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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1958 1
1981 1
1982 1
1983 1
1984 1
1985 1
1986 2
1987 2
1988 5
1989 6
1990 2
1993 8
1994 7
1995 9
1996 3
1997 3
1998 5
1999 9
2000 10
2001 10
2002 2
2003 5
2004 8
2005 9
2006 3
2007 4
2008 6
2009 3
2010 6
2011 2
2012 2
2013 3
2014 3
2015 6
2016 2
2017 3
2018 3
2019 1
2021 3
2022 4
2023 1

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163 results

Results by year

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Page 1
Rare diseases: past achievements and future prospects.
Tumiene B, Kristoffersson U, Hedley V, Kääriäinen H. Tumiene B, et al. Among authors: kaariainen h. J Community Genet. 2021 Apr;12(2):205-206. doi: 10.1007/s12687-021-00529-0. J Community Genet. 2021. PMID: 33945116 Free PMC article. No abstract available.
The Finnish genetic heritage in 2022 - from diagnosis to translational research.
Uusimaa J, Kettunen J, Varilo T, Järvelä I, Kallijärvi J, Kääriäinen H, Laine M, Lapatto R, Myllynen P, Niinikoski H, Rahikkala E, Suomalainen A, Tikkanen R, Tyynismaa H, Vieira P, Zarybnicky T, Sipilä P, Kuure S, Hinttala R. Uusimaa J, et al. Among authors: kaariainen h. Dis Model Mech. 2022 Oct 1;15(10):dmm049490. doi: 10.1242/dmm.049490. Epub 2022 Oct 26. Dis Model Mech. 2022. PMID: 36285626 Free PMC article. Review.
[Hereditary cancer].
Kääriäinen H. Kääriäinen H. Duodecim. 1993;109(10):807-9. Duodecim. 1993. PMID: 8062646 Review. Finnish. No abstract available.
A Web Portal for Communicating Polygenic Risk Score Results for Health Care Use-The P5 Study.
Marjonen H, Marttila M, Paajanen T, Vornanen M, Brunfeldt M, Joensuu A, Halmesvaara O, Aro K, Alanne-Kinnunen M, Jousilahti P, Borodulin K, Koskinen S, Tuomi T, Ilanne-Parikka P, Lindström J, Laine MK, Auro K, Kääriäinen H, Perola M, Kristiansson K. Marjonen H, et al. Among authors: kaariainen h. Front Genet. 2021 Oct 29;12:763159. doi: 10.3389/fgene.2021.763159. eCollection 2021. Front Genet. 2021. PMID: 34777479 Free PMC article. Review.
Polycystic liver and kidney diseases.
Tahvanainen E, Tahvanainen P, Kääriäinen H, Höckerstedt K. Tahvanainen E, et al. Among authors: kaariainen h. Ann Med. 2005;37(8):546-55. doi: 10.1080/07853890500389181. Ann Med. 2005. PMID: 16338757 Review.
Medically assisted reproduction and ethical challenges.
Kääriäinen H, Evers-Kiebooms G, Coviello D. Kääriäinen H, et al. Toxicol Appl Pharmacol. 2005 Sep 1;207(2 Suppl):684-8. doi: 10.1016/j.taap.2005.01.032. Toxicol Appl Pharmacol. 2005. PMID: 15992844 Review.
Benchmarks for cystic fibrosis carrier screening: a European consensus document.
Castellani C, Macek M Jr, Cassiman JJ, Duff A, Massie J, ten Kate LP, Barton D, Cutting G, Dallapiccola B, Dequeker E, Girodon E, Grody W, Highsmith EW, Kääriäinen H, Kruip S, Morris M, Pignatti PF, Pypops U, Schwarz M, Soller M, Stuhrman M, Cuppens H. Castellani C, et al. Among authors: kaariainen h. J Cyst Fibros. 2010 May;9(3):165-78. doi: 10.1016/j.jcf.2010.02.005. Epub 2010 Apr 2. J Cyst Fibros. 2010. PMID: 20363197 Free article.
EuroGentest: DNA-based testing for heritable disorders in Europe.
Javaher P, Kaariainen H, Kristoffersson U, Nippert I, Sequeiros J, Zimmern R, Schmidtke J. Javaher P, et al. Among authors: kaariainen h. Community Genet. 2008;11(2):75-120. doi: 10.1159/000111984. Epub 2008 Jan 17. Community Genet. 2008. PMID: 18204250 Review.
Provision of genetic services in Europe: current practices and issues.
Godard B, Kääriäinen H, Kristoffersson U, Tranebjaerg L, Coviello D, Aymé S. Godard B, et al. Among authors: kaariainen h. Eur J Hum Genet. 2003 Dec;11 Suppl 2:S13-48. doi: 10.1038/sj.ejhg.5201111. Eur J Hum Genet. 2003. PMID: 14718937 Review.
163 results