| Year |
Citation |
Score |
| 2024 |
Lahlou G, Calvet C, Simon F, Michel V, Alciato L, Plion B, Boutet de Monvel J, Lecomte MJ, Beraneck M, Petit C, Safieddine S. Extended timeframe for restoring inner ear function through gene therapy in Usher1G preclinical model. Jci Insight. PMID 38194286 DOI: 10.1172/jci.insight.169504 |
0.311 |
|
| 2023 |
Jean P, Wong Jun Tai F, Singh-Estivalet A, Lelli A, Scandola C, Megharba S, Schmutz S, Roux S, Mechaussier S, Sudres M, Mouly E, Heritier AV, Bonnet C, Mallet A, Novault S, ... ... Petit C, et al. Single-cell transcriptomic profiling of the mouse cochlea: An atlas for targeted therapies. Proceedings of the National Academy of Sciences of the United States of America. 120: e2221744120. PMID 37339214 DOI: 10.1073/pnas.2221744120 |
0.808 |
|
| 2022 |
Calvet C, Peineau T, Benamer N, Cornille M, Lelli A, Plion B, Lahlou G, Fanchette J, Nouaille S, Boutet de Monvel J, Estivalet A, Jean P, Michel V, Sachse M, Michalski N, ... ... Petit C, et al. The SNARE protein SNAP-25 is required for normal exocytosis at auditory hair cell ribbon synapses. Iscience. 25: 105628. PMID 36483015 DOI: 10.1016/j.isci.2022.105628 |
0.814 |
|
| 2022 |
Postal O, Bakay W, Dupont T, Buck A, Petit C, Michalski N, Gourévitch B. Characterizing subcutaneous cortical auditory evoked potentials in mice. Hearing Research. 422: 108566. PMID 35863162 DOI: 10.1016/j.heares.2022.108566 |
0.791 |
|
| 2022 |
AitRaise I, Amalou G, Bousfiha A, Charoute H, Rouba H, Abdelghaffar H, Bonnet C, Petit C, Barakat A. Genetic heterogeneity in GJB2, COL4A3, ATP6V1B1 and EDNRB variants detected among hearing impaired families in Morocco. Molecular Biology Reports. PMID 35301649 DOI: 10.1007/s11033-022-07245-z |
0.304 |
|
| 2021 |
Michalski N, Petit C. Central auditory deficits associated with genetic forms of peripheral deafness. Human Genetics. PMID 34435241 DOI: 10.1007/s00439-021-02339-3 |
0.811 |
|
| 2021 |
Elrharchi S, Riahi Z, Salime S, Charoute H, Elkhattabi L, Boulouiz R, Kabine M, Bonnet C, Petit C, Barakat A. Novel Mutation in AIFM1 Gene Associated with X-Linked Deafness in a Moroccan Family. Human Heredity. 1-5. PMID 33486474 DOI: 10.1159/000512712 |
0.333 |
|
| 2020 |
Boucher S, Wong Jun Tai F, Delmaghani S, Lelli A, Singh-Estivalet A, Dupont T, Niasme-Grare M, Michel V, Wolff N, Bahloul A, Bouyacoub Y, Bouccara D, Fraysse B, Deguine O, Collet L, ... ... Petit C, et al. Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis. Proceedings of the National Academy of Sciences of the United States of America. PMID 33229591 DOI: 10.1073/pnas.2010782117 |
0.802 |
|
| 2020 |
Postal O, Dupont T, Bakay W, Dominique N, Petit C, Michalski N, Gourévitch B. Spontaneous Mouse Behavior in Presence of Dissonance and Acoustic Roughness. Frontiers in Behavioral Neuroscience. 14: 588834. PMID 33132864 DOI: 10.3389/fnbeh.2020.588834 |
0.786 |
|
| 2020 |
Michel V, Pepermans E, Boutet de Monvel J, England P, Nouaille S, Aghaie A, Delhommel F, Wolff N, Perfettini I, Hardelin JP, Petit C, Bahloul A. Interaction of protocadherin-15 with the scaffold protein whirlin supports its anchoring of hair-bundle lateral links in cochlear hair cells. Scientific Reports. 10: 16430. PMID 33009420 DOI: 10.1038/s41598-020-73158-1 |
0.329 |
|
| 2020 |
Song JS, Bahloul A, Petit C, Kim SJ, Moon IJ, Lee J, Ki CS. A Novel Heterozygous Missense Variant (c.667G>T;p.Gly223Cys) in That Interferes With Cadherin-Related 23 and Harmonin Interaction Causes Autosomal Dominant Nonsyndromic Hearing Loss. Annals of Laboratory Medicine. 40: 224-231. PMID 31858762 DOI: 10.3343/Alm.2020.40.3.224 |
0.409 |
|
| 2019 |
Avan P, Le Gal S, Michel V, Dupont T, Hardelin JP, Petit C, Verpy E. Otogelin, otogelin-like, and stereocilin form links connecting outer hair cell stereocilia to each other and the tectorial membrane. Proceedings of the National Academy of Sciences of the United States of America. PMID 31776257 DOI: 10.1073/Pnas.1902781116 |
0.495 |
|
| 2019 |
Dahmani M, Talbi S, Ammar-Khodja F, Ouhab S, Boudjenah F, Djebbar M, Bonnet C, Petit C. ATP6V1B1 recurrent mutations in Algerian deaf patients associated with renal tubular acidosis. International Journal of Pediatric Otorhinolaryngology. 129: 109772. PMID 31733597 DOI: 10.1016/J.Ijporl.2019.109772 |
0.346 |
|
| 2019 |
Dunbar LA, Patni P, Aguilar C, Mburu P, Corns L, Wells HR, Delmaghani S, Parker A, Johnson S, Williams D, Esapa CT, Simon MM, Chessum L, Newton S, Dorning J, ... ... Petit C, et al. Clarin-2 is essential for hearing by maintaining stereocilia integrity and function. Embo Molecular Medicine. e10288. PMID 31448880 DOI: 10.15252/Emmm.201910288 |
0.394 |
|
| 2019 |
Sayeb M, Riahi Z, Laroussi N, Bonnet C, Romdhane L, Mkaouar R, Zaouak A, Marrakchi J, Abdessalem G, Messaoud O, Bouchniba O, Ghilane N, Mokni M, Besbes G, Yacoub-Youssef H, ... Petit C, et al. A Tunisian family with a novel mutation in the gene CYP4F22 for lamellar ichthyosis and co-occurrence of hearing loss in a child due to mutation in the SLC26A4 gene. International Journal of Dermatology. PMID 31020658 DOI: 10.1111/Ijd.14452 |
0.337 |
|
| 2019 |
Defourny J, Aghaie A, Perfettini I, Avan P, Delmaghani S, Petit C. Pejvakin-mediated pexophagy protects auditory hair cells against noise-induced damage. Proceedings of the National Academy of Sciences of the United States of America. PMID 30936319 DOI: 10.1073/Pnas.1821844116 |
0.447 |
|
| 2019 |
Michalski N, Petit C. Genes Involved in the Development and Physiology of Both the Peripheral and Central Auditory Systems. Annual Review of Neuroscience. PMID 30699050 DOI: 10.1146/Annurev-Neuro-070918-050428 |
0.797 |
|
| 2019 |
Richardson GP, Petit C. Hair-Bundle Links: Genetics as the Gateway to Function. Cold Spring Harbor Perspectives in Medicine. PMID 30617060 DOI: 10.1101/Cshperspect.A033142 |
0.468 |
|
| 2018 |
Corns LF, Johnson SL, Roberts T, Ranatunga KM, Hendry A, Ceriani F, Safieddine S, Steel KP, Forge A, Petit C, Furness DN, Kros CJ, Marcotti W. Mechanotransduction is required for establishing and maintaining mature inner hair cells and regulating efferent innervation. Nature Communications. 9: 4015. PMID 30275467 DOI: 10.1038/S41467-018-06307-W |
0.434 |
|
| 2018 |
Dulon D, Papal S, Patni P, Cortese M, Vincent PF, Tertrais M, Emptoz A, Tlili A, Bouleau Y, Michel V, Delmaghani S, Aghaie A, Pepermans E, Allegria-Prevot O, Akil O, ... ... Petit C, et al. Clarin-1 gene transfer rescues auditory synaptopathy in model of Usher syndrome. The Journal of Clinical Investigation. PMID 29985171 DOI: 10.1172/JCI94351 |
0.698 |
|
| 2018 |
Salime S, Riahi Z, Elrharchi S, Elkhattabi L, Charoute H, Nahili H, Rouba H, Kabine M, Bonnet C, Petit C, Barakat A. A novel mutation in SLITRK6 causes deafness and myopia in a Moroccan family. Gene. PMID 29551497 DOI: 10.1016/J.Gene.2018.03.042 |
0.384 |
|
| 2018 |
Trouillet A, Dubus E, Dégardin J, Estivalet A, Ivkovic I, Godefroy D, García-Ayuso D, Simonutti M, Sahly I, Sahel JA, El-Amraoui A, Petit C, Picaud S. Cone degeneration is triggered by the absence of USH1 proteins but prevented by antioxidant treatments. Scientific Reports. 8: 1968. PMID 29386551 DOI: 10.1038/S41598-018-20171-0 |
0.332 |
|
| 2017 |
Michalski N, Goutman JD, Auclair SM, Boutet de Monvel J, Tertrais M, Emptoz A, Parrin A, Nouaille S, Guillon M, Sachse M, Ciric D, Bahloul A, Hardelin JP, Sutton RB, Avan P, ... ... Petit C, et al. Otoferlin acts as a Ca sensor for vesicle fusion and vesicle pool replenishment at auditory hair cell ribbon synapses. Elife. 6. PMID 29111973 DOI: 10.7554/Elife.31013 |
0.775 |
|
| 2017 |
Michel V, Booth KT, Patni P, Cortese M, Azaiez H, Bahloul A, Kahrizi K, Labbé M, Emptoz A, Lelli A, Dégardin J, Dupont T, Aghaie A, Oficjalska-Pham D, Picaud S, ... ... Petit C, et al. CIB2, defective in isolated deafness, is key for auditory hair cell mechanotransduction and survival. Embo Molecular Medicine. PMID 29084757 DOI: 10.15252/Emmm.201708087 |
