Deters, M.A., Laven, A., Castejon, A., Doucette, W.R., Ev, L.S., Krass, I., Mehuys, E., Obarcanin, E., Schwender, H., Läer, S.: Effective Interventions for Diabetes Patients by Community Pharmacists: A Meta-analysis of Pharmaceutical Care Components. Annals of Pharmacotherapy, 52 p. 198-211 (2018)

Grube, L., Dellen, R., Kruse, F., Schwender, H., Stühler, K., Poschmann, G.: Mining the Secretome of C2C12 Muscle Cells: Data Dependent Experimental Approach to Analyze Protein Secretion Using Label-Free Quantification and Peptide Based Analysis. Journal of Proteome Research, 17 p. 879-890 (2018)

Liu, D., Schwender, H., Wang, M., Wang, H., Wang, P., Zhu, H., Zhou, Z., Li, J., Wu, T., Beaty, T.H.: Gene-Gene Interaction Between MSX1 and TP63 in Asian Case-Parent Trios with Nonsyndromic Cleft Lip with or without Cleft Palate. Birth Defects Research, DOI: 10.1002/bdr2.1139 (2018)

Wang, P., Wu, T., Schwender, H., Wang, H., Shi, B., Wang, Z., Yuan, Y., Liu, D., Wang, M., Li, J., Zhou, Z., Zhu, H., Beaty, T.H.: Evidence of Interaction Between Genes in the Folate/Homocysteine Metabolic Pathway in Controlling Risk of Nonsyndromic Oral Cleft. Oral Diseases, DOI: 10.1111/odi.12831 (2018)

Hüls, A., Krämer, U., Carlsten, C., Schikowski, T., Ickstadt, K., Schwender, H.: Comparison of Weighting Approaches for Genetic Risk Scores in Gene-Environment Interaction Studies. BMC Genetics, 18 p. 115 (2017)

Kaisers, W., Schwender, H., Schaal, H.: Sample Size Estimation for Detection of Splicing Events in Transcriptome Sequencing Data. International Journal of Molecular Sciences, 18 p. E1900 (2017)

Kaisers, W., Ptok, J., Schwender, H., Schaal, H.: Validation of Splicing Events in Transcriptome Sequencing Data. International Journal of Molecular Sciences, 18 p. E1110 (2017)

Kaisers, W., Boukamp, P., Stark, H.J., Schwender, H., Tigges, J., Krutmann, J., Schaal, H.: Age, Gender and UV-Exposition Related Effects on Gene Expression in In Vivo Aged Short Term Cultivated Human Dermal Fibroblasts. PLOS ONE, 12 p. e0175657 (2017)

Liu, D., Wang, H., Schwender, H., Marazita, M.L., Wang, Z., Yuan, Y., Wang, P., Liang, K.Y., Wu-Chou, Y.H., Wang, M., Shi, B., Zhu, H., Wu, T., Beaty T.H.: Gene-Gene Interaction of Single Nucleotide Polymorphisms in 16p13.3 may Contribute to the Risk of Non-Syndromic Cleft Lip with or without Cleft Palate in Chinese Case-Parent Trios. American Journal of Medical Genetics, Part A, 173 p. 1489-1494 (2017)

Schäfer, M., Klein, H.U., Schwender, H.: Integrative Analysis of Multiple Genomic Variables Using a Hierarchical Bayesian Model. Bioinformatics, 33 p. 3220-3227 (2017)

Varikuti, D.P., Hoffstaedter, F., Genon, S., Schwender, H., Reid, A.T., Eickhoff, S.B.: Resting-State Test-Retest Reliability of A Priori Defined Canonical Networks over Different Preprocessing Steps. Brain Structure and Function, 222 p. 1447-1468 (2017)

Verhülsdonk, S., Lange-Asschenfeldt, C., Hölft, C., Schwender, H., Supprian, T., Hellen, F., Kalbe, E.: Repressive Coping Does Not Contribute to Anosognosia in First-Diagnosis Patients with Alzheimer Disease. Alzheimer Disease and Associated Disorders, 31 p. 249-255 (2017)

Xiao, Y., Taub, M.A., Ruczinski, I., Begum, F., Hetmanski, J.B., Schwender, H., Leslie, E.J., Koboldt, D.C., Murray, J.C., Marazita, M.L., Beaty, T.H.: Evidence for SNP-SNP Interaction Identified Through Targeted Sequencing of Cleft Case-Parent Trios. Genetic Epidemiology, 41 p. 244-250 (2017)

