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Results by year

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

Year Number of Results
1972 1
1973 1
1975 2
1980 2
1981 2
1983 2
1984 3
1985 8
1986 13
1987 12
1988 12
1989 8
1990 10
1991 5
1992 2
1993 3
1994 2
1995 5
1996 3
1997 9
1998 4
1999 7
2000 6
2001 4
2002 1
2003 3
2004 5
2005 5
2006 3
2007 2
2008 10
2009 3
2010 8
2011 4
2012 11
2013 4
2014 4
2015 2
2016 2
2017 5
2018 5
2019 1
2020 4
2021 4
2022 1
2023 1
2024 0

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Publication date

Search Results

202 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: kristoffersson u. 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.
From Mendel to Medical Genetics.
Kristoffersson U, Macek M. Kristoffersson U, et al. Eur J Hum Genet. 2017 Dec;25(s2):S53-S59. doi: 10.1038/ejhg.2017.157. Eur J Hum Genet. 2017. PMID: 29297875 Free PMC article. No abstract available.
A stroke gene panel for whole-exome sequencing.
Ilinca A, Samuelsson S, Piccinelli P, Soller M, Kristoffersson U, Lindgren AG. Ilinca A, et al. Among authors: kristoffersson u. Eur J Hum Genet. 2019 Feb;27(2):317-324. doi: 10.1038/s41431-018-0274-4. Epub 2018 Oct 24. Eur J Hum Genet. 2019. PMID: 30356112 Free PMC article.
Reflecting on earlier experiences with unsolicited findings: points to consider for next-generation sequencing and informed consent in diagnostics.
Rigter T, Henneman L, Kristoffersson U, Hall A, Yntema HG, Borry P, Tönnies H, Waisfisz Q, Elting MW, Dondorp WJ, Cornel MC. Rigter T, et al. Among authors: kristoffersson u. Hum Mutat. 2013 Oct;34(10):1322-8. doi: 10.1002/humu.22370. Epub 2013 Jul 16. Hum Mutat. 2013. PMID: 23784691 Free PMC article. Review.
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: kristoffersson u. 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.
Issues in human GenEthics.
Saraiva JM, Anionwu E, Belo M, Jenkins T, Kristoffersson U, Marques I, Santos HG, Sequeiros J, Simpson SA, Wertz D, Monteiro C. Saraiva JM, et al. Among authors: kristoffersson u. Genet Med. 2001 May-Jun;3(3):218-9. doi: 10.1097/00125817-200105000-00013. Genet Med. 2001. PMID: 11388765 Free article. No abstract available.
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: kristoffersson u. 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: kristoffersson u. 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.
202 results