| The genome of the Western clawed frog Xenopus tropicalis U Hellsten, RM Harland, MJ Gilchrist, D Hendrix, J Jurka, V Kapitonov, ... Science 328 (5978), 633-636, 2010 | 937 | 2010 |
| Disruption of gastrulation and heparan sulfate biosynthesis in EXT1-deficient mice X Lin, G Wei, Z Shi, L Dryer, JD Esko, DE Wells, MM Matzuk Developmental biology 224 (2), 299-311, 2000 | 543 | 2000 |
| Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1) J Ahn, HJ Lüdecke, S Lindow, WA Horton, B Lee, MJ Wagner, ... Nature genetics 11 (2), 137-143, 1995 | 543 | 1995 |
| Extubation failure in pediatric intensive care: a multiple-center study of risk factors and outcomes SC Kurachek, CJ Newth, MW Quasney, T Rice, RC Sachdeva, NR Patel, ... Critical care medicine 31 (11), 2657-2664, 2003 | 373 | 2003 |
| Ventilator-associated pneumonia in the pediatric intensive care unit: characterizing the problem and implementing a sustainable solution MT Bigham, R Amato, P Bondurrant, J Fridriksson, CD Krawczeski, ... The Journal of pediatrics 154 (4), 582-587. e2, 2009 | 274 | 2009 |
| Genetic heterogeneity in families with hereditary multiple exostoses A Cook, W Raskind, SH Blanton, RM Pauli, RG Gregg, CA Francomano, ... American journal of human genetics 53 (1), 71, 1993 | 267 | 1993 |
| Loss of chromosome arm 8p loci in prostate cancer: mapping by quantitative allelic imbalance D MacGrogan, A Levy, D Bostwick, M Wagner, D Wells, R Bookstein Genes, Chromosomes and Cancer 10 (3), 151-159, 1994 | 220 | 1994 |
| Structure of a human histone cDNA: evidence that basally expressed histone genes have intervening sequences and encode polyadenylylated mRNAs. D Wells, L Kedes Proceedings of the National Academy of Sciences 82 (9), 2834-2838, 1985 | 218 | 1985 |
| A comprehensive compilation and alignment of histones and histone genes D Wells, C McBride Nucleic acids research 17 (Suppl), r311, 1989 | 181 | 1989 |
| Compilation analysis of histones and histone genes DE Wells Nucleic acids research 14 (Suppl), r119, 1986 | 176 | 1986 |
| Chromosomal localization of the human and mouse hyaluronan synthase genes AP Spicer, MF Seldin, AS Olsen, N Brown, DE Wells, NA Doggett, N Itano, ... Genomics 41 (3), 493-497, 1997 | 162 | 1997 |
| Hereditary multiple exostoses (EXT): mutational studies of familial EXT1 cases and EXT-associated malignancies. JT Hecht, D Hogue, Y Wang, SH Blanton, M Wagner, LC Strong, ... American journal of human genetics 60 (1), 80, 1997 | 162 | 1997 |
| Molecular dissection of a contiguous gene syndrome: localization of the genes involved in the Langer—Giedion syndrome HJ Lüdecke, M J. Wagner, J Nardmann, BL Pillo, J E. Parrish, P J. Willems, ... Human molecular genetics 4 (1), 31-36, 1995 | 160 | 1995 |
| Mutation screening of the EXT1 and EXT2 genes in patients with hereditary multiple exostoses C Philippe, DE Porter, ME Emerton, DE Wells, A Hamish, RW Simpson, ... The American Journal of Human Genetics 61 (3), 520-528, 1997 | 154 | 1997 |
| Light induction of a vertebrate clock gene involves signaling through blue-light receptors and MAP kinases N Cermakian, MP Pando, CL Thompson, AB Pinchak, CP Selby, ... Current Biology 12 (10), 844-848, 2002 | 152 | 2002 |
| Accumulation in embryogenesis of five mRNAs enriched in the ectoderm of the sea urchin pluteus AM Bruskin, AL Tyner, DE Wells, RM Showman, WH Klein Developmental biology 87 (2), 308-318, 1981 | 130 | 1981 |
| Identification of intrinsic termination sites in vitro for RNA polymerase II within eukaryotic gene sequences D Reines, D Wells, MJ Chamberlin, CM Kane Journal of molecular biology 196 (2), 299-312, 1987 | 123 | 1987 |
| A hybrid cell mapping panel for regional localization of probes to human chromosome 8 MJ Wagner, Y Ge, M Siciliano, DE Wells Genomics 10 (1), 114-125, 1991 | 105 | 1991 |
| Unusual structure, evolutionary conservation of non-coding sequences and numerous pseudogenes characterize the human H3. 3 histone multigene family D Wells, D Hoffman, L Kedes Nucleic acids research 15 (7), 2871-2889, 1987 | 99 | 1987 |
| Molecular definition of the shortest region of deletion overlap in the Langer-Giedion syndrome HJ Lüdecke, C Johnson, MJ Wagner, DE Wells, C Turleau, N Tommerup, ... American journal of human genetics 49 (6), 1197, 1991 | 92 | 1991 |
Amy K. SaterProfessor of Biology and Biochemistry, University of HoustonDirección de correo verificada de uh.edu
