Literature DB >> 15338609

Genome-wide detection and analysis of recent segmental duplications within mammalian organisms.

J A Bailey1, E E Eichler.   

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Year:  2003        PMID: 15338609     DOI: 10.1101/sqb.2003.68.115

Source DB:  PubMed          Journal:  Cold Spring Harb Symp Quant Biol        ISSN: 0091-7451


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  11 in total

1.  Detection of genotyping errors and pseudo-SNPs via deviations from Hardy-Weinberg equilibrium.

Authors:  Suzanne M Leal
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Review 2.  Explaining human uniqueness: genome interactions with environment, behaviour and culture.

Authors:  Ajit Varki; Daniel H Geschwind; Evan E Eichler
Journal:  Nat Rev Genet       Date:  2008-10       Impact factor: 53.242

3.  Mesangioproliferative glomerulonephritis in an infant with Prader-Willi syndrome.

Authors:  N Printza; E Bersos; D Zafeiriou; M Leontsini; M Stamou; F Papachristou
Journal:  Hippokratia       Date:  2009-04       Impact factor: 0.471

4.  Evolutionary dynamics of segmental duplications from human Y-chromosomal euchromatin/heterochromatin transition regions.

Authors:  Stefan Kirsch; Claudia Münch; Zhaoshi Jiang; Ze Cheng; Lin Chen; Christiane Batz; Evan E Eichler; Werner Schempp
Journal:  Genome Res       Date:  2008-04-29       Impact factor: 9.043

5.  De novo identification of LTR retrotransposons in eukaryotic genomes.

Authors:  Mina Rho; Jeong-Hyeon Choi; Sun Kim; Michael Lynch; Haixu Tang
Journal:  BMC Genomics       Date:  2007-04-03       Impact factor: 3.969

6.  Gene synteny comparisons between different vertebrates provide new insights into breakage and fusion events during mammalian karyotype evolution.

Authors:  Claus Kemkemer; Matthias Kohn; David N Cooper; Lutz Froenicke; Josef Högel; Horst Hameister; Hildegard Kehrer-Sawatzki
Journal:  BMC Evol Biol       Date:  2009-04-24       Impact factor: 3.260

7.  Parental imbalances involving chromosomes 15q and 22q may predispose to the formation of de novo pathogenic microdeletions and microduplications in the offspring.

Authors:  Valeria Capra; Samantha Mascelli; Maria Luisa Garrè; Paolo Nozza; Carlotta Vaccari; Lara Bricco; Frédérique Sloan-Béna; Stefania Gimelli; Cristina Cuoco; Giorgio Gimelli; Elisa Tassano
Journal:  PLoS One       Date:  2013-03-06       Impact factor: 3.240

8.  Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region.

Authors:  Yong-Hui Jiang; Kekio Wauki; Qian Liu; Jan Bressler; Yanzhen Pan; Catherine D Kashork; Lisa G Shaffer; Arthur L Beaudet
Journal:  BMC Genomics       Date:  2008-01-28       Impact factor: 3.969

9.  Evolutionary analysis of the highly dynamic CHEK2 duplicon in anthropoids.

Authors:  Claudia Münch; Stefan Kirsch; António M G Fernandes; Werner Schempp
Journal:  BMC Evol Biol       Date:  2008-10-02       Impact factor: 3.260

10.  Complex evolution of a Y-chromosomal double homeobox 4 (DUX4)-related gene family in hominoids.

Authors:  Julia Schmidt; Stefan Kirsch; Gudrun A Rappold; Werner Schempp
Journal:  PLoS One       Date:  2009-04-30       Impact factor: 3.240

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