A citation-based method for searching scientific literature

Jia Chen, Jiaqi Liu, Yangzhong Zhou, Sen Liu, Gang Liu, Yuzhi Zuo, Zhihong Wu, Nan Wu, Guixing Qiu. J Mol Med (Berl) 2017
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


ZFN, TALEN, and CRISPR/Cas-based methods for genome engineering.
Thomas Gaj, Charles A Gersbach, Carlos F Barbas. Trends Biotechnol 2013
50

Efficient genome editing in zebrafish using a CRISPR-Cas system.
Woong Y Hwang, Yanfang Fu, Deepak Reyon, Morgan L Maeder, Shengdar Q Tsai, Jeffry D Sander, Randall T Peterson, J-R Joanna Yeh, J Keith Joung. Nat Biotechnol 2013
50



The zebrafish reference genome sequence and its relationship to the human genome.
Kerstin Howe, Matthew D Clark, Carlos F Torroja, James Torrance, Camille Berthelot, Matthieu Muffato, John E Collins, Sean Humphray, Karen McLaren, Lucy Matthews,[...]. Nature 2013
50

Chloride channel ClCN7 mutations are responsible for severe recessive, dominant, and intermediate osteopetrosis.
Annalisa Frattini, Alessandra Pangrazio, Lucia Susani, Cristina Sobacchi, Massimiliano Mirolo, Mario Abinun, Marino Andolina, Adrienne Flanagan, Edwin M Horwitz, Ercan Mihci,[...]. J Bone Miner Res 2003
163
50

Adolescent idiopathic scoliosis.
Jack C Cheng, René M Castelein, Winnie C Chu, Aina J Danielsson, Matthew B Dobbs, Theodoros B Grivas, Christina A Gurnett, Keith D Luk, Alain Moreau, Peter O Newton,[...]. Nat Rev Dis Primers 2015
149
50

Hajdu-Cheney syndrome with severe dural ectasia.
Kristiina Avela, Leena Valanne, Ilkka Helenius, Outi Mäkitie. Am J Med Genet A 2011
25
50

TBX6 compound inheritance leads to congenital vertebral malformations in humans and mice.
Nan Yang, Nan Wu, Ling Zhang, Yanxue Zhao, Jiaqi Liu, Xiangyu Liang, Xiaojun Ren, Weiyu Li, Weisheng Chen, Shuangshuang Dong,[...]. Hum Mol Genet 2019
27
50

Engineering of CRISPR-Cas12b for human genome editing.
Jonathan Strecker, Sara Jones, Balwina Koopal, Jonathan Schmid-Burgk, Bernd Zetsche, Linyi Gao, Kira S Makarova, Eugene V Koonin, Feng Zhang. Nat Commun 2019
87
50



The Sry-related gene Sox9 is expressed during chondrogenesis in mouse embryos.
E Wright, M R Hargrave, J Christiansen, L Cooper, J Kun, T Evans, U Gangadharan, A Greenfield, P Koopman. Nat Genet 1995
534
50

A large-scale insertional mutagenesis screen in zebrafish.
A Amsterdam, S Burgess, G Golling, W Chen, Z Sun, K Townsend, S Farrington, M Haldi, N Hopkins. Genes Dev 1999
356
50

The NHGRI GWAS Catalog, a curated resource of SNP-trait associations.
Danielle Welter, Jacqueline MacArthur, Joannella Morales, Tony Burdett, Peggy Hall, Heather Junkins, Alan Klemm, Paul Flicek, Teri Manolio, Lucia Hindorff,[...]. Nucleic Acids Res 2014
50



Hypermineralization and High Osteocyte Lacunar Density in Osteogenesis Imperfecta Type V Bone Indicate Exuberant Primary Bone Formation.
Stéphane Blouin, Nadja Fratzl-Zelman, Francis H Glorieux, Paul Roschger, Klaus Klaushofer, Joan C Marini, Frank Rauch. J Bone Miner Res 2017
29
50

