A citation-based method for searching scientific literature

Nicolas Michalski, Christine Petit. Hum Genet 2022
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Hypertension and cochlear hearing loss.
Tomasz Przewoźny, Anna Gójska-Grymajło, Mariusz Kwarciany, Dariusz Gąsecki, Krzysztof Narkiewicz. Blood Press 2015
29
33

Pharmacological Prevention of Noise-induced Hearing Loss: A Systematic Review.
Avigeet Gupta, Sina Koochakzadeh, Shaun A Nguyen, Emily A Brennan, Ted A Meyer, Paul R Lambert. Otol Neurotol 2021
6
33

NLRP3 mutation and cochlear autoinflammation cause syndromic and nonsyndromic hearing loss DFNA34 responsive to anakinra therapy.
Hiroshi Nakanishi, Yoshiyuki Kawashima, Kiyoto Kurima, Jae Jin Chae, Astin M Ross, Gineth Pinto-Patarroyo, Seema K Patel, Julie A Muskett, Jessica S Ratay, Parna Chattaraj,[...]. Proc Natl Acad Sci U S A 2017
75
33

Familial aggregation of pure tone hearing thresholds in an aging European population.
Jan-Jaap Hendrickx, Jeroen R Huyghe, Vedat Topsakal, Kelly Demeester, Thomas F Wienker, Lut Van Laer, Els Van Eyken, Erik Fransen, Elina Mäki-Torkko, Samuli Hannula,[...]. Otol Neurotol 2013
12
33

Otological aspects of NLRP3-related autoinflammatory disorder focusing on the responsiveness to anakinra.
Bong Jik Kim, Young Ho Kim, Seungmin Lee, Jin Hee Han, Sang-Yeon Lee, Jeon Seong, Dong-Han Lee, Bonggi Kim, Hye-Rim Park, Marge Carandang,[...]. Rheumatology (Oxford) 2021
11
33

Genomic Landscape and Mutational Signatures of Deafness-Associated Genes.
Hela Azaiez, Kevin T Booth, Sean S Ephraim, Bradley Crone, Elizabeth A Black-Ziegelbein, Robert J Marini, A Eliot Shearer, Christina M Sloan-Heggen, Diana Kolbe, Thomas Casavant,[...]. Am J Hum Genet 2018
120
33

PRPS1 loss-of-function variants, from isolated hearing loss to severe congenital encephalopathy: New cases and literature review.
Oriane Mercati, Marie-Thérèse Abi Warde, Geneviève Lina-Granade, Marlène Rio, Solveig Heide, Pascale de Lonlay, Irène Ceballos-Picot, Matthieu P Robert, Vincent Couloigner, Jacques Beltrand,[...]. Eur J Med Genet 2020
6
33

Heritability of hearing loss.
Ellen Kvestad, Nikolai Czajkowski, Norun Hjertager Krog, Bo Engdahl, Kristian Tambs. Epidemiology 2012
31
33

PRPS1 mutations: four distinct syndromes and potential treatment.
Arjan P M de Brouwer, Hans van Bokhoven, Sander B Nabuurs, Willem Frans Arts, John Christodoulou, John Duley. Am J Hum Genet 2010
68
33

The Post-GWAS Era: From Association to Function.
Michael D Gallagher, Alice S Chen-Plotkin. Am J Hum Genet 2018
319
33



Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss.
Christina M Sloan-Heggen, Amanda O Bierer, A Eliot Shearer, Diana L Kolbe, Carla J Nishimura, Kathy L Frees, Sean S Ephraim, Seiji B Shibata, Kevin T Booth, Colleen A Campbell,[...]. Hum Genet 2016
258
33

Heritability of Age-Related Hearing Loss in Middle-Aged and Elderly Chinese: A Population-Based Twin Study.
Haiping Duan, Dongfeng Zhang, Yajun Liang, Chunsheng Xu, Yili Wu, Xiaocao Tian, Zengchang Pang, Qihua Tan, Shuxia Li, Chengxuan Qiu. Ear Hear 2019
12
33

Nucleus Hybrid S12: Multicenter Clinical Trial Results.
Camille C Dunn, Jacob Oleson, Aaron Parkinson, Marlan R Hansen, Bruce J Gantz. Laryngoscope 2020
10
33

The noncoding genome and hearing loss.
Karen B Avraham, Lama Khalaily, Yael Noy, Lara Kamal, Tal Koffler-Brill, Shahar Taiber. Hum Genet 2022
1
100

