tysnes OB, Dietrichs E, Toft M (2015)
Fine mapping and resequencing of the PARK16 locus in Parkinson's disease
J Hum Genet, 60 (7), 357-62
PubMed 25855069

Pihlstrøm L, Toft M (2015)
Cumulative genetic risk and age at onset in Parkinson's disease
Mov Disord, 30 (12), 1712-3
PubMed 26234887

Wang L, Aasly JO, Annesi G, Bardien S, Bozi M, Brice A, Carr J, Chung SJ, Clarke C, Crosiers D, Deutschländer A, Eckstein G, Farrer MJ, Goldwurm S, Garraux G, Hadjigeorgiou GM, Hicks AA, Hattori N, Klein C, Jeon B, Kim YJ, Lesage S, Lin JJ, Lynch T, Lichtner P et al. (2015)
Large-scale assessment of polyglutamine repeat expansions in Parkinson disease
Neurology, 85 (15), 1283-92
PubMed 26354989

Publications 2014

Pihlstrøm L (2014)
[Re: Affection for affection]
Tidsskr Nor Laegeforen, 134 (20), 1920
PubMed 25350431

Pihlstrøm L, Berge V, Rengmark A, Toft M (2014)
Parkinson's disease correlates with promoter methylation in the α-synuclein gene
Mov Disord, 30 (4), 577-80
PubMed 25545759

Pihlstrøm L, Nedregaard B, Krossnes B, Aamodt AH (2014)
[Septic embolus]
Tidsskr Nor Laegeforen, 134 (9), 945
PubMed 24828721

Pihlstrøm L, Rengmark A, Bjørnarå KA, Toft M (2014)
Effective variant detection by targeted deep sequencing of DNA pools: an example from Parkinson's disease
Ann Hum Genet, 78 (3), 243-52
PubMed 24660942

Publications 2012

Pihlstrøm L, Axelsson G, Bjørnarå KA, Dizdar N, Fardell C, Forsgren L, Holmberg B, Larsen JP, Linder J, Nissbrandt H, Tysnes OB, Ohman E, Dietrichs E, Toft M (2012)
Supportive evidence for 11 loci from genome-wide association studies in Parkinson's disease
Neurobiol Aging, 34 (6), 1708.e7-13
PubMed 23153929

Publications 2011

Kvåle G, Fadnes LT, Tryland M, Pihlstrøm L (2011)
Climate change--the biggest health threat of our time
Tidsskr Nor Laegeforen, 131 (17), 1670-2
PubMed 21901045

Pihlstrøm L (2011)
[The sardonic smile]
Tidsskr Nor Laegeforen, 131 (24), 2500-3
PubMed 22170142

Pihlstrøm L, Alfstad KÅ, Solyga V, Ringstad GA, Kerty E (2011)
[A 55-year old man with recurrent brain infarction]
Tidsskr Nor Laegeforen, 131 (11), 1089-91
PubMed 21681238

Pihlstrøm L, Toft M (2011)
Genetic variability in SNCA and Parkinson's disease
Neurogenetics, 12 (4), 283-93
PubMed 21800132

Pihlstrøm L, Toft M (2011)
Parkinson's disease: What remains of the "missing heritability"?
Mov Disord, 26 (11), 1971-3
PubMed 21812035