A citation-based method for searching scientific literature

S Yasunaga, M Grati, M Cohen-Salmon, A El-Amraoui, M Mustapha, N Salem, E El-Zir, J Loiselet, C Petit. Nat Genet 1999
Times Cited: 362







List of co-cited articles
1349 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse.
Isabelle Roux, Saaid Safieddine, Régis Nouvian, M'hamed Grati, Marie-Christine Simmler, Amel Bahloul, Isabelle Perfettini, Morgane Le Gall, Philippe Rostaing, Ghislaine Hamard,[...]. Cell 2006
391
60

Hearing requires otoferlin-dependent efficient replenishment of synaptic vesicles in hair cells.
Tina Pangrsic, Livia Lasarow, Kirsten Reuter, Hideki Takago, Martin Schwander, Dietmar Riedel, Thomas Frank, Lisa M Tarantino, Janice S Bailey, Nicola Strenzke,[...]. Nat Neurosci 2010
138
33

Otoferlin acts as a Ca2+ sensor for vesicle fusion and vesicle pool replenishment at auditory hair cell ribbon synapses.
Nicolas Michalski, Juan D Goutman, Sarah Marie Auclair, Jacques Boutet de Monvel, Margot Tertrais, Alice Emptoz, Alexandre Parrin, Sylvie Nouaille, Marc Guillon, Martin Sachse,[...]. Elife 2017
56
51

A multicenter study on the prevalence and spectrum of mutations in the otoferlin gene (OTOF) in subjects with nonsyndromic hearing impairment and auditory neuropathy.
Montserrat Rodríguez-Ballesteros, Raúl Reynoso, Margarita Olarte, Manuela Villamar, Constantino Morera, Rosamaria Santarelli, Edoardo Arslan, Carme Medá, Carlos Curet, Christiane Völter,[...]. Hum Mutat 2008
117
27

Impairment of SLC17A8 encoding vesicular glutamate transporter-3, VGLUT3, underlies nonsyndromic deafness DFNA25 and inner hair cell dysfunction in null mice.
Jérôme Ruel, Sarah Emery, Régis Nouvian, Tiphaine Bersot, Bénédicte Amilhon, Jana M Van Rybroek, Guy Rebillard, Marc Lenoir, Michel Eybalin, Benjamin Delprat,[...]. Am J Hum Genet 2008
154
22

Hair cell synaptic dysfunction, auditory fatigue and thermal sensitivity in otoferlin Ile515Thr mutants.
Nicola Strenzke, Rituparna Chakrabarti, Hanan Al-Moyed, Alexandra Müller, Gerhard Hoch, Tina Pangrsic, Gulnara Yamanbaeva, Christof Lenz, Kuan-Ting Pan, Elisabeth Auge,[...]. EMBO J 2016
46
47


Identities and frequencies of mutations of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan.
B Y Choi, Z M Ahmed, S Riazuddin, M A Bhinder, M Shahzad, T Husnain, S Riazuddin, A J Griffith, T B Friedman. Clin Genet 2009
62
32

Non-syndromic recessive auditory neuropathy is the result of mutations in the otoferlin (OTOF) gene.
R Varga, P M Kelley, B J Keats, A Starr, S M Leal, E Cohn, W J Kimberling. J Med Genet 2003
162
19

OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9.
S Yasunaga, M Grati, S Chardenoux, T N Smith, T B Friedman, A K Lalwani, E R Wilcox, C Petit. Am J Hum Genet 2000
132
19

Otoferlin: a multi-C2 domain protein essential for hearing.
Tina Pangršič, Ellen Reisinger, Tobias Moser. Trends Neurosci 2012
84
22

Sensorineural deafness and seizures in mice lacking vesicular glutamate transporter 3.
Rebecca P Seal, Omar Akil, Eunyoung Yi, Christopher M Weber, Lisa Grant, Jong Yoo, Amanda Clause, Karl Kandler, Jeffrey L Noebels, Elisabeth Glowatzki,[...]. Neuron 2008
252
18

OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele.
R Varga, M R Avenarius, P M Kelley, B J Keats, C I Berlin, L J Hood, T G Morlet, S M Brashears, A Starr, E S Cohn,[...]. J Med Genet 2006
98
18

Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy.
Sedigheh Delmaghani, Francisco J del Castillo, Vincent Michel, Michel Leibovici, Asadollah Aghaie, Uri Ron, Lut Van Laer, Nir Ben-Tal, Guy Van Camp, Dominique Weil,[...]. Nat Genet 2006
173
17

Otoferlin couples to clathrin-mediated endocytosis in mature cochlear inner hair cells.
Susanne V Duncker, Christoph Franz, Stephanie Kuhn, Uwe Schulte, Dario Campanelli, Niels Brandt, Bernhard Hirt, Bernd Fakler, Nikolaus Blin, Peter Ruth,[...]. J Neurosci 2013
56
30

Otoferlin is a multivalent calcium-sensitive scaffold linking SNAREs and calcium channels.
Nicole Hams, Murugesh Padmanarayana, Weihong Qiu, Colin P Johnson. Proc Natl Acad Sci U S A 2017
26
65

Auditory neuropathy.
A Starr, T W Picton, Y Sininger, L J Hood, C I Berlin. Brain 1996
709
16

Direct interaction of otoferlin with syntaxin 1A, SNAP-25, and the L-type voltage-gated calcium channel Cav1.3.
Neeliyath A Ramakrishnan, Marian J Drescher, Dennis G Drescher. J Biol Chem 2009
82
19

Characterization of the lipid binding properties of Otoferlin reveals specific interactions between PI(4,5)P2 and the C2C and C2F domains.
Murugesh Padmanarayana, Nicole Hams, Lee C Speight, E James Petersson, Ryan A Mehl, Colin P Johnson. Biochemistry 2014
30
50

Probing the functional equivalence of otoferlin and synaptotagmin 1 in exocytosis.
Ellen Reisinger, Chris Bresee, Jakob Neef, Ramya Nair, Kirsten Reuter, Anna Bulankina, Régis Nouvian, Manuel Koch, Johanna Bückers, Lars Kastrup,[...]. J Neurosci 2011
69
21

Restoration of hearing in the VGLUT3 knockout mouse using virally mediated gene therapy.
Omar Akil, Rebecca P Seal, Kevin Burke, Chuansong Wang, Aurash Alemi, Matthew During, Robert H Edwards, Lawrence R Lustig. Neuron 2012
215
15

Disruption of adaptor protein 2μ (AP-2μ) in cochlear hair cells impairs vesicle reloading of synaptic release sites and hearing.
SangYong Jung, Tanja Maritzen, Carolin Wichmann, Zhizi Jing, Andreas Neef, Natalia H Revelo, Hanan Al-Moyed, Sandra Meese, Sonja M Wojcik, Iliana Panou,[...]. EMBO J 2015
56
26

A dual-AAV approach restores fast exocytosis and partially rescues auditory function in deaf otoferlin knock-out mice.
Hanan Al-Moyed, Andreia P Cepeda, SangYong Jung, Tobias Moser, Sebastian Kügler, Ellen Reisinger. EMBO Mol Med 2019
56
26

A prevalent founder mutation and genotype-phenotype correlations of OTOF in Japanese patients with auditory neuropathy.
T Matsunaga, H Mutai, S Kunishima, K Namba, N Morimoto, Y Shinjo, Y Arimoto, Y Kataoka, T Shintani, N Morita,[...]. Clin Genet 2012
51
27

Auditory neuropathy in patients carrying mutations in the otoferlin gene (OTOF).
Montserrat Rodríguez-Ballesteros, Francisco J del Castillo, Yolanda Martín, Miguel A Moreno-Pelayo, Constantino Morera, Félix Prieto, Jaime Marco, Antonio Morant, Jaime Gallo-Terán, Carmelo Morales-Angulo,[...]. Hum Mutat 2003
147
14

