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Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles

Bruder, Carl E G (author)
Piotrowski, Arkadiusz (author)
Gijsbers, Antoinet A C J (author)
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Andersson, Robin (author)
Uppsala universitet,Centrum för bioinformatik
Erickson, Stephen (author)
de Ståhl, Teresita Diaz (author)
Uppsala universitet,Institutionen för genetik och patologi
Menzel, Uwe (author)
Uppsala universitet,Institutionen för genetik och patologi
Sandgren, Johanna (author)
von Tell, Desiree (author)
Poplawski, Andrzej (author)
Crowley, Michael (author)
Crasto, Chiquito (author)
Partridge, E Christopher (author)
Tiwari, Hemant (author)
Allison, David B (author)
Komorowski, Jan (author)
Uppsala universitet,Centrum för bioinformatik
van Ommen, Gert-Jan B (author)
Boomsma, Dorret I (author)
Pedersen, Nancy L (author)
Karolinska Institutet
den Dunnen, Johan T (author)
Wirdefeldt, Karin (author)
Karolinska Institutet
Dumanski, Jan P (author)
Uppsala universitet,Institutionen för genetik och patologi
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 (creator_code:org_t)
Elsevier BV, 2008
2008
English.
In: American Journal of Human Genetics. - : Elsevier BV. - 0002-9297 .- 1537-6605. ; 82:3, s. 763-71
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The exploration of copy-number variation (CNV), notably of somatic cells, is an understudied aspect of genome biology. Any differences in the genetic makeup between twins derived from the same zygote represent an irrefutable example of somatic mosaicism. We studied 19 pairs of monozygotic twins with either concordant or discordant phenotype by using two platforms for genome-wide CNV analyses and showed that CNVs exist within pairs in both groups. These findings have an impact on our views of genotypic and phenotypic diversity in monozygotic twins and suggest that CNV analysis in phenotypically discordant monozygotic twins may provide a powerful tool for identifying disease-predisposition loci. Our results also imply that caution should be exercised when interpreting disease causality of de novo CNVs found in patients based on analysis of a single tissue in routine disease-related DNA diagnostics.

Subject headings

NATURVETENSKAP  -- Biologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences (hsv//eng)

Keyword

Biology
Biologi

Publication and Content Type

ref (subject category)
art (subject category)

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