Photo of Lauri Aaltonen

Lauri Aaltonen, Professor

  • PL 63 (Haartmaninkatu 8)

    00014

    Finland

1992 …2020
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Publications 1992 2020

Article

Gene expression signatures for colorectal cancer microsatellite status and HNPCC

Kruhøffer, M., Jensen, J. L., Laiho, P., Dyrskjot, L., Salovaara, R., Arango, D., Birkenkamp-Demtröder, K., Sørensen, F. B., Christensen, L. L., Buhl, L., Mecklin, J-P., Järvinen, H. J., Thykjaer, T., Wikman, F., Bech-Knudsen, F., Juhola, M., Nupponen, N., Laurberg, S., Andersen, C. L., Aaltonen, L. A. & 1 others, Ørntoft, T. F., 2005, In : British Journal of Cancer. 92, 12, p. 2240-2248 9 p.

Research output: Contribution to journalArticleScientificpeer-review

Genetic and Epigenetic Characterization of Growth Hormone-Secreting Pituitary Tumors

Välimäki, N., Schalin-Jäntti, C., Karppinen, A., Paetau, A., Kivipelto, L., Aaltonen, L. A. & Karhu, A., Dec 2019, In : Molecular Cancer Research. 17, 12, p. 2432-2443 12 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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Genetic mapping of a locus predisposing to human colorectal cancer

Peltomäki, P., AALTONEN, L. A., SISTONEN, P., PYLKKANEN, L., MECKLIN, J. P., JARVINEN, H., GREEN, J. S., JASS, J. R., WEBER, J. L., LEACH, F. S., PETERSEN, G. M., HAMILTON, S. R., DELACHAPELLE, A. & VOGELSTEIN, B., 1993, In : Science. 260, p. 810-812 3 p.

Research output: Contribution to journalArticleScientificpeer-review

Genetic predisposition to uterine leiomyoma is determined by loci for genitourinary development and genome stability

Valimaki, N., Kuisma, H., Pasanen, A., Heikinheimo, O., Sjoberg, J., Butzow, R., Sarvilinna, N., Heinonen, H-R., Tolvanen, J., Bramante, S., Tanskanen, T., Auvinen, J., Uimari, O., Alkodsi, A., Lehtonen, R., Kaasinen, E., Palin, K. & Aaltonen, L. A., 18 Sep 2018, In : eLife. 7, 50 p., 37110.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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Genome-wide association study and meta-analysis in Northern European populations replicate multiple colorectal cancer risk loci

Tanskanen, T., van den Berg, L., Valimaki, N., Aavikko, M., Ness-Jensen, E., Hveem, K., Wettergren, Y., Lindskog, E. B., Tonisson, N., Metspalu, A., Silander, K., Orlando, G., Law, P. J., Tuupanen, S., Gylfe, A. E., Hanninen, U. A., Cajuso, T., Kondelin, J., Sarin, A-P., Pukkala, E. & 40 others, Jousilahti, P., Salomaa, V., Ripatti, S., Palotie, A., Jarvinen, H., Renkonen-Sinisalo, L., Lepisto, A., Bohm, J., Mecklin, J-P., Al-Tassan, N. A., Palles, C., Martin, L., Barclay, E., Tenesa, A., Farrington, S. M., Timofeeva, M. N., Meyer, B. F., Wakil, S. M., Campbell, H., Smith, C. G., Idziaszczyk, S., Maughan, T. S., Kaplan, R., Kerr, R., Kerr, D., Buchanan, D. D., Win, A. K., Hopper, J., Jenkins, M. A., Newcomb, P. A., Gallinger, S., Conti, D., Schumacher, F. R., Casey, G., Cheadle, J. P., Dunlop, M. G., Tomlinson, I. P., Houlston, R. S., Palin, K. & Aaltonen, L. A., 1 Feb 2018, In : International Journal of Cancer. 142, 3, p. 540-546 7 p.

Research output: Contribution to journalArticleScientificpeer-review

Genomic instability in colorectal cancer: relationship to clinicopathological variables and family history

LOTHE, R. A., Peltomäki, P., MELING, G. I., AALTONEN, L. A., NYSTROMLAHTI, M., PYLKKANEN, L., HEIMDAL, K., ANDERSEN, T. I., MOLLER, P., ROGNUM, T. O., FOSSA, S. D., HALDORSEN, T., LANGMARK, F., BROGGER, A., DELACHAPELLE, A. & BORRESEN, A. L., 1993, In : Cancer Research. 53, p. 5849-5852 4 p.

