Literature DB >> 17873655

Microarray analysis for constitutional cytogenetic abnormalities.

Lisa G Shaffer1, Arthur L Beaudet, Arthur R Brothman, Betsy Hirsch, Brynn Levy, Christa Lese Martin, James T Mascarello, Kathleen W Rao.   

Abstract

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Year:  2007        PMID： 17873655     DOI： 10.1097/gim.0b013e31814ce3d9

Source DB:  PubMed          Journal:  Genet Med        ISSN： 1098-3600            Impact factor:   8.822


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  15 in total

1.  Use of array genomic hybridization technology for constitutional genetic diagnosis in Canada.

Authors:  Alessandra Mv Duncan; Bernard Chodirker
Journal:  Paediatr Child Health       Date:  2011-04       Impact factor: 2.253

2.  Genomic characterization of prenatally detected chromosomal structural abnormalities using oligonucleotide array comparative genomic hybridization.

Authors:  Peining Li; Pawel Pomianowski; Miriam S DiMaio; Joanne R Florio; Michael R Rossi; Bixia Xiang; Fang Xu; Hui Yang; Qian Geng; Jiansheng Xie; Maurice J Mahoney
Journal:  Am J Med Genet A       Date:  2011-06-10       Impact factor: 2.802

3.  Detection of Copy Number Variants by Short Multiply Aggregated Sequence Homologies.

Authors:  Vaidehi Jobanputra; Peter Andrews; Vanessa Felice; Avinash Abhyankar; Lukasz Kozon; Dino Robinson; Ferrah London; Inessa Hakker; Kazimierz Wrzeszczynski; Michael Ronemus
Journal:  J Mol Diagn       Date:  2020-10-23       Impact factor: 5.568

Review 4.  Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.

Authors:  David T Miller; Margaret P Adam; Swaroop Aradhya; Leslie G Biesecker; Arthur R Brothman; Nigel P Carter; Deanna M Church; John A Crolla; Evan E Eichler; Charles J Epstein; W Andrew Faucett; Lars Feuk; Jan M Friedman; Ada Hamosh; Laird Jackson; Erin B Kaminsky; Klaas Kok; Ian D Krantz; Robert M Kuhn; Charles Lee; James M Ostell; Carla Rosenberg; Stephen W Scherer; Nancy B Spinner; Dimitri J Stavropoulos; James H Tepperberg; Erik C Thorland; Joris R Vermeesch; Darrel J Waggoner; Michael S Watson; Christa Lese Martin; David H Ledbetter
Journal:  Am J Hum Genet       Date:  2010-05-14       Impact factor: 11.025

5.  CNV-ROC: A cost effective, computer-aided analytical performance evaluator of chromosomal microarrays.

Authors:  Corey W Goodman; Heather J Major; William D Walls; Val C Sheffield; Thomas L Casavant; Benjamin W Darbro
Journal:  J Biomed Inform       Date:  2015-01-13       Impact factor: 6.317

6.  Effects of ozone exposure during microarray posthybridization washes and scanning.

Authors:  Steve Byerly; Kyle Sundin; Rajiv Raja; Jim Stanchfield; Bassem A Bejjani; Lisa G Shaffer
Journal:  J Mol Diagn       Date:  2009-09-18       Impact factor: 5.568

7.  Microarray-based comparative genomic hybridization using sex-matched reference DNA provides greater sensitivity for detection of sex chromosome imbalances than array-comparative genomic hybridization with sex-mismatched reference DNA.

Authors:  Svetlana A Yatsenko; Chad A Shaw; Zhishuo Ou; Amber N Pursley; Ankita Patel; Weimin Bi; Sau Wai Cheung; James R Lupski; A Craig Chinault; Arthur L Beaudet
Journal:  J Mol Diagn       Date:  2009-03-26       Impact factor: 5.568

8.  Expanding diagnostic testing beyond cytogenetics: implications for birth defects research and surveillance.

Authors:  Jodi M Jackson; Charlotte M Druschel; Stuart K Shapira
Journal:  Birth Defects Res A Clin Mol Teratol       Date:  2013-11-06

9.  Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization.

Authors:  Jm Friedman; Shelin Adam; Laura Arbour; Linlea Armstrong; Agnes Baross; Patricia Birch; Cornelius Boerkoel; Susanna Chan; David Chai; Allen D Delaney; Stephane Flibotte; William T Gibson; Sylvie Langlois; Emmanuelle Lemyre; H Irene Li; Patrick MacLeod; Joan Mathers; Jacques L Michaud; Barbara C McGillivray; Millan S Patel; Hong Qian; Guy A Rouleau; Margot I Van Allen; Siu-Li Yong; Farah R Zahir; Patrice Eydoux; Marco A Marra
Journal:  BMC Genomics       Date:  2009-11-16       Impact factor: 3.969

10.  An improved method to extract DNA from 1 ml of uncultured amniotic fluid from patients at less than 16 weeks' gestation.

Authors:  Anne-Laure Mosca-Boidron; Laurence Faivre; Serge Aho; Nathalie Marle; Caroline Truntzer; Thierry Rousseau; Clémence Ragon; Muriel Payet; Christelle Thauvin-Robinet; Julien Thevenon; Salima El Chehadeh; Fréderic Huet; Paul Sagot; Francine Mugneret; Patrick Callier
Journal:  PLoS One       Date:  2013-04-02       Impact factor: 3.240
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