HPPD: A newly recognized autosomal dominant disorder involving hypertelorism, preauricular sinus, punctal pits, and deafness mapping to chromosome 14q31
Sampath, Srirangan, Keats, Bronya J.B., Lacassie, Yves
Published in American journal of medical genetics. Part A (01.05.2011)
Published in American journal of medical genetics. Part A (01.05.2011)
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Dominant and recessive deafness caused by mutations of a novel gene, TMC1 , required for cochlear hair-cell function
Griffith, Andrew J, Kurima, Kiyoto, Peters, Linda M, Yang, Yandan, Riazuddin, Saima, Ahmed, Zubair M, Naz, Sadaf, Arnaud, Deidre, Drury, Stacy, Mo, Jianhong, Makishima, Tomoko, Ghosh, Manju, Menon, P.S.N, Deshmukh, Dilip, Oddoux, Carole, Ostrer, Harry, Khan, Shaheen, Riazuddin, Sheikh, Deininger, Prescott L, Hampton, Lori L, Sullivan, Susan L, Battey, James F, Keats, Bronya J.B, Wilcox, Edward R, Friedman, Thomas B
Published in Nature genetics (01.03.2002)
Published in Nature genetics (01.03.2002)
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Multi-site diagnosis and management of 260 patients with auditory neuropathy/dys-synchrony (auditory neuropathy spectrum disorder)
Berlin, Charles I, Hood, Linda J, Morlet, Thierry, Wilensky, Diane, Li, Li, Mattingly, Kelly Rose, Taylor-Jeanfreau, Jennifer, Keats, Bronya J B, John, Patti St, Montgomery, Elizabeth, Shallop, Jon K, Russell, Benjamin A, Frisch, Stefan A
Published in International journal of audiology (01.01.2010)
Published in International journal of audiology (01.01.2010)
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Modification of Depression by COMT val[superscript 158]Met Polymorphism in Children Exposed to Early Severe Psychosocial Deprivation
Drury, Stacy S, Theall, Katherine P, Smyke, Anna T, Keats, Bronya J. B, Egger, Helen L, Nelson, Charles A, Fox, Nathan A, Marshall, Peter J, Zeanah, Charles H
Published in Child abuse & neglect (01.06.2010)
Published in Child abuse & neglect (01.06.2010)
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Phenotypic variability in Friedreich ataxia: role of the associated GAA triplet repeat expansion
Montermini, L, Richter, A, Morgan, K, Justice, C M, Julien, D, Castellotti, B, Mercier, J, Poirier, J, Capozzoli, F, Bouchard, J P, Lemieux, B, Mathieu, J, Vanasse, M, Seni, M H, Graham, G, Andermann, F, Andermann, E, Melançon, S B, Keats, B J, Di Donato, S, Pandolfo, M
Published in Annals of neurology (01.05.1997)
Published in Annals of neurology (01.05.1997)
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Genetic heterogeneity in Usher syndrome
Keats, Bronya J.B., Savas, Sevtap
Published in American journal of medical genetics. Part A (15.09.2004)
Published in American journal of medical genetics. Part A (15.09.2004)
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Modification of depression by COMT val158met polymorphism in children exposed to early severe psychosocial deprivation
DRURY, Stacy S, THEALL, Katherine P, SMYKE, Anna T, TEATS, Bronya J. B, EGGER, Helen L, NELSON, Charles A, FOX, Nathan A, MARSHALL, Peter J, ZEANAH, Charles H
Published in Child abuse & neglect (01.06.2010)
Published in Child abuse & neglect (01.06.2010)
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Genetic variation of recent Alu insertions in human populations
Batzer, M A, Arcot, S S, Phinney, J W, Alegria-Hartman, M, Kass, D H, Milligan, S M, Kimpton, C, Gill, P, Hochmeister, M, Ioannou, P A, Herrera, R J, Boudreau, D A, Scheer, W D, Keats, B J, Deininger, P L, Stoneking, M
Published in Journal of molecular evolution (01.01.1996)
Published in Journal of molecular evolution (01.01.1996)
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Mouse tales from Kresge: the deafness mouse
Drury, Stacy S, Keats, Bronya J B
Published in Journal of the American Academy of Audiology (01.06.2003)
Published in Journal of the American Academy of Audiology (01.06.2003)
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Structure, diversity, and evolution of the 45-bp VNTR in intron 5 of the USH1C gene
Savas, Sevtap, Frischhertz, Ben, Batzer, Mark A, Deininger, Prescott L, Keats, Bronya J.B
Published in Genomics (San Diego, Calif.) (01.03.2004)
Published in Genomics (San Diego, Calif.) (01.03.2004)
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Early childhood hearing loss: clinical and molecular genetics. An educational slide set of the American College of Medical Genetics
Alford, Raye L, Friedman, Thomas B, Keats, Bronya J B, Kimberling, William J, Proud, Virginia K, Smith, Richard J H, Arnos, Kathleen S, Korf, Bruce R, Rehm, Heidi L, Toriello, Helga V
Published in Genetics in medicine (01.07.2003)
Published in Genetics in medicine (01.07.2003)
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Journal Article
Male Sexual Orientation and Genetic Evidence
Risch, Neil, Squires-Wheeler, Elizabeth, Bronya J. B. Keats, Hamer, Dean H., Hu, Stella, Magnuson, Victoria, Hu, Nan, Angela M. L. Pattatucci
Published in Science (American Association for the Advancement of Science) (24.12.1993)
Published in Science (American Association for the Advancement of Science) (24.12.1993)
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A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C
Petit, Christine, Verpy, Elisabeth, Leibovici, Michel, Zwaenepoel, Ingrid, Liu, Xue-Zhong, Gal, Andreas, Salem, Nabiha, Mansour, Ahmad, Blanchard, Stéphane, Kobayashi, Ichiro, Keats, Bronya J.B, Slim, Rima
Published in Nature genetics (01.09.2000)
Published in Nature genetics (01.09.2000)
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Journal Article
Modification of depression by COMT valmet polymorphism in children exposed to early severe psychosocial deprivation
Drury, Stacy S, Theall, Katherine P, Smyke, Anna T, Keats, Bronya J B, Egger, Helen L, Nelson, Charles A, Fox, Nathan A, Marshall, Peter J, Zeanah, Charles H
Published in Child abuse & neglect (01.06.2010)
Published in Child abuse & neglect (01.06.2010)
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Replication-mediated instability of the GAA triplet repeat mutation in Friedreich ataxia
Pollard, Laura M., Sharma, Rajesh, Gómez, Mariluz, Shah, Sonali, Delatycki, Martin B., Pianese, Luigi, Monticelli, Antonella, Keats, Bronya J.B., Bidichandani, Sanjay I.
Published in Nucleic acids research (01.01.2004)
Published in Nucleic acids research (01.01.2004)
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A dominantly inherited progressive deafness affecting distal auditory nerve and hair cells
Starr, Arnold, Isaacson, Brandon, Michalewski, Henry J, Zeng, Fan-Gang, Kong, Ying-Yee, Beale, Paula, Paulson, George W, Keats, Bronya J B, Lesperance, Marci M
Published in Journal of the Association for Research in Otolaryngology (01.12.2004)
Published in Journal of the Association for Research in Otolaryngology (01.12.2004)
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