Hartung, B., Schwender, H., Pawlik, E., Ritz-Timme, S., Mindiashvili, N., Daldrup, T.: Comparison of Venous Blood Alcohol Concentrations and Breath Alcohol Concentrations Measured with Draeger Alcotest 9510 DE Evidential. Forensic Science International, 258 p. 64-67 (2016)

Hartung, B. Schwender, H. Roth, E.H., Hellen, F., Mindiashvili, N., Rickert, A., Ritz-Timme, S., Grieser, A., Monticelli, F., Daldrup, T.: The Effect of Cannabis on Regular Cannabis Consumers' Ability to Ride a Bicycle. International Journal of Legal Medicine, 130 p. 711-721 (2016)

Bu, L., Chen, Q., Wang, H., Zhang, T., Hetmanski, J.B., Schwender, H., Parker, M., Chou, Y.H., Yeow, V., Chong, S.S., Zhang, B., Jabs, E.W., Scott, A.F., Beaty, T.H.: Novel Evidence of Association with Nonsyndromic Cleft Lip with or without Cleft Palate was Shown for Single Nucleotide Polymorphisms in FOXF2 Gene in an Asian Population. Birth Defects Research A: Clinical and Molecular Teratology, 103 p. 857-862 (2015)

Casjens, S., Schwender, H., Brüning, T., Ickstadt, K.: A Novel Crossover Operator Based on Variable Importance for Evolutionary Multi-Objective Optimization with Tree Representation. Journal of Heuristics, 21 p. 1-24 (2015)

Daldrup, T., Roth, E.H., Schwender, H., Maatz, K.R., Mindiashvili, N., Malczyk, A., Hartung, B.: Zusammenhang zwischen der Höhe der Blutalkoholkonzentration und Beeinträchtigungen beim Führen eines Fahrrades. Blutalkohol, p. 1-9 (2015)

Gabdoulline, R., Kaisers, W., Gaspar, A., Meganathan, K., Doss, M.X., Jagtap, S., Hescheler, J., Sachinidis, A., Schwender, H.: Differences in the Early Development of Human and Mouse Embryonic Stem Cells. PLoS One, 10 p. e0140803 (2015)

Hartung, B., Mindiashvili, N., Maatz, R., Schwender, H., Roth, E.H., Ritz-Timme, S., Moody, J., Malczyk, A., Daldrup, T.: Regarding the Fitness to Ride a Bicycle Under the Acute Influence of Alcohol. International Journal of Legal Medicine, 129 p. 471-480 (2015)

Hartung, B., Ritz-Timme, S., Schwender, H., Mindiahvili, N., Daldrup, T.: Differences Between Male and Female Cyclists' Performances Under the Acute Influence of Alcohol. International Journal of Legal Medicine, 129 p. 1011-1020 (2015)

Hartung, B., Schwender, H., Mindiashvili, N., Ritz-Timme, S., Malczyk, A., Daldrup, T.: The Effect of Alcohol Hangover on the Ability to Ride a Bicycle. International Journal of Legal Medicine, 129 p. 751-758 (2015)

Kaisers, W., Schaal, H., Schwender, H.: rbamtools: an R interface to samtools enabling fast accumulative tabulation of splicing events over multiple RNA-seq samples. Bioinformatics, 31 p. 1663-1664 (2015)

Lang, E., Schäfer, M., Schwender, H., Neumann, N.J., Frank, J.: Occurrence of Malignant Tumours in the Acute Hepatic Porphyrias. Journal of Inherited Metabolic Disease Reports, 22 p. 17-22 (2015)

Obarcanin, E., Krüger, M., Müller, P., Nemitz, V., Schwender, H., Hasanbegovic, S., Kalajdzisalihovic, S., Läer, S.: Pharmaceutical Care of Adolescents with Diabetes Mellitus Type 1: The DIADEMA Study, a Randomized Controlled Trial. International Journal of Clinical Pharmacy, 37 p. 790-798 (2015)

Schäfer, M., Radon, Y., Klein, T., Hermann, S., Schwender, H., Verveer, P.J., Ickstadt, K.: A Bayesian Mixture Model to Quantify Parameters of Spatial Clustering. Computational Statistics and Data Analysis, 92 p. 163-176 (2015)

