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Liisa Myllykangas

  • PL 21 (Haartmaninkatu 3)

    00014

    Finland

19992019
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Publications 1999 2019

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A comprehensive screening of copy number variability in dementia with Lewy bodies

Kun-Rodrigues, C., Orme, T., Carmona, S., Hernandez, D. G., Ross, O. A., Eicher, J. D., Shepherd, C., Parkkinen, L., Darwent, L., Heckman, M. G., Scholz, S. W., Troncoso, J. C., Pletnikova, O., Dawson, T., Rosenthal, L., Ansorge, O., Clarimonm, J., Lleo, A., Morenas-Rodriguez, E., Clark, L. & 48 others, Honig, L. S., Marder, K., Lemstra, A., Rogaeva, E., St George-Hyslop, P., Londos, E., Zetterberg, H., Barber, I., Braae, A., Brown, K., Morgan, K., Troakes, C., Al-Sarraj, S., Lashley, T., Holton, J., Compta, Y., Van Deerlin, V., Serrano, G. E., Beach, T. G., Lesage, S., Galasko, D., Masliah, E., Santana, I., Pastor, P., Diez-Fairen, M., Aguilar, M., Tienari, P. J., Myllykangas, L., Oinas, M., Revesz, T., Lees, A., Boeve, B. F., Petersen, R. C., Ferman, T. J., Escott-Price, V., Graff-Radford, N., Cairns, N. J., Morris, J. C., Pickering-Brown, S., Mann, D., Halliday, G. M., Hardy, J., Trojanowski, J. Q., Dickson, D. W., Singleton, A., Stone, D. J., Guerreiro, R. & Bras, J., Mar 2019, In : Neurobiology of Aging. 75, 10 p., ARTN 223.e1.

Research output: Contribution to journalArticleScientificpeer-review

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A familial frontotemporal dementia associated with C9orf72 repeat expansion and dysplastic gangliocytoma

Ferrari, R., Kero, M., Mok, K., Paetau, A., Tienari, P. J., Tynninen, O., Hardy, J., Momeni, P., Verkkoniemi-Ahola, A. & Myllykangas, L., 1 Feb 2014, In : Neurobiology of Aging. 35, 2, 4 p., 444.e11.

Research output: Contribution to journalArticleScientificpeer-review

Aggregated alpha-synuclein mediates dopaminergic neurotoxicity in vivo

Periquet, M., Fulga, T., Myllykangas, L., Schlossmacher, M. G. & Feany, M. B., 2007, In : Journal of Neuroscience. 27, p. 3338-3346 9 p.

Research output: Contribution to journalArticleScientificpeer-review

A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

Renton, A. E., Majounie, E., Waite, A., Simon-Sanchez, J., Rollinson, S., Gibbs, J. R., Schymick, J. C., Laaksovirta, H., van Swieten, J. C., Myllykangas, L., Kalimo, H., Paetau, A., Abramzon, Y., Remes, A. M., Kaganovich, A., Scholz, S. W., Duckworth, J., Ding, J., Harmer, D. W., Hernandez, D. G. & 31 others, Johnson, J. O., Mok, K., Ryten, M., Trabzuni, D., Guerreiro, R. J., Orrell, R. W., Neal, J., Murray, A., Pearson, J., Jansen, I. E., Sondervan, D., Seelaar, H., Blake, D., Young, K., Halliwell, N., Callister, J. B., Toulson, G., Richardson, A., Gerhard, A., Snowden, J., Mann, D., Neary, D., Nalls, M. A., Peuralinna, T., Jansson, L., Isoviita, V-M., Kaivorinne, A-L., Hölttä-Vuori, M., Ikonen, E., Tienari, P. J. & ITALSGEN Consortium, 2011, In : Neuron. 72, 2, p. 257-268 12 p.

Research output: Contribution to journalArticleScientificpeer-review

alpha-Synuclein pathology in the spinal cord autonomic nuclei associates with alpha-synuclein pathology in the brain: a population-based Vantaa 85+study

Oinas, M., Paetau, A., Myllykangas, L., Notkola, I-L., Kalimo, H. & Polvikoski, T., 2010, In : Acta Neuropathologica. 119, 6, p. 715-722 8 p.

