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Verneri Anttila

20062018
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Publications 2006 2018

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2018

Analysis of shared heritability in common disorders of the brain

Brainstorm Consortium, Anttila, V., Bulik-Sullivan, B., Finucane, H. K., Walters, R. K., Bras, J., Duncan, L., Escott-Price, V., Falcone, G. J., Gormley, P., Malik, R., Patsopoulos, N. A., Ripke, S., Wei, Z., Yu, D., Lee, P. H., Turley, P., Grenier-Boley, B., Chouraki, V., Kamatani, Y. & 33 othersBerr, C., Letenneur, L., Hannequin, D., Amouyel, P., Boland, A., Deleuze, J-F., Duron, E., Vardarajan, B. N., Reitz, C., Goate, A. M., Huentelman, M. J., Kamboh, M. I., Larson, E. B., Rogaeva, E., St George-Hyslop, P., Hakonarson, H., Kukull, W. A., Palta, P., Wedenoja, J., Artto, V., Kaunisto, M., Vepsäläinen, S., Kurki, M. I., Hämäläinen, E., Kaprio, J., Metspalu, A., Keski-Rahkonen, A., Raevuori, A., Ripatti, S., Lönnqvist, J., Daly, M., Palotie, A. & Neale, B. M., 22 Jun 2018, In : Science. 360, 6395, p. 1313-+ 13 p., 8757.

Research output: Contribution to journalArticleScientificpeer-review

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Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

23 Me Res Team, IHGC, Gormley, P., Kurki, M. I., Hiekkala, M. E., Häppölä, P., Palta, P., Surakka, I., Kaunisto, M. A., Hämäläinen, E., Vepsäläinen, S., Havanka, H., Harno, H., Ilmavirta, M., Nissilä, M., Säkö, E., Sumelahti, M-L., Liukkonen, J., Sillanpaa, M., Metsähonkala, L. & 15 othersKoskinen, S., Lehtimaki, T., Raitakari, O., Männikko, M., Jousilahti, P., Anttila, V., Salomaa, V., Artto, V., Färkkilä, M., Daly, M. J., Neale, B. M., Ripatti, S., Kallela, M., Wessman, M. & Palotie, A., 16 May 2018, In : Neuron. 98, 4, p. 743–753 11 p.

Research output: Contribution to journalArticleScientificpeer-review

Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria

23andMe Res Team, Dec 2018, In : PLoS Genetics. 14, 12, 20 p., 1007813.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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Molecular genetic overlap between migraine and major depressive disorder

Int Headache Genetics Consortium, Yang, Y., Zhao, H., Boomsma, D. I., Kallela, M., Wessman, M., Anttila, V., Palta, P., Muona, M., Sarin, A-P., Wedenoja, J., Färkkilä, M., Artto, V., Kaunisto, M., Vepsäläinen, S., Hämäläinen, E., Eriksson, J. G., Heikkilä, K., Kaprio, J., Wessman, M. & 4 othersPalotie, A., Kurki, M. I., Pärn, K. & Neale, B. M., Aug 2018, In : European Journal of Human Genetics. 26, 8, p. 1202-1216 15 p.

Research output: Contribution to journalArticleScientificpeer-review

2017

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

The Autism Spectrum Disorders Working Group of The Psychiatric Genomics Consortium, 22 May 2017, In : Molecular Autism. 8, 17 p., 21.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

Weiner, D. J., Wigdor, E. M., Ripke, S., Walters, R. K., Kosmicki, J. A., Grove, J., Samocha, K. E., Goldstein, J. I., Okbay, A., Bybjerg-Grauholm, J., Werge, T., Hougaard, D. M., Taylor, J., Skuse, D., Devlin, B., Anney, R., Sanders, S. J., Bishop, S., Mortensen, P. B., Borglum, A. D. & 32 othersSmith, G. D., Daly, M. J., Robinson, E. B., Baekvad-Hansen, M., Dumont, A., Hansen, C., Hansen, T. F., Howrigan, D., Mattheisen, M., Moran, J., Mors, O., Nordentoft, M., Norgaard-Pedersen, B., Poterba, T., Poulsen, J., Stevens, C., Anttila, V., Holmans, P., Huang, H., Klei, L., Lee, P. H., Medland, S. E., Neale, B., Weiss, L. A., Zwaigenbaum, L., Yu, T. W., Wittemeyer, K., Willsey, A. J., Rehnström, K., iPSYCH-Broad Autism Grp, Psychiat Genomics Consortium & Palotie, A., Jul 2017, In : Nature Genetics. 49, 7, p. 978-985 11 p.

