| Year |
Citation |
Score |
| 2020 |
Cowley BR, Snyder AC, Acar K, Williamson RC, Yu BM, Smith MA. Slow Drift of Neural Activity as a Signature of Impulsivity in Macaque Visual and Prefrontal Cortex. Neuron. PMID 32810433 DOI: 10.1016/J.Neuron.2020.07.021 |
0.663 |
|
| 2020 |
Issar D, Williamson RC, Khanna SB, Smith MA. A neural network for online spike classification that improves decoding accuracy. Journal of Neurophysiology. PMID 32101491 DOI: 10.1152/jn.00641.2019 |
0.687 |
|
| 2019 |
Williamson RC, Doiron B, Smith MA, Yu BM. Bridging large-scale neuronal recordings and large-scale network models using dimensionality reduction. Current Opinion in Neurobiology. 55: 40-47. PMID 30677702 DOI: 10.1016/J.Conb.2018.12.009 |
0.523 |
|
| 2017 |
Bittner SR, Williamson RC, Snyder AC, Litwin-Kumar A, Doiron B, Chase SM, Smith MA, Yu BM. Population activity structure of excitatory and inhibitory neurons. Plos One. 12: e0181773. PMID 28817581 DOI: 10.1371/Journal.Pone.0181773 |
0.656 |
|
| 2016 |
Williamson RC, Cowley BR, Litwin-Kumar A, Doiron B, Kohn A, Smith MA, Yu BM. Scaling Properties of Dimensionality Reduction for Neural Populations and Network Models. Plos Computational Biology. 12: e1005141. PMID 27926936 DOI: 10.1371/Journal.Pcbi.1005141 |
0.537 |
|
| 2008 |
Humphries SE, Berg K, Gill L, Cumming AM, Robertson FW, Stalenhoef AFH, Williamson R, Børresen A-. The gene for apolipoprotein C-ll is closely linked to the gene for apolipoprotein E on chromosome 19 Clinical Genetics. 26: 389-396. DOI: 10.1111/J.1399-0004.1984.Tb01078.X |
0.326 |
|
| 2006 |
Férec C, Casals T, Chuzhanova N, Macek M, Bienvenu T, Holubova A, King C, McDevitt T, Castellani C, Farrell PM, Sheridan M, Pantaleo SJ, Loumi O, Messaoud T, Cuppens H, ... Williamson R, et al. Gross genomic rearrangements involving deletions in the CFTR gene: characterization of six new events from a large cohort of hitherto unidentified cystic fibrosis chromosomes and meta-analysis of the underlying mechanisms. European Journal of Human Genetics : Ejhg. 14: 567-76. PMID 16493442 DOI: 10.1038/Sj.Ejhg.5201590 |
0.353 |
|
| 2001 |
Agtmael TV, Forrest SM, Williamson R. Genes for left-handedness: how to search for the needle in the haystack? Laterality. 6: 149-164. PMID 15513167 DOI: 10.1080/713754403 |
0.331 |
|
| 2000 |
Delatycki MB, Williamson R, Forrest SM. Friedreich ataxia: an overview Journal of Medical Genetics. 37: 1-8. PMID 10633128 DOI: 10.1136/Jmg.37.1.1 |
0.301 |
|
| 1999 |
Forrest S, Dunn K, Elliott K, Fitzpatrick E, Fullerton J, McCarthy M, Brown J, Hill D, Williamson R. Identifying genes predisposing to atopic eczema. The Journal of Allergy and Clinical Immunology. 104: 1066-70. PMID 10550754 DOI: 10.1016/S0091-6749(99)70090-4 |
0.346 |
|
| 1998 |
Franks S, Gharani N, Waterworth D, Batty S, White D, Williamson R, McCarthy M. Genetics of polycystic ovary syndrome Molecular and Cellular Endocrinology. 145: 123-128. PMID 9922108 DOI: 10.1016/S0303-7207(98)00178-6 |
0.31 |
|
| 1998 |
Delatycki MB, Paris D, Gardner RJ, Forshaw K, Nicholson GA, Nassif N, Williamson R, Forrest SM. Sperm DNA analysis in a Friedreich ataxia premutation carrier suggests both meiotic and mitotic expansion in the FRDA gene. Journal of Medical Genetics. 35: 713-6. PMID 9733027 DOI: 10.1136/Jmg.35.9.713 |
0.324 |
|
| 1997 |
Behrens F, Claussen U, Iyer LM, Green ED, Horsthemke B, Williamson R, Huxley C, Coutelle C. Isolation of DNA from the centromere of human chromosome 7 by microdissection Chromosome Research. 5: 215-220. PMID 9244447 DOI: 10.1023/A:1018459300978 |
0.364 |
|
| 1996 |
Coutelle C, Williamson R. Liposomes and viruses for gene therapy of cystic fibrosis. Journal of Aerosol Medicine-Deposition Clearance and Effects in the Lung. 9: 79-88. PMID 10160212 DOI: 10.1089/Jam.1996.9.79 |
0.304 |
|
| 1996 |
Riley B, Mogudi-Carter M, Jenkins T, Williamson R. No evidence for linkage of chromosome 22 markers to schizophrenia in Southern African Bantu‐speaking families American Journal of Medical Genetics. 67: 515-522. PMID 8950408 DOI: 10.1002/(Sici)1096-8628(19961122)67:6<515::Aid-Ajmg2>3.0.Co;2-G |
0.324 |
|
| 1996 |
