| Suppressed responses to self-triggered sounds in the human auditory cortex MH Martikainen, K Kaneko, R Hari Cerebral cortex 15 (3), 299-302, 2005 | 308 | 2005 |
| Clinical, genetic, and radiological features of extrapyramidal movement disorders in mitochondrial disease MH Martikainen, YS Ng, GS Gorman, CL Alston, EL Blakely, AM Schaefer, ... JAMA neurology 73 (6), 668-674, 2016 | 97 | 2016 |
| Consensus-based statements for the management of mitochondrial stroke-like episodes YS Ng, LA Bindoff, GS Gorman, R Horvath, T Klopstock, M Mancuso, ... Wellcome open research 4, 201, 2019 | 93 | 2019 |
| Successful treatment of POLG‐related mitochondrial epilepsy with antiepileptic drugs and low glycaemic index diet MH Martikainen, M Päivärinta, S Jääskeläinen, K Majamaa Epileptic Disorders 14 (4), 438-441, 2012 | 72 | 2012 |
| A novel mutation m.8561C>G in MT-ATP6/8 causing a mitochondrial syndrome with ataxia, peripheral neuropathy, diabetes mellitus, and hypergonadotropic … L Kytövuori, J Lipponen, H Rusanen, T Komulainen, MH Martikainen, ... Journal of neurology 263, 2188-2195, 2016 | 69 | 2016 |
| Clinical and imaging findings in Parkinson disease associated with the A53E SNCA mutation MH Martikainen, M Päivärinta, M Hietala, V Kaasinen Neurology: Genetics 1 (4), e27, 2015 | 59 | 2015 |
| Deep brain stimulation for monogenic Parkinson’s disease: a systematic review T Kuusimäki, J Korpela, E Pekkonen, MH Martikainen, A Antonini, ... Journal of Neurology 267, 883-897, 2020 | 52 | 2020 |
| Pathogenic variants in MT‐ATP6: A UK‐based Mitochondrial Disease Cohort Study YS Ng, MH Martikainen, GS Gorman, A Blain, E Bugiardini, A Bunting, ... Annals of Neurology, https://doi.org/10.1002/ana.25525, 2019 | 47* | 2019 |
| Mitochondrial disease: mimics and chameleons MH Martikainen, PF Chinnery Practical neurology 15 (6), 424-435, 2015 | 42 | 2015 |
| Using global team science to identify genetic Parkinson's disease worldwide EJ Vollstedt, M Kasten, C Klein, ... Annals of Neurology, https://doi.org/10.1002/ana.25514, 2019 | 36 | 2019 |
| Embracing monogenic Parkinson's disease: the MJFF Global Genetic PD cohort EJ Vollstedt, S Schaake, K Lohmann, S Padmanabhan, A Brice, S Lesage, ... Movement Disorders 38 (2), 286-303, 2023 | 35 | 2023 |
| Prevalence of mitochondrial diabetes in southwestern Finland: a molecular epidemiological study MH Martikainen, T Rönnemaa, K Majamaa Acta diabetologica 50, 737-741, 2013 | 32 | 2013 |
| CD106 (VCAM-1) in testicular immunoregulation S Sainio-Pöllänen, J Sundström, S Erkkilä, A Hänninen, M Vainiopää, ... Journal of reproductive immunology 33 (3), 221-238, 1997 | 31 | 1997 |
| Rapid improvement of a complex migrainous episode with sodium valproate in a patient with CADASIL MH Martikainen, S Roine The Journal of Headache and Pain 13, 95-97, 2012 | 29 | 2012 |
| Decreased male reproductive success in association with mitochondrial dysfunction MH Martikainen, JP Grady, YS Ng, CL Alston, GS Gorman, RW Taylor, ... European Journal of Human Genetics 25 (10), 1162-1164, 2017 | 28 | 2017 |
| Juvenile parkinsonism, hypogonadism and Leigh-like MRI changes in a patient with m. 4296G> A mutation in mitochondrial DNA MH Martikainen, L Kytövuori, K Majamaa Mitochondrion 13 (2), 83-86, 2013 | 28 | 2013 |
| IL‐10 is highly expressed in the cryptorchid cryptepididymal epithelium: a probable mechanism preventing immune responses against autoantigenic spermatozoa in the epididymal tubule E Veräjänkorva, P Pöllänen, A Hänninen, M Martikainen, J Sundström, ... international journal of andrology 25 (3), 129-133, 2002 | 22 | 2002 |
| Impaired information-processing speed and working memory in leukoencephalopathy with brainstem and spinal cord involvement and elevated lactate (LBSL) and DARS2 mutations: a … MH Martikainen, U Ellfolk, K Majamaa Journal of neurology 260, 2078-2083, 2013 | 21 | 2013 |
| Association of mitochondrial DNA haplogroups and vascular complications of diabetes mellitus: a population-based study MH Martikainen, T Rönnemaa, K Majamaa Diabetes and Vascular Disease Research 12 (4), 302-304, 2015 | 19 | 2015 |
| WFS1 variants in Finnish patients with diabetes mellitus, sensorineural hearing impairment or optic atrophy, and in suicide victims L Kytövuori, A Seppänen, MH Martikainen, JS Moilanen, S Kamppari, ... Journal of human genetics 58 (8), 495-500, 2013 | 19 | 2013 |
Riitta HariProf. (emer.) @ Aalto University, School of ARTS & School of SCI; FinlandVerified email at aalto.fi