Younkin, S.G., Scharpf, R.B., Schwender, H., Parker, M.M., Scott, A.F., Marazita, M.L., Beaty, T.H., Ruczinski, I.: A Genome-Wide Study of Inherited Deletions Identified two Regions Associated with Nonsyndromic Isolated Oral Clefts. Birth Defects Research Part A: Clinical and Molecular Teratology, 103 p. 276-283 (2015)

Chen, Q., Wang, H., Schwender, H., Zhang, T., Hetmanski, J.B., Wu-Chou, Y.H., Ye, X., Yeow, V., Chong, S.S., Zhang, B., Jabs, E.W., Parker, M.M., Scott, A.F., Beaty, T.H.: Joint Testing of Genotypic and Gene-Environment Interaction Identified Novel Association for BMP4 with Non-Syndromic CL/P in an Asian Population Using Data from an International Cleft Consortium. PLoS One, 9 p. e109038 (2014)

Herrmann, S., Schwender, H., Ickstadt, K., Müller, P.: A Bayesian Changepoint Analysis of ChIP-Seq Data of Lamin B. Biochimica et Biophysica Acta, 1844 p. 138-144 (2014)

Malina, M., Ickstadt, K., Schwender, H., Posch, M., Bogdan, M.: Detection of Epistatic Effects with Logic Regression and a Classical Linear Regression Model. Statistical Applications in Genetics and Molecular Biology, 13 p. 83-104 (2014)

Neumann, C., Taub, M.A., Younkin, S.G., Beaty, T.H., Ruczinski, I., Schwender, H.: Analytic Power and Sample Size Calculation for the Genotypic Transmission/Disequilibrium Test in Case-Parent Trio Studies. Biometrical Journal, 68 p. 766-773 (2014)

Schwender, H., Li, Q., Neumann, C., Taub, M.A., Younkin, S.G., Berger, P., Scharpf, R.B., Beaty, T.H., Ruczinski, I.: Detecting Disease Variants in Case-Parent Trio Studies Using the Bioconductor Software Package trio. Genetic Epidemiology, 38 p. 516-522 (2014)

Weilandt, M., Koch, A., Rieder, H., Deenen R., Schwender, H., Niegisch, G., Schulz, W.A.: Target Genes of Recurrent Chromosomal Amplification and Deletion in Urothelial Carcinoma. Cancer Genomics \& Proteomics, 11 p. 141-153 (2014)

Wu, T., Schwender, H., Ruczinski, I., Murray, J.C., Marazita, M.L., Munger, R.G., Hetmanski, J.B., Parker, M.M., Wang, P., Murray, T., Taub, M., Li, S., Redett, R.J., Fallin, M.D., Liang, K.Y., {Wu-Chou}, Y.H., Chong, S.S., Yeow, V., Ye, X., Wang, H., Huang, S., Jabs, E.W., Shi, B., Wilcox, A.J., Jee, S.H., Scott, A.F., Beaty, T.B.: Evidence of Gene-Environment Interaction for two Genes on Chromosome 4 and Environmental Tabacco Smoke in Controlling the Risk of Nonsyndromic Cleft Palate. PLoS One, 9 p. e88088 (2014)

Younkin, S.G., Scharpf, R.B., Schwender, H., Parker, M.M., Scott, A.F., Marazita, M.L., Beaty, T.H., Ruczinski, I.: A Genome-Wide Study of De Novo Deletions Identifies a Candidate Locus for Non-Syndromic Isolated Cleft Lip/Palate Risk. BMC Genetics, 15 p. 24 (2014)

Beaty, T.H., Taub, M.A., Scott, A.F, Murray, J.C., Marazita, M.L., Schwender, H., Parker, M.M., Hetmanski, J.B., Balakrishnan, P., Mansilla, M.A., Mangold, E., Ludwig, K.U., Noethen, M.M., Rubini, M., Elcioglu, N., Ruczinski, I.: Confirming Genes Influencing Risk to Cleft Lip with/without Cleft Palate in a Case-Parent Trio Study. Human Genetics, 132 p. 771-781 (2013)

Li, Q., Schwender, H., Louis, T.A., Fallin, M.D., Ruczinski, I.: Efficient Simulation of Epistatic Interactions in Case-Parent Trios. Human Heredity, 75 p. 12-22 (2013)

Taub, M.A., Schwender, H.R., Younkin, S.G., Louis, T.A., Ruczinski, I.: On Multi-Marker Tests for Association in Case-Control Studies. Frontiers in Genetics, 4 p. 252 (2013)

