Per Hoffman
Overview
Explore the profile of Per Hoffman including associated specialties, affiliations and a list of published articles.
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Articles
6
Citations
296
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0
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Recent Articles
1.
Chattopadhyay S, Thomsen H, Yadav P, da Silva Filho M, Weinhold N, Nothen M, et al.
Commun Biol
. 2019 Mar;
2:89.
PMID: 30854481
Inherited genetic susceptibility to multiple myeloma has been investigated in a number of studies. Although 23 individual risk loci have been identified, much of the genetic heritability remains unknown. Here...
2.
Dand N, Mucha S, Tsoi L, Mahil S, Stuart P, Arnold A, et al.
Hum Mol Genet
. 2017 Oct;
26(21):4301-4313.
PMID: 28973304
Psoriasis is a common inflammatory skin disorder for which multiple genetic susceptibility loci have been identified, but few resolved to specific functional variants. In this study, we sought to identify...
3.
Perez-Palma E, Helbig I, Klein K, Anttila V, Horn H, Reinthaler E, et al.
J Med Genet
. 2017 Jul;
54(9):598-606.
PMID: 28756411
Background: Microdeletions are known to confer risk to epilepsy, particularly at genomic rearrangement 'hotspot' loci. However, microdeletion burden not overlapping these regions or within different epilepsy subtypes has not been...
4.
Munz M, Chen H, Jockel-Schneider Y, Adam K, Hoffman P, Berger K, et al.
J Clin Periodontol
. 2017 May;
44(10):962-970.
PMID: 28548211
Aim: The intronic variant rs4252120 in the plasminogen gene (PLG) is known to be associated with aggressive periodontitis (AgP) and atherosclerosis. Here, we examined the chromosomal region spanning PLG for...
5.
Johnson E, Bjelland D, Howrigan D, Abdellaoui A, Breen G, Borglum A, et al.
PLoS Genet
. 2016 Oct;
12(10):e1006343.
PMID: 27792727
It is well known that inbreeding increases the risk of recessive monogenic diseases, but it is less certain whether it contributes to the etiology of complex diseases such as schizophrenia....
6.
Stitziel N, Stirrups K, Masca N, Erdmann J, Ferrario P, Konig I, et al.
N Engl J Med
. 2016 Mar;
374(12):1134-44.
PMID: 26934567
Background: The discovery of low-frequency coding variants affecting the risk of coronary artery disease has facilitated the identification of therapeutic targets. Methods: Through DNA genotyping, we tested 54,003 coding-sequence variants...