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Results by year

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

Year Number of Results
1993 1
1995 2
1997 2
1998 5
1999 1
2000 3
2001 2
2002 2
2003 4
2004 7
2005 3
2006 6
2007 2
2008 1
2009 1
2010 1
2012 1
2014 2
2024 0

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43 results

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Page 1
Meta- and pooled analyses of the methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism and colorectal cancer: a HuGE-GSEC review.
Taioli E, Garza MA, Ahn YO, Bishop DT, Bost J, Budai B, Chen K, Gemignani F, Keku T, Lima CS, Le Marchand L, Matsuo K, Moreno V, Plaschke J, Pufulete M, Thomas SB, Toffoli G, Wolf CR, Moore CG, Little J. Taioli E, et al. Among authors: plaschke j. Am J Epidemiol. 2009 Nov 15;170(10):1207-21. doi: 10.1093/aje/kwp275. Epub 2009 Oct 21. Am J Epidemiol. 2009. PMID: 19846566 Free PMC article. Review.
A microsatellite map of wheat.
Röder MS, Korzun V, Wendehake K, Plaschke J, Tixier MH, Leroy P, Ganal MW. Röder MS, et al. Among authors: plaschke j. Genetics. 1998 Aug;149(4):2007-23. doi: 10.1093/genetics/149.4.2007. Genetics. 1998. PMID: 9691054 Free PMC article.
[Molecular pathology in hereditary colorectal cancer. Recommendations of the Collaborative German Study Group on hereditary colorectal cancer funded by the German Cancer Aid (Deutsche Krebshilfe)].
Rüschoff J, Roggendorf B, Brasch F, Mathiak M, Aust DE, Plaschke J, Mueller W, Poremba C, Kloor M, Keller G, Muders M, Blasenbreu-Vogt S, Rümmele P, Müller A, Büttner R; Collaborative German Study Group on hereditary colorectal cancer funded by the German Cancer Aid (Deutsche Krebshilfe)]. Rüschoff J, et al. Among authors: plaschke j. Pathologe. 2004 May;25(3):178-92. doi: 10.1007/s00292-003-0641-x. Pathologe. 2004. PMID: 15138699 Review. German.
A novel missense mutation in CACNA1A evaluated by in silico protein modeling is associated with non-episodic spinocerebellar ataxia with slow progression.
Bürk K, Kaiser FJ, Tennstedt S, Schöls L, Kreuz FR, Wieland T, Strom TM, Büttner T, Hollstein R, Braunholz D, Plaschke J, Gillessen-Kaesbach G, Zühlke C. Bürk K, et al. Among authors: plaschke j. Eur J Med Genet. 2014 Apr;57(5):207-11. doi: 10.1016/j.ejmg.2014.01.005. Epub 2014 Jan 29. Eur J Med Genet. 2014. PMID: 24486772
Ten novel MSH2 and MLH1 germline mutations in families with HNPCC.
Krüger S, Bier A, Plaschke J, Höhl R, Aust DE, Kreuz FR, Pistorius SR, Saeger HD, Rothhammer V, Al-Taie O, Schackert HK. Krüger S, et al. Among authors: plaschke j. Hum Mutat. 2004 Oct;24(4):351-2. doi: 10.1002/humu.9278. Hum Mutat. 2004. PMID: 15365996
43 results