Margaret J. Kovach - Concepedia

Author

Margaret J. Kovach

Southern Illinois University School of Medicine

Also Known As

M J Kovach, M. J. Kovach, M.J Kovach, M.J. Kovach, Margaret J Kovach, Margaret J. Kovach, Marina Kovach, Schmitz, William

Publications

2.6K

Citations

H-Index

Concepts

All Affiliations

Southern Illinois University School of Medicine University of Tennessee at Chattanooga Washington University in St. Louis Boston Children's Hospital Rockefeller University

About

Margaret J. Kovach is an author at Southern Illinois University School of Medicine specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	2K
2	Natural Sciences	1	1	44
3	Public Health	1	1	22
4	Biology	1	1	44
5	Metabolism	1	1	22

Margaret J. Kovach

Publications

2.5K

Citations

H-Index

Page 1

	Year	Citations
Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein Giles D. Watts, Jill Wymer, Margaret J. Kovach, Nature Genetics Mutant Valosin-containing ProteinAlzheimer's DiseaseInclusion Body MyopathyPathologyDegenerative Disease	2004	1.4K
Chloroplast DNA sequence utility for the lowest phylogenetic and phylogeographic inferences in angiosperms: The tortoise and the hare IV Joey Shaw, Hayden L. Shafer, Opal Rayne Leonard, American Journal of Botany	2014	397
Clinical Delineation and Localization to Chromosome 9p13.3–p12 of a Unique Dominant Disorder in Four Families: Hereditary Inclusion Body Myopathy, Paget Disease of Bone, and Frontotemporal Dementia Margaret J. Kovach, Brook Waggoner, Suzanne M. Leal, Molecular Genetics and Metabolism Mendelian DisorderGenetic DisorderGeneticsClinical DelineationClinical Genetics	2001	197
Clinical and molecular studies in a unique family with autosomal dominant limb-girdle muscular dystrophy and Paget disease of bone Virginia Kimonis, Margaret J. Kovach, Brook Waggoner, Genetics in Medicine Unique FamilyMendelian DisorderGenetic DisorderMolecular StudiesGenetics	2000	140
A Unique Point Mutation in the PMP22 Gene Is Associated with Charcot-Marie-Tooth Disease and Deafness Margaret J. Kovach, Jing‐Ping Lin, Simeon A. Boyadjiev, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderPmp22 Gene IsGeneticsPathogenesis	1999	83
Genetic heterogeneity in autosomal dominant essential tremor Margaret J. Kovach, Jimmy Ruiz, Katerina Kimonis, Genetics in Medicine Mendelian DisorderGenetic DisorderGeneticsParkinson DiseaseGenetic Heterogeneity	2001	63
Kousseff syndrome caused by deletion of chromosome 22q11‐13 Shawnia Forrester, Margaret J. Kovach, Randell E. Smith, American Journal of Medical Genetics	2002	56
Clinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy: exclusion of GNE and three other candidate genes Giles D. Watts, Marielle Thorne, Margaret J. Kovach, Neuromuscular Disorders Chromosome 9PGenetic DisorderMedicineGeneticsPathology	2003	54
Stable transformation of a mosquito cell line results in extraordinarily high copy numbers of the plasmid. Todd Monroe, María C. Mühlmann-Díaz, Margaret J. Kovach, Proceedings of the National Academy of Sciences Stable TransformationGeneticsMolecular BiologyEscherichia ColiMolecular Genetics	1992	44
Manifestations in four males with and an obligate carrier of the Lenz microphthalmia syndrome Shawnia Forrester, Margaret J. Kovach, N.M. Reynolds, American Journal of Medical Genetics	2000	42

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