0.685 |
|
| 2017 |
Delhommel F, Cordier F, Bardiaux B, Bouvier G, Colcombet-Cazenave B, Brier S, Raynal B, Nouaille S, Bahloul A, Chamot-Rooke J, Nilges M, Petit C, Wolff N. Structural Characterization of Whirlin Reveals an Unexpected and Dynamic Supramodule Conformation of Its PDZ Tandem. Structure (London, England : 1993). PMID 28966015 DOI: 10.1016/J.Str.2017.08.013 |
0.352 |
|
| 2017 |
Emptoz A, Michel V, Lelli A, Akil O, Boutet de Monvel J, Lahlou G, Meyer A, Dupont T, Nouaille S, Ey E, Franca de Barros F, Beraneck M, Dulon D, Hardelin JP, Lustig L, ... ... Petit C, et al. Local gene therapy durably restores vestibular function in a mouse model of Usher syndrome type 1G. Proceedings of the National Academy of Sciences of the United States of America. PMID 28835534 DOI: 10.1073/pnas.1708894114 |
0.359 |
|
| 2017 |
Libé-Philippot B, Michel V, Boutet de Monvel J, Le Gal S, Dupont T, Avan P, Métin C, Michalski N, Petit C. Auditory cortex interneuron development requires cadherins operating hair-cell mechanoelectrical transduction. Proceedings of the National Academy of Sciences of the United States of America. PMID 28705869 DOI: 10.1073/Pnas.1703408114 |
0.772 |
|
| 2017 |
Bahloul A, Pepermans E, Raynal B, Wolff N, Cordier F, England P, Nouaille S, Baron B, El-Amraoui A, Hardelin JP, Durand D, Petit C. Conformational switch of harmonin, a submembrane scaffold protein of the hair cell mechanoelectrical transduction machinery. Febs Letters. PMID 28653419 DOI: 10.1002/1873-3468.12729 |
0.397 |
|
| 2017 |
Schietroma C, Parain K, Estivalet A, Aghaie A, Boutet de Monvel J, Picaud S, Sahel JA, Perron M, El-Amraoui A, Petit C. Usher syndrome type 1-associated cadherins shape the photoreceptor outer segment. The Journal of Cell Biology. PMID 28495838 DOI: 10.1083/Jcb.201612030 |
0.372 |
|
| 2017 |
Bousfiha A, Bakhchane A, Charoute H, Riahi Z, Snoussi K, Rouba H, Bonnet C, Petit C, Barakat A. A novel PEX1 mutation in a Moroccan family with Zellweger spectrum disorders. Human Genome Variation. 4: 17009. PMID 28446956 DOI: 10.1038/Hgv.2017.9 |
0.328 |
|
| 2017 |
Cortese M, Papal S, Pisciottano F, Elgoyhen AB, Hardelin JP, Petit C, Franchini LF, El-Amraoui A. Spectrin βV adaptive mutations and changes in subcellular location correlate with emergence of hair cell electromotility in mammalians. Proceedings of the National Academy of Sciences of the United States of America. PMID 28179572 DOI: 10.1073/Pnas.1618778114 |
0.691 |
|
| 2017 |
Michalski N, Goutman JD, Auclair SM, Monvel JBd, Tertrais M, Emptoz A, Parrin A, Nouaille S, Guillon M, Sachse M, Ciric D, Bahloul A, Hardelin J, Sutton RB, Avan P, ... ... Petit C, et al. Author response: Otoferlin acts as a Ca2+ sensor for vesicle fusion and vesicle pool replenishment at auditory hair cell ribbon synapses Elife. DOI: 10.7554/Elife.31013.024 |
0.343 |
|
| 2016 |
Testa F, Melillo P, Bonnet C, Marcelli V, de Benedictis A, Colucci R, Gallo B, Kurtenbach A, Rossi S, Marciano E, Auricchio A, Petit C, Zrenner E, Simonelli F. CLINICAL PRESENTATION AND DISEASE COURSE OF USHER SYNDROME BECAUSE OF MUTATIONS IN MYO7A OR USH2A. Retina (Philadelphia, Pa.). PMID 27828912 DOI: 10.1097/Iae.0000000000001389 |
0.319 |
|
| 2016 |
Abdi S, Bahloul A, Behlouli A, Hardelin JP, Makrelouf M, Boudjelida K, Louha M, Cheknene A, Belouni R, Rous Y, Merad Z, Selmane D, Hasbelaoui M, Bonnet C, Zenati A, ... Petit C, et al. Diversity of the Genes Implicated in Algerian Patients Affected by Usher Syndrome. Plos One. 11: e0161893. PMID 27583663 DOI: 10.1371/Journal.Pone.0161893 |
0.344 |
|
| 2016 |
Bonnet C, Riahi Z, Chantot-Bastaraud S, Smagghe L, Letexier M, Marcaillou C, Lefèvre GM, Hardelin JP, El-Amraoui A, Singh-Estivalet A, Mohand-Saïd S, Kohl S, Kurtenbach A, Sliesoraityte I, Zobor D, ... ... Petit C, et al. An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients. European Journal of Human Genetics : Ejhg. PMID 27460420 DOI: 10.1038/Ejhg.2016.99 |
0.35 |
|
| 2016 |
Delmaghani S, Aghaie A, Bouyacoub Y, El Hachmi H, Bonnet C, Riahi Z, Chardenoux S, Perfettini I, Hardelin JP, Houmeida A, Herbomel P, Petit C. Mutations in CDC14A, Encoding a Protein Phosphatase Involved in Hair Cell Ciliogenesis, Cause Autosomal-Recessive Severe to Profound Deafness. American Journal of Human Genetics. 98: 1266-70. PMID 27259055 DOI: 10.1016/J.Ajhg.2016.04.015 |
0.448 |
|
| 2016 |
Lelli A, Michel V, Boutet de Monvel J, Cortese M, Bosch-Grau M, Aghaie A, Perfettini I, Dupont T, Avan P, El-Amraoui A, Petit C. Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth. The Journal of Cell Biology. 212: 231-44. PMID 26754646 DOI: 10.1085/Jgp.1472Oia7 |
0.674 |
|
| 2016 |
Lelli A, Michel V, De Monvel JB, Cortese M, Bosch-Grau M, Aghaie A, Perfettini I, Dupont T, Avan P, El-Amraoui A, Petit C. Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth Journal of Cell Biology. 212: 231-244. DOI: 10.1083/jcb.201509017 |
0.594 |
|
| 2016 |
Delhommel F, Cordier F, Raynal B, El Bahloul-Jaziri A, Petit C, Delepierre M, Wolff N. Structural Study of Whirlin, A Crucial PDZ Containing Protein Involved in the Mechanotransduction of Auditory Hair Cells Biophysical Journal. 110: 319a. DOI: 10.1016/J.Bpj.2015.11.1713 |
0.355 |
|
| 2015 |
Vincent PF, Bouleau Y, Petit C, Dulon D. Synaptic F-actin network controls otoferlin-dependent exocytosis in auditory inner hair cells. Elife. 4. PMID 26568308 DOI: 10.7554/Elife.10988 |
0.326 |
|
| 2015 |
Delmaghani S, Defourny J, Aghaie A, Beurg M, Dulon D, Thelen N, Perfettini I, Zelles T, Aller M, Meyer A, Emptoz A, Giraudet F, Leibovici M, Dartevelle S, Soubigou G, ... ... Petit C, et al. Hypervulnerability to Sound Exposure through Impaired Adaptive Proliferation of Peroxisomes. Cell. 163: 894-906. PMID 26544938 DOI: 10.1016/J.Cell.2015.10.023 |
0.447 |
|
| 2015 |
Dahmani M, Ammar-Khodja F, Bonnet C, Lefèvre GM, Hardelin JP, Ibrahim H, Mallek Z, Petit C. EPS8L2 is a new causal gene for childhood onset autosomal recessive progressive hearing loss. Orphanet Journal of Rare Diseases. 10: 96. PMID 26282398 DOI: 10.1186/S13023-015-0316-8 |
0.408 |
|
| 2015 |
Pepermans E, Petit C. The tip-link molecular complex of the auditory mechano-electrical transduction machinery. Hearing Research. PMID 26049141 DOI: 10.1016/J.Heares.2015.05.005 |
0.416 |
|
| 2015 |
Ammar-Khodja F, Bonnet C, Dahmani M, Ouhab S, Lefèvre GM, Ibrahim H, Hardelin JP, Weil D, Louha M, Petit C. Diversity of the causal genes in hearing impaired Algerian individuals identified by whole exome sequencing. Molecular Genetics & Genomic Medicine. 3: 189-96. PMID 26029705 DOI: 10.1002/Mgg3.131 |
0.302 |
|
| 2015 |
Michalski N, Petit C. Genetics of auditory mechano-electrical transduction. PflüGers Archiv : European Journal of Physiology. 467: 49-72. PMID 24957570 DOI: 10.1007/S00424-014-1552-9 |
0.807 |
|
| 2015 |
Vincent PF, Bouleau Y, Petit C, Dulon D. Author response: A synaptic F-actin network controls otoferlin-dependent exocytosis in auditory inner hair cells Elife. DOI: 10.7554/Elife.10988.008 |
0.353 |
|
| 2014 |
Pepermans E, Michel V, Goodyear R, Bonnet C, Abdi S, Dupont T, Gherbi S, Holder M, Makrelouf M, Hardelin JP, Marlin S, Zenati A, Richardson G, Avan P, Bahloul A, ... Petit C, et al. The CD2 isoform of protocadherin-15 is an essential component of the tip-link complex in mature auditory hair cells. Embo Molecular Medicine. 6: 984-92. PMID 24940003 DOI: 10.15252/Emmm.201403976 |
0.407 |
|
| 2014 |
Riahi Z, Bonnet C, Zainine R, Louha M, Bouyacoub Y, Laroussi N, Chargui M, Kefi R, Jonard L, Dorboz I, Hardelin JP, Salah SB, Levilliers J, Weil D, McElreavey K, ... ... Petit C, et al. Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness. Plos One. 9: e99797. PMID 24926664 DOI: 10.1371/Journal.Pone.0099797 |
0.307 |
|
| 2014 |
