Mathias Toft

  • Professor, Senior consultant; MD, PhD
  • +47 99 51 41 89
 

Publications 2019

Blauwendraat C, Heilbron K, Vallerga CL, Bandres-Ciga S, von Coelln R, Pihlstrøm L, Simón-Sánchez J, Schulte C, Sharma M, Krohn L, Siitonen A, Iwaki H, Leonard H, Noyce AJ, Tan M, Gibbs JR, Hernandez DG, Scholz SW, Jankovic J, Shulman LM, Lesage S, Corvol JC, Brice A, van Hilten JJ, Marinus J et al. (2019)
Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanisms
Mov Disord, 34 (6), 866-875
DOI 10.1002/mds.27659, PubMed 30957308

Blauwendraat C, Reed X, Krohn L, Heilbron K, Bandres-Ciga S, Tan M, Gibbs JR, Hernandez DG, Kumaran R, Langston R, Bonet-Ponce L, Alcalay RN, Hassin-Baer S, Greenbaum L, Iwaki H, Leonard HL, Grenn FP, Ruskey JA, Sabir M, Ahmed S, Makarious MB, Pihlstrøm L, Toft M, van Hilten JJ, Marinus J et al. (2019)
Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia
Brain (in press)
DOI 10.1093/brain/awz350, PubMed 31755958

Fernandez-Santiago R, Martin-Flores N, Antonelli F, Cerquera C, Moreno V, Bandres-Ciga S, Manduchi E, Tolosa E, Singleton AB, Moore JH, Noyce AJ, Kaiyrzhanov R, Middlehurst B, Kia DA, Tan M, Houlden H, Morris HR, Plun-Favreau H, Holmans P, Hardy J, Trabzuni D, Bras J, Quinn J, Mok KY, Kinghorn KJ et al. (2019)
SNCA and mTOR Pathway Single Nucleotide Polymorphisms Interact to Modulate the Age at Onset of Parkinson's Disease
Mov. Disord., 34 (9), 1333-1344

Flengsrud K, Toft M, Dietrichs E (2019)
Essential tremor
Tidsskr Nor Laegeforen, 139 (8)
DOI 10.4045/tidsskr.18.0904, PubMed 31062562

Flengsrud K, Toft M, Dietrichs E (2019)
Essential tremor
Tidsskr. Nor. Laegeforen., 139 (8), 722-725

Iqbal Z, Koht J, Pihlstrøm L, Henriksen SP, Cappelletti C, Russel MB, Norberto de Souza O, Skogseid IM, Toft M (2019)
Missense mutations in DYT-TOR1A dystonia
Neurol Genet, 5 (4), e343
DOI 10.1212/NXG.0000000000000343, PubMed 31321303

Iqbal Z, Toft M (2019)
TMEM230 variants in Parkinson's disease
Nat Genet, 51 (3), 366
DOI 10.1038/s41588-019-0353-7, PubMed 30804555

Iwaki H, Blauwendraat C, Leonard HL, Kim JJ, Liu G, Maple-Grødem J, Corvol JC, Pihlstrøm L, van Nimwegen M, Hutten SJ, Nguyen KH, Rick J, Eberly S, Faghri F, Auinger P, Scott KM, Wijeyekoon R, Van Deerlin VM, Hernandez DG, Gibbs JR, International Parkinson's Disease Genomics Consortium, Chitrala KN, Day-Williams AG, Brice A, Alves G et al. (2019)
Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts
Mov Disord
DOI 10.1002/mds.27845, PubMed 31505070

Iwaki H, Blauwendraat C, Leonard HL, Liu G, Maple-Grødem J, Corvol JC, Pihlstrøm L, van Nimwegen M, Hutten SJ, Nguyen KH, Rick J, Eberly S, Faghri F, Auinger P, Scott KM, Wijeyekoon R, Van Deerlin VM, Hernandez DG, Day-Williams AG, Brice A, Alves G, Noyce AJ, Tysnes OB, Evans JR, Breen DP et al. (2019)
Genetic risk of Parkinson disease and progression:: An analysis of 13 longitudinal cohorts
Neurol Genet, 5 (4), e348
DOI 10.1212/NXG.0000000000000348, PubMed 31404238

