Literature DB >> 20572109

The future of prenatal cytogenetic diagnostics: a personal perspective.

Charles Lee1.   

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Year:  2010        PMID: 20572109      PMCID: PMC2893288          DOI: 10.1002/pd.2547

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


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  20 in total

1.  Microarray analysis of cell-free fetal DNA in amniotic fluid: a prenatal molecular karyotype.

Authors:  Paige B Larrabee; Kirby L Johnson; Ekaterina Pestova; Madhuri Lucas; Kim Wilber; Erik S LeShane; Umadevi Tantravahi; Janet M Cowan; Diana W Bianchi
Journal:  Am J Hum Genet       Date:  2004-07-13       Impact factor: 11.025

2.  Prenatal detection of unbalanced chromosomal rearrangements by array CGH.

Authors:  L Rickman; H Fiegler; C Shaw-Smith; R Nash; V Cirigliano; G Voglino; B L Ng; C Scott; J Whittaker; M Adinolfi; N P Carter; M Bobrow
Journal:  J Med Genet       Date:  2005-09-30       Impact factor: 6.318

Review 3.  Copy number variations and clinical cytogenetic diagnosis of constitutional disorders.

Authors:  Charles Lee; A John Iafrate; Arthur R Brothman
Journal:  Nat Genet       Date:  2007-07       Impact factor: 38.330

4.  Runs of homozygosity in European populations.

Authors:  Ruth McQuillan; Anne-Louise Leutenegger; Rehab Abdel-Rahman; Christopher S Franklin; Marijana Pericic; Lovorka Barac-Lauc; Nina Smolej-Narancic; Branka Janicijevic; Ozren Polasek; Albert Tenesa; Andrew K Macleod; Susan M Farrington; Pavao Rudan; Caroline Hayward; Veronique Vitart; Igor Rudan; Sarah H Wild; Malcolm G Dunlop; Alan F Wright; Harry Campbell; James F Wilson
Journal:  Am J Hum Genet       Date:  2008-08-28       Impact factor: 11.025

5.  Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances.

Authors:  S Solinas-Toldo; S Lampel; S Stilgenbauer; J Nickolenko; A Benner; H Döhner; T Cremer; P Lichter
Journal:  Genes Chromosomes Cancer       Date:  1997-12       Impact factor: 5.006

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.  Somatic mosaicism for copy number variation in differentiated human tissues.

Authors:  Arkadiusz Piotrowski; Carl E G Bruder; Robin Andersson; Teresita Diaz de Ståhl; Uwe Menzel; Johanna Sandgren; Andrzej Poplawski; Desiree von Tell; Chiquito Crasto; Adam Bogdan; Rafal Bartoszewski; Zsuzsa Bebok; Maciej Krzyzanowski; Zbigniew Jankowski; E Christopher Partridge; Jan Komorowski; Jan P Dumanski
Journal:  Hum Mutat       Date:  2008-09       Impact factor: 4.878

8.  High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays.

Authors:  D Pinkel; R Segraves; D Sudar; S Clark; I Poole; D Kowbel; C Collins; W L Kuo; C Chen; Y Zhai; S H Dairkee; B M Ljung; J W Gray; D G Albertson
Journal:  Nat Genet       Date:  1998-10       Impact factor: 38.330

9.  Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization.

Authors:  Trilochan Sahoo; Sau Wai Cheung; Patricia Ward; Sandra Darilek; Ankita Patel; Daniela del Gaudio; Sung Hae L Kang; Seema R Lalani; Jiangzhen Li; Sallie McAdoo; Audrey Burke; Chad A Shaw; Pawel Stankiewicz; A Craig Chinault; Ignatia B Van den Veyver; Benjamin B Roa; Arthur L Beaudet; Christine M Eng
Journal:  Genet Med       Date:  2006-11       Impact factor: 8.822

10.  Single-cell chromosomal imbalances detection by array CGH.

Authors:  Cedric Le Caignec; Claudia Spits; Karen Sermon; Martine De Rycke; Bernard Thienpont; Sophie Debrock; Catherine Staessen; Yves Moreau; Jean-Pierre Fryns; Andre Van Steirteghem; Inge Liebaers; Joris R Vermeesch
Journal:  Nucleic Acids Res       Date:  2006-05-12       Impact factor: 16.971

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