Research output: Contribution to journalArticleScientificpeer-review

Germline and somatic mutation analysis of MLH3 in MSI-positive colorectal cancer

Loukola, A., Vilkki, S., Singh, J., Launonen, T. & Aaltonen, LA., Aug 2000, In : The American Journal of Pathology. 157, 2, p. 347-352 6 p.

Research output: Contribution to journalArticleScientificpeer-review

Germline CDKN1B/p27Kip1 mutation in multiple endocrine neoplasia

Georgitsi, M., Raitila, A., Karhu, A., van der Luijt, R. B., Aalfs, C. M., Sane, T., Vierimaa, O., Mäkinen, M. J., Tuppurainen, K., Paschke, R., Gimm, O., Koch, C. A., Gundogdu, S., Lucassen, A., Tischkowitz, M., Izatt, L., Aylwin, S., Bano, G., Hodgson, S., De Menis, E. & 3 others, Launonen, V., Vahteristo, P. & Aaltonen, L. A., 2007, In : Journal of Clinical Endocrinology and Metabolism. 92, 8, p. 3321-3325 5 p.

Research output: Contribution to journalArticleScientificpeer-review

Germline fumarate hydratase mutations in patients with ovarian mucinous cystadenoma

Ylisaukko-oja, S. K., Cybulski, C., Lehtonen, R., Kiuru, M., Matyjasik, J., Szymanska, A., Szymanska-Pasternak, J., Dyrskjot, L., Butzow, R., Orntoft, T. F., Launonen, V., Lubinski, J. & Aaltonen, L. A., 2006, In : European Journal of Human Genetics. 14, 7, p. 880-883 4 p.

Research output: Contribution to journalArticleScientificpeer-review

Germline MSH6 Mutation in a Patient With Two Independent Primary Glioblastomas

Forsstrom, L. M., Sumi, K., Makinen, M. J., Oh, J. E., Herva, R., Kleihues, P., Ohgaki, H. & Aaltonen, L. A., Oct 2017, In : Journal of Neuropathology and Experimental Neurology. 76, 10, p. 848-853 6 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access

Germline mutations in BMPR1A/ALK3 cause a subset of cases of juvenile polyposis syndrome and of Cowden and Bannayan-Riley-Ruvalcaba syndromes

Zhou, X. P., Woodford-Richens, K., Lehtonen, R., Kurose, K., Aldred, M., Hampel, H., Launonen, V., Virta, S., Pilarski, R., Salovaara, R., Bodmer, W. F., Conrad, B. A., Dunlop, M., Hodgson, S. V., Iwama, T., Jarvinen, H., Kellokumpu, I., Kim, J. C., Leggett, B., Markie, D. & 9 others, Mecklin, J. P., Neale, K., Phillips, R., Piris, J., Rozen, P., Houlston, R. S., Aaltonen, L. A., Tomlinson, I. P. M. & Eng, C., 2001, In : American Journal of Human Genetics. 69, p. 704-711 8 p.

Research output: Contribution to journalArticleScientificpeer-review

Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer

Tomlinson, I. P. M., Alam, N. A., Rowan, A. J., Barclay, E., Jaeger, E. E. M., Kelsell, D., Leigh, I., Gorman, P., Lamlum, H., Rahman, S., Roylance, R. R., Olpin, S., Bevan, S., Barker, K., Hearle, N., Houlston, R. S., Kiuru, M., Lehtonen, R., Karhu, A., Vilkki, S. & 12 others, Laiho, P., Eklund, C., Vierimaa, O., Aittomaki, K., Hietala, M., Sistonen, P., Paetau, A., Salovaara, R., Herva, R., Launonen, V., Aaltonen, L. A. & Multiple Leiomyoma Consortium, 2002, In : Nature Genetics. 30, p. 406-410 5 p.

