| Year |
Citation |
Score |
| 2019 |
Williamson R, McShane T, Grunstein M, Flavell RA. "Cytoplasmic" DNA from primary embryonic cell cultures is not informational. Febs Letters. 20: 108-110. PMID 11946394 DOI: 10.1016/0014-5793(72)80029-2 |
0.335 |
|
| 2008 |
Higgins AW, Alkuraya FS, Bosco AF, Brown KK, Bruns GA, Donovan DJ, Eisenman R, Fan Y, Farra CG, Ferguson HL, Gusella JF, Harris DJ, Herrick SR, Kelly C, Kim HG, ... ... Williamson RE, et al. Characterization of apparently balanced chromosomal rearrangements from the developmental genome anatomy project. American Journal of Human Genetics. 82: 712-22. PMID 18319076 DOI: 10.1016/J.Ajhg.2008.01.011 |
0.322 |
|
| 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 |
0.398 |
|
| 2007 |
Williamson RE, Darrow KN, Michaud S, Jacobs JS, Jones MC, Eberl DF, Maas RL, Liberman MC, Morton CC. Methylthioadenosine phosphorylase (MTAP) in hearing: gene disruption by chromosomal rearrangement in a hearing impaired individual and model organism analysis. American Journal of Medical Genetics. Part A. 143: 1630-9. PMID 17534888 DOI: 10.1002/Ajmg.A.31724 |
0.334 |
|
| 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 |
0.424 |
|
| 2002 |
Fullerton J, Paprocki P, Foote S, Mackey DA, Williamson R, Forrest S. Identity-by-descent approach to gene localisation in eight individuals affected by keratoconus from north-west Tasmania, Australia. Human Genetics. 110: 462-70. PMID 12073017 DOI: 10.1007/S00439-002-0705-7 |
0.351 |
|
| 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 |
0.381 |
|
| 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 |
0.346 |
|
| 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 |
0.411 |
|
| 1998 |
Franks S, Gharani N, Waterworth D, Batty S, White D, Williamson R, McCarthy M. Current developments in the molecular genetics of the polycystic ovary syndrome. Trends in Endocrinology and Metabolism: Tem. 9: 51-4. PMID 18406240 DOI: 10.1016/S1043-2760(98)00018-6 |
0.325 |
|
| 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 |
0.351 |
|
| 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 |
0.386 |
|
| 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 |
0.464 |
|
| 1997 |
Gharani N, Waterworth DM, Batty S, White D, Gilling-Smith C, Conway GS, McCarthy M, Franks S, Williamson R. Association of the Steroid Synthesis Gene Cyp11a with Polycystic Ovary Syndrome and Hyperandrogenism Human Molecular Genetics. 6: 397-402. PMID 9147642 DOI: 10.1093/Hmg/6.3.397 |
0.327 |
|
| 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 |
0.343 |
|
| 1996 |
Wildenauer DB, Schwab SG, Albus M, Hallmayer J, Lerer B, Maier W, Blackwood D, Muir W, Clair DS, Morris S, Moises HW, Yang L, Kristbjarnarson H, Helgason T, Wiese C, ... ... Williamson R, et al. Additional support for schizophrenia linkage on chromosomes 6 and 8: A multicenter study American Journal of Medical Genetics. 67: 580-594. PMID 8950417 DOI: 10.1002/(Sici)1096-8628(19961122)67:6<580::Aid-Ajmg11>3.0.Co;2-P |
0.338 |
|
| 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 |
0.381 |
|
| 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 |
0.415 |
|
| 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 |
0.347 |
|
| 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 |
0.379 |
|
| 1995 |
Hart SL, Mayall E, Stern M, Munkonge FM, Frost A, Huang L, Vasilliou M, Williamson R, Alton EW, Coutelle C. The introduction of two silent mutations into a CFTR cDNA construct allows improved detection of exogenous mRNA in gene transfer experiments. Human Molecular Genetics. 4: 1597-602. PMID 8541845 DOI: 10.1093/Hmg/4.9.1597 |
0.337 |
|
| 1995 |
Thomas MR, Tutschek B, Frost A, Rodeck CH, Yazdani N, Craft I, Williamson R. The time of appearance and disappearance of fetal DNA from the maternal circulation. Prenatal Diagnosis. 15: 641-6. PMID 8532624 DOI: 10.1002/Pd.1970150709 |
0.314 |
|
| 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 |
0.445 |
|
| 1995 |
Hillermann R, See CG, Pook M, Wilkes D, Carvajal J, Doudney K, Williamson R, Chamberlain S. Physical evidence for the position of the Friedreich's ataxia locus FRDA proximal to D9S5. Cytogenetic and Genome Research. 71: 214-216. PMID 7587379 DOI: 10.1159/000134112 |
