| Rare variant discovery by deep whole-genome sequencing of 1,070 Japanese individuals M Nagasaki, J Yasuda, F Katsuoka, N Nariai, K Kojima, Y Kawai, ... Nature communications 6 (1), 8018, 2015 | 435 | 2015 |
| iPSCORE: a resource of 222 iPSC lines enabling functional characterization of genetic variation across a variety of cell types AD Panopoulos, M D'Antonio, P Benaglio, R Williams, SI Hashem, ... Stem cell reports 8 (4), 1086-1100, 2017 | 185 | 2017 |
| Large-scale profiling reveals the influence of genetic variation on gene expression in human induced pluripotent stem cells C DeBoever, H Li, D Jakubosky, P Benaglio, J Reyna, KM Olson, ... Cell stem cell 20 (4), 533-546. e7, 2017 | 182 | 2017 |
| Japonica array: improved genotype imputation by designing a population-specific SNP array with 1070 Japanese individuals Y Kawai, T Mimori, K Kojima, N Nariai, I Danjoh, R Saito, J Yasuda, ... Journal of human genetics 60 (10), 581-587, 2015 | 156 | 2015 |
| Systematic analysis of binding of transcription factors to noncoding variants J Yan, Y Qiu, AM Ribeiro dos Santos, Y Yin, YE Li, N Vinckier, N Nariai, ... Nature 591 (7848), 147-151, 2021 | 135 | 2021 |
| Probabilistic protein function prediction from heterogeneous genome-wide data N Nariai, ED Kolaczyk, S Kasif Plos one 2 (3), e337, 2007 | 135 | 2007 |
| Using protein-protein interactions for refining gene networks estimated from microarray data by Bayesian networks N Nariai, S Kim, S Imoto, S Miyano Biocomputing 2004, 336-347, 2003 | 120 | 2003 |
| iJGVD: an integrative Japanese genome variation database based on whole-genome sequencing Y Yamaguchi-Kabata, N Nariai, Y Kawai, Y Sato, K Kojima, M Tateno, ... Human genome variation 2 (1), 1-4, 2015 | 113 | 2015 |
| Pancreatic islet chromatin accessibility and conformation reveals distal enhancer networks of type 2 diabetes risk WW Greenwald, J Chiou, J Yan, Y Qiu, N Dai, A Wang, N Nariai, ... Nature communications 10 (1), 2078, 2019 | 107 | 2019 |
| HLA-VBSeq: accurate HLA typing at full resolution from whole-genome sequencing data N Nariai, K Kojima, S Saito, T Mimori, Y Sato, Y Kawai, ... BMC genomics 16, 1-6, 2015 | 100 | 2015 |
| Transposon mutagenesis identifies genes that transform neural stem cells into glioma-initiating cells H Koso, H Takeda, CCK Yew, JM Ward, N Nariai, K Ueno, M Nagasaki, ... Proceedings of the National Academy of Sciences 109 (44), E2998-E3007, 2012 | 83 | 2012 |
| Estimating gene regulatory networks and protein–protein interactions of Saccharomyces cerevisiae from multiple genome-wide data N Nariai, Y Tamada, S Imoto, S Miyano Bioinformatics 21 (suppl_2), ii206-ii212, 2005 | 61 | 2005 |
| TIGAR2: sensitive and accurate estimation of transcript isoform expression with longer RNA-Seq reads N Nariai, K Kojima, T Mimori, Y Sato, Y Kawai, Y Yamaguchi-Kabata, ... BMC genomics 15, 1-9, 2014 | 56 | 2014 |
| Integration of relational and hierarchical network information for protein function prediction X Jiang, N Nariai, M Steffen, S Kasif, ED Kolaczyk BMC Bioinformatics 9 (1), 350, 2008 | 48 | 2008 |
| TIGAR: transcript isoform abundance estimation method with gapped alignment of RNA-Seq data by variational Bayesian inference N Nariai, O Hirose, K Kojima, M Nagasaki Bioinformatics 29 (18), 2292-2299, 2013 | 47 | 2013 |
| Wnt3a stimulates maturation of impaired neutrophils developed from severe congenital neutropenia patient-derived pluripotent stem cells T Hiramoto, Y Ebihara, Y Mizoguchi, K Nakamura, K Yamaguchi, K Ueno, ... Proceedings of the National Academy of Sciences 110 (8), 3023-3028, 2013 | 45 | 2013 |
| Systematic genetic analysis of the MHC region reveals mechanistic underpinnings of HLA type associations with disease M D'Antonio, J Reyna, D Jakubosky, MKR Donovan, MJ Bonder, H Matsui, ... Elife 8, e48476, 2019 | 44 | 2019 |
| Pgltools: a genomic arithmetic tool suite for manipulation of Hi-C peak and other chromatin interaction data WW Greenwald, H Li, EN Smith, P Benaglio, N Nariai, KA Frazer BMC bioinformatics 18, 1-6, 2017 | 43 | 2017 |
| Establishing the involvement of the novel gene AGBL5 in retinitis pigmentosa by whole genome sequencing K Branham, H Matsui, P Biswas, AA Guru, M Hicks, JJ Suk, H Li, ... Physiological Genomics 48 (12), 922-927, 2016 | 41 | 2016 |
| iSVP: an integrated structural variant calling pipeline from high-throughput sequencing data T Mimori, N Nariai, K Kojima, M Takahashi, A Ono, Y Sato, ... BMC systems biology 7, 1-8, 2013 | 39 | 2013 |
Takahiro MimoriWaseda UniversityZweryfikowany adres z aoni.waseda.jp