Nalls MA, Blauwendraat C, Vallerga CL, Heilbron K, Bandres-Ciga S, Chang D, Tan M, Kia DA, Noyce AJ, Xue A, Bras J, Young E, von Coelln R, Simón-Sánchez J, Schulte C, Sharma M, Krohn L, Pihlstrøm L, Siitonen A, Iwaki H, Leonard H, Faghri F, Gibbs JR, Hernandez DG, Scholz SW et al. (2019)
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
Lancet Neurol, 18 (12), 1091-1102
DOI 10.1016/S1474-4422(19)30320-5, PubMed 31701892

Puschmann A, Jiménez-Ferrer I, Lundblad-Andersson E, Mårtensson E, Hansson O, Odin P, Widner H, Brolin K, Mzezewa R, Kristensen J, Soller M, Rödström EY, Ross OA, Toft M, Breedveld GJ, Bonifati V, Brodin L, Zettergren A, Sydow O, Linder J, Wirdefeldt K, Svenningsson P, Nissbrandt H, Belin AC, Forsgren L et al. (2019)
Low prevalence of known pathogenic mutations in dominant PD genes: A Swedish multicenter study
Parkinsonism Relat Disord, 66, 158-165
DOI 10.1016/j.parkreldis.2019.07.032, PubMed 31422003

Rongve A, Witoelar A, Ruiz A, Athanasiu L, Abdelnour C, Clarimon J, Heilmann-Heimbach S, Hernández I, Moreno-Grau S, de Rojas I, Morenas-Rodríguez E, Fladby T, Sando SB, Bråthen G, Blanc F, Bousiges O, Lemstra AW, van Steenoven I, Londos E, Almdahl IS, Pålhaugen L, Eriksen JA, Djurovic S, Stordal E, Saltvedt I et al. (2019)
GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study
Sci Rep, 9 (1), 7013
DOI 10.1038/s41598-019-43458-2, PubMed 31065058

Rongve A, Witoelar A, Ruiz A, Athanasiu L, Abdelnour C, Clarimon J, Heilmann-Heimbach S, Hernández I, Moreno-Grau S, de Rojas I, Morenas-Rodríguez E, Fladby T, Sando SB, Bråthen G, Blanc F, Bousiges O, Lemstra AW, van Steenoven I, Londos E, Almdahl IS, Pålhaugen L, Eriksen JA, Djurovic S, Stordal E, Saltvedt I et al. (2019)
Author Correction: GBA and APOE ε4 associate with sporadic dementia with Lewy bodies in European genome wide association study
Sci Rep, 9 (1), 15168
DOI 10.1038/s41598-019-51827-0, PubMed 31619746

Publications 2018

Berge-Seidl V, Pihlstrøm L, Wszolek ZK, Ross OA, Toft M (2018)
No evidence for DNM3 as genetic modifier of age at onset in idiopathic Parkinson's disease
Neurobiol Aging, 74, 236.e1-236.e5
DOI 10.1016/j.neurobiolaging.2018.09.022, PubMed 30340792

Bjerknes S, Toft M, Konglund AE, Pham U, Waage TR, Pedersen L, Skjelland M, Haraldsen I, Andersson S, Dietrichs E, Skogseid IM (2018)
Multiple Microelectrode Recordings in STN-DBS Surgery for Parkinson's Disease: A Randomized Study
Mov Disord Clin Pract, 5 (3), 296-305
DOI 10.1002/mdc3.12621, PubMed 30009214

Bjørnarå KA, Pihlstrøm L, Dietrichs E, Toft M (2018)
Risk variants of the α-synuclein locus and REM sleep behavior disorder in Parkinson's disease: a genetic association study
BMC Neurol, 18 (1), 20
DOI 10.1186/s12883-018-1023-6, PubMed 29466944

Blauwendraat C, Reed X, Kia DA, Gan-Or Z, Lesage S, Pihlstrøm L, Guerreiro R, Gibbs JR, Sabir M, Ahmed S, Ding J, Alcalay RN, Hassin-Baer S, Pittman AM, Brooks J, Edsall C, Hernandez DG, Chung SJ, Goldwurm S, Toft M, Schulte C, Bras J, Wood NW, Brice A, Morris HR et al. (2018)
Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease
JAMA Neurol, 75 (11), 1416-1422
DOI 10.1001/jamaneurol.2018.1885, PubMed 30039155