0.331 |
|
| 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 |
0.454 |
|
| 1995 |
Davies GE, Howard CM, Farrer MJ, Coleman MM, Bennett LB, Cullen LM, Wyse RKH, Burn J, Williamson R, Kessling AM. Genetic variation in the COL6A1 region is associated with congenital heart defects in trisomy 21 (Down's syndrome) Annals of Human Genetics. 59: 253-269. PMID 7486833 DOI: 10.1111/J.1469-1809.1995.Tb00746.X |
0.338 |
|
| 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 |
0.355 |
|
| 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 |
0.359 |
|
| 1994 |
Davies GE, Howard CM, Farrer MJ, Coleman MM, Cullen LM, Williamson R, Wyse RKH, Kessling AM. Unusual genotypes in the COL6A1 gene in parents of children with trisomy 21 and major congenital heart defects Human Genetics. 93: 443-446. PMID 7909528 DOI: 10.1007/Bf00201672 |
0.325 |
|
| 1994 |
Thomas MR, Williamson R, Craft I, Yazdani N, Rodeck CH. Y chromosome sequence DNA amplified from peripheral blood of women in early pregnancy. Lancet (London, England). 343: 413-4. PMID 7905562 DOI: 10.1016/S0140-6736(94)91248-3 |
0.353 |
|
| 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 |
0.365 |
|
| 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 |
0.424 |
|
| 1993 |
al-Mahdawi S, Chamberlain S, Cleland J, Nihoyannopoulos P, Gilligan D, French J, Choudhury L, Williamson R, Oakley C. Identification of a mutation in the beta cardiac myosin heavy chain gene in a family with hypertrophic cardiomyopathy. Heart. 69: 136-141. PMID 8435239 DOI: 10.1136/Hrt.69.2.136 |
0.319 |
|
| 1993 |
Wall WJ, Williamson R, Petrou M, Papaioannou D, Parkin BH. Variation of short tandem repeats within and between populations Human Molecular Genetics. 2: 1023-1029. PMID 8364538 DOI: 10.1093/Hmg/2.7.1023 |
0.307 |
|
| 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 |
0.372 |
|
| 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 |
0.379 |
|
| 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 |
0.417 |
|
| 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 |
0.387 |
|
| 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 |
0.409 |
|
| 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 |
0.411 |
|
| 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 |
0.393 |
|
| 1992 |
Duthie A, Doherty DG, Williams C, Scott‐Jupp R, Warner JO, Tanner MS, Williamson R, Mowat AP. Genotype analysis for ΔF508, G551D and R553X mutations in children and young adults with cystic fibrosis with and without chronic liver disease Hepatology. 15: 660-664. PMID 1551644 DOI: 10.1002/Hep.1840150418 |
0.318 |
|
| 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 |
0.378 |
|
| 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 |
0.468 |
|
| 1992 |
Scambler PJ, Kelly D, Lindsay E, Williamson R, Goldberg R, Shprintzen R, Wilson DI, Goodship JA, Cross IE, Burn J. Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus The Lancet. 339: 1138-1139. PMID 1349369 DOI: 10.1016/0140-6736(92)90734-K |
0.358 |
|
| 1992 |
Ratcliff R, Evans MJ, Doran J, Wainwright BJ, Williamson R, Colledge WH. Disruption of the cystic fibrosis transmembrane conductance regulator gene in embryonic stem cells by gene targeting. Transgenic Research. 1: 177-81. PMID 1284482 DOI: 10.1007/Bf02522536 |
0.343 |
|
| 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 |
0.457 |
|
| 1991 |
Westbrook CA, Neuman WL, Hewitt J, Kidd KK, Le Beau MM, Williamson R. Report of the chromosome 5 workshop. Genomics. 10: 1105-9. PMID 1916818 DOI: 10.1016/0888-7543(91)90211-V |
0.365 |
|
| 1991 |
Mullan MJ, Giuffra L, Hardy JA, Ovenstone I, Haynes AR, James LA, Williamson R, Newton PJ, Owen MJ, Roques P. Clinical and pathologic features of chromosome 21-linked familial Alzheimer's disease. Annals of the New York Academy of Sciences. 640: 177-80. PMID 1776736 DOI: 10.1111/J.1749-6632.1991.Tb00212.X |
0.319 |
|
| 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 |
0.376 |
|
| 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 |
0.389 |
|