AudioGene: refining the natural history of KCNQ4, GSDME, WFS1, and COCH-associated hearing loss.
Ryan K Thorpe, W Daniel Walls, Rae Corrigan, Amanda Schaefer, Kai Wang, Patrick Huygen, Thomas L Casavant, Richard J H Smith. Hum Genet 2022
3
33

Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment.
Andries Paul Nagtegaal, Linda Broer, Nuno R Zilhao, Johanna Jakobsdottir, Charles E Bishop, Marco Brumat, Mark W Christiansen, Massimiliano Cocca, Yan Gao, Nancy L Heard-Costa,[...]. Sci Rep 2019
17
33

Is type 2 diabetes mellitus associated with alterations in hearing? A systematic review and meta-analysis.
Olubunmi V Akinpelu, Mario Mujica-Mota, Sam J Daniel. Laryngoscope 2014
68
33


Gene Therapy for Human Sensorineural Hearing Loss.
Yin Ren, Lukas D Landegger, Konstantina M Stankovic. Front Cell Neurosci 2019
36
33

American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss.
Raye L Alford, Kathleen S Arnos, Michelle Fox, Jerry W Lin, Christina G Palmer, Arti Pandya, Heidi L Rehm, Nathaniel H Robin, Daryl A Scott, Christine Yoshinaga-Itano. Genet Med 2014
129
33


Viral vectors for gene delivery to the inner ear.
Casey A Maguire, David P Corey. Hear Res 2020
14
33

Comprehensive genetic testing for hereditary hearing loss using massively parallel sequencing.
A Eliot Shearer, Adam P DeLuca, Michael S Hildebrand, Kyle R Taylor, José Gurrola, Steve Scherer, Todd E Scheetz, Richard J H Smith. Proc Natl Acad Sci U S A 2010
217
33

International Pediatric Otolaryngology Group (IPOG) consensus recommendations: Hearing loss in the pediatric patient.
Bryan J Liming, John Carter, Alan Cheng, Daniel Choo, John Curotta, Daniela Carvalho, John A Germiller, Stephen Hone, Margaret A Kenna, Natalie Loundon,[...]. Int J Pediatr Otorhinolaryngol 2016
57
33

Gene therapy for hearing loss.
Ryotaro Omichi, Seiji B Shibata, Cynthia C Morton, Richard J H Smith. Hum Mol Genet 2019
40
33

GWAS Identifies 44 Independent Associated Genomic Loci for Self-Reported Adult Hearing Difficulty in UK Biobank.
Helena R R Wells, Maxim B Freidin, Fatin N Zainul Abidin, Antony Payton, Piers Dawes, Kevin J Munro, Cynthia C Morton, David R Moore, Sally J Dawson, Frances M K Williams. Am J Hum Genet 2019
54
33

Human induced pluripotent stem cells and CRISPR/Cas-mediated targeted genome editing: Platforms to tackle sensorineural hearing loss.
Miodrag Stojkovic, Dongjun Han, Minjin Jeong, Petra Stojkovic, Konstantina M Stankovic. Stem Cells 2021
12
33

Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness.
T R Prezant, J V Agapian, M C Bohlman, X Bu, S Oztas, W Q Qiu, K S Arnos, G A Cortopassi, L Jaber, J I Rotter. Nat Genet 1993
885
33

Generation of inner ear hair cells by direct lineage conversion of primary somatic cells.
Louise Menendez, Talon Trecek, Suhasni Gopalakrishnan, Litao Tao, Alexander L Markowitz, Haoze V Yu, Xizi Wang, Juan Llamas, Chichou Huang, James Lee,[...]. Elife 2020
31
33

KChIPs and Kv4 alpha subunits as integral components of A-type potassium channels in mammalian brain.
Kenneth J Rhodes, Karen I Carroll, M Amy Sung, Lisa C Doliveira, Michael M Monaghan, Sharon L Burke, Brian W Strassle, Lynn Buchwalder, Milena Menegola, Jie Cao,[...]. J Neurosci 2004
203
33

Biochemical Evidence for a Nuclear Modifier Allele (A10S) in TRMU (Methylaminomethyl-2-thiouridylate-methyltransferase) Related to Mitochondrial tRNA Modification in the Phenotypic Manifestation of Deafness-associated 12S rRNA Mutation.
Feilong Meng, Xiaohui Cang, Yanyan Peng, Ronghua Li, Zhengyue Zhang, Fushan Li, Qingqing Fan, Anna S Guan, Nathan Fischel-Ghosian, Xiaoli Zhao,[...]. J Biol Chem 2017
36
33

