Verkerk AJ - Search Results

1

A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14.

Solouki AM, Verhoeven VJ, van Duijn CM, Verkerk AJ, Ikram MK, Hysi PG, Despriet DD, van Koolwijk LM, Ho L, Ramdas WD, Czudowska M, Kuijpers RW, Amin N, Struchalin M, Aulchenko YS, van Rij G, Riemslag FC, Young TL, Mackey DA, Spector TD, Gorgels TG, Willemse-Assink JJ, Isaacs A, Kramer R, Swagemakers SM, Bergen AA, van Oosterhout AA, Oostra BA, Rivadeneira F, Uitterlinden AG, Hofman A, de Jong PT, Hammond CJ, Vingerling JR, Klaver CC. Solouki AM, et al. Among authors: verkerk aj. Nat Genet. 2010 Oct;42(10):897-901. doi: 10.1038/ng.663. Epub 2010 Sep 12. Nat Genet. 2010. PMID: 20835239 Free PMC article.

2

Limited size of the fragile X site shown by fluorescence in situ hybridization.

Verkerk AJ, Eussen BH, Van Hemel JO, Oostra BA. Verkerk AJ, et al. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):187-91. doi: 10.1002/ajmg.1320430131. Am J Med Genet. 1992. PMID: 1605191

3

Intragenic probe used for diagnostics in fragile X families.

Verkerk AJ, deVries BB, Niermeijer MF, Fu YH, Nelson DL, Warren ST, Majoor-Krakauer DF, Halley DJ, Oostra BA. Verkerk AJ, et al. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):192-6. doi: 10.1002/ajmg.1320430132. Am J Med Genet. 1992. PMID: 1605192

4

The fragile X syndrome: isolation of the FMR-1 gene and characterization of the fragile X mutation.

Oostra BA, Verkerk AJ. Oostra BA, et al. Among authors: verkerk aj. Chromosoma. 1992 Apr;101(7):381-7. doi: 10.1007/BF00582832. Chromosoma. 1992. PMID: 1618021 Review.

5

Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE.

Parrish JE, Oostra BA, Verkerk AJ, Richards CS, Reynolds J, Spikes AS, Shaffer LG, Nelson DL. Parrish JE, et al. Among authors: verkerk aj. Nat Genet. 1994 Nov;8(3):229-35. doi: 10.1038/ng1194-229. Nat Genet. 1994. PMID: 7874164

6

Mental status and fragile X expression in relation to FMR-1 gene mutation.

de Vries BB, Wiegers AM, de Graaff E, Verkerk AJ, Van Hemel JO, Halley DJ, Fryns JP, Curfs LM, Niermeijer MF, Oostra BA. de Vries BB, et al. Among authors: verkerk aj. Eur J Hum Genet. 1993;1(1):72-9. doi: 10.1159/000472389. Eur J Hum Genet. 1993. PMID: 8069653

7

Characterization and localization of the FMR-1 gene product associated with fragile X syndrome.

Verheij C, Bakker CE, de Graaff E, Keulemans J, Willemsen R, Verkerk AJ, Galjaard H, Reuser AJ, Hoogeveen AT, Oostra BA. Verheij C, et al. Among authors: verkerk aj. Nature. 1993 Jun 24;363(6431):722-4. doi: 10.1038/363722a0. Nature. 1993. PMID: 8515814

8

CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder.

Verkerk AJ, Mathews CA, Joosse M, Eussen BH, Heutink P, Oostra BA; Tourette Syndrome Association International Consortium for Genetics. Verkerk AJ, et al. Genomics. 2003 Jul;82(1):1-9. doi: 10.1016/s0888-7543(03)00097-1. Genomics. 2003. PMID: 12809671

9

Genetic and clinical analysis of a large Dutch Gilles de la Tourette family.

Verkerk AJ, Cath DC, van der Linde HC, Both J, Heutink P, Breedveld G, Aulchenko YS, Oostra BA. Verkerk AJ, et al. Mol Psychiatry. 2006 Oct;11(10):954-64. doi: 10.1038/sj.mp.4001877. Epub 2006 Aug 8. Mol Psychiatry. 2006. PMID: 16894393

10

Functional annotation of the human retinal pigment epithelium transcriptome.

Booij JC, van Soest S, Swagemakers SM, Essing AH, Verkerk AJ, van der Spek PJ, Gorgels TG, Bergen AA. Booij JC, et al. Among authors: verkerk aj. BMC Genomics. 2009 Apr 20;10:164. doi: 10.1186/1471-2164-10-164. BMC Genomics. 2009. PMID: 19379482 Free PMC article.

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