Robinson WP - Search Results

1

Extensive epigenetic reprogramming in human somatic tissues between fetus and adult.

Yuen RK, Neumann SM, Fok AK, Peñaherrera MS, McFadden DE, Robinson WP, Kobor MS. Yuen RK, et al. Among authors: robinson wp. Epigenetics Chromatin. 2011 May 5;4:7. doi: 10.1186/1756-8935-4-7. Epigenetics Chromatin. 2011. PMID: 21545704 Free PMC article.

2

Comparison of phenotype in uniparental disomy and deletion Prader-Willi syndrome: sex specific differences.

Mitchell J, Schinzel A, Langlois S, Gillessen-Kaesbach G, Schuffenhauer S, Michaelis R, Abeliovich D, Lerer I, Christian S, Guitart M, McFadden DE, Robinson WP. Mitchell J, et al. Among authors: robinson wp. Am J Med Genet. 1996 Oct 16;65(2):133-6. doi: 10.1002/(SICI)1096-8628(19961016)65:2<133::AID-AJMG10>3.0.CO;2-R. Am J Med Genet. 1996. PMID: 8911605

3

Skewed X-chromosome inactivation is common in fetuses or newborns associated with confined placental mosaicism.

Lau AW, Brown CJ, Peñaherrera M, Langlois S, Kalousek DK, Robinson WP. Lau AW, et al. Among authors: robinson wp. Am J Hum Genet. 1997 Dec;61(6):1353-61. doi: 10.1086/301651. Am J Hum Genet. 1997. PMID: 9399909 Free PMC article.

4

The mechanisms involved in formation of deletions and duplications of 15q11-q13.

Robinson WP, Dutly F, Nicholls RD, Bernasconi F, Peñaherrera M, Michaelis RC, Abeliovich D, Schinzel AA. Robinson WP, et al. J Med Genet. 1998 Feb;35(2):130-6. doi: 10.1136/jmg.35.2.130. J Med Genet. 1998. PMID: 9580159 Free PMC article.

5

Frequency of meiotic trisomy depends on involved chromosome and mode of ascertainment.

Robinson WP, Bernasconi F, Lau A, McFadden DE. Robinson WP, et al. Am J Med Genet. 1999 May 7;84(1):34-42. Am J Med Genet. 1999. PMID: 10213044

6

Clinical and molecular findings in two patients with russell-silver syndrome and UPD7: comparison with non-UPD7 cases.

Bernard LE, Peñaherrera MS, Van Allen MI, Wang MS, Yong SL, Gareis F, Langlois S, Robinson WP. Bernard LE, et al. Among authors: robinson wp. Am J Med Genet. 1999 Nov 26;87(3):230-6. Am J Med Genet. 1999. PMID: 10564876

7

Somatic segregation errors predominantly contribute to the gain or loss of a paternal chromosome leading to uniparental disomy for chromosome 15.

Robinson WP, Christian SL, Kuchinka BD, Peñaherrera MS, Das S, Schuffenhauer S, Malcolm S, Schinzel AA, Hassold TJ, Ledbetter DH. Robinson WP, et al. Clin Genet. 2000 May;57(5):349-58. doi: 10.1034/j.1399-0004.2000.570505.x. Clin Genet. 2000. PMID: 10852369

8

An association between skewed X-chromosome inactivation and abnormal outcome in mosaic trisomy 16 confined predominantly to the placenta.

Peñaherrera MS, Barrett IJ, Brown CJ, Langlois S, Yong SL, Lewis S, Bruyère H, Howard-Peebles PN, Kalousek DK, Robinson WP. Peñaherrera MS, et al. Among authors: robinson wp. Clin Genet. 2000 Dec;58(6):436-46. doi: 10.1034/j.1399-0004.2000.580603.x. Clin Genet. 2000. PMID: 11149612

9

Recurrent trisomy 15 in a female carrier of der(15)t(Y;15)(q12;p13).

Rajcan-Separovic E, Robinson WP, Stephenson M, Pantzar T, Arbour L, McFadden D, Guscott J. Rajcan-Separovic E, et al. Among authors: robinson wp. Am J Med Genet. 2001 Apr 1;99(4):320-4. doi: 10.1002/1096-8628(2001)9999:9999<::aid-ajmg1173>3.0.co;2-1. Am J Med Genet. 2001. PMID: 11252000

10

The origin of abnormalities in recurrent aneuploidy/polyploidy.

Robinson WP, McFadden DE, Stephenson MD. Robinson WP, et al. Am J Hum Genet. 2001 Dec;69(6):1245-54. doi: 10.1086/324468. Epub 2001 Oct 23. Am J Hum Genet. 2001. PMID: 11675616 Free PMC article.

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