Aktan-Collan K[au] - Search Results

Year	Number of Results
2000	3
2001	3
2005	1
2007	2
2009	1
2011	2
2013	2
2018	2
2019	1
2023	0

1

Lay Perspectives on Receiving Different Types of Genomic Secondary Findings: a Qualitative Vignette Study.

Vornanen M, Aktan-Collan K, Hallowell N, Konttinen H, Haukkala A. Vornanen M, et al. Among authors: aktan collan k. J Genet Couns. 2019 Apr;28(2):343-354. doi: 10.1007/s10897-018-0288-7. Epub 2018 Dec 14. J Genet Couns. 2019. PMID: 30964582

2

"I would like to discuss it further with an expert": a focus group study of Finnish adults' perspectives on genetic secondary findings.

Vornanen M, Aktan-Collan K, Hallowell N, Konttinen H, Kääriäinen H, Haukkala A. Vornanen M, et al. Among authors: aktan collan k. J Community Genet. 2018 Jul;9(3):305-314. doi: 10.1007/s12687-018-0356-6. Epub 2018 Jan 16. J Community Genet. 2018. PMID: 29340884 Free PMC article.

3

Sharing genetic risk with next generation: mutation-positive parents' communication with their offspring in Lynch Syndrome.

Aktan-Collan KI, Kääriäinen HA, Kolttola EM, Pylvänäinen K, Järvinen HJ, Haukkala AH, Mecklin JP. Aktan-Collan KI, et al. Fam Cancer. 2011 Mar;10(1):43-50. doi: 10.1007/s10689-010-9386-x. Fam Cancer. 2011. PMID: 20857224

4

Adolescents at risk for MODY3 diabetes prefer genetic testing before adulthood.

Liljeström B, Tuomi T, Isomaa B, Sarelin L, Aktan-Collan K, Kääriäinen H. Liljeström B, et al. Among authors: aktan collan k. Diabetes Care. 2007 Jun;30(6):1571-3. doi: 10.2337/dc06-1744. Epub 2007 Mar 10. Diabetes Care. 2007. PMID: 17351287 No abstract available.

5

A microduplication on chromosome 17p13.1p13.3 including the PAFAH1B1 (LIS1) gene.

Avela K, Aktan-Collan K, Horelli-Kuitunen N, Knuutila S, Somer M. Avela K, et al. Among authors: aktan collan k. Am J Med Genet A. 2011 Apr;155A(4):875-9. doi: 10.1002/ajmg.a.33944. Epub 2011 Mar 15. Am J Med Genet A. 2011. PMID: 21595003

6

Revised guidelines for the clinical management of Lynch syndrome (HNPCC): recommendations by a group of European experts.

Vasen HF, Blanco I, Aktan-Collan K, Gopie JP, Alonso A, Aretz S, Bernstein I, Bertario L, Burn J, Capella G, Colas C, Engel C, Frayling IM, Genuardi M, Heinimann K, Hes FJ, Hodgson SV, Karagiannis JA, Lalloo F, Lindblom A, Mecklin JP, Møller P, Myrhoj T, Nagengast FM, Parc Y, Ponz de Leon M, Renkonen-Sinisalo L, Sampson JR, Stormorken A, Sijmons RH, Tejpar S, Thomas HJ, Rahner N, Wijnen JT, Järvinen HJ, Möslein G; Mallorca group. Vasen HF, et al. Among authors: aktan collan k. Gut. 2013 Jun;62(6):812-23. doi: 10.1136/gutjnl-2012-304356. Epub 2013 Feb 13. Gut. 2013. PMID: 23408351 Free PMC article.

7

Predictive genetic testing for hereditary non-polyposis colorectal cancer: uptake and long-term satisfaction.

Aktan-Collan K, Mecklin JP, Järvinen H, Nyström-Lahti M, Peltomäki P, Söderling I, Uutela A, de la Chapelle A, Kääriäinen H. Aktan-Collan K, et al. Int J Cancer. 2000 Jan 20;89(1):44-50. Int J Cancer. 2000. PMID: 10719730 Free article.

8

Psychosocial consequences of predictive genetic testing for Lynch syndrome and associations to surveillance behaviour in a 7-year follow-up study.

Aktan-Collan K, Kääriäinen H, Järvinen H, Peltomäki P, Pylvänäinen K, Mecklin JP, Haukkala A. Aktan-Collan K, et al. Fam Cancer. 2013 Dec;12(4):639-46. doi: 10.1007/s10689-013-9628-9. Fam Cancer. 2013. PMID: 23512527

9

Evaluation of a counselling protocol for predictive genetic testing for hereditary non-polyposis colorectal cancer.

Aktan-Collan K, Mecklin JP, de la Chapelle A, Peltomäki P, Uutela A, Kääriäinen H. Aktan-Collan K, et al. J Med Genet. 2000 Feb;37(2):108-13. doi: 10.1136/jmg.37.2.108. J Med Genet. 2000. PMID: 10662810 Free PMC article.

10

Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer.

Järvinen HJ, Aarnio M, Mustonen H, Aktan-Collan K, Aaltonen LA, Peltomäki P, De La Chapelle A, Mecklin JP. Järvinen HJ, et al. Among authors: aktan collan k. Gastroenterology. 2000 May;118(5):829-34. doi: 10.1016/s0016-5085(00)70168-5. Gastroenterology. 2000. PMID: 10784581 Clinical Trial.

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