S. Hussain Askree MBBS PhD
- Department of Human Genetics
Adjunct Assistant Professor
-
MNG Laboratories, a LAbCorp Company
5424 Glenridge Drive
Academic Appointment
- Adjunct Assistant Professor, Human Genetics, Emory University
Education
Degrees
- Ph.D. from University of Georgia
- M.B.B.S. from Rawalpindi Medical College
Research
Publications
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Genetic landscape and novel disease mechanisms from a large LGMD cohort of 4656 patients.
Ann Clin Transl Neurol Volume: 5 Page(s): 1574 - 1587
12/01/2018 Authors: Nallamilli BRR; Chakravorty S; Kesari A; Tanner A; Ankala A; Schneider T; da Silva C; Beadling R; Alexander JJ; Askree SH -
Variants of uncertain significance in newborn screening disorders: implications for large-scale genomic sequencing.
Genet Med Volume: 19 Page(s): 77 - 82
01/01/2017 Authors: Narravula A; Garber KB; Askree SH; Hegde M; Hall PL -
Next-Generation Sequencing as a Diagnostic Tool for Hereditary Breast and Ovarian Cancer
Volume: 17 Page(s): 761 - 761
11/01/2015 Authors: Dai Z; Bean LJ; Collins C; Askree SH; Alexander JJ; Hegde M; Tanner A -
Detection limit of intragenic deletions with targeted array comparative genomic hybridization.
BMC Genet Volume: 14 Page(s): 116
12/05/2013 Authors: Askree SH; Chin ELH; Bean LH; Coffee B; Tanner A; Hegde M -
Genotype and biochemical phenotypes in short-chain acyl-coenzyme A dehydrogenase deficiency
Volume: 105 Page(s): 303 - 303
03/01/2012 Authors: Askree SH; Oglesbee D; Gavrilov D; Raymond K; Tortorelli S; Rinaldo P; Matern D -
Aberrant firing of replication origins potentially explains intragenic nonrecurrent rearrangements within genes, including the human DMD gene.
Genome Res Volume: 22 Page(s): 25 - 34
01/01/2012 Authors: Ankala A; Kohn JN; Hegde A; Meka A; Ephrem CLH; Askree SH; Bhide S; Hegde MR -
Parent-of-origin testing for 15q11-q13 gains by quantitative DNA methylation analysis.
J Mol Diagn Volume: 14 Page(s): 192 - 198
01/01/2012 Authors: Askree SH; Dharamrup S; Hjelm LN; Coffee B -
Allelic dropout can cause false-positive results for Prader-Willi and Angelman syndrome testing.
J Mol Diagn Volume: 13 Page(s): 108 - 112
01/01/2011 Authors: Hussain Askree S; Hjelm LN; Ali Pervaiz M; Adam M; Bean LJH; Hedge M; Coffee B -
Aberrant DNA Methylation as a Marker for Human Disease in Newborns
Volume: 12 Page(s): 865 - 865
11/01/2010 Authors: Coffee B; Askree S; Dharamrup S; Bean L; Hegde M -
A genome-wide screen for Saccharomyces cerevisiae deletion mutants that affect telomere length.
Proc Natl Acad Sci U S A Volume: 101 Page(s): 8658 - 8663
06/08/2004 Authors: Askree SH; Yehuda T; Smolikov S; Gurevich R; Hawk J; Coker C; Krauskopf A; Kupiec M; McEachern MJ