A citation-based method for searching scientific literature

Xi Gu, Daqi Wang, Zhijiao Xu, Jinghan Wang, Luo Guo, Renjie Chai, Genglin Li, Yilai Shu, Huawei Li. Genome Biol 2021
Times Cited: 14







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



Times Cited
  Times     Co-cited
Similarity


Allele-specific gene editing prevents deafness in a model of dominant progressive hearing loss.
Bence György, Carl Nist-Lund, Bifeng Pan, Yukako Asai, K Domenica Karavitaki, Benjamin P Kleinstiver, Sara P Garcia, Mikołaj P Zaborowski, Paola Solanes, Sofia Spataro,[...]. Nat Med 2019
97
57

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
170
57

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
173
50

Treatment of autosomal dominant hearing loss by in vivo delivery of genome editing agents.
Xue Gao, Yong Tao, Veronica Lamas, Mingqian Huang, Wei-Hsi Yeh, Bifeng Pan, Yu-Juan Hu, Johnny H Hu, David B Thompson, Yilai Shu,[...]. Nature 2018
262
42

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
224
35

Gene Therapy Restores Balance and Auditory Functions in a Mouse Model of Usher Syndrome.
Kevin Isgrig, Jack W Shteamer, Inna A Belyantseva, Meghan C Drummond, Tracy S Fitzgerald, Sarath Vijayakumar, Sherri M Jones, Andrew J Griffith, Thomas B Friedman, Lisa L Cunningham,[...]. Mol Ther 2017
94
35

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
87
35

AAV2.7m8 is a powerful viral vector for inner ear gene therapy.
Kevin Isgrig, Devin S McDougald, Jianliang Zhu, Hong Jun Wang, Jean Bennett, Wade W Chien. Nat Commun 2019
63
35

Identification of Adeno-Associated Viral Vectors That Target Neonatal and Adult Mammalian Inner Ear Cell Subtypes.
Yilai Shu, Yong Tao, Zhengmin Wang, Yong Tang, Huawei Li, Pu Dai, Guangping Gao, Zheng-Yi Chen. Hum Gene Ther 2016
52
35

Gene editing in a Myo6 semi-dominant mouse model rescues auditory function.
Yuanyuan Xue, Xinde Hu, Daqi Wang, Di Li, Yige Li, Fang Wang, Mingqian Huang, Xi Gu, Zhijiao Xu, Jinan Zhou,[...]. Mol Ther 2022
6
83

Cationic lipid-mediated delivery of proteins enables efficient protein-based genome editing in vitro and in vivo.
John A Zuris, David B Thompson, Yilai Shu, John P Guilinger, Jeffrey L Bessen, Johnny H Hu, Morgan L Maeder, J Keith Joung, Zheng-Yi Chen, David R Liu. Nat Biotechnol 2015
831
28

Screened AAV variants permit efficient transduction access to supporting cells and hair cells.
Xinde Hu, Jinghan Wang, Xuan Yao, Qingquan Xiao, Yuanyuan Xue, Shaoran Wang, Linyu Shi, Yilai Shu, Huawei Li, Hui Yang. Cell Discov 2019
10
40

In vivo base editing restores sensory transduction and transiently improves auditory function in a mouse model of recessive deafness.
Wei-Hsi Yeh, Olga Shubina-Oleinik, Jonathan M Levy, Bifeng Pan, Gregory A Newby, Michael Wornow, Rachel Burt, Jonathan C Chen, Jeffrey R Holt, David R Liu. Sci Transl Med 2020
63
28

Virally mediated Kcnq1 gene replacement therapy in the immature scala media restores hearing in a mouse model of human Jervell and Lange-Nielsen deafness syndrome.
Qing Chang, Jianjun Wang, Qi Li, Yeunjung Kim, Binfei Zhou, Yunfeng Wang, Huawei Li, Xi Lin. EMBO Mol Med 2015
64
28

Neonatal AAV gene therapy rescues hearing in a mouse model of SYNE4 deafness.
Shahar Taiber, Roie Cohen, Ofer Yizhar-Barnea, David Sprinzak, Jeffrey R Holt, Karen B Avraham. EMBO Mol Med 2021
12
33

Improved TMC1 gene therapy restores hearing and balance in mice with genetic inner ear disorders.
Carl A Nist-Lund, Bifeng Pan, Amy Patterson, Yukako Asai, Tianwen Chen, Wu Zhou, Hong Zhu, Sandra Romero, Jennifer Resnik, Daniel B Polley,[...]. Nat Commun 2019
68
28

