A citation-based method for searching scientific literature

Ishani Dasgupta, Terence R Flotte, Allison M Keeler. Hum Gene Ther 2021
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


A programmable dual-RNA-guided DNA endonuclease in adaptive bacterial immunity.
Martin Jinek, Krzysztof Chylinski, Ines Fonfara, Michael Hauer, Jennifer A Doudna, Emmanuelle Charpentier. Science 2012
50

Induced Liver Regeneration Enhances CRISPR/Cas9-Mediated Gene Repair in Tyrosinemia Type 1.
Qing-Shuo Zhang, Amita Tiyaboonchai, Sean Nygaard, Kevin Baradar, Angela Major, Niveditha Balaji, Markus Grompe. Hum Gene Ther 2021
4
50

GUIDE-seq enables genome-wide profiling of off-target cleavage by CRISPR-Cas nucleases.
Shengdar Q Tsai, Zongli Zheng, Nhu T Nguyen, Matthew Liebers, Ved V Topkar, Vishal Thapar, Nicolas Wyvekens, Cyd Khayter, A John Iafrate, Long P Le,[...]. Nat Biotechnol 2015
33

CRISPR/Cas9 β-globin gene targeting in human haematopoietic stem cells.
Daniel P Dever, Rasmus O Bak, Andreas Reinisch, Joab Camarena, Gabriel Washington, Carmencita E Nicolas, Mara Pavel-Dinu, Nivi Saxena, Alec B Wilkens, Sruthi Mantri,[...]. Nature 2016
417
33

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
830
33

Rational Selection of CRISPR-Cas Triggering Homology-Directed Repair in Human Cells.
Fanfan Li, Chenchen Zhou, Tianxiang Tu, Yuanyuan Liu, Xiujuan Lv, Bang Wang, Zongming Song, Qifeng Zhao, Changbao Liu, Feng Gu,[...]. Hum Gene Ther 2021
2
50


Genome-Editing Strategies for Treating Human Retinal Degenerations.
Joel Quinn, Ayesha Musa, Ariel Kantor, Michelle E McClements, Jasmina Cehajic-Kapetanovic, Robert E MacLaren, Kanmin Xue. Hum Gene Ther 2021
7
16

Double nicking by RNA-guided CRISPR Cas9 for enhanced genome editing specificity.
F Ann Ran, Patrick D Hsu, Chie-Yu Lin, Jonathan S Gootenberg, Silvana Konermann, Alexandro E Trevino, David A Scott, Azusa Inoue, Shogo Matoba, Yi Zhang,[...]. Cell 2013
16

Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegia.
Francesc Pérez-Brangulí, Himanshu K Mishra, Iryna Prots, Steven Havlicek, Zacharias Kohl, Domenica Saul, Christine Rummel, Jonatan Dorca-Arevalo, Martin Regensburger, Daniela Graef,[...]. Hum Mol Genet 2014
50
16


Neural Subtype Specification from Human Pluripotent Stem Cells.
Yunlong Tao, Su-Chun Zhang. Cell Stem Cell 2016
123
16

Motor neuron disease. SMN2 splicing modifiers improve motor function and longevity in mice with spinal muscular atrophy.
Nikolai A Naryshkin, Marla Weetall, Amal Dakka, Jana Narasimhan, Xin Zhao, Zhihua Feng, Karen K Y Ling, Gary M Karp, Hongyan Qi, Matthew G Woll,[...]. Science 2014
284
16

In vivo genome editing improves motor function and extends survival in a mouse model of ALS.
Thomas Gaj, David S Ojala, Freja K Ekman, Leah C Byrne, Prajit Limsirichai, David V Schaffer. Sci Adv 2017
68
16

Approach for in vivo delivery of CRISPR/Cas system: a recent update and future prospect.
Yu-Fan Chuang, Andrew J Phipps, Fan-Li Lin, Valerie Hecht, Alex W Hewitt, Peng-Yuan Wang, Guei-Sheung Liu. Cell Mol Life Sci 2021
6
16

Systemic gene delivery in large species for targeting spinal cord, brain, and peripheral tissues for pediatric disorders.
Adam K Bevan, Sandra Duque, Kevin D Foust, Pablo R Morales, Lyndsey Braun, Leah Schmelzer, Curtis M Chan, Mary McCrate, Louis G Chicoine, Brian D Coley,[...]. Mol Ther 2011
216
16

Gene targeting of a disease-related gene in human induced pluripotent stem and embryonic stem cells.
Jizhong Zou, Morgan L Maeder, Prashant Mali, Shondra M Pruett-Miller, Stacey Thibodeau-Beganny, Bin-Kuan Chou, Guibin Chen, Zhaohui Ye, In-Hyun Park, George Q Daley,[...]. Cell Stem Cell 2009
385
16

40 Years of CSF Toxicity Studies in ALS: What Have We Learnt About ALS Pathophysiology?
Koy Chong Ng Kee Kwong, Pratap K Harbham, Bhuvaneish T Selvaraj, Jenna M Gregory, Suvankar Pal, Giles E Hardingham, Siddharthan Chandran, Arpan R Mehta. Front Mol Neurosci 2021
3
33