Carvajal JJ, Pook MA, Santos Md, Doudney K, Hillermann R, Minogue S, Williamson R, Hsuan JJ, Chamberlain S. The Friedreich's ataxia gene encodes a novel phosphatidylinositol–4–phosphate 5–kinase Nature Genetics. 14: 157-162. PMID 8841185 DOI: 10.1038/Ng1096-157 |
0.351 |
|
| 1996 |
Franks S, White D, Gilling-Smith C, Carey A, Waterworth D, Williamson R. Hypersecretion of androgens by polycystic ovaries: The role of genetic factors in the regulation of cytochrome P450c17α BaillièRe's Clinical Endocrinology and Metabolism. 10: 193-203. PMID 8773744 DOI: 10.1016/S0950-351X(96)80057-7 |
0.315 |
|
| 1996 |
Wheeler VC, Prodromou C, Pearl LH, Williamson R, Coutelle C. Synthesis of a modified gene encoding human ornithine transcarbamylase for expression in mammalian mitochondrial and universal translation systems: a novel approach towards correction of a genetic defect Gene. 169: 251-255. PMID 8647457 DOI: 10.1016/0378-1119(95)00812-8 |
0.33 |
|
| 1995 |
Dow E, Cross S, Wolgemuth DJ, Lyonnet S, Mulligan LM, Mascari M, Ladda R, Williamson R. Second locus for Hirschsprung disease/Waardenburg syndrome in a large Mennonite kindred. American Journal of Medical Genetics. 53: 75-80. PMID 7802041 DOI: 10.1002/Ajmg.1320530116 |
0.365 |
|
| 1995 |
Carvajal JJ, Pook MA, Doudney K, Hillermann R, Wilkes D, Al-Mahdawi S, Williamson R, Chamberlain S. Friedreich's ataxia: a defect in signal transduction? Human Molecular Genetics. 4: 1411-1419. PMID 7581382 DOI: 10.1093/Hmg/4.8.1411 |
0.384 |
|
| 1994 |
Twells R, Yenchitsomanus P, Sirinavin C, Allotey R, Roungvarin N, Viriyavejakul A, Cemal C, Weber J, Farrall M, Rodprasert P, Prayoonwiwat N, Williamson R, Chamberlain S. Autosomal dominant cerebellar ataxia with dementla: evidence for a fourth disease locus Human Molecular Genetics. 3: 177-180. PMID 8162021 DOI: 10.1093/Hmg/3.1.177 |
0.3 |
|
| 1994 |
Westbrook CA, Le Beau MM, Neuman WL, Keinanen M, Yamaoka LH, Speer MC, Espinosa R, Nakamura Y, Williamson R, Mullan M. Physical and genetic map of 5q31: use of fluorescence in situ hybridization data to identify errors in the CEPH database. Centre d'Etude de Polymorphisme Humain. Cytogenetics and Cell Genetics. 67: 86-93. PMID 7913678 DOI: 10.1159/000133805 |
0.302 |
|
| 1994 |
Carey AH, Waterworth D, Patel K, White D, Little J, Novelli P, Franks S, Williamson R. Polycystic ovaries and premature male pattern baldness are associated with one allele of the steroid metabolism gene CYP17 Human Molecular Genetics. 3: 1873-1876. PMID 7849715 DOI: 10.1093/Hmg/3.10.1873 |
0.32 |
|
| 1993 |
Buxton J, Davies J, Shelbourne P, Yokobata K, Williamson R, Johnson K. Isolation and ordering of bacteriophage genomic clones corresponding to two YACs from 19q13.3. Molecular and Cellular Probes. 7: 75-80. PMID 8455645 DOI: 10.1006/Mcpr.1993.1010 |
0.338 |
|
| 1993 |
Ramsay M, Williamson R, Estivill X, Wainwright BJ, Ho MF, Halford S, Kere J, Savilahti E, Chapelle Adl, Schwartz M. Haplotype analysis to determine the position of a mutation among closely linked DNA markers Human Molecular Genetics. 2: 1007-1014. PMID 8364537 DOI: 10.1093/Hmg/2.7.1007 |
0.321 |
|
| 1993 |
Wijmenga C, Wright TJ, Baan MJ, Padberg GW, Williamson R, van Ommen GJ, Hewitt JE, Hofker MH, Frants RR. Physical mapping and YAC-cloning connects four genetically distinct 4qter loci (D4S163, D4S139, D4F35S1 and D4F104S1) in the FSHD gene-region. Human Molecular Genetics. 2: 1667-72. PMID 8268920 DOI: 10.1093/Hmg/2.10.1667 |
0.313 |
|
| 1993 |
Stanier P, Forbes SA, Arnason A, Bjornsson A, Sveinbjornsdottir E, Williamson R, Moore G. The localization of a gene causing X-linked cleft palate and ankyloglossia (CPX) in an Icelandic kindred is between DXS326 and DXYS1X. Genomics. 17: 549-555. PMID 8244369 DOI: 10.1006/Geno.1993.1370 |
0.334 |
|
| 1993 |
Halford S, Wadey R, Roberts C, Daw SCM, Whiting JA, O'Donnell H, Dunham I, Bentley D, Lindsay E, BaldInI A, Francis F, Lehrach H, Williamson R, Wilson DI, Goodship J, et al. Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease Human Molecular Genetics. 2: 2099-2107. PMID 8111380 DOI: 10.1093/Hmg/2.12.2099 |
0.325 |
|
| 1993 |
