Literature DB >> 17065419

Diagnostic genome profiling: unbiased whole genome or targeted analysis?

Joris A Veltman1, Bert B A de Vries.   

Abstract

Mesh：

Year:  2006        PMID： 17065419      PMCID： PMC1876178          DOI： 10.2353/jmoldx.2006.060131

Source DB:  PubMed          Journal:  J Mol Diagn        ISSN： 1525-1578            Impact factor:   5.568


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  28 in total

1.  Assembly of microarrays for genome-wide measurement of DNA copy number.

Authors:  A M Snijders; N Nowak; R Segraves; S Blackwood; N Brown; J Conroy; G Hamilton; A K Hindle; B Huey; K Kimura; S Law; K Myambo; J Palmer; B Ylstra; J P Yue; J W Gray; A N Jain; D Pinkel; D G Albertson
Journal:  Nat Genet       Date:  2001-11       Impact factor: 38.330

2.  DNA microarrays for comparative genomic hybridization based on DOP-PCR amplification of BAC and PAC clones.

Authors:  Heike Fiegler; Philippa Carr; Eleanor J Douglas; Deborah C Burford; Sarah Hunt; Carol E Scott; James Smith; David Vetrie; Patricia Gorman; Ian P M Tomlinson; Nigel P Carter
Journal:  Genes Chromosomes Cancer       Date:  2003-04       Impact factor: 5.006

3.  A set of BAC clones spanning the human genome.

Authors:  Martin Krzywinski; Ian Bosdet; Duane Smailus; Readman Chiu; Carrie Mathewson; Natasja Wye; Sarah Barber; Mabel Brown-John; Susanna Chan; Steve Chand; Alison Cloutier; Noreen Girn; Darlene Lee; Amara Masson; Michael Mayo; Teika Olson; Pawan Pandoh; Anna-Liisa Prabhu; Eric Schoenmakers; Miranda Tsai; Donna Albertson; Wan Lam; Chik-On Choy; Kazutoyo Osoegawa; Shaying Zhao; Pieter J de Jong; Jacqueline Schein; Steven Jones; Marco A Marra
Journal:  Nucleic Acids Res       Date:  2004-07-09       Impact factor: 16.971

4.  A tiling resolution DNA microarray with complete coverage of the human genome.

Authors:  Adrian S Ishkanian; Chad A Malloff; Spencer K Watson; Ronald J DeLeeuw; Bryan Chi; Bradley P Coe; Antoine Snijders; Donna G Albertson; Daniel Pinkel; Marco A Marra; Victor Ling; Calum MacAulay; Wan L Lam
Journal:  Nat Genet       Date:  2004-02-15       Impact factor: 38.330

Review 5.  Application of array-based comparative genomic hybridization to clinical diagnostics.

Authors:  Bassem A Bejjani; Lisa G Shaffer
Journal:  J Mol Diagn       Date:  2006-11       Impact factor: 5.568

6.  Large-scale copy number polymorphism in the human genome.

Authors:  Jonathan Sebat; B Lakshmi; Jennifer Troge; Joan Alexander; Janet Young; Pär Lundin; Susanne Månér; Hillary Massa; Megan Walker; Maoyen Chi; Nicholas Navin; Robert Lucito; John Healy; James Hicks; Kenny Ye; Andrew Reiner; T Conrad Gilliam; Barbara Trask; Nick Patterson; Anders Zetterberg; Michael Wigler
Journal:  Science       Date:  2004-07-23       Impact factor: 47.728

7.  Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features.

Authors:  C Shaw-Smith; R Redon; L Rickman; M Rio; L Willatt; H Fiegler; H Firth; D Sanlaville; R Winter; L Colleaux; M Bobrow; N P Carter
Journal:  J Med Genet       Date:  2004-04       Impact factor: 6.318

8.  Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities.

Authors:  Lisenka E L M Vissers; Bert B A de Vries; Kazutoyo Osoegawa; Irene M Janssen; Ton Feuth; Chik On Choy; Huub Straatman; Walter van der Vliet; Erik H L P G Huys; Anke van Rijk; Dominique Smeets; Conny M A van Ravenswaaij-Arts; Nine V Knoers; Ineke van der Burgt; Pieter J de Jong; Han G Brunner; Ad Geurts van Kessel; Eric F P M Schoenmakers; Joris A Veltman
Journal:  Am J Hum Genet       Date:  2003-11-18       Impact factor: 11.025

Review 9.  Genomic microarrays in the spotlight.

