Center for Sensory Neuroscience

Research Output

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Letter
2010

Clarin-1 protein expression in photoreceptors

Cosgrove, D. & Zallocchi, M., Jan 1 2010, In : Hearing Research. 259, 1-2, 1 p.

Research output: Contribution to journalLetter

2 Scopus citations
2009

A novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family

Shearer, A. E., Hildebrand, M. S., Bromhead, C. J., Kahrizi, K., Webster, J. A., Azadeh, B., Kimberling, W. J., Anousheh, A., Nazeri, A., Stephan, D., Najmabadi, H., Smith, R. J. H. & Bahlo, M., Mar 1 2009, In : American Journal of Medical Genetics, Part A. 149, 3, p. 555-558 4 p.

Research output: Contribution to journalLetter

13 Scopus citations
2004

Increasing evidence for syndromic phenotypes associated with RPGR mutations [3] (multiple letters)

Iannaccone, A., Wang, X., Jablonski, M. M., Kuo, S. F., Baldi, A., Cosgrove, D., Morton, C. C., Swaroop, A. & Koenekoop, R. K., Apr 2004, In : American journal of ophthalmology. 137, 4, p. 785-786 2 p.

Research output: Contribution to journalLetter

21 Scopus citations
2003

Non-syndromic recessive auditory neuropathy is the result of mutations in the otoferlin (OTOF) gene [2]

Varga, R., Kelley, P. M., Keats, B. J., Starr, A., Leal, S. M., Cohn, E. & Kimberling, W. J., Jan 1 2003, In : Journal of medical genetics. 40, 1, p. 45-50 6 p.

Research output: Contribution to journalLetter

165 Scopus citations
2002

Distinctive audiometric features between USH2A and USH2B subtypes of Usher syndrome [2]

Hmani-Aifa, M., Ben Arab, S., Kharrat, K., Orten, D. J., Boulila-Elgaied, A., Drira, M., Hachicha, S., Kimberling, W. J. & Ayadi, H., May 21 2002, In : Journal of medical genetics. 39, 4, p. 281-283 3 p.

Research output: Contribution to journalLetter

13 Scopus citations
1999

Deafness linked to DFNA2: One locus but how many genes? [5]

Van Hauwe, P., Coucke, P. J., Declau, F., Kunst, H., Ensink, R. J., Marres, H. A., Cremers, C. W. R. J., Djelantik, B., Smith, S. D., Kelley, P., Van de Heyning, P. H. & Van Camp, G., Mar 22 1999, In : Nature Genetics. 21, 3, 1 p.

Research output: Contribution to journalLetter

32 Scopus citations

Genetic heterogeneity associated with branchio-oto-renal syndrome [1]

Kumar, S., Kimberling, W. J., Marres, H. A. M. & Cremers, C. W. R. J., Mar 19 1999, In : American journal of medical genetics. 83, 3, p. 207-208 2 p.

Research output: Contribution to journalLetter

7 Scopus citations
1995

Reading disability, attention-deficit hyperactivity disorder, and the immune system [5]

Warren, R. P., Odell, J. D., Warren, W. L., Burger, R. A., Maciulis, A., Daniels, W. W. & Torres, A. R., Jan 1 1995, In : Science. 268, 5212, p. 786-787 2 p.

Research output: Contribution to journalLetter

11 Scopus citations

Response [6]

Cardon, L. R., Smith, S. D., Fulker, D. W., Kimberling, W. J., Pennington, B. F. & DeFries, J. C., Jan 1 1995, In : Science. 268, 5212, p. 787-788 2 p.

Research output: Contribution to journalLetter

1989

Polycystic Kidney Disease

Cheng, T. O., Lavie, C. J., Klein, A. L., Seward, J. B., Tajik, A. J., Hossack, K. F., Schrier, R. W., Gabow, P. A., Carbonara, P. A., Restagno, G., Kimberling, W. J., Friedman, E. A. & Grantham, J. J., Mar 16 1989, In : New England Journal of Medicine. 320, 11, p. 737-739 3 p.

Research output: Contribution to journalLetter

1 Scopus citations
1988

Letter to the editor: Reassignment of a cancer family syndrome gene to chromosome 18

Boman, B. M., Lynch, H. T., Kimberling, W. J. & Wildrick, D. M., Aug 1988, In : Cancer genetics and cytogenetics. 34, 1, p. 153-154 2 p.

Research output: Contribution to journalLetter

18 Scopus citations
1983

Familial Atypical Multiple Mole Melanoma Syndrome (FAMMM)

Fusaro, R. M., Lynch, H. T. & Kimberling, W. J., Jan 1983, In : Archives of Dermatology. 119, 1, p. 2-3 2 p.

Research output: Contribution to journalLetter

5 Scopus citations
1978

HUMORAL IMMUNITY IN MYASTHENIA GRAVIS: RELATIONSHIP TO DISEASE SEVERITY AND STEROID TREATMENT

Bradley, R. J., Dwyer, D., Morley, B. J., Robinson, G., Kemp, G. E. & Oh, S. J., Jul 8 1978, In : The Lancet. 312, 8080, 1 p.

Research output: Contribution to journalLetter

18 Scopus citations
1977

DIAGNOSTIC RADIATION AND CHROMOSOME ABERRATIONS

Patil, S. R., Hecht, F., Lubs, H. A., Kimberling, W., Brown, J., Gerald, P. S. & Summitt, R. L., Jan 15 1977, In : The Lancet. 309, 8003, 1 p.

Research output: Contribution to journalLetter

2 Scopus citations

Effects of dietary choline on nicotinic acetylcholine receptors in brain [22]

Morley, B. J., Robinson, G. R., Brown, G. B., Kemp, G. E. & Bradley, R. J., Dec 1 1977, In : Nature. 266, 5605, p. 848-850 3 p.

Research output: Contribution to journalLetter

29 Scopus citations
1972

REGISTRY OF DATA ON ROBERTSONIAN (CENTRIC-FUSION) TRANSLOCATIONS

Hecht, F. & Kimberling, W. J., Jun 17 1972, In : The Lancet. 299, 7764, 1 p.

Research output: Contribution to journalLetter

3 Scopus citations
1971

TESTOSTERONE-BINDING PROTEIN PROBABLY NOT Y-LINKED

Hecht, F. & Kimberling, W., Jun 19 1971, In : The Lancet. 297, 7712, 1 p.

Research output: Contribution to journalLetter