Kamiya K, Michel V, Giraudet F, Riederer B, Foucher I, Papal S, Perfettini I, Le Gal S, Verpy E, Xia W, Seidler U, Georgescu MM, Avan P, El-Amraoui A, Petit C. An unusually powerful mode of low-frequency sound interference due to defective hair bundles of the auditory outer hair cells. Proceedings of the National Academy of Sciences of the United States of America. 111: 9307-12. PMID 24920589 DOI: 10.1073/Pnas.1405322111 |
0.401 |
|
| 2014 |
Behlouli A, Bonnet C, Abdi S, Bouaita A, Lelli A, Hardelin JP, Schietroma C, Rous Y, Louha M, Cheknane A, Lebdi H, Boudjelida K, Makrelouf M, Zenati A, Petit C. EPS8, encoding an actin-binding protein of cochlear hair cell stereocilia, is a new causal gene for autosomal recessive profound deafness. Orphanet Journal of Rare Diseases. 9: 55. PMID 24741995 DOI: 10.1186/1750-1172-9-55 |
0.43 |
|
| 2014 |
El-Amraoui A, Petit C. The retinal phenotype of Usher syndrome: pathophysiological insights from animal models. Comptes Rendus Biologies. 337: 167-77. PMID 24702843 DOI: 10.1016/J.Crvi.2013.12.004 |
0.43 |
|
| 2014 |
El-Amraoui A, Kamiya K, Michel V, Giraudet F, Gerogescu M, Avan P, Petit C. A novel mode of off-frequency hearing as a result of defective outer hair cells hair bundles unveiled by Nherf1-/- mice Journal of the Acoustical Society of America. 135: 2188-2188. DOI: 10.1121/1.4877127 |
0.417 |
|
| 2013 |
Meyer A, Petit C, Safieddine S. [Gene therapy for human hearing loss: challenges and promises]. MéDecine Sciences : M/S. 29: 883-9. PMID 24148127 DOI: 10.1051/Medsci/20132910016 |
0.399 |
|
| 2013 |
Avan P, Büki B, Petit C. Auditory distortions: origins and functions. Physiological Reviews. 93: 1563-619. PMID 24137017 DOI: 10.1152/Physrev.00029.2012 |
0.4 |
|
| 2013 |
Zhao Y, Zhao F, Zong L, Zhang P, Guan L, Zhang J, Wang D, Wang J, Chai W, Lan L, Li Q, Han B, Yang L, Jin X, Yang W, ... ... Petit C, et al. Exome sequencing and linkage analysis identified tenascin-C (TNC) as a novel causative gene in nonsyndromic hearing loss. Plos One. 8: e69549. PMID 23936043 DOI: 10.1371/Journal.Pone.0069549 |
0.309 |
|
| 2013 |
Bonnet C, Louha M, Loundon N, Michalski N, Verpy E, Smagghe L, Hardelin JP, Rouillon I, Jonard L, Couderc R, Gherbi S, Garabedian EN, Denoyelle F, Petit C, Marlin S. Biallelic nonsense mutations in the otogelin-like gene (OTOGL) in a child affected by mild to moderate hearing impairment. Gene. 527: 537-40. PMID 23850727 DOI: 10.1016/J.Gene.2013.06.044 |
0.786 |
|
| 2013 |
Lepelletier L, de Monvel JB, Buisson J, Desdouets C, Petit C. Auditory hair cell centrioles undergo confined Brownian motion throughout the developmental migration of the kinocilium. Biophysical Journal. 105: 48-58. PMID 23823223 DOI: 10.1016/J.Bpj.2013.05.009 |
0.393 |
|
| 2013 |
Papal S, Cortese M, Legendre K, Sorusch N, Dragavon J, Sahly I, Shorte S, Wolfrum U, Petit C, El-Amraoui A. The giant spectrin βV couples the molecular motors to phototransduction and Usher syndrome type I proteins along their trafficking route. Human Molecular Genetics. 22: 3773-88. PMID 23704327 DOI: 10.1093/Hmg/Ddt228 |
0.652 |
|
| 2013 |
El-Amraoui A, Petit C. Cadherin defects in inherited human diseases. Progress in Molecular Biology and Translational Science. 116: 361-84. PMID 23481203 DOI: 10.1016/B978-0-12-394311-8.00016-9 |
0.347 |
|
| 2013 |
Boulay AC, del Castillo FJ, Giraudet F, Hamard G, Giaume C, Petit C, Avan P, Cohen-Salmon M. Hearing is normal without connexin30. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 430-4. PMID 23303923 DOI: 10.1523/Jneurosci.4240-12.2013 |
0.651 |
|
| 2013 |
Meyer A, Danos O, Akil O, Petit C, Safieddine S. In Vivo Gene Transfer into Neonatal Mice Cochlea Using Adeno- Associated Viral Vectors Otolaryngology–Head and Neck Surgery. 149: P102-P102. DOI: 10.1177/0194599813495815A205 |
0.434 |
|
| 2012 |
Lukashkin AN, Legan PK, Weddell TD, Lukashkina VA, Goodyear RJ, Welstead LJ, Petit C, Russell IJ, Richardson GP. A mouse model for human deafness DFNB22 reveals that hearing impairment is due to a loss of inner hair cell stimulation. Proceedings of the National Academy of Sciences of the United States of America. 109: 19351-6. PMID 23129639 DOI: 10.1073/pnas.1210159109 |
0.383 |
|
| 2012 |
Sahly I, Dufour E, Schietroma C, Michel V, Bahloul A, Perfettini I, Pepermans E, Estivalet A, Carette D, Aghaie A, Ebermann I, Lelli A, Iribarne M, Hardelin JP, Weil D, ... ... Petit C, et al. Localization of Usher 1 proteins to the photoreceptor calyceal processes, which are absent from mice. The Journal of Cell Biology. 199: 381-99. PMID 23045546 DOI: 10.1083/Jcb.201202012 |
0.356 |
|
| 2012 |
Safieddine S, El-Amraoui A, Petit C. The auditory hair cell ribbon synapse: from assembly to function. Annual Review of Neuroscience. 35: 509-28. PMID 22715884 DOI: 10.1146/Annurev-Neuro-061010-113705 |
0.434 |
|
| 2012 |
Delmaghani S, Aghaie A, Michalski N, Bonnet C, Weil D, Petit C. Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness. Human Molecular Genetics. 21: 3835-44. PMID 22678063 DOI: 10.1093/Hmg/Dds212 |
0.817 |
|
| 2011 |
Caberlotto E, Michel V, de Monvel JB, Petit C. Coupling of the mechanotransduction machinery and F-actin polymerization in the cochlear hair bundles. Bioarchitecture. 1: 169-174. PMID 22069509 DOI: 10.4161/bioa.1.4.17532 |
0.322 |
|
| 2011 |
Bonnet C, Grati M, Marlin S, Levilliers J, Hardelin JP, Parodi M, Niasme-Grare M, Zelenika D, Délépine M, Feldmann D, Jonard L, El-Amraoui A, Weil D, Delobel B, Vincent C, ... ... Petit C, et al. Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis. Orphanet Journal of Rare Diseases. 6: 21. PMID 21569298 DOI: 10.1186/1750-1172-6-21 |
0.313 |
|
| 2011 |
Reisinger E, Bresee C, Neef J, Nair R, Reuter K, Bulankina A, Nouvian R, Koch M, Bückers J, Kastrup L, Roux I, Petit C, Hell SW, Brose N, Rhee JS, et al. Probing the functional equivalence of otoferlin and synaptotagmin 1 in exocytosis. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 31: 4886-95. PMID 21451027 DOI: 10.1523/Jneurosci.5122-10.2011 |
0.373 |
|
| 2011 |
Caberlotto E, Michel V, Foucher I, Bahloul A, Goodyear RJ, Pepermans E, Michalski N, Perfettini I, Alegria-Prévot O, Chardenoux S, Do Cruzeiro M, Hardelin JP, Richardson GP, Avan P, Weil D, ... Petit C, et al. Usher type 1G protein sans is a critical component of the tip-link complex, a structure controlling actin polymerization in stereocilia. Proceedings of the National Academy of Sciences of the United States of America. 108: 5825-30. PMID 21436032 DOI: 10.1073/Pnas.1017114108 |
0.816 |
|
| 2011 |
Verpy E, Leibovici M, Michalski N, Goodyear RJ, Houdon C, Weil D, Richardson GP, Petit C. Stereocilin connects outer hair cell stereocilia to one another and to the tectorial membrane. The Journal of Comparative Neurology. 519: 194-210. PMID 21165971 DOI: 10.1002/Cne.22509 |
0.805 |
|
| 2011 |
Richardson GP, de Monvel JB, Petit C. How the genetics of deafness illuminates auditory physiology. Annual Review of Physiology. 73: 311-34. PMID 21073336 DOI: 10.1146/Annurev-Physiol-012110-142228 |
0.499 |
|
| 2010 |
El-Amraoui A, Petit C. [Stem cell therapy in the inner ear: recent achievements and prospects]. MéDecine Sciences : M/S. 26: 981-5. PMID 21106181 DOI: 10.1051/Medsci/20102611981 |
0.396 |
|
| 2010 |
Beurg M, Michalski N, Safieddine S, Bouleau Y, Schneggenburger R, Chapman ER, Petit C, Dulon D. Control of exocytosis by synaptotagmins and otoferlin in auditory hair cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 30: 13281-90. PMID 20926654 DOI: 10.1523/Jneurosci.2528-10.2010 |
0.789 |
|
| 2010 |
Bahloul A, Michel V, Hardelin JP, Nouaille S, Hoos S, Houdusse A, England P, Petit C. Cadherin-23, myosin VIIa and harmonin, encoded by Usher syndrome type I genes, form a ternary complex and interact with membrane phospholipids. Human Molecular Genetics. 19: 3557-65. PMID 20639393 DOI: 10.1093/Hmg/Ddq271 |
0.462 |
|
| 2010 |
Boutet de Monvel J, Petit C. Wrapping up stereocilia rootlets. Cell. 141: 748-50. PMID 20510920 DOI: 10.1016/J.Cell.2010.05.022 |