Davies GE, Howard CM, Gorman LM, Farrer MJ, Holland AJ, Williamson R, Kessling AM. Polymorphisms and linkage disequilibrium in the COL6A1 and COL6A2 gene cluster : novel DNA polymorphisms in the region of a candidate gene for congenital heart defects in Down's syndrome Human Genetics. 90: 521-525. PMID 8094066 DOI: 10.1007/Bf00217452 |
0.341 |
|
| 1993 |
Wright TJ, Wijmenga C, Clark LN, Frants RR, Williamson R, Hewitt JE. Fine mapping of the FSHD gene region orientates the rearranged fragment detected by the probe p13E-11. Human Molecular Genetics. 2: 1673-8. PMID 7903581 DOI: 10.1093/Hmg/2.10.1673 |
0.337 |
|
| 1992 |
Carey AH, Claussen U, Lüdecke H, Horsthemke B, Ellis D, Oakey H, Wilson D, Burn J, Williamson R, Scambler PJ. Interstitial deletions in DiGeorge syndrome detected with microclones from 22q11 Mammalian Genome. 3: 101-105. PMID 1617213 DOI: 10.1007/Bf00431253 |
0.321 |
|
| 1992 |
Davies J, Yamagata H, Shelbourne P, Buxton J, Ogihara T, Nokelainen P, Nakagawa M, Williamson R, Johnson K, Miki T. Comparison of the myotonic dystrophy associated CTG repeat in European and Japanese populations. Journal of Medical Genetics. 29: 766-769. PMID 1453423 DOI: 10.1136/Jmg.29.11.766 |
0.328 |
|
| 1992 |
Wijmenga C, Hewitt JE, Sandkuijl LA, Clark LN, Wright TJ, Dauwerse HG, Gruter AM, Hofker MH, Moerer P, Williamson R. Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy. Nature Genetics. 2: 26-30. PMID 1363881 DOI: 10.1038/Ng0992-26 |
0.37 |
|
| 1991 |
Wilkes D, Shaw J, Anand R, Riley J, Winter P, Wallis J, Driesel AG, Williamson R, Chamberlain S. Identification of CpG islands in a physical map encompassing the Friedreich's ataxia locus. Genomics. 9: 90-95. PMID 2004770 DOI: 10.1016/0888-7543(91)90224-3 |
0.378 |
|
| 1991 |
Williamson R. Cystic fibrosis - A strategy for the future Advances in Experimental Medicine and Biology. 290: 1-7. PMID 1719752 DOI: 10.1007/978-1-4684-5934-0_1 |
0.333 |
|
| 1991 |
Tata F, Stanier P, Wicking C, Halford S, Kruyer H, Lench NJ, Scambler PJ, Hansen C, Braman JC, Williamson R, Wainwright BJ. Cloning The Mouse Homolog Of The Human Cystic-Fibrosis Transmembrane Conductance Regulator Gene Genomics. 10: 301-307. PMID 1712752 DOI: 10.1016/0888-7543(91)90312-3 |
0.328 |
|
| 1991 |
Hewitt JE, Clark LN, Ivens A, Williamson R. Structure and sequence of the human homeobox gene HOX7. Genomics. 11: 670-8. PMID 1685479 DOI: 10.1016/0888-7543(91)90074-O |
0.319 |
|
| 1991 |
Williamson R. The application of molecular genetics to antenatal diagnosis of inherited disease Pathology. 23: 17. DOI: 10.1016/S0031-3025(16)36216-X |
0.314 |
|
| 1991 |
Williamson R. Polymerase chain reaction Pathology. 23: 17. DOI: 10.1016/S0031-3025(16)36213-4 |
0.314 |
|
| 1990 |
Wallis J, Williamson R, Chamberlain S. Identification of a hypervariable microsatellite polymorphism within D9S15 tightly linked to Friedreich's ataxia Human Genetics. 85: 98-100. PMID 2358306 DOI: 10.1007/Bf00276331 |
0.353 |
|
| 1990 |
Watson EK, Mayall ES, Simova L, Thompson EM, Warner JO, Williamson R, Williams C. The incidence of delta F508 CF mutation, and associated haplotypes, in a sample of English CF families. Human Genetics. 85: 435-436. PMID 2210766 DOI: 10.1007/Bf02428303 |
0.321 |
|
| 1990 |
Shaw J, Lichter P, Driesel AJ, Williamson R, Chamberlain S. Regional localisation of the Friedreich ataxia locus to human chromosome 9q13----q21.1. Cytogenetic and Genome Research. 53: 221-224. PMID 2209091 DOI: 10.1159/000132936 |
0.343 |
|
| 1990 |
Simova L, Williams C, Efremov GD, Gordova-Muratovska A, Suštić S, Watson EK, Williamson R. ΔF508 frequency and associated haplotypes near the cystic fibrosis locus in the Yugoslav population Human Genetics. 85: 432-433. PMID 1976597 DOI: 10.1007/Bf02428301 |
0.346 |
|
| 1990 |
Ivens A, Flavin N, Williamson R, Dixon M, Bates G, Buckingham M, Robert B. The human homeobox gene HOX7 maps to chromosome 4p16.1 and may be implicated in Wolf-Hirschhorn syndrome. Human Genetics. 84: 473-476. PMID 1969845 DOI: 10.1007/Bf00195823 |
0.371 |
|
| 1989 |
Poustka AM, Lehrach H, Williamson R, Bates G. A long-range restriction map encompassing the cystic fibrosis locus and its closely linked genetic markers. Genomics. 2: 337-45. PMID 2906041 DOI: 10.1016/0888-7543(88)90023-7 |
0.313 |
|
| 1989 |
