Owen R - Search Results

1

Regions of homozygosity identified by oligonucleotide SNP arrays: evaluating the incidence and clinical utility.

Wang JC, Ross L, Mahon LW, Owen R, Hemmat M, Wang BT, El Naggar M, Kopita KA, Randolph LM, Chase JM, Matas Aguilera MJ, Siles JL, Church JA, Hauser N, Shen JJ, Jones MC, Wierenga KJ, Jiang Z, Haddadin M, Boyar FZ, Anguiano A, Strom CM, Sahoo T. Wang JC, et al. Among authors: owen r. Eur J Hum Genet. 2015 May;23(5):663-71. doi: 10.1038/ejhg.2014.153. Epub 2014 Aug 13. Eur J Hum Genet. 2015. PMID: 25118026 Free PMC article.

2

Genotype-phenotype analysis of recombinant chromosome 4 syndrome: an array-CGH study and literature review.

Hemmat M, Hemmat O, Anguiano A, Boyar FZ, El Naggar M, Wang JC, Wang BT, Sahoo T, Owen R, Haddadin M. Hemmat M, et al. Among authors: owen r. Mol Cytogenet. 2013 May 2;6(1):17. doi: 10.1186/1755-8166-6-17. Mol Cytogenet. 2013. PMID: 23639048 Free PMC article.

3

Mosaic isochromosome 15q and maternal uniparental isodisomy for chromosome 15 in a patient with morbid obesity and variant PWS-like phenotype.

Wang JC, Vaccarello-Cruz M, Ross L, Owen R, Pratt VM, Lightman K, Liu Y, Hafezi K, Cherif D, Sahoo T. Wang JC, et al. Among authors: owen r. Am J Med Genet A. 2013 Jul;161A(7):1695-701. doi: 10.1002/ajmg.a.35939. Epub 2013 May 17. Am J Med Genet A. 2013. PMID: 23686718

4

Abnormalities in spontaneous abortions detected by G-banding and chromosomal microarray analysis (CMA) at a national reference laboratory.

Wang BT, Chong TP, Boyar FZ, Kopita KA, Ross LP, El-Naggar MM, Sahoo T, Wang JC, Hemmat M, Haddadin MH, Owen R, Anguiano AL. Wang BT, et al. Among authors: owen r. Mol Cytogenet. 2014 May 22;7:33. doi: 10.1186/1755-8166-7-33. eCollection 2014. Mol Cytogenet. 2014. PMID: 24914406 Free PMC article.

5

Inherited and de novo 22q11.2 distal duplications in two patients with autistic features, speech delay and no dysmorphology.

Hantash FM, Wang BT, Owen R, Ross LP, Mahon LW, Boyar FZ, Anguiano A, Strom CM. Hantash FM, et al. Among authors: owen r. J Pediatr Genet. 2012 Jun;1(2):115-24. doi: 10.3233/PGE-2012-019. J Pediatr Genet. 2012. PMID: 27625811 Free PMC article.

6

Enrichment of small pathogenic deletions at chromosome 9p24.3 and 9q34.3 involving DOCK8, KANK1, EHMT1 genes identified by using high-resolution oligonucleotide-single nucleotide polymorphism array analysis.

Wang JC, Mahon LW, Ross LP, Anguiano A, Owen R, Boyar FZ. Wang JC, et al. Among authors: owen r. Mol Cytogenet. 2016 Nov 15;9:82. doi: 10.1186/s13039-016-0291-3. eCollection 2016. Mol Cytogenet. 2016. PMID: 27891178 Free PMC article.

7

Improving the Accuracy of Prenatal Screening with DNA Copy-Number Analysis.

Strom CM, Maxwell MD, Owen R. Strom CM, et al. Among authors: owen r. N Engl J Med. 2017 Jan 12;376(2):188-189. doi: 10.1056/NEJMc1604205. N Engl J Med. 2017. PMID: 28076705 No abstract available.

8

Maternal chromosome Xp deletion identified by prenatal cell-free DNA screening.

Ilagan BJ, Maxwell MD, Fisher BM, Milanovich J, Owen R, Anderson B, Zhang K, Strom CM. Ilagan BJ, et al. Among authors: owen r. Prenat Diagn. 2017 Sep;37(9):935-937. doi: 10.1002/pd.5103. Epub 2017 Jul 25. Prenat Diagn. 2017. PMID: 28654736 No abstract available.

9

Clinical array comparative genomic hybridization: a new paradigm.

Chan P, Anguiano A, Hensley K, Keo N, Liu Y, Sarno R, Strom CM, Owen R. Chan P, et al. Among authors: owen r. Expert Opin Med Diagn. 2008 Apr;2(4):449-59. doi: 10.1517/17530059.2.4.449. Expert Opin Med Diagn. 2008. PMID: 23495710

10

Molecular combing compared to Southern blot for measuring D4Z4 contractions in FSHD.

Vasale J, Boyar F, Jocson M, Sulcova V, Chan P, Liaquat K, Hoffman C, Meservey M, Chang I, Tsao D, Hensley K, Liu Y, Owen R, Braastad C, Sun W, Walrafen P, Komatsu J, Wang JC, Bensimon A, Anguiano A, Jaremko M, Wang Z, Batish S, Strom C, Higgins J. Vasale J, et al. Among authors: owen r. Neuromuscul Disord. 2015 Dec;25(12):945-51. doi: 10.1016/j.nmd.2015.08.008. Epub 2015 Aug 21. Neuromuscul Disord. 2015. PMID: 26420234

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