| Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein GDJ Watts, J Wymer, MJ Kovach, SG Mehta, S Mumm, D Darvish, ... Nature genetics 36 (4), 377-381, 2004 | 1594 | 2004 |
| Chloroplast DNA sequence utility for the lowest phylogenetic and phylogeographic inferences in angiosperms: The tortoise and the hare IV ABM Joey Shaw, Hayden L Shafer, O Rayne Leonard, Margaret J Kovach, Mark Schorr American journal of botany 101 (11), 1987-2004, 2014 | 259 | 2014 |
| 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 … MJ Kovach, B Waggoner, SM Leal, D Gelber, R Khardori, MA Levenstien, ... Molecular genetics and metabolism 74 (4), 458-475, 2001 | 252 | 2001 |
| Clinical and molecular studies in a unique family with autosomal dominant limb-girdle muscular dystrophy and Paget disease of bone VE Kimonis, MJ Kovach, B Waggoner, S Leal, A Salam, L Rimer, K Davis, ... Genetics in Medicine 2 (4), 232-241, 2000 | 165 | 2000 |
| A unique point mutation in the PMP22 gene is associated with Charcot-Marie-Tooth disease and deafness MJ Kovach, JP Lin, S Boyadjiev, K Campbell, L Mazzeo, K Herman, ... The American Journal of Human Genetics 64 (6), 1580-1593, 1999 | 106 | 1999 |
| Genetic heterogeneity in autosomal dominant essential tremor MJ Kovach, J Ruiz, K Kimonis, S Mueed, S Sinha, C Higgins, S Elble, ... Genetics in medicine 3 (3), 197-199, 2001 | 87 | 2001 |
| Clinical and genetic heterogeneity in chromosome 9p associated hereditary inclusion body myopathy: exclusion of GNE and three other candidate genes GDJ Watts, M Thorne, MJ Kovach, A Pestronk, VE Kimonis Neuromuscular Disorders 13 (7-8), 559-567, 2003 | 73 | 2003 |
| Anticipation in a unique family with Charcot‐Marie‐Tooth syndrome and deafness: Delineation of the clinical features and review of the literature MJ Kovach, KCM Campbell, K Herman, B Waggoner, D Gelber, ... American journal of medical genetics 108 (4), 295-303, 2002 | 71 | 2002 |
| Stable transformation of a mosquito cell line results in extraordinarily high copy numbers of the plasmid. TJ Monroe, MC Muhlmann-Diaz, MJ Kovach, JO Carlson, JS Bedford, ... Proceedings of the National Academy of Sciences 89 (13), 5725-5729, 1992 | 54 | 1992 |
| Manifestations in four males with and an obligate carrier of the Lenz microphthalmia syndrome S Forrester, MJ Kovach, NM Reynolds, R Urban, V Kimonis American journal of medical genetics 98 (1), 92-100, 2001 | 42 | 2001 |
| Heterogeneity in familial dominant Paget disease of bone and muscular dystrophy B Waggoner, MJ Kovach, M Winkelman, D Cai, R Khardori, D Gelber, ... American journal of medical genetics 108 (3), 187-191, 2002 | 34 | 2002 |
| A Drosophila metallothionein promoter is inducible in mosquito cells MJ Kovach, JO Carlson, BJ Beaty Insect molecular biology 1 (1), 37-43, 1992 | 32 | 1992 |
| Placental 11β-Hydroxysteroid dehydrogenase type 2 expression: Correlations with birth weight and placental metal concentrations SR C. Mikelson, M.J. Kovach, J. Troisi, S. Symes, D. Adair, R.K. Miller, C ... Placenta 36, 1212-1217, 2015 | 24 | 2015 |
| Kousseff syndrome caused by deletion of chromosome 22q11‐13 S Forrester, MJ Kovach, RE Smith, L Rimer, M Wesson, VE Kimonis American journal of medical genetics 112 (4), 338-342, 2002 | 18 | 2002 |
| Site-specific Photo-cross-linking between λ Integrase and Its DNA Recombination Target MJ Kovach, R Tirumalai, A Landy Journal of Biological Chemistry 277 (17), 14530-14538, 2002 | 14 | 2002 |
| Clinical heterogeneity in autosomal dominant optic atrophy in two 3q28-qter linked central Illinois families AS Chen, MJ Kovach, K Herman, A Avakian, W Frank, S Forrester, JP Lin, ... Genetics in Medicine 2 (5), 283-289, 2000 | 8 | 2000 |
| Feminism and First Nations: Conflict or Concert? L Brown, C Jamieson, M Kovach Canadian Review of Social Policy, 68-78, 1995 | 7 | 1995 |
| Inclusion body myopathy–Paget bone disease–frontotemporal dementia syndrome caused by mutated valosin containing protein GD Watts, J Wymer, SG Mehta Nat Genet 36, 377-381, 2004 | 4 | 2004 |
| Clinical and molecular studies in 5 families with limb girdle muscular dystrophy/hereditary inclusion body myopathy, Paget disease of bone and frontotemporal dementia. GDJ Watts, M Thorne, MJ Kovach, A Pestronck, VE Kimonis AMERICAN JOURNAL OF HUMAN GENETICS 71 (4), 549-549, 2002 | | 2002 |
| Clinical delineation and localization to chromosome 9p13. 3-p12 of a unique dominant disorder: Hereditary inclusion body myopathy, Paget disease of bone and frontotemporal … VE Kimonis, M Kovach, B Waggoner, SM Leal, Z Simmons, R Khardori, ... AMERICAN JOURNAL OF HUMAN GENETICS 69 (4), 225-225, 2001 | | 2001 |
Joey ShawUC Foundation Professor, University of Tennessee at ChattanoogaVerified email at utc.edu