Williamson R. Gene mapping in cystic fibrosis and its clinical applications Acta Paediatrica Scandinavica, Supplement. 78: 7-9. PMID 2701928 DOI: 10.1111/Apa.1989.78.S363.7 |
0.34 |
|
| 1989 |
Wallis J, Shaw J, Wilkes D, Farrall M, Williamson R, Chamberlain S, Skare JC, Milunsky A. Prenatal diagnosis of friedreich ataxia American Journal of Medical Genetics. 34: 458-461. PMID 2574535 DOI: 10.1002/Ajmg.1320340327 |
0.316 |
|
| 1989 |
Estivill X, Casals T, Morral N, Chillon M, Bosch A, Nunes V, Gasparini P, Seia A, Pignatti PF, Novelli G, Dallapiccola B, Fernandez E, Benitez J, Williamson R. Δf508 Gene Deletion In Cystic Fibrosis In Southern Europe The Lancet. 334: 1404-1404. PMID 2574355 DOI: 10.1016/S0140-6736(89)92024-2 |
0.324 |
|
| 1989 |
Claustres M, Williams C, Williamson R. Amplification of DNA for detection of cystic fibrosis-linked polymorphisms. The Journal of Pediatrics. 115: 749-752. PMID 2572686 DOI: 10.1016/S0022-3476(89)80655-9 |
0.305 |
|
| 1989 |
Nunes V, Casals T, Gallano P, Giménez FJ, Kere J, Williamson R, Estivill X. Detection of a rare allele with the pMP6d-9/MspI RFLP near the cystic fibrosis locus. Human Genetics. 83: 305-6. PMID 2571567 DOI: 10.1007/Bf00285181 |
0.315 |
|
| 1989 |
Nimmo E, Padua RA, Hughes D, Brook JD, Williamson R, Johnson KJ. Confirmation and refinement of the localisation of the c-MEL locus on chromosome 19 by physical and genetic mapping. Human Genetics. 81: 382-384. PMID 2564840 DOI: 10.1007/Bf00283697 |
0.37 |
|
| 1989 |
Goate AM, Haynes AR, Owen MJ, Farrall M, James LA, Lai LY, Mullan MJ, Roques P, Rossor MN, Williamson R. Predisposing locus for Alzheimer's disease on chromosome 21. Lancet. 1: 352-5. PMID 2563508 DOI: 10.1016/S0140-6736(89)91725-X |
0.304 |
|
| 1989 |
Chan AM, Hilkens J, Kroezen V, Mitchell PJ, Scambler P, Wainwright BJ, Williamson R, Cooper CS. Molecular cloning and localization to chromosome 6 of mouse INT1L1 gene. Somatic Cell and Molecular Genetics. 15: 555-62. PMID 2531931 DOI: 10.1007/Bf01534916 |
0.37 |
|
| 1988 |
Brueton L, Huson SM, Winter RM, Williamson R, Opitz JM, Reynolds JF. Chromosomal localisation of a developmental gene in man: direct DNA analysis demonstrates that Greig cephalopolysyndactyly maps to 7p13. American Journal of Medical Genetics. 31: 799-804. PMID 3239571 DOI: 10.1002/Ajmg.1320310412 |
0.35 |
|
| 1988 |
Johnson K, Nimmo E, Jones P, Weiss M, Savontaus ML, Anvret M, Bartlett R, Roses A, Shaw D, Harper PS, Koivunen-Tapio E, Williamson R. Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19q. Human Genetics. 80: 379-381. PMID 3198115 DOI: 10.1007/Bf00273655 |
0.356 |
|
| 1988 |
Ivens A, Moore G, Williamson R. Molecular approaches to dysmorphology. Journal of Medical Genetics. 25: 473-479. PMID 2902228 DOI: 10.1136/Jmg.25.7.473 |
0.322 |
|
| 1988 |
Lench N, Stanier P, Williamson R. Simple non-invasive method to obtain DNA for gene analysis. The Lancet. 331: 1356-1358. PMID 2898042 DOI: 10.1016/S0140-6736(88)92178-2 |
0.33 |
|
| 1988 |
Ivens A, Moore GE, Chambers J, Arnason A, Jensson O, Bjornsson A, Williamson R. X-linked cleft palate: the gene is localized between polymorphic DNA markers DXYS12 and DXS17. Human Genetics. 78: 356-8. PMID 2896158 DOI: 10.1007/Bf00291735 |
0.349 |
|
| 1988 |
Stanier P, Estivill X, Lench N, Williamson R. Detection of a rare-cutter RFLP in a CpG-rich island near the cystic fibrosis locus. Human Genetics. 80: 309-310. PMID 2461342 DOI: 10.1007/Bf01790107 |
0.31 |
|
| 1987 |
Azoulay M, Henry I, Tata F, Weil D, Grzeschik KH, Chaves ME, McIntyre N, Williamson R, Humphries SE, Junien C. The structural gene for lecithin:cholesterol acyl transferase (LCAT) maps to 16q22. Annals of Human Genetics. 51: 129-36. PMID 3674753 DOI: 10.1111/J.1469-1809.1987.Tb01054.X |
0.363 |
|
| 1987 |
Law HY, Stanier P, Williamson R, Modell B, Ward RH, Petrou M, Old J, Farrall M. Two unusual cases of first trimester prenatal diagnosis of cystic fibrosis using DNA probes. Prenatal Diagnosis. 7: 215-21. PMID 3588540 DOI: 10.1002/Pd.1970070309 |
0.313 |
|
| 1987 |
Horsthemke B, Beisiegel U, Dunning A, Havinga JR, Williamson R, Humphries S. Unequal crossing-over between two alu-repetitive DNA sequences in the low-density-lipoprotein-receptor gene. A possible mechanism for the defect in a patient with familial hypercholesterolaemia. Febs Journal. 164: 77-81. PMID 3549308 DOI: 10.1111/J.1432-1033.1987.Tb10995.X |