Gene Transfer with AAV9-PHP.B Rescues Hearing in a Mouse Model of Usher Syndrome 3A and Transduces Hair Cells in a Non-human Primate.
Bence György, Elise J Meijer, Maryna V Ivanchenko, Kelly Tenneson, Frederick Emond, Killian S Hanlon, Artur A Indzhykulian, Adrienn Volak, K Domenica Karavitaki, Panos I Tamvakologos,[...]. Mol Ther Methods Clin Dev 2018
75
28

Single and Dual Vector Gene Therapy with AAV9-PHP.B Rescues Hearing in Tmc1 Mutant Mice.
Jason Wu, Paola Solanes, Carl Nist-Lund, Sofia Spataro, Olga Shubina-Oleinik, Irina Marcovich, Hannah Goldberg, Bernard L Schneider, Jeffrey R Holt. Mol Ther 2021
16
28

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
63
28

Cochlear gene therapy with ancestral AAV in adult mice: complete transduction of inner hair cells without cochlear dysfunction.
Jun Suzuki, Ken Hashimoto, Ru Xiao, Luk H Vandenberghe, M Charles Liberman. Sci Rep 2017
103
28

Local gene therapy durably restores vestibular function in a mouse model of Usher syndrome type 1G.
Alice Emptoz, Vincent Michel, Andrea Lelli, Omar Akil, Jacques Boutet de Monvel, Ghizlene Lahlou, Anaïs Meyer, Typhaine Dupont, Sylvie Nouaille, Elody Ey,[...]. Proc Natl Acad Sci U S A 2017
67
21

Gene Therapy Restores Hair Cell Stereocilia Morphology in Inner Ears of Deaf Whirler Mice.
Wade W Chien, Kevin Isgrig, Soumen Roy, Inna A Belyantseva, Meghan C Drummond, Lindsey A May, Tracy S Fitzgerald, Thomas B Friedman, Lisa L Cunningham. Mol Ther 2016
58
21


Clarin-1 gene transfer rescues auditory synaptopathy in model of Usher syndrome.
Didier Dulon, Samantha Papal, Pranav Patni, Matteo Cortese, Philippe Fy Vincent, Margot Tertrais, Alice Emptoz, Abdelaziz Tlili, Yohan Bouleau, Vincent Michel,[...]. J Clin Invest 2018
60
21

Delivery of therapeutics to the inner ear: The challenge of the blood-labyrinth barrier.
Sophie Nyberg, N Joan Abbott, Xiaorui Shi, Peter S Steyger, Alain Dabdoub. Sci Transl Med 2019
99
21

Search-and-replace genome editing without double-strand breaks or donor DNA.
Andrew V Anzalone, Peyton B Randolph, Jessie R Davis, Alexander A Sousa, Luke W Koblan, Jonathan M Levy, Peter J Chen, Christopher Wilson, Gregory A Newby, Aditya Raguram,[...]. Nature 2019
21

Perinatal Gjb2 gene transfer rescues hearing in a mouse model of hereditary deafness.
Takashi Iizuka, Kazusaku Kamiya, Satoru Gotoh, Yoshinobu Sugitani, Masaaki Suzuki, Tetsuo Noda, Osamu Minowa, Katsuhisa Ikeda. Hum Mol Genet 2015
51
21

Advances and challenges in adeno-associated viral inner-ear gene therapy for sensorineural hearing loss.
Kamakshi Bankoti, Charles Generotti, Tiffany Hwa, Lili Wang, Bert W O'Malley, Daqing Li. Mol Ther Methods Clin Dev 2021
7
42

Adeno-associated virus-mediated gene delivery into the scala media of the normal and deafened adult mouse ear.
L A Kilpatrick, Q Li, J Yang, J C Goddard, D M Fekete, H Lang. Gene Ther 2011
71
21

AAV-ie enables safe and efficient gene transfer to inner ear cells.
Fangzhi Tan, Cenfeng Chu, Jieyu Qi, Wenyan Li, Dan You, Ke Li, Xin Chen, Weidong Zhao, Cheng Cheng, Xiaoyi Liu,[...]. Nat Commun 2019
86
21

Efficient viral transduction in mouse inner ear hair cells with utricle injection and AAV9-PHP.B.
John Lee, Carl Nist-Lund, Paola Solanes, Hannah Goldberg, Jason Wu, Bifeng Pan, Bernard L Schneider, Jeffrey R Holt. Hear Res 2020
32
21

