Literature DB >> 30355123

Copy Number Variation and Risk of Stroke.

Caspar Grond-Ginsbach1, Philipp Erhart2, Bowang Chen3, Manja Kloss1, Stefan T Engelter4,5, John W Cole6.   

Abstract

Entities:  

Keywords:  comparative genomic hybridization; genomics; incidental findings; polymorphism, single nucleotide; stroke

Mesh：

Year:  2018        PMID： 30355123      PMCID： PMC6209107          DOI： 10.1161/STROKEAHA.118.020371

Source DB:  PubMed          Journal:  Stroke        ISSN： 0039-2499            Impact factor:   7.914


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  45 in total

Review 1.  Association of cervical artery dissection with connective tissue abnormalities in skin and arteries.

Authors:  T Brandt; M Morcher; I Hausser
Journal:  Front Neurol Neurosci       Date:  2005

2.  Identification of DNA copy number aberrations by array comparative genomic hybridization in patients with ruptured intracranial aneurysms.

Authors:  Jin Soo Choi; Seong-Rim Kim; Yang-Whan Jeon; Kweon-Haeng Lee; Hyoung Kyun Rha
Journal:  J Clin Neurosci       Date:  2008-12-03       Impact factor: 1.961

Review 3.  Role of DNA copy number variation in dyslipidemias.

Authors:  Michael A Iacocca; Robert A Hegele
Journal:  Curr Opin Lipidol       Date:  2018-04       Impact factor: 4.776

4.  Detecting associations of rare variants with common diseases: collapsing or haplotyping?

Authors:  Meng Wang; Shili Lin
Journal:  Brief Bioinform       Date:  2015-01-17       Impact factor: 11.622

5.  Copy number variation in glutathione S-transferases M1 and T1 and ischemic vascular disease: four studies and meta-analyses.

Authors:  Marianne S Nørskov; Ruth Frikke-Schmidt; Steffen Loft; Henrik Sillesen; Peer Grande; Børge G Nordestgaard; Anne Tybjaerg-Hansen
Journal:  Circ Cardiovasc Genet       Date:  2011-05-11

6.  Cerebral small-vessel disease associated with COL4A1 and COL4A2 gene duplications.

Authors:  Dimitri Renard; Manuele Miné; Eva Pipiras; Pierre Labauge; Andrée Delahaye; Brigitte Benzacken; Elisabeth Tournier-Lasserve
Journal:  Neurology       Date:  2014-08-06       Impact factor: 9.910

7.  Large germline deletions and duplication in isolated cerebral cavernous malformation patients.

Authors:  U Felbor; S Gaetzner; D J Verlaan; R Vijzelaar; G A Rouleau; A M Siegel
Journal:  Neurogenetics       Date:  2007-01-09       Impact factor: 2.660

8.  Recurrent chromosome 16p13.1 duplications are a risk factor for aortic dissections.

Authors:  Shao-Qing Kuang; Dong-Chuan Guo; Siddharth K Prakash; Merry-Lynn N McDonald; Ralph J Johnson; Min Wang; Ellen S Regalado; Ludivine Russell; Jiu-Mei Cao; Callie Kwartler; Kurt Fraivillig; Joseph S Coselli; Hazim J Safi; Anthony L Estrera; Suzanne M Leal; Scott A LeMaire; John W Belmont; Dianna M Milewicz
Journal:  PLoS Genet       Date:  2011-06-16       Impact factor: 5.917

9.  Obesity in adults with 22q11.2 deletion syndrome.

Authors:  Sarah L Voll; Erik Boot; Nancy J Butcher; Samantha Cooper; Tracy Heung; Eva W C Chow; Candice K Silversides; Anne S Bassett
Journal:  Genet Med       Date:  2016-08-18       Impact factor: 8.822

Review 10.  Loss of chromosome Y (LOY) in blood cells is associated with increased risk for disease and mortality in aging men.

Authors:  Lars A Forsberg
Journal:  Hum Genet       Date:  2017-04-19       Impact factor: 4.132
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  2 in total

1.  The copy number variation and stroke (CaNVAS) risk and outcome study.

Authors:  John W Cole; Taiwo Adigun; Rufus Akinyemi; Onoja Matthew Akpa; Steven Bell; Bowang Chen; Jordi Jimenez Conde; Uxue Lazcano Dobao; Israel Fernandez; Myriam Fornage; Cristina Gallego-Fabrega; Christina Jern; Michael Krawczak; Arne Lindgren; Hugh S Markus; Olle Melander; Mayowa Owolabi; Kristina Schlicht; Martin Söderholm; Vinodh Srinivasasainagendra; Carolina Soriano Tárraga; Martin Stenman; Hemant Tiwari; Margaret Corasaniti; Natalie Fecteau; Beth Guizzardi; Haley Lopez; Kevin Nguyen; Brady Gaynor; Timothy O'Connor; O Colin Stine; Steven J Kittner; Patrick McArdle; Braxton D Mitchell; Huichun Xu; Caspar Grond-Ginsbach
Journal:  PLoS One       Date:  2021-04-19       Impact factor: 3.752

2.  Genetic analysis reveals novel variants for vascular cognitive impairment.

Authors:  Saana Mönkäre; Liina Kuuluvainen; Johanna Schleutker; Jose Bras; Susanna Roine; Minna Pöyhönen; Rita Guerreiro; Liisa Myllykangas
Journal:  Acta Neurol Scand       Date:  2022-03-20       Impact factor: 3.915
  2 in total

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