0.34 |
|
| 1987 |
Chamberlain S, Worrall CS, South S, Shaw J, Farrall M, Williamson R. Exclusion of the Friedreich ataxia gene from chromosome 19 Human Genetics. 76: 186-190. PMID 3475247 DOI: 10.1007/Bf00284919 |
0.355 |
|
| 1987 |
Estivill X, Williamson R. A rapid method to identify cosmids containing rare restriction sites. Nucleic Acids Research. 15: 1415-1425. PMID 3029714 DOI: 10.1093/Nar/15.4.1415 |
0.336 |
|
| 1987 |
Vissing H, Grosveld F, Solomon E, Moore G, Lench N, Shennan N, Williamson R. Progress towards construction of a total restriction fragment map of a human chromosome. Nucleic Acids Research. 15: 1363-1375. PMID 3029713 DOI: 10.1093/Nar/15.4.1363 |
0.343 |
|
| 1987 |
Estivill X, Scambler PJ, Wainwright BJ, Hawley K, Frederick P, Schwartz M, Baiget M, Kere J, Williamson R, Farrall M. Patterns of polymorphism and linkage disequilibrium for cystic fibrosis. Genomics. 1: 257-263. PMID 2895728 DOI: 10.1016/0888-7543(87)90052-8 |
0.328 |
|
| 1987 |
Davies KA, Lorand L, Waterfield M, Wainwright B, Farrall M, Williamson R. Isolation of a polymorphic genomic clone from chromosome 7 - Physical and genetic linkage studies to markers around the cystic fibrosis locus Human Genetics. 77: 122-126. PMID 2888718 DOI: 10.1007/Bf00272377 |
0.361 |
|
| 1987 |
Scambler PJ, McPherson MA, Bates G, Bradbury NA, Dormer RL, Williamson R. Biochemical and genetic exclusion of calmodulin as the site of the basic defect in cystic fibrosis Human Genetics. 76: 278-282. PMID 2885258 DOI: 10.1007/Bf00283623 |
0.316 |
|
| 1987 |
Moore GE, Ivens A, Chambers J, Farrall M, Williamson R, Page DC, Bjornsson A, Arnason A, Jensson O. Linkage of an X-chromosome cleft palate gene. Nature. 326: 91-2. PMID 2881212 DOI: 10.1038/326091A0 |
0.34 |
|
| 1987 |
Tata F, Chaves ME, Markham AF, Scrace GD, Waterfield MD, McIntyre N, Williamson R, Humphries SE. The isolation and characterisation of cDNA and genomic clones for human lecithin: cholesterol acyltransferase. Biochimica Et Biophysica Acta. 910: 142-8. PMID 2823898 DOI: 10.1016/0167-4781(87)90066-2 |
0.311 |
|
| 1986 |
Scambler PJ, Wainwright BJ, Walson E, Bates G, Bell G, Williamson R, Farrall M. Isolation of a further anonymous informative DNA sequence from chromosome seven closely linked to cystic flbrosis Nucleic Acids Research. 14: 1951-1956. PMID 3960715 DOI: 10.1093/Nar/14.5.1951 |
0.364 |
|
| 1986 |
Klinger K, Stanislovitis P, Hoffman N, Watkins PC, Schwartz R, Doherty R, Scambler P, Farrall M, Williamson R, Wainwright B. Genetic homogeneity of cystic fibrosis Nucleic Acids Research. 14: 8681-8686. PMID 3786136 DOI: 10.1093/Nar/14.21.8681 |
0.331 |
|
| 1986 |
Scambler PJ, Law HY, Williamson R, Cooper CS. Chromosome mediated gene transfer of six DNA markers linked to the cystic fibrosis locus on human chromosome seven Nucleic Acids Research. 14: 7159-7174. PMID 3763403 DOI: 10.1093/Nar/14.18.7159 |
0.382 |
|
| 1986 |
Williamson R, Bell G, Bell J, Bates G, Davies KA, Estivill X, Farrall M, Kruyer H, Law HY, Lench N. Molecular genetics and the basic defect causing cystic fibrosis Cold Spring Harbor Symposia On Quantitative Biology. 51: 309-315. PMID 3472728 DOI: 10.1101/Sqb.1986.051.01.036 |
0.376 |
|
| 1986 |
Barni N, Talmud PJ, Carlsson P, Azoulay M, Darnfors C, Harding D, Weil D, Grzeschik KH, Bjursell G, Junien C, Williamson R, Humphries SE. The isolation of genomic recombinants for the human apolipoprotein B gene and the mapping of three common DNA polymorphisms of the gene--a useful marker for human chromosome 2. Human Genetics. 73: 313-319. PMID 3017840 DOI: 10.1007/Bf00279093 |
0.367 |
|
| 1986 |
Scambler PJ, Bell J, Bell G, Williamson R. Isolation of a polymorphic DNA sequence (λ 82B, D8S2) from chromosome eight Nucleic Acids Research. 14: 1927-1927. PMID 3005992 DOI: 10.1093/Nar/14.4.1927 |
0.331 |
|
| 1986 |
Estivill X, Schmidtke J, Williamson R, Wainwright B. Chromosome assignment and restriction fragment length polymorphism analysis of the anonymous DNA probe B79a at 7q22 (HMG8 assignment D7S13). Human Genetics. 74: 320-322. PMID 2877942 DOI: 10.1007/Bf00282558 |
