| Year |
Citation |
Score |
| 2019 |
Hashimoto K, Hickman TT, Suzuki J, Ji L, Kohrman DC, Corfas G, Liberman MC. Protection from noise-induced cochlear synaptopathy by virally mediated overexpression of NT3. Scientific Reports. 9: 15362. PMID 31653916 DOI: 10.1038/S41598-019-51724-6 |
0.327 |
|
| 2019 |
Kohrman DC, Wan G, Cassinotti L, Corfas G. Hidden Hearing Loss: A Disorder with Multiple Etiologies and Mechanisms. Cold Spring Harbor Perspectives in Medicine. PMID 30617057 DOI: 10.1101/Cshperspect.A035493 |
0.324 |
|
| 2018 |
Altschuler RA, Kanicki A, Martin C, Kohrman DC, Miller RA. Rapamycin but not acarbose decreases age-related loss of outer hair cells in the mouse Cochlea. Hearing Research. 370: 11-15. PMID 30245283 DOI: 10.1016/J.Heares.2018.09.003 |
0.357 |
|
| 2018 |
Avenarius MR, Jung JY, Askew C, Jones SM, Hunker KL, Azaiez H, Rehman AU, Schraders M, Najmabadi H, Kremer H, Smith RJH, Géléoc GSG, Dolan DF, Raphael Y, Kohrman DC. Grxcr2 is required for stereocilia morphogenesis in the cochlea. Plos One. 13: e0201713. PMID 30157177 DOI: 10.1371/Journal.Pone.0201713 |
0.484 |
|
| 2015 |
Kommareddi P, Nair T, Kakaraparthi BN, Galano MM, Miller D, Laczkovich I, Thomas T, Lu L, Rule K, Kabara L, Kanicki A, Hughes ED, Jones JM, Hoenerhoff M, Fisher SG, ... ... Kohrman DC, et al. Hair Cell Loss, Spiral Ganglion Degeneration, and Progressive Sensorineural Hearing Loss in Mice with Targeted Deletion of Slc44a2/Ctl2. Journal of the Association For Research in Otolaryngology : Jaro. PMID 26463873 DOI: 10.1007/S10162-015-0547-3 |
0.454 |
|
| 2015 |
Altschuler RA, Dolan DF, Halsey K, Kanicki A, Deng N, Martin C, Eberle J, Kohrman DC, Miller RA, Schacht J. Age-related changes in auditory nerve-inner hair cell connections, hair cell numbers, auditory brain stem response and gap detection in UM-HET4 mice. Neuroscience. 292: 22-33. PMID 25665752 DOI: 10.1016/J.Neuroscience.2015.01.068 |
0.391 |
|
| 2014 |
Imtiaz A, Kohrman DC, Naz S. A frameshift mutation in GRXCR2 causes recessively inherited hearing loss. Human Mutation. 35: 618-24. PMID 24619944 DOI: 10.1002/Humu.22545 |
0.53 |
|
| 2013 |
Kohrman DC, Raphael Y. Gene therapy for deafness. Gene Therapy. 20: 1119-23. PMID 23864018 DOI: 10.1038/Gt.2013.39 |
0.411 |
|
| 2012 |
Schacht J, Altschuler R, Burke DT, Chen S, Dolan D, Galecki AT, Kohrman D, Miller RA. Alleles that modulate late life hearing in genetically heterogeneous mice. Neurobiology of Aging. 33: 1842.e15-29. PMID 22305187 DOI: 10.1016/J.Neurobiolaging.2011.12.034 |
0.422 |
|
| 2010 |
Odeh H, Hunker KL, Belyantseva IA, Azaiez H, Avenarius MR, Zheng L, Peters LM, Gagnon LH, Hagiwara N, Skynner MJ, Brilliant MH, Allen ND, Riazuddin S, Johnson KR, Raphael Y, ... ... Kohrman DC, et al. Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouse. American Journal of Human Genetics. 86: 148-60. PMID 20137774 DOI: 10.1016/J.Ajhg.2010.01.016 |
0.732 |
|
| 2008 |
Shen YC, Jeyabalan AK, Wu KL, Hunker KL, Kohrman DC, Thompson DL, Liu D, Barald KF. The transmembrane inner ear (tmie) gene contributes to vestibular and lateral line development and function in the zebrafish (Danio rerio). Developmental Dynamics : An Official Publication of the American Association of Anatomists. 237: 941-52. PMID 18330929 DOI: 10.1002/Dvdy.21486 |
0.491 |
|
| 2006 |
Gong TW, Karolyi IJ, Macdonald J, Beyer L, Raphael Y, Kohrman DC, Camper SA, Lomax MI. Age-related changes in cochlear gene expression in normal and shaker 2 mice. Journal of the Association For Research in Otolaryngology : Jaro. 7: 317-28. PMID 16794912 DOI: 10.1007/S10162-006-0046-7 |
0.481 |
|
| 2004 |
Odeh H, Hagiwara N, Skynner M, Mitchem KL, Beyer LA, Allen ND, Brilliant MH, Lebart MC, Dolan DF, Raphael Y, Kohrman DC. Characterization of two transgene insertional mutations at pirouette, a mouse deafness locus. Audiology & Neuro-Otology. 9: 303-14. PMID 15347914 DOI: 10.1159/000080701 |
