Susanne Schulz

Prof. Dr. Susanne Schulz

Department of Operative Dentistry and Periodontology, Martin Luther University, Halle-Wittenberg, Germany
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Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 March 2019 in Archives of Oral Biology
Verified
Journal Article
Closed access
SSSusanne Schulz
Susanne Schulz
MPMartin Porsch
Martin Porsch
Ivo GrosseIvo Grosse
Ivo Grosse
KHKatrin Hoffmann
Katrin Hoffmann
HSHans-Günter Schaller
Hans-Günter Schaller
SRStefan Reichert
Stefan Reichert

1 January 2016 in Human Immunology
Verified
Journal Article
Closed access
SSSusanne Schulz
Susanne Schulz
UIUta Dorothee Immel
Uta Dorothee Immel
LJLouise Just
Louise Just
HSHans-Günter Schaller
Hans-Günter Schaller
CGChristiane Gläser
Christiane Gläser
SRStefan Reichert
Stefan Reichert

9 August 2010 in BMC Medical Genetics
Verified
Journal Article
Open access
PDF file
FEFlorian D Ernst
Florian D Ernst
KUKatharina Uhr
Katharina Uhr
ATAlexander Teumer
Alexander Teumer
JFJutta Fanghänel
Jutta Fanghänel
SSSusanne Schulz
Susanne Schulz
TKThomas Kocher
Thomas Kocher
Background: The human chromosomal region9p21.3has been shown to be strongly associated with Coronary Heart Disease (CHD) in several Genome-wide Association Studies (GWAS). Recently, this region has also been shown to be associated with Aggressive Periodontitis (AgP), strengthening the hypothesis that the established epidemiological association between periodontitis and CHD is caused by a shared genetic background, in addition to common environmental and behavioural risk factors. However, the size of the analyzed cohorts in this primary analysis was small compared to other association studies on complex diseases. Using our own AgP cohort, we attempted to confirm the described associations for the chromosomal region9p21.3.Methods: We analyzed our cohort consisting of patients suffering from the most severe form of AgP, generalized AgP (gAgP) (n = 130) and appropriate periodontally healthy control individuals (n = 339) by genotyping four tagging SNPs (rs2891168, rs1333042, rs1333048 and rs496892), located in the chromosomal region9p21.3, that have been associated with AgP.Results: The results confirmed significant associations between three of the four SNPs and gAgP. The combination of our results with those from the study which described this association for the first time in a meta-analysis of the four tagging SNPs produced clearly lower p-values compared with the results of each individual study. According to these results, the most plausible genetic model for the association of all four tested SNPs with gAgP seems to be the multiplicative one.Conclusion: We positively replicated the finding of an association between the chromosomal region9p21.3and gAgP. This result strengthens support for the hypothesis that shared susceptibility genes within this chromosomal locus might be involved in the pathogenesis of both CHD and gAgP.

1 December 2016 in Cytokine
Verified
Journal Article
Closed access
SSSusanne Schulz
Susanne Schulz
HLHenriette Lüdike
Henriette Lüdike
MLMadlen Lierath
Madlen Lierath
ASAxel Schlitt
Axel Schlitt
KWKarl Werdan
Karl Werdan
SRStefan Reichert
Stefan Reichert

11 November 2008 in International Journal of Immunogenetics
Verified
Journal Article
Closed access
PDF file
SSSusanne Schulz
Susanne Schulz
NZN. Zissler
N. Zissler
WAW. Altermann
W. Altermann
JKJ. Klapproth
J. Klapproth
UZU. Zimmermann
U. Zimmermann
SRS. Reichert
S. Reichert

1 October 2011 in Human Immunology
Verified
Journal Article
Closed access
SSSusanne Schulz
Susanne Schulz
JSJamal M. Stein
Jamal M. Stein
WAWolfgang Altermann
Wolfgang Altermann
JKJana Klapproth
Jana Klapproth
UZUta Zimmermann
Uta Zimmermann
SRStefan Reichert
Stefan Reichert