Research output: Contribution to journalArticleScientificpeer-review

Shared genetic risk between migraine and coronary artery disease: A genome-wide analysis of common variants

Winsvold, B. S., Bettella, F., Witoelar, A., Anttila, V., Gormley, P., Kurth, T., Terwindt, G. M., Freilinger, T. M., Frei, O., Shadrin, A., Wang, Y., Dale, A. M., van den Maagdenberg, A. M. J. M., Chasman, D. I., Nyholt, D. R., Palotie, A., Andreassen, O. A., Zwart, J-A. & Int Headache Genetics Consortium, 28 Sep 2017, In : PLoS One. 12, 9, 15 p., 0185663.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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SNP Variants in Major Histocompatibility Complex Are Associate with Sarcoidosis Susceptibility - A Joint Analysis in Four European Populations

Wolin, A., Lahtela, L. E., Anttila, V., Petrek, M., Grunewald, J., van Moorsel, C. H. M., Eklund, A., Grutters, J. C., Kolek, V., Mrazek, F., Kishore, A., Padyukov, L., Pietinalho, A., Ronninger, M., Seppanen, M., Selroos, O. & Lokki, M-L., 19 Apr 2017, In : Frontiers in Immunology. 8, 11 p., 422.

Research output: Contribution to journalArticleScientificpeer-review

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2015

Candidate-gene association study searching for genetic factors involved in migraine chronification

Louter, M. A., Fernandez-Morales, J., de Vries, B., Winsvold, B., Anttila, V., Fernandez-Cadenas, I., Vila-Pueyo, M., Sintas, C., van Duijn, C. M., Cormand, B., Alvarez-Sabin, J., Montaner, J., Ferrari, M. D., van den Maagdenberg, A. M. J. M., Palotie, A., Zwart, J. A., Macaya, A., Terwindt, G. M. & Pozo-Rosich, P., May 2015, In : Cephalalgia. 35, 6, p. 500-507 8 p.

Research output: Contribution to journalArticleScientificpeer-review

Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies

Nyholt, D. R., Anttila, V., Winsvold, B. S., Kurth, T., Stefansson, H., Kallela, K. M., Malik, R., de Vries, B., Terwindt, G. M., Ikram, M. A., Stam, A. H., Ligthart, L., Freilinger, T., Alexander, M., Muller-Myhsok, B., Schreiber, S., Meitinger, T., Aromaa, A., Eriksson, J. G., Kaprio, J. & 17 othersBoomsma, D. I., van Duijn, C., Raitakari, O., Jaervelin, M-R., Zwart, J-A., Quaye, L., Strachan, D. P., Kubisch, C., Ferrari, M. D., van den Maagdenberg, A. M. J. M., Dichgans, M., Wessman, M., Smith, G. D., Stefansson, K., Chasman, D. I., Palotie, A. & Int Headache Genetics Consortium, May 2015, In : Cephalalgia. 35, 6, p. 489-499 11 p.

Research output: Contribution to journalArticleScientificpeer-review

Genetic analysis for a shared biological basis between migraine and coronary artery disease

Int Headache Genetics Consortium, Jun 2015, In : Neurology Genetics. 1, 1, 10 p., 10.

Research output: Contribution to journalArticleScientificpeer-review

Genome wide association study identifies variants in NBEA associated with migraine in bipolar disorder

Jacobsen, K. K., Nievergelt, C. M., Zayats, T., Greenwood, T. A., Anttila, V., Akiskal, H. S., Haavik, J., Fasmer, O. B., Kelsoe, J. R., Johansson, S., Oedegaard, K. J., BiGs Consortium IHG Consortium, Liu, C., Wedenoja, J. O., Kaunisto, M. A., Heikkilä, K. V., Kaprio, J. A., Wessman, M., Kallela, M., Färkkilä, M. & 4 othersArtto, V., Eriksson, J., Palotie, A. V. & Daly, M., 1 Feb 2015, In : Journal of Affective Disorders. 172, p. 453-461 9 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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Shared genetic basis for migraine and ischemic stroke: A genome-wide analysis of common variants

