A citation-based method for searching scientific literature

Xianding Sun, Ruobin Zhang, Mi Liu, Hangang Chen, Liang Chen, Fengtao Luo, Dali Zhang, Junlan Huang, Fangfang Li, Zhenhong Ni, Huabing Qi, Nan Su, Min Jin, Jing Yang, Qiaoyan Tan, Xiaolan Du, Bo Chen, Haiyang Huang, Shuai Chen, Liangjun Yin, Xiaoling Xu, Chuxia Deng, Lingfei Luo, Yangli Xie, Lin Chen. J Bone Miner Res 2019
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


Consequences of mutations in the non-coding RMRP RNA in cartilage-hair hypoplasia.
Pia Hermanns, Alison A Bertuch, Terry K Bertin, Brian Dawson, Mark E Schmitt, Chad Shaw, Bernhard Zabel, Brendan Lee. Hum Mol Genet 2005
73
33

An RNA-dependent RNA polymerase formed by TERT and the RMRP RNA.
Yoshiko Maida, Mami Yasukawa, Miho Furuuchi, Timo Lassmann, Richard Possemato, Naoko Okamoto, Vivi Kasim, Yoshihide Hayashizaki, William C Hahn, Kenkichi Masutomi. Nature 2009
261
33

The human long non-coding RNA gene RMRP has pleiotropic effects and regulates cell-cycle progression at G2.
Svetlana Vakkilainen, Tiina Skoog, Elisabet Einarsdottir, Anna Middleton, Minna Pekkinen, Tiina Öhman, Shintaro Katayama, Kaarel Krjutškov, Panu E Kovanen, Markku Varjosalo,[...]. Sci Rep 2019
7
42

Mutations in the RNA component of RNase MRP cause a pleiotropic human disease, cartilage-hair hypoplasia.
M Ridanpää, H van Eenennaam, K Pelin, R Chadwick, C Johnson, B Yuan, W vanVenrooij, G Pruijn, R Salmela, S Rockas,[...]. Cell 2001
297
33

RMRP is a non-coding RNA essential for early murine development.
Joseph Rosenbluh, Deepak Nijhawan, Zhao Chen, Kwok-Kin Wong, Kenkichi Masutomi, William C Hahn. PLoS One 2011
35
33

Severely incapacitating mutations in patients with extreme short stature identify RNA-processing endoribonuclease RMRP as an essential cell growth regulator.
Christian T Thiel, Denise Horn, Bernhard Zabel, Arif B Ekici, Kelly Salinas, Erich Gebhart, Franz Rüschendorf, Heinrich Sticht, Jürgen Spranger, Dietmar Müller,[...]. Am J Hum Genet 2005
90
22

Small RNAs derived from lncRNA RNase MRP have gene-silencing activity relevant to human cartilage-hair hypoplasia.
Leslie E Rogler, Brian Kosmyna, David Moskowitz, Remon Bebawee, Joseph Rahimzadeh, Katrina Kutchko, Alain Laederach, Luigi D Notarangelo, Silvia Giliani, Eric Bouhassira,[...]. Hum Mol Genet 2014
60
22


RMRP mutations in cartilage-hair hypoplasia.
Pia Hermanns, Alyssa Tran, Elda Munivez, Susan Carter, Bernhard Zabel, Brendan Lee, Jules G Leroy. Am J Med Genet A 2006
39
22

A 30-Year Prospective Follow-Up Study Reveals Risk Factors for Early Death in Cartilage-Hair Hypoplasia.
Svetlana Vakkilainen, Mervi Taskinen, Paula Klemetti, Eero Pukkala, Outi Mäkitie. Front Immunol 2019
12
22

A Wide Spectrum of Autoimmune Manifestations and Other Symptoms Suggesting Immune Dysregulation in Patients With Cartilage-Hair Hypoplasia.
Svetlana Vakkilainen, Riikka Mäkitie, Paula Klemetti, Helena Valta, Mervi Taskinen, Eystein Sverre Husebye, Outi Mäkitie. Front Immunol 2018
7
28


