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Andrew J Griffith
Andrew J Griffith
Unknown affiliation
Verified email at nidcd.nih.gov
Title
Cited by
Cited by
Year
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23
JM Bork, LM Peters, S Riazuddin, SL Bernstein, ZM Ahmed, SL Ness, ...
The American Journal of Human Genetics 68 (1), 26-37, 2001
6312001
Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29
ER Wilcox, QL Burton, S Naz, S Riazuddin, TN Smith, B Ploplis, ...
Cell 104 (1), 165-172, 2001
5562001
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function
K Kurima, LM Peters, Y Yang, S Riazuddin, ZM Ahmed, S Naz, D Arnaud, ...
Nature genetics 30 (3), 277-284, 2002
4792002
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F
ZM Ahmed, S Riazuddin, SL Bernstein, Z Ahmed, S Khan, AJ Griffith, ...
The American Journal of Human Genetics 69 (1), 25-34, 2001
4712001
Binding of Ku protein to DNA. Measurement of affinity for ends and demonstration of binding to nicks.
PR Blier, AJ Griffith, J Craft, JA Hardin
journal of Biological Chemistry 268 (10), 7594-7601, 1993
4231993
Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness
HJ Park, S Shaukat, XZ Liu, SH Hahn, S Naz, M Ghosh, HN Kim, SK Moon, ...
Journal of medical genetics 40 (4), 242-248, 2003
4052003
Mechanotransduction in mouse inner ear hair cells requires transmembrane channel–like genes
Y Kawashima, GSG Géléoc, K Kurima, V Labay, A Lelli, Y Asai, ...
The Journal of clinical investigation 121 (12), 4796-4809, 2011
4012011
TMC1 and TMC2 are components of the mechanotransduction channel in hair cells of the mammalian inner ear
B Pan, GS Géléoc, Y Asai, GC Horwitz, K Kurima, K Ishikawa, ...
Neuron 79 (3), 504-515, 2013
3972013
Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia
IA Belyantseva, ET Boger, S Naz, GI Frolenkov, JR Sellers, ZM Ahmed, ...
Nature cell biology 7 (2), 148-156, 2005
3712005
Expert specification of the ACMG/AMP variant interpretation guidelines for genetic hearing loss
AM Oza, MT DiStefano, SE Hemphill, BJ Cushman, AR Grant, RK Siegert, ...
Human mutation 39 (11), 1593-1613, 2018
3482018
PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23
ZM Ahmed, S Riazuddin, J Ahmad, SL Bernstein, Y Guo, MF Sabar, ...
Human molecular genetics 12 (24), 3215-3223, 2003
3272003
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)
WT McGuirt, SD Prasad, AJ Griffith, HPM Kunst, GE Green, KB Shpargel, ...
Nature genetics 23 (4), 413-419, 1999
3191999
The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15
ZM Ahmed, R Goodyear, S Riazuddin, A Lagziel, PK Legan, M Behra, ...
Journal of Neuroscience 26 (26), 7022-7034, 2006
3062006
SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct …
SP Pryor, AC Madeo, JC Reynolds, NJ Sarlis, KS Arnos, WE Nance, ...
Journal of medical genetics 42 (2), 159-165, 2005
3032005
Human nonsyndromic sensorineural deafness
TB Friedman, AJ Griffith
Annual review of genomics and human genetics 4 (1), 341-402, 2003
2992003
Genetic insights into the morphogenesis of inner ear hair cells
GI Frolenkov, IA Belyantseva, TB Friedman, AJ Griffith
Nature Reviews Genetics 5 (7), 489-498, 2004
2822004
Beethoven, a mouse model for dominant, progressive hearing loss DFNA36
S Vreugde, A Erven, CJ Kros, W Marcotti, H Fuchs, K Kurima, ER Wilcox, ...
Nature genetics 30 (3), 257-258, 2002
2772002
Mutations of MYO6 are associated with recessive deafness, DFNB37
ZM Ahmed, RJ Morell, S Riazuddin, A Gropman, S Shaukat, MM Ahmad, ...
The American Journal of Human Genetics 72 (5), 1315-1322, 2003
2272003
Modification of human hearing loss by plasma-membrane calcium pump PMCA2
JM Schultz, Y Yang, AJ Caride, AG Filoteo, AR Penheiter, A Lagziel, ...
New England Journal of Medicine 352 (15), 1557-1564, 2005
2052005
Actin-bundling protein TRIOBP forms resilient rootlets of hair cell stereocilia essential for hearing
S Kitajiri, T Sakamoto, IA Belyantseva, RJ Goodyear, R Stepanyan, ...
Cell 141 (5), 786-798, 2010
1962010
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