Pare G - Search Results

1

Identification of a methylation profile for DNMT1-associated autosomal dominant cerebellar ataxia, deafness, and narcolepsy.

Kernohan KD, Cigana Schenkel L, Huang L, Smith A, Pare G, Ainsworth P; Care4Rare Canada Consortium; Boycott KM, Warman-Chardon J, Sadikovic B. Kernohan KD, et al. Among authors: pare g. Clin Epigenetics. 2016 Sep 5;8(1):91. doi: 10.1186/s13148-016-0254-x. eCollection 2016. Clin Epigenetics. 2016. PMID: 27602171 Free PMC article.

2

Genomics and epigenomics in pediatric oncology and clinical laboratory genetics.

Sadikovic B, Pare G. Sadikovic B, et al. Among authors: pare g. Clin Biochem. 2014 Jun;47(9):731-2. doi: 10.1016/j.clinbiochem.2014.05.033. Epub 2014 May 20. Clin Biochem. 2014. PMID: 24858242 No abstract available.

3

Gender and BCR-ABL transcript type are correlated with molecular response to imatinib treatment in patients with chronic myeloid leukemia.

Lin HX, Sjaarda J, Dyck J, Stringer R, Hillis C, Harvey M, Carter R, Ainsworth P, Leber B, Pare G, Sadikovic B. Lin HX, et al. Among authors: pare g. Eur J Haematol. 2016 Apr;96(4):360-6. doi: 10.1111/ejh.12597. Epub 2015 Jul 3. Eur J Haematol. 2016. PMID: 26059983

4

DNA methylation analysis in constitutional disorders: Clinical implications of the epigenome.

Schenkel LC, Rodenhiser DI, Ainsworth PJ, Paré G, Sadikovic B. Schenkel LC, et al. Among authors: pare g. Crit Rev Clin Lab Sci. 2016;53(3):147-65. doi: 10.3109/10408363.2015.1113496. Epub 2016 Jan 12. Crit Rev Clin Lab Sci. 2016. PMID: 26758403 Review.

5

Clinical Validation of Fragile X Syndrome Screening by DNA Methylation Array.

Schenkel LC, Schwartz C, Skinner C, Rodenhiser DI, Ainsworth PJ, Pare G, Sadikovic B. Schenkel LC, et al. Among authors: pare g. J Mol Diagn. 2016 Nov;18(6):834-841. doi: 10.1016/j.jmoldx.2016.06.005. Epub 2016 Aug 29. J Mol Diagn. 2016. PMID: 27585064 Free article.

6

Clinical evaluation of a hemochromatosis next-generation sequencing gene panel.

Lanktree MB, Sadikovic B, Waye JS, Levstik A, Lanktree BB, Yudin J, Crowther MA, Pare G, Adams PC. Lanktree MB, et al. Among authors: pare g. Eur J Haematol. 2017 Mar;98(3):228-234. doi: 10.1111/ejh.12820. Epub 2016 Nov 11. Eur J Haematol. 2017. PMID: 27753142

7

The defining DNA methylation signature of Floating-Harbor Syndrome.

Hood RL, Schenkel LC, Nikkel SM, Ainsworth PJ, Pare G, Boycott KM, Bulman DE, Sadikovic B. Hood RL, et al. Among authors: pare g. Sci Rep. 2016 Dec 9;6:38803. doi: 10.1038/srep38803. Sci Rep. 2016. PMID: 27934915 Free PMC article.

8

Identification of epigenetic signature associated with alpha thalassemia/mental retardation X-linked syndrome.

Schenkel LC, Kernohan KD, McBride A, Reina D, Hodge A, Ainsworth PJ, Rodenhiser DI, Pare G, Bérubé NG, Skinner C, Boycott KM, Schwartz C, Sadikovic B. Schenkel LC, et al. Among authors: pare g. Epigenetics Chromatin. 2017 Mar 10;10:10. doi: 10.1186/s13072-017-0118-4. eCollection 2017. Epigenetics Chromatin. 2017. PMID: 28293299 Free PMC article.

9

Clinical Validation of a Genome-Wide DNA Methylation Assay for Molecular Diagnosis of Imprinting Disorders.

Aref-Eshghi E, Schenkel LC, Lin H, Skinner C, Ainsworth P, Paré G, Siu V, Rodenhiser D, Schwartz C, Sadikovic B. Aref-Eshghi E, et al. Among authors: pare g. J Mol Diagn. 2017 Nov;19(6):848-856. doi: 10.1016/j.jmoldx.2017.07.002. Epub 2017 Aug 12. J Mol Diagn. 2017. PMID: 28807811 Free article.

10

The defining DNA methylation signature of Kabuki syndrome enables functional assessment of genetic variants of unknown clinical significance.

Aref-Eshghi E, Schenkel LC, Lin H, Skinner C, Ainsworth P, Paré G, Rodenhiser D, Schwartz C, Sadikovic B. Aref-Eshghi E, et al. Among authors: pare g. Epigenetics. 2017;12(11):923-933. doi: 10.1080/15592294.2017.1381807. Epub 2017 Nov 7. Epigenetics. 2017. PMID: 28933623 Free PMC article.

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