Highly efficient targeted mutagenesis in one-cell mouse embryos mediated by the TALEN and CRISPR/Cas systems.
Akihiro Yasue, Silvia Naomi Mitsui, Takahito Watanabe, Tetsushi Sakuma, Seiichi Oyadomari, Takashi Yamamoto, Sumihare Noji, Taro Mito, Eiji Tanaka. Sci Rep 2014
49
50

Chiari I malformation redefined: clinical and radiographic findings for 364 symptomatic patients.
T H Milhorat, M W Chou, E M Trinidad, R W Kula, M Mandell, C Wolpert, M C Speer. Neurosurgery 1999
749
50

Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu,[...]. N Engl J Med 2013
50

Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene.
J W Foster, M A Dominguez-Steglich, S Guioli, C Kwok, P A Weller, M Stevanović, J Weissenbach, S Mansour, I D Young, P N Goodfellow. Nature 1994
50

The genetic implication of scoliosis in osteogenesis imperfecta: a review.
Gang Liu, Jia Chen, Yangzhong Zhou, Yuzhi Zuo, Sen Liu, Weisheng Chen, Zhihong Wu, Nan Wu. J Spine Surg 2017
3
50

Return of genetic testing results in the era of whole-genome sequencing.
Bartha Maria Knoppers, Ma'n H Zawati, Karine Sénécal. Nat Rev Genet 2015
90
50

One-step generation of mice carrying mutations in multiple genes by CRISPR/Cas-mediated genome engineering.
Haoyi Wang, Hui Yang, Chikdu S Shivalila, Meelad M Dawlaty, Albert W Cheng, Feng Zhang, Rudolf Jaenisch. Cell 2013
50


Osteoprotection Through the Deletion of the Transcription Factor Rorβ in Mice.
Joshua N Farr, Megan M Weivoda, Kristy M Nicks, Daniel G Fraser, Brittany A Negley, Jennifer L Onken, Brianne S Thicke, Ming Ruan, Hong Liu, Douglas Forrest,[...]. J Bone Miner Res 2018
7
50

CasX enzymes comprise a distinct family of RNA-guided genome editors.
Jun-Jie Liu, Natalia Orlova, Benjamin L Oakes, Enbo Ma, Hannah B Spinner, Katherine L M Baney, Jonathan Chuck, Dan Tan, Gavin J Knott, Lucas B Harrington,[...]. Nature 2019
125
50

Inducible and multiplex gene regulation using CRISPR-Cpf1-based transcription factors.
Y Esther Tak, Benjamin P Kleinstiver, James K Nuñez, Jonathan Y Hsu, Joy E Horng, Jingyi Gong, Jonathan S Weissman, J Keith Joung. Nat Methods 2017
95
50

A two-color acid-free cartilage and bone stain for zebrafish larvae.
M B Walker, C B Kimmel. Biotech Histochem 2007
368
50

Enhanced mammalian genome editing by new Cas12a orthologs with optimized crRNA scaffolds.
Fei Teng, Jing Li, Tongtong Cui, Kai Xu, Lu Guo, Qingqin Gao, Guihai Feng, Chuanyuan Chen, Dali Han, Qi Zhou,[...]. Genome Biol 2019
27
50

Development of the endochondral skeleton.
Fanxin Long, David M Ornitz. Cold Spring Harb Perspect Biol 2013
287
50

The lateral meningocele syndrome mutation causes marked osteopenia in mice.
Ernesto Canalis, Jungeun Yu, Lauren Schilling, Siu-Pok Yee, Stefano Zanotti. J Biol Chem 2018
15
50

Deficiency of ATP6V1H Causes Bone Loss by Inhibiting Bone Resorption and Bone Formation through the TGF-β1 Pathway.
Xiaohong Duan, Jin Liu, Xueni Zheng, Zhe Wang, Yanli Zhang, Ying Hao, Tielin Yang, Hongwen Deng. Theranostics 2016
21
50

