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 | 236 | 2012 |
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 | 205 | 2020 |
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 | 176 | 2013 |
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 | 138 | 2013 |
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 | 65 | 2012 |
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 | 46 | 2015 |
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 | 44 | 2012 |
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 | 30 | 2008 |
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 | 29 | 2015 |
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 | 29 | 2012 |
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 | 13 | 2013 |
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 | 10 | 2012 |
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 | 7 | 2012 |
Personalization in Skipforward, an Ontology-Based Distributed Annotation System. M Kiesel, F Mittag SPIM 781, 90-97, 2011 | 2 | 2011 |
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 | 1 | 2023 |
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 | 1 | 2013 |
ReduxExp: A justification-based explanationsupport server TR Roth-Berghofer, F Mittag Proceedings of AI-2008. The twenty-eighth SGAI international conference on …, 2008 | 1 | 2008 |
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 |