0.387 |
|
| 2010 |
Wang DY, Wang YC, Weil D, Zhao YL, Rao SQ, Zong L, Ji YB, Liu Q, Li JQ, Yang HM, Shen Y, Benedict-Alderfer C, Zheng QY, Petit C, Wang QJ. Screening mutations of OTOF gene in Chinese patients with auditory neuropathy, including a familial case of temperature-sensitive auditory neuropathy. Bmc Medical Genetics. 11: 79. PMID 20504331 DOI: 10.1186/1471-2350-11-79 |
0.396 |
|
| 2010 |
Etournay R, Lepelletier L, Boutet de Monvel J, Michel V, Cayet N, Leibovici M, Weil D, Foucher I, Hardelin JP, Petit C. Cochlear outer hair cells undergo an apical circumference remodeling constrained by the hair bundle shape. Development (Cambridge, England). 137: 1373-83. PMID 20332152 DOI: 10.1242/Dev.045138 |
0.453 |
|
| 2010 |
Marlin S, Feldmann D, Nguyen Y, Rouillon I, Loundon N, Jonard L, Bonnet C, Couderc R, Garabedian EN, Petit C, Denoyelle F. Temperature-sensitive auditory neuropathy associated with an otoferlin mutation: Deafening fever! Biochemical and Biophysical Research Communications. 394: 737-42. PMID 20230791 DOI: 10.1016/j.bbrc.2010.03.062 |
0.322 |
|
| 2010 |
El-Amraoui A, Petit C. Cadherins as targets for genetic diseases. Cold Spring Harbor Perspectives in Biology. 2: a003095. PMID 20182609 DOI: 10.1101/Cshperspect.A003095 |
0.402 |
|
| 2010 |
del Castillo FJ, Cohen-Salmon M, Charollais A, Caille D, Lampe PD, Chavrier P, Meda P, Petit C. Consortin, a trans-Golgi network cargo receptor for the plasma membrane targeting and recycling of connexins. Human Molecular Genetics. 19: 262-75. PMID 19864490 DOI: 10.1093/Hmg/Ddp490 |
0.35 |
|
| 2010 |
Ashmore JF, Culley S, Boutet de Monvel J, Petit C, Safieddine S. Two Photon Imaging of Calcium Signalling at the Mouse Inner Hair Cell Ribbon Synapse Biophysical Journal. 98: 508a. DOI: 10.1016/J.Bpj.2009.12.2767 |
0.339 |
|
| 2009 |
Bahloul A, Simmler MC, Michel V, Leibovici M, Perfettini I, Roux I, Weil D, Nouaille S, Zuo J, Zadro C, Licastro D, Gasparini P, Avan P, Hardelin JP, Petit C. Vezatin, an integral membrane protein of adherens junctions, is required for the sound resilience of cochlear hair cells. Embo Molecular Medicine. 1: 125-38. PMID 20049712 DOI: 10.1002/Emmm.200900015 |
0.503 |
|
| 2009 |
Michalski N, Michel V, Caberlotto E, Lefèvre GM, van Aken AF, Tinevez JY, Bizard E, Houbron C, Weil D, Hardelin JP, Richardson GP, Kros CJ, Martin P, Petit C. Harmonin-b, an actin-binding scaffold protein, is involved in the adaptation of mechanoelectrical transduction by sensory hair cells. PflüGers Archiv : European Journal of Physiology. 459: 115-30. PMID 19756723 DOI: 10.1007/S00424-009-0711-X |
0.8 |
|
| 2009 |
Roux I, Hosie S, Johnson SL, Bahloul A, Cayet N, Nouaille S, Kros CJ, Petit C, Safieddine S. Myosin VI is required for the proper maturation and function of inner hair cell ribbon synapses. Human Molecular Genetics. 18: 4615-28. PMID 19744958 DOI: 10.1093/Hmg/Ddp429 |
0.417 |
|
| 2009 |
Dulon D, Safieddine S, Jones SM, Petit C. Otoferlin is critical for a highly sensitive and linear calcium-dependent exocytosis at vestibular hair cell ribbon synapses. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 29: 10474-87. PMID 19710301 DOI: 10.1523/Jneurosci.1009-09.2009 |
0.359 |
|
| 2009 |
Petit C, Richardson GP. Linking genes underlying deafness to hair-bundle development and function. Nature Neuroscience. 12: 703-10. PMID 19471269 DOI: 10.1038/nn.2330 |
0.377 |
|
| 2009 |
Legendre K, Petit C, El-Amraoui A. [The outer hair cell of the mammalian cochlea: an outstanding amplifier]. MéDecine Sciences : M/S. 25: 117-20. PMID 19239835 DOI: 10.1051/Medsci/2009252117 |
0.403 |
|
| 2009 |
Lagresle-Peyrou C, Six EM, Picard C, Rieux-Laucat F, Michel V, Ditadi A, Demerens-de Chappedelaine C, Morillon E, Valensi F, Simon-Stoos KL, Mullikin JC, Noroski LM, Besse C, Wulffraat NM, Ferster A, ... ... Petit C, et al. Human adenylate kinase 2 deficiency causes a profound hematopoietic defect associated with sensorineural deafness. Nature Genetics. 41: 106-11. PMID 19043416 DOI: 10.1038/ng.278 |
0.397 |
|
| 2008 |
Leibovici M, Safieddine S, Petit C. Mouse models for human hereditary deafness. Current Topics in Developmental Biology. 84: 385-429. PMID 19186249 DOI: 10.1016/S0070-2153(08)00608-X |
0.489 |
|
| 2008 |
Wei D, Levic S, Nie L, Gao WQ, Petit C, Jones EG, Yamoah EN. Cells of adult brain germinal zone have properties akin to hair cells and can be used to replace inner ear sensory cells after damage. Proceedings of the National Academy of Sciences of the United States of America. 105: 21000-5. PMID 19064919 DOI: 10.1073/Pnas.0808044105 |
0.409 |
|
| 2008 |
Verpy E, Weil D, Leibovici M, Goodyear RJ, Hamard G, Houdon C, Lefèvre GM, Hardelin JP, Richardson GP, Avan P, Petit C. Stereocilin-deficient mice reveal the origin of cochlear waveform distortions. Nature. 456: 255-8. PMID 18849963 DOI: 10.1038/nature07380 |
0.364 |
|
| 2008 |
Hilgert N, Alasti F, Dieltjens N, Pawlik B, Wollnik B, Uyguner O, Delmaghani S, Weil D, Petit C, Danis E, Yang T, Pandelia E, Petersen MB, Goossens D, Favero JD, et al. Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11. Clinical Genetics. 74: 223-32. PMID 18616530 DOI: 10.1111/J.1399-0004.2008.01053.X |
0.397 |
|
| 2008 |
Yanicostas C, Ernest S, Dayraud C, Petit C, Soussi-Yanicostas N. Essential requirement for zebrafish anosmin-1a in the migration of the posterior lateral line primordium. Developmental Biology. 320: 469-79. PMID 18585376 DOI: 10.1016/J.Ydbio.2008.06.008 |
0.338 |
|
| 2008 |
Lefèvre G, Michel V, Weil D, Lepelletier L, Bizard E, Wolfrum U, Hardelin JP, Petit C. A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth. Development (Cambridge, England). 135: 1427-37. PMID 18339676 DOI: 10.1242/Dev.012922 |
0.494 |
|
| 2008 |
Beurg M, Safieddine S, Roux I, Bouleau Y, Petit C, Dulon D. Calcium- and otoferlin-dependent exocytosis by immature outer hair cells. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 28: 1798-803. PMID 18287496 DOI: 10.1523/Jneurosci.4653-07.2008 |
0.309 |
|
| 2007 |
Etournay R, Zwaenepoel I, Perfettini I, Legrain P, Petit C, El-Amraoui A. Shroom2, a myosin-VIIa- and actin-binding protein, directly interacts with ZO-1 at tight junctions. Journal of Cell Science. 120: 2838-50. PMID 17666436 DOI: 10.1242/Jcs.002568 |
0.422 |
|
| 2007 |
Lévêque M, Marlin S, Jonard L, Procaccio V, Reynier P, Amati-Bonneau P, Baulande S, Pierron D, Lacombe D, Duriez F, Francannet C, Mom T, Journel H, Catros H, Drouin-Garraud V, ... ... Petit C, et al. Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip. European Journal of Human Genetics : Ejhg. 15: 1145-55. PMID 17637808 DOI: 10.1038/Sj.Ejhg.5201891 |
0.301 |
|
| 2007 |
Michalski N, Michel V, Bahloul A, Lefèvre G, Barral J, Yagi H, Chardenoux S, Weil D, Martin P, Hardelin JP, Sato M, Petit C. Molecular characterization of the ankle-link complex in cochlear hair cells and its role in the hair bundle functioning. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 6478-88. PMID 17567809 DOI: 10.1523/Jneurosci.0342-07.2007 |
0.816 |
|
| 2007 |
Cohen-Salmon M, Regnault B, Cayet N, Caille D, Demuth K, Hardelin JP, Janel N, Meda P, Petit C. Connexin30 deficiency causes instrastrial fluid-blood barrier disruption within the cochlear stria vascularis. Proceedings of the National Academy of Sciences of the United States of America. 104: 6229-34. PMID 17400755 DOI: 10.1073/Pnas.0605108104 |
0.419 |
|
| 2007 |
Hoskins BE, Cramer CH, Silvius D, Zou D, Raymond RM, Orten DJ, Kimberling WJ, Smith RJ, Weil D, Petit C, Otto EA, Xu PX, Hildebrandt F. Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome. American Journal of Human Genetics. 80: 800-4. PMID 17357085 DOI: 10.1086/513322 |
0.338 |
|
| 2006 |
Delmaghani S, del Castillo FJ, Michel V, Leibovici M, Aghaie A, Ron U, Van Laer L, Ben-Tal N, Van Camp G, Weil D, Langa F, Lathrop M, Avan P, Petit C. Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy. Nature Genetics. 38: 770-8. PMID 16804542 DOI: 10.1038/Ng1829 |