Research output: Contribution to journalArticleScientificpeer-review

Alzheimer disease PS-1 exon 9 deletion defined

Prihar, G., Verkkoniemi, A., Perez-Tur, J., Crook, R., Lincoln, S., Moulden, H., Somer, M., Paetau, A., Kalimo, H., Grover, A., Myllykangas, L., Hutton, M., Hardy, J. & Haltia, M., 1999, In : Nature Medicine. 5, p. 1090-1090 1 p.

Research output: Contribution to journalArticleScientificpeer-review

Alzheimerin taudin patofysiologia - mitä uutta?

Tanila, H., Hiltunen, M. & Myllykangas, L., 2018, In : Duodecim. 134, 24, p. 2511-2518 8 p.

Research output: Contribution to journalArticleProfessional

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Alzheimer risk loci and associated neuropathology in a population-based study (Vantaa 85+)

Mäkelä, M., Kaivola, K., Valori, M., Paetau, A., Polvikoski, T., Singleton, A. B., Traynor, B. J., Stone, D. J., Peuralinna, T., Tienari, P. J., Tanskanen, M. & Myllykangas, L., Feb 2018, In : Neurology Genetics. UNSP e211 .

Research output: Contribution to journalArticleScientificpeer-review

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Amygdala alpha-Synuclein Pathology in the Population-Based Vantaa 85+Study

Raunio, A. K., Myllykangas, L., Kero, M., Polvikoski, T., Paetau, A. & Oinas, M., 2017, In : Journal of Alzheimer's Disease. 58, 3, p. 669-674 6 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access

Amyloid precursor protein (APP) A673T mutation in the elderly Finnish population.

Kero, M., Paetau, A., Polvikoski, T., Tanskanen, M., Sulkava, R., Jansson, L., Myllykangas, L. T. & Tienari, P., 2013, In : Neurobiology of Aging. 34, 5, p. 1518.e1-1518.e3 3 p.

Research output: Contribution to journalArticleScientificpeer-review

Amyloid tracers binding sites in autosomal dominant and sporadic Alzheimer's disease

Ni, R., Gillberg, P-G., Bogdanovic, N., Viitanen, M., Myllykangas, L., Nennesmo, I., Langstrom, B. & Nordberg, A., Apr 2017, In : Alzheimer's & Dementia. 13, 4, p. 419-430 12 p.

Research output: Contribution to journalArticleScientificpeer-review

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Analysis of C9orf72 repeat expansions in a large international cohort of dementia with Lewy bodies

Kun-Rodrigues, C., Ross, O. A., Orme, T., Shepherd, C., Parkkinen, L., Darwent, L., Hernandez, D., Ansorge, O., Clark, L. N., Honig, L. S., Marder, K., Lemstra, A., Scheltens, P., van der Flier, W., Louwersheimer, E., Holstege, H., Rogaeva, E., St George-Hyslop, P., Londos, E., Zetterberg, H. & 44 others, Barber, I., Braae, A., Brown, K., Morgan, K., Maetzler, W., Berg, D., Troakes, C., Al-Sarraj, S., Lashley, T., Holton, J., Compta, Y., Van Deerlin, V., Trojanowski, J. Q., Serrano, G. E., Beach, T. G., Clarimon, J., Lleo, A., Morenas-Rodriguez, E., Lesage, S., Galasko, D., Masliah, E., Santana, I., Diez, M., Pastor, P., Tienari, P. J., Myllykangas, L., Oinas, M., Revesz, T., Lees, A., Boeve, B. F., Petersen, R. C., Ferman, T. J., Escott-Price, V., Graff-Radford, N., Cairns, N. J., Morris, J. C., Stone, D. J., Pickering-Brown, S., Mann, D., Dickson, D. W., Halliday, G. M., Singleton, A., Guerreiro, R. & Bras, J., Jan 2017, In : Neurobiology of Aging. 49, 3 p., ARTN 214.e13.

Research output: Contribution to journalArticleScientificpeer-review

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A Novel Loss-of-Function GRN Mutation p.(Tyr229*): Clinical and Neuropathological Features

Kuuluvainen, L., Pöyhönen, M., Pasanen, P., Siitonen, M., Rummukainen, J., Tienari, P. J., Paetau, A. & Myllykangas, L., 2017, In : Journal of Alzheimer's Disease. 55, 3, p. 1167-1174 8 p.

