Sahoo T - 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: sahoo t. 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

Concurrent triplication and uniparental isodisomy: evidence for microhomology-mediated break-induced replication model for genomic rearrangements.

Sahoo T, Wang JC, Elnaggar MM, Sanchez-Lara P, Ross LP, Mahon LW, Hafezi K, Deming A, Hinman L, Bruno Y, Bartley JA, Liehr T, Anguiano A, Jones M. Sahoo T, et al. Eur J Hum Genet. 2015 Jan;23(1):61-6. doi: 10.1038/ejhg.2014.53. Epub 2014 Apr 9. Eur J Hum Genet. 2015. PMID: 24713661 Free PMC article.

3

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: sahoo t. Mol Cytogenet. 2014 May 22;7:33. doi: 10.1186/1755-8166-7-33. eCollection 2014. Mol Cytogenet. 2014. PMID: 24914406 Free PMC article.

4

Discordant noninvasive prenatal testing and cytogenetic results: a study of 109 consecutive cases.

Wang JC, Sahoo T, Schonberg S, Kopita KA, Ross L, Patek K, Strom CM. Wang JC, et al. Among authors: sahoo t. Genet Med. 2015 Mar;17(3):234-6. doi: 10.1038/gim.2014.92. Epub 2014 Aug 7. Genet Med. 2015. PMID: 25101914 Free article.

5

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: sahoo t. Mol Cytogenet. 2013 May 2;6(1):17. doi: 10.1186/1755-8166-6-17. Mol Cytogenet. 2013. PMID: 23639048 Free PMC article.

6

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: sahoo t. 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

7

Constitutional chromothripsis involving chromosome 19 in a child with subtle dysmorphic features.

Wang JC, Fisker T, Sahoo T. Wang JC, et al. Among authors: sahoo t. Am J Med Genet A. 2015 Apr;167A(4):910-3. doi: 10.1002/ajmg.a.36962. Epub 2015 Mar 3. Am J Med Genet A. 2015. PMID: 25736334 No abstract available.

8

Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12.

Nagamani SC, Erez A, Shen J, Li C, Roeder E, Cox S, Karaviti L, Pearson M, Kang SH, Sahoo T, Lalani SR, Stankiewicz P, Sutton VR, Cheung SW. Nagamani SC, et al. Among authors: sahoo t. Eur J Hum Genet. 2010 Mar;18(3):278-84. doi: 10.1038/ejhg.2009.174. Epub 2009 Oct 21. Eur J Hum Genet. 2010. PMID: 19844256 Free PMC article.

9

Identification of novel deletions of 15q11q13 in Angelman syndrome by array-CGH: molecular characterization and genotype-phenotype correlations.

Sahoo T, Bacino CA, German JR, Shaw CA, Bird LM, Kimonis V, Anselm I, Waisbren S, Beaudet AL, Peters SU. Sahoo T, et al. Eur J Hum Genet. 2007 Sep;15(9):943-9. doi: 10.1038/sj.ejhg.5201859. Epub 2007 May 23. Eur J Hum Genet. 2007. PMID: 17522620 Free article.

10

Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader-Willi syndrome.

Duker AL, Ballif BC, Bawle EV, Person RE, Mahadevan S, Alliman S, Thompson R, Traylor R, Bejjani BA, Shaffer LG, Rosenfeld JA, Lamb AN, Sahoo T. Duker AL, et al. Among authors: sahoo t. Eur J Hum Genet. 2010 Nov;18(11):1196-201. doi: 10.1038/ejhg.2010.102. Epub 2010 Jun 30. Eur J Hum Genet. 2010. PMID: 20588305 Free PMC article.

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