Reik W - Search Results

1

Beckwith-Wiedemann syndrome and assisted reproduction technology (ART).

Maher ER, Brueton LA, Bowdin SC, Luharia A, Cooper W, Cole TR, Macdonald F, Sampson JR, Barratt CL, Reik W, Hawkins MM. Maher ER, et al. Among authors: reik w. J Med Genet. 2003 Jan;40(1):62-4. doi: 10.1136/jmg.40.1.62. J Med Genet. 2003. PMID: 12525545 Free PMC article. No abstract available.

2

Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome.

Cooper WN, Luharia A, Evans GA, Raza H, Haire AC, Grundy R, Bowdin SC, Riccio A, Sebastio G, Bliek J, Schofield PN, Reik W, Macdonald F, Maher ER. Cooper WN, et al. Among authors: reik w. Eur J Hum Genet. 2005 Sep;13(9):1025-32. doi: 10.1038/sj.ejhg.5201463. Eur J Hum Genet. 2005. PMID: 15999116

3

Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologies.

Lim D, Bowdin SC, Tee L, Kirby GA, Blair E, Fryer A, Lam W, Oley C, Cole T, Brueton LA, Reik W, Macdonald F, Maher ER. Lim D, et al. Among authors: reik w. Hum Reprod. 2009 Mar;24(3):741-7. doi: 10.1093/humrep/den406. Epub 2008 Dec 10. Hum Reprod. 2009. PMID: 19073614

4

Epigenetic modification and uniparental inheritance of H19 in Beckwith-Wiedemann syndrome.

Catchpoole D, Lam WW, Valler D, Temple IK, Joyce JA, Reik W, Schofield PN, Maher ER. Catchpoole D, et al. Among authors: reik w. J Med Genet. 1997 May;34(5):353-9. doi: 10.1136/jmg.34.5.353. J Med Genet. 1997. PMID: 9152830 Free PMC article.

5

Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome.

Reik W, Maher ER. Reik W, et al. Trends Genet. 1997 Aug;13(8):330-4. doi: 10.1016/s0168-9525(97)01200-6. Trends Genet. 1997. PMID: 9260520 Review.

6

Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation.

Lam WW, Hatada I, Ohishi S, Mukai T, Joyce JA, Cole TR, Donnai D, Reik W, Schofield PN, Maher ER. Lam WW, et al. Among authors: reik w. J Med Genet. 1999 Jul;36(7):518-23. J Med Genet. 1999. PMID: 10424811 Free PMC article.

7

Beckwith-Wiedemann syndrome: imprinting in clusters revisited.

Maher ER, Reik W. Maher ER, et al. Among authors: reik w. J Clin Invest. 2000 Feb;105(3):247-52. doi: 10.1172/JCI9340. J Clin Invest. 2000. PMID: 10675349 Free PMC article. Review. No abstract available.

8

Mutation analysis of H19 and NAP1L4 (hNAP2) candidate genes and IGF2 DMR2 in Beckwith-Wiedemann syndrome.

Catchpoole D, Smallwood AV, Joyce JA, Murrell A, Lam W, Tang T, Munroe D, Reik W, Schofield PN, Maher ER. Catchpoole D, et al. Among authors: reik w. J Med Genet. 2000 Mar;37(3):212-5. doi: 10.1136/jmg.37.3.212. J Med Genet. 2000. PMID: 10777363 Free PMC article. No abstract available.

9

Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.

Engel JR, Smallwood A, Harper A, Higgins MJ, Oshimura M, Reik W, Schofield PN, Maher ER. Engel JR, et al. Among authors: reik w. J Med Genet. 2000 Dec;37(12):921-6. doi: 10.1136/jmg.37.12.921. J Med Genet. 2000. PMID: 11106355 Free PMC article.

10

Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndrome.

Diaz-Meyer N, Day CD, Khatod K, Maher ER, Cooper W, Reik W, Junien C, Graham G, Algar E, Der Kaloustian VM, Higgins MJ. Diaz-Meyer N, et al. Among authors: reik w. J Med Genet. 2003 Nov;40(11):797-801. doi: 10.1136/jmg.40.11.797. J Med Genet. 2003. PMID: 14627666 Free PMC article.

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