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Results: 15

1.

A CGG-Repeat Expansion Mutation in ZNF713 Causes FRA7A: Association with Autistic Spectrum Disorder in two Families.

Metsu S, Rainger JK, Debacker K, Bernhard B, Rooms L, Grafodatskaya D, Weksberg R, Fombonne E, Taylor MS, Scherer SW, Kooy RF, FitzPatrick DR.

Hum Mutat. 2014 Sep 4. doi: 10.1002/humu.22683. [Epub ahead of print]

PMID:
25196122
[PubMed - as supplied by publisher]
2.

Comparative chromosome painting of pronghorn (Antilocapra americana) and saola (Pseudoryx nghetinhensis) karyotypes with human and dromedary camel probes.

Kulemzina AI, Perelman PL, Grafodatskaya DA, Nguyen TT, Thompson M, Roelke-Parker ME, Graphodatsky AS.

BMC Genet. 2014 Jun 12;15:68. doi: 10.1186/1471-2156-15-68.

PMID:
24923361
[PubMed - in process]
Free PMC Article
3.

Multilocus loss of DNA methylation in individuals with mutations in the histone H3 lysine 4 demethylase KDM5C.

Grafodatskaya D, Chung BH, Butcher DT, Turinsky AL, Goodman SJ, Choufani S, Chen YA, Lou Y, Zhao C, Rajendram R, Abidi FE, Skinner C, Stavropoulos J, Bondy CA, Hamilton J, Wodak S, Scherer SW, Schwartz CE, Weksberg R.

BMC Med Genomics. 2013 Jan 28;6:1. doi: 10.1186/1755-8794-6-1.

PMID:
23356856
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

The health risks of ART.

Grafodatskaya D, Cytrynbaum C, Weksberg R.

EMBO Rep. 2013 Feb;14(2):129-35. doi: 10.1038/embor.2012.222. Epub 2013 Jan 22. No abstract available.

PMID:
23337626
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarray.

Chen YA, Lemire M, Choufani S, Butcher DT, Grafodatskaya D, Zanke BW, Gallinger S, Hudson TJ, Weksberg R.

Epigenetics. 2013 Feb;8(2):203-9. doi: 10.4161/epi.23470. Epub 2013 Jan 11.

PMID:
23314698
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Cross-reactive DNA microarray probes lead to false discovery of autosomal sex-associated DNA methylation.

Chen YA, Choufani S, Grafodatskaya D, Butcher DT, Ferreira JC, Weksberg R.

Am J Hum Genet. 2012 Oct 5;91(4):762-4. doi: 10.1016/j.ajhg.2012.06.020. No abstract available.

PMID:
23040499
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Phenotypic spectrum associated with duplication of Xp11.22-p11.23 includes Autism Spectrum Disorder.

Chung BH, Drmic I, Marshall CR, Grafodatskaya D, Carter M, Fernandez BA, Weksberg R, Roberts W, Scherer SW.

Eur J Med Genet. 2011 Sep-Oct;54(5):e516-20. doi: 10.1016/j.ejmg.2011.05.008. Epub 2011 Jun 29.

PMID:
21689796
[PubMed - indexed for MEDLINE]
8.

WNT2 promoter methylation in human placenta is associated with low birthweight percentile in the neonate.

Ferreira JC, Choufani S, Grafodatskaya D, Butcher DT, Zhao C, Chitayat D, Shuman C, Kingdom J, Keating S, Weksberg R.

Epigenetics. 2011 Apr;6(4):440-9. Epub 2011 Apr 1.

PMID:
21474991
[PubMed - indexed for MEDLINE]
Free Article
9.

Isolation of MECP2-null Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation.

Cheung AY, Horvath LM, Grafodatskaya D, Pasceri P, Weksberg R, Hotta A, Carrel L, Ellis J.

Hum Mol Genet. 2011 Jun 1;20(11):2103-15. doi: 10.1093/hmg/ddr093. Epub 2011 Mar 3.

PMID:
21372149
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Assessment of methylation level prediction accuracy in methyl-DNA immunoprecipitation and sodium bisulfite based microarray platforms.

Rajendram R, Ferreira JC, Grafodatskaya D, Choufani S, Chiang T, Pu S, Butcher DT, Wodak SJ, Weksberg R.

Epigenetics. 2011 Apr;6(4):410-5. Epub 2011 Apr 1.

PMID:
21343703
[PubMed - indexed for MEDLINE]
Free Article
11.

A novel approach identifies new differentially methylated regions (DMRs) associated with imprinted genes.

Choufani S, Shapiro JS, Susiarjo M, Butcher DT, Grafodatskaya D, Lou Y, Ferreira JC, Pinto D, Scherer SW, Shaffer LG, Coullin P, Caniggia I, Beyene J, Slim R, Bartolomei MS, Weksberg R.

Genome Res. 2011 Mar;21(3):465-76. doi: 10.1101/gr.111922.110. Epub 2011 Feb 7.

PMID:
21324877
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Sequence overlap between autosomal and sex-linked probes on the Illumina HumanMethylation27 microarray.

Chen YA, Choufani S, Ferreira JC, Grafodatskaya D, Butcher DT, Weksberg R.

Genomics. 2011 Apr;97(4):214-22. doi: 10.1016/j.ygeno.2010.12.004. Epub 2011 Jan 4.

PMID:
21211562
[PubMed - indexed for MEDLINE]
Free Article
13.

Autism spectrum disorders and epigenetics.

Grafodatskaya D, Chung B, Szatmari P, Weksberg R.

J Am Acad Child Adolesc Psychiatry. 2010 Aug;49(8):794-809. doi: 10.1016/j.jaac.2010.05.005. Epub 2010 Jul 3. Review.

PMID:
20643313
[PubMed - indexed for MEDLINE]
14.

EBV transformation and cell culturing destabilizes DNA methylation in human lymphoblastoid cell lines.

Grafodatskaya D, Choufani S, Ferreira JC, Butcher DT, Lou Y, Zhao C, Scherer SW, Weksberg R.

Genomics. 2010 Feb;95(2):73-83. doi: 10.1016/j.ygeno.2009.12.001. Epub 2009 Dec 18.

PMID:
20005943
[PubMed - indexed for MEDLINE]
Free Article
15.

Search for the sex-determining switch in monotremes: mapping WT1, SF1, LHX1, LHX2, FGF9, WNT4, RSPO1 and GATA4 in platypus.

Grafodatskaya D, Rens W, Wallis MC, Trifonov V, O'Brien PC, Clarke O, Graves JA, Ferguson-Smith MA.

Chromosome Res. 2007;15(6):777-85. Epub 2007 Aug 29.

PMID:
17717721
[PubMed - indexed for MEDLINE]

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