Chromosome 17 deletions and p53 gene mutations in colorectal carcinomas SJ Baker, ER Fearon, JM Nigro, SR Hamilton, AC Preisinger, JM Jessup, ... Science 244 (4901), 217-221, 1989 | 2934 | 1989 |
DNA duplication associated with Charcot-Marie-Tooth disease type 1A JR Lupski, RM de Oca-Luna, S Slaugenhaupt, L Pentao, V Guzzetta, ... Cell 66 (2), 219-232, 1991 | 1533 | 1991 |
A genetic linkage map of the human genome H Donis-Keller, P Green, C Helms, S Cartinhour, B Weiffenbach, ... Cell 51 (2), 319-337, 1987 | 1263 | 1987 |
Identification of mutations in the COL4A5 collagen gene in Alport syndrome DF Barker, SL Hostikka, J Zhou, LT Chow, AR Oliphant, SC Gerken, ... Science 248 (4960), 1224-1227, 1990 | 1050 | 1990 |
Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17 D Barker, E Wright, K Nguyen, L Cannon, P Fain, D Goldgar, DT Bishop, ... Science 236 (4805), 1100-1102, 1987 | 923 | 1987 |
Duplication in chromosome 17p11. 2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a) P Raeymaekers, V Timmerman, E Nelis, P De Jonghe, JE Hoogenduk, ... Neuromuscular disorders 1 (2), 93-97, 1991 | 750 | 1991 |
Cystic fibrosis locus defined by a genetically linked polymorphic DNA marker LC Tsui, M Buchwald, D Barker, JC Braman, R Knowlton, JW Schumm, ... Science 230 (4729), 1054-1057, 1985 | 705 | 1985 |
Restriction sites containing CpG show a higher frequency of polymorphism in human DNA D Barker, M Schafer, R White Cell 36 (1), 131-138, 1984 | 690 | 1984 |
Metagenomic analyses of alcohol induced pathogenic alterations in the intestinal microbiome and the effect of Lactobacillus rhamnosus GG treatment L Bull-Otterson, W Feng, I Kirpich, Y Wang, X Qin, Y Liu, L Gobejishvili, ... PloS one 8 (1), e53028, 2013 | 562 | 2013 |
A polymorphic DNA marker linked to cystic fibrosis is located on chromosome 7 RG Knowlton, O Cohen-Haguenauer, N Van Cong, J Frézal, VA Brown, ... Nature 318 (6044), 380-382, 1985 | 430 | 1985 |
Construction of linkage maps with DNA markers for human chromosomes R White, M Leppert, DT Bishop, D Barker, J Berkowitz, C Brown, ... Nature 313 (5998), 101-105, 1985 | 424 | 1985 |
Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like … KE Heath, A Campos-Barros, A Toren, G Rozenfeld-Granot, LE Carlsson, ... The American Journal of Human Genetics 69 (5), 1033-1045, 2001 | 391 | 2001 |
Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17 JM Vance, GA Nicholson, LH Yamaoka, J Stajich, CS Stewart, MC Speer, ... Experimental neurology 104 (2), 186-189, 1989 | 271 | 1989 |
Paternal origin of new mutations in von Recklinghausen neurofibromatosis D Jadayel, P Fain, M Upadhyaya, MA Ponder, SM Huson, J Carey, ... Nature 343 (6258), 558-559, 1990 | 252 | 1990 |
Genetic and biochemical characterization of the birA gene and its product: evidence for a direct role of biotin holoenzyme synthetase in repression of the biotin operon in … DF Barker, AM Campbell Journal of molecular biology 146 (4), 469-492, 1981 | 240 | 1981 |
A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22. L Tranebjaerg, C Schwartz, H Eriksen, S Andreasson, V Ponjavic, A Dahl, ... Journal of medical genetics 32 (4), 257-263, 1995 | 235 | 1995 |
PROPERTIES OF THE TRANSLOCATABLE TETRACYCLINE-RESISTANCE ELEMENT Tn10 IN ESCHERICHIA COLI AND BACTERIOPHAGE LAMBDA N Kleckner, DF Barker, DG Ross, D Botstein Genetics 90 (3), 427-461, 1978 | 226 | 1978 |
Single-copy sequence hybridizes to polymorphic and homologous loci on human X and Y chromosomes. D Page, B de Martinville, D Barker, A Wyman, R White, U Francke, ... Proceedings of the National Academy of Sciences 79 (17), 5352-5356, 1982 | 225 | 1982 |
The birA gene of Escherichia coli encodes a biotin holoenzyme synthetase DF Barker, AM Campbell Journal of molecular biology 146 (4), 451-467, 1981 | 221 | 1981 |
A mapped set of DNA markers for human chromosome 17 Y Nakamura, M Lathrop, P O'Connell, M Leppert, D Barker, E Wright, ... Genomics 2 (4), 302-309, 1988 | 183 | 1988 |