Stephen D. M. Brown, PhD, FRS, FMedSci - Publications

Affiliations: 
Medical Research Council Harwell, Didcot, England, United Kingdom 
Area:
Genetics
Website:
https://en.m.wikipedia.org/wiki/Stephen_D._M._Brown

20 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2012 Brown SD, Moore MW. The International Mouse Phenotyping Consortium: past and future perspectives on mouse phenotyping. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 23: 632-40. PMID 22940749 DOI: 10.1007/S00335-012-9427-X  0.375
2012 Brown SD, Moore MW. Towards an encyclopaedia of mammalian gene function: the International Mouse Phenotyping Consortium. Disease Models & Mechanisms. 5: 289-92. PMID 22566555 DOI: 10.1242/Dmm.009878  0.309
2011 Bhutta MF, Hedge EA, Parker A, Cheeseman MT, Brown SD. Oto-endoscopy: a reliable and validated technique for phenotyping otitis media in the mouse. Hearing Research. 272: 5-12. PMID 20870016 DOI: 10.1016/J.Heares.2010.09.002  0.346
2009 Brown A, Brown S, Ellisor D, Hagan N, Normand E, Zervas M. A practical approach to genetic inducible fate mapping: a visual guide to mark and track cells in vivo. Journal of Visualized Experiments : Jove. PMID 20042997 DOI: 10.3791/1687  0.302
2009 Schofield PN, Bubela T, Weaver T, Portilla L, Brown SD, Hancock JM, Einhorn D, Tocchini-Valentini G, Hrabe de Angelis M, Rosenthal N. Post-publication sharing of data and tools. Nature. 461: 171-3. PMID 19741686 DOI: 10.1038/461171A  0.399
2006 Parkinson N, Hardisty-Hughes RE, Tateossian H, Tsai HT, Brooker D, Morse S, Lalane Z, MacKenzie F, Fray M, Glenister P, Woodward AM, Polley S, Barbaric I, Dear N, Hough TA, ... ... Brown SD, et al. Mutation at the Evi1 locus in Junbo mice causes susceptibility to otitis media. Plos Genetics. 2: e149. PMID 17029558 DOI: 10.1371/Journal.Pgen.0020149  0.347
2006 Brown SD, Hancock JM, Gates H. Understanding mammalian genetic systems: the challenge of phenotyping in the mouse. Plos Genetics. 2: e118. PMID 16933996 DOI: 10.1371/Journal.Pgen.0020118  0.538
2000 O'Carroll D, Scherthan H, Peters AH, Opravil S, Haynes AR, Laible G, Rea S, Schmid M, Lebersorger A, Jerratsch M, Sattler L, Mattei MG, Denny P, Brown SD, Schweizer D, et al. Isolation and characterization of Suv39h2, a second histone H3 methyltransferase gene that displays testis-specific expression. Molecular and Cellular Biology. 20: 9423-33. PMID 11094092 DOI: 10.1128/Mcb.20.24.9423-9433.2000  0.405
1999 Liu XY, Dangel AW, Kelley RI, Zhao W, Denny P, Botcherby M, Cattanach B, Peters J, Hunsicker PR, Mallon AM, Strivens MA, Bate R, Miller W, Rhodes M, Brown SD, et al. The gene mutated in bare patches and striated mice encodes a novel 3beta-hydroxysteroid dehydrogenase. Nature Genetics. 22: 182-7. PMID 10369263 DOI: 10.1038/9700  0.393
1997 Gibson F, Brown SD. Isolation of coding sequences from yeast artificial chromosome (Yac). Clones by exon amplification Methods in Molecular Biology (Clifton, N.J.). 67: 301-313. PMID 9031155 DOI: 10.1385/0-89603-483-6:301  0.336
1995 Adler DA, Quaderi NA, Brown SD, Chapman VM, Moore J, Tate P, Disteche CM. The X-linked methylated DNA binding protein, Mecp2, is subject to X inactivation in the mouse. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 6: 491-2. PMID 8589515 DOI: 10.1007/Bf00356163  0.343
1993 Hamvas RM, Larin Z, Brockdorff N, Rastan S, Lehrach H, Chartier FL, Brown SD. YAC clone contigs surrounding the Zfx and Pola loci on the mouse X chromosome. Genomics. 17: 52-8. PMID 8406471 DOI: 10.1006/Geno.1993.1282  0.44
1992 Chartier FL, Keer JT, Sutcliffe MJ, Henriques DA, Mileham P, Brown SD. Construction of a mouse yeast artificial chromosome library in a recombination-deficient strain of yeast. Nature Genetics. 1: 132-6. PMID 1302006 DOI: 10.1038/Ng0592-132  0.346
1991 Irving NG, Hardy JA, Brown SD. The multipoint genetic mapping of mouse chromosome 16. Genomics. 9: 386-9. PMID 1672298 DOI: 10.1016/0888-7543(91)90271-F  0.454
1990 Keer JT, Hamvas RM, Brockdorff N, Page D, Rastan S, Brown SD. Genetic mapping in the region of the mouse X-inactivation center. Genomics. 7: 566-72. PMID 1974879 DOI: 10.1016/0888-7543(90)90200-E  0.582
1989 Brown SD. The mouse genome at Oxford: what can mouse gene mapping do for mammalian genetics? Bioessays. 11: 191-193. PMID 2695087 DOI: 10.1002/Bies.950110610  0.423
1988 Brown SD, Brockdorff N, Cavanna JS, Fisher EM, Greenfield AJ, Lyon MF, Nasir J. The long-range mapping of mammalian chromosomes. Current Topics in Microbiology and Immunology. 137: 3-12. PMID 3416640 DOI: 10.1007/978-3-642-50059-6_1  0.569
1988 Cavanna JS, Coulton G, Morgan JE, Brockdorff N, Forrest SM, Davies KE, Brown SD. Molecular and genetic mapping of the mouse mdx locus. Genomics. 3: 337-41. PMID 3243547 DOI: 10.1016/0888-7543(88)90124-3  0.495
1987 Brockdorff N, Cross GS, Cavanna JS, Fisher EM, Lyon MF, Davies KE, Brown SD. The mapping of a cDNA from the human X-linked Duchenne muscular dystrophy gene to the mouse X chromosome. Nature. 328: 166-8. PMID 3600793 DOI: 10.1038/328166A0  0.647
1987 Brockdorff N, Fisher EM, Cavanna JS, Lyon MF, Brown SD. Construction of a detailed molecular map of the mouse X chromosome by microcloning and interspecific crosses. The Embo Journal. 6: 3291-3297. DOI: 10.1002/J.1460-2075.1987.Tb02648.X  0.585
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