Optimized knock-in of point mutations in zebrafish using CRISPR/Cas9.
Sergey V Prykhozhij, Charlotte Fuller, Shelby L Steele, Chansey J Veinotte, Babak Razaghi, Johane M Robitaille, Christopher R McMaster, Adam Shlien, David Malkin, Jason N Berman. Nucleic Acids Res 2018
12
50

Identification of zebrafish insertional mutants with defects in visual system development and function.
Jeffrey M Gross, Brian D Perkins, Adam Amsterdam, Ana Egaña, Tristan Darland, Jonathan I Matsui, Salvatore Sciascia, Nancy Hopkins, John E Dowling. Genetics 2005
106
50

Crispr-Cas9 engineered osteogenesis imperfecta type V leads to severe skeletal deformities and perinatal lethality in mice.
Frank Rauch, Yeqing Geng, Lisa Lamplugh, Bahareh Hekmatnejad, Marie-Hélène Gaumond, Janice Penney, Yojiro Yamanaka, Pierre Moffatt. Bone 2018
16
50

Impaired gastric acidification negatively affects calcium homeostasis and bone mass.
Thorsten Schinke, Arndt F Schilling, Anke Baranowsky, Sebastian Seitz, Robert P Marshall, Tilman Linn, Michael Blaeker, Antje K Huebner, Ansgar Schulz, Ronald Simon,[...]. Nat Med 2009
118
50

Haploinsufficiency of Sox9 results in defective cartilage primordia and premature skeletal mineralization.
W Bi, W Huang, D J Whitworth, J M Deng, Z Zhang, R R Behringer, B de Crombrugghe. Proc Natl Acad Sci U S A 2001
421
50

Secondary impairments in young adults with spina bifida.
M Verhoef, H A Barf, M W M Post, F W A van Asbeck, R H J M Gooskens, A J H Prevo. Dev Med Child Neurol 2004
87
50

Enhanced proofreading governs CRISPR-Cas9 targeting accuracy.
Janice S Chen, Yavuz S Dagdas, Benjamin P Kleinstiver, Moira M Welch, Alexander A Sousa, Lucas B Harrington, Samuel H Sternberg, J Keith Joung, Ahmet Yildiz, Jennifer A Doudna. Nature 2017
453
50

ESF1 is required for 18S rRNA synthesis in Saccharomyces cerevisiae.
Wen-Tao Peng, Nevan J Krogan, Dawn P Richards, Jack F Greenblatt, Timothy R Hughes. Nucleic Acids Res 2004
14
50

Generate TALE/TALEN as Easily and Rapidly as Generating CRISPR.
Shuyan Zhang, Huiting Chen, Jinke Wang. Mol Ther Methods Clin Dev 2019
4
50

A large-scale zebrafish gene knockout resource for the genome-wide study of gene function.
Gaurav K Varshney, Jing Lu, Derek E Gildea, Haigen Huang, Wuhong Pei, Zhongan Yang, Sunny C Huang, David Schoenfeld, Nam H Pho, David Casero,[...]. Genome Res 2013
69
50

Developmental regulation of the growth plate.
Henry M Kronenberg. Nature 2003
50

PFKFB4 control of AKT signaling is essential for premigratory and migratory neural crest formation.
Ana Leonor Figueiredo, Frédérique Maczkowiak, Caroline Borday, Patrick Pla, Meghane Sittewelle, Caterina Pegoraro, Anne H Monsoro-Burq. Development 2017
18
50

The need for mouse models in osteoporosis genetics research.
Cheryl L Ackert-Bicknell, Matthew A Hibbs. Bonekey Rep 2012
3
50

Mutations in OSTM1 (grey lethal) define a particularly severe form of autosomal recessive osteopetrosis with neural involvement.
Alessandra Pangrazio, Pietro Luigi Poliani, André Megarbane, Gérard Lefranc, Edoardo Lanino, Maja Di Rocco, Francesca Rucci, Franco Lucchini, Maria Ravanini, Fabio Facchetti,[...]. J Bone Miner Res 2006
71
50




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.