Wang, H., Zhang, T., Wu, T., Hetmanski, J.B., Ruczinski, I., Schwender, H., Murray, T., Fallin, M.D., Redett, R.J., Raymond, G.V., Jin, S.C., Wu-Chou, Y.H., Chen, P.K., Yeow, V., Chong, S.S., Cheah, F.S., Jee, S.H., Jabs, E.W., Liang, K.Y., Scott, A.F., Beaty, T. H.: The FGF&FGFR Gene Family and Risk of Cleft Lip With/Without Cleft Palate. The Cleft Palate-Craniofacial Journal, 50 p. 96-103 (2013)

Binder, H., Müller, T., Schwender, H., Golka, K., Steffens, M., Hengstler, J.G., Ickstadt, K., Schumacher, M.: Cluster-Localized Sparse Logistic Regression for {SNP} Data. Statistical Applications in Genetics and Molecular Biology, 11 p. 13 (2012)

Chen, Q., Wang, H., Hetmanski, J.B., Zhang, T., Ruczinski, I., Schwender, H., Liang, K.Y., Fallin, M.D., Redett, R.J., Raymond, G.V., Wu-Chou, Y.H., Chen, P.K., Yeow, V., Chong, S.S., Cheah, F.S., Jabs, E.W., Scott, A.F., Beaty, T.H.: BMP4 was Associated with NSCL/P in an Asian Population. PLoS One, 7 p. e35347 (2012)

Murray, T., Taub, M.A., Ruczinski, I., Scott, A.F., Hetmanski, J.B., Schwender, H., Patel, P.J., Zhang, T.X., Munger, R.G., Wilcox, A.J., Ye, X., Wang, H., Wu, T., Wu-Chou, Y.H., Shi, B., Jee, S.H., Chong, S.S., Yeow, V., Murray, J.C., Marazita, M.L., Beaty, T.H.: Examining Markers in 8q24 Markers to Explain Differences in Evidence for Association with Cleft Lip with/without Cleft Palate Between Asians and Europeans. Genetic Epidemiology, 36 p. 392-399 (2012)

Scharpf, R.B., Beaty, T.H., Schwender, H., Younkin, S.G., Scott, A.F., Ruczinski, I.: Fast Detection of De Novo Copy Number Variants from SNP Arrays for Case-Parent Trios. BMC Bioinformatics, 13 p. 330 (2012)

Schwender, H.: Imputing Missing Genotypes with Weighted K Nearest Neighbors. Journal of Toxicology and Environmental Health, Part A, 75 p. 438-446 (2012)

Schwender, H.: Applied Survival Analysis, 2. Auflage, von Hosmer, D. W., Lemeshow, S., May, S.. Statistical Papers, 53 p. 247-248 (2012)

Schwender, H., Selinski, S., Blaszkewicz, M., Marchan, R., Ickstadt, K., Golka, K., Hengstler, J.G.: Distinct SNP Combinations Confer Susceptibility to Urinary Bladder Cancer in Smokers and Non-Smokers. PLoS ONE, 7 p. e51880 (2012)

Schwender, H., Taub, M.A., Beaty, T.H., Marazita, M.L., Ruczinski, I.: Rapid Testing of SNPs and Gene-Environment Interactions in Case-Parent Trio Data Based on Exact Analytic Parameter Estimation. Biometrics, 68 p. 766-773 (2012)

Taub, M.A., Schwender, H., Beaty, T.H., Louis, T.A., Ruczinski, I.: Incorporating Genotype Uncertainties into the Genotypic {TDT} for Main Effects and Gene-Environment Interactions. Genetic Epidemiology, 36 p. 225-234 (2012)

Beaty, T.H., Ruczinski, I., Murray, J.C., Marazita, M.L., Munger, R.G., Hetmanski, J.B., Murray, T., Redett, R.J., Fallin, M.D., Liang, K.Y., Wu, T., Patel, P.J., Jin, S.C., Zhang, T.X., Schwender, H., Wu-Chou, Y.H., Chen, P.K., Chong, S.S., Cheah, F., Yeow, V., Ye, X., Wang, H., Huang, S., Jabs, E.W., Shi, B., Wilcox, A.J., Lie, R.T., Jee, S.H., Christensen, K., Doheny, K.F., Pugh, E.W., Ling, H., Scott, A.F.: Evidence for Gene-Environment Interaction in a Genome Wide Study of Isolated, Non-Syndromic Cleft Palate. Genetic Epidemiology, 35 p. 469-478 (2011)