Kristiansen M, Maple-Grødem J, Alves G, Arepalli S, Hernandez DG, Iwaki H, Nalls MA, Singleton A, Tysnes OB, Toft M, Pihlstrøm L (2018)
A paradoxical relationship between family history, onset age, and genetic risk in Parkinson's disease
Mov Disord, 34 (2), 298-299
DOI 10.1002/mds.27555, PubMed 30484896

Pihlstrøm L, Blauwendraat C, Cappelletti C, Berge-Seidl V, Langmyhr M, Henriksen SP, van de Berg WDJ, Gibbs JR, Cookson MR, International Parkinson Disease Genomics Consortium, North American Brain Expression Consortium, Singleton AB, Nalls MA, Toft M (2018)
A comprehensive analysis of SNCA-related genetic risk in sporadic parkinson disease
Ann Neurol, 84 (1), 117-129
DOI 10.1002/ana.25274, PubMed 30146727

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
DOI 10.1016/j.neulet.2017.08.040, PubMed 28830825

Blauwendraat C, Kia DA, Pihlstrøm L, Gan-Or Z, Lesage S, Gibbs JR, Ding J, Alcalay RN, Hassin-Baer S, Pittman AM, Brooks J, Edsall C, Chung SJ, Goldwurm S, Toft M, Schulte C, International Parkinson's Disease Genomics Consortium (IPDGC), COURAGE-PD Consortium, Hernandez D, Singleton AB, Nalls MA, Brice A, Scholz SW, Wood NW (2017)
Insufficient evidence for pathogenicity of SNCA His50Gln (H50Q) in Parkinson's disease
Neurobiol Aging, 64, 159.e5-159.e8
DOI 10.1016/j.neurobiolaging.2017.12.012, PubMed 29398121

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
DOI 10.1371/journal.pone.0174667, PubMed 28362824

Iqbal Z, Rydning SL, Wedding IM, Koht J, Pihlstrøm L, Rengmark AH, Henriksen SP, Tallaksen CME, Toft M (2017)
Correction: Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia
PLoS One, 12 (10), e0186571
DOI 10.1371/journal.pone.0186571, PubMed 29023604

Publications 2016

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
DOI 10.1038/ejhg.2016.79, PubMed 27329738

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
DOI 10.1002/mds.26505, 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
DOI 10.1016/j.parkreldis.2016.05.010, PubMed 27185167

Toft M, Ross OA (2016)
Exome Variant Mining in Familial Parkinson Disease: Will Replication Find the Gold?
JAMA Neurol, 73 (1), 21-2
DOI 10.1001/jamaneurol.2015.3536, PubMed 26595415

Publications 2015

Iqbal Z, Toft M (2015)
CHCHD2 and Parkinson's disease
Lancet Neurol, 14 (7), 680-1
DOI 10.1016/S1474-4422(15)00096-4, PubMed 26067113

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
DOI 10.1016/j.jalz.2014.12.009, PubMed 25936935

Pham U, Solbakk AK, Skogseid IM, Toft M, Pripp AH, Konglund AE, Andersson S, Haraldsen IR, Aarsland D, Dietrichs E, Malt UF (2015)
Personality changes after deep brain stimulation in Parkinson's disease
Parkinsons Dis, 2015, 490507
DOI 10.1155/2015/490507, PubMed 25705545

Pham UH, Andersson S, Toft M, Pripp AH, Konglund AE, Dietrichs E, Malt UF, Skogseid IM, Haraldsen IR, Solbakk AK (2015)
Self-Reported Executive Functioning in Everyday Life in Parkinson's Disease after Three Months of Subthalamic Deep Brain Stimulation
Parkinsons Dis, 2015, 461453
DOI 10.1155/2015/461453, PubMed 26167329

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
DOI 10.1038/jhg.2015.34, PubMed 25855069

Pihlstrøm L, Toft M (2015)
Cumulative genetic risk and age at onset in Parkinson's disease
Mov Disord, 30 (12), 1712-3
DOI 10.1002/mds.26366, 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
DOI 10.1212/WNL.0000000000002016, PubMed 26354989

Publications 2014

Bjerknes S, Skogseid IM, Sæhle T, Dietrichs E, Toft M (2014)
Surgical site infections after deep brain stimulation surgery: frequency, characteristics and management in a 10-year period
PLoS One, 9 (8), e105288
DOI 10.1371/journal.pone.0105288, PubMed 25122445