0.492 |
|
| 2006 |
Albert S, Blons H, Jonard L, Feldmann D, Chauvin P, Loundon N, Sergent-Allaoui A, Houang M, Joannard A, Schmerber S, Delobel B, Leman J, Journel H, Catros H, Dollfus H, ... ... Petit C, et al. SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations. European Journal of Human Genetics : Ejhg. 14: 773-9. PMID 16570074 DOI: 10.1038/Sj.Ejhg.5201611 |
0.381 |
|
| 2006 |
Petit C. From deafness genes to hearing mechanisms: harmony and counterpoint. Trends in Molecular Medicine. 12: 57-64. PMID 16406841 DOI: 10.1016/J.Molmed.2005.12.006 |
0.406 |
|
| 2006 |
Rouillon I, Marcolla A, Roux I, Marlin S, Feldmann D, Couderc R, Jonard L, Petit C, Denoyelle F, Garabédian EN, Loundon N. Results of cochlear implantation in two children with mutations in the OTOF gene. International Journal of Pediatric Otorhinolaryngology. 70: 689-696. PMID 16226319 DOI: 10.1016/J.Ijporl.2005.09.006 |
0.395 |
|
| 2006 |
Roux I, Safieddine S, Guillaumie K, Nouvian R, Grati M, Rostaing P, Hardelin J, Triller A, Moser T, Darchen F, Petit C. Otoferlin, defective in DFNB9 human deafness, is a synaptic protein of sensory hair cells involved in exocytosis Journal of Physiology-Paris. 99: 2-3. DOI: 10.1016/J.Jphysparis.2005.12.068 |
0.408 |
|
| 2005 |
Adato A, Lefèvre G, Delprat B, Michel V, Michalski N, Chardenoux S, Weil D, El-Amraoui A, Petit C. Usherin, the defective protein in Usher syndrome type IIA, is likely to be a component of interstereocilia ankle links in the inner ear sensory cells. Human Molecular Genetics. 14: 3921-32. PMID 16301217 DOI: 10.1093/hmg/ddi416 |
0.824 |
|
| 2005 |
El-Amraoui A, Petit C. Usher I syndrome: unravelling the mechanisms that underlie the cohesion of the growing hair bundle in inner ear sensory cells. Journal of Cell Science. 118: 4593-603. PMID 16219682 DOI: 10.1242/Jcs.02636 |
0.509 |
|
| 2005 |
Hyenne V, Louvet-Vallée S, El-Amraoui A, Petit C, Maro B, Simmler MC. Vezatin, a protein associated to adherens junctions, is required for mouse blastocyst morphogenesis. Developmental Biology. 287: 180-91. PMID 16199027 DOI: 10.1016/J.Ydbio.2005.09.004 |
0.371 |
|
| 2005 |
El-Amraoui A, Lefèvre G, Hardelin JP, Petit C. [Usher syndrome type I and the differentiation of inner ear sensory cells' hair bundles]. MéDecine Sciences : M/S. 21: 737-40. PMID 16115459 DOI: 10.1051/Medsci/2005218-9737 |
0.505 |
|
| 2005 |
Feldmann D, Denoyelle F, Blons H, Lyonnet S, Loundon N, Rouillon I, Hadj-Rabia S, Petit C, Couderc R, Garabédian EN, Marlin S. The GJB2 mutation R75Q can cause nonsyndromic hearing loss DFNA3 or hereditary palmoplantar keratoderma with deafness. American Journal of Medical Genetics. Part A. 137: 225-7. PMID 16059934 DOI: 10.1002/Ajmg.A.30765 |
0.366 |
|
| 2005 |
del Castillo FJ, RodrÃguez-Ballesteros M, Alvarez A, Hutchin T, Leonardi E, de Oliveira CA, Azaiez H, Brownstein Z, Avenarius MR, Marlin S, Pandya A, Shahin H, Siemering KR, Weil D, Wuyts W, ... ... Petit C, et al. A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment. Journal of Medical Genetics. 42: 588-94. PMID 15994881 DOI: 10.1136/Jmg.2004.028324 |
0.327 |
|
| 2005 |
Etournay R, El-Amraoui A, Bahloul A, Blanchard S, Roux I, Pézeron G, Michalski N, Daviet L, Hardelin JP, Legrain P, Petit C. PHR1, an integral membrane protein of the inner ear sensory cells, directly interacts with myosin 1c and myosin VIIa. Journal of Cell Science. 118: 2891-9. PMID 15976448 DOI: 10.1242/Jcs.02424 |
0.795 |
|
| 2005 |
Marlin S, Feldmann D, Blons H, Loundon N, Rouillon I, Albert S, Chauvin P, Garabédian EN, Couderc R, Odent S, Joannard A, Schmerber S, Delobel B, Leman J, Journel H, ... ... Petit C, et al. GJB2 and GJB6 mutations: genotypic and phenotypic correlations in a large cohort of hearing-impaired patients. Archives of Otolaryngology--Head & Neck Surgery. 131: 481-7. PMID 15967879 DOI: 10.1001/Archotol.131.6.481 |
0.323 |
|
| 2005 |
Michel V, Goodyear RJ, Weil D, Marcotti W, Perfettini I, Wolfrum U, Kros CJ, Richardson GP, Petit C. Cadherin 23 is a component of the transient lateral links in the developing hair bundles of cochlear sensory cells. Developmental Biology. 280: 281-94. PMID 15882573 DOI: 10.1016/J.Ydbio.2005.01.014 |
0.44 |
|
| 2005 |
Leibovici M, Verpy E, Goodyear RJ, Zwaenepoel I, Blanchard S, Lainé S, Richardson GP, Petit C. Initial characterization of kinocilin, a protein of the hair cell kinocilium. Hearing Research. 203: 144-53. PMID 15855039 DOI: 10.1016/J.Heares.2004.12.002 |
0.487 |
|
| 2005 |
Adato A, Michel V, Kikkawa Y, Reiners J, Alagramam KN, Weil D, Yonekawa H, Wolfrum U, El-Amraoui A, Petit C. Interactions in the network of Usher syndrome type 1 proteins. Human Molecular Genetics. 14: 347-56. PMID 15590703 DOI: 10.1093/hmg/ddi031 |
0.302 |
|
| 2005 |
Delprat B, Michel V, Goodyear R, Yamasaki Y, Michalski N, El-Amraoui A, Perfettini I, Legrain P, Richardson G, Hardelin JP, Petit C. Myosin XVa and whirlin, two deafness gene products required for hair bundle growth, are located at the stereocilia tips and interact directly. Human Molecular Genetics. 14: 401-10. PMID 15590698 DOI: 10.1093/hmg/ddi036 |
0.804 |
|
| 2004 |
Masmoudi S, Charfedine I, Rebeh I, Rebai A, Tlili A, Ghorbel A, Belguith H, Petit C, Drira M, Ayadi H. Refined mapping of the autosomal recessive non-syndromic deafness locus DFNB13 using eight novel microsatellite markers. Clinical Genetics. 66: 358-364. PMID 15355440 DOI: 10.1111/J.1399-0004.2004.00311.X |
0.324 |
|
| 2004 |
Feldmann D, Denoyelle F, Chauvin P, Garabédian EN, Couderc R, Odent S, Joannard A, Schmerber S, Delobel B, Leman J, Journel H, Catros H, Le Maréchal C, Dollfus H, Eliot MM, ... ... Petit C, et al. Large deletion of the GJB6 gene in deaf patients heterozygous for the GJB2 gene mutation: genotypic and phenotypic analysis. American Journal of Medical Genetics. Part A. 127: 263-7. PMID 15150777 DOI: 10.1002/Ajmg.A.20588 |
0.34 |
|
| 2004 |
Sousa S, Cabanes D, El-Amraoui A, Petit C, Lecuit M, Cossart P. Unconventional myosin VIIa and vezatin, two proteins crucial for Listeria entry into epithelial cells. Journal of Cell Science. 117: 2121-30. PMID 15090598 DOI: 10.1242/Jcs.01066 |
0.38 |
|
| 2004 |
Hardelin JP, Denoyelle F, Levilliers J, Simmler MC, Petit C. [Hereditary deafness: molecular genetics]. MéDecine Sciences : M/S. 20: 311-6. PMID 15067576 DOI: 10.1051/Medsci/2004203311 |
0.378 |
|
| 2004 |
Hildebrand MS, de Silva MG, Klockars T, Rose E, Price M, Smith RJ, McGuirt WT, Christopoulos H, Petit C, Dahl HH. Characterisation of DRASIC in the mouse inner ear. Hearing Research. 190: 149-60. PMID 15051137 DOI: 10.1016/S0378-5955(04)00015-2 |
0.473 |
|
| 2004 |
Cohen-Salmon M, Maxeiner S, Krüger O, Theis M, Willecke K, Petit C. Expression of the connexin43- and connexin45-encoding genes in the developing and mature mouse inner ear. Cell and Tissue Research. 316: 15-22. PMID 14986102 DOI: 10.1007/S00441-004-0861-2 |
0.385 |
|
| 2004 |
Modamio-Høybjør S, Moreno-Pelayo MA, MencÃa A, del Castillo I, Chardenoux S, Morais D, Lathrop M, Petit C, Moreno F. A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA50, maps to chromosome 7q32 between the DFNB17 and DFNB13 deafness loci. Journal of Medical Genetics. 41: e14. PMID 14757864 DOI: 10.1136/Jmg.2003.012500 |
0.403 |
|
| 2004 |
Feldmann D, Denoyelle F, Loundon N, Weil D, Garabedian EN, Couderc R, Joannard A, Schmerber S, Delobel B, Leman J, Journel H, Catros H, Ferrec C, Drouin-Garraud V, Obstoy MF, ... ... Petit C, et al. Clinical evidence of the nonpathogenic nature of the M34T variant in the connexin 26 gene. European Journal of Human Genetics : Ejhg. 12: 279-84. PMID 14694360 DOI: 10.1038/Sj.Ejhg.5201147 |
0.384 |
|
| 2004 |