| 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 |
0.371 |
|
| 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 |
0.358 |
|
| 1991 |
Williamson R. Polymerase chain reaction Pathology. 23: 17. DOI: 10.1016/S0031-3025(16)36213-4 |
0.351 |
|
| 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 |
0.427 |
|
| 1990 |
Ferrari M, Antonelli M, Bellini F, Borgo G, Castiglione O, Curcio L, Dallapiccola B, Devoto M, Estivill X, Gasparini P, Giunta A, Marianelli L, Mastella G, Novelli G, Pignatti P, ... ... Williamson R, et al. Genetic differences in cystic fibrosis patients with and without pancreatic insufficiency. An Italian collaborative study. Human Genetics. 84: 435-438. PMID 2323776 DOI: 10.1007/Bf00195815 |
0.325 |
|
| 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 |
0.389 |
|
| 1990 |
Santis G, Osborne L, Knight R, Ramsay M, Williamson R, Hodson M. Cystic fibrosis haplotype association and the ΔF508 mutation in adult British CF patients Human Genetics. 85: 424-425. PMID 2210760 DOI: 10.1007/Bf02428295 |
0.354 |
|
| 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 |
0.429 |
|
| 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 |
0.429 |
|
| 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 |
0.466 |
|
| 1990 |
Gasparini P, Novelli G, Estivill X, Olivieri D, Savoia A, Ruzzo A, Nunes V, Borgo G, Antonelli M, Williamson R. The genotype of a new linked DNA marker, MP6d-9, is related to the clinical course of cystic fibrosis. Journal of Medical Genetics. 27: 17-20. PMID 1968514 DOI: 10.1136/Jmg.27.1.17 |
0.345 |
|
| 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 |
0.374 |
|
| 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 |
0.405 |
|
| 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 |
0.372 |
|
| 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 |
0.375 |
|
| 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 |
0.357 |
|
| 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 |
0.373 |
|
| 1989 |
Feldman GL, Lewiston N, Fernbach SD, O'Brien WE, Williamson R, Wainwright BJ, Beaudet AL. Prenatal diagnosis of cystic fibrosis by using linked DNA markers in 138 pregnancies at 1-in-4 risk. American Journal of Medical Genetics. 33: 238-41. PMID 2569827 DOI: 10.1002/Ajmg.1320330219 |
0.326 |
|
| 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 |
0.467 |
|
| 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 |
0.375 |
|
| 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 |
0.459 |
|
| 1989 |
Williamson R. Molecular genetics and the transformation of clinical chemistry. Clinical Chemistry. 35: 2165-2168. DOI: 10.1093/Clinchem/35.11.2165 |
0.339 |
|
| 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 |
0.437 |
|
| 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 |
0.434 |
|
| 1988 |
Bennett CP, Burn J, Moore GE, Chambers J, Williamson R, Wilkinson J. Exclusion of calcitonin as a candidate gene for the basic defect in a family with autosomal dominant supravalvular aortic stenosis. Journal of Medical Genetics. 25: 311-2. PMID 3164411 DOI: 10.1136/Jmg.25.5.311 |
0.344 |
|
| 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 |
0.379 |
|
| 1988 |
Williams C, Weber L, Williamson R, Hjelm M. Guthrie Spots For Dna-Based Carrier Testing In Cystic Fibrosis The Lancet. 332: 693. PMID 2901556 DOI: 10.1016/S0140-6736(88)90512-0 |
0.31 |
|
| 1988 |
Williams C, Williamson R, Coutelle C, Loeffler F, Smith J, Ivinson A. Same-day, first-trimester antenatal diagnosis for cystic fibrosis by gene amplification. The Lancet. 332: 102-103. PMID 2898671 DOI: 10.1016/S0140-6736(88)90031-1 |
0.317 |
|
| 1988 |
Feldman GL, Williamson R, Beaudet AL, O'Brien WE. Prenatal diagnosis of cystic fibrosis by DNA amplification for detection of KM-19 polymorphism. Lancet. 2: 102. PMID 2898670 DOI: 10.1016/S0140-6736(88)90030-X |
0.347 |
|
| 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 |
0.388 |
|
| 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 |
0.448 |
|
| 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 |
0.357 |
|
| 1988 |