Research output: Contribution to journalArticleScientificpeer-review

Germline mutations in young non-smoking women with lung adenocarcinoma

Donner, I., Katainen, R., Sipilä, L. J., Aavikko, M., Pukkala, E. & Aaltonen, L. A., Aug 2018, In : Lung Cancer. 122, p. 76-82 7 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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Global metabolomic profiling of uterine leiomyomas

Heinonen, H-R., Mehine, M., Mäkinen, N., Pasanen, A., Pitkänen, E., Karhu, A., Sarvilinna, N. S., Sjöberg, J., Heikinheimo, O., Bützow, R., Aaltonen, L. A. & Kaasinen, E., 5 Dec 2017, In : British Journal of Cancer. 117, 12, p. 1855-1864 10 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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High Familial Risk in Nodular Lymphocyte-Predominant Hodgkin Lymphoma

Saarinen, S., Pukkala, E., Vahteristo, P., Makinen, M. J., Franssila, K. & Aaltonen, L. A., 1 Mar 2013, In : Journal of Clinical Oncology. 31, 7, p. 938-943 6 p.

Research output: Contribution to journalArticleScientificpeer-review

High Frequency of RPL22 Mutations in Microsatellite-Unstable Colorectal and Endometrial Tumors

Ferreira, A. M., Tuominen, I., van Dijk-Bos, K., Sanjabi, B., van der Sluis, T., van der Zee, A. G., Hollema, H., Zazula, M., Sijmons, R. H., Aaltonen, L. A., Westers, H. & Hofstra, R. M. W., Dec 2014, In : Human Mutation. 35, 12, p. 1442-1445 4 p.

Research output: Contribution to journalArticleScientificpeer-review

High frequency of TTK mutations in microsatellite-unstable colorectal cancer and evaluation of their effect on spindle assembly checkpoint

Niittymaki, I., Gylfe, A., Laine, L., Laakso, M., Lehtonen, H. J., Kondelin, J., Tolvanen, J., Nousiainen, K., Pouwels, J., Jarvinen, H., Nuorva, K., Mecklin, J-P., Makinen, M., Ristimaki, A., Orntoft, T. F., Hautaniemi, S., Karhu, A., Kallio, M. J. & Aaltonen, L. A., 2011, In : Carcinogenesis. 32, 3, p. 305-311 7 p.

Research output: Contribution to journalArticleScientificpeer-review

HOXB13 G84E Mutation in Finland: Population-Based Analysis of Prostate, Breast, and Colorectal Cancer Risk

Laitinen, V. H., Wahlfors, T., Saaristo, L., Rantapero, T., Pelttari, L. M., Kilpivaara, O., Laasanen, S-L., Kallioniemi, A., Nevanlinna, H., Aaltonen, L., Vessella, R. L., Auvinen, A., Visakorpi, T., Tammela, T. L. J. & Schleutker, J., Mar 2013, In : Cancer Epidemiology, Biomarkers & Prevention. 22, 3, p. 452-460 9 p.

Research output: Contribution to journalArticleScientificpeer-review

Identification of 33 candidate oncogenes by screening for base-specific mutations

Tuupanen, S., Hanninen, U. A., Kondelin, J., von Nandelstadh, P., Cajuso, T., Gylfe, A. E., Katainen, R., Tanskanen, T., Ristolainen, H., Bohm, J., Mecklin, J-P., Järvinen, H., Renkonen-Sinisalo, L., Andersen, C. L., Taipale, M., Taipale, J., Vahteristo, P., Lehti, K., Pitkanen, E. & Aaltonen, L. A., 14 Oct 2014, In : British Journal of Cancer. 111, 8, p. 1657-1662 6 p.

Research output: Contribution to journalArticleScientificpeer-review

Identification of Candidate Oncogenes in Human Colorectal Cancers With Microsatellite Instability

Gylfe, A. E., Kondelin, J., Turunen, M., Ristolainen, H., Katainen, R., Pitkänen, E., Kaasinen, E., Rantanen, V., Tanskanen, T., Varjosalo, M., Lehtonen, H., Palin, K., Taipale, M., Taipale, J., Renkonen-Sinisalo, L., Järvinen, H., Bohm, J., Mecklin, J-P., Ristimäki, A., Kilpivaara, O. & 4 others, Tuupanen, S., Karhu, A., Vahteristo, P. & Aaltonen, L. A., Sep 2013, In : Gastroenterology. 145, 3, p. 540-+ 26 p.

Research output: Contribution to journalArticleScientificpeer-review

Identification of homozygous deletion in ACAN and other candidate variants in familial classical Hodgkin lymphoma by exome sequencing

Ristolainen, H., Kilpivaara, O., Kamper, P., Taskinen, M., Saarinen, S., Leppa, S., d'Amore, F. & Aaltonen, L. A., Aug 2015, In : British Journal of Haematology. 170, 3, p. 428-431 4 p.