0.344 |
|
| 1986 |
Farrall M, Rodeck C, Stanier P, Lissens W, Watson E, Law HY, Warren R, Super M, Scambler P, Wainwright B, Williamson R. FIRST-TRIMESTER PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS WITH LINKED DNA PROBES The Lancet. 327: 1402-1405. PMID 2872515 DOI: 10.1016/S0140-6736(86)91553-9 |
0.344 |
|
| 1985 |
Williamson R. Cloned genes and their use in the analysis of inherited disease Biochemical Society Transactions. 13: 807-811. PMID 3905449 DOI: 10.1042/Bst0130807 |
0.301 |
|
| 1985 |
Wainwright BJ, Scambler PJ, Schmidtke J, Watson EA, Law HY, Farrall M, Cooke HJ, Eiberg H, Williamson R. Localization of cystic fibrosis locus to human chromosome 7cen-q22. Nature. 318: 384-5. PMID 2999612 DOI: 10.1038/318384A0 |
0.358 |
|
| 1985 |
Humphries SE, Tata F, Henry I, Barichard F, Holm M, Junien C, Williamson R. The isolation, characterisation, and chromosomal assignment of the gene for human 3-hydroxy-3-methylglutaryl coenzyme A reductase, (HMG-CoA reductase) Human Genetics. 71: 254-258. PMID 2998972 DOI: 10.1007/Bf00284585 |
0.369 |
|
| 1985 |
Horsthemke B, Kessling AM, Seed M, Wynn V, Williamson R, Humphries SE. Identification of a deletion in the low density lipoprotein (LDL) receptor gene in a patient with familial hypercholesterolaemia. Human Genetics. 71: 75-78. PMID 2993159 DOI: 10.1007/Bf00295672 |
0.311 |
|
| 1985 |
Tata F, Henry I, Markham AF, Wallis SC, Weil D, Grzeschik KH, Junien C, Williamson R, Humphries SE. Isolation and characterisation of a cDNA clone for human apolipoprotein CI and assignment of the gene to chromosome 19. Human Genetics. 69: 345-349. PMID 2985493 DOI: 10.1007/Bf00291654 |
0.345 |
|
| 1985 |
Scambler P, Robbins T, Gilliam C, Boylston A, Tippett P, Williamson R, Davies KE. Linkage studies between polymorphic markers on chromosome 4 and cystic fibrosis. Human Genetics. 69: 250-4. PMID 2984105 DOI: 10.1007/Bf00293035 |
0.375 |
|
| 1985 |
Humphries SE, Horsthemke B, Seed M, Holm M, Wynn V, Kessling AM, Donald JA, Jowett N, Galton DJ, Williamson R. A common DNA polymorphism of the low-density lipoprotein (LDL) receptor gene and its use in diagnosis. The Lancet. 325: 1003-1005. PMID 2859461 DOI: 10.1016/S0140-6736(85)91611-3 |
0.305 |
|
| 1984 |
Jeanpierre M, Weil D, Hors-Cayla MC, Williamson R, Junien C, Humphries SE. Gene for apolipoprotein CII is on human chromosome 19. Somatic Cell and Molecular Genetics. 10: 645-649. PMID 6594769 DOI: 10.1007/Bf01535231 |
0.358 |
|
| 1984 |
Pembrey ME, Davies KE, Winter RM, Elles RG, Williamson R, Fazzone TA, Walker C. Clinical use of DNA markers linked to the gene for Duchenne muscular dystrophy. Archives of Disease in Childhood. 59: 208-16. PMID 6585184 DOI: 10.1136/Adc.59.3.208 |
0.348 |
|
| 1984 |
Humphries SE, Williams L, Myklebost O, Stalenhoef AF, Demacker PN, Baggio G, Crepaldi G, Galton DJ, Williamson R. Familial apolipoprotein CII deficiency: a preliminary analysis of the gene defect in two independent families. Human Genetics. 67: 151-5. PMID 6547689 DOI: 10.1007/Bf00272990 |
0.329 |
|
| 1984 |
Humphries SE, Imam AM, Robbins TP, Cook M, Carritt B, Ingle C, Williamson R. The identification of a DNA polymorphism of the alpha fibrinogen gene, and the regional assignment of the human fibrinogen genes to 4q26-qter. Human Genetics. 68: 148-53. PMID 6500566 DOI: 10.1007/Bf00279305 |
0.351 |
|
| 1984 |
Humphries SE, Donald JA, McFadden JJP, Shull S, Williamson R, Jowett NI, Galton DJ, Julsrud JO, Berg K, Heiberg A, Ball S, Fey G, Seed M, Wynn V. The use of polymorphic DNA and protein markers for the third complement component for determining linkage of familial hypercholesterolaemia Atherosclerosis. 52: 267-278. PMID 6497930 DOI: 10.1016/0021-9150(84)90056-X |
0.34 |
|
| 1984 |
Drayna D, Davies K, Hartley D, Mandel JL, Camerino G, Williamson R, White R. Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms. Proceedings of the National Academy of Sciences of the United States of America. 81: 2836-2839. PMID 6326147 DOI: 10.1073/Pnas.81.9.2836 |
0.363 |
|
| 1984 |
Davies KE, Harper K, Bonthron D, Krumlauf R, Polkey A, Pembrey ME, Williamson R. Use of a chromosome 21 cloned DNA probe for the analysis of non-disjunction in Down syndrome. Human Genetics. 66: 54-6. PMID 6230306 DOI: 10.1007/Bf00275186 |
