S. M. Forrest - Concepedia

Author

S. M. Forrest

Also Known As

Murdoch, S FORREST, S Forrest, S M Forrest, S. Forrest, S. M. Forrest, S.M. Forrest, Susan M Forrest, Susan M. Forrest, SusanM. Forrest

Publications

2.4K

Citations

H-Index

Concepts

All Affiliations

Royal Children's Hospital John Radcliffe Hospital The University of Melbourne AGRF Ltd Victorian Clinical Genetics Services

About

S. M. Forrest is an author at Royal Children's Hospital specializing in medicine, genetics, and neuromuscular pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	18	1.7K
2	Natural Sciences	2	2	49
3	Public Health	2	2	85
4	Health Sciences	1	1	42
5	Social Sciences	1	1	11

S. M. Forrest

Publications

2.1K

Citations

H-Index

Page 1

	Year	Citations
Very mild muscular dystrophy associated with the deletion of 46% of dystrophin Sarah England, L. V. B. Nicholson, Mark Johnson, Nature UrologyMedicineMild Muscular DystrophyDegenerative DiseaseNeuromusculoskeletal Disorder	1990	597
Preferential deletion of exons in Duchenne and Becker muscular dystrophies S. M. Forrest, Gareth Cross, Andreas Speer, Nature KinesiologyMedicineDegenerative DiseasePreferential DeletionNeuromuscular Pathology	1987	196
Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies S. M. Forrest, Gareth Cross, Tracey Flint, Genomics Mendelian DisorderGenetic DisorderMedicineGeneticsDegenerative Disease	1988	178
A duplication at chromosome 11q12.2-11q12.3 is associated with spinocerebellar ataxia type 20 Melanie A. Knight, Dena Hernández, Scott J. Diede, Human Molecular Genetics Sca20 RegionNeurodegenerative DiseasesDevelopmental BiologyMendelian DisorderGenetic Disorder	2008	138
Maternal uniparental disomy of chromosome 13 in a phenotypically normal child. Howard R. Slater, J H Shaw, G.W. Dawson, Journal of Medical Genetics ChromatinInfertilityCytogeneticsGenetic DisorderGenetics	1994	121
A new autosomal dominant pure cerebellar ataxia Elsdon Storey, R. J. M. Gardner, Melanie A. Knight, Neurology Mendelian DisorderNeurological DisorderMedicineGeneticsGenetic Disorder	2001	83
Population-Specific Polymorphisms of the Human FMO3 Gene: Significance for Detoxication John R. Cashman, Beverly R. Akerman, S. M. Forrest, Drug Metabolism and Disposition	2000	74
Mutation detection in phenylketonuria by using chemical cleavage of mismatch: importance of using probes from both normal and patient samples. S. M. Forrest, H H Dahl, David W. Howells, PubMed	1991	67
X-linked recessive panhypopituitarism associated with a regional duplication in Xq25-q26. Maria Lagerström‐Fermér, Mats Sundvall, Elsy Johnsen, PubMed	1997	66
EFFECTIVE STRATEGY FOR PRENATAL PREDICTION OF DUCHENNE AND BECKER MUSCULAR DYSTROPHY S. M. Forrest, Gareth Cross, Nick Thomas, The Lancet Developmental BiologyMotor DevelopmentPediatricsMaternal HealthPreterm Birth	1987	53

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