Research output: Contribution to journalArticleScientificpeer-review

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A novel transthyretin Lys70Glu (p.Lys90Glu) mutation presenting with vitreous amyloidosis and carpal tunnel syndrome

Raivio, V. E., Jonasson, J., Myllykangas, L., Ala-Mello, S., Kankuri-Tammilehto, M., Kiuru-Enari, S., Westermark, P., Tanskanen, M. & Kivela, T., 2 Jan 2016, In : Amyloid. 23, 1, p. 46-50 5 p.

Research output: Contribution to journalArticleScientificpeer-review

APOE and A beta PP Gene Variation in Cortical and Cerebrovascular Amyloid-beta Pathology and Alzheimer's Disease: A Population-Based Analysis

Peuralinna, T., Tanskanen, M., Mäkelä, M., Polvikoski, T., Paetau, A., Kalimo, H., Sulkava, R., Hardy, J., Lai, S-L., Arepalli, S., Hernandez, D., Traynor, B. J., Singleton, A., Tienari, P. J. & Myllykangas, L., 2011, In : Journal of Alzheimer's Disease. 26, 2, p. 377-385 9 p.

Research output: Contribution to journalArticleScientificpeer-review

ApoE epsilon 3-haplotype modulates Alzheimer beta-amyloid deposition in the brain

Myllykangas, L., Polvikoski, T., Reunanen, K., Wavrant-DeVrieze, F., Ellis, C., Hernandez, D., Sulkava, R., Kontula, K., Verkkoniemi, A., Notkola, I. L., Hardy, J., Perez-Tur, J., Haltia, M. J. & Tienari, P. J., 2002, In : American journal of medical genetics. Part C, Seminars in medical genetics. 114, p. 288-291 4 p.

Research output: Contribution to journalArticleScientificpeer-review

Apolipoprotein E (APOE) and lipoprotein lipase (LPL) gene variants and carotid atherosclerotic lesions in the oldest old: a population-based autopsy study

Myllykangas, L., Lammie, G. A., Notkola, I-L., Sulkava, R. & Polvikoski, T., 2009, In : Archives of Gerontology and Geriatrics. 49, 1, p. 108-112 5 p.

Research output: Contribution to journalArticleScientificpeer-review

Association of lipoprotein lipase Ser447Ter polymorphism with brain infarction: a population-based neuropathological study

Myllykangas, L., Polvikoski, T., Sulkava, R., Notkola, I. L., Rastas, S., Verkkoniemi, A., Tienari, P. J., Niinisto, L., Hardy, J., Perez-Tur, J., Kontula, K. & Haltia, M., 2001, In : Annals of Medicine. 33, p. 486-492 7 p.

Research output: Contribution to journalArticleScientificpeer-review

C9orf72 hexanucleotide repeat length in older population: normal variation and effects on cognition

Kaivola, K., Kiviharju, A., Jansson, L., Rantalainen, V., Eriksson, J. G., Strandberg, T. E., Laaksovirta, H., Renton, A. E., Traynor, B. J., Myllykangas, L. & Tienari, P., Dec 2019, In : Neurobiology of Aging. 84, p. 242.e7-242.e12 6 p.

Research output: Contribution to journalArticleScientificpeer-review

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CADASIL and CARASIL

Tikka, S., Baumann, M., Siitonen, M., Pasanen, P., Poyhonen, M., Myllykangas, L., Viitanen, M., Fukutake, T., Cognat, E., Joutel, A. & Kalimo, H., Sep 2014, In : Brain Pathology. 24, 5, p. 525-544 20 p.

Research output: Contribution to journalArticleScientificpeer-review

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CAIDE Dementia Risk Score, Alzheimer and cerebrovascular pathology: a population-based autopsy study

Hooshmand, B., Polvikoski, T., Kivipelto, M., Myllykangas, L., Mäkelä, M., Tanskanen, M., Oinas, M., Paetau, A. & Solomon, A., Jun 2018, In : Journal of internal medicine. 283, 6, p. 597-603 7 p.

