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Items: 1 to 20 of 35


The Role of scaRNAs in Adjusting Alternative mRNA Splicing in Heart Development.

Nagasawa C, Ogren A, Kibiryeva N, Marshall J, O'Brien JE, Kenmochi N, Bittel DC.

J Cardiovasc Dev Dis. 2018 May 8;5(2). pii: E26. doi: 10.3390/jcdd5020026. Review.


Biology and clinical relevance of noncoding sno/scaRNAs.

Cao T, Rajasingh S, Samanta S, Dawn B, Bittel DC, Rajasingh J.

Trends Cardiovasc Med. 2018 Feb;28(2):81-90. doi: 10.1016/j.tcm.2017.08.002. Epub 2017 Aug 12. Review.


A Hypothesis for Using Pathway Genetic Load Analysis for Understanding Complex Outcomes in Bilirubin Encephalopathy.

Riordan SM, Bittel DC, Le Pichon JB, Gazzin S, Tiribelli C, Watchko JF, Wennberg RP, Shapiro SM.

Front Neurosci. 2016 Aug 18;10:376. doi: 10.3389/fnins.2016.00376. eCollection 2016.


scaRNAs regulate splicing and vertebrate heart development.

Patil P, Kibiryeva N, Uechi T, Marshall J, O'Brien JE Jr, Artman M, Kenmochi N, Bittel DC.

Biochim Biophys Acta. 2015 Aug;1852(8):1619-29. doi: 10.1016/j.bbadis.2015.04.016. Epub 2015 Apr 23.


Hyperactivity in the Gunn rat model of neonatal jaundice: age-related attenuation and emergence of gait deficits.

Stanford JA, Shuler JM, Fowler SC, Stanford KG, Ma D, Bittel DC, Le Pichon JB, Shapiro SM.

Pediatr Res. 2015 Mar;77(3):434-9. doi: 10.1038/pr.2014.199. Epub 2014 Dec 17.


MicroRNA-421 Dysregulation is Associated with Tetralogy of Fallot.

Bittel DC, Kibiryeva N, Marshall JA, O'Brien JE.

Cells. 2014 Jul 11;3(3):713-23. doi: 10.3390/cells3030713.


A tissue-specific gene expression template portrays heart development and pathology.

Rodemoyer A, Kibiryeva N, Bair A, Marshall J, O'Brien JE Jr, Bittel DC.

Hum Genomics. 2014 Mar 11;8:6. doi: 10.1186/1479-7364-8-6.


Ultra high-resolution gene centric genomic structural analysis of a non-syndromic congenital heart defect, Tetralogy of Fallot.

Bittel DC, Zhou XG, Kibiryeva N, Fiedler S, O'Brien JE Jr, Marshall J, Yu S, Liu HY.

PLoS One. 2014 Jan 31;9(1):e87472. doi: 10.1371/journal.pone.0087472. eCollection 2014. Erratum in: PLoS One. 2014;9(5):e99148.


Genome-wide gene expression in a patient with 15q13.3 homozygous microdeletion syndrome.

Le Pichon JB, Yu S, Kibiryeva N, Graf WD, Bittel DC.

Eur J Hum Genet. 2013 Oct;21(10):1093-9. doi: 10.1038/ejhg.2013.1. Epub 2013 Jan 30.


Noncoding RNA expression in myocardium from infants with tetralogy of Fallot.

O'Brien JE Jr, Kibiryeva N, Zhou XG, Marshall JA, Lofland GK, Artman M, Chen J, Bittel DC.

Circ Cardiovasc Genet. 2012 Jun;5(3):279-86. doi: 10.1161/CIRCGENETICS.111.961474. Epub 2012 Apr 23.


Gene expression in cardiac tissues from infants with idiopathic conotruncal defects.

Bittel DC, Butler MG, Kibiryeva N, Marshall JA, Chen J, Lofland GK, O'Brien JE Jr.

BMC Med Genomics. 2011 Jan 5;4:1. doi: 10.1186/1755-8794-4-1.


1.39 Mb inherited interstitial deletion in 12p13.33 associated with developmental delay.

Abdelmoity AT, Hall JJ, Bittel DC, Yu S.

Eur J Med Genet. 2011 Mar-Apr;54(2):198-203. doi: 10.1016/j.ejmg.2010.11.010. Epub 2010 Dec 7.


TPH2 polymorphisms and expression in Prader-Willi syndrome subjects with differing genetic subtypes.

Henkhaus RS, Bittel DC, Butler MG.

J Neurodev Disord. 2010 Sep;2(3):144-8. doi: 10.1007/s11689-010-9051-6. Epub 2010 May 21.


An interstitial 15q11-q14 deletion: expanded Prader-Willi syndrome phenotype.

Butler MG, Bittel DC, Kibiryeva N, Cooley LD, Yu S.

Am J Med Genet A. 2010 Feb;152A(2):404-8. doi: 10.1002/ajmg.a.33197. Erratum in: Am J Med Genet A. 2010 May;152A(5):1331-2.


Quantitative real-time polymerase chain reaction for the verification of genomic imbalances detected by microarray-based comparative genomic hybridization.

Yu S, Kielt M, Stegner AL, Kibiryeva N, Bittel DC, Cooley LD.

Genet Test Mol Biomarkers. 2009 Dec;13(6):751-60. doi: 10.1089/gtmb.2009.0056.


Validation of the Agilent 244K oligonucleotide array-based comparative genomic hybridization platform for clinical cytogenetic diagnosis.

Yu S, Bittel DC, Kibiryeva N, Zwick DL, Cooley LD.

Am J Clin Pathol. 2009 Sep;132(3):349-60. doi: 10.1309/AJCP1BOUTWF6ERYS.


Methylation-specific multiplex ligation-dependent probe amplification analysis of subjects with chromosome 15 abnormalities.

Bittel DC, Kibiryeva N, Butler MG.

Genet Test. 2007 Winter;11(4):467-75. doi: 10.1089/gte.2007.0061.


Array comparative genomic hybridization (aCGH) analysis in Prader-Willi syndrome.

Butler MG, Fischer W, Kibiryeva N, Bittel DC.

Am J Med Genet A. 2008 Apr 1;146A(7):854-60. doi: 10.1002/ajmg.a.32249.


Whole genome microarray analysis of gene expression in subjects with fragile X syndrome.

Bittel DC, Kibiryeva N, Butler MG.

Genet Med. 2007 Jul;9(7):464-72.

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