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Publications 1989 2019

2019

Heterozygous IQSEC2 loss increased activated Arf6 in severe female neurocognitive seizure phenotype

Jackson, M., Loring, K., Homan, C., Thai, M., Määttänen, L., Arvio, M., Järvelä, I., Shaw, M., Gardner, A., Gecz, J. & Schoubridge, C., 15 Sep 2019, (Accepted/In press) In : Life Science Alliance.

Research output: Contribution to journalArticleScientificpeer-review

Music-performance regulates microRNAs in professional musicians

Nair, P. S., Kuusi, T., Ahvenainen, M., Philips, A. K. & Järvelä, I., 29 Mar 2019, In : PeerJ. 7, 26 p., 6660.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population

Polla, D., Rahikkala, E., Bode, M., Määttä, T., Varilo, T., Loman, T., Philips, A. K., Kurki, M. I., Palotie, A., Korkko, J., Avela, K., Pirson, I., Jacquemin, V., Abramowicz, M., de Brouwer, A. P. M., Kuismin, O., van Bokhoven, H. & Järvelä, I. E., 26 Mar 2019, In : European Journal of Human Genetics.

Research output: Contribution to journalArticleScientificpeer-review

The causes of death of professional musicians in the classical genre

Kuusi, T., Haukka, J. K., Myllykangas, L. T. & Järvelä, I. E., 25 Jan 2019, (Accepted/In press) In : Medical Problems of Performing Artists. 34 , 2, p. 92

Research output: Contribution to journalArticleScientificpeer-review

2018

Genomics Approaches for Studying Musical Aptitude and Related Traits

Järvelä, I., Oct 2018, The Oxford Handbook of Music and Neuroscience. Thaut, M. H. & Hodges, D. A. (eds.). Oxford University Press Pakistan, (Oxford Handbooks Online).

Research output: Chapter in Book/Report/Conference proceedingChapterScientificpeer-review

Genomics studies on musical aptitude, music perception and practice

Järvelä, I., Jul 2018, In : Annals of the New York Academy of Sciences. 1423, 1, p. 82-91 10 p.

Research output: Contribution to journalArticleScientificpeer-review

Musiikillisen luovuuden perimänlaajuinen tutkimus

Oikkonen, J., Kuusi, T. & Järvelä, I., 29 Jun 2018, In : Musiikki. 44, 1, p. 45-57 13 p.

Research output: Contribution to journalArticleGeneral public

2017

Exploring genome-wide DNA methylation patterns in Aicardi syndrome

Piras, I. S., Mills, G., Llaci, L., Naymik, M., Ramsey, K., Belnap, N., Balak, C. D., Jepsen, W. M., Szelinger, S., Siniard, A. L., Lewis, C. R., LaFleur, M., Richholt, R. F., De Both, M. D., Avela, K., Rangasamy, S., Craig, D. W., Narayanan, V., Jarvela, I., Huentelman, M. J. & 1 othersSchrauwen, I., Nov 2017, In : Epigenomics. 9, 11, p. 1373-1386 14 p.

