Lu XY - Search Results

1

Genomic imbalances in neonates with birth defects: high detection rates by using chromosomal microarray analysis.

Lu XY, Phung MT, Shaw CA, Pham K, Neil SE, Patel A, Sahoo T, Bacino CA, Stankiewicz P, Kang SH, Lalani S, Chinault AC, Lupski JR, Cheung SW, Beaudet AL. Lu XY, et al. Pediatrics. 2008 Dec;122(6):1310-8. doi: 10.1542/peds.2008-0297. Pediatrics. 2008. PMID: 19047251 Free PMC article.

2

Identification of chromosome abnormalities in subtelomeric regions by microarray analysis: a study of 5,380 cases.

Shao L, Shaw CA, Lu XY, Sahoo T, Bacino CA, Lalani SR, Stankiewicz P, Yatsenko SA, Li Y, Neill S, Pursley AN, Chinault AC, Patel A, Beaudet AL, Lupski JR, Cheung SW. Shao L, et al. Among authors: lu xy. Am J Med Genet A. 2008 Sep 1;146A(17):2242-51. doi: 10.1002/ajmg.a.32399. Am J Med Genet A. 2008. PMID: 18663743 Free PMC article.

3

Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGH.

Bi W, Breman AM, Venable SF, Eng PA, Sahoo T, Lu XY, Patel A, Beaudet AL, Cheung SW, White LD. Bi W, et al. Among authors: lu xy. Prenat Diagn. 2008 Oct;28(10):943-9. doi: 10.1002/pd.2087. Prenat Diagn. 2008. PMID: 18792925

4

Increased LIS1 expression affects human and mouse brain development.

Bi W, Sapir T, Shchelochkov OA, Zhang F, Withers MA, Hunter JV, Levy T, Shinder V, Peiffer DA, Gunderson KL, Nezarati MM, Shotts VA, Amato SS, Savage SK, Harris DJ, Day-Salvatore DL, Horner M, Lu XY, Sahoo T, Yanagawa Y, Beaudet AL, Cheung SW, Martinez S, Lupski JR, Reiner O. Bi W, et al. Among authors: lu xy. Nat Genet. 2009 Feb;41(2):168-77. doi: 10.1038/ng.302. Epub 2009 Jan 11. Nat Genet. 2009. PMID: 19136950 Free PMC article.

5

Array-CGH analysis of cell-free fetal DNA in 10 mL of amniotic fluid supernatant.

Lapaire O, Lu XY, Johnson KL, Jarrah Z, Stroh H, Cowan JM, Tantravahi U, Bianchi DW. Lapaire O, et al. Among authors: lu xy. Prenat Diagn. 2007 Jul;27(7):616-21. doi: 10.1002/pd.1752. Prenat Diagn. 2007. PMID: 17510923

6

A familial Cri-du-Chat/5p deletion syndrome resulted from rare maternal complex chromosomal rearrangements (CCRs) and/or possible chromosome 5p chromothripsis.

Gu H, Jiang JH, Li JY, Zhang YN, Dong XS, Huang YY, Son XM, Lu X, Chen Z. Gu H, et al. PLoS One. 2013 Oct 15;8(10):e76985. doi: 10.1371/journal.pone.0076985. eCollection 2013. PLoS One. 2013. PMID: 24143197 Free PMC article.

7

Publisher Correction: Epigenetic alterations of repeated relapses in patient-matched childhood ependymomas.

Zhao S, Li J, Zhang H, Qi L, Du Y, Kogiso M, Braun FK, Xiao S, Huang Y, Li J, Teo WY, Lindsay H, Baxter P, Su JMF, Adesina A, Laczik M, Genevini P, Veillard AC, Schvartzman S, Berguet G, Ding SR, Du L, Stephan C, Yang J, Davies PJA, Lu X, Chintagumpala M, Parsons DW, Perlaky L, Xia YF, Man TK, Huang Y, Sun D, Li XN. Zhao S, et al. Nat Commun. 2022 Dec 22;13(1):7871. doi: 10.1038/s41467-022-35539-0. Nat Commun. 2022. PMID: 36550163 Free PMC article. No abstract available.

8

Effects of leading-edge serration shape on noise reduction in rod-airfoil interactions.

Yu FY, Wan ZH, Hu YS, Sun DJ, Lu XY. Yu FY, et al. Among authors: lu xy. J Acoust Soc Am. 2025 Jan 1;157(1):215-233. doi: 10.1121/10.0034845. J Acoust Soc Am. 2025. PMID: 39812628

9

Cr-MOF composited with facet-engineered bimetallic alloys for inducing photocatalytic conversion of CO₂ to C₂H₄.

Lu XY, Wang P, Qiu ZF, Sun WY. Lu XY, et al. Chem Commun (Camb). 2025 Jan 10. doi: 10.1039/d4cc04659e. Online ahead of print. Chem Commun (Camb). 2025. PMID: 39791375

10

Added Value of Dynamic Contrast-Enhanced Ultrasound Analysis for Differential Diagnosis of Small (≤20 mm) Solid Pancreatic Lesions.

Lu XY, Cao JY, Chen S, Wang Y, Wei L, Gong W, Lou WH, Dong Y. Lu XY, et al. Ultrasound Med Biol. 2025 Jan 2:S0301-5629(24)00439-3. doi: 10.1016/j.ultrasmedbio.2024.11.015. Online ahead of print. Ultrasound Med Biol. 2025. PMID: 39753466

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