Research output: Contribution to journalArticleScientificpeer-review

Identification of Lynch Syndrome Among Patients With Colorectal Cancer

EPICOLON Consortium, 17 Oct 2012, In : JAMA : The Journal of the American Medical Association. 308, 15, p. 1555-1565 11 p.

Research output: Contribution to journalArticleScientificpeer-review

Impact of constitutional TET2 haploinsufficiency on molecular and clinical phenotype in humans

Kaasinen, E., Kuismin, O., Rajamäki, K., Ristolainen, H., Aavikko, M., Kondelin, J., Saarinen, S., Berta, D. G., Katainen, R., Hirvonen, E. A. M., Karhu, A., Taira, A., Tanskanen, T., Alkodsi, A., Taipale, M., Morgunova, E., Franssila, K., Lehtonen, R., Mäkinen, M., Aittomäki, K. & 15 others, Palotie, A., Kurki, M., Pietiläinen, O., Hilpert, M., Saarentaus, E., Niinimäki, J., Junttila, J., Kaikkonen, K., Vahteristo, P., Skoda, R. C., Seppänen, M. R. J., Eklund, K. K., Taipale, J., Kilpivaara, O. & Aaltonen, L. A., 19 Mar 2019, In : Nature Communications. 10, 17 p., 1252.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
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Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease

Aaltonen, L. A., Salovaara, R., Kristo, P., Canzian, F., Hemminki, A., Peltomäki, P., Chadwick, R. B., Kääriäinen, H., Eskelinen, M., Jarvinen, H., Mecklin, J. P., de la Chapelle, A., Percesepe, A., Ahtola, H., Harkonen, N., Julkunen, R., Kangas, E., Ojala, S., Tulikoura, J. & ValKamo, E., 1998, In : New England Journal of Medicine. 338, 21, p. 1481-1487 7 p.

Research output: Contribution to journalArticleScientificpeer-review

Increased HIF1 alpha in SDH and FH deficient tumors does not cause microsatellite instability

Lehtonen, H. J., Mäkinen, M. J., Kiuru, M., Laiho, P., Herva, R., van Minderhout, I., Hogendoorn, P. C. W., Cornelisse, C., Devilee, P., Launonen, V. & Aaltonen, L. A., 2007, In : International Journal of Cancer. 121, 6, p. 1386-1389 4 p.

Research output: Contribution to journalArticleScientificpeer-review

Increased risk of cancer in patients with fumarate hydratase germline mutation

Lehtonen, H., Kiuru, M., Ylisaukko-oja, S., Salovaara, R., Herva, R., Koivisto, P., Vierimaa, O., Aittomäki, K., Pukkala, E., Launonen, V., Aaltonen, L. A. & Lehtonen, H., 2006, In : Journal of Medical Genetics. 43, 6, p. 523-526 4 p.

Research output: Contribution to journalArticleScientificpeer-review

Induction of cyclooxygenase-2 in a mouse model of Peutz-Jeghers polyposis

Rossi, D. J., Ylikorkala, A., Korsisaari, N., Salovaara, R., Luukko, K., Launonen, V., Henkemeyer, M., Ristimaki, A., Aaltonen, L. A. & Makela, T. P., 2002, In : Proceedings of the National Academy of Sciences of the United States of America. 99, p. 12327-12332 6 p.

Research output: Contribution to journalArticleScientificpeer-review

In response: SMAD4 levels and allelic imbalance in 18q21 in colorectal cancer

Arango, D., Alhopuro, P. & Aaltonen, L. A., 2006, In : Clinical Cancer Research. 12, 5, p. 1654-1655 2 p.

Research output: Contribution to journalArticleScientific

Open Access

Intestinal cancer in patients with a germline mutation in the down-regulated in adenoma (DRA) gene

Hemminki, A., Hoglund, P., Pukkala, E., Salovaara, R., Jarvinen, H., Norio, R. & Aaltonen, L. A., 1998, In : Oncogene. 16, p. 681-684 4 p.

Research output: Contribution to journalArticleScientificpeer-review

KSHV-Initiated Notch Activation Leads to Membrane-Type-1MatrixMetalloproteinase-Dependent Lymphatic Endothelial-to-Mesenchymal Transition

Cheng, F., Pekkonen, P. M., Laurinavicius, S., Sugiyama, N., Henderson, S., Günther, T., Rantanen, V., Kaivanto, E., Aavikko, M., Sarek, G., Hautaniemi, S., Biberfeld, P., Aaltonen, L. A., Grundhoff, A., Boshoff, C., Alitalo, K., Lehti, K. & Ojala, P., 2011, In : Cell Host & Microbe. 10, 6, p. 577-590 14 p.