Research output: Contribution to journalArticleScientificpeer-review

Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci

Aung, T., Ozaki, M., Lee, M. C., Schlotzer-Schrehardt, U., Thorleifsson, G., Mizoguchi, T., Igo, R. P., Haripriya, A., Williams, S. E., Astakhov, Y. S., Orr, A. C., Burdon, K. P., Nakano, S., Mori, K., Abu-Amero, K., Hauser, M., Li, Z., Prakadeeswari, G., Bailey, J. N. C., Cherecheanu, A. P. & 269 othersKang, J. H., Nelson, S., Hayashi, K., Manabe, S., Kazama, S., Zarnowski, T., Inoue, K., Irkec, M., Coca-Prados, M., Sugiyama, K., Jarvela, I., Schlottmann, P., Lerner, S. F., Lamari, H., Nilgun, Y., Bikbov, M., Park, K. H., Cha, S. C., Yamashiro, K., Zenteno, J. C., Jonas, J. B., Kumar, R. S., Perera, S. A., Chan, A. S. Y., Kobakhidze, N., George, R., Vijaya, L., Do, T., Edward, D. P., de Juan Marcos, L., Pakravan, M., Moghimi, S., Ideta, R., Bach-Holm, D., Kappelgaard, P., Wirostko, B., Thomas, S., Gaston, D., Bedard, K., Greer, W. L., Yang, Z., Chen, X., Huang, L., Sang, J., Jia, H., Jia, L., Qiao, C., Zhang, H., Liu, X., Zhao, B., Wang, Y-X., Xu, L., Leruez, S., Reynier, P., Chichua, G., Tabagari, S., Uebe, S., Zenkel, M., Berner, D., Mossboeck, G., Weisschuh, N., Hoja, U., Welge-Luessen, U-C., Mardin, C., Founti, P., Chatzikyriakidou, A., Pappas, T., Anastasopoulos, E., Lambropoulos, A., Ghosh, A., Shetty, R., Porporato, N., Saravanan, V., Venkatesh, R., Shivkumar, C., Kalpana, N., Sarangapani, S., Kanavi, M. R., Beni, A. N., Yazdani, S., Lashay, A., Naderifar, H., Khatibi, N., Fea, A., Lavia, C., Dallorto, L., Rolle, T., Frezzotti, P., Paoli, D., Salvi, E., Manunta, P., Mori, Y., Miyata, K., Higashide, T., Chihara, E., Ishiko, S., Yoshida, A., Yanagi, M., Kiuchi, Y., Ohashi, T., Sakurai, T., Sugimoto, T., Chuman, H., Aihara, M., Inatani, M., Miyake, M., Gotoh, N., Matsuda, F., Yoshimura, N., Ikeda, Y., Ueno, M., Sotozono, C., Jeoung, J. W., Sagong, M., Park, K. H., Ahn, J., Cruz-Aguilar, M., Ezzouhairi, S. M., Rafei, A., Chong, Y. F., Ng, X. Y., Goh, S. R., Chen, Y., Yong, V. H. K., Khan, M. I., Olawoye, O. O., Ashaye, A. O., Ugbede, I., Onakoya, A., Kizor-Akaraiwe, N., Teekhasaenee, C., Suwan, Y., Supakontanasan, W., Okeke, S., Uche, N. J., Asimadu, I., Ayub, H., Akhtar, F., Kosior-Jarecka, E., Lukasik, U., Lischinsky, I., Castro, V., Perez Grossmann, R., Megevand, G. S., Roy, S., Dervan, E., Silke, E., Rao, A., Sahay, P., Fornero, P., Cuello, O., Sivori, D., Zompa, T., Mills, R. A., Souzeau, E., Mitchell, P., Wang, J. J., Hewitt, A. W., Coote, M., Crowston, J. G., Astakhov, S. Y., Akopov, E. L., Emelyanov, A., Vysochinskaya, V., Kazakbaeva, G., Fayzrakhmanov, R., Al-Obeidan, S. A., Owaidhah, O., Aljasim, L. A., Chowbay, B., Foo, J. N., Soh, R. Q., Sim, K. S., Xie, Z., Cheong, A. W. O., Mok, S. Q., Soo, H. M., Chen, X. Y., Peh, S. Q., Heng, K. K., Husain, R., Ho, S-L., Hillmer, A. M., Cheng, C-Y., Escudero-Dominguez, F. A., Gonzalez-Sarmiento, R., Martinon-Torres, F., Salas, A., Pathanapitoon, K., Hansapinyo, L., Wanichwecharugruang, B., Kitnarong, N., Sakuntabhai, A., Nguyn, H. X., Nguyn, G. T. T., Nguyn, T. V., Zenz, W., Binder, A., Klobassa, D. S., Hibberd, M. L., Davila, S., Herms, S., Nothen, M. M., Moebus, S., Rautenbach, R. M., Ziskind, A., Carmichael, T. R., Ramsay, M., Alvarez, L., Garcia, M., Gonzalez-Iglesias, H., Rodriguez-Calvo, P. P., Fernandez-Vega Cueto, L., Oguz, C., Tamcelik, N., Atalay, E., Batu, B., Aktas, D., Kasim, B., Wilson, M. R., Coleman, A. L., Liu, Y., Challa, P., Herndon, L., Kuchtey, R. W., Kuchtey, J., Curtin, K., Chaya, C. J., Crandall, A., Zangwill, L. M., Wong, T. Y., Nakano, M., Kinoshita, S., den Hollander, A. I., Vesti, E., Fingert, J. H., Lee, R. K., Sit, A. J., Shingleton, B. J., Wang, N., Cusi, D., Qamar, R., Kraft, P., Pericak-Vance, M. A., Raychaudhuri, S., Heegaard, S., Kivela, T., Reis, A., Kruse, F. E., Weinreb, R. N., Pasquale, L. R., Haines, J. L., Thorsteinsdottir, U., Jonasson, F., Allingham, R. R., Milea, D., Ritch, R., Kubota, T., Tashiro, K., Vithana, E. N., Micheal, S., Topouzis, F., Craig, J. E., Dubina, M., Sundaresan, P., Stefansson, K., Wiggs, J. L., Pasutto, F. & Khor, C. C., Jul 2017, In : Nature Genetics. 49, 7, p. 993-+ 15 p.

