P30 HD002528/HD/NICHD NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1998	1
1999	3
2000	1
2001	1
2002	1
2004	1
2005	6
2006	7
2007	17
2008	34
2009	42
2010	44
2011	62
2012	88
2013	69
2014	89
2015	63
2016	54
2017	50
2018	37
2019	19
2020	15
2021	11
2022	9
2023	2
2024	0

1

Imprinting disorders in humans: a review.

Butler MG. Butler MG. Curr Opin Pediatr. 2020 Dec;32(6):719-729. doi: 10.1097/MOP.0000000000000965. Curr Opin Pediatr. 2020. PMID: 33148967 Free PMC article. Review.

2

The 15q11.2 BP1-BP2 microdeletion syndrome: a review.

Cox DM, Butler MG. Cox DM, et al. Int J Mol Sci. 2015 Feb 13;16(2):4068-82. doi: 10.3390/ijms16024068. Int J Mol Sci. 2015. PMID: 25689425 Free PMC article. Review.

3

Rare FMR1 gene mutations causing fragile X syndrome: A review.

Sitzmann AF, Hagelstrom RT, Tassone F, Hagerman RJ, Butler MG. Sitzmann AF, et al. Am J Med Genet A. 2018 Jan;176(1):11-18. doi: 10.1002/ajmg.a.38504. Epub 2017 Nov 27. Am J Med Genet A. 2018. PMID: 29178241 Free PMC article. Review.

4

Aspirin and multiple sclerosis.

Tsau S, Emerson MR, Lynch SG, LeVine SM. Tsau S, et al. BMC Med. 2015 Jun 29;13:153. doi: 10.1186/s12916-015-0394-4. BMC Med. 2015. PMID: 26123634 Free PMC article. Review.

5

Stromal contributions to the carcinogenic process.

Spaw M, Anant S, Thomas SM. Spaw M, et al. Mol Carcinog. 2017 Apr;56(4):1199-1213. doi: 10.1002/mc.22583. Epub 2016 Nov 5. Mol Carcinog. 2017. PMID: 27787930 Free PMC article. Review.

6

Clinical and genetic aspects of the 15q11.2 BP1-BP2 microdeletion disorder.

Butler MG. Butler MG. J Intellect Disabil Res. 2017 Jun;61(6):568-579. doi: 10.1111/jir.12382. Epub 2017 Apr 7. J Intellect Disabil Res. 2017. PMID: 28387067 Free PMC article. Review.

7

Prader-Willi Syndrome: Clinical Genetics and Diagnostic Aspects with Treatment Approaches.

Butler MG, Manzardo AM, Forster JL. Butler MG, et al. Curr Pediatr Rev. 2016;12(2):136-66. doi: 10.2174/1573396312666151123115250. Curr Pediatr Rev. 2016. PMID: 26592417 Free PMC article. Review.

8

Clinically relevant known and candidate genes for obesity and their overlap with human infertility and reproduction.

Butler MG, McGuire A, Manzardo AM. Butler MG, et al. J Assist Reprod Genet. 2015 Apr;32(4):495-508. doi: 10.1007/s10815-014-0411-0. Epub 2015 Jan 29. J Assist Reprod Genet. 2015. PMID: 25631154 Free PMC article. Review.

9

The 7q11.23 Microduplication Syndrome: A Clinical Report with Review of Literature.

Abbas E, Cox DM, Smith T, Butler MG. Abbas E, et al. J Pediatr Genet. 2016 Sep;5(3):129-40. doi: 10.1055/s-0036-1584361. Epub 2016 Jun 15. J Pediatr Genet. 2016. PMID: 27617154 Free PMC article. Review.

10

Single Gene and Syndromic Causes of Obesity: Illustrative Examples.

Butler MG. Butler MG. Prog Mol Biol Transl Sci. 2016;140:1-45. doi: 10.1016/bs.pmbts.2015.12.003. Epub 2016 Mar 23. Prog Mol Biol Transl Sci. 2016. PMID: 27288824 Free PMC article. Review.

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