Genetic mapping of a gene causing hypertension in the stroke-prone spontaneously hypertensive rat HJ Jacob, K Lindpaintner, SE Lincoln, K Kusumi, RK Bunker, YP Mao, ... Cell 67 (1), 213-224, 1991 | 1026 | 1991 |
The diastrophic dysplasia gene encodes a novel sulfate transporter: positional cloning by fine-structure linkage disequilibrium mapping J Hästbacka, A de la Chapelle, MM Mahtani, G Clines, MP Reeve-Daly, ... Cell 78 (6), 1073-1087, 1994 | 863 | 1994 |
Disruption of the nuclear hormone receptor RORα in staggerer mice BA Hamilton, WN Frankel, AW Kerrebrock, TL Hawkins, W FitzHugh, ... Nature 379 (6567), 736-739, 1996 | 576 | 1996 |
Mutations in the human delta homologue, DLL3, cause axial skeletal defects in spondylocostal dysostosis MP Bulman, K Kusumi, TM Frayling, C McKeown, C Garrett, ES Lander, ... Nature genetics 24 (4), 438-441, 2000 | 477 | 2000 |
Immunization of chimpanzees confers protection against challenge with human immunodeficiency virus. M Girard, MP Kieny, A Pinter, F Barre-Sinoussi, P Nara, H Kolbe, ... Proceedings of the National Academy of Sciences 88 (2), 542-546, 1991 | 449 | 1991 |
Ducky mouse phenotype of epilepsy and ataxia is associated with mutations in the Cacna2d2 gene and decreased calcium channel current in cerebellar Purkinje cells J Barclay, N Balaguero, M Mione, SL Ackerman, VA Letts, J Brodbeck, ... Journal of Neuroscience 21 (16), 6095-6104, 2001 | 391 | 2001 |
The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8 S Ranta, Y Zhang, B Ross, L Lonka, E Takkunen, A Messer, J Sharp, ... Nature genetics 23 (2), 233-236, 1999 | 363 | 1999 |
The mouse pudgy mutation disrupts Delta homologue Dll3 and initiation of early somite boundaries K Kusumi, E Sun, AW Kerrebrock, RT Bronson, DC Chi, M Bulotsky, ... Nature genetics 19 (3), 274-278, 1998 | 353 | 1998 |
Klippel-Feil syndrome: clinical features and current understanding of etiology. MR Tracy, JP Dormans, K Kusumi Clinical Orthopaedics and Related Research (1976-2007) 424, 183-190, 2004 | 329 | 2004 |
Mutation of the LUNATIC FRINGE gene in humans causes spondylocostal dysostosis with a severe vertebral phenotype DB Sparrow, G Chapman, MA Wouters, NV Whittock, S Ellard, D Fatkin, ... The American Journal of Human Genetics 78 (1), 28-37, 2006 | 266 | 2006 |
A mechanism for gene-environment interaction in the etiology of congenital scoliosis DB Sparrow, G Chapman, AJ Smith, MZ Mattar, JA Major, VC O'Reilly, ... Cell 149 (2), 295-306, 2012 | 235 | 2012 |
Human immunodeficiency virus type 1 envelope gene structure and diversity in vivo and after cocultivation in vitro K Kusumi, B Conway, S Cunningham, A Berson, C Evans, AK Iversen, ... Journal of virology 66 (2), 875-885, 1992 | 192 | 1992 |
Abnormal vertebral segmentation and the notch signaling pathway in man PD Turnpenny, B Alman, AS Cornier, PF Giampietro, A Offiah, O Tassy, ... Developmental dynamics: an official publication of the American Association …, 2007 | 187 | 2007 |
Direct isolation of polymorphic markers linked to a trait by genetically directed representational difference analysis NA Lisitsyn, JA Segre, K Kusumi, NM Lisitsyn, JH Nadeau, WN Frankel, ... Nature genetics 6 (1), 57-63, 1994 | 165 | 1994 |
Novel mutations in DLL3, a somitogenesis gene encoding a ligand for the Notch signalling pathway, cause a consistent pattern of abnormal vertebral segmentation in … PD Turnpenny, N Whittock, J Duncan, S Dunwoodie, K Kusumi, S Ellard Journal of medical genetics 40 (5), 333-339, 2003 | 153 | 2003 |
Identification of cord blood-derived mesenchymal stem/stromal cell populations with distinct growth kinetics, differentiation potentials, and gene expression profiles V Markov, K Kusumi, MG Tadesse, DA William, DM Hall, V Lounev, ... Stem cells and development 16 (1), 53-74, 2007 | 149 | 2007 |
Transcriptomic analysis of tail regeneration in the lizard Anolis carolinensis reveals activation of conserved vertebrate developmental and repair mechanisms ED Hutchins, GJ Markov, WL Eckalbar, RM George, JM King, ... PloS one 9 (8), e105004, 2014 | 146 | 2014 |
Hereditary multiple exostoses: one center’s experience and review of etiology KA Pierz, JR Stieber, K Kusumi, JP Dormans Clinical Orthopaedics and Related Research® 401, 49-59, 2002 | 134 | 2002 |
A Histological Comparison of the Original and Regenerated Tail in the Green Anole, Anolis carolinensis RE Fisher, LA Geiger, LK Stroik, ED Hutchins, RM George, DF Denardo, ... The Anatomical Record: Advances in Integrative Anatomy and Evolutionary …, 2012 | 123 | 2012 |
Developmental anomalies of the cervical spine in patients with fibrodysplasia ossificans progressiva are distinctly different from those in patients with Klippel-Feil syndrome … AA Schaffer, FS Kaplan, MR Tracy, ML O'Brien, JP Dormans, EM Shore, ... Spine 30 (12), 1379-1385, 2005 | 114 | 2005 |