Research output: Contribution to journalArticleScientificpeer-review

GenRank: A R/Bioconductor package for prioritization of candidate genes

Kanduri, C. & Järvelä, I., 2017, In : F1000Research. 6, 9 p., 463.

Research output: Contribution to journalArticleScientificpeer-review

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Identification of C12orf4 as a gene for autosomal recessive intellectual disability

Philips, A. K., Pinelli, M., de Bie, C. I., Mustonen, A., Maatta, T., Arts, H. H., Wu, K., Roepman, R., Moilanen, J. S., Raza, S., Varilo, T., Scala, G., Cocozza, S., Gilissen, C., van Gassen, K. L. I. & Jarvela, I., Jan 2017, In : Clinical Genetics. 91, 1, p. 100-105 6 p.

Research output: Contribution to journalArticleScientificpeer-review

Laktoosi-intoleranssi

Järvelä, I., 2017, Lääkärin käsikirja. Jousimaa, J., Alenius, H., Atula, S., Berghem, N., Kattainen, A., Kunnamo, I., Pelttari, H. & Teikari, M. (eds.). 12. uud. p. ed. Helsinki: Duodecim, p. 441-442 2 p.

Research output: Chapter in Book/Report/Conference proceedingChapterProfessional

Lisää genetiikan osaamista yleislääkäreille

Järvelä, I., 2017, In : Suomen lääkärilehti. 72, 38, p. 2072-2073 2 p.

Research output: Contribution to journalArticleProfessional

Open Access
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Mitä geenitutkimukset kertovat musikaalisuuden perinnöllisyydestä?

Järvelä, I., 16 Aug 2017, Kiehtovat geenit : mihin geenitietoa käytetään?. Jokela, M., Oja-Leikas, M. & Rova, M. (eds.). 1. p. ed. Helsinki: Duodecim, p. 167-171 5 p.

Research output: Chapter in Book/Report/Conference proceedingChapterProfessional

2016

Convergent evidence for the molecular basis of musical traits

Oikkonen, J., Onkamo, P., Järvelä, I. & Kanduri, C., 22 Dec 2016, In : Scientific Reports. 6, 10 p., 39707.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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Creative Activities in Music - A Genome-Wide Linkage Analysis

Oikkonen, J., Kuusi, T., Peltonen, P., Raijas, P., Ukkola-Vuoti, L., Karma, K., Onkamo, P. & Jarvela, I., 24 Feb 2016, In : PLoS One. 11, 2, 21 p., 0148679.

Research output: Contribution to journalArticleScientificpeer-review

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Detecting signatures of positive selection associated with musical aptitude in the human genome

Liu, X., Kanduri, C., Oikkonen, J., Karma, K., Raijas, P., Ukkola-Vuoti, L., Teo, Y-Y. & Jarvela, I., 16 Feb 2016, In : Scientific Reports. 6, 9 p., 21198.

Research output: Contribution to journalArticleScientificpeer-review

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The landscape of copy number variations in Finnish families with autism spectrum disorders

Kanduri, C., Kantojärvi, K., Salo, P. M., Vanhala, R., Buck, G., Blancher, C., Lahdesmaki, H. & Jarvela, I., Jan 2016, In : Autism Research. 9, 1, p. 9-16 8 p.

Research output: Contribution to journalArticleScientificpeer-review

2015

A genome-wide linkage and association study of musical aptitude identifies loci containing genes related to inner ear development and neurocognitive functions

Oikkonen, J., Huang, Y., Onkamo, P., Ukkola-Vuoti, L., Raijas, P., Karma, K., Vieland, V. J. & Jarvela, I., Feb 2015, In : Molecular Psychiatry. 20, 2, p. 275-282 8 p.

