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Florian Mittag
Florian Mittag
Professor for Artificial Intelligence in Visual Computing at Coburg University of Applied Sciences
Bestätigte E-Mail-Adresse bei hs-coburg.de
Titel
Zitiert von
Zitiert von
Jahr
Using genome-wide complex trait analysis to quantify ‘missing heritability’in Parkinson's disease
MF Keller, M Saad, J Bras, F Bettella, N Nicolaou, J Simón-Sánchez, ...
Human molecular genetics 21 (22), 4996-5009, 2012
2332012
SBML Level 3: an extensible format for the exchange and reuse of biological models
SM Keating, D Waltemath, M König, F Zhang, A Dräger, C Chaouiya, ...
Molecular systems biology 16 (8), e9110, 2020
1962020
Path2Models: large-scale generation of computational models from biochemical pathway maps
F Büchel, N Rodriguez, N Swainston, C Wrzodek, T Czauderna, R Keller, ...
BMC systems biology 7, 1-19, 2013
1752013
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease
P Holmans, V Moskvina, L Jones, M Sharma, ...
Human molecular genetics 22 (5), 1039-1049, 2013
1382013
Use of support vector machines for disease risk prediction in genome‐wide association studies: Concerns and opportunities
F Mittag, F Büchel, M Saad, A Jahn, C Schulte, Z Bochdanovits, ...
Human mutation 33 (12), 1708-1718, 2012
652012
JSBML 1.0: providing a smorgasbord of options to encode systems biology models
N Rodriguez, A Thomas, L Watanabe, IY Vazirabad, V Kofia, HF Gómez, ...
Bioinformatics 31 (20), 3383-3386, 2015
462015
Linking the epigenome to the genome: correlation of different features to DNA methylation of CpG islands
C Wrzodek, F Büchel, G Hinselmann, J Eichner, F Mittag, A Zell
PloS one 7 (4), e35327, 2012
432012
Generating and using gaze-based document annotations
G Buscher, A Dengel, L Van Elst, F Mittag
CHI'08 extended abstracts on Human factors in computing systems, 3045-3050, 2008
302008
Influence of feature encoding and choice of classifier on disease risk prediction in genome-wide association studies
F Mittag, M Römer, A Zell
PloS one 10 (8), e0135832, 2015
292015
Qualitative translation of relations from BioPAX to SBML qual
F Büchel, C Wrzodek, F Mittag, A Dräger, J Eichner, N Rodriguez, ...
Bioinformatics 28 (20), 2648-2653, 2012
292012
International Parkinson’s Disease Genomics Consortium (IPDGC) Wellcome Trust Case Control Consortium 2 (WTCCC2), 2012. Using genome-wide complex trait analysis to quantify …
MF Keller, M Saad, J Bras, F Bettella, N Nicolaou, J Simón-Sánchez, ...
Hum. Mol. Genet 21 (4996), e5009, 0
17
Integrative pathway-based approach for genome-wide association studies: identification of new pathways for rheumatoid arthritis and type 1 diabetes
F Buechel, F Mittag, C Wrzodek, A Zell, T Gasser, M Sharma
PLoS One 8 (10), e78577, 2013
132013
International Parkinson’s Disease Genomics C, Wellcome Trust Case Control C. Using genome-wide complex trait analysis to quantify ‘missing heritability’in Parkinson’s disease
MF Keller, M Saad, J Bras, F Bettella, N Nicolaou, J Simon-Sanchez, ...
Hum Mol Genet 21, 4996-5009, 2012
102012
Wellcome Trust Case Control Consortium 2 (WTCCC2) Using genome-wide complex trait analysis to quantify ‘missing heritability’in Parkinson’s disease
MF Keller, M Saad, J Bras, F Bettella, N Nicolaou, J Simón-Sánchez, ...
Hum Mol Genet 21 (22), 4996-5009, 2012
72012
Personalization in Skipforward, an Ontology-Based Distributed Annotation System.
M Kiesel, F Mittag
SPIM 781, 90-97, 2011
22011
Which Country Is This? Automatic Country Ranking of Street View Photos
T Menzner, F Mittag, JL Leidner
European Conference on Information Retrieval, 275-280, 2023
12023
Using genome-wide complex trait analysis to quantify'missing heritability'in Parkinsons disease (vol 22, pg 1696, 2013)
MF Keller, M Saad, J Bras, F Bettella, N Nicolaou, J Simon-Sanchez, ...
Human Molecular Genetics 22 (14), 2973-2973, 2013
12013
ReduxExp: A justification-based explanationsupport server
TR Roth-Berghofer, F Mittag
Proceedings of AI-2008. The twenty-eighth SGAI international conference on …, 2008
12008
Disease risk prediction in genome-wide association studies
F Mittag
München: Verlag Dr. Hut, 2016
2016
Using genome-wide complex trait analysis to quantify missing heritability in Parkinsons disease (vol 21, pg 4996, 2012)
MF Keller, M Saad, J Bras, F Bettella, N Nicolaou, J Simon-Sanchez, ...
HUMAN MOLECULAR GENETICS 22 (8), 1696-1696, 2013
2013
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