Literature DB >> 19287164

Copy number variation and mosaicism.

A J Notini1, J M Craig, S J White.   

Abstract

Mosaicism is the presence of cells within an organism that have a different genetic composition despite deriving from a single zygote. The consequence of this depends on the number and type of cells that are affected as well as the specific DNA involved. There are several diseases where mosaicism is known to occur, but the currently observed frequency is presumably an underestimation due to the difficulty of detecting changes in only a percentage of cells. Recent advances in technology have provided a greater insight into the frequency and mechanisms of mosaicism in all forms. This review will cover the different techniques that can be used for detecting copy number variation (CNV) in mosaic form, and describe some of the insights that different diseases have given on the true frequencies and mechanisms responsible for somatic rearrangements. It will conclude with a discussion of the implications of the recent description of CNV in identical twins, and what remains to be elucidated in the world of mosaic CNV. Copyright 2009 S. Karger AG, Basel.

Mesh:

Year:  2009        PMID: 19287164     DOI: 10.1159/000184717

Source DB:  PubMed          Journal:  Cytogenet Genome Res        ISSN: 1424-8581            Impact factor:   1.636


  25 in total

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Authors:  Stefan White; Jacqueline Hewitt; Erin Turbitt; Yvonne van der Zwan; Remko Hersmus; Stenvert Drop; Peter Koopman; Vincent Harley; Martine Cools; Leendert Looijenga; Andrew Sinclair
Journal:  Eur J Hum Genet       Date:  2011-11-09       Impact factor: 4.246

2.  Copy number detection in discordant monozygotic twins of Congenital Diaphragmatic Hernia (CDH) and Esophageal Atresia (EA) cohorts.

Authors:  Danielle Veenma; Erwin Brosens; Elisabeth de Jong; Cees van de Ven; Connie Meeussen; Titia Cohen-Overbeek; Marjan Boter; Hubertus Eussen; Hannie Douben; Dick Tibboel; Annelies de Klein
Journal:  Eur J Hum Genet       Date:  2011-11-09       Impact factor: 4.246

3.  New mutations and intellectual function.

Authors:  James R Lupski
Journal:  Nat Genet       Date:  2010-12       Impact factor: 38.330

4.  TGFBR2 deletion in a 20-month-old female with developmental delay and microcephaly.

Authors:  Ian M Campbell; Katarzyna E Kolodziejska; Michael M Quach; Varina Louise Wolf; Sau Wai Cheung; Seema R Lalani; Melissa B Ramocki; Pawel Stankiewicz
Journal:  Am J Med Genet A       Date:  2011-05-12       Impact factor: 2.802

5.  Mosaic uniparental disomies and aneuploidies as large structural variants of the human genome.

Authors:  Benjamín Rodríguez-Santiago; Núria Malats; Nathaniel Rothman; Lluís Armengol; Montse Garcia-Closas; Manolis Kogevinas; Olaya Villa; Amy Hutchinson; Julie Earl; Gaëlle Marenne; Kevin Jacobs; Daniel Rico; Adonina Tardón; Alfredo Carrato; Gilles Thomas; Alfonso Valencia; Debra Silverman; Francisco X Real; Stephen J Chanock; Luis A Pérez-Jurado
Journal:  Am J Hum Genet       Date:  2010-07-09       Impact factor: 11.025

6.  Missing genetic variations in GNE myopathy: rearrangement hotspots encompassing 5'UTR and founder allele.

Authors:  Wenhua Zhu; Satomi Mitsuhashi; Takahiro Yonekawa; Satoru Noguchi; Josiah Chai Yui Huei; Atchayaram Nalini; Veeramani Preethish-Kumar; Masayoshi Yamamoto; Kenji Murakata; Madoka Mori-Yoshimura; Sachiko Kamada; Hiroyuki Yahikozawa; Masato Karasawa; Seigo Kimura; Fumitada Yamashita; Ichizo Nishino
Journal:  J Hum Genet       Date:  2016-11-10       Impact factor: 3.172

7.  Parental somatic mosaicism for CNV deletions - A need for more sensitive and precise detection methods in clinical diagnostics settings.

Authors:  Qian Liu; Justyna A Karolak; Christopher M Grochowski; Theresa A Wilson; Jill A Rosenfeld; Carlos A Bacino; Seema R Lalani; Ankita Patel; Amy Breman; Janice L Smith; Sau Wai Cheung; James R Lupski; Weimin Bi; Pawel Stankiewicz
Journal:  Genomics       Date:  2020-05-06       Impact factor: 5.736

Review 8.  Genetic, environmental and stochastic factors in monozygotic twin discordance with a focus on epigenetic differences.

Authors:  Witold Czyz; Julia M Morahan; George C Ebers; Sreeram V Ramagopalan
Journal:  BMC Med       Date:  2012-08-17       Impact factor: 8.775

9.  Association between reduced copy-number at T-cell receptor gamma (TCRgamma) and childhood allergic asthma: A possible role for somatic mosaicism.

Authors:  Kyle M Walsh; Michael B Bracken; William K Murk; Josephine Hoh; Andrew T Dewan
Journal:  Mutat Res       Date:  2010-05-27       Impact factor: 2.433

10.  Quantitative Assessment of Parental Somatic Mosaicism for Copy-Number Variant (CNV) Deletions.

Authors:  Qian Liu; Christopher M Grochowski; Weimin Bi; James R Lupski; Paweł Stankiewicz
Journal:  Curr Protoc Hum Genet       Date:  2020-06
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