Desnos C, Schonn JS, Huet S, Tran VS, El-Amraoui A, Raposo G, Fanget I, Chapuis C, Ménasché G, de Saint Basile G, Petit C, Cribier S, Henry JP, Darchen F. Rab27A and its effector MyRIP link secretory granules to F-actin and control their motion towards release sites. The Journal of Cell Biology. 163: 559-70. PMID 14610058 DOI: 10.1083/Jcb.200302157 |
0.33 |
|
| 2003 |
Moreno-Pelayo MA, Modamio-Høybjør S, MencÃa A, del Castillo I, Chardenoux S, Fernández-Burriel M, Lathrop M, Petit C, Moreno F. DFNA49, a novel locus for autosomal dominant non-syndromic hearing loss, maps proximal to DFNA7/DFNM1 region on chromosome 1q21-q23. Journal of Medical Genetics. 40: 832-6. PMID 14627674 DOI: 10.1136/Jmg.40.11.832 |
0.409 |
|
| 2003 |
Reiners J, Reidel B, El-Amraoui A, Boëda B, Huber I, Petit C, Wolfrum U. Differential distribution of harmonin isoforms and their possible role in Usher-1 protein complexes in mammalian photoreceptor cells. Investigative Ophthalmology & Visual Science. 44: 5006-5015. PMID 14578428 DOI: 10.1167/Iovs.03-0483 |
0.39 |
|
| 2003 |
Waselle L, Coppola T, Fukuda M, Iezzi M, El-Amraoui A, Petit C, Regazzi R. Involvement of the Rab27 binding protein Slac2c/MyRIP in insulin exocytosis. Molecular Biology of the Cell. 14: 4103-13. PMID 14517322 DOI: 10.1091/Mbc.E03-01-0022 |
0.326 |
|
| 2003 |
Delmaghani S, Aghaie A, Compain-Nouaille S, Ataie A, Lemainque A, Zeinali S, Lathrop M, Weil D, Petit C. DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21-12.1. European Journal of Human Genetics. 11: 816-818. PMID 14512974 DOI: 10.1038/Sj.Ejhg.5201045 |
0.361 |
|
| 2003 |
Michel V, Hardelin JP, Petit C. Molecular mechanism of a frequent genetic form of deafness. The New England Journal of Medicine. 349: 716-7. PMID 12917317 DOI: 10.1056/Nejmc030327 |
0.34 |
|
| 2003 |
Mburu P, Mustapha M, Varela A, Weil D, El-Amraoui A, Holme RH, Rump A, Hardisty RE, Blanchard S, Coimbra RS, Perfettini I, Parkinson N, Mallon AM, Glenister P, Rogers MJ, ... ... Petit C, et al. Defects in whirlin, a PDZ domain molecule involved in stereocilia elongation, cause deafness in the whirler mouse and families with DFNB31. Nature Genetics. 34: 421-8. PMID 12833159 DOI: 10.1038/Ng1208 |
0.516 |
|
| 2003 |
Jawaheer D, Juo SHH, Le Caignec C, David A, Petit C, Gregersen P, Dowbak S, Damle A, McElreavey K, Ostrer H. Mapping a gene for 46,XY gonadal dysgenesis by linkage analysis Clinical Genetics. 63: 530-535. PMID 12786760 DOI: 10.1034/J.1399-0004.2003.00082.X |
0.316 |
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| 2003 |
Liu XZ, Ouyang XM, Xia XJ, Zheng J, Pandya A, Li F, Du LL, Welch KO, Petit C, Smith RJ, Webb BT, Yan D, Arnos KS, Corey D, Dallos P, et al. Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss. Human Molecular Genetics. 12: 1155-62. PMID 12719379 DOI: 10.1093/Hmg/Ddg127 |
0.43 |
|
| 2003 |
Masmoudi S, Tlili A, Majava M, Ghorbel AM, Chardenoux S, Lemainque A, Zina ZB, Moala J, Männikkö M, Weil D, Lathrop M, Ala-Kokko L, Drira M, Petit C, Ayadi H. Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1 European Journal of Human Genetics. 11: 185-188. PMID 12634867 DOI: 10.1038/Sj.Ejhg.5200934 |
0.323 |
|
| 2003 |
Weil D, El-Amraoui A, Masmoudi S, Mustapha M, Kikkawa Y, Lainé S, Delmaghani S, Adato A, Nadifi S, Zina ZB, Hamel C, Gal A, Ayadi H, Yonekawa H, Petit C. Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin. Human Molecular Genetics. 12: 463-71. PMID 12588794 DOI: 10.1093/Hmg/Ddg051 |
0.342 |
|
| 2003 |
Dellovade TL, Hardelin JP, Soussi-Yanicostas N, Pfaff DW, Schwanzel-Fukuda M, Petit C. Anosmin-1 immunoreactivity during embryogenesis in a primitive eutherian mammal. Brain Research. Developmental Brain Research. 140: 157-67. PMID 12586422 DOI: 10.1016/S0165-3806(02)00544-8 |
0.311 |
|
| 2003 |
Bruzzone R, Veronesi V, Gomès D, Bicego M, Duval N, Marlin S, Petit C, D'Andrea P, White TW. Loss-of-function and residual channel activity of connexin26 mutations associated with non-syndromic deafness Febs Letters. 533: 79-88. PMID 12505163 DOI: 10.1016/S0014-5793(02)03755-9 |
0.395 |
|
| 2003 |
Teubner B, Michel V, Pesch J, Lautermann J, Cohen-Salmon M, Söhl G, Jahnke K, Winterhager E, Herberhold C, Hardelin JP, Petit C, Willecke K. Connexin30 (Gjb6)-deficiency causes severe hearing impairment and lack of endocochlear potential. Human Molecular Genetics. 12: 13-21. PMID 12490528 DOI: 10.1093/Hmg/Ddg001 |
0.493 |
|
| 2003 |
Modamio-Høybjør S, Moreno-Pelayo MA, MencÃa A, del Castillo I, Chardenoux S, Armenta D, Lathrop M, Petit C, Moreno F. A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28-29. Human Genetics. 112: 24-8. PMID 12483295 DOI: 10.1007/S00439-002-0836-X |
0.363 |
|
| 2002 |
Boëda B, El-Amraoui A, Bahloul A, Goodyear R, Daviet L, Blanchard S, Perfettini I, Fath KR, Shorte S, Reiners J, Houdusse A, Legrain P, Wolfrum U, Richardson G, Petit C. Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle. The Embo Journal. 21: 6689-99. PMID 12485990 DOI: 10.1093/Emboj/Cdf689 |
0.346 |
|
| 2002 |
Chapiro E, Feldmann D, Denoyelle F, Sternberg D, Jardel C, Eliot MM, Bouccara D, Weil D, Garabédian EN, Couderc R, Petit C, Marlin S. Two large French pedigrees with non syndromic sensorineural deafness and the mitochondrial DNA T7511C mutation: evidence for a modulatory factor. European Journal of Human Genetics : Ejhg. 10: 851-6. PMID 12461693 DOI: 10.1038/Sj.Ejhg.5200894 |
0.363 |
|
| 2002 |
Ouyang XM, Xia XJ, Verpy E, Du LL, Pandya A, Petit C, Balkany T, Nance WE, Liu XZ. Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness. Human Genetics. 111: 26-30. PMID 12136232 DOI: 10.1007/S00439-002-0736-0 |
0.369 |
|
| 2002 |
Cohen-Salmon M, Ott T, Michel V, Hardelin JP, Perfettini I, Eybalin M, Wu T, Marcus DC, Wangemann P, Willecke K, Petit C. Targeted ablation of connexin26 in the inner ear epithelial gap junction network causes hearing impairment and cell death. Current Biology : Cb. 12: 1106-11. PMID 12121617 DOI: 10.1016/S0960-9822(02)00904-1 |
0.363 |
|
| 2002 |
Medlej-Hashim M, Mustapha M, Chouery E, Weil D, Parronaud J, Salem N, Delague V, Loiselet J, Lathrop M, Petit C, Mégarbané A. Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutations. European Journal of Human Genetics : Ejhg. 10: 391-4. PMID 12080392 DOI: 10.1038/Sj.Ejhg.5200813 |
0.365 |
|
| 2002 |
Coimbra RS, Weil D, Brottier P, Blanchard S, Levi M, Hardelin JP, Weissenbach J, Petit C. A subtracted cDNA library from the zebrafish (Danio rerio) embryonic inner ear. Genome Research. 12: 1007-11. PMID 12045154 DOI: 10.1101/Gr.227502 |
0.332 |
|
| 2002 |
Mustapha M, Chouery E, Chardenoux S, Naboulsi M, Paronnaud J, Lemainque A, Mégarbané A, Loiselet J, Weil D, Lathrop M, Petit C. DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34. European Journal of Human Genetics : Ejhg. 10: 210-2. PMID 11973626 DOI: 10.1038/Sj.Ejhg.5200780 |
0.377 |
|
| 2002 |
Zwaenepoel I, Mustapha M, Leibovici M, Verpy E, Goodyear R, Liu XZ, Nouaille S, Nance WE, Kanaan M, Avraham KB, Tekaia F, Loiselet J, Lathrop M, Richardson G, Petit C. Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22. Proceedings of the National Academy of Sciences of the United States of America. 99: 6240-5. PMID 11972037 DOI: 10.1073/Pnas.082515999 |
0.306 |
|
| 2002 |
El-Amraoui A, Schonn JS, Küssel-Andermann P, Blanchard S, Desnos C, Henry JP, Wolfrum U, Darchen F, Petit C. MyRIP, a novel Rab effector, enables myosin VIIa recruitment to retinal melanosomes. Embo Reports. 3: 463-70. PMID 11964381 DOI: 10.1093/Embo-Reports/Kvf090 |
0.373 |
|
| 2002 |
Mustapha M, Chouery E, Torchard-Pagnez D, Nouaille S, Khrais A, Sayegh FN, Mégarbané A, Loiselet J, Lathrop M, Petit C, Weil D. A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25. Human Genetics. 110: 348-50. PMID 11941484 DOI: 10.1007/S00439-002-0690-X |
0.383 |
|
| 2002 |
Mustapha M, Salem N, Delague V, Chouery E, Ghassibeh M, Rai M, Loiselet J, Petit C, Mégarbané A. Autosomal recessive non-syndromic hearing loss in the Lebanese population: prevalence of the 30delG mutation and report of two novel mutations in the connexin 26 (GJB2) gene. Journal of Medical Genetics. 38: E36. PMID 11584050 DOI: 10.1136/Jmg.38.10.E36 |
