| Imaging tumor-stroma interactions during chemotherapy reveals contributions of the microenvironment to resistance ES Nakasone, HA Askautrud, T Kees, JH Park, V Plaks, AJ Ewald, M Fein, ... Cancer cell 21 (4), 488-503, 2012 | 533 | 2012 |
| An improved approach for construction of bacterial artificial chromosome libraries K Osoegawa, PY Woon, B Zhao, E Frengen, M Tateno, JJ Catanese, ... Genomics 52 (1), 1-8, 1998 | 436 | 1998 |
| Bacterial artificial chromosome libraries for mouse sequencing and functional analysis K Osoegawa, M Tateno, PY Woon, E Frengen, AG Mammoser, ... Genome research 10 (1), 116-128, 2000 | 405 | 2000 |
| A bacterial artificial chromosome library for sequencing the complete human genome K Osoegawa, AG Mammoser, C Wu, E Frengen, C Zeng, JJ Catanese, ... Genome research 11 (3), 483-496, 2001 | 364 | 2001 |
| GRIN2B encephalopathy: novel findings on phenotype, variant clustering, functional consequences and treatment aspects K Platzer, H Yuan, H Schütz, A Winschel, W Chen, C Hu, H Kusumoto, ... Journal of medical genetics 54 (7), 460-470, 2017 | 239 | 2017 |
| Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy JR Lemke, K Geider, KL Helbig, HO Heyne, H Schütz, J Hentschel, ... Neurology 86 (23), 2171-2178, 2016 | 195 | 2016 |
| A Dominant STIM 1 Mutation Causes S tormorken Syndrome D Misceo, A Holmgren, WE Louch, PA Holme, M Mizobuchi, RJ Morales, ... Human mutation 35 (5), 556-564, 2014 | 190 | 2014 |
| A modular, positive selection bacterial artificial chromosome vector with multiple cloning sites E Frengen, D Weichenhan, B Zhao, K Osoegawa, M van Geel, PJ de Jong Genomics 58 (3), 250-253, 1999 | 185 | 1999 |
| A core MYC gene expression signature is prominent in basal-like breast cancer but only partially overlaps the core serum response S Chandriani, E Frengen, VH Cowling, SA Pendergrass, CM Perou, ... PloS one 4 (8), e6693, 2009 | 165 | 2009 |
| YY1 haploinsufficiency causes an intellectual disability syndrome featuring transcriptional and chromatin dysfunction M Gabriele, AT Vulto-van Silfhout, PL Germain, A Vitriolo, R Kumar, ... The American Journal of Human Genetics 100 (6), 907-925, 2017 | 143 | 2017 |
| Human TGF-β1 deficiency causes severe inflammatory bowel disease and encephalopathy D Kotlarz, B Marquardt, T Barøy, WS Lee, L Konnikova, S Hollizeck, ... Nature genetics 50 (3), 344-348, 2018 | 132 | 2018 |
| Alternative transcripts of the candidate tumor suppressor gene, WWOX, are expressed at high levels in human breast tumors K Driouch, H Prydz, R Monese, H Johansen, R Lidereau, E Frengen Oncogene 21 (12), 1832-1840, 2002 | 126 | 2002 |
| A highly redundant BAC library of Atlantic salmon (Salmo salar): an important tool for salmon projects J Thorsen, B Zhu, E Frengen, K Osoegawa, PJ de Jong, BF Koop, ... BMC genomics 6, 1-8, 2005 | 106 | 2005 |
| A novel type of rhizomelic chondrodysplasia punctata, RCDP5, is caused by loss of the PEX5 long isoform T Barøy, J Koster, P Strømme, MS Ebberink, D Misceo, S Ferdinandusse, ... Human molecular genetics 24 (20), 5845-5854, 2015 | 90 | 2015 |
| Increasing the resolution of the comet assay using fluorescent in situ hybridization—a review S Shaposhnikov, E Frengen, AR Collins Mutagenesis 24 (5), 383-389, 2009 | 76 | 2009 |
| Mutated thyroid hormone transporter OATP1C1 associates with severe brain hypometabolism and juvenile neurodegeneration P Strømme, S Groeneweg, EC Lima de Souza, C Zevenbergen, ... Thyroid 28 (11), 1406-1415, 2018 | 73 | 2018 |
| Modular bacterial artificial chromosome vectors for transfer of large inserts into mammalian cells E Frengen, B Zhao, S Howe, D Weichenhan, K Osoegawa, E Gjernes, ... Genomics 68 (2), 118-126, 2000 | 72 | 2000 |
| Identification of novel splice variants of the human catalytic subunit cβ of cAMP‐dependent protein kinase S Ørstavik, N Reinton, E Frengen, BT Langeland, T Jahnsen, ... European Journal of Biochemistry 268 (19), 5066-5073, 2001 | 69 | 2001 |
| Spastic paraplegia type 7 is associated with multiple mitochondrial DNA deletions IM Wedding, J Koht, GT Tran, D Misceo, KK Selmer, A Holmgren, ... PloS one 9 (1), e86340, 2014 | 62 | 2014 |
| Porcine SINEs: characterization and use in species-specific amplification E Frengen, P Thomsen, T Kristensen, S Kran, R Miller, W Davies Genomics 10 (4), 949-956, 1991 | 62 | 1991 |