Auditory neuropathy--neural and synaptic mechanisms.
Tobias Moser, Arnold Starr. Nat Rev Neurol 2016
148
14

Audibility, speech perception and processing of temporal cues in ribbon synaptic disorders due to OTOF mutations.
Rosamaria Santarelli, Ignacio del Castillo, Elona Cama, Pietro Scimemi, Arnold Starr. Hear Res 2015
32
43

Dual AAV-mediated gene therapy restores hearing in a DFNB9 mouse model.
Omar Akil, Frank Dyka, Charlotte Calvet, Alice Emptoz, Ghizlene Lahlou, Sylvie Nouaille, Jacques Boutet de Monvel, Jean-Pierre Hardelin, William W Hauswirth, Paul Avan,[...]. Proc Natl Acad Sci U S A 2019
74
18

Ferlins: regulators of vesicle fusion for auditory neurotransmission, receptor trafficking and membrane repair.
Angela Lek, Frances J Evesson, R Bryan Sutton, Kathryn N North, Sandra T Cooper. Traffic 2012
93
13

Q829X, a novel mutation in the gene encoding otoferlin (OTOF), is frequently found in Spanish patients with prelingual non-syndromic hearing loss.
V Migliosi, S Modamio-Høybjør, M A Moreno-Pelayo, M Rodríguez-Ballesteros, M Villamar, D Tellería, I Menéndez, F Moreno, I Del Castillo. J Med Genet 2002
89
14

Tmc gene therapy restores auditory function in deaf mice.
Charles Askew, Cylia Rochat, Bifeng Pan, Yukako Asai, Hena Ahmed, Erin Child, Bernard L Schneider, Patrick Aebischer, Jeffrey R Holt. Sci Transl Med 2015
146
13

Unconventional molecular regulation of synaptic vesicle replenishment in cochlear inner hair cells.
Christian Vogl, Benjamin H Cooper, Jakob Neef, Sonja M Wojcik, Kerstin Reim, Ellen Reisinger, Nils Brose, Jeong-Seop Rhee, Tobias Moser, Carolin Wichmann. J Cell Sci 2015
47
27

Mechanotransduction in mouse inner ear hair cells requires transmembrane channel-like genes.
Yoshiyuki Kawashima, Gwenaëlle S G Géléoc, Kiyoto Kurima, Valentina Labay, Andrea Lelli, Yukako Asai, Tomoko Makishima, Doris K Wu, Charles C Della Santina, Jeffrey R Holt,[...]. J Clin Invest 2011
251
12

Exocytosis at the hair cell ribbon synapse apparently operates without neuronal SNARE proteins.
Régis Nouvian, Jakob Neef, Anna V Bulankina, Ellen Reisinger, Tina Pangršič, Thomas Frank, Stefan Sikorra, Nils Brose, Thomas Binz, Tobias Moser. Nat Neurosci 2011
78
15

Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
Kiyoto Kurima, Linda M Peters, Yandan Yang, Saima Riazuddin, Zubair M Ahmed, Sadaf Naz, Deidre Arnaud, Stacy Drury, Jianhong Mo, Tomoko Makishima,[...]. Nat Genet 2002
282
12

A synthetic AAV vector enables safe and efficient gene transfer to the mammalian inner ear.
Lukas D Landegger, Bifeng Pan, Charles Askew, Sarah J Wassmer, Sarah D Gluck, Alice Galvin, Ruth Taylor, Andrew Forge, Konstantina M Stankovic, Jeffrey R Holt,[...]. Nat Biotechnol 2017
156
12

Gene therapy restores auditory and vestibular function in a mouse model of Usher syndrome type 1c.
Bifeng Pan, Charles Askew, Alice Galvin, Selena Heman-Ackah, Yukako Asai, Artur A Indzhykulian, Francine M Jodelka, Michelle L Hastings, Jennifer J Lentz, Luk H Vandenberghe,[...]. Nat Biotechnol 2017
157
12

