A citation-based method for searching scientific literature

Zi-Bing Jin, Zhongshan Li, Zhenwei Liu, Yi Jiang, Xue-Bi Cai, Jinyu Wu. Biol Rev Camb Philos Soc 2018
Times Cited: 17







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



Times Cited
  Times     Co-cited
Similarity


Genotype-phenotype correlation and mutation spectrum in a large cohort of patients with inherited retinal dystrophy revealed by next-generation sequencing.
Xiu-Feng Huang, Fang Huang, Kun-Chao Wu, Juan Wu, Jie Chen, Chi-Pui Pang, Fan Lu, Jia Qu, Zi-Bing Jin. Genet Med 2015
122
35

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
29

Trio-based exome sequencing arrests de novo mutations in early-onset high myopia.
Zi-Bing Jin, Jinyu Wu, Xiu-Feng Huang, Chun-Yun Feng, Xue-Bi Cai, Jian-Yang Mao, Lue Xiang, Kun-Chao Wu, Xueshan Xiao, Bethany A Kloss,[...]. Proc Natl Acad Sci U S A 2017
36
23

Genome-Wide Detection of Copy Number Variations in Unsolved Inherited Retinal Disease.
Xiu-Feng Huang, Jian-Yang Mao, Zhi-Qin Huang, Feng-Qin Rao, Fei-Fei Cheng, Fen-Fen Li, Qing-Feng Wang, Zi-Bing Jin. Invest Ophthalmol Vis Sci 2017
20
23

A framework for the interpretation of de novo mutation in human disease.
Kaitlin E Samocha, Elise B Robinson, Stephan J Sanders, Christine Stevens, Aniko Sabo, Lauren M McGrath, Jack A Kosmicki, Karola Rehnström, Swapan Mallick, Andrew Kirby,[...]. Nat Genet 2014
526
17


Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
17

mirTrios: an integrated pipeline for detection of de novo and rare inherited mutations from trios-based next-generation sequencing.
Jinchen Li, Yi Jiang, Tao Wang, Huiqian Chen, Qing Xie, Qianzhi Shao, Xia Ran, Kun Xia, Zhong Sheng Sun, Jinyu Wu. J Med Genet 2015
22
17


A method and server for predicting damaging missense mutations.
Ivan A Adzhubei, Steffen Schmidt, Leonid Peshkin, Vasily E Ramensky, Anna Gerasimova, Peer Bork, Alexey S Kondrashov, Shamil R Sunyaev. Nat Methods 2010
17

The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.
Aaron McKenna, Matthew Hanna, Eric Banks, Andrey Sivachenko, Kristian Cibulskis, Andrew Kernytsky, Kiran Garimella, David Altshuler, Stacey Gabriel, Mark Daly,[...]. Genome Res 2010
17

Retinitis pigmentosa.
Dyonne T Hartong, Eliot L Berson, Thaddeus P Dryja. Lancet 2006
17

Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
17

The next-generation sequencing revolution and its impact on genomics.
Daniel C Koboldt, Karyn Meltz Steinberg, David E Larson, Richard K Wilson, Elaine R Mardis. Cell 2013
552
17

Parental influence on human germline de novo mutations in 1,548 trios from Iceland.
Hákon Jónsson, Patrick Sulem, Birte Kehr, Snaedis Kristmundsdottir, Florian Zink, Eirikur Hjartarson, Marteinn T Hardarson, Kristjan E Hjorleifsson, Hannes P Eggertsson, Sigurjon Axel Gudjonsson,[...]. Nature 2017
151
17

Mutation spectrum and genotype-phenotype correlation of inherited retinal dystrophy in Taiwan.
Zhen-Ji Chen, Keng-Hung Lin, Shi-Huang Lee, Ren-Juan Shen, Zhuo-Kun Feng, Xiao-Fang Wang, Xiu-Feng Huang, Zhi-Qin Huang, Zi-Bing Jin. Clin Exp Ophthalmol 2020
7
42

Rate of de novo mutations and the importance of father's age to disease risk.
Augustine Kong, Michael L Frigge, Gisli Masson, Soren Besenbacher, Patrick Sulem, Gisli Magnusson, Sigurjon A Gudjonsson, Asgeir Sigurdsson, Aslaug Jonasdottir, Adalbjorg Jonasdottir,[...]. Nature 2012
11

