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Results: 1 to 20 of 242

1.

Copy number variations at the Prader-Willi syndrome region on chromosome 15 and associations with obesity in whites.

Chen Y, Liu YJ, Pei YF, Yang TL, Deng FY, Liu XG, Li DY, Deng HW.

Obesity (Silver Spring). 2011 Jun;19(6):1229-34. doi: 10.1038/oby.2010.323. Epub 2011 Jan 13.

PMID:
21233802
[PubMed - indexed for MEDLINE]
2.

Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region.

Jiang YH, Wauki K, Liu Q, Bressler J, Pan Y, Kashork CD, Shaffer LG, Beaudet AL.

BMC Genomics. 2008 Jan 28;9:50. doi: 10.1186/1471-2164-9-50.

PMID:
18226259
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndrome.

Duker AL, Ballif BC, Bawle EV, Person RE, Mahadevan S, Alliman S, Thompson R, Traylor R, Bejjani BA, Shaffer LG, Rosenfeld JA, Lamb AN, Sahoo T.

Eur J Hum Genet. 2010 Nov;18(11):1196-201. doi: 10.1038/ejhg.2010.102. Epub 2010 Jun 30.

PMID:
20588305
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Whole genome microarray analysis of gene expression in Prader-Willi syndrome.

Bittel DC, Kibiryeva N, Sell SM, Strong TV, Butler MG.

Am J Med Genet A. 2007 Mar 1;143(5):430-42.

PMID:
17236194
[PubMed - indexed for MEDLINE]
5.

Insulin resistance and obesity-related factors in Prader-Willi syndrome: comparison with obese subjects.

Talebizadeh Z, Butler MG.

Clin Genet. 2005 Mar;67(3):230-9.

PMID:
15691361
[PubMed - indexed for MEDLINE]
6.

Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13).

Christian SL, Fantes JA, Mewborn SK, Huang B, Ledbetter DH.

Hum Mol Genet. 1999 Jun;8(6):1025-37.

PMID:
10332034
[PubMed - indexed for MEDLINE]
Free Article
7.

The C15orf2 gene in the Prader-Willi syndrome region is subject to genomic imprinting and positive selection.

Wawrzik M, Unmehopa UA, Swaab DF, van de Nes J, Buiting K, Horsthemke B.

Neurogenetics. 2010 May;11(2):153-61. doi: 10.1007/s10048-009-0231-z. Epub 2009 Dec 19.

PMID:
20020165
[PubMed - indexed for MEDLINE]
8.

Deletions and duplications of the 15q11-q13 region in spermatozoa from Prader-Willi syndrome fathers.

Molina O, Blanco J, Vidal F.

Mol Hum Reprod. 2010 May;16(5):320-8. doi: 10.1093/molehr/gaq005. Epub 2010 Jan 18.

PMID:
20083560
[PubMed - indexed for MEDLINE]
Free Article
9.

Microarray analysis of gene/transcript expression in Prader-Willi syndrome: deletion versus UPD.

Bittel DC, Kibiryeva N, Talebizadeh Z, Butler MG.

J Med Genet. 2003 Aug;40(8):568-74.

PMID:
12920063
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

A nonimprinted Prader-Willi Syndrome (PWS)-region gene regulates a different chromosomal domain in trans but the imprinted pws loci do not alter genome-wide mRNA levels.

Stefan M, Portis T, Longnecker R, Nicholls RD.

Genomics. 2005 May;85(5):630-40.

PMID:
15820315
[PubMed - indexed for MEDLINE]
11.

Identification of a testis-specific gene (C15orf2) in the Prader-Willi syndrome region on chromosome 15.

Färber C, Gross S, Neesen J, Buiting K, Horsthemke B.

Genomics. 2000 Apr 15;65(2):174-83.

PMID:
10783265
[PubMed - indexed for MEDLINE]
12.

Identification of a novel paternally expressed gene in the Prader-Willi syndrome region.

Wevrick R, Kerns JA, Francke U.

Hum Mol Genet. 1994 Oct;3(10):1877-82.

PMID:
7849716
[PubMed - indexed for MEDLINE]
13.

Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndrome.

Schüle B, Albalwi M, Northrop E, Francis DI, Rowell M, Slater HR, Gardner RJ, Francke U.

BMC Med Genet. 2005 May 6;6:18.

PMID:
15877813
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Ethnic differentiation of copy number variation on chromosome 16p12.3 for association with obesity phenotypes in European and Chinese populations.

Yang TL, Guo Y, Li SM, Li SK, Tian Q, Liu YJ, Deng HW.

Int J Obes (Lond). 2013 Feb;37(2):188-90. doi: 10.1038/ijo.2012.31. Epub 2012 Mar 6.

PMID:
22391884
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis.

Jarick I, Vogel CI, Scherag S, Schäfer H, Hebebrand J, Hinney A, Scherag A.

Hum Mol Genet. 2011 Feb 15;20(4):840-52. doi: 10.1093/hmg/ddq518. Epub 2010 Dec 2.

PMID:
21131291
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria.

Gunay-Aygun M, Schwartz S, Heeger S, O'Riordan MA, Cassidy SB.

Pediatrics. 2001 Nov;108(5):E92.

PMID:
11694676
[PubMed - indexed for MEDLINE]
18.

Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome.

Bittel DC, Kibiryeva N, Butler MG.

Pediatrics. 2006 Oct;118(4):e1276-83. Epub 2006 Sep 18.

PMID:
16982806
[PubMed - indexed for MEDLINE]
Free Article
19.

De novo interstitial duplication of the 15q11.2-q14 PWS/AS region of maternal origin: Clinical description, array CGH analysis, and review of the literature.

Kitsiou-Tzeli S, Tzetis M, Sofocleous C, Vrettou C, Xaidara A, Giannikou K, Pampanos A, Mavrou A, Kanavakis E.

Am J Med Genet A. 2010 Aug;152A(8):1925-32. doi: 10.1002/ajmg.a.33447.

PMID:
20575009
[PubMed - indexed for MEDLINE]
20.

Mosaic isochromosome 15q and maternal uniparental isodisomy for chromosome 15 in a patient with morbid obesity and variant PWS-like phenotype.

Wang JC, Vaccarello-Cruz M, Ross L, Owen R, Pratt VM, Lightman K, Liu Y, Hafezi K, Cherif D, Sahoo T.

Am J Med Genet A. 2013 Jul;161A(7):1695-701. doi: 10.1002/ajmg.a.35939. Epub 2013 May 17.

PMID:
23686718
[PubMed - indexed for MEDLINE]

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