Aaltonen LA - Search Results

1

Nordic collaborative study of the BARD1 Cys557Ser allele in 3956 patients with cancer: enrichment in familial BRCA1/BRCA2 mutation-negative breast cancer but not in other malignancies.

Karppinen SM, Barkardottir RB, Backenhorn K, Sydenham T, Syrjäkoski K, Schleutker J, Ikonen T, Pylkäs K, Rapakko K, Erkko H, Johannesdottir G, Gerdes AM, Thomassen M, Agnarsson BA, Grip M, Kallioniemi A, Kere J, Aaltonen LA, Arason A, Møller P, Kruse TA, Borg A, Winqvist R. Karppinen SM, et al. Among authors: aaltonen la. J Med Genet. 2006 Nov;43(11):856-62. doi: 10.1136/jmg.2006.041731. Epub 2006 Jul 6. J Med Genet. 2006. PMID: 16825437 Free PMC article.

2

Evidence that the MCC-APC gene region in 5q21 is not the site for susceptibility to hereditary nonpolyposis colorectal carcinoma.

Peltomäki P, Sistonen P, Mecklin JP, Pylkkänen L, Aaltonen L, Nordling S, Kere J, Järvinen H, Hamilton SR, Petersen G, et al. Peltomäki P, et al. Cancer Res. 1992 Aug 15;52(16):4530-3. Cancer Res. 1992. PMID: 1643645

3

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

Hemminki A, Peltomäki P, Mecklin JP, Järvinen H, Salovaara R, Nyström-Lahti M, de la Chapelle A, Aaltonen LA. Hemminki A, et al. Among authors: aaltonen la. Nat Genet. 1994 Dec;8(4):405-10. doi: 10.1038/ng1294-405. Nat Genet. 1994. PMID: 7894494

4

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

Lothe RA, Peltomäki P, Meling GI, Aaltonen LA, Nyström-Lahti M, Pylkkänen L, Heimdal K, Andersen TI, Møller P, Rognum TO, et al. Lothe RA, et al. Among authors: aaltonen la. Cancer Res. 1993 Dec 15;53(24):5849-52. Cancer Res. 1993. PMID: 8261392

5

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

Hemminki A, Höglund P, Pukkala E, Salovaara R, Järvinen H, Norio R, Aaltonen LA. Hemminki A, et al. Among authors: aaltonen la. Oncogene. 1998 Feb 5;16(5):681-4. doi: 10.1038/sj.onc.1201538. Oncogene. 1998. PMID: 9482116

6

A missense mutation in the BRCA2 gene in three siblings with ovarian cancer.

Roth S, Kristo P, Auranen A, Shayehgi M, Seal S, Collins N, Barfoot R, Rahman N, Klemi PJ, Grénman S, Sarantaus L, Nevanlinna H, Butzow R, Ashworth A, Stratton MR, Aaltonen LA. Roth S, et al. Among authors: aaltonen la. Br J Cancer. 1998 Apr;77(8):1199-202. doi: 10.1038/bjc.1998.202. Br J Cancer. 1998. PMID: 9579822 Free PMC article.

7

Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients.

Wang ZJ, Churchman M, Avizienyte E, McKeown C, Davies S, Evans DG, Ferguson A, Ellis I, Xu WH, Yan ZY, Aaltonen LA, Tomlinson IP. Wang ZJ, et al. Among authors: aaltonen la. J Med Genet. 1999 May;36(5):365-8. J Med Genet. 1999. PMID: 10353780 Free PMC article.

8

Strategies for screening for hereditary non-polyposis colorectal cancer.

Loukola A, de la Chapelle A, Aaltonen LA. Loukola A, et al. Among authors: aaltonen la. J Med Genet. 1999 Nov;36(11):819-22. J Med Genet. 1999. PMID: 10544224 Free PMC article.

9

PPP2R1B gene in chronic lymphocytic leukemias and mantle cell lymphomas.

Zhu Y, Loukola A, Monni O, Kuokkanen K, Franssila K, Elonen E, Vilpo J, Joensuu H, Kere J, Aaltonen L, Knuutila S. Zhu Y, et al. Leuk Lymphoma. 2001 Mar;41(1-2):177-83. doi: 10.3109/10428190109057968. Leuk Lymphoma. 2001. PMID: 11342371

10

DNA methylation patterns in hereditary human cancers mimic sporadic tumorigenesis.

Esteller M, Fraga MF, Guo M, Garcia-Foncillas J, Hedenfalk I, Godwin AK, Trojan J, Vaurs-Barrière C, Bignon YJ, Ramus S, Benitez J, Caldes T, Akiyama Y, Yuasa Y, Launonen V, Canal MJ, Rodriguez R, Capella G, Peinado MA, Borg A, Aaltonen LA, Ponder BA, Baylin SB, Herman JG. Esteller M, et al. Among authors: aaltonen la. Hum Mol Genet. 2001 Dec 15;10(26):3001-7. doi: 10.1093/hmg/10.26.3001. Hum Mol Genet. 2001. PMID: 11751682

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