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Results by year

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

Year Number of Results
1969 1
1970 1
1972 3
1973 3
1976 4
1977 4
1978 4
1979 4
1980 4
1981 5
1982 3
1983 9
1984 2
1985 2
1986 6
1987 8
1988 9
1989 1
1990 4
1991 6
1992 4
1993 14
1994 9
1995 10
1996 21
1997 15
1998 19
1999 17
2000 24
2001 20
2002 19
2003 12
2004 13
2005 29
2006 19
2007 17
2008 24
2009 17
2010 12
2011 8
2012 6
2013 10
2014 8
2015 6
2016 4
2017 5
2018 2
2024 0

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423 results

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Page 1
Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database.
Thompson BA, Spurdle AB, Plazzer JP, Greenblatt MS, Akagi K, Al-Mulla F, Bapat B, Bernstein I, Capellá G, den Dunnen JT, du Sart D, Fabre A, Farrell MP, Farrington SM, Frayling IM, Frebourg T, Goldgar DE, Heinen CD, Holinski-Feder E, Kohonen-Corish M, Robinson KL, Leung SY, Martins A, Moller P, Morak M, Nystrom M, Peltomaki P, Pineda M, Qi M, Ramesar R, Rasmussen LJ, Royer-Pokora B, Scott RJ, Sijmons R, Tavtigian SV, Tops CM, Weber T, Wijnen J, Woods MO, Macrae F, Genuardi M. Thompson BA, et al. Nat Genet. 2014 Feb;46(2):107-115. doi: 10.1038/ng.2854. Epub 2013 Dec 22. Nat Genet. 2014. PMID: 24362816 Free PMC article.
Response.
Smith CG, West H, Harris R, Idziaszczyk S, Maughan TS, Kaplan R, Richman S, Quirke P, Seymour M, Moskvina V, Steinke V, Propping P, Hes FJ, Wijnen J, Cheadle JP. Smith CG, et al. Among authors: propping p. J Natl Cancer Inst. 2014 Apr 26;106(5):dju087. doi: 10.1093/jnci/dju087. J Natl Cancer Inst. 2014. PMID: 24771876 No abstract available.
Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer.
Mangold E, Pagenstecher C, Friedl W, Mathiak M, Buettner R, Engel C, Loeffler M, Holinski-Feder E, Müller-Koch Y, Keller G, Schackert HK, Krüger S, Goecke T, Moeslein G, Kloor M, Gebert J, Kunstmann E, Schulmann K, Rüschoff J, Propping P. Mangold E, et al. Among authors: propping p. Int J Cancer. 2005 Sep 20;116(5):692-702. doi: 10.1002/ijc.20863. Int J Cancer. 2005. PMID: 15849733 Free article.
Hexosaminidase--pseudodeficiency?
Kappler J, Gieselmann V, Propping P. Kappler J, et al. Among authors: propping p. Am J Hum Genet. 1990 Nov;47(5):880-2. Am J Hum Genet. 1990. PMID: 2145759 Free PMC article. No abstract available.
Pharmacogenetics of schizophrenia.
Cichon S, Nöthen MM, Rietschel M, Propping P. Cichon S, et al. Among authors: propping p. Am J Med Genet. 2000 Spring;97(1):98-106. doi: 10.1002/(sici)1096-8628(200021)97:1<98::aid-ajmg12>3.0.co;2-w. Am J Med Genet. 2000. PMID: 10813809 Review.
Hereditary nonpolyposis colorectal cancer (HNPCC)/Lynch syndrome.
Steinke V, Engel C, Büttner R, Schackert HK, Schmiegel WH, Propping P. Steinke V, et al. Among authors: propping p. Dtsch Arztebl Int. 2013 Jan;110(3):32-8. doi: 10.3238/arztebl.2013.0032. Epub 2013 Jan 18. Dtsch Arztebl Int. 2013. PMID: 23413378 Free PMC article. Review.
Genetics of schizophrenia: A consensus paper of the WFSBP Task Force on Genetics.
Giegling I, Hosak L, Mössner R, Serretti A, Bellivier F, Claes S, Collier DA, Corrales A, DeLisi LE, Gallo C, Gill M, Kennedy JL, Leboyer M, Maier W, Marquez M, Massat I, Mors O, Muglia P, Nöthen MM, Ospina-Duque J, Owen MJ, Propping P, Shi Y, St Clair D, Thibaut F, Cichon S, Mendlewicz J, O'Donovan MC, Rujescu D. Giegling I, et al. Among authors: propping p. World J Biol Psychiatry. 2017 Oct;18(7):492-505. doi: 10.1080/15622975.2016.1268715. Epub 2017 Jan 23. World J Biol Psychiatry. 2017. PMID: 28112043 Review.
Pharmacogenetics.
Propping P. Propping P. Rev Physiol Biochem Pharmacol. 1978;83:123-73. doi: 10.1007/3-540-08907-1_4. Rev Physiol Biochem Pharmacol. 1978. PMID: 81508 Review. No abstract available.
423 results