Whole-genome sequencing in autism identifies hot spots for de novo germline mutation.
Jacob J Michaelson, Yujian Shi, Madhusudan Gujral, Hancheng Zheng, Dheeraj Malhotra, Xin Jin, Minghan Jian, Guangming Liu, Douglas Greer, Abhishek Bhandari,[...]. Cell 2012
334
11

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010
11


The contribution of de novo coding mutations to autism spectrum disorder.
Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A Stessman, Kali T Witherspoon, Laura Vives, Karynne E Patterson,[...]. Nature 2014
11

MutationTaster evaluates disease-causing potential of sequence alterations.
Jana Marie Schwarz, Christian Rödelsperger, Markus Schuelke, Dominik Seelow. Nat Methods 2010
11

Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes.
Xin He, Stephan J Sanders, Li Liu, Silvia De Rubeis, Elaine T Lim, James S Sutcliffe, Gerard D Schellenberg, Richard A Gibbs, Mark J Daly, Joseph D Buxbaum,[...]. PLoS Genet 2013
133
11

The Sequence Alignment/Map format and SAMtools.
Heng Li, Bob Handsaker, Alec Wysoker, Tim Fennell, Jue Ruan, Nils Homer, Gabor Marth, Goncalo Abecasis, Richard Durbin. Bioinformatics 2009
11

Whole-genome sequencing of quartet families with autism spectrum disorder.
Ryan K C Yuen, Bhooma Thiruvahindrapuram, Daniele Merico, Susan Walker, Kristiina Tammimies, Ny Hoang, Christina Chrysler, Thomas Nalpathamkalam, Giovanna Pellecchia, Yi Liu,[...]. Nat Med 2015
300
11

miR-183/96 plays a pivotal regulatory role in mouse photoreceptor maturation and maintenance.
Lue Xiang, Xue-Jiao Chen, Kun-Chao Wu, Chang-Jun Zhang, Gao-Hui Zhou, Ji-Neng Lv, Lan-Fang Sun, Fei-Fei Cheng, Xue-Bi Cai, Zi-Bing Jin. Proc Natl Acad Sci U S A 2017
43
11

'RetinoGenetics': a comprehensive mutation database for genes related to inherited retinal degeneration.
Xia Ran, Wei-Jun Cai, Xiu-Feng Huang, Qi Liu, Fan Lu, Jia Qu, Jinyu Wu, Zi-Bing Jin. Database (Oxford) 2014
41
11

Non-syndromic retinitis pigmentosa.
Sanne K Verbakel, Ramon A C van Huet, Camiel J F Boon, Anneke I den Hollander, Rob W J Collin, Caroline C W Klaver, Carel B Hoyng, Ronald Roepman, B Jeroen Klevering. Prog Retin Eye Res 2018
233
11

Next generation sequencing-based molecular diagnosis of retinitis pigmentosa: identification of a novel genotype-phenotype correlation and clinical refinements.
Feng Wang, Hui Wang, Han-Fang Tuan, Duy H Nguyen, Vincent Sun, Vafa Keser, Sara J Bowne, Lori S Sullivan, Hongrong Luo, Ling Zhao,[...]. Hum Genet 2014
158
11


Gene Correction Reverses Ciliopathy and Photoreceptor Loss in iPSC-Derived Retinal Organoids from Retinitis Pigmentosa Patients.
Wen-Li Deng, Mei-Ling Gao, Xin-Lan Lei, Ji-Neng Lv, Huan Zhao, Kai-Wen He, Xi-Xi Xia, Ling-Yun Li, Yu-Chen Chen, Yan-Ping Li,[...]. Stem Cell Reports 2018
94
11

SLC7A14 linked to autosomal recessive retinitis pigmentosa.
Zi-Bing Jin, Xiu-Feng Huang, Ji-Neng Lv, Lue Xiang, Dong-Qing Li, Jiangfei Chen, Changjiang Huang, Jinyu Wu, Fan Lu, Jia Qu. Nat Commun 2014
54
11

Epilepsy and synaptic proteins.
Yuko Fukata, Masaki Fukata. Curr Opin Neurobiol 2017
36
11