Chen, C.C.M., Schwender, H., Keith, J., Nunkesser, R., Mengersen, K., Macrossan, P.: Methods for Identifying SNP Interactions: A Review on Variations of Logic Regression, Random Forest and {Bayesian} Logistic Regression. IEEE/ACM Transactions on Computational Biology and Bioinformatics, 8 p. 1580-1591 (2011)

Golka, K., Selinski, S., Lehmann, M.L., Blaszkewicz, M., Marchan, R., Ickstadt, K., Schwender, H., Bolt, H.M., Hengstler, J.H.: Genetic Variants in Urinary Bladder Cancer: Collective Power of the Wimp SNPs. Archives of Toxicology, 85 p. 539-554 (2011)

Schwender, H., Bowers, K., Fallin, M.D., Ruczinski, I.: Importance measures for epistatic interactions in case-parent trios. Annals of Human Genetics, 75 p. 122-132 (2011)

Schwender, H., Ruczinski, I., Ickstadt, K.: Testing SNPs and Sets of SNPs for Importance in Association Studies. Biostatistics, 12 p. 18-32 (2011)

Selinski, S., Blaszkewicz, M., Lehmann, M.L., Ovsiannikov, D., Moormann, O., Guballa, C., Kress, A., Truss, M.C., Gerullis, H., Otto, T., Barski, D., Niegisch, G., Albers, P., Frees, S., Brenner, W., Thüroff, J.W., Angeli-Greaves, M., Seidel, T., Roth, G., Dietrich, H., Ebbinghaus, R., Prager, H.M., Bolt, H.M., Falkenstein, M., Zimmermann, A., Klein, T., Reckwitz, T., Roemer, H.C., Löhlein, D., Weistenhöfer, W., Schöps, W., Rizvi, S.A.H., Aslam, M., Banfi, G., Romics, I., Steffens, M., Ekici, A.B., Winterpacht, A., Ickstadt, K., Schwender, H., Hengstler, J.G., Golka, K.: Genotyping NAT2 with only two SNPs (rs1041983 and rs1801280) Outperforms the Tagging {SNP} rs1495741 and is Equivalent to The Conventional 7-SNP NAT2 Genotype. Pharmacogenetics and Genomics, 21 p. 673-678 (2011)

Beaty, T.H., Murray, J.C., Marazita, M.L., Munger, R.G., Ruczinski, I., Hetmanski, J.B., Liang, K.Y., Wu, T., Murray, T., Fallin, M.D., Redett, R.A., Raymond, G., Schwender, H., Jin, S.C., Cooper, M.E., Dunnwald, M., Mansilla, M.A., Leslie, E., Bullard, S., Lidral, A.C., Moreno, L.M., Menezes, R., Vieira, A.R., Petrin, A., Wilcox, A.J., Lie, R.T., Jabs, E.W., Wu-Chou, Y.H., Chen, P.K., Wang, H., Ye, X., Huang, S., Yeow, V., Chong, S.S., Jee, S.H., Shi, B., Christensen, K., Melbye, M., Doheny, K.F., Pugh, E.W., Ling, H., Castilla, E.E., Czeizel, A.E., Ma, L., Field, L.L., Brody, L., Pangilinan, F., Mills, J.L., Molloy, A.M., Kirke, P.N., Scott, J.M., Arcos-Burgos, M., Scott, A.F.: A Genome-Wide Association Study of Cleft Lip With and Without Cleft Palate Identifies Risk Variants near {MAFB} and {ABCA4}. Nature Genetics, 42 p. 525-529 (2010)

Lehmann, M.L., Selinski, S., Blaszkewicz, M., Orlich, M., Ovsiannikov, D., Moormann, O., Guballa, C., Kress, A., Truss, M. C., Gerullis, H., Otto, T., Barski, D., Niegisch, G., Albers, P., Frees, S. , Brenner, W., Thüroff, J. W., Angeli-Greaves, M., Seidel, T., Roth, G., Dietrich, H., Ebbinghaus, R., Prager, H. M., Bolt, H. M., Falkenstein, M., Zimmermann, A., Klein, T., Reckwitz, T., Roemer, H. C., Löhlein, D., Weistenhöfer, W., Schöps, W., Beg, A. E., Aslam, M., Banfi, G., Romics, I., Ickstadt, K., Schwender, H., Winterpacht, A., Hengstler, J. G., Golka, K.: Rs710521[A] on Chromosome 3q28 close to {TP63} is Associated with Increased Urinary Bladder Cancer Risk. Archives of Toxicology, 84 p. 967-978 (2010)

