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Kenneth Johnson
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Network (preview)
28
Davisson, Muriel
18
Zheng, Qing Yin
16
Cook, Susan
11
Bronson, Roderick
11
Ward-Bailey, Patricia
8
Donahue, Leah Rae
8
Gagnon, Leona
7
Erway, Lawrence
5
Longo-Guess, Chantal
4
Hawes, Norman
3
Jones, Sherri
3
Jones, Timothy
3
Lane, Priscilla
3
Sweet, Hope
3
Harris, Belinda
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All Publications
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2008: Johnson Kenneth R; Longo-Guess Chantal; Gagnon Leona H; Yu Heping; Zheng Qing Yin
A locus on distal chromosome 11 (ahl8) and its interaction with Cdh23 ahl underlie the early onset, age-related hearing loss of DBA/2J mice.
Genomics 2008;92(4):219-25.
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2007: Longo-Guess Chantal; Gagnon Leona H; Bergstrom David E; Johnson Kenneth R
A missense mutation in the conserved C2B domain of otoferlin causes deafness in a new mouse model of DFNB9.
Hearing research 2007;234(1-2):21-8.
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2007: Longo-Guess Chantal M; Gagnon Leona H; Fritzsch Bernd; Johnson Kenneth R
Targeted knockout and lacZ reporter expression of the mouse Tmhs deafness gene and characterization of the hscy-2J mutation.
Mammalian genome : official journal of the International Mammalian Genome Society 2007;18(9):646-56.
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2007: Johnson Kenneth R; Marden Coleen C; Ward-Bailey Patricia; Gagnon Leona H; Bronson Roderick T; Donahue Leah Rae
Congenital hypothyroidism, dwarfism, and hearing impairment caused by a missense mutation in the mouse dual oxidase 2 gene, Duox2.
Molecular endocrinology (Baltimore, Md.) 2007;21(7):1593-602.
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2006: Gagnon Leona H; Longo-Guess Chantal M; Berryman Mark; Shin Jung-Bum; Saylor Katherine W; Yu Heping; Gillespie Peter G; Johnson Kenneth R
The chloride intracellular channel protein CLIC5 is expressed at high levels in hair cell stereocilia and is essential for normal inner ear function.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2006;26(40):10188-98.
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2006: Johnson Kenneth R; Zheng Qing Yin; Noben-Trauth Konrad
Strain background effects and genetic modifiers of hearing in mice.
Brain research 2006;1091(1):79-88.
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2006: Jones Sherri M; Jones Timothy A; Johnson Kenneth R; Yu Heping; Erway Lawrence C; Zheng Qing Y
A comparison of vestibular and auditory phenotypes in inbred mouse strains.
Brain research 2006;1091(1):40-6.
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2005: Jones Sherri M; Johnson Kenneth R; Yu Heping; Erway Lawrence C; Alagramam Kumar N; Pollak Natasha; Jones Timothy A
A quantitative survey of gravity receptor function in mutant mouse strains.
Journal of the Association for Research in Otolaryngology : JARO 2005;6(4):297-310.
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2005: Longo-Guess Chantal M; Gagnon Leona H; Cook Susan A; Wu Jian; Zheng Qing Y; Johnson Kenneth R
A missense mutation in the previously undescribed gene Tmhs underlies deafness in hurry-scurry (hscy) mice.
Proceedings of the National Academy of Sciences of the United States of America 2005;102(22):7894-9.
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2005: Johnson K R; Zheng Q Y; Weston M D; Ptacek L J; Noben-Trauth K
The Mass1frings mutation underlies early onset hearing impairment in BUB/BnJ mice, a model for the auditory pathology of Usher syndrome IIC.
Genomics 2005;85(5):582-90.
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2004: Jones Sherri M; Erway Lawrence C; Johnson Kenneth R; Yu Heping; Jones Timothy A
Gravity receptor function in mice with graded otoconial deficiencies.
Hearing research 2004;191(1-2):34-40.
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2004: Lorenz-Depiereux Bettina; Guido Victoria E; Johnson Kenneth R; Zheng Qing Yin; Gagnon Leona H; Bauschatz Joiel D; Davisson Muriel T; Washburn Linda L; Donahue Leah Rae; Strom Tim M; Eicher Eva M
New intragenic deletions in the Phex gene clarify X-linked hypophosphatemia-related abnormalities in mice.
Mammalian genome : official journal of the International Mammalian Genome Society 2004;15(3):151-61.
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2003: Johnson Kenneth R; Gagnon Leona H; Webb Lisa S; Peters Luanne L; Hawes Norman L; Chang Bo; Zheng Qing Yin
Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene.
Human molecular genetics 2003;12(23):3075-86.
