![]() ![]() | SCHRÖDER, V., SKROZIC, A., ERZ, D., KAYSEN, A., FRITZ, J., LOUREIRO, J. M., MCINTYRE, D., PAULY, L., KEMP, J., SCHMITZ, S. K., WAGNER, S., REYES, M., SOARE-LELUBRE, R., SATAGOPAM, V., VEGA MORENO, C. G., GAWRON, P., ROOMP, K., MARTINS CONDE, P., KLUCKEN, J., ... KRÜGER, R. (04 January 2024). Programme Dementia Prevention (pdp): A Nationwide Program for Personalized Prevention in Luxembourg. Journal of Alzheimer's Disease, 97 (2), 791-804. doi:10.3233/JAD-230794 ![]() |
![]() ![]() | HANSEN, B., LACZNY, C. C., AHO, V., Frachet-Bour, A., Habier, J., OSTASZEWSKI, M., Michalsen, A., Hanslian, E., Koppold, D. A., Hartmann, A. M., Steckhan, N., Mollenhauer, B., Schade, S., RUMP, K., SCHNEIDER, J., & WILMES, P. (18 August 2023). Protocol for a multicentre cross-sectional, longitudinal ambulatory clinical trial in rheumatoid arthritis and Parkinson's disease patients analysing the relation between the gut microbiome, fasting and immune status in Germany (ExpoBiome). BMJ Open, 13 (8), 071380. doi:10.1136/bmjopen-2022-071380 ![]() |
![]() ![]() | NEININGER, K., MAY, P., Altieri, B., Lippert, J. L., ROOMP, K., Dalmazi, G. D., Canu, L., Ceccato, F., Riester, A., Herterich, S. L., Fassnacht, M., SCHNEIDER, J., & Ronchi, C. L. (03 May 2021). Evaluation of the Molecular Pathogenesis of Adrenocortical Tumors by Whole-Genome Sequencing. Journal of the Endocrine Society, 5 (Issue Supplement_1), 68. doi:10.1210/jendso/bvab048.137 ![]() |
![]() ![]() | NOOR, F., Biemann, R., ROOMP, K., SCHNEIDER, J., & Isermann, B. (20 October 2020). Gene expression profile of CD14+ blood monocytes following lifestyle-induced weight loss in individuals with metabolic syndrome. Scientific Reports, 10 (1), 17855. doi:10.1038/s41598-020-74973-2 ![]() |
![]() ![]() | HIPP EPOUSE D'AMICO, G., Vaillant, M., Diederich, N. J., ROOMP, K., SATAGOPAM, V., BANDA, P., Sandt, E., Mommaerts, K., SCHMITZ, S., Longhino, L., Schweicher, A., Hanff, A.-M., Nicolai, B., KOLBER, P. L., REITER, D., PAVELKA, L., BINCK, S., PAULY, C., GEFFERS, L., ... KRÜGER, R. (29 October 2018). The Luxembourg Parkinson’s Study: A Comprehensive Approach for Stratification and Early Diagnosis. Frontiers in Aging Neuroscience, 10, 326. doi:10.3389/fnagi.2018.00326 ![]() |
![]() ![]() | Staaf, J., Labmayr, V., Paulmichl, K., Manell, H., SCHNEIDER, R., & ROOMP, K. (2017). Pancreatic Fat Is Associated With Metabolic Syndrome and Visceral Fat but Not Beta-Cell Function or Body Mass Index in Pediatric Obesity. Pancreas. doi:10.1097/MPA.0000000000000771 ![]() |
![]() ![]() | ROOMP, K., & Rand, J. (2015). Rebound hyperglycaemia in diabetic cats. Journal of Feline Medicine and Surgery, 1-10. doi:10.1177/1098612X15588967 ![]() |
![]() ![]() | ROOMP, K., & Rand, J. (2012). Evaluation of detemir in diabetic cats managed with a protocol for intensive blood glucose control. Journal of Feline Medicine and Surgery, 14 (8), 566-572. doi:10.1177/1098612X12446211 ![]() |
![]() ![]() | CRESPO, I., RUMP, K., JURKOWSKI, W., Kitano, H., & DEL SOL MESA, A. (2012). Gene regulatory network analysis supports inflammation as a key neurodegeneration process in prion disease. BMC Systems Biology, 6 (132). doi:10.1186/1752-0509-6-132 ![]() |