Johnson KJ, Jones PJ, Spurr N, Nimmo E, Davies J, Creed H, Weiss M, Williamson R. Linkage relationships of the protein kinase C gamma gene which exclude it as a candidate for myotonic dystrophy. Cytogenetic and Genome Research. 48: 13-15. PMID 2460293 DOI: 10.1159/000132577 |
0.317 |
|
| 1987 |
Davies KE, Gusella JF, Tsui LC, Williamson R, Page DC, Ferguson-Smith MA. Valuable libraries. Nature. 326: 124. PMID 3821885 DOI: 10.1038/326124e0 |
0.347 |
|
| 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 |
0.449 |
|
| 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 |
0.374 |
|
| 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 |
0.412 |
|
| 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 |
0.443 |
|
| 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 |
0.407 |
|
| 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 |
0.432 |
|
| 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 |
0.387 |
|
| 1987 |
Berger W, Hein J, Gedschold J, Bauer I, Speer A, Farrall M, Williamson R, Coutelle C. Crossovers in two German cystic fibrosis families determine probe order for MET, 7C22 and XV-2c/CS.7 Human Genetics. 77: 197-199. PMID 2888722 DOI: 10.1007/Bf00272392 |
0.32 |
|
| 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 |
0.464 |
|
| 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 |
0.38 |
|
| 1987 |
Nimmo ER, Padua RA, Hughes D, Williamson R, Johnson K. A c-DNA probe for the oncogene c-MEL (pC7–1) recognises a polymorphism with NcoI Nucleic Acids Research. 15: 3940-3940. PMID 2884641 DOI: 10.1093/Nar/15.9.3940 |
0.301 |
|
| 1987 |
Bates GP, Williamson R. RFLP for pHM20 (D2S12), an anonymous DNA sequence localised to 2p23-2pter. Nucleic Acids Research. 15: 864. PMID 2881265 DOI: 10.1093/Nar/15.2.864 |
0.339 |
|
| 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 |
0.379 |
|
| 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 |
0.369 |
|
| 1987 |
Robbins TP, Scambler PJ, Davies KE, Williamson R. An anonymous clone E9pl (D4S112) localised to 4q26-qter detects an Msp I RFLP. Nucleic Acids Research. 15: 8122. PMID 2444927 DOI: 10.1093/nar/15.19.8122 |
0.418 |
|
| 1986 |
Wainwright B, Lench N, Bartlett R, Roses A, Williamson R. RFLP identified by the anonymous DNA segment pBAM34 at 19q13.3-qter [HGM8 assignment D19S6] Nucleic Acids Research. 14: 3149-3149. PMID 3960744 DOI: 10.1093/Nar/14.7.3149 |
0.359 |
|
| 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 |
0.457 |
|
| 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 |
0.407 |
|
| 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 |
0.487 |
|
| 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 |
0.465 |
|
| 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 |
0.458 |
|
| 1986 |
Davison PJ, Norton P, Wallis SC, Gill L, Cook M, Williamson R, Humphries SE. There are two gene sequences for human apolipoprotein CI (apo CI) on chromosome 19, one of which is 4 KB from the gene for apo E Biochemical and Biophysical Research Communications. 136: 876-884. PMID 3013172 DOI: 10.1016/0006-291X(86)90414-6 |
0.336 |
|
| 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 |
0.426 |
|
| 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 |
0.43 |
|
| 1986 |
Davies KE, Williamson R. Towards a complete linkage map of the human X chromosome. Horizons in Biochemistry and Biophysics. 8: 1-50. PMID 2875929 |
0.564 |
|
| 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 |
0.421 |
|
| 1986 |
Williamson R. Dna Analysis And The Diagnosis Of Inherited Disease Pediatric Research. 20: 1031-1031. DOI: 10.1203/00006450-198610000-00050 |
0.314 |
|
| 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 |
0.354 |
|
| 1985 |
Davies KE, Briand P, Ionasescu V, Ionasescu G, Williamson R, Brown C, Cavard C, Cathelineau L. Gene for OTC: characterisation and linkage to Duchenne muscular dystrophy. Nucleic Acids Research. 13: 155-65. PMID 3839070 DOI: 10.1093/Nar/13.1.155 |
0.463 |
|
| 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 |
0.445 |
|
| 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 |
0.464 |
|
| 1985 |
Eiberg H, Mohr J, Schmiegelow K, Nielsen LS, Williamson R. Linkage relationships of paraoxonase (PON) with other markers: indication of PON-cystic fibrosis synteny. Clinical Genetics. 28: 265-71. PMID 2998653 DOI: 10.1111/J.1399-0004.1985.Tb00400.X |