Research output: Contribution to journalArticleScientificpeer-review

KSHV-Initiated Notch Activation Leads to Membrane-Type-1 Matrix Metalloproteinase-Dependent Lymphatic Endothelial-to-Mesenchymal Transition

Cheng, F., Pekkonen, P., Laurinavicius, S., Sugiyama, N., Henderson, S., Guenther, T., Rantanen, V., Kaivanto, E., Aavikko, M., Sarek, G., Hautaniemi, S., Biberfeld, P., Aaltonen, L., Grundhoff, A., Boshoff, C., Alitalo, K., Lehti, K. & Ojala, P. M., 2011, In : Cell Host & Microbe. 10, 6, p. 577-590 14 p.

Research output: Contribution to journalArticleScientificpeer-review

Large genomic deletions in AIP in pituitary adenoma predisposition

Georgitsi, M., Heliövaara, E., Paschke, R., Kumar, A. V. K., Tischkowitz, M., Vierimaa, O., Salmela, P., Sane, T., De Menis, E., Cannavo, S., Gundogdu, S., Lucassen, A., Izatt, L., Aylwin, S., Bano, G., Hodgson, S., Koch, C. A., Karhu, A. & Aaltonen, L. A., 2008, In : Journal of Clinical Endocrinology and Metabolism. 93, 10, p. 4146-4151 6 p.

Research output: Contribution to journalArticleScientificpeer-review

Little evidence for involvement of MLH3 in colorectal cancer predisposition

Hienonen, T., Laiho, P., Salovaara, R., Mecklin, J. P., Järvinen, H., Sistonen, P., Peltomäki, P., Lehtonen, R., Nupponen, N. N., Launonen, V., Karhu, A. & Aaltonen, L. A., 2003, In : International Journal of Cancer. 106, p. 292-296 5 p.

Research output: Contribution to journalArticleScientificpeer-review

LKB1 exonic and whole gene deletions are a common cause of Peutz-Jeghers syndrome: [electronic letter]

Volikos, E., Robinson, J., Aittomäki, K., Mecklin, J-P., Järvinen, H., Westerman, A. M., de Rooij, F. W. M., Vogel, T., Moeslein, G., Launonen, V., Tomlinson, I. P. M., Silver, A. R. J. & Aaltonen, L. A., 2006, In : Journal of Medical Genetics. 43, 5, p. e18 3 p.

Research output: Contribution to journalArticleScientificpeer-review

LKB1 somatic mutations in sporadic tumors

Avizienyte, E., Loukola, A., Roth, S., Hemminki, A., Tarkkanen, M., Salovaara, R., Arola, J., Butzow, R., Husgafvel-Pursiainen, K., Kokkola, A., Jarvinen, H. & Aaltonen, L. A., 1999, In : The American Journal of Pathology. 154, 3, p. 677-681 5 p.

Research output: Contribution to journalArticleScientificpeer-review

Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridization and targeted linkage analysis

Hemminki, A., Tomlinson, I., Markie, D., Jarvinen, H., Sistonen, P., Bjorkqvist, A. M., Knuutila, S., Salovaara, R., Bodmer, W., Shibata, D., delaChapelle, A. & Aaltonen, L. A., 1997, In : Nature Genetics. 15, p. 87-90 4 p.

Research output: Contribution to journalArticleScientificpeer-review

Loss of SUFU Function in Familial Multiple Meningioma

Aavikko, M., Li, S-P., Saarinen, S., Alhopuro, P., Kaasinen, E., Morgunova, E., Li, Y., Vesanen, K., Smith, M. J., Evans, D. G. R., Pöyhönen, M., Kiuru, A., Auvinen, A., Aaltonen, L. A., Taipale, J. & Vahteristo, P., 7 Sep 2012, In : American Journal of Human Genetics. 91, 3, p. 520-526 7 p.

Research output: Contribution to journalArticleScientificpeer-review

Loss of the wild type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancer

Hemminki, A., Peltomäki, P., MECKLIN, J. P., Järvinen, H., Salovaara, R., Nyström-Lahti, M., de la Chapelle, A. & Aaltonen, L. A., 1994, In : Nature Genetics. 8, p. 405-410 6 p.

