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

Year Number of Results
1988 1
1989 2
1990 2
1991 2
1992 2
1993 5
1995 1
1996 1
1997 3
1998 1
1999 1
2000 3
2001 3
2002 1
2003 4
2004 2
2005 4
2006 3
2007 2
2008 2
2009 1
2010 1
2011 1
2013 1
2014 4
2015 1
2016 3
2017 3
2018 2
2019 3
2021 1
2022 1
2023 2
2024 1

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66 results

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Page 1
Update on genetic predisposition to colorectal cancer and polyposis.
Valle L, de Voer RM, Goldberg Y, Sjursen W, Försti A, Ruiz-Ponte C, Caldés T, Garré P, Olsen MF, Nordling M, Castellvi-Bel S, Hemminki K. Valle L, et al. Among authors: nordling m. Mol Aspects Med. 2019 Oct;69:10-26. doi: 10.1016/j.mam.2019.03.001. Epub 2019 Mar 18. Mol Aspects Med. 2019. PMID: 30862463 Free article. Review.
Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population.
Lagerstedt-Robinson K, Rohlin A, Aravidis C, Melin B, Nordling M, Stenmark-Askmalm M, Lindblom A, Nilbert M. Lagerstedt-Robinson K, et al. Among authors: nordling m. Oncol Rep. 2016 Nov;36(5):2823-2835. doi: 10.3892/or.2016.5060. Epub 2016 Sep 1. Oncol Rep. 2016. PMID: 27601186 Free article.
Response to Yang et al.
Olkinuora A, Nieminen TT, Nordling M, Peltomäki P. Olkinuora A, et al. Among authors: nordling m. Genet Med. 2019 Nov;21(11):2652-2653. doi: 10.1038/s41436-019-0530-1. Epub 2019 May 2. Genet Med. 2019. PMID: 31043712 Free article. No abstract available.
Gene-specific ACMG/AMP classification criteria for germline APC variants: Recommendations from the ClinGen InSiGHT Hereditary Colorectal Cancer/Polyposis Variant Curation Expert Panel.
Spier I, Yin X, Richardson M, Pineda M, Laner A, Ritter D, Boyle J, Mur P, Hansen TVO, Shi X, Mahmood K, Plazzer JP, Ognedal E, Nordling M, Farrington SM, Yamamoto G, Baert-Desurmont S, Martins A, Borras E, Tops C, Webb E, Beshay V, Genuardi M, Pesaran T, Capellá G, Tavtigian SV, Latchford A, Frayling IM, Plon SE, Greenblatt M, Macrae FA, Aretz S; InSiGHT-ClinGen Hereditary Colon Cancer/Polyposis Variant Curation Expert Panel. Spier I, et al. Among authors: nordling m. Genet Med. 2024 Feb;26(2):100992. doi: 10.1016/j.gim.2023.100992. Epub 2023 Oct 4. Genet Med. 2024. PMID: 37800450 Free article.
Biallelic germline nonsense variant of MLH3 underlies polyposis predisposition.
Olkinuora A, Nieminen TT, Mårtensson E, Rohlin A, Ristimäki A, Koskenvuo L, Lepistö A; Swedish Extended Genetic Analysis of Colorectal Neoplasia (SWEN) Study Group; Gebre-Medhin S, Nordling M, Peltomäki P. Olkinuora A, et al. Among authors: nordling m. Genet Med. 2019 Aug;21(8):1868-1873. doi: 10.1038/s41436-018-0405-x. Epub 2018 Dec 21. Genet Med. 2019. PMID: 30573798 Free PMC article.
A mutation in POLE predisposing to a multi-tumour phenotype.
Rohlin A, Zagoras T, Nilsson S, Lundstam U, Wahlström J, Hultén L, Martinsson T, Karlsson GB, Nordling M. Rohlin A, et al. Among authors: nordling m. Int J Oncol. 2014 Jul;45(1):77-81. doi: 10.3892/ijo.2014.2410. Epub 2014 Apr 29. Int J Oncol. 2014. PMID: 24788313 Free PMC article.
GREM1 and POLE variants in hereditary colorectal cancer syndromes.
Rohlin A, Eiengård F, Lundstam U, Zagoras T, Nilsson S, Edsjö A, Pedersen J, Svensson J, Skullman S, Karlsson BG, Björk J, Nordling M. Rohlin A, et al. Among authors: nordling m. Genes Chromosomes Cancer. 2016 Jan;55(1):95-106. doi: 10.1002/gcc.22314. Epub 2015 Oct 23. Genes Chromosomes Cancer. 2016. PMID: 26493165 Free PMC article.
66 results