Petry, I.B., Fieber, E., Schmidt, M., Gehrmann, M., Gebhard, S., Hermes, M., Schormann, W., Selinski, S., Freis, E., Schwender, H., Brulport, M., Ickstadt, K., Rahnenführer, J., Maccoux, L., West, J., Kölbl, H., Schuler, M., Hengstler, J.G.: ERBB2 Induces an Anti-Apoptotic Expression Pattern of Bcl-2 Family Members in Node Negative Breast Cancer. Clinical Cancer Research, 16 p. 451-460 (2010)

Schwender, H., Ruczinski, I.: Logic Regression and Its Extensions. In: Computational Methods for Genetics of Complex Traits. Band 72 von Advances in Genetics. Academic Press, p. 25-45 (2010)

Freis, E., Selinski, S., Weibert, B., Krahn, U., Schmidt, M., Gehrmann, M., Hermes, M., Maccoux, L., West, J., Schwender, H., Rahnenführer, J., Hengstler, J.G., Ickstadt, K.: Effects of Metagene Calculation on Survival: An Integrative Approach Using Cluster, Promoter Analysis. In: Proceedings of the Sixth International Workshop on Computational Systems Biology. p. 47-50 (2009)

Schäfer, M., Schwender, H., Merk, S., Haferlach, C., Ickstadt, K., Dugas, M.: Integrated Analysis of Copy Number Alterations and Gene Expression: A Bivariate Assessment of Equally Directed Abnormalities. Bioinformatics, 25 p. 3228-3235 (2009)

Schwender, H.: Multiple Testing Procedures with Applications to Genomics von Dudoit, S., van der Laan, M.J.. Statistical Papers, 50 p. 681-682 (2009)

Ickstadt, K., Schäfer, M., Fritsch, A., Schwender, H., Abel, J., Bolt, H.M., Brüning, T., Ko, Y.D., Vetter, H., Harth, V.: Statistical Methods for Detecting Genetic Interactions: A Head and Neck Squamous Cell Cancer Study. Journal of Toxicology and Environmental Health Part A, 71 p. 803-815 (2008)

Müller, T., Schwender, H., Ickstadt, K.: Finding SNP Interactions. In: Proceedings of the Fifth International Workshop on Computational Systems Biology. p. 109-112 (2008)

Schwender, H., Ickstadt, K.: Empirical Bayes Analysis of Single Nucleotide Polymorphisms. BMC Bioinformatics, 9 p. 144 (2008)

Schwender, H., Ickstadt, K.: Identification of SNP Interactions Using Logic Regression. Biostatistics, 9 p. 187-198 (2008)

Schwender, H., Ickstadt, K., Rahnenführer, J.: Classification with High-Dimensional Genetic Data: Assigning Patients and Genetic Features to Known Classes. Biometrical Journal, 50 p. 911-926 (2008)

Nunkesser, R., Bernholt, T., Schwender, H., Ickstadt, K., Wegener, I.: Detecting High-Order Interactions of Single Nucleotide Polymorphisms Using Genetic Programming. Bioinformatics, 23 p. 3280-3288 (2007)

Ickstadt, K., Müller, T., Schwender, H.: Analyzing SNPs: Are There Needles in the Haystack?. Chance, 19 p. 21-26 (2006)

Schwender, H., Belousov, A.: Comparison of Preprocessing Methods for Affymetrix Microarrays. Chance, 19 p. 15-20 (2006)

Schwender, H., Krause, A., Ickstadt, K.: Identifying Interesting Genes with siggenes. RNews, 6 p. 45-50 (2006)

Schwender, H., Rabstein, S., Ickstadt, K.: Do you Speak Genomish?. Chance, 19 p. 3-8 (2006)

Schwender, H.: Modifying Microarray Analysis Methods for Categorical Data - SAM and PAM for SNPs. In: Classification - The Ubiquitous Challenge. Springer, Heidelberg, p. 370-377 (2005)

Schwender, H., Zucknick, M., Ickstadt, K., Bolt, H.M.: A Pilot Study on the Application of Statistical Classification Procedures to Molecular Epidemiological Data. Toxicology Letters, 151 p. 291-299 (2004)