0.348 |
|
| 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 |
0.368 |
|
| 1985 |
Ingle C, Williamson R, de la Chapelle A, Herva RR, Haapala K, Bates G, Willard HF, Pearson P, Davies KE. Mapping DNA sequences in a human X-chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation. American Journal of Human Genetics. 37: 451-62. PMID 2988331 |
0.52 |
|
| 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 |
0.43 |
|
| 1985 |
Kalsheker N, Chiswell D, Markham A, Imam A, Wallis S, Williamson R, Humphries SE. Possible Applications of Recombinant DNA Technology to the Diagnosis and Study of Variants of α1-Antitrypsin Annals of Clinical Biochemistry. 22: 25-32. PMID 2984979 DOI: 10.1177/000456328502200102 |
0.342 |
|
| 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 |
0.601 |
|
| 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 |
0.362 |
|
| 1985 |
Old JM, Briand PL, Purvis-Smith S, Howard NJ, Wilcken B, Hammond J, Pearson P, Cathelineau L, Williamson R, Davies KE. Prenatal exclusion of ornithine transcarbamylase deficiency by direct gene analysis. Lancet (London, England). 1: 73-5. PMID 2857026 DOI: 10.1016/S0140-6736(85)91966-X |
0.526 |
|
| 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 |
0.441 |
|
| 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 |
0.564 |
|
| 1984 |
Hartley DA, Davies KE, Drayna D, White RL, Williamson R. A cytological map of the human X chromosome--evidence for non-random recombination. Nucleic Acids Research. 12: 5277-85. PMID 6547776 DOI: 10.1093/nar/12.13.5277 |
0.545 |
|
| 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 |
0.394 |
|
| 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 |
0.43 |
|
| 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 |
0.42 |
|
| 1984 |
Williamson R, Davies KE, Donald J, Gilliam C, Wallis S, Humphries S. The implications of genetic variation in human pathology. Biochemical Society Symposium. 49: 183-8. PMID 6400491 |
0.496 |
|
| 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 |
0.599 |
|
| 1984 |
Wieacker P, Davies KE, Cooke HJ, Pearson PL, Williamson R, Bhattacharya S, Zimmer J, Ropers HH. Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids. American Journal of Human Genetics. 36: 265-76. PMID 6324578 |
0.539 |
|
| 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 |
0.603 |
|
| 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 |
0.444 |
|
| 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 |
0.596 |
|
| 1983 |
Imam AM, Eaton MA, Williamson R, Humphries S. Isolation and characterisation of cDNA clones for the A alpha- and gamma-chains of human fibrinogen. Nucleic Acids Research. 11: 7427-34. PMID 6689067 DOI: 10.1093/Nar/11.21.7427 |
0.312 |
|
| 1983 |
Harper PS, O'Brien T, Murray JM, Davies KE, Pearson P, Williamson R. The use of linked DNA polymorphisms for genotype prediction in families with Duchenne muscular dystrophy. Journal of Medical Genetics. 20: 252-4. PMID 6684693 DOI: 10.1136/Jmg.20.4.252 |
0.488 |
|
| 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 |
0.549 |
|
| 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 |
0.469 |
|
| 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 |
0.587 |
|
| 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 |
0.555 |
|
| 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 |
0.596 |
|
| 1983 |
Kingston HM, Harper PS, Pearson PL, Davies KE, Williamson R, Page D. Localisation of gene for Becker muscular dystrophy. Lancet (London, England). 2: 1200. PMID 6139558 DOI: 10.1016/S0140-6736(83)91252-7 |
0.494 |
|
| 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 |
0.519 |
|
| 1983 |
Davies KE, Gilliam TC, Williamson R. Cystic fibrosis is not caused by a defect in the gene coding for human complement C3. Molecular Biology & Medicine. 1: 185-90. PMID 6094950 |
0.501 |
|
| 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 |
0.583 |
|
| 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 |
0.388 |
|
| 1982 |