Rescue of the spinal muscular atrophy phenotype in a mouse model by early postnatal delivery of SMN.
Kevin D Foust, Xueyong Wang, Vicki L McGovern, Lyndsey Braun, Adam K Bevan, Amanda M Haidet, Thanh T Le, Pablo R Morales, Mark M Rich, Arthur H M Burghes,[...]. Nat Biotechnol 2010
507
16

HIV-1 remission following CCR5Δ32/Δ32 haematopoietic stem-cell transplantation.
Ravindra K Gupta, Sultan Abdul-Jawad, Laura E McCoy, Hoi Ping Mok, Dimitra Peppa, Maria Salgado, Javier Martinez-Picado, Monique Nijhuis, Annemarie M J Wensing, Helen Lee,[...]. Nature 2019
235
16

Quantification of zinc finger nuclease-associated toxicity.
Tatjana I Cornu, Toni Cathomen. Methods Mol Biol 2010
30
16


Drug screening for ALS using patient-specific induced pluripotent stem cells.
Naohiro Egawa, Shiho Kitaoka, Kayoko Tsukita, Motoko Naitoh, Kazutoshi Takahashi, Takuya Yamamoto, Fumihiko Adachi, Takayuki Kondo, Keisuke Okita, Isao Asaka,[...]. Sci Transl Med 2012
352
16

Pluripotent stem cell-based models of spinal muscular atrophy.
Emanuele Frattini, Margherita Ruggieri, Sabrina Salani, Irene Faravelli, Chiara Zanetta, Monica Nizzardo, Chiara Simone, Francesca Magri, Stefania Corti. Mol Cell Neurosci 2015
23
16

ALS Clinical Trials Review: 20 Years of Failure. Are We Any Closer to Registering a New Treatment?
Dmitry Petrov, Colin Mansfield, Alain Moussy, Olivier Hermine. Front Aging Neurosci 2017
180
16

Specification of motoneurons from human embryonic stem cells.
Xue-Jun Li, Zhong-Wei Du, Ewa D Zarnowska, Matthew Pankratz, Lauren O Hansen, Robert A Pearce, Su-Chun Zhang. Nat Biotechnol 2005
545
16

Double-strand breaks and translocations in cancer.
B Elliott, M Jasin. Cell Mol Life Sci 2002
117
16

Impaired mitochondrial dynamics underlie axonal defects in hereditary spastic paraplegias.
Kyle Denton, Yongchao Mou, Chong-Chong Xu, Dhruvi Shah, Jaerak Chang, Craig Blackstone, Xue-Jun Li. Hum Mol Genet 2018
26
16

Induced Pluripotent Stem Cells and Their Use in Human Models of Disease and Development.
Peter Karagiannis, Kazutoshi Takahashi, Megumu Saito, Yoshinori Yoshida, Keisuke Okita, Akira Watanabe, Haruhisa Inoue, Jun K Yamashita, Masaya Todani, Masato Nakagawa,[...]. Physiol Rev 2019
77
16

CRISPR-mediated gene correction links the ATP7A M1311V mutations with amyotrophic lateral sclerosis pathogenesis in one individual.
Yeomin Yun, Sung-Ah Hong, Ka-Kyung Kim, Daye Baek, Dongsu Lee, Ashwini M Londhe, Minhyung Lee, Jihyeon Yu, Zachary T McEachin, Gary J Bassell,[...]. Commun Biol 2020
5
20

Human C9ORF72 Hexanucleotide Expansion Reproduces RNA Foci and Dipeptide Repeat Proteins but Not Neurodegeneration in BAC Transgenic Mice.
Owen M Peters, Gabriela Toro Cabrera, Helene Tran, Tania F Gendron, Jeanne E McKeon, Jake Metterville, Alexandra Weiss, Nicholas Wightman, Johnny Salameh, Juyhun Kim,[...]. Neuron 2015
165
16

Treatment of a Mouse Model of ALS by In Vivo Base Editing.
Colin K W Lim, Michael Gapinske, Alexandra K Brooks, Wendy S Woods, Jackson E Powell, M Alejandra Zeballos C, Jackson Winter, Pablo Perez-Pinera, Thomas Gaj. Mol Ther 2020
50
16

Delivery systems of CRISPR/Cas9-based cancer gene therapy.
Alessio Biagioni, Anna Laurenzana, Francesca Margheri, Anastasia Chillà, Gabriella Fibbi, Mario Del Rosso. J Biol Eng 2018
18
16

Modeling ALS with iPSCs reveals that mutant SOD1 misregulates neurofilament balance in motor neurons.
Hong Chen, Kun Qian, Zhongwei Du, Jingyuan Cao, Andrew Petersen, Huisheng Liu, Lisle W Blackbourn, CindyTzu-Ling Huang, Anthony Errigo, Yingnan Yin,[...]. Cell Stem Cell 2014
185
16