Malik, R., Freilinger, T., Anttila, V., Vander Heiden, J., Traylor, M., de Vries, B., Holliday, E. G., Terwindt, G. M., Sturm, J., Bis, J. C., Hopewell, J. C., Ferrari, M. D., Rannikmae, K., Wessman, M., Kallela, M., Kubisch, C., Fornage, M., Meschia, J. F., Lehtimaki, T., Sudlow, C. & 32 othersClarke, R., Chasman, D. I., Mitchell, B. D., Maguire, J., Kaprio, J., Farrall, M., Raitakari, O. T., Kurth, T., Ikram, M. A., Reiner, A. P., Longstreth, W. T., Rothwell, P. M., Strachan, D. P., Sharma, P., Seshadri, S., Quaye, L., Cherkas, L., Schuerks, M., Rosand, J., Ligthart, L., Boncoraglio, G. B., Smith, G. D., van Duijn, C. M., Stefansson, K., Worrall, B. B., Nyholt, D. R., Markus, H. S., van den Maagdenberg, A. M. J. M., Cotsapas, C., Palotie, A., Int Headache Genetics Consortium & METASTROKE Collaboration Int Strok, 26 May 2015, In : Neurology. 84, 21, p. 2132-2145 14 p.

Research output: Contribution to journalArticleScientificpeer-review

The genetic architecture of pediatric cognitive abilities in the Philadelphia Neurodevelopmental Cohort

Robinson, E. B., Kirby, A., Ruparel, K., Yang, J., McGrath, L., Anttila, V., Neale, B. M., Merikangas, K., Lehner, T., Sleiman, P. M. A., Daly, M., Gur, R., Gur, R. & Hakonarson, H., Apr 2015, In : Molecular Psychiatry. 20, 4, p. 454-458 5 p.

Research output: Contribution to journalArticleScientificpeer-review

2014

High Risk Population Isolate Reveals Low Frequency Variants Predisposing to Intracranial Aneurysms

Kurki, M. I., Gaal, E. I., Kettunen, J., Lappalainen, T., Menelaou, A., Anttila, V., van't Hof, F. N. G., von und zu Fraunberg, M., Helisalmi, S., Hiltunen, M., Lehto, H., Laakso, A., Kivisaari, R., Koivisto, T., Ronkainen, A., Rinne, J., Kiemeney, L. A. L., Vermeulen, S. H., Kaunisto, M. A., Eriksson, J. G. & 15 othersAromaa, A., Perola, M., Lehtimaki, T., Raitakari, O. T., Salomaa, V., Gunel, M., Dermitzakis, E. T., Ruigrok, Y. M., Rinkel, G. J. E., Niemela, M., Hernesniemi, J., Ripatti, S., de Bakker, P. I. W., Palotie, A. & Jaaskelainen, J. E., Jan 2014, In : PLoS Genetics. 10, 1, 12 p., 1004134.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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Selectivity in Genetic Association with Sub-classified Migraine in Women

Chasman, D. I., Anttila, V., Buring, J. E., Ridker, P. M., Schuerks, M., Kurth, T. & Int Headache Genetics Consortium, May 2014, In : PLoS Genetics. 10, 5, 11 p., 1004366.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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2013

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Lee, S. H., Ripke, S., Neale, B. M., Faraone, S. V., Purcell, S. M., Perlis, R. H., Mowry, B. J., Thapar, A., Goddard, M. E., Witte, J. S., Absher, D., Agartz, I., Akil, H., Amin, F., Andreassen, O. A., Anjorin, A., Anney, R., Anttila, V., Arking, D. E., Asherson, P. & 32 othersAzevedo, M. H., Backlund, L., Badner, J. A., Bailey, A. J., Banaschewski, T., Barchas, J. D., Barnes, M. R., Barrett, T. B., Bass, N., Battaglia, A., Bauer, M., Bayes, M., Bellivier, F., Bergen, S. E., Berrettini, W., Betancur, C., Bettecken, T., Biederman, J., Binder, E. B., Black, D. W., Blackwood, D. H. R., Bloss, C. S., Boehnke, M., Boomsma, D. I., Breen, G., Breuer, R., Bruggeman, R., Cormican, P., Buccola, N. G., Palotie, A., Cross-Disorder Grp Psychiat Genomi & Int Inflammatory Bowel Dis Genetic, Sep 2013, In : Nature Genetics. 45, 9, p. 984-+ 12 p.

