Fan Y - Search Results

1

A novel sporadic 614-Kb duplication of the 22q11.2 chromosome in a child with amyoplasia.

Liewluck T, Sacharow SJ, Fan Y, Lopez-Alberola R. Liewluck T, et al. Among authors: fan y. J Child Neurol. 2011 Aug;26(8):1005-8. doi: 10.1177/0883073810394846. Epub 2011 May 13. J Child Neurol. 2011. PMID: 21572057

2

Familial 16q24.3 microdeletion involving ANKRD11 causes a KBG-like syndrome.

Sacharow S, Li D, Fan YS, Tekin M. Sacharow S, et al. Am J Med Genet A. 2012 Mar;158A(3):547-52. doi: 10.1002/ajmg.a.34436. Epub 2012 Feb 3. Am J Med Genet A. 2012. PMID: 22307766

3

Detection of pathogenic gene copy number variations in patients with mental retardation by genomewide oligonucleotide array comparative genomic hybridization.

Fan YS, Jayakar P, Zhu H, Barbouth D, Sacharow S, Morales A, Carver V, Benke P, Mundy P, Elsas LJ. Fan YS, et al. Hum Mutat. 2007 Nov;28(11):1124-32. doi: 10.1002/humu.20581. Hum Mutat. 2007. PMID: 17621639

4

Frequent detection of parental consanguinity in children with developmental disorders by a combined CGH and SNP microarray.

Fan YS, Ouyang X, Peng J, Sacharow S, Tekin M, Barbouth D, Bodamer O, Yusupov R, Navarrete C, Heller AH, Pena SDj. Fan YS, et al. Mol Cytogenet. 2013 Sep 20;6(1):38. doi: 10.1186/1755-8166-6-38. Mol Cytogenet. 2013. PMID: 24053112 Free PMC article.

5

Co-existence of other copy number variations with 22q11.2 deletion or duplication: a modifier for variable phenotypes of the syndrome?

Li D, Tekin M, Buch M, Fan YS. Li D, et al. Mol Cytogenet. 2012 Apr 9;5(1):18. doi: 10.1186/1755-8166-5-18. Mol Cytogenet. 2012. PMID: 22487416 Free PMC article.

6

Monosomy chromosome 21 compensated by 21q22.11q22.3 duplication in a case with small size and minor anomalies.

Su M, Benke PJ, Bademci G, Cengiz FB, Ouyang X, Peng J, Casas CE, Tekin M, Fan YS. Su M, et al. Mol Cytogenet. 2018 Aug 1;11:43. doi: 10.1186/s13039-018-0390-4. eCollection 2018. Mol Cytogenet. 2018. PMID: 30123325 Free PMC article.

7

EUS-FNA with rescue fluorescence in situ hybridization for the diagnosis of pancreatic carcinoma in patients with inconclusive on-site cytopathology results.

Kubiliun N, Ribeiro A, Fan YS, Rocha-Lima CM, Sleeman D, Merchan J, Barkin J, Levi J. Kubiliun N, et al. Gastrointest Endosc. 2011 Sep;74(3):541-7. doi: 10.1016/j.gie.2011.04.043. Epub 2011 Jul 12. Gastrointest Endosc. 2011. PMID: 21752364

8

Searching for mammary analogue [corrected] secretory carcinoma of salivary gland among its mimics.

Pinto A, Nosé V, Rojas C, Fan YS, Gomez-Fernandez C. Pinto A, et al. Mod Pathol. 2014 Jan;27(1):30-7. doi: 10.1038/modpathol.2013.84. Epub 2013 Jun 28. Mod Pathol. 2014. PMID: 23807775 Free article.

9

Endoscopic ultrasound guided fine needle aspiration with fluorescence in situ hybridization analysis in 104 patients with pancreatic mass.

Ribeiro A, Peng J, Casas C, Fan YS. Ribeiro A, et al. J Gastroenterol Hepatol. 2014 Aug;29(8):1654-8. doi: 10.1111/jgh.12575. J Gastroenterol Hepatol. 2014. PMID: 24628622

10

HER2 FISH classification of equivocal HER2 IHC breast cancers with use of the 2013 ASCO/CAP practice guideline.

Fan YS, Casas CE, Peng J, Watkins M, Fan L, Chapman J, Ikpatt OF, Gomez C, Zhao W, Reis IM. Fan YS, et al. Breast Cancer Res Treat. 2016 Feb;155(3):457-62. doi: 10.1007/s10549-016-3717-z. Epub 2016 Feb 19. Breast Cancer Res Treat. 2016. PMID: 26895325

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