Research output: Contribution to journalArticleScientificpeer-review

Association and Promoter Analysis of AVPR1A in Finnish Autism Families

Kantojärvi, K., Oikkonen, J., Kotala, I., Kallela, J., Vanhala, R., Onkamo, P. & Jarvela, I., Oct 2015, In : Autism Research. 8, 5, p. 634-639 6 p.

Research output: Contribution to journalArticleScientificpeer-review

Geenitutkimukset muuttavat laboratorioiden toimintaa

Järvelä, I., 29 May 2015, In : Suomen lääkärilehti. 70, 22, p. 1549-1550 2 p.

Research output: Contribution to journalArticleScientific

The effect of listening to music on human transcriptome

Kanduri, C., Raijas, P., Ahvenainen, M., Philips, A. K., Ukkola-Vuoti, L., Lahdesmaki, H. & Jarvela, I., 12 Mar 2015, In : PeerJ. 3, 17 p., 830.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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The effect of music performance on the transcriptome of professional musicians

Kanduri, C., Kuusi, T., Ahvenainen, M., Philips, A. K., Lahdesmaki, H. & Jarvela, I., 25 Mar 2015, In : Scientific Reports. 5, 7 p., 9506.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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The genetic variant rs4073 A→T of the Interleukin-8 promoter region is associated with the earlier onset of exudative age-related macular degeneration

Hautamäki, A., Seitsonen, S., Holopainen, J. M., Moilanen, J. A., Kivioja, J., Onkamo, P., Järvelä, I. & Immonen, I., 2015, In : Acta Ophthalmologica. 93, 8, p. 726-733 8 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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Variants in CUL4B are Associated with Cerebral Malformations

Vulto-van Silfhout, A. T., Nakagawa, T., Bahi-Buisson, N., Haas, S. A., Hu, H., Bienek, M., Vissers, L. E. L. M., Gilissen, C., Tzschach, A., Busche, A., Muesebeck, J., Rump, P., Mathijssen, I. B., Avela, K., Somer, M., Doagu, F., Philips, A. K., Rauch, A., Baumer, A., Voesenek, K. & 25 othersPoirier, K., Vigneron, J., Amram, D., Odent, S., Nawara, M., Obersztyn, E., Lenart, J., Charzewska, A., Lebrun, N., Fischer, U., Nillesen, W. M., Yntema, H. G., Jarvela, I., Ropers, H-H., de Vries, B. B. A., Brunner, H. G., van Bokhoven, H., Raymond, F. L., Willemsen, M. A. A. P., Chelly, J., Xiong, Y., Barkovich, A. J., Kalscheuer, V. M., Kleefstra, T. & de Brouwer, A. P. M., Jan 2015, In : Human Mutation. 36, 1, p. 106-117 12 p.

Research output: Contribution to journalArticleScientificpeer-review

2014

Geenitutkimukset, musiikki ja musikaalisuus

Järvelä, I. & Kuusi, T., 2014, In : Trio : DocMus-tohtorikoulun julkaisu. p. 6-16 11 p.

Research output: Contribution to journalArticleGeneral public

Genomics approaches to study musical aptitude

Oikkonen, J. & Jarvela, I., Nov 2014, In : BioEssays. 36, 11, p. 1102-1108 7 p.

Research output: Contribution to journalArticleScientificpeer-review

Laktoosi-intoleranssi

Järvelä, I. & Kolho, K-L., 2014, Lääkärin käsikirja. Jousimaa, J., Alenius, H., Atula, S., Kattainen, A., Pelttari, H., Kunnamo, I. & Teikari, M. (eds.). 11. uud. ed. Helsinki: Duodecim, p. 418-419 2 p.

Research output: Chapter in Book/Report/Conference proceedingChapterProfessional

Monivammaisuuden taustalla Allan-Herndon-Dudleyn oireyhtymä

Arvio, M., Philips, A. K., Ahvenainen, M., Somer, M., Kalscheuer, V. & Järvelä, I., 2014, In : Duodecim. 130, 21, p. 2202-2205 4 p.

Research output: Contribution to journalArticleScientificpeer-review

The IL-8, VEGF, and CFH Polymorphisms and Bevacizumab in Age-related Macular Degeneration

Hautamaki, A., Kivioja, J., Seitsonen, S., Savolainen, E-R., Liinamaa, M. J., Luoma, A., Jarvela, I. & Immonen, I., Apr 2014, In : Ophthalmology. 121, 4, p. 973-974 4 p.