Research output: Contribution to journalArticleScientificpeer-review

Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity

Cousminer, D. L., Berry, D. J., Timpson, N. J., Ang, W., Thiering, E., Byrne, E. M., Taal, H. R., Huikari, V., Bradfield, J. P., Kerkhof, M., Groen-Blokhuis, M. M., Kreiner-Moller, E., Marinelli, M., Holst, C., Leinonen, J. T., Perry, J. R. B., Surakka, I., Pietiläinen, O., Kettunen, J., Anttila, V. & 32 othersKaakinen, M., Sovio, U., Pouta, A., Das, S., Lagou, V., Power, C., Prokopenko, I., Evans, D. M., Kemp, J. P., St Pourcain, B., Ring, S., Palotie, A., Kajantie, E., Osmond, C., Lehtimaki, T., Viikari, J. S., Kahonen, M., Warrington, N. M., Lye, S. J., Palmer, L. J., Tiesler, C. M. T., Flexeder, C., Montgomery, G. W., Medland, S. E., Hofman, A., Hakonarson, H., Kaprio, J., Eriksson, J. G., Ripatti, S., Widen, E., ReproGen Consortium & Early Growth Genetics EGG, 1 Jul 2013, In : Human Molecular Genetics. 22, 13, p. 2735-2747 13 p.

Research output: Contribution to journalArticleScientificpeer-review

Genome-wide meta-analysis identifies new susceptibility loci for migraine

Anttila, V., Winsvold, B. S., Gormley, P., Kurth, T., Bettella, F., McMahon, G., Kallela, K. M. J., Malik, R., de Vries, B., Terwindt, G., Medland, S. E., Todt, U., McArdle, W. L., Quaye, L., Koiranen, M., Ikram, M. A., Lehtimaki, T., Stam, A. H., Ligthart, L., Wedenoja, J. & 33 othersDunham, I., Neale, B. M., Palta, P., Hämäläinen, E., Schuerks, M., Rose, L. M., Buring, J. E., Ridker, P. M., Steinberg, S., Stefansson, H., Jakobsson, F., Lawlor, D. A., Evans, D. M., Ring, S. M., Färkkilä, M., Artto, V., Kaunisto, M. A., Freilinger, T., Schoenen, J., Frants, R. R., Pelzer, N., Weller, C. M., Zielman, R., Heath, A. C., Madden, P. A. F., Heikkila, K., Eriksson, J. G., Kaprio, J., Wessman, M., Palotie, A., North Amer Brain Expression, UK Brain Expression Consortium & Int Headache Genetics Consortium, Aug 2013, In : Nature Genetics. 45, 8, p. 912-U255 8 p.

Research output: Contribution to journalArticleScientificpeer-review

Probing the Brain of Comorbidity

Palotie, A., Kallela, K. M. J. & Anttila, V., 1 May 2013, In : Science translational medicine. 5, 183, p. Article Number: 183fs15 3 p.

Research output: Contribution to journalArticleScientific

2012

A Potential Novel Spontaneous Preterm Birth Gene, AR, Identified by Linkage and Association Analysis of X Chromosomal Markers

Karjalainen, M. K., Huusko, J. M., Ulvila, J., Sotkasiira, J., Luukkonen, A., Teramo, K., Plunkett, J., Anttila, V., Palotie, A., Haataja, R., Muglia, L. J. & Hallman, M., 5 Dec 2012, In : PLoS One. 7, 12, p. Article Number: e51378 11 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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Genome-wide association analysis identifies susceptibility loci for migraine without aura

Freilinger, T., Anttila, V., de Vries, B., Malik, R., Kallela, K. M. J., Terwindt, G. M., Pozo-Rosich, P., Winsvold, B., Nyholt, D. R., van Oosterhout, W. P. J., Artto, V., Todt, U., Hämäläinen, E., Fernandez-Morales, J., Louter, M. A., Kaunisto, M. A., Schoenen, J., Raitakari, O., Lehtimaki, T., Vila-Pueyo, M. & 24 othersGoebel, H., Wichmann, E., Sintas, C., Uitterlinden, A. G., Hofman, A., Rivadeneira, F., Heinze, A., Tronvik, E., van Duijn, C. M., Kaprio, J., Cormand, B., Wessman, M., Frants, R. R., Meitinger, T., Mueller-Myhsok, B., Zwart, J-A., Färkkilä, M., Macaya, A., Ferrari, M. D., Kubisch, C., Palotie, A., Dichgans, M., van den Maagdenberg, A. M. J. M. & Int Headache Genetics Consortium, 2012, In : Nature Genetics. 44, 7, p. 777-U205 8 p.