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2003: Donahue Leah Rae; Chang Bo; Mohan Subburaman; Miyakoshi Nao; Wergedal Jon E; Baylink David J; Hawes Norman L; Rosen Clifford J; Ward-Bailey Patricia; Zheng Qing Y; Bronson Roderick T; Johnson Kenneth R; Davisson Muriel T
A missense mutation in the mouse Col2a1 gene causes spondyloepiphyseal dysplasia congenita, hearing loss, and retinoschisis.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2003;18(9):1612-21.
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2003: Johnson Kenneth R; Lane Priscilla W; Cook Susan A; Harris Belinda S; Ward-Bailey Patricia F; Bronson Roderick T; Lyons Bonnie L; Shultz Leonard D; Davisson Muriel T
Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5.
Genomics 2003;81(1):6-14.
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2002: Johnson Kenneth R; Zheng Qing Yin
Ahl2, a second locus affecting age-related hearing loss in mice.
Genomics 2002;80(5):461-4.
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2002: Ikeda Akihiro; Zheng Qing Yin; Zuberi Aamir R; Johnson Kenneth R; Naggert Jürgen K; Nishina Patsy M
Microtubule-associated protein 1A is a modifier of tubby hearing (moth1).
Nature genetics 2002;30(4):401-5.
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2001: Zheng Q Y; Johnson K R
Hearing loss associated with the modifier of deaf waddler (mdfw) locus corresponds with age-related hearing loss in 12 inbred strains of mice.
Hearing research 2001;154(1-2):45-53.
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2001: Johnson K R; Zheng Q Y; Bykhovskaya Y; Spirina O; Fischel-Ghodsian N
A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice.
Nature genetics 2001;27(2):191-4.
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2001: Cook S A; Akeson E C; Calvano C; Johnson K R; Mandell J; Hawes N L; Bronson R T; Roderick T H; Davisson M T
Mouse paracentric inversion In(3)55Rk mutates the urate oxidase gene.
Cytogenetics and cell genetics 2001;93(1-2):77-82.
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2000: Davisson M T; Johnson K R; Bronson R T; Ward-Bailey P F; Cook S A; Harris B S; Donahue L R
Grey intense: a new mouse mutation affecting pigmentation.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(12):1139-41.
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2000: Johnson K R; Zheng Q Y; Erway L C
A major gene affecting age-related hearing loss is common to at least ten inbred strains of mice.
Genomics 2000;70(2):171-80.
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2000: Letts V A; Valenzuela A; Dunbar C; Zheng Q Y; Johnson K R; Frankel W N
A new spontaneous mouse mutation in the Kcne1 gene.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(10):831-5.
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2000: Ward-Bailey P F; Wood B; Johnson K R; Bronson R T; Donahue L R; Davisson M T
Neuromuscular ataxia: a new spontaneous mutation in the mouse.
Mammalian genome : official journal of the International Mammalian Genome Society 2000;11(10):820-3.
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1999: Ikeda A; Zheng Q Y; Rosenstiel P; Maddatu T; Zuberi A R; Roopenian D C; North M A; Naggert J K; Johnson K R; Nishina P M
Genetic modification of hearing in tubby mice: evidence for the existence of a major gene (moth1) which protects tubby mice from hearing loss.
Human molecular genetics 1999;8(9):1761-7.
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1999: Zheng Q Y; Johnson K R; Erway L C
Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses.
Hearing research 1999;130(1-2):94-107.
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1999: Johnson K R; Cook S A; Erway L C; Matthews A N; Sanford L P; Paradies N E; Friedman R A
Inner ear and kidney anomalies caused by IAP insertion in an intron of the Eya1 gene in a mouse model of BOR syndrome.
Human molecular genetics 1999;8(4):645-53.
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1999: Smith R S; Johnson K R; Hawes N L; Harris B S; Sundberg J P; Davisson M T
Lens epithelial proliferation cataract in segmental trisomy involving mouse Chromosomes 4 and 17.
Mammalian genome : official journal of the International Mammalian Genome Society 1999;10(2):102-6.
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1998: Sweet H O; Brilliant M H; Cook S A; Johnson K R; Davisson M T
A new allelic series for the underwhite gene on mouse chromosome 15.
The Journal of heredity 1998;89(6):546-51.
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1998: Johnson K R; Cook S A; Zheng Q Y
The original shaker-with-syndactylism mutation (sy) is a contiguous gene deletion syndrome.
Mammalian genome : official journal of the International Mammalian Genome Society 1998;9(11):889-92.
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1998: Johnson K R; Sweet H O; Donahue L R; Ward-Bailey P; Bronson R T; Davisson M T
A new spontaneous mouse mutation of Hoxd13 with a polyalanine expansion and phenotype similar to human synpolydactyly.
Human molecular genetics 1998;7(6):1033-8.
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1998: Bronson R T; Donahue L R; Johnson K R; Tanner A; Lane P W; Faust J R
Neuronal ceroid lipofuscinosis (nclf), a new disorder of the mouse linked to chromosome 9.
