Andreas Fiebig
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Explore the profile of Andreas Fiebig including associated specialties, affiliations and a list of published articles.
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9
Citations
1371
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Recent Articles
1.
Ellinghaus E, Ellinghaus D, Krusche P, Greiner A, Schreiber C, Nikolaus S, et al.
Sci Rep
. 2017 Apr;
7:45652.
PMID: 28374850
Chronic venous disease (CVD) is a multifactorial condition representing one of the most common disorders among populations of Western countries. The heritability of about 17% suggests genetic risk factors in...
2.
Lionel A, Crosbie J, Barbosa N, Goodale T, Thiruvahindrapuram B, Rickaby J, et al.
Sci Transl Med
. 2011 Aug;
3(95):95ra75.
PMID: 21832240
Attention deficit hyperactivity disorder (ADHD) is a common and persistent condition characterized by developmentally atypical and impairing inattention, hyperactivity, and impulsiveness. We identified de novo and rare copy number variations...
3.
Noor A, Whibley A, Marshall C, Gianakopoulos P, Piton A, Carson A, et al.
Sci Transl Med
. 2010 Sep;
2(49):49ra68.
PMID: 20844286
Autism is a common neurodevelopmental disorder with a complex mode of inheritance. It is one of the most highly heritable of the complex disorders, although the underlying genetic factors remain...
4.
Fiebig A, Krusche P, Wolf A, Krawczak M, Timm B, Nikolaus S, et al.
Hum Genet
. 2010 Apr;
127(6):669-74.
PMID: 20354728
Varicose veins without skin changes have a prevalence of approximately 20% in Northern and Western Europe whereas advanced chronic venous insufficiency affects about 3% of the population. Genetic risk factors...
5.
Chase A, Ernst T, Fiebig A, Collins A, Grand F, Erben P, et al.
Haematologica
. 2009 Oct;
95(1):20-6.
PMID: 19797732
Background: The formation of fusion genes plays roles in both oncogenesis and evolution by facilitating the acquisition of novel functions. Here we describe the first example of a human polymorphic...
6.
Salmela E, Lappalainen T, Fransson I, Andersen P, Dahlman-Wright K, Fiebig A, et al.
PLoS One
. 2008 Oct;
3(10):e3519.
PMID: 18949038
Background: Genome-wide data provide a powerful tool for inferring patterns of genetic variation and structure of human populations. Principal Findings: In this study, we analysed almost 250,000 SNPs from a...
7.
Fiebig A, Jepsen S, Loos B, Scholz C, Schafer C, Ruhling A, et al.
Genomics
. 2008 Aug;
92(5):309-15.
PMID: 18723088
Polymorphisms in the interleukin-1 (IL1) gene have been suggested to influence transcription of IL1A (interleukin-1alpha) and IL1B (interleukin-1beta) and thereby the pathophysiology of periodontitis. This case-control association study on 415...
8.
Marshall C, Noor A, Vincent J, Lionel A, Feuk L, Skaug J, et al.
Am J Hum Genet
. 2008 Feb;
82(2):477-88.
PMID: 18252227
Structural variation (copy number variation [CNV] including deletion and duplication, translocation, inversion) of chromosomes has been identified in some individuals with autism spectrum disorder (ASD), but the full etiologic role...
9.
Fiebig A, Stegemann S, Bock R
Nucleic Acids Res
. 2004 Jul;
32(12):3615-22.
PMID: 15240834
Chloroplast RNA editing proceeds by C-to-U transitions at highly specific sites. Here, we provide a phylogenetic analysis of RNA editing in a small plastid gene, petL, encoding subunit VI of...