Control of exocytosis by synaptotagmins and otoferlin in auditory hair cells.
Maryline Beurg, Nicolas Michalski, Saaid Safieddine, Yohan Bouleau, Ralf Schneggenburger, Edwin R Chapman, Christine Petit, Didier Dulon. J Neurosci 2010
80
15

Screening of OTOF mutations in Iran: a novel mutation and review.
Nejat Mahdieh, Atefeh Shirkavand, Bahareh Rabbani, Mustafa Tekin, Bahman Akbari, Mohammad Taghi Akbari, Sirous Zeinali. Int J Pediatr Otorhinolaryngol 2012
31
35

Otoferlin deficiency in zebrafish results in defects in balance and hearing: rescue of the balance and hearing phenotype with full-length and truncated forms of mouse otoferlin.
Paroma Chatterjee, Murugesh Padmanarayana, Nazish Abdullah, Chelsea L Holman, Jane LaDu, Robert L Tanguay, Colin P Johnson. Mol Cell Biol 2015
25
44


Temperature-sensitive auditory neuropathy associated with an otoferlin mutation: Deafening fever!
Sandrine Marlin, Delphine Feldmann, Yann Nguyen, Isabelle Rouillon, Natalie Loundon, Laurence Jonard, Crystel Bonnet, Remy Couderc, Eréa Noel Garabedian, Christine Petit,[...]. Biochem Biophys Res Commun 2010
48
22

Increased activity of Diaphanous homolog 3 (DIAPH3)/diaphanous causes hearing defects in humans with auditory neuropathy and in Drosophila.
Cynthia J Schoen, Sarah B Emery, Marc C Thorne, Hima R Ammana, Elzbieta Sliwerska, Jameson Arnett, Michael Hortsch, Frances Hannan, Margit Burmeister, Marci M Lesperance. Proc Natl Acad Sci U S A 2010
67
14

Otoferlin interacts with myosin VI: implications for maintenance of the basolateral synaptic structure of the inner hair cell.
Paulina Heidrych, Ulrike Zimmermann, Stephanie Kuhn, Christoph Franz, Jutta Engel, Susanne V Duncker, Bernhard Hirt, Carsten M Pusch, Peter Ruth, Markus Pfister,[...]. Hum Mol Genet 2009
76
13

Hair cell synaptic ribbons are essential for synchronous auditory signalling.
Darina Khimich, Régis Nouvian, Rémy Pujol, Susanne Tom Dieck, Alexander Egner, Eckart D Gundelfinger, Tobias Moser. Nature 2005
355
10

Defective membrane repair in dysferlin-deficient muscular dystrophy.
Dimple Bansal, Katsuya Miyake, Steven S Vogel, Séverine Groh, Chien-Chang Chen, Roger Williamson, Paul L McNeil, Kevin P Campbell. Nature 2003
691
10

OTOF mutation screening in Japanese severe to profound recessive hearing loss patients.
Yoh-ichiro Iwasa, Shin-ya Nishio, Hidekane Yoshimura, Yukihiko Kanda, Kozo Kumakawa, Satoko Abe, Yasushi Naito, Kyoko Nagai, Shin-ichi Usami. BMC Med Genet 2013
25
40

Novel OTOF mutations in Brazilian patients with auditory neuropathy.
Jihane Romanos, Lilian Kimura, Mariana Lopes Fávero, Fernanda Attanasio R Izarra, Maria Teresa Balester de Mello Auricchio, Ana Carla Batissoco, Karina Lezirovitz, Ronaldo Serafim Abreu-Silva, Regina Célia Mingroni-Netto. J Hum Genet 2009
43
23

The genetic basis of auditory neuropathy spectrum disorder (ANSD).
Vinaya K C Manchaiah, Fei Zhao, Ali A Danesh, Rachel Duprey. Int J Pediatr Otorhinolaryngol 2011
70
14

Newborn hearing screening--a silent revolution.
Cynthia C Morton, Walter E Nance. N Engl J Med 2006
884
10


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.