Bjørnarå KA, Dietrichs E, Toft M (2014)
Clinical features associated with sleep disturbances in Parkinson's disease
Clin Neurol Neurosurg, 124, 37-43
DOI 10.1016/j.clineuro.2014.06.027, PubMed 25016237

Børretzen MN, Bjerknes S, Sæhle T, Skjelland M, Skogseid IM, Toft M, Dietrichs E (2014)
Long-term follow-up of thalamic deep brain stimulation for essential tremor - patient satisfaction and mortality
BMC Neurol, 14, 120
DOI 10.1186/1471-2377-14-120, PubMed 24903550

Koht J, Rengmark A, Opladen T, Bjørnarå KA, Selberg T, Tallaksen CM, Blau N, Toft M (2014)
Clinical and genetic studies in a family with a novel mutation in the sepiapterin reductase gene
Acta Neurol Scand Suppl (198), 7-12
DOI 10.1111/ane.12230, PubMed 24588500

Lilleeng B, Brønnick K, Toft M, Dietrichs E, Larsen JP (2014)
Progression and survival in Parkinson's disease with subthalamic nucleus stimulation
Acta Neurol Scand, 130 (5), 292-8
DOI 10.1111/ane.12224, PubMed 24495107

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
DOI 10.1002/mds.26073, PubMed 25545759

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
DOI 10.1111/ahg.12060, PubMed 24660942

Toft M (2014)
Advances in genetic diagnosis of neurological disorders
Acta Neurol Scand Suppl (198), 20-5
DOI 10.1111/ane.12232, PubMed 24588502

Publications 2013

Karlsson MK, Sharma P, Aasly J, Toft M, Skogar O, Sæbø S, Lönneborg A (2013)
Found in transcription: accurate Parkinson's disease classification in peripheral blood
J Parkinsons Dis, 3 (1), 19-29
DOI 10.3233/JPD-120159, PubMed 23938308

Toft M, Dietrichs E (2013)
Medication costs following subthalamic nucleus deep brain stimulation for Parkinson's disease
Mov Disord, 29 (2), 275-6
DOI 10.1002/mds.25504, PubMed 23696136

Publications 2012

Bjørnarå KA, Dietrichs E, Toft M (2012)
REM sleep behavior disorder in Parkinson's disease--is there a gender difference?
Parkinsonism Relat Disord, 19 (1), 120-2
DOI 10.1016/j.parkreldis.2012.05.027, PubMed 22726815

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
DOI 10.1016/j.neurobiolaging.2012.10.019, PubMed 23153929

Publications 2011

Pihlstrøm L, Toft M (2011)
Genetic variability in SNCA and Parkinson's disease
Neurogenetics, 12 (4), 283-93
DOI 10.1007/s10048-011-0292-7, PubMed 21800132

Pihlstrøm L, Toft M (2011)
Parkinson's disease: What remains of the "missing heritability"?
Mov Disord, 26 (11), 1971-3
DOI 10.1002/mds.23898, PubMed 21812035

Toft M (2011)
The Wilson films--MS tremor
Mov Disord, 26 (14), 2471-2
DOI 10.1002/mds.24010, PubMed 22170271

Toft M (2011)
Dopaminergic Neurons Generated Directly From Human Fibroblasts
Mov. Disord., 26 (11), 1975

Toft M (2011)
International consortium identifies new genetic risk factors for Parkinson's disease
Mov Disord, 26 (4), 606
DOI 10.1002/mds.23725, PubMed 21648125

Toft M, Dietrichs E (2011)
Aggravated stuttering following subthalamic deep brain stimulation in Parkinson's disease--two cases
BMC Neurol, 11, 44
DOI 10.1186/1471-2377-11-44, PubMed 21477305

Toft M, Dietrichs E (2011)
Levodopa-responsive parkinsonism in probable extrapontine myelinolysis of the mesencephalon
Mov Disord, 26 (12), 2180-1
DOI 10.1002/mds.23876, PubMed 22021157

Toft M, Lilleeng B, Ramm-Pettersen J, Skogseid IM, Gundersen V, Gerdts R, Pedersen L, Skjelland M, Røste GK, Dietrichs E (2011)
Long-term efficacy and mortality in Parkinson's disease patients treated with subthalamic stimulation
Mov Disord, 26 (10), 1931-4
DOI 10.1002/mds.23817, PubMed 21656853

