J. MacMillan - Concepedia

Author

J. MacMillan

Also Known As

J C MacMillan, J C Macmillan, J MACMILLAN, J MacMillan, J Macmillan, J. C. MacMillan, J. C. Macmillan, J. MacMILLAN, J. MacMillan, J.C MacMillan

Publications

1.4K

Citations

H-Index

Concepts

All Affiliations

University of Wales Royal Children's Hospital Griffith University Royal Brisbane and Women's Hospital University Hospital of Wales

About

J. MacMillan is an author at University of Wales specializing in medicine, genetics, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	18	711
2	Public Health	3	3	50
3	Social Sciences	2	2	73
4	Cell Biology	2	2	93
5	Nursing	1	1	70

J. MacMillan

Publications

1.2K

Citations

H-Index

Page 1

	Year	Citations
Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy. Helen G. Harley, S A Rundle, J. MacMillan, PubMed	1993	379
Molecular analysis and clinical correlations of the Huntington's disease mutation J. MacMillan, Russell G. Snell, Audrey Tyler, The Lancet Mendelian DisorderGenetic DisorderGeneticsMolecular BiologyDegenerative Disease	1993	95
Huntingtin Protein Colocalizes with Lesions of Neurodegenerative Diseases: An Investigation in Huntington's, Alzheimer's, and Pick's Diseases Sim K. Singhrao, P. Thomas, J.D. Wood, Experimental Neurology Neurodegenerative DiseasesAlzheimer's DiseaseMolecular BiologyDegenerative DiseaseNeurochemical Biomarkers	1998	78
Telemedicine and clinical genetics: Establishing a successful service Michael Gattas, J. MacMillan, I Meinecke, Journal of Telemedicine and Telecare Wireless TelemedicinePrimary CareConventional ClinicTelegenetic ConsultationTelemedicine	2001	73
Obtaining Patients' Views of Nursing Care to Inform the Development of a Patient Satisfaction Scale Lois H Thomas, J. MacMillan, Elaine McColl, International Journal for Quality in Health Care NursingQuality Of LifePatient SatisfactionPrimary CareNursing Care	1995	70
Association between migraine and a functional polymorphism at the dopamine β-hydroxylase locus Francesca Fernandez, Natalie Colson, Sharon Quinlan, Neurogenetics Cluster HeadacheMolecular NeuroscienceNeuropharmacologyDopamine β-Hydroxylase LocusNeuroscience	2009	62
A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine Rod A. Lea, Dale R. Nyholt, Rob Curtain, Neurogenetics Genome-wide Association StudyCluster HeadacheGeneticsNeurologyGenomics	2005	52
Charcot-Marie-Tooth disease 1A (CMT1A) associated with a maternal duplication of chromosome 17p11.2?12 Meena Upadhyaya, Susan Roberts, James M. Farnham, Human Genetics Mendelian DisorderMaternal DuplicationGenetic DisorderGeneticsPathology	1993	46
Identification of an expanded CAG repeat in the Huntington's disease gene (IT15) in a family reported to have benign hereditary chorea. J. MacMillan, Patrick J. Morrison, N C Nevin, Journal of Medical Genetics GeneticsDisease GeneGenetic EpidemiologyMolecular BiologyPathology	1993	44
Single‐gene neurological disorders in south wales: An epidemiological study J. MacMillan, Peter S. Harper Annals of Neurology	1991	35

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