Increasing the efficiency of homology-directed repair for CRISPR-Cas9-induced precise gene editing in mammalian cells.
Van Trung Chu, Timm Weber, Benedikt Wefers, Wolfgang Wurst, Sandrine Sander, Klaus Rajewsky, Ralf Kühn. Nat Biotechnol 2015
660
16

Impaired lipid metabolism in astrocytes underlies degeneration of cortical projection neurons in hereditary spastic paraplegia.
Yongchao Mou, Yi Dong, Zhenyu Chen, Kyle R Denton, Michael O Duff, Craig Blackstone, Su-Chun Zhang, Xue-Jun Li. Acta Neuropathol Commun 2020
4
25

Evolution and classification of the CRISPR-Cas systems.
Kira S Makarova, Daniel H Haft, Rodolphe Barrangou, Stan J J Brouns, Emmanuelle Charpentier, Philippe Horvath, Sylvain Moineau, Francisco J M Mojica, Yuri I Wolf, Alexander F Yakunin,[...]. Nat Rev Microbiol 2011
16

Generation of isogenic pluripotent stem cells differing exclusively at two early onset Parkinson point mutations.
Frank Soldner, Josée Laganière, Albert W Cheng, Dirk Hockemeyer, Qing Gao, Raaji Alagappan, Vikram Khurana, Lawrence I Golbe, Richard H Myers, Susan Lindquist,[...]. Cell 2011
500
16

Genetic Correction of SOD1 Mutant iPSCs Reveals ERK and JNK Activated AP1 as a Driver of Neurodegeneration in Amyotrophic Lateral Sclerosis.
Akshay Bhinge, Seema C Namboori, Xiaoyu Zhang, Antonius M J VanDongen, Lawrence W Stanton. Stem Cell Reports 2017
69
16

Therapeutic rAAVrh10 Mediated SOD1 Silencing in Adult SOD1(G93A) Mice and Nonhuman Primates.
Florie Borel, Gwladys Gernoux, Brynn Cardozo, Jake P Metterville, Gabriela C Toro Cabrera, Lina Song, Qin Su, Guang Ping Gao, Mai K Elmallah, Robert H Brown,[...]. Hum Gene Ther 2016
57
16

Induced pluripotent stem cell lines derived from human somatic cells.
Junying Yu, Maxim A Vodyanik, Kim Smuga-Otto, Jessica Antosiewicz-Bourget, Jennifer L Frane, Shulan Tian, Jeff Nie, Gudrun A Jonsdottir, Victor Ruotti, Ron Stewart,[...]. Science 2007
16

Induction of pluripotent stem cells from adult human fibroblasts by defined factors.
Kazutoshi Takahashi, Koji Tanabe, Mari Ohnuki, Megumi Narita, Tomoko Ichisaka, Kiichiro Tomoda, Shinya Yamanaka. Cell 2007
16

Introduction to stem cells and regenerative medicine.
George Kolios, Yuben Moodley. Respiration 2013
99
16

Gain of Toxicity from ALS/FTD-Linked Repeat Expansions in C9ORF72 Is Alleviated by Antisense Oligonucleotides Targeting GGGGCC-Containing RNAs.
Jie Jiang, Qiang Zhu, Tania F Gendron, Shahram Saberi, Melissa McAlonis-Downes, Amanda Seelman, Jennifer E Stauffer, Paymaan Jafar-Nejad, Kevin Drenner, Derek Schulte,[...]. Neuron 2016
280
16

Modeling ALS with motor neurons derived from human induced pluripotent stem cells.
Samuel Sances, Lucie I Bruijn, Siddharthan Chandran, Kevin Eggan, Ritchie Ho, Joseph R Klim, Matt R Livesey, Emily Lowry, Jeffrey D Macklis, David Rushton,[...]. Nat Neurosci 2016
140
16

Therapeutic AAV9-mediated suppression of mutant SOD1 slows disease progression and extends survival in models of inherited ALS.
Kevin D Foust, Desirée L Salazar, Shibi Likhite, Laura Ferraiuolo, Dara Ditsworth, Hristelina Ilieva, Kathrin Meyer, Leah Schmelzer, Lyndsey Braun, Don W Cleveland,[...]. Mol Ther 2013
124
16

Highly efficient endogenous human gene correction using designed zinc-finger nucleases.
Fyodor D Urnov, Jeffrey C Miller, Ya-Li Lee, Christian M Beausejour, Jeremy M Rock, Sheldon Augustus, Andrew C Jamieson, Matthew H Porteus, Philip D Gregory, Michael C Holmes. Nature 2005
16

A SMN2 Splicing Modifier Rescues the Disease Phenotypes in an In Vitro Human Spinal Muscular Atrophy Model.
Ye Seul Son, Kwangman Choi, Hana Lee, Ohman Kwon, Kwang Bo Jung, Sunwha Cho, Jiyeon Baek, Bora Son, Sung-Min Kang, Mingu Kang,[...]. Stem Cells Dev 2019
10
16

Methods for gene transfer to the central nervous system.
Boris Kantor, Rachel M Bailey, Keon Wimberly, Sahana N Kalburgi, Steven J Gray. Adv Genet 2014
44
16



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.