| Year |
Citation |
Score |
| 2008 |
Cryns K, Shamir A, Van Acker N, Levi I, Daneels G, Goris I, Bouwknecht JA, Andries L, Kass S, Agam G, Belmaker H, Bersudsky Y, Steckler T, Moechars D. IMPA1 is essential for embryonic development and lithium-like pilocarpine sensitivity. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 33: 674-84. PMID 17460611 DOI: 10.1038/Sj.Npp.1301431 |
0.321 |
|
| 2007 |
Cryns K, Shamir A, Shapiro J, Daneels G, Goris I, Van Craenendonck H, Straetemans R, Belmaker RH, Agam G, Moechars D, Steckler T. Lack of lithium-like behavioral and molecular effects in IMPA2 knockout mice. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 32: 881-91. PMID 16841073 DOI: 10.1038/Sj.Npp.1301154 |
0.31 |
|
| 2005 |
Snoeckx RL, Huygen PL, Feldmann D, Marlin S, Denoyelle F, Waligora J, Mueller-Malesinska M, Pollak A, Ploski R, Murgia A, Orzan E, Castorina P, Ambrosetti U, Nowakowska-Szyrwinska E, Bal J, ... ... Cryns K, et al. GJB2 mutations and degree of hearing loss: a multicenter study. American Journal of Human Genetics. 77: 945-57. PMID 16380907 DOI: 10.1086/497996 |
0.459 |
|
| 2004 |
Cryns K, Orzan E, Murgia A, Huygen PL, Moreno F, del Castillo I, Chamberlin GP, Azaiez H, Prasad S, Cucci RA, Leonardi E, Snoeckx RL, Govaerts PJ, Van de Heyning PH, Van de Heyning CM, et al. A genotype-phenotype correlation for GJB2 (connexin 26) deafness. Journal of Medical Genetics. 41: 147-54. PMID 14985372 DOI: 10.1136/Jmg.2003.013896 |
0.447 |
|
| 2004 |
Cryns K, van Alphen AM, van Spaendonck MP, van de Heyning PH, Timmermans JP, de Zeeuw CI, van Camp G. Circling behavior in the Ecl mouse is caused by lateral semicircular canal defects. The Journal of Comparative Neurology. 468: 587-95. PMID 14689488 DOI: 10.1002/Cne.10975 |
0.53 |
|
| 2004 |
Pennings RJ, Huygen PL, van den Ouweland JM, Cryns K, Dikkeschei LD, Van Camp G, Cremers CW. Sex-related hearing impairment in Wolfram syndrome patients identified by inactivating WFS1 mutations. Audiology & Neuro-Otology. 9: 51-62. PMID 14676474 DOI: 10.1159/000074187 |
0.419 |
|
| 2004 |
Cryns K, Van Camp G. Deafness genes and their diagnostic applications. Audiology & Neuro-Otology. 9: 2-22. PMID 14676470 DOI: 10.1159/000074183 |
0.43 |
|
| 2003 |
Cryns K, Sivakumaran TA, Van den Ouweland JM, Pennings RJ, Cremers CW, Flothmann K, Young TL, Smith RJ, Lesperance MM, Van Camp G. Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease. Human Mutation. 22: 275-87. PMID 12955714 DOI: 10.1002/Humu.10258 |
0.441 |
|
| 2003 |
Van Laer L, Cryns K, Smith RJ, Van Camp G. Nonsyndromic hearing loss. Ear and Hearing. 24: 275-88. PMID 12923419 DOI: 10.1097/01.Aud.0000079805.04016.03 |
0.419 |
|
| 2003 |
van ven Ouweland JM, Cryns K, Pennings RJ, Walraven I, Janssen GM, Maassen JA, Veldhuijzen BF, Arntzenius AB, Lindhout D, Cremers CW, Van Camp G, Dikkeschei LD. Molecular characterization of WFS1 in patients with Wolfram syndrome. The Journal of Molecular Diagnostics : Jmd. 5: 88-95. PMID 12707373 DOI: 10.1016/S1525-1578(10)60457-6 |
0.407 |
|
| 2003 |
Pennings RJ, Bom SJ, Cryns K, Flothmann K, Huygen PL, Kremer H, Van Camp G, Cremers CW. Progression of low-frequency sensorineural hearing loss (DFNA6/14-WFS1). Archives of Otolaryngology--Head & Neck Surgery. 129: 421-6. PMID 12707188 DOI: 10.1001/Archotol.129.4.421 |
0.474 |
|
| 2003 |
Cryns K, Thys S, Van Laer L, Oka Y, Pfister M, Van Nassauw L, Smith RJ, Timmermans JP, Van Camp G. The WFS1 gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells. Histochemistry and Cell Biology. 119: 247-56. PMID 12649740 DOI: 10.1007/S00418-003-0495-6 |
0.558 |
|
| 2002 |
Bom SJ, Van Camp G, Cryns K, Admiraal RJ, Huygen PL, Cremers CW. Autosomal dominant low-frequency hearing impairment (DFNA6/14): a clinical and genetic family study. Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology. 23: 876-84. PMID 12438850 DOI: 10.1097/00129492-200211000-00012 |
0.381 |
|
| 2002 |
Cryns K, Pfister M, Pennings RJ, Bom SJ, Flothmann K, Caethoven G, Kremer H, Schatteman I, Köln KA, Tóth T, Kupka S, Blin N, Nürnberg P, Thiele H, van de Heyning PH, et al. Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations. Human Genetics. 110: 389-94. PMID 12073007 DOI: 10.1007/S00439-002-0719-1 |
0.482 |
|
| 2002 |
Cryns K, Van Spaendonck MP, Flothmann K, van Alphen AM, Van De Heyning PH, Timmermans JP, De Zeeuw CI, Van Camp G. Vestibular dysfunction in the epistatic circler mouse is caused by phenotypic interaction of one recessive gene and three modifier genes. Genome Research. 12: 613-7. PMID 11932245 DOI: 10.1101/Gr.218402 |
0.514 |
|
| 2001 |
Bespalova IN, Van Camp G, Bom SJ, Brown DJ, Cryns K, DeWan AT, Erson AE, Flothmann K, Kunst HP, Kurnool P, Sivakumaran TA, Cremers CW, Leal SM, Burmeister M, Lesperance MM. Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss. Human Molecular Genetics. 10: 2501-8. PMID 11709537 DOI: 10.1093/Hmg/10.22.2501 |
0.484 |
|
| 2000 |
Van Spaendonck MP, Cryns K, Van De Heyning PH, Scheuermann DW, Van Camp G, Timmermans JP. High resolution imaging of the mouse inner ear by microtomography: a new tool in inner ear research. The Anatomical Record. 259: 229-36. PMID 10820324 DOI: 10.1002/(Sici)1097-0185(20000601)259:2<229::Aid-Ar12>3.0.Co;2-L |
0.447 |
|
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