Research output: Contribution to journalArticleScientificpeer-review

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Capillary Amyloid-beta Protein Deposition in a Population-Based Study (Vantaa 85+)

Makela, M., Paetau, A., Polvikoski, T., Myllykangas, L. & Tanskanen, M., 2015, In : Journal of Alzheimer's Disease. 49, 1, p. 149-157 9 p.

Research output: Contribution to journalArticleScientificpeer-review

Cardiovascular risk factors and Alzheimer's disease: a genetic association study in a population aged 85 or over

Myllykangas, L., Polvikoski, T., Sulkava, R., Verkkoniemi, A., Tienari, P., Niinisto, L., Kontula, K., Hardy, J., Haltia, M. & Perez-Tur, J., 2000, In : Neuroscience Letters. 292, p. 195-198 4 p.

Research output: Contribution to journalArticleScientificpeer-review

Cathepsin D-deficient Drosophila recapitulate the key features of neuronal ceroid lipofuscinoses

Myllykangas, L., Tyynelä, J., Page-McCaw, A., Rubin, G. M., Haltia, M. & Feany, M. B., 2005, In : Neurobiology of Disease. 19, 1/2, p. 194-199 6 p.

Research output: Contribution to journalArticleScientificpeer-review

Cathepsin D expression level affects alpha-synuclein processing, aggregation, and toxicity in vivo

Cullen, V., Lindfors, M., Ng, J., Paetau, A., Swinton, E., Kolodziej, P., Boston, H., Saftig, P., Woulfe, J., Feany, M. B., Myllykangas, L., Schlossmacher, M. G. & Tyynelä, J., 2009, In : Molecular brain.

Research output: Contribution to journalArticleScientificpeer-review

Causes of death of professional musicians in the classical genre

Kuusi, T., Haukka, J., Myllykangas, L. & Järvelä, I., Jun 2019, In : Medical Problems of Performing Artists. 34 , 2, p. 92-97 6 p.

Research output: Contribution to journalArticleScientificpeer-review

Chromosome 21 BACE2 haplotype associates with Alzheimer's disease: a two-stage study

Myllykangas, L., Wavrant-De Vrieze, F., Polvikoski, T., Notkola, I-L., Sulkava, R., Niinistö, L., Edland, S. D., Arepalli, S., Adighibe, O., Compton, D., Hardy, J., Haltia, M. & Tienari, P. J., 2005, In : Journal of the Neurological Sciences. 236, p. 17-24 8 p.

Research output: Contribution to journalArticleScientificpeer-review

Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study

Laaksovirta, H., Peuralinna, T., Schymick, J. C., Scholz, S. W., Lai, S-L., Myllykangas, L., Sulkava, R., Jansson, L., Hernandez, D. G., Gibbs, J. R., Nalls, M. A., Heckerman, D., Tienari, P. J. & Traynor, B. J., 2010, In : Lancet Neurology. 9, 10, p. 978-985 8 p.

Research output: Contribution to journalArticleScientificpeer-review

Contribution of APOE promoter polymorphisms to Alzheimer's disease risk

Lambert, J. C., Araria-Goumidi, L., Myllykangas, L., Ellis, C., Wang, J. C., Bullido, M. J., Harris, J. M., Artiga, M. J., Hernandez, D., Kwon, J. M., Frigard, B., Petersen, R. C., Cumming, A. M., Pasquier, F., Sastre, I., Tienari, P., Frank, A., Sulkava, R., Morris, J. C., St Clair, D. & 11 others, Mann, D. M., Wavrant-DeVrieze, F., Ezquerra-Trabalon, M., Amouyel, P., Hardy, J., Haltia, M., Valdivieso, F., Goate, A. M., Perez-Tur, J., Lendon, C. L. & Chartier-Harlin, M. C., 2002, In : Neurology. 59, p. 59-66 8 p.

Research output: Contribution to journalArticleScientificpeer-review

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Genetic association of alpha(2)-macroglobulin with Alzheimer's disease in a Finnish elderly population

Myllykangas, L., Polvikoski, T., Sulkava, R., Verkkoniemi, A., Crook, R., Tienari, P. J., Pusa, A. K., Niinisto, L., O'Brien, P., Kontula, K., Hardy, J., Haltia, M. & Perez-Tur, J., 1999, In : Annals of Neurology. 46, p. 382-390 9 p.