![]() ![]() | ROOMP, K., & Domingues, F. S. (2011). Predicting interactions between T cell receptors and MHC-peptide complexes. Molecular Immunology, 48 (4), 553-562. doi:10.1016/j.molimm.2010.10.014 ![]() |
![]() ![]() | JURKOWSKI, W., ROOMP, K., CRESPO, I., SCHNEIDER, J., & DEL SOL MESA, A. (2011). PPARγ population shift produces disease-related changes in molecular networks associated with metabolic syndrome. Cell Death and Disease, 2 (8), 192. doi:10.1038/cddis.2011.74 ![]() |
![]() ![]() | Lange, C. M., ROOMP, K., Dragan, A., Nattermann, J., Michalk, M., Spengler, U., Weich, V., Lengauer, T., Zeuzem, S., Berg, T., & Sarrazin, C. (2010). HLA class I allele associations with HCV genetic variants in patients with chronic HCV genotypes 1a or 1b infection. Journal of Hepatology, 53 (6), 1022-1028. doi:10.1016/j.jhep.2010.06.011 ![]() |
![]() ![]() | ROOMP, K., Antes, I., & Lengauer, T. (2010). Predicting MHC class I epitopes in large datasets. BMC Bioinformatics, 11 (90), 1-2. doi:10.1186/1471-2105-11-90 ![]() |
Däumer, M., Awerkiew, S., Aragon, S. S., Kartashev, V., Poplavskaja, T., Klein, R., Sichtig, N., Thiele, B., Lengauer, T., ROOMP, K., Pfister, H., & Kaiser, R. (2010). Short communication: selection of thymidine analogue resistance mutational patterns in children infected from a common HIV type 1 subtype G source. AIDS Research and Human Retroviruses, 26 (3), 275-278. doi:10.1089/aid.2009.0233 ![]() |
![]() ![]() | ROOMP, K., & Rand, J. (2009). Intensive blood glucose control is safe and effective in diabetic cats using home monitoring and treatment with glargine. Journal of Feline Medicine and Surgery, 11 (8), 668-682. doi:10.1016/j.jfms.2009.04.010 ![]() |
ROOMP, K., & Rand, J. S. (2008). The somogyi effect is rare in diabetic cats managed using glargine and a protocol aimed at tight glycemic control. Journal of Veterinary Internal Medicine, 22 (3), 790-791. doi:10.1111/j.1939-1676.2008.0103.x ![]() |
ROOMP, K., & Rand, J. S. (2008). Evaluation of intensive blood glucose control using glargine in diabetic cats. Journal of Veterinary Internal Medicine, 22 (3), 790. ![]() |
ROOMP, K., & Rand, J. S. (2008). Factors predictive of non-insulin dependence in diabetic cats initially treated with insulin. Journal of Veterinary Internal Medicine, 22 (3), 791. doi:10.1111/j.1939-1676.2008.0103.x ![]() |
![]() ![]() | Ahlenstiel, G., ROOMP, K., Daumer, M., Nattermann, J., Vogel, M., Rockstroh, J. K., Beerenwinkel, N., Kaiser, R., Nischalke, H. D., Sauerbruch, T., Lengauer, T., & Spengler, U. (2007). Selective pressures of HLA genotypes and antiviral therapy on human immunodeficiency virus type 1 sequence mutation at a population level. Clinical and Vaccine Immunology, 14 (10), 1266-1273. doi:10.1128/CVI.00169-07 ![]() |
![]() ![]() | ROOMP, K., Beerenwinkel, N., Sing, T., Schülter, E., Büch, J., Sierra-Aragon, S., Däumer, M., Hoffmann, D., Kaiser, R., Lengauer, T., & Selbig, J. (2006). Arevir: A Secure Platform for Designing Personalized Antiretroviral Therapies Against HIV. In U. Leser, F. Naumann, ... B. Eckman (Eds.), Data Integration in the Life Sciences (pp. 185-194). Springer-Verlag Berlin Heidelberg. doi:10.1007/11799511_16 ![]() |
