| The allelic landscape of human blood cell trait variation and links to common complex disease WJ Astle, H Elding, T Jiang, D Allen, D Ruklisa, AL Mann, D Mead, ... Cell 167 (5), 1415-1429. e19, 2016 | 1171 | 2016 |
| Genetic drivers of epigenetic and transcriptional variation in human immune cells L Chen, B Ge, FP Casale, L Vasquez, T Kwan, D Garrido-Martín, S Watt, ... Cell 167 (5), 1398-1414. e24, 2016 | 649 | 2016 |
| The polygenic and monogenic basis of blood traits and diseases D Vuckovic, EL Bao, P Akbari, CA Lareau, A Mousas, T Jiang, MH Chen, ... Cell 182 (5), 1214-1231. e11, 2020 | 426 | 2020 |
| Shared genetic effects on chromatin and gene expression indicate a role for enhancer priming in immune response K Alasoo, J Rodrigues, S Mukhopadhyay, AJ Knights, AL Mann, K Kundu, ... Nature genetics 50 (3), 424-431, 2018 | 279 | 2018 |
| A map of transcriptional heterogeneity and regulatory variation in human microglia AMH Young, N Kumasaka, F Calvert, TR Hammond, A Knights, ... Nature genetics 53 (6), 861-868, 2021 | 135 | 2021 |
| Freiburg RNA tools: a central online resource for RNA-focused research and teaching M Raden, SM Ali, OS Alkhnbashi, A Busch, F Costa, JA Davis, ... Nucleic acids research 46 (W1), W25-W29, 2018 | 125 | 2018 |
| Tumors induce de novo steroid biosynthesis in T cells to evade immunity B Mahata, J Pramanik, L van der Weyden, K Polanski, G Kar, A Riedel, ... Nature communications 11 (1), 3588, 2020 | 67 | 2020 |
| MoDPepInt: an interactive web server for prediction of modular domain–peptide interactions K Kundu, M Mann, F Costa, R Backofen Bioinformatics 30 (18), 2668-2669, 2014 | 46 | 2014 |
| Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program Y Hu, AM Stilp, CP McHugh, S Rao, D Jain, X Zheng, J Lane, ... The American Journal of Human Genetics 108 (5), 874-893, 2021 | 44 | 2021 |
| Genetic perturbation of PU. 1 binding and chromatin looping at neutrophil enhancers associates with autoimmune disease S Watt, L Vasquez, K Walter, AL Mann, K Kundu, L Chen, Y Sims, S Ecker, ... Nature communications 12 (1), 2298, 2021 | 36 | 2021 |
| Semi-supervised prediction of SH2-peptide interactions from imbalanced high-throughput data K Kundu, F Costa, M Huber, M Reth, R Backofen PloS one 8 (5), e62732, 2013 | 36 | 2013 |
| Immune disease variants modulate gene expression in regulatory CD4+ T cells L Bossini-Castillo, DA Glinos, N Kunowska, G Golda, AA Lamikanra, ... Cell genomics 2 (4), 2022 | 32 | 2022 |
| Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits A Gilly, D Suveges, K Kuchenbaecker, M Pollard, L Southam, ... Nature communications 9 (1), 4674, 2018 | 32 | 2018 |
| Mitochondrial DNA variants modulate N-formylmethionine, proteostasis and risk of late-onset human diseases N Cai, A Gomez-Duran, E Yonova-Doing, K Kundu, AI Burgess, ZJ Golder, ... Nature medicine 27 (9), 1564-1575, 2021 | 31 | 2021 |
| Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for 12 immune-mediated diseases K Kundu, M Tardaguila, AL Mann, S Watt, H Ponstingl, L Vasquez, ... Nature genetics 54 (3), 251-262, 2022 | 29 | 2022 |
| Cluster based prediction of PDZ-peptide interactions K Kundu, R Backofen BMC genomics 15, 1-11, 2014 | 29 | 2014 |
| Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative G Butler-Laporte, G Povysil, JA Kosmicki, ET Cirulli, T Drivas, S Furini, ... PLoS genetics 18 (11), e1010367, 2022 | 27 | 2022 |
| GRIN3B missense mutation as an inherited risk factor for schizophrenia: whole-exome sequencing in a family with a familiar history of psychotic disorders T Hornig, B Gruening, K Kundu, T Houwaart, R Backofen, K Biber, ... Genetics Research 99, e1, 2017 | 24 | 2017 |
| A graph kernel approach for alignment-free domain–peptide interaction prediction with an application to human SH3 domains K Kundu, F Costa, R Backofen Bioinformatics 29 (13), i335-i343, 2013 | 24 | 2013 |
| Whole-exome sequencing identifies rare genetic variants associated with human plasma metabolites L Bomba, K Walter, Q Guo, P Surendran, K Kundu, S Nongmaithem, ... The American Journal of Human Genetics 109 (6), 1038-1054, 2022 | 19 | 2022 |
Rolf BackofenProfessor für Bioinformatik, Universität FreiburgVerified email at informatik.uni-freiburg.de
