Franke B - Search Results

1

Confirmation of dyslexia susceptibility loci on chromosomes 1p and 2p, but not 6p in a Dutch sib-pair collection.

de Kovel CG, Franke B, Hol FA, Lebrec JJ, Maassen B, Brunner H, Padberg GW, Platko J, Pauls D. de Kovel CG, et al. Among authors: franke b. Am J Med Genet B Neuropsychiatr Genet. 2008 Apr 5;147(3):294-300. doi: 10.1002/ajmg.b.30598. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 17886254

2

A deletion encompassing Zic3 in bent tail, a mouse model for X-linked neural tube defects.

Klootwijk R, Franke B, van der Zee CE, de Boer RT, Wilms W, Hol FA, Mariman EC. Klootwijk R, et al. Among authors: franke b. Hum Mol Genet. 2000 Jul 1;9(11):1615-22. doi: 10.1093/hmg/9.11.1615. Hum Mol Genet. 2000. PMID: 10861288

3

Genetic variation analysis of MLP, TFAP2A, and CSK in patients with neural tube defects.

Klootwijk R, Hol FA, Wu M, Willemen JJ, Groenen P, Hamel B, Straatman H, Steegers-Theunissen RP, Mariman EC, Franke B. Klootwijk R, et al. Among authors: franke b. J Med Genet. 2003 Apr;40(4):e43. doi: 10.1136/jmg.40.4.e43. J Med Genet. 2003. PMID: 12676916 Free PMC article. No abstract available.

4

No evidence for involvement of IL-4R and CD11B from the IBD1 region and STAT6 in the IBD2 region in Crohn's disease.

de Jong DJ, Franke B, Naber AH, Willemen JJ, Heister AJ, Brunner HG, de Kovel CG, Hol FA. de Jong DJ, et al. Among authors: franke b. Eur J Hum Genet. 2003 Nov;11(11):884-7. doi: 10.1038/sj.ejhg.5201058. Eur J Hum Genet. 2003. PMID: 14571275

5

Genetic variants in ZIC1, ZIC2, and ZIC3 are not major risk factors for neural tube defects in humans.

Klootwijk R, Groenen P, Schijvenaars M, Hol F, Hamel B, Straatman H, Steegers-Theunissen R, Mariman E, Franke B. Klootwijk R, et al. Among authors: franke b. Am J Med Genet A. 2004 Jan 1;124A(1):40-7. doi: 10.1002/ajmg.a.20402. Am J Med Genet A. 2004. PMID: 14679585

6

Phenotype of the neural tube defect mouse model bent tail is not sensitive to maternal folinic acid, myo-inositol, or zinc supplementation.

Franke B, Klootwijk R, Lemmers B, de Kovel CG, Steegers-Theunissen RP, Mariman EC. Franke B, et al. Birth Defects Res A Clin Mol Teratol. 2003 Dec;67(12):979-84. doi: 10.1002/bdra.10132. Birth Defects Res A Clin Mol Teratol. 2003. PMID: 14745918

7

Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family.

de Kovel CG, Hol FA, Heister JG, Willemen JJ, Sandkuijl LA, Franke B, Padberg GW. de Kovel CG, et al. Among authors: franke b. J Med Genet. 2004 Sep;41(9):652-7. doi: 10.1136/jmg.2003.012294. J Med Genet. 2004. PMID: 15342694 Free PMC article.

8

Novel association in chromosome 4q27 region with rheumatoid arthritis and confirmation of type 1 diabetes point to a general risk locus for autoimmune diseases.

Zhernakova A, Alizadeh BZ, Bevova M, van Leeuwen MA, Coenen MJ, Franke B, Franke L, Posthumus MD, van Heel DA, van der Steege G, Radstake TR, Barrera P, Roep BO, Koeleman BP, Wijmenga C. Zhernakova A, et al. Among authors: franke b, franke l. Am J Hum Genet. 2007 Dec;81(6):1284-8. doi: 10.1086/522037. Epub 2007 Oct 24. Am J Hum Genet. 2007. PMID: 17999365 Free PMC article.

9

DSM-IV combined type ADHD shows familial association with sibling trait scores: a sampling strategy for QTL linkage.

Chen W, Zhou K, Sham P, Franke B, Kuntsi J, Campbell D, Fleischman K, Knight J, Andreou P, Arnold R, Altink M, Boer F, Boholst MJ, Buschgens C, Butler L, Christiansen H, Fliers E, Howe-Forbes R, Gabriëls I, Heise A, Korn-Lubetzki I, Marco R, Medad S, Minderaa R, Müller UC, Mulligan A, Psychogiou L, Rommelse N, Sethna V, Uebel H, McGuffin P, Plomin R, Banaschewski T, Buitelaar J, Ebstein R, Eisenberg J, Gill M, Manor I, Miranda A, Mulas F, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Sonuga-Barke E, Steinhausen HC, Taylor E, Thompson M, Faraone SV, Asherson P. Chen W, et al. Among authors: franke b. Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1450-60. doi: 10.1002/ajmg.b.30672. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18189238

10

Identification of novel dyslexia candidate genes through the analysis of a chromosomal deletion.

Poelmans G, Engelen JJ, Van Lent-Albrechts J, Smeets HJ, Schoenmakers E, Franke B, Buitelaar JK, Wuisman-Frerker M, Erens W, Steyaert J, Schrander-Stumpel C. Poelmans G, et al. Among authors: franke b. Am J Med Genet B Neuropsychiatr Genet. 2009 Jan 5;150B(1):140-7. doi: 10.1002/ajmg.b.30787. Am J Med Genet B Neuropsychiatr Genet. 2009. PMID: 18521840

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