R03 HD073731/HD/NICHD NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2013	5
2014	6
2015	1
2016	4
2025	0

1

DNA Methylation: Insights into Human Evolution.

Hernando-Herraez I, Garcia-Perez R, Sharp AJ, Marques-Bonet T. Hernando-Herraez I, et al. PLoS Genet. 2015 Dec 10;11(12):e1005661. doi: 10.1371/journal.pgen.1005661. eCollection 2015 Dec. PLoS Genet. 2015. PMID: 26658498 Free PMC article. Review.

2

The genetics of microdeletion and microduplication syndromes: an update.

Watson CT, Marques-Bonet T, Sharp AJ, Mefford HC. Watson CT, et al. Annu Rev Genomics Hum Genet. 2014;15:215-244. doi: 10.1146/annurev-genom-091212-153408. Epub 2014 Apr 16. Annu Rev Genomics Hum Genet. 2014. PMID: 24773319 Free PMC article. Review.

3

Epigenome-wide differences in pathology-free regions of multiple sclerosis-affected brains.

Huynh JL, Garg P, Thin TH, Yoo S, Dutta R, Trapp BD, Haroutunian V, Zhu J, Donovan MJ, Sharp AJ, Casaccia P. Huynh JL, et al. Nat Neurosci. 2014 Jan;17(1):121-30. doi: 10.1038/nn.3588. Epub 2013 Nov 24. Nat Neurosci. 2014. PMID: 24270187 Free PMC article.

4

Genome-wide DNA methylation profiling in the superior temporal gyrus reveals epigenetic signatures associated with Alzheimer's disease.

Watson CT, Roussos P, Garg P, Ho DJ, Azam N, Katsel PL, Haroutunian V, Sharp AJ. Watson CT, et al. Genome Med. 2016 Jan 19;8(1):5. doi: 10.1186/s13073-015-0258-8. Genome Med. 2016. PMID: 26803900 Free PMC article.

5

Genome-wide analysis of parent-of-origin effects in non-syndromic orofacial clefts.

Garg P, Ludwig KU, Böhmer AC, Rubini M, Steegers-Theunissen R, Mossey PA, Mangold E, Sharp AJ. Garg P, et al. Eur J Hum Genet. 2014 Jun;22(6):822-30. doi: 10.1038/ejhg.2013.235. Epub 2013 Oct 30. Eur J Hum Genet. 2014. PMID: 24169523 Free PMC article.

6

Digital genotyping of macrosatellites and multicopy genes reveals novel biological functions associated with copy number variation of large tandem repeats.

Brahmachary M, Guilmatre A, Quilez J, Hasson D, Borel C, Warburton P, Sharp AJ. Brahmachary M, et al. PLoS Genet. 2014 Jun 19;10(6):e1004418. doi: 10.1371/journal.pgen.1004418. eCollection 2014 Jun. PLoS Genet. 2014. PMID: 24945355 Free PMC article.

7

DNA Methylation Signatures of Early Childhood Malnutrition Associated With Impairments in Attention and Cognition.

Peter CJ, Fischer LK, Kundakovic M, Garg P, Jakovcevski M, Dincer A, Amaral AC, Ginns EI, Galdzicka M, Bryce CP, Ratner C, Waber DP, Mokler D, Medford G, Champagne FA, Rosene DL, McGaughy JA, Sharp AJ, Galler JR, Akbarian S. Peter CJ, et al. Biol Psychiatry. 2016 Nov 15;80(10):765-774. doi: 10.1016/j.biopsych.2016.03.2100. Epub 2016 Mar 26. Biol Psychiatry. 2016. PMID: 27184921 Free PMC article.

8

DNA methylation profiling in X;autosome translocations supports a role for L1 repeats in the spread of X chromosome inactivation.

Bala Tannan N, Brahmachary M, Garg P, Borel C, Alnefaie R, Watson CT, Thomas NS, Sharp AJ. Bala Tannan N, et al. Hum Mol Genet. 2014 Mar 1;23(5):1224-36. doi: 10.1093/hmg/ddt553. Epub 2013 Nov 1. Hum Mol Genet. 2014. PMID: 24186870 Free PMC article.

9

Polymorphic tandem repeats within gene promoters act as modifiers of gene expression and DNA methylation in humans.

Quilez J, Guilmatre A, Garg P, Highnam G, Gymrek M, Erlich Y, Joshi RS, Mittelman D, Sharp AJ. Quilez J, et al. Nucleic Acids Res. 2016 May 5;44(8):3750-62. doi: 10.1093/nar/gkw219. Epub 2016 Apr 7. Nucleic Acids Res. 2016. PMID: 27060133 Free PMC article.

10

Expansion of a 12-kb VNTR containing the REXO1L1 gene cluster underlies the microscopically visible euchromatic variant of 8q21.2.

Tyson C, Sharp AJ, Hrynchak M, Yong SL, Hollox EJ, Warburton P, Barber JC. Tyson C, et al. Eur J Hum Genet. 2014 Apr;22(4):458-63. doi: 10.1038/ejhg.2013.185. Epub 2013 Sep 18. Eur J Hum Genet. 2014. PMID: 24045839 Free PMC article.

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