0.381 |
|
| 2001 |
Bruzzone R, Gomès D, Denoyelle F, Duval N, Perea J, Veronesi V, Weil D, Petit C, Gabellec M-, D'andrea P, White TW. Functional analysis of a dominant mutation of human connexin26 associated with nonsyndromic deafness. Cell Communication and Adhesion. 8: 425-431. PMID 12064630 DOI: 10.3109/15419060109080765 |
0.36 |
|
| 2001 |
Petit C. USHER SYNDROME: From Genetics to Pathogenesis Annual Review of Genomics and Human Genetics. 2: 271-297. PMID 11701652 DOI: 10.1146/Annurev.Genom.2.1.271 |
0.465 |
|
| 2001 |
Verpy E, Masmoudi S, Zwaenepoel I, Leibovici M, Hutchin TP, Del Castillo I, Nouaille S, Blanchard S, Lainé S, Popot JL, Moreno F, Mueller RF, Petit C. Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locus. Nature Genetics. 29: 345-9. PMID 11687802 DOI: 10.1038/Ng726 |
0.393 |
|
| 2001 |
El-Amraoui A, Cohen-Salmon M, Petit C, Simmler M. Spatiotemporal expression of otogelin in the developing and adult mouse inner ear. Hearing Research. 158: 151-159. PMID 11506947 DOI: 10.1016/S0378-5955(01)00312-4 |
0.435 |
|
| 2001 |
Marlin S, Garabédian EN, Roger G, Moatti L, Matha N, Lewin P, Petit C, Denoyelle F. Connexin 26 gene mutations in congenitally deaf children: pitfalls for genetic counseling. Archives of Otolaryngology--Head & Neck Surgery. 127: 927-33. PMID 11493200 DOI: 10.1001/Archotol.127.8.927 |
0.313 |
|
| 2001 |
Boëda B, Weil D, Petit C. A specific promoter of the sensory cells of the inner ear defined by transgenesis Human Molecular Genetics. 10: 1581-1589. PMID 11468276 DOI: 10.1093/Hmg/10.15.1581 |
0.44 |
|
| 2001 |
Zwaenepoel I, Verpy E, Blanchard S, Meins M, Apfelstedt-Sylla E, Gal A, Petit C. Identification of three novel mutations in the USH1C gene and detection of thirty-one polymorphisms used for haplotype analysis. Human Mutation. 17: 34-41. PMID 11139240 DOI: 10.1002/1098-1004(2001)17:1<34::Aid-Humu4>3.0.Co;2-O |
0.34 |
|
| 2000 |
Simmler MC, Zwaenepoel, Verpy E, Guillaud L, Elbaz C, Petit C, Panthier JJ. Twister mutant mice are defective for otogelin, a component specific to inner ear acellular membranes. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 11: 961-966. PMID 11178734 DOI: 10.1007/S003350010197 |
0.453 |
|
| 2000 |
Masmoudi S, Elgaied-Boulila A, Kassab I, Ben Arab S, Blanchard S, Bouzouita JE, Drira M, Kassab A, Hachicha S, Petit C, Ayadi H. Determination of the frequency of connexin26 mutations in inherited sensorineural deafness and carrier rates in the Tunisian population using DGGE. Journal of Medical Genetics. 37: E39. PMID 11073548 DOI: 10.1136/Jmg.37.11.E39 |
0.373 |
|
| 2000 |
Ernest S, Rauch GJ, Haffter P, Geisler R, Petit C, Nicolson T. Mariner is defective in myosin VIIA: a zebrafish model for human hereditary deafness. Human Molecular Genetics. 9: 2189-96. PMID 10958658 DOI: 10.1093/Hmg/9.14.2189 |
0.489 |
|
| 2000 |
Ben Arab S, Hmani M, Denoyelle F, Boulila-Elgaied A, Chardenoux S, Hachicha S, Petit C, Ayadi H. Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates. Clinical Genetics. 57: 439-43. PMID 10905664 DOI: 10.1034/J.1399-0004.2000.570607.X |
0.335 |
|
| 2000 |
Yasunaga S, Grati M, Chardenoux S, Smith TN, Friedman TB, Lalwani AK, Wilcox ER, Petit C. OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9. American Journal of Human Genetics. 67: 591-600. PMID 10903124 DOI: 10.1086/303049 |
0.355 |
|
| 2000 |
Küssel-Andermann P, El-Amraoui A, Safieddine S, Hardelin J, Nouaille S, Camonis J, Petit C. Unconventional myosin VIIA is a novel A-kinase-anchoring protein. Journal of Biological Chemistry. 275: 29654-29659. PMID 10889203 DOI: 10.1074/Jbc.M004393200 |
0.415 |
|
| 2000 |
Yasunaga S, Grati M, Petit C. DFNB9 and DFNB12 Advances in Oto-Rhino-Laryngology. 56: 164-167. PMID 10868229 DOI: 10.1159/000059097 |
0.358 |
|
| 2000 |
Casademont I, Chevrier D, Denoyelle F, Petit C, Guesdon J-. A simple and reliable method for the detection of the 30delG mutation of the CX26 gene. Molecular and Cellular Probes. 14: 149-152. PMID 10860712 DOI: 10.1006/Mcpr.2000.0297 |
0.335 |
|
| 2000 |
Simmler MC, Cohen-Salmon M, El-Amraoui A, Guillaud L, Benichou JC, Petit C, Panthier JJ. Targeted disruption of otog results in deafness and severe imbalance. Nature Genetics. 24: 139-43. PMID 10655058 DOI: 10.1038/72793 |
0.455 |
|
| 2000 |
Ardouin O, Legouis R, Fasano L, David-Watine B, Korn H, Hardelin J, Petit C. Characterization of the two zebrafish orthologues of the KAL-1 gene underlying X chromosome-linked Kallmann syndrome. Mechanisms of Development. 90: 89-94. PMID 10585565 DOI: 10.1016/S0925-4773(99)00222-1 |
0.37 |
|
| 1999 |
Marlin S, Blanchard S, Slim R, Lacombe D, Denoyelle F, Alessandri J, Calzolari E, Drouin-Garraud V, Ferraz FG, Fourmaintraux A, Philip N, Toublanc J, Petit C. Townes‐Brocks syndrome: Detection of a SALL1 mutation hot spot and evidence for a position effect in one patient Human Mutation. 14: 377-386. PMID 10533063 DOI: 10.1002/(Sici)1098-1004(199911)14:5<377::Aid-Humu3>3.0.Co;2-A |
0.337 |
|
| 1999 |
Hardelin J, Julliard AK, Moniot B, Soussi-Yanicostas N, Verney C, Schwanzel-Fukuda M, Lievre CA, Petit C. Anosmin-1 is a regionally restricted component of basement membranes and interstitial matrices during organogenesis: implications for the developmental anomalies of X chromosome-linked Kallmann syndrome. Developmental Dynamics. 215: 26-44. PMID 10340754 DOI: 10.1002/(Sici)1097-0177(199905)215:1<26::Aid-Dvdy4>3.0.Co;2-D |
0.359 |
|
| 1999 |
Hmani M, Ghorbel A, Boulila-Elgaied A, Zina ZB, Kammoun W, Drira M, Chaabouni M, Petit C, Ayadi H. A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23-24.2. European Journal of Human Genetics. 7: 363-367. PMID 10234513 DOI: 10.1038/Sj.Ejhg.5200307 |
0.353 |
|
| 1999 |
Kubisch C, Schroeder BC, Friedrich T, Lütjohann B, El-Amraoui A, Marlin S, Petit C, Jentsch TJ. KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness. Cell. 96: 437-46. PMID 10025409 DOI: 10.1016/S0092-8674(00)80556-5 |
0.302 |
|
| 1999 |
Mustapha M, Weil D, Chardenoux S, Elias S, El-Zir E, Beckmann JS, Loiselet J, Petit C. An α-Tectorin Gene Defect Causes a Newly Identified Autosomal Recessive Form of Sensorineural Pre-Lingual Non-Syndromic Deafness, DFNB21 Human Molecular Genetics. 8: 409-412. PMID 9949200 DOI: 10.1093/Hmg/8.3.409 |
0.39 |
|
| 1999 |
Verpy E, Leibovici M, Petit C. Characterization of otoconin-95, the major protein of murine otoconia, provides insights into the formation of these inner ear biominerals Proceedings of the National Academy of Sciences of the United States of America. 96: 529-534. PMID 9892667 DOI: 10.1073/Pnas.96.2.529 |
0.422 |
|
| 1998 |
Mustapha M, Salem N, Weil D, el-Zir E, Loiselet J, Petit C. Identification of a locus on chromosome 7q31, DFNB14, responsible for prelingual sensorineural non-syndromic deafness. European Journal of Human Genetics : Ejhg. 6: 548-51. PMID 9887371 DOI: 10.1038/Sj.Ejhg.5200261 |
0.317 |
|
| 1998 |
Kalatzis V, Sahly I, El-Amraoui A, Petit C. Eya1 expression in the developing ear and kidney: towards the understanding of the pathogenesis of Branchio-Oto-Renal (BOR) syndrome. Developmental Dynamics. 213: 486-499. PMID 9853969 DOI: 10.1002/(Sici)1097-0177(199812)213:4<486::Aid-Aja13>3.0.Co;2-L |
0.402 |
|
| 1998 |
Mustapha M, Chardenoux S, Nieder A, Salem N, Weissenbach J, el-Zir E, Loiselet J, Petit C. A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36. European Journal of Human Genetics : Ejhg. 6: 245-50. PMID 9781028 DOI: 10.1038/Sj.Ejhg.5200177 |
0.324 |
|
| 1998 |
Saouda M, Mansour A, Moglabey YB, Zir EE, Mustapha M, Chaib H, Nehmé A, Mégarbané A, Loiselet J, Petit C, Slim R. The Usher syndrome in the Lebanese population and further refinement of the USH2A candidate region. Human Genetics. 103: 193-198. PMID 9760205 DOI: 10.1007/S004390050806 |
