Züchner S - Search Results

1

Vitamin D receptor and Alzheimer's disease: a genetic and functional study.

Wang L, Hara K, Van Baaren JM, Price JC, Beecham GW, Gallins PJ, Whitehead PL, Wang G, Lu C, Slifer MA, Züchner S, Martin ER, Mash D, Haines JL, Pericak-Vance MA, Gilbert JR. Wang L, et al. Among authors: zuchner s. Neurobiol Aging. 2012 Aug;33(8):1844.e1-9. doi: 10.1016/j.neurobiolaging.2011.12.038. Epub 2012 Feb 4. Neurobiol Aging. 2012. PMID: 22306846

2

Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease.

Oliveira SA, Li YJ, Noureddine MA, Zuchner S, Qin X, Pericak-Vance MA, Vance JM. Oliveira SA, et al. Among authors: zuchner s. Am J Hum Genet. 2005 Aug;77(2):252-64. doi: 10.1086/432588. Epub 2005 Jun 28. Am J Hum Genet. 2005. PMID: 15986317 Free PMC article.

3

SNPselector: a web tool for selecting SNPs for genetic association studies.

Xu H, Gregory SG, Hauser ER, Stenger JE, Pericak-Vance MA, Vance JM, Züchner S, Hauser MA. Xu H, et al. Among authors: zuchner s. Bioinformatics. 2005 Nov 15;21(22):4181-6. doi: 10.1093/bioinformatics/bti682. Epub 2005 Sep 22. Bioinformatics. 2005. PMID: 16179360 Free PMC article.

4

Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31.

Züchner S, Wang G, Tran-Viet KN, Nance MA, Gaskell PC, Vance JM, Ashley-Koch AE, Pericak-Vance MA. Züchner S, et al. Am J Hum Genet. 2006 Aug;79(2):365-9. doi: 10.1086/505361. Epub 2006 May 26. Am J Hum Genet. 2006. PMID: 16826527 Free PMC article.

5

Effect of heterogeneity on the chromosome 10 risk in late-onset Alzheimer disease.

Liang X, Martin ER, Schnetz-Boutaud N, Bartlett J, Anderson B, Züchner S, Gwirtsman H, Schmechel D, Carney R, Gilbert JR, Pericak-Vance MA, Haines JL. Liang X, et al. Among authors: zuchner s. Hum Mutat. 2007 Nov;28(11):1065-73. doi: 10.1002/humu.20567. Hum Mutat. 2007. PMID: 17573676

6

Variation in the miRNA-433 binding site of FGF20 confers risk for Parkinson disease by overexpression of alpha-synuclein.

Wang G, van der Walt JM, Mayhew G, Li YJ, Züchner S, Scott WK, Martin ER, Vance JM. Wang G, et al. Among authors: zuchner s. Am J Hum Genet. 2008 Feb;82(2):283-9. doi: 10.1016/j.ajhg.2007.09.021. Epub 2008 Jan 31. Am J Hum Genet. 2008. PMID: 18252210 Free PMC article.

7

Linkage and association study of late-onset Alzheimer disease families linked to 9p21.3.

Züchner S, Gilbert JR, Martin ER, Leon-Guerrero CR, Xu PT, Browning C, Bronson PG, Whitehead P, Schmechel DE, Haines JL, Pericak-Vance MA. Züchner S, et al. Ann Hum Genet. 2008 Nov;72(Pt 6):725-31. doi: 10.1111/j.1469-1809.2008.00474.x. Epub 2008 Aug 28. Ann Hum Genet. 2008. PMID: 18761660 Free PMC article.

8

Multiple rare SAPAP3 missense variants in trichotillomania and OCD.

Züchner S, Wendland JR, Ashley-Koch AE, Collins AL, Tran-Viet KN, Quinn K, Timpano KC, Cuccaro ML, Pericak-Vance MA, Steffens DC, Krishnan KR, Feng G, Murphy DL. Züchner S, et al. Mol Psychiatry. 2009 Jan;14(1):6-9. doi: 10.1038/mp.2008.83. Mol Psychiatry. 2009. PMID: 19096451 Free PMC article. Review. No abstract available.

9

Genomic convergence to identify candidate genes for Alzheimer disease on chromosome 10.

Liang X, Slifer M, Martin ER, Schnetz-Boutaud N, Bartlett J, Anderson B, Züchner S, Gwirtsman H, Gilbert JR, Pericak-Vance MA, Haines JL. Liang X, et al. Among authors: zuchner s. Hum Mutat. 2009 Mar;30(3):463-71. doi: 10.1002/humu.20953. Hum Mutat. 2009. PMID: 19241460 Free PMC article.

10

Copy number variations are a rare cause of non-CMT1A Charcot-Marie-Tooth disease.

Huang J, Wu X, Montenegro G, Price J, Wang G, Vance JM, Shy ME, Züchner S. Huang J, et al. Among authors: zuchner s. J Neurol. 2010 May;257(5):735-41. doi: 10.1007/s00415-009-5401-2. Epub 2009 Dec 1. J Neurol. 2010. PMID: 19949810 Free PMC article.

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