Decreased telomere length in children with cartilage-hair hypoplasia.
Svetlana Kostjukovits, Sofie Degerman, Minna Pekkinen, Paula Klemetti, Mattias Landfors, Göran Roos, Mervi Taskinen, Outi Mäkitie. J Med Genet 2017
13
22

Cartilage hair hypoplasia with cutaneous lymphomatoid granulomatosis.
D Sathishkumar, J E Gach, M Ogboli, M Desai, T Cole, W Högler, J Motwani, A Norton, B Morland, I Colmenero. Clin Exp Dermatol 2018
3
66

Diffuse large B-cell lymphoma chemotherapy reveals a combined immunodeficiency syndrome in cartilage hair hypoplasia.
Alexandre Nguyen, Nicolas Martin Silva, Hubert de Boysson, Gandhi Damaj, Achille Aouba. Swiss Med Wkly 2018
3
66

Combating cancer predisposition in association with idiopathic immune deficiency: a recurrent nodal and cutaneous T-cell lymphoproliferative disease in a patient with cartilage-hair hypoplasia.
Mervi Taskinen, Leila Jeskanen, Marja-Liisa Karjalainen-Lindsberg, Antti Mäkitie, Outi Mäkitie, Annamari Ranki. Clin Lymphoma Myeloma Leuk 2013
9
22

The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita.
T Vulliamy, A Marrone, F Goldman, A Dearlove, M Bessler, P J Mason, I Dokal. Nature 2001
681
22

Cartilage hair hypoplasia mutations that lead to RMRP promoter inefficiency or RNA transcript instability.
Eiji Nakashima, Joseph R Tran, Tim J M Welting, Ger J M Pruijn, Yuichiro Hirose, Gen Nishimura, Hirofumi Ohashi, Shepherd H Schurman, Jun Cheng, Fabio Candotti,[...]. Am J Med Genet A 2007
25
22


Intrinsic and extrinsic causes of malignancies in patients with primary immunodeficiency disorders.
Fabian Hauck, Rebecca Voss, Christian Urban, Markus G Seidel. J Allergy Clin Immunol 2018
50
22




lncRNA RMRP knockdown suppress hepatocellular carcinoma biological activities via regulation miRNA-206/TACR1.
Zhao Hongfeng, Ju Andong, Sun Liwen, Bi Mingping, Yang Xiaowei, Li Mingyong, Yue Aimin. J Cell Biochem 2020
10
22


LncRNA-RMRP promotes carcinogenesis by acting as a miR-206 sponge and is used as a novel biomarker for gastric cancer.
Yongfu Shao, Meng Ye, Qier Li, Weiliang Sun, Guoliang Ye, Xinjun Zhang, Yunben Yang, Bingxiu Xiao, Junming Guo. Oncotarget 2016
119
22

lncRNA-RMRP promotes proliferation, migration and invasion of bladder cancer via miR-206.
H-L Cao, Z-J Liu, P-L Huang, Y-L Yue, J-N Xi. Eur Rev Med Pharmacol Sci 2019
13
22

Long noncoding-RNA component of mitochondrial RNA processing endoribonuclease is involved in the progression of cholangiocarcinoma by regulating microRNA-217.
Lingyu Tang, Yuting Wang, Huishan Wang, Boming Xu, Hao Ji, Guolong Xu, Xianxiu Ge, Quanpeng Li, Lin Miao. Cancer Sci 2019
15
22

Wnt/β-catenin regulates an ancient signaling network during zebrafish scale development.
Andrew J Aman, Alexis N Fulbright, David M Parichy. Elife 2018
27
22


Zebrafish Craniofacial Development: A Window into Early Patterning.
Lindsey Mork, Gage Crump. Curr Top Dev Biol 2015
52
22