Research output: Contribution to journalArticleScientificpeer-review

Genetic modifiers of degeneration in the cathepsin D deficient Drosophila model for neuronal ceroid lipofuscinosis

Kuronen, M., Talvitie, M., Lehesjoki, A-E. & Myllykangas, L., 2009, In : Neurobiology of Disease. 36, 3, p. 488-493 6 p.

Research output: Contribution to journalArticleScientificpeer-review

Genetics of dementia in a Finnish cohort

Pasanen, P., Myllykangas, L., Pöyhönen, M., Kiviharju, A., Siitonen, M., Hardy, J., Bras, J., Paetau, A., Tienari, P. J., Guerreiro, R. & Verkkoniemi-Ahola, A., Jun 2018, In : European Journal of Human Genetics. 26, 6, p. 827-837 11 p.

Research output: Contribution to journalArticleScientificpeer-review

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene

ITALSGEN Consortium, Genomic Translation ALS Care GTAC, ALS Sequencing Consortium, NYGC ALS Consortium, Answer ALS Fdn, Clinical Res ALS Related Disorders, SLAGEN Consortium, French ALS Consortium & Project MinE ALS Sequencing Consor, 21 Mar 2018, In : Neuron. 97, 6, p. 1268-+ 21 p.

Research output: Contribution to journalArticleScientificpeer-review

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Genome-wide association study of neocortical Lewy-related pathology

Peuralinna, T., Myllykangas, L., Oinas, M., Nails, M. A., Keage, H. A. D., Isoviita, V-M., Valori, M. V. P., Polvikoski, T., Paetau, A., Sulkava, R., Ince, P. G., Zaccai, J., Brayne, C., Traynor, B. J., Hardy, J., Singleton, A. B. & Tienari, P. J., 18 Aug 2015, In : Annals of Clinical and Translational Neurology. 2, 9, p. 920–931 12 p.

Research output: Contribution to journalArticleScientificpeer-review

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Heritability and genetic variance of dementia with Lewy bodies

Int Parkinson's Dis Genomics Cons, Guerreiro, R., Escott-Price, V., Tienari, P. J., Myllykangas, L. & Oinas, M., Jul 2019, In : Neurobiology of Disease. 127, p. 492-501 10 p.

Research output: Contribution to journalArticleScientificpeer-review

Heterozygous TYROBP deletion (PLOSLFIN) is not a strong risk factor for cognitive impairment

Kaivola, K., Jansson, L., Saarentaus, E., Kiviharju, A., Rantalainen, V., Eriksson, J. G., Strandberg, T. E., Polvikoski, T., Myllykangas, L. & Tienari, P. J., Apr 2018, In : Neurobiology of Aging. 64, 4 p., ARTN 159.e1.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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Hippocampal Sclerosis in the Oldest Old: A Finnish Population-Based Study

Kero, M., Raunio, A., Polvikoski, T., Tienari, P. J., Paetau, A. & Myllykangas, L., 2018, In : Journal of Alzheimer's Disease. 63, 1, p. 263-272 10 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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Homozygosity analysis in amyotrophic lateral sclerosis

Mok, K., Laaksovirta, H., Tienari, P. J., Peuralinna, T., Myllykangas, L., Chio, A., Traynor, B. J., Nalls, M. A., Gurunlian, N., Shatunov, A., Restagno, G., Mora, G., Leigh, P. N., Shaw, C. E., Morrison, K. E., Shaw, P. J., Al-Chalabi, A., Hardy, J. & Orrell, R. W., Dec 2013, In : European Journal of Human Genetics. 21, 12, p. 1429-1435 7 p.