Publications 2010

Toft M, Ross OA (2010)
Copy number variation in Parkinson's disease
Genome Med, 2 (9), 62
DOI 10.1186/gm183, PubMed 20828427

Aasly JO, Vilariño-Güell C, Dachsel JC, Webber PJ, West AB, Haugarvoll K, Johansen KK, Toft M, Nutt JG, Payami H, Kachergus JM, Lincoln SJ, Felic A, Wider C, Soto-Ortolaza AI, Cobb SA, White LR, Ross OA, Farrer MJ (2010)
Novel pathogenic LRRK2 p.Asn1437His substitution in familial Parkinson's disease
Mov Disord, 25 (13), 2156-63
DOI 10.1002/mds.23265, PubMed 20669305

Publications 2008

Haugarvoll K, Toft M, Skipper L, Heckman MG, Crook JE, Soto A, Ross OA, Hulihan MM, Kachergus JM, Sando SB, White LR, Lynch T, Gibson JM, Uitti RJ, Wszolek ZK, Aasly JO, Farrer MJ (2008)
Fine-mapping and candidate gene investigation within the PARK10 locus
Eur J Hum Genet, 17 (3), 336-43
DOI 10.1038/ejhg.2008.187, PubMed 18854859

Ross OA, Toft M, Haugarvoll K (2008)
Corticobasal syndrome and primary progressive aphasia as manifestations of lrrk2 gene mutations
Neurology, 71 (4), 303; author reply 303-4
DOI 10.1212/01.wnl.0000320511.30222.dd, PubMed 18645174

Toft M, Lilleeng B, Ramm-Pettersen J, Røste GK, Pedersen L, Skogseid IM, Dietrichs E (2008)
[Treatment of movement disorders with deep brain stimulation]
Tidsskr Nor Laegeforen, 128 (17), 1972-6
PubMed 18787575

Publications 2007

Haugarvoll K, Toft M, Ross OA, Stone JT, Heckman MG, White LR, Lynch T, Gibson JM, Wszolek ZK, Uitti RJ, Aasly JO, Farrer MJ (2007)
ELAVL4, PARK10, and the Celts
Mov Disord, 22 (4), 585-7
DOI 10.1002/mds.21336, PubMed 17230446

Haugarvoll K, Toft M, Ross OA, White LR, Aasly JO, Farrer MJ (2007)
Variants in the LRRK1 gene and susceptibility to Parkinson's disease in Norway
Neurosci Lett, 416 (3), 299-301
DOI 10.1016/j.neulet.2007.02.020, PubMed 17324517

Toft M (2007)
A patient's journey - The reluctant patient: Parkinson's disease - A doctor's perspective
Br. Med. J., 335 (7627), 990

Toft M, Mata IF, Ross OA, Kachergus J, Hulihan MM, Haugarvoll K, Stone JT, Blazquez M, Gibson JM, Aasly JO, White LR, Lynch T, Adler CH, Gwinn-Hardy K, Farrer MJ (2007)
Pathogenicity of the Lrrk2 R1514Q substitution in Parkinson's disease
Mov Disord, 22 (3), 389-92
DOI 10.1002/mds.21217, PubMed 17216639

White LR, Toft M, Kvam SN, Farrer MJ, Aasly JO (2007)
MAPK-pathway activity, Lrrk2 G2019S, and Parkinson's disease
J Neurosci Res, 85 (6), 1288-94
DOI 10.1002/jnr.21240, PubMed 17385669

Publications 2006

Dächsel JC, Ross OA, Mata IF, Kachergus J, Toft M, Cannon A, Baker M, Adamson J, Hutton M, Dickson DW, Farrer MJ (2006)
Lrrk2 G2019S substitution in frontotemporal lobar degeneration with ubiquitin-immunoreactive neuronal inclusions
Acta Neuropathol, 113 (5), 601-6
DOI 10.1007/s00401-006-0178-1, PubMed 17151837

Farrer MJ, Haugarvoll K, Ross OA, Stone JT, Milkovic NM, Cobb SA, Whittle AJ, Lincoln SJ, Hulihan MM, Heckman MG, White LR, Aasly JO, Gibson JM, Gosal D, Lynch T, Wszolek ZK, Uitti RJ, Toft M (2006)
Genomewide association, Parkinson disease, and PARK10
Am J Hum Genet, 78 (6), 1084-8; author reply 1092-4
DOI 10.1086/504728, PubMed 16685661

