Ehrlich M - Search Results

1

Diagnosis by sequencing: correction of misdiagnosis from FSHD2 to LGMD2A by whole-exome analysis.

Leidenroth A, Sorte HS, Gilfillan G, Ehrlich M, Lyle R, Hewitt JE. Leidenroth A, et al. Among authors: ehrlich m. Eur J Hum Genet. 2012 Sep;20(9):999-1003. doi: 10.1038/ejhg.2012.42. Epub 2012 Feb 29. Eur J Hum Genet. 2012. PMID: 22378277 Free PMC article.

2

Analysis of allele-specific RNA transcription in FSHD by RNA-DNA FISH in single myonuclei.

Masny PS, Chan OY, de Greef JC, Bengtsson U, Ehrlich M, Tawil R, Lock LF, Hewitt JE, Stocksdale J, Martin JH, van der Maarel SM, Winokur ST. Masny PS, et al. Among authors: ehrlich m. Eur J Hum Genet. 2010 Apr;18(4):448-56. doi: 10.1038/ejhg.2009.183. Epub 2009 Nov 4. Eur J Hum Genet. 2010. PMID: 19888305 Free PMC article.

3

Deciphering transcription dysregulation in FSH muscular dystrophy.

Ehrlich M, Lacey M. Ehrlich M, et al. J Hum Genet. 2012 Aug;57(8):477-84. doi: 10.1038/jhg.2012.74. Epub 2012 Jun 21. J Hum Genet. 2012. PMID: 22718021 Free PMC article. Review.

4

Methylation of the FSHD syndrome-linked subtelomeric repeat in normal and FSHD cell cultures and tissues.

Tsien F, Sun B, Hopkins NE, Vedanarayanan V, Figlewicz D, Winokur S, Ehrlich M. Tsien F, et al. Among authors: ehrlich m. Mol Genet Metab. 2001 Nov;74(3):322-31. doi: 10.1006/mgme.2001.3219. Mol Genet Metab. 2001. PMID: 11708861

5

Testing the position-effect variegation hypothesis for facioscapulohumeral muscular dystrophy by analysis of histone modification and gene expression in subtelomeric 4q.

Jiang G, Yang F, van Overveld PG, Vedanarayanan V, van der Maarel S, Ehrlich M. Jiang G, et al. Among authors: ehrlich m. Hum Mol Genet. 2003 Nov 15;12(22):2909-21. doi: 10.1093/hmg/ddg323. Epub 2003 Sep 23. Hum Mol Genet. 2003. PMID: 14506132

6

FSH dystrophy and a subtelomeric 4q haplotype: a new assay and associations with disease.

Tsumagari K, Chen D, Hackman JR, Bossler AD, Ehrlich M. Tsumagari K, et al. Among authors: ehrlich m. J Med Genet. 2010 Nov;47(11):745-51. doi: 10.1136/jmg.2009.076703. Epub 2010 Aug 15. J Med Genet. 2010. PMID: 20710047 Free PMC article.

7

Risks and rewards of big-data in epigenomics research: an interview with Melanie Ehrlich.

Ehrlich M. Ehrlich M. Epigenomics. 2022 Mar;14(6):351-358. doi: 10.2217/epi-2022-0056. Epub 2022 Mar 8. Epigenomics. 2022. PMID: 35255735

8

Cytogenetic and immuno-FISH analysis of the 4q subtelomeric region, which is associated with facioscapulohumeral muscular dystrophy.

Yang F, Shao C, Vedanarayanan V, Ehrlich M. Yang F, et al. Among authors: ehrlich m. Chromosoma. 2004 May;112(7):350-9. doi: 10.1007/s00412-004-0280-x. Epub 2004 May 11. Chromosoma. 2004. PMID: 15138770

9

Hybridization analysis of D4Z4 repeat arrays linked to FSHD.

Ehrlich M, Jackson K, Tsumagari K, Camaño P, Lemmers RJ. Ehrlich M, et al. Chromosoma. 2007 Apr;116(2):107-16. doi: 10.1007/s00412-006-0080-6. Epub 2006 Nov 28. Chromosoma. 2007. PMID: 17131163 Free PMC article.

10

Epigenetics of a tandem DNA repeat: chromatin DNaseI sensitivity and opposite methylation changes in cancers.

Tsumagari K, Qi L, Jackson K, Shao C, Lacey M, Sowden J, Tawil R, Vedanarayanan V, Ehrlich M. Tsumagari K, et al. Among authors: ehrlich m. Nucleic Acids Res. 2008 Apr;36(7):2196-207. doi: 10.1093/nar/gkn055. Epub 2008 Feb 16. Nucleic Acids Res. 2008. PMID: 18281700 Free PMC article.

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