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Genetic landscape and novel disease mechanisms from a large LGMD cohort of 4656 patients.
Ann Clin Transl Neurol. 2018 Dec 1;5(12):1574-1587. doi: 10.1002/acn3.649. eCollection 2018 Dec.
Ann Clin Transl Neurol. 2018.
PMID: 30564623
Free PMC article.
Detection limit of intragenic deletions with targeted array comparative genomic hybridization.
Askree SH, Chin EL, Bean LH, Coffee B, Tanner A, Hegde M.
Askree SH, et al.
BMC Genet. 2013 Dec 5;14:116. doi: 10.1186/1471-2156-14-116.
BMC Genet. 2013.
PMID: 24304607
Free PMC article.
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Variants of uncertain significance in newborn screening disorders: implications for large-scale genomic sequencing.
Narravula A, Garber KB, Askree SH, Hegde M, Hall PL.
Narravula A, et al. Among authors: askree sh.
Genet Med. 2017 Jan;19(1):77-82. doi: 10.1038/gim.2016.67. Epub 2016 Jun 16.
Genet Med. 2017.
PMID: 27308838
Free article.
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Aberrant firing of replication origins potentially explains intragenic nonrecurrent rearrangements within genes, including the human DMD gene.
Ankala A, Kohn JN, Hegde A, Meka A, Ephrem CL, Askree SH, Bhide S, Hegde MR.
Ankala A, et al. Among authors: askree sh.
Genome Res. 2012 Jan;22(1):25-34. doi: 10.1101/gr.123463.111. Epub 2011 Nov 16.
Genome Res. 2012.
PMID: 22090376
Free PMC article.
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Parent-of-origin testing for 15q11-q13 gains by quantitative DNA methylation analysis.
Askree SH, Dharamrup S, Hjelm LN, Coffee B.
Askree SH, et al.
J Mol Diagn. 2012 May-Jun;14(3):192-8. doi: 10.1016/j.jmoldx.2012.01.005. Epub 2012 Mar 14.
J Mol Diagn. 2012.
PMID: 22426236
Free article.
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A genome-wide screen for Saccharomyces cerevisiae deletion mutants that affect telomere length.
Askree SH, Yehuda T, Smolikov S, Gurevich R, Hawk J, Coker C, Krauskopf A, Kupiec M, McEachern MJ.
Askree SH, et al.
Proc Natl Acad Sci U S A. 2004 Jun 8;101(23):8658-63. doi: 10.1073/pnas.0401263101. Epub 2004 May 25.
Proc Natl Acad Sci U S A. 2004.
PMID: 15161972
Free PMC article.
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