Research output: Contribution to journalArticleScientificpeer-review

Genome-Wide Association Study to Identify Common Variants Associated with Brachial Circumference: A Meta-Analysis of 14 Cohorts

Boraska, V., Day-Williams, A., Franklin, C. S., Elliott, K. S., Panoutsopoulou, K., Tachmazidou, I., Albrecht, E., Bandinelli, S., Beilin, L. J., Bochud, M., Cadby, G., Ernst, F., Evans, D. M., Hayward, C., Hicks, A. A., Huffman, J., Huth, C., James, A. L., Klopp, N., Kolcic, I. & 46 othersKutalik, Z., Lawlor, D. A., Musk, A. W., Pehlic, M., Pennell, C. E., Perry, J. R. B., Peters, A., Polasek, O., St Pourcain, B., Ring, S. M., Salvi, E., Schipf, S., Staessen, J. A., Teumer, A., Timpson, N., Vitart, V., Warrington, N. M., Yaghootkar, H., Zemunik, T., Zgaga, L., An, P., Anttila, V., Borecki, I. B., Holmen, J., Ntalla, I., Palotie, A., Pietiläinen, K. H., Wedenoja, J., Winsvold, B. S., Dedoussis, G. V., Kaprio, J., Province, M. A., Zwart, J-A., Burnier, M., Campbell, H., Cusi, D., Smith, G. D., Frayling, T. M., Gieger, C., Palmer, L. J., Pramstaller, P. P., Rudan, I., Voelzke, H., Wichmann, H. E., Wright, A. F. & Zeggini, E., 2012, In : PLoS One. 7, 3, p. Article Number: e31369 10 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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IFITM3 restricts the morbidity and mortality associated with influenza

Everitt, A. R., Clare, S., Pertel, T., John, S. P., Wash, R. S., Smith, S. E., Chin, C. R., Feeley, E. M., Sims, J. S., Adams, D. J., Wise, H. M., Kane, L., Goulding, D., Digard, P., Anttila, V., Baillie, J. K., Walsh, T. S., Hume, D. A., Palotie, A., Xue, Y. & 11 othersColonna, V., Tyler-Smith, C., Dunning, J., Gordon, S. B., Smyth, R. L., Openshaw, P. J., Dougan, G., Brass, A. L., Kellam, P., GenISIS Investigators & MOSAIC Investigators, 26 Apr 2012, In : Nature. 484, 7395, p. 519-U146 7 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

2011

Genome-wide association study reveals three susceptibility loci for common migraine in the general population

Chasman, D. I., Schuerks, M., Anttila, V., de Vries, B., Schminke, U., Launer, L. J., Terwindt, G. M., van den Maagdenberg, A. M. J. M., Fendrich, K., Voelzke, H., Ernst, F., Griffiths, L. R., Buring, J. E., Kallela, M., Freilinger, T., Kubisch, C., Ridker, P. M., Palotie, A., Ferrari, M. D., Hoffmann, W. & 3 othersZee, R. Y. L., Kurth, T. & IHGC, 2011, In : Nature Genetics. 43, 7, p. 695-U116 5 p.

Research output: Contribution to journalArticleScientificpeer-review

2010

A visual migraine aura locus maps to 9q21-q22

Tikka-Kleemola, P. J., Artto, V., Vepsalainen, S., Sobel, E. M., Raty, S., Kaunisto, M., Anttila, V., Hämäläinen, E., Sumelahti, M. -L., Ilmavirta, M., Färkkilä, M., Kallela, K. M. J., Palotie, A. & Wessman, M., 2010, In : Neurology. 74, 15, p. 1171-1177 7 p.

Research output: Contribution to journalArticleScientificpeer-review

Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging

Surakka, I., Kristiansson, K., Anttila, V., Inouye, M., Barnes, C., Moutsianas, L., Salomaa, V., Daly, M., Palotie, A., Peltonen, L. & Ripatti, S., 2010, In : Genome Research. 20, 10, p. 1344-1351 8 p.

Research output: Contribution to journalArticleScientificpeer-review

Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1

Anttila, V., Stefansson, H., Kallela, M., Todt, U., Terwindt, G. M., Calafato, M. S., Nyholt, D. R., Dimas, A. S., Freilinger, T., Mueller-Myhsok, B., Artto, V., Inouye, M., Alakurtti, K., Kaunisto, M. A., Hämäläinen, E., de Vries, B., Stam, A. H., Weller, C. M., Heinze, A., Heinze-Kuhn, K. & 31 othersGoebel, I., Borck, G., Goebel, H., Steinberg, S., Wolf, C., Bjoernsson, A., Gudmundsson, G., Kirchmann, M., Hauge, A., Werge, T., Schoenen, J., Eriksson, J. G., Hagen, K., Stovner, L., Wichmann, E., Meitinger, T., Alexander, M., Moebus, S., Schreiber, S., Aulchenko, Y. S., Breteler, M. M. B., Uitterlinden, A. G., Hofman, A., van Duijn, C. M., Tikka-Kleemola, P., Kaprio, J., Färkkilä, M., Palotie, L., Wessman, M., Palotie, A. & Int Headache Genetics Consortium, 2010, In : Nature Genetics. 42, 10, p. 869-873 5 p.

