Butler MG - Search Results

1

Relationships between UBE3A and SNORD116 expression and features of autism in chromosome 15 imprinting disorders.

Baker EK, Butler MG, Hartin SN, Ling L, Bui M, Francis D, Rogers C, Field MJ, Slee J, Gamage D, Amor DJ, Godler DE. Baker EK, et al. Among authors: butler mg. Transl Psychiatry. 2020 Oct 29;10(1):362. doi: 10.1038/s41398-020-01034-7. Transl Psychiatry. 2020. PMID: 33116122 Free PMC article.

2

Imprinting disorders: non-Mendelian mechanisms affecting growth.

Butler MG. Butler MG. J Pediatr Endocrinol Metab. 2002 Dec;15 Suppl 5(Suppl 5):1279-88. J Pediatr Endocrinol Metab. 2002. PMID: 12510981 Free PMC article. Review.

3

Methylation-specific multiplex ligation-dependent probe amplification analysis of subjects with chromosome 15 abnormalities.

Bittel DC, Kibiryeva N, Butler MG. Bittel DC, et al. Among authors: butler mg. Genet Test. 2007 Winter;11(4):467-75. doi: 10.1089/gte.2007.0061. Genet Test. 2007. PMID: 18294067 Free PMC article.

4

Genomic imprinting disorders in humans: a mini-review.

Butler MG. Butler MG. J Assist Reprod Genet. 2009 Sep-Oct;26(9-10):477-86. doi: 10.1007/s10815-009-9353-3. Epub 2009 Oct 21. J Assist Reprod Genet. 2009. PMID: 19844787 Free PMC article. Review.

5

Methylation-specific multiplex ligation-dependent probe amplification and identification of deletion genetic subtypes in Prader-Willi syndrome.

Henkhaus RS, Kim SJ, Kimonis VE, Gold JA, Dykens EM, Driscoll DJ, Butler MG. Henkhaus RS, et al. Among authors: butler mg. Genet Test Mol Biomarkers. 2012 Mar;16(3):178-86. doi: 10.1089/gtmb.2011.0115. Epub 2011 Oct 6. Genet Test Mol Biomarkers. 2012. PMID: 21977908 Free PMC article.

6

Increased plasma chemokine levels in children with Prader-Willi syndrome.

Butler MG, Hossain W, Sulsona C, Driscoll DJ, Manzardo AM. Butler MG, et al. Am J Med Genet A. 2015 Mar;167A(3):563-71. doi: 10.1002/ajmg.a.36908. Am J Med Genet A. 2015. PMID: 25691409 Free PMC article.

7

High plasma neurotensin levels in children with Prader-Willi syndrome.

Butler MG, Nelson TA, Driscoll DJ, Manzardo AM. Butler MG, et al. Am J Med Genet A. 2015 Aug;167A(8):1773-8. doi: 10.1002/ajmg.a.37103. Epub 2015 Apr 5. Am J Med Genet A. 2015. PMID: 25847417 Free PMC article.

8

Higher plasma orexin A levels in children with Prader-Willi syndrome compared with healthy unrelated sibling controls.

Manzardo AM, Johnson L, Miller JL, Driscoll DJ, Butler MG. Manzardo AM, et al. Among authors: butler mg. Am J Med Genet A. 2016 Aug;170(8):2097-102. doi: 10.1002/ajmg.a.37749. Epub 2016 May 23. Am J Med Genet A. 2016. PMID: 27214028

9

Prader-Willi syndrome and atypical submicroscopic 15q11-q13 deletions with or without imprinting defects.

Hassan M, Butler MG. Hassan M, et al. Among authors: butler mg. Eur J Med Genet. 2016 Nov;59(11):584-589. doi: 10.1016/j.ejmg.2016.09.017. Epub 2016 Sep 19. Eur J Med Genet. 2016. PMID: 27659713 Free PMC article.

10

Three siblings with Prader-Willi syndrome caused by imprinting center microdeletions and review.

Hartin SN, Hossain WA, Weisensel N, Butler MG. Hartin SN, et al. Among authors: butler mg. Am J Med Genet A. 2018 Apr;176(4):886-895. doi: 10.1002/ajmg.a.38627. Epub 2018 Feb 13. Am J Med Genet A. 2018. PMID: 29437285 Free PMC article.

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