Research output: Contribution to journalArticleScientificpeer-review

X-exome sequencing in Finnish families with Intellectual Disability - four novel mutations and two novel syndromic phenotypes

Philips, A. K., Siren, A., Avela, K., Somer, M., Peippo, M., Ahvenainen, M., Doagu, F., Arvio, M., Kaariainen, H., Van Esch, H., Froyen, G., Haas, S. A., Hu, H., Kalscheuer, V. M. & Jarvela, I., 11 Apr 2014, In : Orphanet journal of rare diseases. 9, 13 p., 49.

Research output: Contribution to journalArticleScientificpeer-review

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2013

Genome-Wide Copy Number Variation Analysis in Extended Families and Unrelated Individuals Characterized for Musical Aptitude and Creativity in Music

Ukkola-Vuoti, L., Kanduri, C., Oikkonen, J., Buck, G., Blancher, C., Raijas, P., Karma, K., Lahdesmaki, H. & Järvelä, I., 27 Feb 2013, In : PLoS One. 8, 2, 9 p., e56356.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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Interleukin 8 promoter polymorphism predict the initial response to bevacizumab treatment for exudative age-related macular degeneration

Hautamäki, A., Kivioja, J., Vavuli, S., Kakko, S., Savolainen, E-R., Savolainen, M., Liinamaa, M. J., Seitsonen, S., Onkamo, P., Järvelä, I. & Immonen, I., Oct 2013, In : Retina. 33, 9, p. 1815-1827 13 p.

Research output: Contribution to journalArticleScientificpeer-review

Kehitysvammaisuuden ja autismin geenitutkimusten nykytilanne

Järvelä, I., 22 Feb 2013, In : Suomen lääkärilehti. 68, 8, p. 575-579a 6 p.

Research output: Contribution to journalReview ArticleScientificpeer-review

Lääketieteellisen genetiikan osaamista tarvitsee yhä useampi lääkäri

Varilo, T., Pyörälä, E., Varilo, S., Hietala, M. & Järvelä, I., 2013, In : Suomen lääkärilehti. 68, 18, p. 1368-1369 2 p.

Research output: Contribution to journalArticleProfessional

The genome-wide landscape of copy number variations in the MUSGEN study provides evidence for a founder effect in the isolated Finnish population

Kanduri, C., Ukkola-Vuoti, L., Oikkonen, J., Buck, G., Blancher, C., Raijas, P., Karma, K., Lahdesmaki, H. & Järvelä, I., Dec 2013, In : European Journal of Human Genetics. 21, 12, p. 1411-1416 6 p.

Research output: Contribution to journalArticleScientificpeer-review

2012

Acquisition of Complement Factor H Is Important for Pathogenesis of Streptococcus pyogenes Infections: Evidence from Bacterial In Vitro Survival and Human Genetic Association

Haapasalo, K., Vuopio, J., Syrjänen, J., Suvilehto, J., Massinen, S., Karppelin, M., Järvelä, I., Meri, S., Kere, J. & Jokiranta, T. S., 2 Dec 2012, In : Journal of Immunology. 188, 1, p. 426-435 10 p.

Research output: Contribution to journalArticleScientificpeer-review

A novel mutation W388X underlying properdin deficiency in a Finnish family.

Helminen, M., Seitsonen, S., Jarva, H., Meri, S. & Järvelä, I., 2012, In : Scandinavian Journal of Immunology. 75, 4, p. 445-448 4 p.

Research output: Contribution to journalArticleScientificpeer-review

Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders

Leblond, C. S., Heinrich, J., Delorme, R., Proepper, C., Betancur, C., Huguet, G., Konyukh, M., Chaste, P., Ey, E., Rastam, M., Anckarsater, H., Nygren, G., Gillberg, I. C., Melke, J., Toro, R., Regnault, B., Fauchereau, F., Mercati, O., Lemiere, N., Skuse, D. & 40 othersPoot, M., Holt, R., Monaco, A. P., Jarvela, I., Kantojärvi, K., Vanhala, R., Curran, S., Collier, D. A., Bolton, P., Chiocchetti, A., Klauck, S. M., Poustka, F., Freitag, C. M., Waltes, R., Kopp, M., Duketis, E., Bacchelli, E., Minopoli, F., Ruta, L., Battaglia, A., Mazzone, L., Maestrini, E., Sequeira, A. F., Oliveira, B., Vicente, A., Oliveira, G., Pinto, D., Scherer, S. W., Zelenika, D., Delepine, M., Lathrop, M., Bonneau, D., Guinchat, V., Devillard, F., Assouline, B., Mouren, M-C., Leboyer, M., Gillberg, C., Boeckers, T. M. & Bourgeron, T., 2012, In : PLoS Genetics. 8, 2, p. e1002521 17 p.

