Berger W - Search Results

1

Glutathione S-transferase genotypes modify lung function decline in the general population: SAPALDIA cohort study.

Imboden M, Downs SH, Senn O, Matyas G, Brändli O, Russi EW, Schindler C, Ackermann-Liebrich U, Berger W, Probst-Hensch NM; SAPALDIA Team. Imboden M, et al. Among authors: berger w. Respir Res. 2007 Jan 11;8(1):2. doi: 10.1186/1465-9921-8-2. Respir Res. 2007. PMID: 17217536 Free PMC article.

2

Circulating alpha1-antitrypsin in the general population: determinants and association with lung function.

Senn O, Russi EW, Schindler C, Imboden M, von Eckardstein A, Brändli O, Zemp E, Ackermann-Liebrich U, Berger W, Rochat T, Luisetti M, Probst-Hensch NM; SAPALDIA Team. Senn O, et al. Among authors: berger w. Respir Res. 2008 Apr 25;9(1):35. doi: 10.1186/1465-9921-9-35. Respir Res. 2008. PMID: 18439253 Free PMC article.

3

Glutathione S-transferase polymorphisms, passive smoking, obesity, and heart rate variability in nonsmokers.

Probst-Hensch NM, Imboden M, Felber Dietrich D, Barthélemy JC, Ackermann-Liebrich U, Berger W, Gaspoz JM, Schwartz J. Probst-Hensch NM, et al. Among authors: berger w. Environ Health Perspect. 2008 Nov;116(11):1494-9. doi: 10.1289/ehp.11402. Epub 2008 Jul 18. Environ Health Perspect. 2008. PMID: 19057702 Free PMC article.

4

Decreased PM10 exposure attenuates age-related lung function decline: genetic variants in p53, p21, and CCND1 modify this effect.

Imboden M, Schwartz J, Schindler C, Curjuric I, Berger W, Liu SL, Russi EW, Ackermann-Liebrich U, Rochat T, Probst-Hensch NM; SAPALDIA Team. Imboden M, et al. Among authors: berger w. Environ Health Perspect. 2009 Sep;117(9):1420-7. doi: 10.1289/ehp.0800430. Epub 2009 May 26. Environ Health Perspect. 2009. PMID: 19750108 Free PMC article.

5

SERPINA1 gene variants in individuals from the general population with reduced alpha1-antitrypsin concentrations.

Zorzetto M, Russi E, Senn O, Imboden M, Ferrarotti I, Tinelli C, Campo I, Ottaviani S, Scabini R, von Eckardstein A, Berger W, Brändli O, Rochat T, Luisetti M, Probst-Hensch N; SAPALDIA Team. Zorzetto M, et al. Among authors: berger w. Clin Chem. 2008 Aug;54(8):1331-8. doi: 10.1373/clinchem.2007.102798. Epub 2008 May 29. Clin Chem. 2008. PMID: 18515255

6

Association of STR polymorphisms in CMA1 and IL-4 with asthma and atopy: the SAPALDIA cohort.

Hersberger M, Thun GA, Imboden M, Brandstätter A, Waechter V, Summerer M, Schmid-Grendelmeier P, Bircher A, Rohrer L, Berger W, Russi EW, Rochat T, Kronenberg F, Probst-Hensch N. Hersberger M, et al. Among authors: berger w. Hum Immunol. 2010 Nov;71(11):1154-60. doi: 10.1016/j.humimm.2010.08.008. Epub 2010 Aug 22. Hum Immunol. 2010. PMID: 20736038

7

The association of a variant in the cell cycle control gene CCND1 and obesity on the development of asthma in the Swiss SAPALDIA study.

Thun GA, Imboden M, Berger W, Rochat T, Probst-Hensch NM. Thun GA, et al. Among authors: berger w. J Asthma. 2013 Mar;50(2):147-54. doi: 10.3109/02770903.2012.757776. Epub 2013 Jan 13. J Asthma. 2013. PMID: 23311506 Free article.

8

Large genomic fibrillin-1 (FBN1) gene deletions provide evidence for true haploinsufficiency in Marfan syndrome.

Mátyás G, Alonso S, Patrignani A, Marti M, Arnold E, Magyar I, Henggeler C, Carrel T, Steinmann B, Berger W. Mátyás G, et al. Among authors: berger w. Hum Genet. 2007 Aug;122(1):23-32. doi: 10.1007/s00439-007-0371-x. Epub 2007 May 10. Hum Genet. 2007. PMID: 17492313 Free article.

9

Novel mutations in CACNA1F and NYX in Dutch families with X-linked congenital stationary night blindness.

Zeitz C, Minotti R, Feil S, Mátyás G, Cremers FP, Hoyng CB, Berger W. Zeitz C, et al. Among authors: berger w. Mol Vis. 2005 Mar 2;11:179-83. Mol Vis. 2005. PMID: 15761389 Free article.

10

Identification and in silico analyses of novel TGFBR1 and TGFBR2 mutations in Marfan syndrome-related disorders.

Mátyás G, Arnold E, Carrel T, Baumgartner D, Boileau C, Berger W, Steinmann B. Mátyás G, et al. Among authors: berger w. Hum Mutat. 2006 Aug;27(8):760-9. doi: 10.1002/humu.20353. Hum Mutat. 2006. PMID: 16791849

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