0.375 |
|
| 1984 |
Wallis SC, Donald JA, Forrest LA, Williamson R, Humphries SE. The isolation of a genomic clone containing the apolipoprotein CII gene and the detection of linkage disequilibrium between two common DNA polymorphisms around the gene Human Genetics. 68: 286-289. PMID 6096256 DOI: 10.1007/Bf00292585 |
0.359 |
|
| 1984 |
Gilliam TC, Scambler P, Robbins T, Ingle C, Williamson R, Davies KE. The positions of three restriction fragment length polymorphisms on chromosome 4 relative to known genetic markers. Human Genetics. 68: 154-8. PMID 6094335 DOI: 10.1007/Bf00279306 |
0.36 |
|
| 1983 |
O'Brien T, Harper PS, Davies KE, Murray JM, Sarfarazi M, Williamson R. Absence of genetic heterogeneity in Duchenne muscular dystrophy shown by a linkage study using two cloned DNA sequences. Journal of Medical Genetics. 20: 249-51. PMID 6684692 DOI: 10.1136/Jmg.20.4.249 |
0.332 |
|
| 1983 |
Williamson R, Darling SM. Methods to analyse the human genome. The Journal of Pathology. 141: 193-200. PMID 6663387 DOI: 10.1002/Path.1711410303 |
0.382 |
|
| 1983 |
Davies KE, Jackson J, Williamson R, Harper PS, Ball S, Sarfarazi M, Meredith L, Fey G. Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe. Journal of Medical Genetics. 20: 259-63. PMID 6620325 DOI: 10.1136/Jmg.20.4.259 |
0.362 |
|
| 1983 |
Sarfarazi M, Harper PS, Kingston HM, Murray JM, O'Brien T, Davies KE, Williamson R, Tippett P, Sanger R. Genetic linkage relationship between the Xg blood group system and two X chromosome DNA polymorphisms in families with Duchenne and Becker muscular dystrophy. Human Genetics. 65: 169-71. PMID 6317539 DOI: 10.1007/Bf00286656 |
0.321 |
|
| 1983 |
Davies KE, Pearson PL, Harper PS, Murray JM, O'Brien T, Sarfarazi M, Williamson R. Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome. Nucleic Acids Research. 11: 2303-12. PMID 6304647 DOI: 10.1093/Nar/11.8.2303 |
0.363 |
|
| 1983 |
Davies KE, Harper PS, Williamson R. Cloned gene probes for carrier detection in muscular dystrophy. Lancet (London, England). 2: 108. PMID 6134944 DOI: 10.1016/S0140-6736(83)90095-8 |
0.316 |
|
| 1982 |
Murray JM, Davies KE, Harper PS, Meredith L, Mueller CR, Williamson R. Linkage relationship of a cloned DNA sequence on the short arm of the X chromosome to Duchenne muscular dystrophy. Nature. 300: 69-71. PMID 6982420 DOI: 10.1038/300069A0 |
0.354 |
|
| 1982 |
Darling SM, Crampton JM, Williamson R. Organization of a family of highly repetitive sequences within the human genome. Journal of Molecular Biology. 154: 51-63. PMID 6896218 DOI: 10.1016/0022-2836(82)90416-8 |
0.315 |
|
| 1982 |
Hill ME, Davies KE, Harper P, Williamson R. The Mendelian inheritance of a human X chromosome-specific DNA sequence polymorphism and its use in linkage studies of genetic disease. Human Genetics. 60: 222-6. PMID 6286461 DOI: 10.1007/Bf00303007 |
0.374 |
|
| 1981 |
Davies KE, Young BD, Elles RG, Hill ME, Williamson R. Cloning of a representative genomic library of the human X chromosome after sorting by flow cytometry. Nature. 293: 374-6. PMID 6456416 DOI: 10.1038/293374A0 |
0.335 |
|
| 1981 |
Jackson IJ, Freund RM, Wasylyk B, Malcolm ADB, Williamson R. The Isolation, Mapping and Transcription in vitro of a β0‐Thalassaemia Globin Gene Febs Journal. 121: 27-31. PMID 6276172 DOI: 10.1111/J.1432-1033.1981.Tb06424.X |
0.328 |
|
| 1981 |
Humphries SE, Whittall R, Minty A, Buckingham M, Williamson R. There are approximately 20 actin gene in the human genome. Nucleic Acids Research. 9: 4895-4908. PMID 6273789 DOI: 10.1093/Nar/9.19.4895 |
0.334 |
|
| 1981 |
Westaway D, Williamson R. An intron nucleotide sequence variant in a cloned β+-thalassaemia globin gene Nucleic Acids Research. 9: 1777-1788. PMID 6264391 DOI: 10.1093/Nar/9.8.1777 |
0.33 |
|
| 1981 |
Hill MEE, Ellis RG, Davies KE, Williamson R. Cloning Of A Library Representative Of The Human X-Chromosome Biochemical Society Transactions. 9. DOI: 10.1042/Bst009130Pe |
0.303 |
|
| 1980 |
Williamson R, Little P, Flavell R. The structure of the human gamma-globin gene locus and its relation to the delta/beta-globin gene locus. Annals of the New York Academy of Sciences. 344: 73-5. PMID 6930884 DOI: 10.1111/J.1749-6632.1980.Tb33650.X |