![]() ![]() | Beerenwinkel, N., Sing, T., Lengauer, T., Rahnenführer, ROOMP, K., Savenkov, I., Fischer, R., Hoffmann, D., Selbig, J., Korn, K., Walter, H., Berg, T., Braun, P., Fätkenheuer, Oette, M., Rockstroh, J., Kupfer, B., Kaiser, R., & Däumer. (2005). Computational methods for the design of effective therapies against drug resistant HIV strains. Bioinformatics, 21 (21), 3943-50. doi:10.1093/bioinformatics/bti654 ![]() |
![]() ![]() | Wellington, C. L., Yang, Y. Z., Zhou, S., Clee, S. M., Tan, B., Hirano, K., Zwarts, K., Kwok, A., Gelfer, A., Marcil, M., Newman, S., ROOMP, K., Singaraja, R., Collins, J. A., Zhang, L. H., Groen, A. K., Hovingh, K., Brownlie, A., Tafuri, S., ... Hayden, M. R. (2002). Truncation mutations in ABCA1 suppress normal upregulation of full-length ABCA1 by 9-cis-retinoic acid and 22-R-hydroxycholesterol. Journal of Lipid Research, 43 (11), 1939-1949. doi:10.1194/jlr.M200277-JLR200 ![]() |
![]() ![]() | Nishida, Y., Hirano, K., Tsukamoto, K., Nagano, M., Ikegami, C., ROOMP, K., Ishihara, M., Sakane, N., Zhang, Z., Tsujii Ki, K., Matsuyama, A., Ohama, T., Matsuura, F., Ishigami, M., Sakai, N., Hiraoka, H., Hattori, H., Wellington, C., Yoshida, Y., ... Matsuzawa, Y. (2002). Expression and functional analyses of novel mutations of ATP-binding cassette transporter-1 in Japanese patients with high-density lipoprotein deficiency. Biochemical and Biophysical Research Communications, 290 (2), 713-721. doi:10.1006/bbrc.2001.6219 ![]() |
Zwarts, K. Y., Clee, S. M., Zwinderman, A. H., Engert, J. C., Singaraja, R., Loubser, O., James, E., ROOMP, K., Hudson, T. J., Jukema, J. W., Kastelein, J. J., & Hayden, M. R. (2002). ABCA1 regulatory variants influence coronary artery disease independent of effects on plasma lipid levels. Clinical Genetics, 61 (2), 115-125. doi:10.1034/j.1399-0004.2002.610206.x ![]() |
![]() ![]() | Clee, S. M., Zwinderman, A. H., Engert, J. C., Zwarts, K. Y., Molhuizen, H. O., ROOMP, K., Jukema, J. W., van Wijland, M., van Dam, M., Hudson, T. J., Brooks-Wilson, A., Genest Jr., J., Kastelein, J. J., & Hayden, M. R. (2001). Common genetic variation in ABCA1 is associated with altered lipoprotein levels and a modified risk for coronary artery disease. Circulation, 103 (9), 1198-1205. doi:10.1161/01.CIR.103.9.1198 ![]() |
Clee, S. M., Kastelein, J. J., van Dam, M., Marcil, M., ROOMP, K., Zwarts, K. Y., Collins, J. A., Roelants, R., Tamasawa, N., Stulc, T., Suda, T., Ceska, R., Boucher, B., Rondeau, C., DeSouich, C., Brooks-Wilson, A., Molhuizen, H. O., Frohlich, J., Genest Jr., J., & Hayden, M. R. (2000). Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes. Journal of Clinical Investigation, 106 (10), 1263-1270. doi:10.1172/JCI10727 ![]() |
Brooks-Wilson, A., Marcil, M., Clee, S. M., Zhang, L. H., RUMP, K., van Dam, M., Yu, L., Brewer, C., Collins, J. A., Molhuizen, H. O., Loubser, O., Ouelette, B. F., Fichter, K., Ashbourne-Excoffon, K. J., Sensen, C. W., Scherer, S., Mott, S., Denis, M., Martindale, D., ... Hayden, M. R. (August 1999). Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency. Nature Genetics, 22 (4), 336-45. doi:10.1038/11905 ![]() |