Robert Williamson - Concepedia

Author

Robert Williamson

Also Known As

Bruce Wallace, R Williamson, R. B. Williamson, R. Brady Williamson, R.B Williamson, R.B. Williamson, ROBERT WILLIAMSON, Robert B. Williamson, Robert Brady Williamson, Robert WILLIAMSON

289

Publications

19K

Citations

H-Index

254

Concepts

All Affiliations

Royal Children's Hospital Murdoch Children's Research Institute St. Mary's Hospital St Mary's Hospital The University of Melbourne

About

Robert Williamson is an author at Royal Children's Hospital specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Engineering	16	21	821
2	Education	7	7	142
3	Health Sciences	3	3	80
4	Law	1	1	15
5	Management	1	1	51

Robert Williamson

152

Publications

17.5K

Citations

H-Index

Page 1

	Year	Citations
Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease Alison Goate, Marie‐Christine Chartier‐Harlin, Jeremy Brown, Nature Alzheimer's DiseaseGeneticsMissense MutationMolecular BiologyPrion Disease	1991	4.6K
A Mutation in the Interferon-γ –Receptor Gene and Susceptibility to Mycobacterial Infection Melanie J. Newport, Clare Huxley, Sara Huston, New England Journal of Medicine	1996	1.2K
Liposome-mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosis Natasha J. Caplen, Eric W.F.W. Alton, Peter G. Mddleton, Nature Medicine FibrosisMolecular PhysiologyAllergyImmunologyNasal Epithelium	1995	707
Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy Cisca Wijmenga, Jane Hewitt, Lodewijk A. Sandkuijl, Nature Genetics ChromatinMendelian DisorderGenetic DisorderGeneticsMolecular Biology	1992	662
Localization of cystic fibrosis locus to human chromosome 7cen–q22 Brandon J. Wainwright, Peter Scambler, Jörg Schmidtke, Nature ChromatinChromatin StructureCytogeneticsGenetic DisorderGenetics	1985	487
Polycystic ovaries and premature male pattern baldness are associated with one allele of the steroid metabolism gene CYP17 Adam Carey, Dawn Waterworth, Kirty Patel, Human Molecular Genetics	1994	463
A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands Xavier Estivill, Martin Farrall, Peter Scambler, Nature Genetic DisorderMedicineGeneticsCystic Fibrosis LocusPathology	1987	335
Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystropothhy Jane Hewitt, Robert Lyle, Lorraine N. Clark, Human Molecular Genetics BiologyRare DiseasesRepeat SequencesMendelian DisorderGenetic Disorder	1994	322
Linkage and association of insulin gene VNTR regulatory polymorphism with polycystic ovary syndrome Dawn Waterworth, Simon T. Bennett, Neda Gharani, The Lancet Metabolic SyndromeGenetic DeterminantGeneticsDiabetesGenetic Epidemiology	1997	320
Mapping of mutation causing Friedreich's ataxia to human chromosome 9 Susan Chamberlain, Jacqui Shaw, Alison Rowland, Nature Mendelian DisorderGenetic DisorderGeneticsHuman Chromosome 9Pathology	1988	316

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