0.32 |
|
| 1998 |
Kalatzis V, Petit C. The fundamental and medical impacts of recent progress in research on hereditary hearing loss. Human Molecular Genetics. 7: 1589-97. PMID 9735380 DOI: 10.1093/Hmg/7.10.1589 |
0.369 |
|
| 1998 |
Marlin S, Denoyelle F, Busquet D, Garabedian N, Petit C. A particular case of deafness-oligodontia syndrome. International Journal of Pediatric Otorhinolaryngology. 44: 63-9. PMID 9720683 DOI: 10.1016/S0165-5876(98)00029-9 |
0.321 |
|
| 1998 |
Dodé C, Weil D, Levilliers J, Crozet F, Chaı̈b H, Levi-Acobas F, Guilford P, Petit C. Sequence Characterization of a Newly Identified Human α-Tubulin Gene (TUBA2) Genomics. 47: 125-130. PMID 9465305 DOI: 10.1006/Geno.1997.5081 |
0.345 |
|
| 1997 |
Cohen-Salmon M, El-Amraoui A, Leibovici M, Petit C. Otogelin: A glycoprotein specific to the acellular membranes of the inner ear Proceedings of the National Academy of Sciences of the United States of America. 94: 14450-14455. PMID 9405633 DOI: 10.1073/Pnas.94.26.14450 |
0.365 |
|
| 1997 |
Abdelhak S, Kalatzis V, Heilig R, Compain S, Samson D, Vincent C, Levi-Acobas F, Cruaud C, Merrer ML, Mathieu M, König R, Vigneron J, Weissenbach J, Petit C, Weil D. Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1 Human Molecular Genetics. 6: 2247-2255. PMID 9361030 DOI: 10.1093/Hmg/6.13.2247 |
0.342 |
|
| 1997 |
Schiebel K, Winkelmann M, Mertz A, Xu X, Page DC, Weil D, Petit C, Rappold GA. Abnormal XY interchange between a novel isolated protein kinase gene, PRKY and its homologue, PRKX, accounts for one third of all (Y+)XX males and (Y-)XY females Human Molecular Genetics. 6: 1985-1989. PMID 9302280 DOI: 10.1093/Hmg/6.11.1985 |
0.307 |
|
| 1997 |
Cohen-Salmon M, Crozet F, Rebillard G, Petit C. Cloning and characterization of the mouse collapsin response mediator protein-1, crmpl Mammalian Genome. 8: 349-351. PMID 9107681 DOI: 10.1007/S003359900438 |
0.309 |
|
| 1997 |
Lévy G, Levi-Acobas F, Blanchard S, Gerber S, Larget-Piet D, Chenal V, Liu XZ, Newton V, Steel KP, Brown SDM, Munnich A, Kaplan J, Petit C, Weil D. Myosin VIIA Gene: Heterogeneity of the Mutations Responsible for Usher Syndrome Type IB Human Molecular Genetics. 6: 111-116. PMID 9002678 DOI: 10.1093/Hmg/6.1.111 |
0.352 |
|
| 1997 |
Chaïb H, Kaplan J, Gerber S, Vincent C, Ayadi H, Slim R, Munnich A, Weissenbach J, Petit C. A Newly Identified Locus for Usher Syndrome Type I, USH1E, Maps to Chromosome 21q21 Human Molecular Genetics. 6: 27-31. PMID 9002666 DOI: 10.1093/Hmg/6.1.27 |
0.328 |
|
| 1997 |
Vincent C, Kalatzis V, Abdelhak S, Chaïb H, Compain S, Helias J, Vaneecloo F, Petit C. BOR and BO syndromes are allelic defects of EYA1. European Journal of Human Genetics. 5: 242-246. DOI: 10.1007/Bf03405924 |
0.333 |
|
| 1996 |
Tesson F, Donger C, Denjoy I, Berthet M, Bennaceur M, Petit C, Coumel P, Schwartz K, Guicheney P. Exclusion of KCNE1 (IsK) as a candidate gene for Jervell and Lange-Nielsen syndrome. Journal of Molecular and Cellular Cardiology. 28: 2051-2055. PMID 8899564 DOI: 10.1006/Jmcc.1996.0198 |
0.374 |
|
| 1996 |
Chaïb H, Place C, Salem N, Dodé C, Chardenoux S, Weissenbach J, Zir EE, Loiselet J, Petit C. Mapping of DFNB12, a Gene for a Non-Syndromal Autosomal Recessive Deafness, to Chromosome 10q21–22 Human Molecular Genetics. 5: 1061-1064. PMID 8817348 DOI: 10.1093/Hmg/5.7.1061 |
0.389 |
|
| 1996 |
Kalatzis V, Abdelhak S, Compain S, Vincent C, Petit C. Characterization of a translocation-associated deletion defines the candidate region for the gene responsible for branchio-oto-renal syndrome. Genomics. 34: 422-425. PMID 8786145 DOI: 10.1006/Geno.1996.0307 |
0.31 |
|
| 1996 |
Weil D, Levy G, Sahly I, Levi-Acobas F, Blanchard S, El-Amraoui A, Crozet F, Philippe H, Abitbol M, Petit C. Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia. Proceedings of the National Academy of Sciences of the United States of America. 93: 3232-3237. PMID 8622919 DOI: 10.1073/Pnas.93.8.3232 |
0.45 |
|
| 1995 |
Legouis R, Hardelin JP, Petit C, Ayer-Le Lièvre C. Early expression of the KAL gene during embryonic development of the chick. Anatomy and Embryology. 190: 549-62. PMID 7893008 DOI: 10.1007/Bf00190105 |
0.336 |
|
| 1995 |
Cohen-Salmon M, Tronche F, del Castillo I, Petit C. Characterization of the promoter of the human KAL gene, responsible for the X-chromosome-linked Kallmann syndrome. Gene. 164: 235-42. PMID 7590336 DOI: 10.1016/0378-1119(95)00481-K |
0.31 |
|
| 1995 |
Hardelin J, Petit C. A molecular approach to the pathophysiology of the X chromosome-linked Kallmann's syndrome. BaillièRe's Clinical Endocrinology and Metabolism. 9: 489-507. PMID 7575329 DOI: 10.1016/S0950-351X(95)80553-2 |
0.354 |
|
| 1994 |
Guilford P, Arab SB, Blanchard S, Levilliers J, Weissenbach J, Belkahia A, Petit C. A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q. Nature Genetics. 6: 24-28. PMID 8136828 DOI: 10.1038/Ng0194-24 |
0.331 |
|
| 1994 |
Chaib H, Lina-Granade G, Guilford P, Plauchu H, Levilliers J, Morgon A, Petit C. A gene responsible for a dominant form of neurosensory non-syndromic deafness maps to the NSRD1 recessive deafness gene interval Human Molecular Genetics. 3: 2219-2222. PMID 7881423 DOI: 10.1093/Hmg/3.12.2219 |
0.372 |
|
| 1994 |
Vincent C, Kalatzis V, Compain S, Levilliers J, Slim R, Graia F, Pereira MdL, Nivelon A, Croquette M, Lacombe D, Vigneron J, Helias J, Broyer M, Callen DF, Haan EA, ... ... Petit C, et al. A proposed new contiguous gene syndrome on 8q consists of Branchio-Oto-Renal (BOR) syndrome, Duane syndrome, a dominant form of hydrocephalus and trapeze aplasia; implications for the mapping of the BOR gene Human Molecular Genetics. 3: 1859-1866. PMID 7849713 DOI: 10.1093/Hmg/3.10.1859 |
0.316 |
|
| 1993 |
Petit C. Molecular basis of the X-chromosome-linked Kallmann's syndrome Trends in Endocrinology and Metabolism. 4: 8-13. PMID 18407127 DOI: 10.1016/1043-2760(93)90057-L |
0.339 |
|
| 1993 |
Soussi-Yanicostas N, Whalen RG, Petit C. Five skeletal myosin heavy chain genes are organized as a multigene complex in the human genome. Human Molecular Genetics. 2: 563-9. PMID 8518795 DOI: 10.1093/Hmg/2.5.563 |
0.315 |
|
| 1993 |
Hardelin J, Levilliers J, Blanchard S, Carel J, Leutenegger M, Pinard-Bertelletto J, Bouloux P, Petit C. Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome Human Molecular Genetics. 2: 373-377. PMID 8504298 DOI: 10.1093/Hmg/2.4.373 |
0.339 |
|
| 1993 |
Hardelin JP, Levilliers J, Young J, Pholsena M, Legouis R, Kirk J, Bouloux P, Petit C, Schaison G. Xp22.3 deletions in isolated familial Kallmann's syndrome. The Journal of Clinical Endocrinology and Metabolism. 76: 827-831. PMID 8473391 DOI: 10.1210/Jcem.76.4.8473391 |
0.331 |
|
| 1993 |
Legouis R, Cohen-Salmon M, del Castillo I, Levilliers J, Capy L, Mornow JP, Petit C. Characterization of the chicken and quail homologues of the human gene responsible for the X-linked Kallmann syndrome. Genomics. 17: 516-8. PMID 8406507 DOI: 10.1006/Geno.1993.1360 |
0.331 |
|
| 1990 |
Petit C, Melki J, Levilliers J, Serville F, Weissenbach J, Maroteaux P. An interstitial deletion in Xp22.3 in a family with X-linked recessive chondrodysplasia punctata and short stature. Human Genetics. 85: 247-250. PMID 2370057 DOI: 10.1007/Bf00193206 |
0.301 |
|
| 1986 |
Petit C, Levilliers J, Ott M, Weiss MC. Tissue-specific expression of the rat albumin gene: genetic control of its extinction in microcell hybrids Proceedings of the National Academy of Sciences of the United States of America. 83: 2561-2565. PMID 3458217 DOI: 10.1073/Pnas.83.8.2561 |
0.337 |
|
| 1977 |
Antoine JC, Petit C, Bach M, Bach JF, Salomon JC, Avrameas S. T cell dependence of cells synthesizing immunoglobulin without detectable antibody function induced after an antigenic stimulation. European Journal of Immunology. 7: 336-341. PMID 302205 DOI: 10.1002/Eji.1830070603 |
0.307 |
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