American journal of medical genetics 1998;77(4):289-97.
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1998: Johnson K R; Davisson M T
Encyclopedia of the mouse genome VII. Mouse chromosome 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1998;8 Spec No():S343-52.
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1997: Johnson K R; Erway L C; Cook S A; Willott J F; Zheng Q Y
A major gene affecting age-related hearing loss in C57BL/6J mice.
Hearing research 1997;114(1-2):83-92.
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1996: Donahue L R; Cook S A; Johnson K R; Bronson R T; Davisson M T
Megencephaly: a new mouse mutation on chromosome 6 that causes hypertrophy of the brain.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(12):871-6.
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1996: Sweet H O; Bronson R T; Johnson K R; Cook S A; Davisson M T
Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(11):798-802.
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1996: Ward-Bailey P F; Johnson K R; Handel M A; Harris B S; Davisson M T
A new mouse mutation causing male sterility and histoincompatibility.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(11):793-7.
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1996: Schweitzer P A; Noben-Trauth N; Pelsue S C; Johnson K R; Wolf S F; Shultz L D
Genetic mapping of the IL-12 alpha chain gene (Il12a) on mouse chromosome 3.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(5):394-5.
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1996: Noben-Trauth N; Schweitzer P A; Johnson K R; Wolf S F; Knowles B B; Shultz L D
The interleukin-12 beta subunit (p40) maps to mouse chromosome 11.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(5):392.
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1996: Sweet H O; Marks S C; MacKay C A; Johnson K R; Davisson M T
Dense incisors (din): a new mouse mutation on chromosome 16 affecting tooth eruption and body size.
The Journal of heredity 1996;87(2):162-7.
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1996: Johnson K R; Davisson M T
Encyclopedia of the mouse genome V. Mouse chromosome 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;6 Spec No():S300-8.
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1995: Johnson K R; Lane P W; Ward-Bailey P; Davisson M T
Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac.
Genomics 1995;29(2):457-64.
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1995: Rice D S; Williams R W; Ward-Bailey P; Johnson K R; Harris B S; Davisson M T; Goldowitz D
Mapping the Bst mutation on mouse chromosome 16: a model for human optic atrophy.
Mammalian genome : official journal of the International Mammalian Genome Society 1995;6(8):546-8.
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1995: Cook S A; Johnson K R; Bronson R T; Davisson M T
Neuromuscular degeneration (nmd): a mutation on mouse chromosome 19 that causes motor neuron degeneration.
Mammalian genome : official journal of the International Mammalian Genome Society 1995;6(3):187-91.
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1994: Johnson K R; Cook S A; Davisson M T
Identification and genetic mapping of 151 dispersed members of 16 ribosomal protein multigene families in the mouse.
Mammalian genome : official journal of the International Mammalian Genome Society 1994;5(11):670-87.
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1994: Johnson K R; Davisson M T
Mouse chromosome 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1994;5 Spec No():S259-65.
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1993: Davisson M T; Johnson K R
Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1993;4 Spec No():S253-60.
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1993: Johnson K R; Cook S A; Ward-Bailey P; Bustin M; Davisson M T
Identification and genetic mapping of the murine gene and 20 related sequences encoding chromosomal protein HMG-17.
Mammalian genome : official journal of the International Mammalian Genome Society 1993;4(2):83-9.
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1993: Johnson K R; Cook S A; Ward-Bailey P; Davisson M T
Genetic mapping of variable length rDNA segments to centromeric regions of mouse chromosomes 11, 12, 15, 16, and 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1993;4(1):49-52.
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1992: Johnson K R; Lu S; Murtha M T; Ruddle F H; Davisson M T
Genetic mapping of a new homeobox gene to mouse chromosome 7.
Genomics 1992;14(4):1107-9.
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1992: Johnson K R; Davisson M T
A multipoint genetic linkage map of mouse chromosome 18.
Genomics 1992;13(4):1143-9.
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1992: Johnson K R; Cook S A; Davisson M T
Chromosomal localization of the murine gene and two related sequences encoding high-mobility-group I and Y proteins.
Genomics 1992;12(3):503-9.
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1992: Davisson M T; Johnson K R
Mouse chromosome 18.
Mammalian genome : official journal of the International Mammalian Genome Society 1992;3 Spec No():S261-5.
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1992: Johnson K R; Cook S A; Bustin M; Davisson M T
Genetic mapping of the murine gene and 14 related sequences encoding chromosomal protein HMG-14.
Mammalian genome : official journal of the International Mammalian Genome Society 1992;3(11):625-32.
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1991: Johnson K R
Improved oligonucleotide labeling and hybridization assay for endogenous nonecotropic murine leukemia proviruses.
Mammalian genome : official journal of the International Mammalian Genome Society 1991;1(4):260-2.
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