0.749 |
|
| 2003 |
Karolyi IJ, Probst FJ, Beyer L, Odeh H, Dootz G, Cha KB, Martin DM, Avraham KB, Kohrman D, Dolan DF, Raphael Y, Camper SA. Myo15 function is distinct from Myo6, Myo7a and pirouette genes in development of cochlear stereocilia. Human Molecular Genetics. 12: 2797-805. PMID 12966030 DOI: 10.1093/Hmg/Ddg308 |
0.729 |
|
| 2002 |
Naz S, Giguere CM, Kohrman DC, Mitchem KL, Riazuddin S, Morell RJ, Ramesh A, Srisailpathy S, Deshmukh D, Riazuddin S, Griffith AJ, Friedman TB, Smith RJ, Wilcox ER. Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locus. American Journal of Human Genetics. 71: 632-6. PMID 12145746 DOI: 10.1086/342193 |
0.538 |
|
| 2002 |
Mitchem KL, Hibbard E, Beyer LA, Bosom K, Dootz GA, Dolan DF, Johnson KR, Raphael Y, Kohrman DC. Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6. Human Molecular Genetics. 11: 1887-98. PMID 12140191 DOI: 10.1093/Hmg/11.16.1887 |
0.574 |
|
| 2000 |
Beyer LA, Odeh H, Probst FJ, Lambert EH, Dolan DF, Camper SA, Kohrman DC, Raphael Y. Hair cells in the inner ear of the pirouette and shaker 2 mutant mice. Journal of Neurocytology. 29: 227-40. PMID 11276175 DOI: 10.1023/A:1026515619443 |
0.379 |
|
| 1999 |
Gong TWL, Winnicki RS, Kohrman DC, Lomax MI. A novel mouse kinesin of the UNC-104/KIF1 subfamily encoded by the Kif1b gene Gene. 239: 117-127. PMID 10571041 DOI: 10.1016/S0378-1119(99)00370-4 |
0.446 |
|
| 1998 |
Plummer NW, Galt J, Jones JM, Burgess DL, Sprunger LK, Kohrman DC, Meisler MH. Exon organization, coding sequence, physical mapping, and polymorphic intragenic markers for the human neuronal sodium channel gene SCN8A. Genomics. 54: 287-96. PMID 9828131 DOI: 10.1006/Geno.1998.5550 |
0.699 |
|
| 1996 |
Kohrman DC, Smith MR, Goldin AL, Harris J, Meisler MH. A missense mutation in the sodium channel Scn8a is responsible for cerebellar ataxia in the mouse mutant jolting. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 16: 5993-9. PMID 8815882 DOI: 10.1523/Jneurosci.16-19-05993.1996 |
0.622 |
|
| 1996 |
Griffith AJ, Burgess DL, Kohrman DC, Yu J, Blaschak J, Blanton SH, Boehnke M, Hecht JT, Overhauser J, Meisler MH. Localization of the homolog of a mouse craniofacial mutant to human chromosome 18q11 and evaluation of linkage to human CLP and CPO. Genomics. 34: 299-303. PMID 8786128 DOI: 10.1006/Geno.1996.0290 |
0.638 |
|
| 1996 |
Kohrman DC, Harris JB, Meisler MH. Mutation detection in the med and med(J) alleles of the sodium channel Scn8a: Unusual splicing due to a minor class AT-AC intron Journal of Biological Chemistry. 271: 17576-17581. PMID 8663325 DOI: 10.1074/Jbc.271.29.17576 |
0.628 |
|
| 1996 |
Griffith AJ, Radice GL, Burgess DL, Kohrman DC, Hansen GM, Justice MJ, Johnson KR, Davisson MT, Meisler MH. Location of the 9257 and ataxia mutations on mouse chromosome 18. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 7: 417-9. PMID 8662222 DOI: 10.1007/S003359900124 |
0.642 |
|
| 1995 |
Burgess DL, Kohrman DC, Galt J, Plummer NW, Jones JM, Spear B, Meisler MH. Mutation of a new sodium channel gene, Scn8a, in the mouse mutant 'motor endplate disease'. Nature Genetics. 10: 461-5. PMID 7670495 DOI: 10.1038/Ng0895-461 |
0.739 |
|
| 1995 |
Kohrman DC, Plummer NW, Schuster T, Jones JM, Jang W, Burgess DL, Galt J, Spear BT, Meisler MH. Insertional mutation of the motor endplate disease (med) locus on mouse chromosome 15. Genomics. 26: 171-7. PMID 7601440 DOI: 10.1016/0888-7543(95)80198-U |
0.746 |
|
| 1992 |
Silverstein GH, Kohrman DC, Christensen JB, Brockman WW, Imperiale MJ. An SV40 transformation revertant due to a host mutation: isolation and complementation analysis. Virology. 187: 723-33. PMID 1312274 DOI: 10.1016/0042-6822(92)90475-5 |
0.302 |
|
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