Authors:  Kiran K Mantripragada; Patrick G Buckley; Teresita Diaz de Ståhl; Jan P Dumanski
Journal:  Trends Genet       Date:  2004-02       Impact factor: 11.639

10.  Integration of cytogenetic landmarks into the draft sequence of the human genome.

Authors:  V G Cheung; N Nowak; W Jang; I R Kirsch; S Zhao; X N Chen; T S Furey; U J Kim; W L Kuo; M Olivier; J Conroy; A Kasprzyk; H Massa; R Yonescu; S Sait; C Thoreen; A Snijders; E Lemyre; J A Bailey; A Bruzel; W D Burrill; S M Clegg; S Collins; P Dhami; C Friedman; C S Han; S Herrick; J Lee; A H Ligon; S Lowry; M Morley; S Narasimhan; K Osoegawa; Z Peng; I Plajzer-Frick; B J Quade; D Scott; K Sirotkin; A A Thorpe; J W Gray; J Hudson; D Pinkel; T Ried; L Rowen; G L Shen-Ong; R L Strausberg; E Birney; D F Callen; J F Cheng; D R Cox; N A Doggett; N P Carter; E E Eichler; D Haussler; J R Korenberg; C C Morton; D Albertson; G Schuler; P J de Jong; B J Trask
Journal:  Nature       Date:  2001-02-15       Impact factor: 49.962
View more
  10 in total

1.  Diagnostic array comparative genomic hybridization: is it ready for prime time?

Authors:  Susan J Done; Susan B Done
Journal:  J Mol Diagn       Date:  2006-11       Impact factor: 5.568

2.  Targeted versus whole-genome array comparative genome hybridization: The Atlantic divide.

Authors:  Jean Amos Wilson; David Barton
Journal:  J Mol Diagn       Date:  2007-04       Impact factor: 5.568

3.  Whole-genome array comparative genome hybridization: the preferred diagnostic choice in postnatal clinical cytogenetics.

Authors:  Joris A Veltman; Bert B A de Vries
Journal:  J Mol Diagn       Date:  2007-04       Impact factor: 5.568

4.  Microarrays as a diagnostic tool in prenatal screening strategies: ethical reflection.

Authors:  Antina de Jong; Wybo J Dondorp; Merryn V E Macville; Christine E M de Die-Smulders; Jan M M van Lith; Guido M W R de Wert
Journal:  Hum Genet       Date:  2014-02       Impact factor: 4.132

5.  Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow.

Authors:  Malgorzata Srebniak; Marjan Boter; Grétel Oudesluijs; Marieke Joosten; Lutgarde Govaerts; Diane Van Opstal; Robert-Jan H Galjaard
Journal:  Eur J Hum Genet       Date:  2011-06-22       Impact factor: 4.246

Review 6.  Anaplastic thyroid cancer: molecular pathogenesis and emerging therapies.

Authors:  Robert C Smallridge; Laura A Marlow; John A Copland
Journal:  Endocr Relat Cancer       Date:  2008-11-05       Impact factor: 5.678

Review 7.  Novel microdeletion syndromes detected by chromosome microarrays.

Authors:  Anne M Slavotinek
Journal:  Hum Genet       Date:  2008-05-30       Impact factor: 4.132

8.  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

9.  Bacterial artificial chromosome-emulation oligonucleotide arrays for targeted clinical array-comparative genomic hybridization analyses.

Authors:  Zhishuo Ou; Sung-Hae L Kang; Chad A Shaw; Condie E Carmack; Lisa D White; Ankita Patel; Arthur L Beaudet; Sau Wai Cheung; A Craig Chinault
Journal:  Genet Med       Date:  2008-04       Impact factor: 8.822

10.  Diagnosing idiopathic learning disability: a cost-effectiveness analysis of microarray technology in the National Health Service of the United Kingdom.

Authors:  Sarah Wordsworth; James Buchanan; Regina Regan; Val Davison; Kim Smith; Sara Dyer; Carolyn Campbell; Edward Blair; Eddy Maher; Jenny Taylor; Samantha J L Knight
Journal:  Genomic Med       Date:  2007-06-05
  10 in total

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