White SJ - Search Results

1

Contribution of Fcgamma receptor IIIA gene 158V/F polymorphism and copy number variation to the risk of ACPA-positive rheumatoid arthritis.

Thabet MM, Huizinga TW, Marques RB, Stoeken-Rijsbergen G, Bakker AM, Kurreeman FA, White SJ, Toes RE, van der Helm-van Mil AH. Thabet MM, et al. Among authors: white sj. Ann Rheum Dis. 2009 Nov;68(11):1775-80. doi: 10.1136/ard.2008.099309. Epub 2008 Nov 19. Ann Rheum Dis. 2009. PMID: 19019892 Review.

2

Counting copy number and calories.

White S. White S. Nat Genet. 2015 Aug;47(8):852-3. doi: 10.1038/ng.3365. Nat Genet. 2015. PMID: 26220133

3

Multiallelic copy number variation in the complement component 4A (C4A) gene is associated with late-stage age-related macular degeneration (AMD).

Grassmann F, Cantsilieris S, Schulz-Kuhnt AS, White SJ, Richardson AJ, Hewitt AW, Vote BJ, Schmied D, Guymer RH, Weber BH, Baird PN. Grassmann F, et al. Among authors: white sj. J Neuroinflammation. 2016 Apr 18;13(1):81. doi: 10.1186/s12974-016-0548-0. J Neuroinflammation. 2016. PMID: 27090374 Free PMC article.

4

Glucocorticoid-induced leucine zipper (GILZ) inhibits B cell activation in systemic lupus erythematosus.

Jones SA, Toh AE, Odobasic D, Oudin MA, Cheng Q, Lee JP, White SJ, Russ BE, Infantino S, Light A, Tarlinton DM, Harris J, Morand EF. Jones SA, et al. Among authors: white sj. Ann Rheum Dis. 2016 Apr;75(4):739-47. doi: 10.1136/annrheumdis-2015-207744. Epub 2015 Nov 26. Ann Rheum Dis. 2016. PMID: 26612340

5

Genotyping Multiallelic Copy Number Variation with Multiplex Ligation-Dependent Probe Amplification (MLPA).

de Boer S, White SJ. de Boer S, et al. Among authors: white sj. Methods Mol Biol. 2017;1492:147-153. doi: 10.1007/978-1-4939-6442-0_9. Methods Mol Biol. 2017. PMID: 27822861

6

Copy number variation in the genome; the human DMD gene as an example.

White SJ, den Dunnen JT. White SJ, et al. Cytogenet Genome Res. 2006;115(3-4):240-6. doi: 10.1159/000095920. Cytogenet Genome Res. 2006. PMID: 17124406 Review.

7

Variation of CNV distribution in five different ethnic populations.

White SJ, Vissers LE, Geurts van Kessel A, de Menezes RX, Kalay E, Lehesjoki AE, Giordano PC, van de Vosse E, Breuning MH, Brunner HG, den Dunnen JT, Veltman JA. White SJ, et al. Cytogenet Genome Res. 2007;118(1):19-30. doi: 10.1159/000106437. Cytogenet Genome Res. 2007. PMID: 17901696

8

Copy number variation in regions flanked (or unflanked) by duplicons among patients with developmental delay and/or congenital malformations; detection of reciprocal and partial Williams-Beuren duplications.

Kriek M, White SJ, Szuhai K, Knijnenburg J, van Ommen GJ, den Dunnen JT, Breuning MH. Kriek M, et al. Among authors: white sj. Eur J Hum Genet. 2006 Feb;14(2):180-9. doi: 10.1038/sj.ejhg.5201540. Eur J Hum Genet. 2006. PMID: 16391556

9

Methods to detect CNVs in the human genome.

Aten E, White SJ, Kalf ME, Vossen RH, Thygesen HH, Ruivenkamp CA, Kriek M, Breuning MH, den Dunnen JT. Aten E, et al. Among authors: white sj. Cytogenet Genome Res. 2008;123(1-4):313-21. doi: 10.1159/000184723. Epub 2009 Mar 11. Cytogenet Genome Res. 2008. PMID: 19287170

10

Copy number variation and mosaicism.

Notini AJ, Craig JM, White SJ. Notini AJ, et al. Among authors: white sj. Cytogenet Genome Res. 2008;123(1-4):270-7. doi: 10.1159/000184717. Epub 2009 Mar 11. Cytogenet Genome Res. 2008. PMID: 19287164 Review.

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