The genetic landscape of the epileptic encephalopathies of infancy and childhood.
Amy McTague, Katherine B Howell, J Helen Cross, Manju A Kurian, Ingrid E Scheffer. Lancet Neurol 2016
258
11

De novo mutations in human genetic disease.
Joris A Veltman, Han G Brunner. Nat Rev Genet 2012
450
11

ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology.
Ingrid E Scheffer, Samuel Berkovic, Giuseppe Capovilla, Mary B Connolly, Jacqueline French, Laura Guilhoto, Edouard Hirsch, Satish Jain, Gary W Mathern, Solomon L Moshé,[...]. Epilepsia 2017
11

Expanding the Phenotypic and Genotypic Landscape of Nonsyndromic High Myopia: A Cross-Sectional Study in 731 Chinese Patients.
Xue-Bi Cai, Yi-Han Zheng, De-Fu Chen, Fang-Yue Zhou, Lu-Qi Xia, Xin-Ran Wen, Yi-Min Yuan, Fang Han, Shun-Yu Piao, Wenjuan Zhuang,[...]. Invest Ophthalmol Vis Sci 2019
9
22

Standards and Guidelines for the Interpretation and Reporting of Sequence Variants in Cancer: A Joint Consensus Recommendation of the Association for Molecular Pathology, American Society of Clinical Oncology, and College of American Pathologists.
Marilyn M Li, Michael Datto, Eric J Duncavage, Shashikant Kulkarni, Neal I Lindeman, Somak Roy, Apostolia M Tsimberidou, Cindy L Vnencak-Jones, Daynna J Wolff, Anas Younes,[...]. J Mol Diagn 2017
590
11


The Third Revolution in Sequencing Technology.
Erwin L van Dijk, Yan Jaszczyszyn, Delphine Naquin, Claude Thermes. Trends Genet 2018
275
11

Analysis of genetic inheritance in a family quartet by whole-genome sequencing.
Jared C Roach, Gustavo Glusman, Arian F A Smit, Chad D Huff, Robert Hubley, Paul T Shannon, Lee Rowen, Krishna P Pant, Nathan Goodman, Michael Bamshad,[...]. Science 2010
688
11

Clinical application of next-generation sequencing to the practice of neurology.
Jessica Rexach, Hane Lee, Julian A Martinez-Agosto, Andrea H Németh, Brent L Fogel. Lancet Neurol 2019
30
11

A global reference for human genetic variation.
Adam Auton, Lisa D Brooks, Richard M Durbin, Erik P Garrison, Hyun Min Kang, Jan O Korbel, Jonathan L Marchini, Shane McCarthy, Gil A McVean, Gonçalo R Abecasis. Nature 2015
11

De Novo Mutations Reflect Development and Aging of the Human Germline.
J M Goldmann, J A Veltman, C Gilissen. Trends Genet 2019
23
11

Somatic and gonadal mosaicism in X-linked retinitis pigmentosa.
Zi-Bing Jin, Feng Gu, Hirokazu Matsuda, Nobuhiro Yukawa, Xu Ma, Nobuhisa Nao-i. Am J Med Genet A 2007
17
11

Comprehensive molecular diagnosis of Bardet-Biedl syndrome by high-throughput targeted exome sequencing.
Dong-Jun Xing, Hong-Xing Zhang, Na Huang, Kun-Chao Wu, Xiu-Feng Huang, Fang Huang, Yi Tong, Chi-Pui Pang, Jia Qu, Zi-Bing Jin. PLoS One 2014
18
11


Genetics of Nonsyndromic Craniosynostosis.
Andrew T Timberlake, John A Persing. Plast Reconstr Surg 2018
21
5

De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus.
Charuta Gavankar Furey, Jungmin Choi, Sheng Chih Jin, Xue Zeng, Andrew T Timberlake, Carol Nelson-Williams, M Shahid Mansuri, Qiongshi Lu, Daniel Duran, Shreyas Panchagnula,[...]. Neuron 2018
51
5

Infantile hydrocephalus: a review of epidemiology, classification and causes.
Hannah M Tully, William B Dobyns. Eur J Med Genet 2014
113
5


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.