H.M. Kozman - Concepedia

Author

H.M. Kozman

Women's and Children's Hospital

Also Known As

H Kozman, H M Kozman, H. KOZMAN, H. Kozman, H. M. Kozman, H.M. Kozman, Helen Kozman, Helen M. Kozman

Publications

885

Citations

H-Index

Concepts

All Affiliations

Women's and Children's Hospital The University of Adelaide Boston Children's Hospital Perron Institute for Neurological and Translational Science University College London

About

H.M. Kozman is an author at Women's and Children's Hospital specializing in genetics, medicine, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	12	512
2	Molecular Biology	4	4	295
3	Natural Sciences	1	1	61
4	Public Health	1	1	10
5	Biostatistics	1	1	10

H.M. Kozman

Publications

875

Citations

H-Index

Page 1

	Year	Citations
Autosomal dominant distal myopathy: linkage to chromosome 14. Nigel G. Laing, B.A. Laing, Christopher S. Meredith, PubMed	1995	143
Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site. Robert I. Richards, K. Holman, H.M. Kozman, Journal of Medical Genetics Developmental BiologyLinkage MappingFragile XFragile X GenotypeMedicine	1991	138
A New DNA Marker Tightly Linked to the Fragile X Locus ( <i>FRAXA</i> ) G K Suthers, David F. Callen, V.J. Hyland, Science GeneticsGenomic MechanismMolecular BiologyMolecular GeneticsDisease Gene Identification	1989	61
Refined genetic localization for central core disease. John C. Mulley, H.M. Kozman, Hilary A. Phillips, PubMed	1993	53
Dinucleotide repeat polymorphism at the D16S288 locus Yang Shen, K. Holman, Andrew Thompson, Nucleic Acids Research Allelic VariantGeneticsHuman PolymorphismMolecular BiologyMolecular Genetics	1991	51
Fine Genetic Mapping of the Batten Disease Locus (CLN3) by Haplotype Analysis and Demonstration of Allelic Association with Chromosome 16p Microsatellite Loci Hannah M. Mitchison, Andrew Thompson, John C. Mulley, Genomics Genetic AnalysisAllelic VariantHaplotype DeterminationFine Genetic MappingGenetics	1993	48
Integration of Transcript and Genetic Maps of Chromosome 16 at Near-1-Mb Resolution: Demonstration of a “Hot Spot” for Recombination at 16p12 David F. Callen, Sharon Lane, H.M. Kozman, Genomics ChromatinNear-1-mb ResolutionGeneticsMolecular BiologyChromosome Biology	1995	45
Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers. Robert I. Richards, Yang Shen, K. Holman, PubMed	1991	44
Identification of a highly polymorphic marker within intron 7 of the <i>ALAS2</i> gene and suggestion of at least two loci for X-linked sideroblastic anemia Timothy C. Cox, H.M. Kozman, Wendy H. Raskind, Human Molecular Genetics	1992	33
Genetic Mapping of the Batten Disease Locus (CLN3) to the Interval D16S288-D16S383 by Analysis of Haplotypes and Allelic Association Hannah M. Mitchison, Peter E.M. Taschner, Angela O'Rawe, Genomics Allelic VariantAllelic AssociationGenetic DisorderGeneticsPathology	1994	32

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