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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
2024 1

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164 results

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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.
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 Free 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.
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.
Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities. Background Document to the ESHG recommendations on genetic testing and common disorders.
Becker F, van El CG, Ibarreta D, Zika E, Hogarth S, Borry P, Cambon-Thomsen A, Cassiman JJ, Evers-Kiebooms G, Hodgson S, Janssens AC, Kaariainen H, Krawczak M, Kristoffersson U, Lubinski J, Patch C, Penchaszadeh VB, Read A, Rogowski W, Sequeiros J, Tranebjaerg L, van Langen IM, Wallace H, Zimmern R, Schmidtke J, Cornel MC. Becker F, et al. Among authors: kaariainen h. Eur J Hum Genet. 2011 Apr;19 Suppl 1(Suppl 1):S6-44. doi: 10.1038/ejhg.2010.249. Eur J Hum Genet. 2011. PMID: 21412252 Free PMC article. Review. No abstract available.
Familial pericentric inversion inv(8)(p23q11).
Boyd H, Kaste J, Hovi E, Ritanen-Mohammed UM, Kääriäinen H, de la Chapelle A, Lehesjoki AE. Boyd H, et al. Among authors: kaariainen h. J Med Genet. 1994 Mar;31(3):201-5. doi: 10.1136/jmg.31.3.201. J Med Genet. 1994. PMID: 8014967 Free PMC article.
Community genetics. Its definition 2010.
Ten Kate LP, Al-Gazali L, Anand S, Bittles A, Cassiman JJ, Christianson A, Cornel MC, Hamamy H, Kääriäinen H, Kristoffersson U, Marais D, Penchaszadeh VB, Rahman P, Schmidtke J. Ten Kate LP, et al. Among authors: kaariainen h. J Community Genet. 2010 Mar;1(1):19-22. doi: 10.1007/s12687-010-0007-z. Epub 2010 Mar 31. J Community Genet. 2010. PMID: 21475671 Free PMC article.
164 results