Phenotypic and expression analysis of a novel spontaneous myosin VI null mutant mouse.
Eiji Mochizuki, Kazuhiro Okumura, Masashi Ishikawa, Sachi Yoshimoto, Junya Yamaguchi, Yuta Seki, Kenta Wada, Michinari Yokohama, Tatsuo Ushiki, Hisashi Tokano,[...]. Exp Anim 2010
11
18

A novel nonsense mutation in MYO6 is associated with progressive nonsyndromic hearing loss in a Danish DFNA22 family.
Kirsten M Sanggaard, Klaus W Kjaer, Hans Eiberg, Gudrun Nürnberg, Peter Nürnberg, Katrin Hoffman, Hanne Jensen, Charlotte Sørum, Nanna D Rendtorff, Lisbeth Tranebjaerg. Am J Med Genet A 2008
33
14

A humanized mouse model, demonstrating progressive hearing loss caused by MYO6 p.C442Y, is inherited in a semi-dominant pattern.
Jinghan Wang, Jun Shen, Luo Guo, Cheng Cheng, Renjie Chai, Yilai Shu, Huawei Li. Hear Res 2019
7
28

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
155
14

RNA Interference Prevents Autosomal-Dominant Hearing Loss.
Seiji B Shibata, Paul T Ranum, Hideaki Moteki, Bifeng Pan, Alexander T Goodwin, Shawn S Goodman, Paul J Abbas, Jeffrey R Holt, Richard J H Smith. Am J Hum Genet 2016
64
14


Unconventional myosins in inner-ear sensory epithelia.
T Hasson, P G Gillespie, J A Garcia, R B MacDonald, Y Zhao, A G Yee, M S Mooseker, D P Corey. J Cell Biol 1997
427
14

Evoked Potentials Reveal Noise Exposure-Related Central Auditory Changes Despite Normal Audiograms.
Naomi F Bramhall, Christopher E Niemczak, Sean D Kampel, Curtis J Billings, Garnett P McMillan. Am J Audiol 2020
11
18

Rescue of hearing and vestibular function by antisense oligonucleotides in a mouse model of human deafness.
Jennifer J Lentz, Francine M Jodelka, Anthony J Hinrich, Kate E McCaffrey, Hamilton E Farris, Matthew J Spalitta, Nicolas G Bazan, Dominik M Duelli, Frank Rigo, Michelle L Hastings. Nat Med 2013
139
14

Development of the ear and hearing.
J W Hall. J Perinatol 2000
48
14


Functional alteration of ribbon synapses in inner hair cells by noise exposure causing hidden hearing loss.
Huihui Liu, Jiawen Lu, Zhongying Wang, Lei Song, Xueling Wang, Geng-Lin Li, Hao Wu. Neurosci Lett 2019
20
14


Mutations of MYO6 are associated with recessive deafness, DFNB37.
Zubair M Ahmed, Robert J Morell, Saima Riazuddin, Andrea Gropman, Shahzad Shaukat, Mussaber M Ahmad, Saidi A Mohiddin, Lameh Fananapazir, Rafael C Caruso, Tayyab Husnain,[...]. Am J Hum Genet 2003
134
14

MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing loss.
S Melchionda, N Ahituv, L Bisceglia, T Sobe, F Glaser, R Rabionet, M L Arbones, A Notarangelo, E Di Iorio, M Carella,[...]. Am J Hum Genet 2001
169
14

Targeted Allele Suppression Prevents Progressive Hearing Loss in the Mature Murine Model of Human TMC1 Deafness.
Hidekane Yoshimura, Seiji B Shibata, Paul T Ranum, Hideaki Moteki, Richard J H Smith. Mol Ther 2019
39
14

Direct Delivery of Antisense Oligonucleotides to the Middle and Inner Ear Improves Hearing and Balance in Usher Mice.
Jennifer J Lentz, Bifeng Pan, Abhilash Ponnath, Christopher M Tran, Carl Nist-Lund, Alice Galvin, Hannah Goldberg, Katelyn N Robillard, Francine M Jodelka, Hamilton E Farris,[...]. Mol Ther 2020
14
14

In vivo base editing of post-mitotic sensory cells.
Wei-Hsi Yeh, Hao Chiang, Holly A Rees, Albert S B Edge, David R Liu. Nat Commun 2018
115
14

In Silico Reconstruction of the Viral Evolutionary Lineage Yields a Potent Gene Therapy Vector.
Eric Zinn, Simon Pacouret, Vadim Khaychuk, Heikki T Turunen, Livia S Carvalho, Eva Andres-Mateos, Samiksha Shah, Rajani Shelke, Anna C Maurer, Eva Plovie,[...]. Cell Rep 2015
187
14


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.