Metabolic plasticity in stem cell homeostasis and differentiation.
Clifford D L Folmes, Petras P Dzeja, Timothy J Nelson, Andre Terzic. Cell Stem Cell 2012
424
33

Cellular Metabolism and Induced Pluripotency.
Jun Wu, Alejandro Ocampo, Juan Carlos Izpisua Belmonte. Cell 2016
87
33

Genetics of Childhood Hearing Loss.
Calli Ober Mitchell, Cynthia Casson Morton. Otolaryngol Clin North Am 2021
3
33

Global hearing health care: new findings and perspectives.
Blake S Wilson, Debara L Tucci, Michael H Merson, Gerard M O'Donoghue. Lancet 2017
257
33


Functional characterization of the mitochondrial 12S rRNA C1494T mutation associated with aminoglycoside-induced and non-syndromic hearing loss.
Hui Zhao, Wie-Yen Young, Qingfeng Yan, Ronghua Li, Juyang Cao, Qiuju Wang, Xiaoming Li, Jennifer L Peters, Dongyi Han, Min-Xin Guan. Nucleic Acids Res 2005
70
33

Contribution of the tRNAIle 4317A→G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A→G mutation.
Feilong Meng, Zheyun He, Xiaowen Tang, Jing Zheng, Xiaofen Jin, Yi Zhu, Xiaoyan Ren, Mi Zhou, Meng Wang, Shasha Gong,[...]. J Biol Chem 2018
25
33

Reprogramming LCLs to iPSCs Results in Recovery of Donor-Specific Gene Expression Signature.
Samantha M Thomas, Courtney Kagan, Bryan J Pavlovic, Jonathan Burnett, Kristen Patterson, Jonathan K Pritchard, Yoav Gilad. PLoS Genet 2015
23
33


An efficient nonviral method to generate integration-free human-induced pluripotent stem cells from cord blood and peripheral blood cells.
Keisuke Okita, Tatsuya Yamakawa, Yasuko Matsumura, Yoshiko Sato, Naoki Amano, Akira Watanabe, Naoki Goshima, Shinya Yamanaka. Stem Cells 2013
457
33

A more efficient method to generate integration-free human iPS cells.
Keisuke Okita, Yasuko Matsumura, Yoshiko Sato, Aki Okada, Asuka Morizane, Satoshi Okamoto, Hyenjong Hong, Masato Nakagawa, Koji Tanabe, Ken-ichi Tezuka,[...]. Nat Methods 2011
33

Structural basis of gating modulation of Kv4 channel complexes.
Yoshiaki Kise, Go Kasuya, Hiroyuki H Okamoto, Daichi Yamanouchi, Kan Kobayashi, Tsukasa Kusakizako, Tomohiro Nishizawa, Koichi Nakajo, Osamu Nureki. Nature 2021
14
33

Complex I mutations synergize to worsen the phenotypic expression of Leber's hereditary optic neuropathy.
Yanchun Ji, Juanjuan Zhang, Yuanyuan Lu, Qiuzi Yi, Mengquan Chen, Shipeng Xie, Xiaoting Mao, Yun Xiao, Feilong Meng, Minglian Zhang,[...]. J Biol Chem 2020
14
33


Genetic Correction of Induced Pluripotent Stem Cells From a Deaf Patient With MYO7A Mutation Results in Morphologic and Functional Recovery of the Derived Hair Cell-Like Cells.
Zi-Hua Tang, Jia-Rong Chen, Jing Zheng, Hao-Song Shi, Jie Ding, Xiao-Dan Qian, Cui Zhang, Jian-Ling Chen, Cui-Cui Wang, Liang Li,[...]. Stem Cells Transl Med 2016
47
33

Molecular architecture of the chick vestibular hair bundle.
Jung-Bum Shin, Jocelyn F Krey, Ahmed Hassan, Zoltan Metlagel, Andrew N Tauscher, James M Pagana, Nicholas E Sherman, Erin D Jeffery, Kateri J Spinelli, Hongyu Zhao,[...]. Nat Neurosci 2013
121
33

Genome-scale CRISPR-Cas9 knockout screening in human cells.
Ophir Shalem, Neville E Sanjana, Ella Hartenian, Xi Shi, David A Scott, Tarjei Mikkelson, Dirk Heckl, Benjamin L Ebert, David E Root, John G Doench,[...]. Science 2014
33


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.