Research output: Contribution to journalArticleScientificpeer-review

Integrating common and rare genetic variation in diverse human populations

Altshuler, D. M., Gibbs, R. A., Peltonen, L., Dermitzakis, E., Schaffner, S. F., Yu, F., Bonnen, P. E., de Bakker, P. I. W., Deloukas, P., Gabriel, S. B., Gwilliam, R., Hunt, S., Inouye, M., Jia, X., Palotie, A., Parkin, M., Whittaker, P., Chang, K., Hawes, A., Lewis, L. R. & 31 othersRen, Y., Wheeler, D., Muzny, D. M., Barnes, C., Darvishi, K., Hurles, M., Korn, J. M., Kristiansson, K., Lee, C., McCarroll, S. A., Nemesh, J., Keinan, A., Montgomery, S. B., Pollack, S., Price, A. L., Soranzo, N., Gonzaga-Jauregui, C., Anttila, V., Brodeur, W., Daly, M. J., Leslie, S., McVean, G., Moutsianas, L., Nguyen, H., Zhang, Q., Ghori, M. J. R., McGinnis, R., McLaren, W., Takeuchi, F., Grossman, S. R. & Int HapMap 3 Consortium, 2010, In : Nature. 467, 7311, p. 52-58 7 p.

Research output: Contribution to journalArticleScientificpeer-review

2009

Valsalva maneuver as migraine inducer: a case report of a woman with patent foramen ovale and an ischemic stroke

Artto, V., Anttila, V., Rantanen, K., Kallela, M. & Färkkilä, M., 2009, In : Headache. 49, 1, p. 146-147 2 p.

Research output: Contribution to journalArticleScientificpeer-review

2008

A high-density association screen of 155 ion transport genes for involvement with common migraine

Nyholt, D. R., LaForge, K. S., Kallela, M., Alakurtti, K., Anttila, V., Färkkilä, M., Hämäläinen, E., Kaprio, J., Kaunisto, M. A., Heath, A. C., Montgomery, G. W., Göbel, H., Todt, U., Ferrari, M. D., Launer, L. J., Frants, R. R., Terwindt, G. M., de Vries, B., Verschuren, W. M. M., Brand, J. & 14 othersFreilinger, T., Pfaffenrath, V., Straube, A., Ballinger, D. G., Zhan, Y., Daly, M. J., Cox, D. R., Dichgans, M., van den Maagdenberg, A. M. J. M., Kubisch, C., Martin, N. G., Wessman, M., Peltonen, L. & Palotie, A., 2008, In : Human Molecular Genetics. 17, 21, p. 3318-3331 14 p.

Research output: Contribution to journalArticleScientificpeer-review

Consistently replicating locus linked to migraine on 10q22-q23

Anttila, V., Nyholt, D. R., Kallela, M., Artto, V., Vepsäläinen, S., Jakkula, E., Wennerström, A., Tikka-Kleemola, P., Kaunisto, M. A., Hämäläinen, E., Widen, E., Terwilliger, J., Merikangas, K., Montgomery, G. W., Martin, N. G., Daly, M., Kaprio, J., Peltonen, L., Färkkilä, M., Wessman, M. & 1 othersPalotie, A., 2008, In : American Journal of Human Genetics. 82, 5, p. 1051-1063 13 p.

Research output: Contribution to journalArticleScientificpeer-review

2006

Trait components provide tools to dissect the genetic susceptibility of migraine

Anttila, V., Kallela, M., Oswell, G., Kaunisto, M., Nyholt, D. R., Hämäläinen, E., Havanka, H., Ilmavirta, M., Terwilliger, J., Sobel, E., Peltonen, L., Kaprio, J., Färkkilä, M., Wessman, M. & Palotie, A., 2006, In : American Journal of Human Genetics. 79, 1, p. 85-99 15 p.

Research output: Contribution to journalArticleScientificpeer-review

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