Arrand JE, Murray AM, Williamson R. The purification of human DNA fragments containing benzpyrene adducts. Biochimica Et Biophysica Acta. 698: 49-55. PMID 6288102 DOI: 10.1016/0167-4781(82)90183-X |
0.333 |
|
| 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 |
0.607 |
|
| 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 |
0.568 |
|
| 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 |
0.387 |
|
| 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 |
0.409 |
|
| 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 |
0.394 |
|
| 1981 |
Williamson R, Eskdale J, Coleman DV, Niazi M, Loeffler FE, Modell BM. Direct gene analysis of chorionic villi: A possible technique for first-trimester antenatal diagnosis of haemoglobinopathies. The Lancet. 318: 1125-1127. PMID 6118574 DOI: 10.1016/S0140-6736(81)90583-3 |
0.307 |
|
| 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 |
0.538 |
|
| 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 |
0.381 |
|
| 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 |
0.429 |
|
| 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 |
0.351 |
|
| 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 |
0.346 |
|
| 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 |
0.386 |
|
| 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 |
0.35 |
|
| 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 |
0.432 |
|
| 1980 |
Whitelaw E, Pagnier J, Verdier G, Henni T, Godet J, Williamson R. Mapping the alpha-globin genes in an Algerian HbH patient and his family. Blood. 55: 511-516. DOI: 10.1182/Blood.V55.3.511.Bloodjournal553511 |
0.33 |
|
| 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 |
0.374 |
|
| 1979 |
Courtney M, Williamson R. A nuclear precursor to human γ-globin messenger RNA Nucleic Acids Research. 7: 1121-1130. PMID 514808 DOI: 10.1093/Nar/7.5.1121 |
0.307 |
|
| 1979 |
Flavell RA, Bernards R, Kooter JM, de Boer E, Little PF, Annison G, Williamson R. The structure of the human beta-globin gene in beta-thalassaemia. Nucleic Acids Research. 6: 2749-60. PMID 461203 DOI: 10.1093/Nar/6.8.2749 |
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 |
0.398 |
|
| 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 |
0.409 |
|
| 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 |
0.369 |
|
| 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 |
0.37 |
|
| 1977 |
Comi P, Giglioni B, Barbarano L, Ottolenghi S, Williamson R, Novakova M, Masera G. Transcriptional and Post‐transcriptional Defects in β0‐Thalassaemia Febs Journal. 79: 617-622. PMID 923569 DOI: 10.1111/J.1432-1033.1977.Tb11846.X |
0.327 |
|
| 1977 |
Williamson R. Human globin gene expression in controls and thalassaemic patients Biochemical Society Transactions. 5: 478-479. PMID 902868 DOI: 10.1042/Bst0050478 |
0.309 |
|
| 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 |
0.374 |
|
| 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 |
0.387 |
|
| 1977 |
Godet J, Verdier G, Nigon V, Belhani M, Richard F, Colonna P, Mitchell J, Williamson R, Tolstoshev P. beta-O-thalassemia from Algeria: genetic and molecular characterization Blood. 50: 463-470. DOI: 10.1182/Blood.V50.3.463.463 |
0.316 |
|
| 1976 |
Tolstoshev P, Mitchell J, Lanyon G, Williamson R, Ottolenghi S, Comi P, Giglioni B, Masera G, Modell B, Weatherall DJ, Clegg JB. Presence of gene for beta globin in homozygous beta0 thalassaemia. Nature. 259: 95-98. PMID 1246358 DOI: 10.1038/259095A0 |
0.32 |
|
| 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 |
0.374 |
|
| 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 |
0.366 |
|
| 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 |
0.425 |
|
| 1976 |
Williamson R. Direct measurement of the number of globin genes British Medical Bulletin. 32: 246-250. PMID 788833 DOI: 10.1093/Oxfordjournals.Bmb.A071370 |
0.311 |
|
| 1975 |
Lanyon WG, Ottolenghi S, Williamson R. Human globin gene expression and linkage in bone marrow and fetal liver. Proceedings of the National Academy of Sciences of the United States of America. 72: 258-262. PMID 1054502 DOI: 10.1073/Pnas.72.1.258 |
0.326 |
|
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