Research output: Contribution to journalArticleScientificpeer-review

Low-level microsatellite instability in most colorectal carcinomas

Laiho, P., Launonen, T., Lahermo, P., Esteller, M., Guo, MZ., Herman, JG., Mecklin, JP., Jarvinen, H., Sistonen, P., Kim, KM., Shibata, D., Houlston, RS. & Aaltonen, LA., 15 Feb 2002, In : Cancer Research. 62, 4, p. 1166-1170 5 p.

Research output: Contribution to journalArticleScientificpeer-review

Low-Penetrance Susceptibility Variants in Familial Colorectal Cancer

Niittymaki, I., Kaasinen, E., Tuupanen, S., Karhu, A., Jarvinen, H., Mecklin, J-P., Tomlinson, I. P. M., Di Bernardo, M. C., Houlston, R. S. & Aaltonen, L. A., 2010, In : Cancer Epidemiology, Biomarkers & Prevention. 19, 6, p. 1478-1483 6 p.

Research output: Contribution to journalArticleScientificpeer-review

MDM2 SNP309 accelerates colorectal tumour formation in women

Bond, G. L., Menin, C., Bertorelle, R., Alhopuro, P., Aaltonen, L. A. & Levine, A. J., 2006, In : Journal of Medical Genetics. 43, 12, p. 950-952 3 p.

Research output: Contribution to journalArticleScientificpeer-review

Mechanisms of inactivation of the receptor tyrosine kinase EPHB2 in colorectal tumors

Alazzouzi, H., Davalos, V., Kokko, A., Domingo, E., Woerner, S. M., Wilson, A. J., Konrad, L., Laiho, P., Espin, E., Armengol, M., Imai, K., Yamamoto, H., Mariadason, J. M., Gebert, J. F., Aaltonen, L. A., Schwartz, S. & Arango, D., 2005, In : Cancer Research. 65, 22, p. 10170-10173 4 p.

Research output: Contribution to journalArticleScientificpeer-review

MED12, the Mediator Complex Subunit 12 Gene, Is Mutated at High Frequency in Uterine Leiomyomas

Mäkinen, N., Mehine, M., Tolvanen, J., Kaasinen, E., Li, Y., Lehtonen, H. J., Gentile, M., Yan, J., Enge, M., Taipale, M., Aavikko, M., Katainen, R., Virolainen, E., Böhling, T., Koski, T. A., Launonen, V., Sjöberg, J., Taipale, J., Vahteristo, P. & Aaltonen, L. A., 2011, In : Science Progress. 334, 6053, p. 252-255 4 p.

Research output: Contribution to journalArticleScientificpeer-review

MED12 exon 2 mutations are common in uterine leiomyomas from South African patients

Mäkinen, N., Heinonen, H-R., Moore, S., Tomlinson, I. P. M., van der Spuy, Z. M. & Aaltonen, L. A., Dec 2011, In : Oncotarget. 2, 12, p. 966-969 4 p.

Research output: Contribution to journalArticleScientificpeer-review

MED12 exon 2 mutations in histopathological uterine leiomyoma variants

Mäkinen, N., Vahteristo, P., Kämpjärvi, K., Arola, J., Butzow, R. & Aaltonen, L. A., Nov 2013, In : European Journal of Human Genetics. 21, 11, p. 1300-1303 4 p.

Research output: Contribution to journalArticleScientificpeer-review

MED12 mutation frequency in unselected sporadic uterine leiomyomas

Heinonen, H-R., Sarvilinna, N. S., Sjoberg, J., Kampjarvi, K., Pitkanen, E., Vahteristo, P., Makinen, N. & Aaltonen, L. A., Oct 2014, In : Fertility and Sterility : official journal of the American Fertility Society . 102, 4, p. 1137-1142 6 p.

Research output: Contribution to journalArticleScientificpeer-review

MED12 mutations and FH inactivation are mutually exclusive in uterine leiomyomas

Kampjarvi, K., Makinen, N., Mehine, M., Valipakka, S., Uimari, O., Pitkanen, E., Heinonen, H-R., Heikkinen, T., Tolvanen, J., Ahtikoski, A., Frizzell, N., Sarvilinna, N., Sjoberg, J., Butzow, R., Aaltonen, L. A. & Vahteristo, P., 14 Jun 2016, In : British Journal of Cancer. 114, 12, p. 1405-1411 7 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access