| The Collaborative Cross, a community resource for the genetic analysis of complex traits Nature genetics 36 (11), 1133-1137, 2004 | 1217 | 2004 |
| A mouse model for Down syndrome exhibits learning and behaviour deficits RH Reeves, NG Irving, TH Moran, A Wohn, C Kitt, SS Sisodia, C Schmidt, ... Nature genetics 11 (2), 177-184, 1995 | 1101 | 1995 |
| Down syndrome SE Antonarakis, BG Skotko, MS Rafii, A Strydom, SE Pape, DW Bianchi, ... Nature Reviews Disease Primers 6 (1), 9, 2020 | 857 | 2020 |
| TSLC1 is a tumor-suppressor gene in human non-small-cell lung cancer M Kuramochi, H Fukuhara, T Nobukuni, T Kanbe, T Maruyama, HP Ghosh, ... Nature genetics 27 (4), 427-430, 2001 | 592 | 2001 |
| Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethonin ES Moreira, TJ Wiltshire, G Faulkner, A Nilforoushan, M Vainzof, ... Nature genetics 24 (2), 163-166, 2000 | 444 | 2000 |
| Segmental trisomy as a mouse model for Down syndrome. MT Davisson, C Schmidt, RH Reeves, NG Irving, EC Akeson, BS Harris, ... Progress in clinical and biological research 384, 117-133, 1993 | 424 | 1993 |
| Discovery and genetic localization of Down syndrome cerebellar phenotypes using the Ts65Dn mouse LL Baxter, TH Moran, JT Richtsmeier, J Troncoso, RH Reeves Human molecular genetics 9 (2), 195-202, 2000 | 409 | 2000 |
| A chromosome 21 critical region does not cause specific Down syndrome phenotypes LE Olson, JT Richtsmeier, J Leszl, RH Reeves Science 306 (5696), 687-690, 2004 | 407 | 2004 |
| Parallels of craniofacial maldevelopment in Down syndrome and Ts65Dn mice JT Richtsmeier, LL Baxter, RH Reeves Developmental dynamics: an official publication of the American Association …, 2000 | 347 | 2000 |
| Down syndrome and Alzheimer's disease: Common pathways, common goals D Hartley, T Blumenthal, M Carrillo, G DiPaolo, L Esralew, K Gardiner, ... Alzheimer's & Dementia 11 (6), 700-709, 2015 | 339 | 2015 |
| Understanding the basis for Down syndrome phenotypes RJ Roper, RH Reeves PLoS genetics 2 (3), e50, 2006 | 311 | 2006 |
| Transcript level alterations reflect gene dosage effects across multiple tissues in a mouse model of down syndrome P Kahlem, M Sultan, R Herwig, M Steinfath, D Balzereit, B Eppens, ... Genome research 14 (7), 1258-1267, 2004 | 308 | 2004 |
| The Pit-1 transcription factor gene is a candidate for the murine Snell dwarf mutation SA Camper, TL Saunders, RW Katz, RH Reeves Genomics 8 (3), 586-590, 1990 | 263 | 1990 |
| Too much of a good thing: mechanisms of gene action in Down syndrome RH Reeves, LL Baxter, JT Richtsmeier TRENDS in Genetics 17 (2), 83-88, 2001 | 259 | 2001 |
| Defective cerebellar response to mitogenic Hedgehog signaling in Down's syndrome mice RJ Roper, LL Baxter, NG Saran, DK Klinedinst, PA Beachy, RH Reeves Proceedings of the National Academy of Sciences 103 (5), 1452-1456, 2006 | 258 | 2006 |
| Astrocytosis and axonal proliferation in the hippocampus of S100b transgenic mice. RH Reeves, J Yao, MR Crowley, S Buck, X Zhang, P Yarowsky, ... Proceedings of the National Academy of Sciences 91 (12), 5359-5363, 1994 | 258 | 1994 |
| The “Down syndrome critical region” is sufficient in the mouse model to confer behavioral, neurophysiological, and synaptic phenotypes characteristic of Down syndrome NP Belichenko, PV Belichenko, AM Kleschevnikov, A Salehi, RH Reeves, ... Journal of Neuroscience 29 (18), 5938-5948, 2009 | 248 | 2009 |
| Trisomy for the Down syndrome ‘critical region’is necessary but not sufficient for brain phenotypes of trisomic mice LE Olson, RJ Roper, CL Sengstaken, EA Peterson, V Aquino, Z Galdzicki, ... Human molecular genetics 16 (7), 774-782, 2007 | 246 | 2007 |
| NPTX2 and cognitive dysfunction in Alzheimer’s Disease MF Xiao, D Xu, MT Craig, KA Pelkey, CC Chien, Y Shi, J Zhang, ... elife 6, e23798, 2017 | 238 | 2017 |
| Protection from doxorubicin-induced cardiac toxicity in mice with a null allele of carbonyl reductase LE Olson, D Bedja, SJ Alvey, AJ Cardounel, KL Gabrielson, RH Reeves Cancer research 63 (20), 6602-6606, 2003 | 238 | 2003 |
