Geraedts J - Search Results

1

mtDNA point mutations are present at various levels of heteroplasmy in human oocytes.

Jacobs L, Gerards M, Chinnery P, Dumoulin J, de Coo I, Geraedts J, Smeets H. Jacobs L, et al. Among authors: geraedts j. Mol Hum Reprod. 2007 Mar;13(3):149-54. doi: 10.1093/molehr/gal112. Epub 2007 Jan 26. Mol Hum Reprod. 2007. PMID: 17259224

2

Transmission and prenatal diagnosis of the T9176C mitochondrial DNA mutation.

Jacobs LJ, de Coo IF, Nijland JG, Galjaard RJ, Los FJ, Schoonderwoerd K, Niermeijer MF, Geraedts JP, Scholte HR, Smeets HJ. Jacobs LJ, et al. Among authors: geraedts jp. Mol Hum Reprod. 2005 Mar;11(3):223-8. doi: 10.1093/molehr/gah152. Epub 2005 Feb 11. Mol Hum Reprod. 2005. PMID: 15709156

3

The transmission of OXPHOS disease and methods to prevent this.

Jacobs LJ, de Wert G, Geraedts JP, de Coo IF, Smeets HJ. Jacobs LJ, et al. Among authors: geraedts jp. Hum Reprod Update. 2006 Mar-Apr;12(2):119-36. doi: 10.1093/humupd/dmi042. Epub 2005 Sep 30. Hum Reprod Update. 2006. PMID: 16199488 Review.

4

PGD and heteroplasmic mitochondrial DNA point mutations: a systematic review estimating the chance of healthy offspring.

Hellebrekers DM, Wolfe R, Hendrickx AT, de Coo IF, de Die CE, Geraedts JP, Chinnery PF, Smeets HJ. Hellebrekers DM, et al. Among authors: geraedts jp. Hum Reprod Update. 2012 Jul;18(4):341-9. doi: 10.1093/humupd/dms008. Epub 2012 Mar 28. Hum Reprod Update. 2012. PMID: 22456975 Review.

5

Multiplex PCR of polymorphic markers flanking the CFTR gene; a general approach for preimplantation genetic diagnosis of cystic fibrosis.

Dreesen JC, Jacobs LJ, Bras M, Herbergs J, Dumoulin JC, Geraedts JP, Evers JL, Smeets HJ. Dreesen JC, et al. Among authors: geraedts jp. Mol Hum Reprod. 2000 May;6(5):391-6. doi: 10.1093/molehr/6.5.391. Mol Hum Reprod. 2000. PMID: 10775641

6

Preimplantation genetic diagnosis of spinocerebellar ataxia 3 by (CAG)(n) repeat detection.

Drüsedau M, Dreesen JC, De Die-Smulders C, Hardy K, Bras M, Dumoulin JC, Evers JL, Smeets HJ, Geraedts JP, Herbergs J. Drüsedau M, et al. Among authors: geraedts jp. Mol Hum Reprod. 2004 Jan;10(1):71-5. doi: 10.1093/molehr/gah008. Mol Hum Reprod. 2004. PMID: 14665709

7

Pearson syndrome and the role of deletion dimers and duplications in the mtDNA.

Jacobs LJ, Jongbloed RJ, Wijburg FA, de Klerk JB, Geraedts JP, Nijland JG, Scholte HR, de Coo IF, Smeets HJ. Jacobs LJ, et al. Among authors: geraedts jp. J Inherit Metab Dis. 2004;27(1):47-55. doi: 10.1023/B:BOLI.0000016601.49372.18. J Inherit Metab Dis. 2004. PMID: 14970745

8

DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.

Jongbloed R, Marcelis C, Velter C, Doevendans P, Geraedts J, Smeets H. Jongbloed R, et al. Among authors: geraedts j. Hum Mutat. 2002 Nov;20(5):382-91. doi: 10.1002/humu.10131. Hum Mutat. 2002. PMID: 12402336

9

Differential gene expression in cumulus cells as a prognostic indicator of embryo viability: a microarray analysis.

van Montfoort AP, Geraedts JP, Dumoulin JC, Stassen AP, Evers JL, Ayoubi TA. van Montfoort AP, et al. Mol Hum Reprod. 2008 Mar;14(3):157-68. doi: 10.1093/molehr/gam088. Epub 2008 Jan 18. Mol Hum Reprod. 2008. PMID: 18204071

10

Preimplantation genetic diagnosis in mitochondrial DNA disorders: challenge and success.

Sallevelt SC, Dreesen JC, Drüsedau M, Spierts S, Coonen E, van Tienen FH, van Golde RJ, de Coo IF, Geraedts JP, de Die-Smulders CE, Smeets HJ. Sallevelt SC, et al. Among authors: geraedts jp. J Med Genet. 2013 Feb;50(2):125-32. doi: 10.1136/jmedgenet-2012-101172. J Med Genet. 2013. PMID: 23339111

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