Chen YA - Search Results

1

Mosaicism for genome-wide paternal uniparental disomy with features of multiple imprinting disorders: diagnostic and management issues.

Inbar-Feigenberg M, Choufani S, Cytrynbaum C, Chen YA, Steele L, Shuman C, Ray PN, Weksberg R. Inbar-Feigenberg M, et al. Among authors: chen ya. Am J Med Genet A. 2013 Jan;161A(1):13-20. doi: 10.1002/ajmg.a.35651. Epub 2012 Dec 13. Am J Med Genet A. 2013. PMID: 23239666

2

NSD1 mutations generate a genome-wide DNA methylation signature.

Choufani S, Cytrynbaum C, Chung BH, Turinsky AL, Grafodatskaya D, Chen YA, Cohen AS, Dupuis L, Butcher DT, Siu MT, Luk HM, Lo IF, Lam ST, Caluseriu O, Stavropoulos DJ, Reardon W, Mendoza-Londono R, Brudno M, Gibson WT, Chitayat D, Weksberg R. Choufani S, et al. Among authors: chen ya. Nat Commun. 2015 Dec 22;6:10207. doi: 10.1038/ncomms10207. Nat Commun. 2015. PMID: 26690673 Free PMC article.

3

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. Chen YA, et al. Genomics. 2011 Apr;97(4):214-22. doi: 10.1016/j.ygeno.2010.12.004. Epub 2011 Jan 4. Genomics. 2011. PMID: 21211562 Free article.

4

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. Chen YA, et al. Epigenetics. 2013 Feb;8(2):203-9. doi: 10.4161/epi.23470. Epub 2013 Jan 11. Epigenetics. 2013. PMID: 23314698 Free PMC article.

5

High frequency of copy number variations (CNVs) in the chromosome 11p15 region in patients with Beckwith-Wiedemann syndrome.

Baskin B, Choufani S, Chen YA, Shuman C, Parkinson N, Lemyre E, Micheil Innes A, Stavropoulos DJ, Ray PN, Weksberg R. Baskin B, et al. Among authors: chen ya. Hum Genet. 2014 Mar;133(3):321-30. doi: 10.1007/s00439-013-1379-z. Epub 2013 Oct 24. Hum Genet. 2014. PMID: 24154661

6

Genome-Wide DNA Methylation Analysis of Chinese Patients with Systemic Lupus Erythematosus Identified Hypomethylation in Genes Related to the Type I Interferon Pathway.

Yeung KS, Chung BH, Choufani S, Mok MY, Wong WL, Mak CC, Yang W, Lee PP, Wong WH, Chen YA, Grafodatskaya D, Wong RW, Lau CS, Chan DT, Weksberg R, Lau YL. Yeung KS, et al. Among authors: chen ya. PLoS One. 2017 Jan 13;12(1):e0169553. doi: 10.1371/journal.pone.0169553. eCollection 2017. PLoS One. 2017. PMID: 28085900 Free PMC article.

7

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. Chen YA, et al. Am J Hum Genet. 2012 Oct 5;91(4):762-4. doi: 10.1016/j.ajhg.2012.06.020. Am J Hum Genet. 2012. PMID: 23040499 Free PMC article. No abstract available.

8

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. Grafodatskaya D, et al. Among authors: chen ya. BMC Med Genomics. 2013 Jan 28;6:1. doi: 10.1186/1755-8794-6-1. BMC Med Genomics. 2013. PMID: 23356856 Free PMC article.

9

Investigation of correlations between DNA methylation, suicidal behavior and aging.

Jeremian R, Chen YA, De Luca V, Vincent JB, Kennedy JL, Zai CC, Strauss J. Jeremian R, et al. Among authors: chen ya. Bipolar Disord. 2017 Feb;19(1):32-40. doi: 10.1111/bdi.12466. Epub 2017 Mar 9. Bipolar Disord. 2017. PMID: 28276657

10

Basic income guarantee: a review of implications for oral health.

Chen YA, Quiñonez C. Chen YA, et al. J Public Health Dent. 2018 Dec;78(1):56-62. doi: 10.1111/jphd.12239. Epub 2017 Aug 3. J Public Health Dent. 2018. PMID: 28771733 Review.

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