Research output: Contribution to journalArticleScientificpeer-review

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Suomalaisten musikaalisuus

Raijas, P., Oikkonen, J., Ukkola-Vuoti, L., Onkamo, P. & Järvelä, I., 2012, In : Musiikki. 2012, 1, p. 86-90 5 p.

Research output: Contribution to journalArticleGeneral public

2011

Association of the arginine vasopressin receptor 1A (AVPR1A) haplotypes with listening to music

Ukkola-Vuoti, L., Oikkonen, J., Onkamo, P., Karma, K., Raijas, P. & Jarvela, I., 2011, In : Journal of Human Genetics. 56, 4, p. 324-329 6 p.

Research output: Contribution to journalArticleScientificpeer-review

Avokulmaglaukooman geenitutkimuksen nykytilanne Suomessa

Forsman, E., Lemmelä, S., Puska, P. & Järvelä, I., 2011, In : Duodecim. 127, 14, p. 1426-31 5 p.

Research output: Contribution to journalReview ArticleScientificpeer-review

Lactase non-persistent genotype influences milk consumption and gastrointestinal symptoms in Northern Russians

Khabarova, Y., Tornianen, S., Tuomisto, S., Jarvela, I., Karhunen, P., Isokoski, M. & Mattila, K., 13 Nov 2011, In : BMC Gastroenterology. 11, 19 p., 124.

Research output: Contribution to journalArticleScientificpeer-review

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Lactase persistence genotypes and malaria susceptibility in Fulani of Mali

Lokki, A. I., Jarvela, I., Israelsson, E., Maiga, B., Troye-Blomberg, M., Dolo, A., Doumbo, O. K., Meri, S. & Holmberg, V., 14 Jan 2011, In : Malaria Journal. 10, 6 p., 9.

Research output: Contribution to journalArticleScientificpeer-review

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Laktoosi-intoleranssi

Järvelä, I. & Kolho, K-L., 2011, Lääkärin käsikirja. Jousimaa, J., Alenius, H., Atula, S., Kattainen, A., Kunnamo, I. & Teikari, M. (eds.). 10. uud. ed. Helsinki: Duodecim, p. 359-360 2 p.

Research output: Chapter in Book/Report/Conference proceedingChapterProfessional

2010

Analysis of 9p24 and 11p12-13 regions in autism spectrum disorders: rs1340513 in the JMJD2C gene is associated with ASDs in Finnish sample

Kantojärvi, K., Onkamo, P., Vanhala, R., Alen, R., Hedman, M., Sajantila, A., Nieminen-von Wendt, T. & Järvelä, I., 2010, In : Psychiatric Genetics. 20, 3, p. 102-108 7 p.

Research output: Contribution to journalArticleScientificpeer-review

Lack of Complement Inhibitors in the Outer Intracranial Artery Aneurysm Wall Associates with Complement Terminal Pathway Activation.

Tulamo, R. M., Frösen, J., Paetau, A., Seitsonen, S., Hernesniemi, J., Niemelä, M. R., Järvelä, I. & Meri, S., 2010, In : The American Journal of Pathology. 177, 6, p. 3224-3232 9 p.

Research output: Contribution to journalArticleScientificpeer-review

Linkage and candidate gene studies of autism spectrum disorders in European populations

Holt, R., Barnby, G., Maestrini, E., Bacchelli, E., Brocklebank, D., Sousa, I., Mulder, E. J., Kantojarvi, K., Jarvela, I., Klauck, S. M., Poustka, F., Bailey, A. J., Monaco, A. P. & EU Autism MOLGEN Consortium, 2010, In : European Journal of Human Genetics. 18, 9, p. 1013-1019 7 p.

Research output: Contribution to journalArticleScientificpeer-review

Properdiinigeenin mutaatio meningiitin taustalla

Seitsonen, S., Helminen, M., Jarva, H., Meri, S. & Järvelä, I. E., 2010, In : Duodecim. 126, 9, p. 1071-5

Research output: Contribution to journalArticleScientificpeer-review