0.33 |
|
| 1980 |
Little PFR, Annison G, Darling S, Williamson R, Camba L, Modell B. Model for antenatal diagnosis of β -thalassaemia and other monogenic disorders by molecular analysis of linked DNA polymorphisms Nature. 285: 144-147. PMID 6246441 DOI: 10.1038/285144A0 |
0.355 |
|
| 1980 |
Jackson IJ, Williamson R. Mapping of the human globin genes. British Journal of Haematology. 46: 341-349. PMID 6160868 DOI: 10.1111/J.1365-2141.1980.Tb05980.X |
0.301 |
|
| 1980 |
Woods D, Crampton J, Clarke B, Williamson R. The construction of a recombinant cDNA library representative of the po1y(A)+ mRNA population from normal human lymphocytes Nucleic Acids Research. 8: 5157-5168. PMID 6110205 DOI: 10.1093/Nar/8.22.5157 |
0.3 |
|
| 1980 |
Little PF, Williamson R, Annison G, Flavell RA, De Boer E, Bernini LF, Ottolenghi S, Saglio G, Mazza U. Polymorphism of human gamma-globin genes in Mediterranean populations. Nature. 282: 316-8. PMID 503205 DOI: 10.1038/282316A0 |
0.34 |
|
| 1980 |
Bernards R, Little PF, Annison G, Williamson R, Flavell RA. Structure of the human G gamma-A gamma-delta-beta-globin gene locus. Proceedings of the National Academy of Sciences of the United States of America. 76: 4827-31. PMID 291902 DOI: 10.1073/Pnas.76.10.4827 |
0.305 |
|
| 1980 |
Little P, Whitelaw E, Annison G, Williamson R, Kooter J, Flavell R, Goossens M, Sergeant G, Montgomery D. The detection and use of hemoglobin mutants in the direct analysis of human globin genes Blood. 55: 1060-1062. DOI: 10.1182/Blood.V55.6.1060.1060 |
0.364 |
|
| 1979 |
Senno LD, Conconi F, Little PFR, Williamson R. Restriction enzyme analysis of the β-globin gene in DNA from β°-thalassaemic subjects from Ferrara Biochemical and Biophysical Research Communications. 91: 548-553. PMID 518653 DOI: 10.1016/0006-291X(79)91557-2 |
0.32 |
|
| 1979 |
Little PF, Flavell RA, Kooter JM, Annison G, Williamson R. Structure of the human fetal globin gene locus. Nature. 278: 227-31. PMID 423971 DOI: 10.1038/278227A0 |
0.342 |
|
| 1978 |
Flavell RA, Kooter JM, De Boer E, Little PF, Williamson R. Analysis of the beta-delta-globin gene loci in normal and Hb Lepore DNA: direct determination of gene linkage and intergene distance. Cell. 15: 25-41. PMID 699045 DOI: 10.1016/0092-8674(78)90080-6 |
0.344 |
|
| 1978 |
Coutelle C, Ioannou P, Williamson R. Use of matrix-immobilised recombinant plasmids to purify chain-specific rabbit globin complementary DNAs Gene. 3: 113-122. PMID 350711 DOI: 10.1016/0378-1119(78)90055-0 |
0.308 |
|
| 1978 |
Little P, Curtis P, Coutelle C, Berg JVD, Dalgleish R, Malcolm S, Courtney M, Westaway D, Williamson R. Isolation and partial sequence of recombinant plasmids containing human alpha-, beta- and gamma-globin cDNA fragments. Nature. 273: 640-643. PMID 318161 DOI: 10.1038/273640A0 |
0.314 |
|
| 1977 |
Mitchell GJ, Williamson R. Genes for ϒ-globin in human adult erythroid DNA Nucleic Acids Research. 4: 3557-3562. PMID 563063 DOI: 10.1093/Nar/4.10.3557 |
0.321 |
|
| 1977 |
Tolstoshev P, Williamson R, Eskdale J, Verdier G, Godet J, Nigon V, Trabuchet G, Benabadji M. Demonstration of two alpha-globin genes per human haploid genome for normals and Hb J Mexico. European Journal of Biochemistry / Febs. 78: 161-5. PMID 71990 DOI: 10.1111/J.1432-1033.1977.Tb11725.X |
0.323 |
|
| 1976 |
Ottolenghi S, Comi P, Giglioni B, Tolstoshev P, Lanyon WG, Mitchell GJ, Williamson R, Russo G, Musumeci S, Schiliro G, Tsistrakis GA, Charache S, Wood WG, Clegg JB, Weatherall DJ. δβ-Thalassemia is due to a gene deletion Cell. 9: 71-80. PMID 975241 DOI: 10.1016/0092-8674(76)90053-2 |
0.324 |
|
| 1976 |
Jackson JF, Tolstoshev P, Williamson R, Hendrick D. Chicken globin gene number Nucleic Acids Research. 3: 2019-2026. PMID 967685 DOI: 10.1093/Nar/3.8.2019 |
0.31 |
|
| 1976 |
Old J, Clegg JB, Weatherall DJ, Ottolenghi S, Comi P, Giglioni B, Mitchell J, Tolstoshev P, Williamson R. A direct estimate of the number of human γ-globin genes Cell. 8: 13-18. PMID 954089 DOI: 10.1016/0092-8674(76)90180-X |
0.356 |
|
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