Research output: Contribution to journalArticleScientificpeer-review

Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study

Guerreiro, R., Ross, O. A., Kun-Rodrigues, C., Hernandez, D. G., Orme, T., Eicher, J. D., Shepherd, C. E., Parkkinen, L., Darwent, L., Heckman, M. G., Scholz, S. W., Troncoso, J. C., Pletnikova, O., Ansorge, O., Clarimon, J., Lleo, A., Morenas-Rodriguez, E., Clark, L., Honig, L. S., Marder, K. & 45 others, Lemstra, A., Rogaeva, E., St George-Hyslop, P., Londos, E., Zetterberg, H., Barber, I., Braae, A., Brown, K., Morgan, K., Troakes, C., Al-Sarraj, S., Lashley, T., Holton, J., Compta, Y., Van Deerlin, V., Serrano, G. E., Beach, T. G., Lesage, S., Galasko, D., Masliah, E., Santana, I., Pastor, P., Diez-Fairen, M., Aguilar, M., Tienari, P. J., Myllykangas, L., Oinas, M., Revesz, T., Lees, A., Boeve, B. F., Petersen, R. C., Ferman, T. J., Escott-Price, V., Graff-Radford, N., Cairns, N. J., Morris, J. C., Pickering-Brown, S., Mann, D., Halliday, G. M., Hardy, J., Trojanowski, J. Q., Dickson, D. W., Singleton, A., Stone, D. J. & Bras, J., Jan 2018, In : Lancet Neurology. 17, 1, p. 64-74 11 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access

Matrix metalloproteinase-19 expressed in cerebral amyloid angiopathy

Tanskanen, M., Myllykangas, L. T., Saarialho-Kere, U. & Paetau, A., 2011, In : Amyloid. 18, 1, p. 3-9 7 p.

Research output: Contribution to journalArticleScientificpeer-review

Melatonin receptor type 1A gene linked to Alzheimer's disease in old age

Sulkava, S., Muggalla, P., Sulkava, R., Ollila, H. M., Peuralinna, T., Myllykangas, L., Kaivola, K., Stone, D. J., Traynor, B. J., Renton, A. E., Rivera, A. M., Helisalmi, S., Soininen, H., Polvikoski, T., Hiltunen, M., Tienari, P. J., Huttunen, H. J. & Paunio, T., Jul 2018, In : Sleep. 41, 7, 10 p., 103.

Research output: Contribution to journalArticleScientificpeer-review

Open Access

Multi-infarct dementia of Swedish type is caused by a 3 ' UTR mutation of COL4A1

Siitonen, M., Borjesson-Hanson, A., Pöyhönen, M., Ora, A., Pasanen, P., Bras, J., Kern, S., Kern, J., Andersen, O., Stanescu, H., Kleta, R., Baumann, M., Kalaria, R., Kalimo, H., Singleton, A., Hardy, J., Viitanen, M., Myllykangas, L. & Guerreiro, R., May 2017, In : Brain : a journal of neurology. 140, 4 p., 29.

Research output: Contribution to journalArticleScientific

Open Access

Neurofibrillary tau pathology modulated by genetic variation of [alpha]-synuclein

Peuralinna, T., Oinas, M., Polvikoski, T., Paetau, A., Sulkava, R., Niinistö, L., Kalimo, H., Hernandez, D., Hardy, J., Singleton, A., Tienari, P. J. & Myllykangas, L., 2008, In : Annals of Neurology. 64, 3, p. 348-352 5 p.

Research output: Contribution to journalArticleScientificpeer-review

Neuropathologic Findings of Dementia with Lewy Bodies (DLB) in a Population-based Vantaa 85+Study

Oinas, M., Polvikoski, T., Sulkava, R., Myllykangas, L., Juva, K., Notkola, I-L., Rastas, S., Niinisto, L., Kalimo, H. & Paetau, A., 2009, In : Journal of Alzheimer's Disease. 18, p. 677-689 13 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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No association between TAU haplotype and Alzheimer's disease in population or clinic based series or in familial disease

Baker, M., Graff-Radford, D., DeVrieze, F. W., Graff-Radford, N., Petersen, R. C., Kokmen, E., Boeve, B., Myllykangas, L., Polvikoski, T., Sulkava, R., Verkoniemmi, A., Tienari, P., Haltia, M., Hardy, J., Hutton, M. & Perez-Tur, J., 2000, In : Neuroscience Letters. 285, p. 147-149 3 p.

Research output: Contribution to journalArticleScientificpeer-review

Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene

Kousi, M., Anttila, V., Schulz, A., Calafato, S., Jakkula, E., Riesch, E., Myllykangas, L., Kalimo, H., Topcu, M., Gokben, S., Alehan, F., Lemke, J. R., Alber, M., Palotie, A., Kopra, O. & Lehesjoki, A-E., 2012, In : Journal of Medical Genetics. 49, 6, p. 391-399 9 p.

Research output: Contribution to journalArticleScientificpeer-review