Papapetropoulos S, Singer C, Ross OA, Toft M, Johnson JL, Farrer MJ, Mash DC (2006)
Clinical heterogeneity of the LRRK2 G2019S mutation
Arch Neurol, 63 (9), 1242-6
DOI 10.1001/archneur.63.9.1242, PubMed 16966501

Ross OA, Toft M, Whittle AJ, Johnson JL, Papapetropoulos S, Mash DC, Litvan I, Gordon MF, Wszolek ZK, Farrer MJ, Dickson DW (2006)
Lrrk2 and Lewy body disease
Ann Neurol, 59 (2), 388-93
DOI 10.1002/ana.20731, PubMed 16437559

Publications 2005

Biancalana V, Toft M, Le Ber I, Tison F, Scherrer E, Thibodeau S, Mandel JL, Brice A, Farrer MJ, Dürr A (2005)
FMR1 premutations associated with fragile X-associated tremor/ataxia syndrome in multiple system atrophy
Arch Neurol, 62 (6), 962-6
DOI 10.1001/archneur.62.6.962, PubMed 15956167

Gosal D, Ross OA, Wiley J, Irvine GB, Johnston JA, Toft M, Mata IF, Kachergus J, Hulihan M, Taylor JP, Lincoln SJ, Farrer MJ, Lynch T, Mark Gibson J (2005)
Clinical traits of LRRK2-associated Parkinson's disease in Ireland: a link between familial and idiopathic PD
Parkinsonism Relat Disord, 11 (6), 349-52
DOI 10.1016/j.parkreldis.2005.05.004, PubMed 16102999

Haugen T, Toft M, Müller CR, Aasly J (2005)
[Malignant hyperthermia--a hereditary and potentially life-threatening condition]
Tidsskr Nor Laegeforen, 125 (20), 2792-4
PubMed 16244682

Kachergus J, Mata IF, Hulihan M, Taylor JP, Lincoln S, Aasly J, Gibson JM, Ross OA, Lynch T, Wiley J, Payami H, Nutt J, Maraganore DM, Czyzewski K, Styczynska M, Wszolek ZK, Farrer MJ, Toft M (2005)
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations
Am J Hum Genet, 76 (4), 672-80
DOI 10.1086/429256, PubMed 15726496

Toft M, Farrer M (2005)
Premutation alleles and fragile X-associated tremor/ataxia syndrome
JAMA, 293 (3), 296; author reply 296-7
DOI 10.1001/jama.293.3.296-a, PubMed 15657320

Toft M, Mata IF, Kachergus JM, Ross OA, Farrer MJ (2005)
LRRK2 mutations and Parkinsonism
Lancet, 365 (9466), 1229-30
DOI 10.1016/S0140-6736(05)74809-1, PubMed 15811454

Toft M, Sando SB, Melquist S, Ross OA, White LR, Aasly JO, Farrer MJ (2005)
LRRK2 mutations are not common in Alzheimer's disease
Mech Ageing Dev, 126 (11), 1201-5
DOI 10.1016/j.mad.2005.06.010, PubMed 16087219

Toft M, Aasly J, Bisceglio G, Adler CH, Uitti RJ, Krygowska-Wajs A, Lynch T, Wszolek ZK, Farrer MJ (2005)
Parkinsonism, FXTAS, and FMR1 premutations
Mov Disord, 20 (2), 230-3
DOI 10.1002/mds.20297, PubMed 15390127

Aasly JO, Toft M, Fernandez-Mata I, Kachergus J, Hulihan M, White LR, Farrer M (2005)
Clinical features of LRRK2-associated Parkinson's disease in central Norway
Ann Neurol, 57 (5), 762-5
DOI 10.1002/ana.20456, PubMed 15852371

Publications 2004

Skipper L, Wilkes K, Toft M, Baker M, Lincoln S, Hulihan M, Ross OA, Hutton M, Aasly J, Farrer M (2004)
Linkage disequilibrium and association of MAPT H1 in Parkinson disease
Am J Hum Genet, 75 (4), 669-77
DOI 10.1086/424492, PubMed 15297935

Toft M, Aasly J (2004)
[The genetics of Parkinson disease]
Tidsskr Nor Laegeforen, 124 (7), 922-4
PubMed 15060636

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