Zebrafish as an Emerging Model for Osteoporosis: A Primary Testing Platform for Screening New Osteo-Active Compounds.
Dylan J M Bergen, Erika Kague, Chrissy L Hammond. Front Endocrinol (Lausanne) 2019
33
22

Osterix/Sp7 limits cranial bone initiation sites and is required for formation of sutures.
Erika Kague, Paula Roy, Garrett Asselin, Gui Hu, Jacqueline Simonet, Alexandra Stanley, Craig Albertson, Shannon Fisher. Dev Biol 2016
29
22


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
22

Examination of a palatogenic gene program in zebrafish.
Mary E Swartz, Kelly Sheehan-Rooney, Michael J Dixon, Johann K Eberhart. Dev Dyn 2011
72
22

Heritable targeted gene disruption in zebrafish using designed zinc-finger nucleases.
Yannick Doyon, Jasmine M McCammon, Jeffrey C Miller, Farhoud Faraji, Catherine Ngo, George E Katibah, Rainier Amora, Toby D Hocking, Lei Zhang, Edward J Rebar,[...]. Nat Biotechnol 2008
593
22

Medaka and zebrafish, an evolutionary twin study.
Makoto Furutani-Seiki, Joachim Wittbrodt. Mech Dev 2004
145
22

Specification and morphogenesis of the zebrafish larval head skeleton.
C B Kimmel, C T Miller, C B Moens. Dev Biol 2001
125
22

Power and challenges of using zebrafish as a model for skeletal tissue imaging.
Bart Bruneel, Paul Eckhard Witten. Connect Tissue Res 2015
21
22

Small teleost fish provide new insights into human skeletal diseases.
P E Witten, M P Harris, A Huysseune, C Winkler. Methods Cell Biol 2017
43
22

Hedgehog signaling is required for cranial neural crest morphogenesis and chondrogenesis at the midline in the zebrafish skull.
Naoyuki Wada, Yashar Javidan, Sarah Nelson, Thomas J Carney, Robert N Kelsh, Thomas F Schilling. Development 2005
207
22


Embryonic fate map of first pharyngeal arch structures in the sox10: kaede zebrafish transgenic model.
Max Dougherty, George Kamel, Valeriy Shubinets, Graham Hickey, Michael Grimaldi, Eric C Liao. J Craniofac Surg 2012
34
22

Scleraxis genes are required for normal musculoskeletal development and for rib growth and mineralization in zebrafish.
Erika Kague, Simon M Hughes, Elizabeth A Lawrence, Stephen Cross, Elizabeth Martin-Silverstone, Chrissy L Hammond, Yaniv Hinits. FASEB J 2019
12
22

Diverse Autoantibody Reactivity in Cartilage-Hair Hypoplasia.
Catherine M Biggs, Svetlana Kostjukovits, Kerry Dobbs, Saila Laakso, Paula Klemetti, Helena Valta, Mervi Taskinen, Outi Mäkitie, Luigi D Notarangelo. J Clin Immunol 2017
2
50

Fatal adult-onset antibody deficiency syndrome in a patient with cartilage hair hypoplasia.
Julia Horn, Michael Schlesier, Klaus Warnatz, Antje Prasse, Andrea Superti-Furga, Hans-Hartmut Peter, Ulrich Salzer. Hum Immunol 2010
6
16


Mutual interactions between subunits of the human RNase MRP ribonucleoprotein complex.
Tim J M Welting, Walther J van Venrooij, Ger J M Pruijn. Nucleic Acids Res 2004
71
11

Extended follow-up of the Finnish cartilage-hair hypoplasia cohort confirms high incidence of non-Hodgkin lymphoma and basal cell carcinoma.
Mervi Taskinen, Annamari Ranki, Eero Pukkala, Leila Jeskanen, Ilkka Kaitila, Outi Mäkitie. Am J Med Genet A 2008
55
11


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.