A citation-based method for searching scientific literature




D A Clayton. Proc Natl Acad Sci U S A 1994
Times Cited: 61




List of shared articles



Times cited

snoRNPs: Functions in Ribosome Biogenesis.
Sandeep Ojha, Sulochan Malla, Shawn M Lyons. Biomolecules 2020
14

Broadening the phenotypic spectrum of POP1-skeletal dysplasias: identification of POP1 mutations in a mild and severe skeletal dysplasia.
J Barraza-García, C I Rivera-Pedroza, A Hisado-Oliva, A Belinchón-Martínez, L Sentchordi-Montané, E L Duncan, G R Clark, A Del Pozo, K Ibáñez-Garikano, A Offiah,[...]. Clin Genet 2017
7

Of proteins and RNA: the RNase P/MRP family.
Olga Esakova, Andrey S Krasilnikov. RNA 2010
147

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


Evolutionary comparison provides evidence for pathogenicity of RMRP mutations.
Luisa Bonafé, Emmanouil T Dermitzakis, Sheila Unger, Cheryl R Greenberg, Belinda A Campos-Xavier, Andreas Zankl, Catherine Ucla, Stylianos E Antonarakis, Andrea Superti-Furga, Alexandre Reymond. PLoS Genet 2005
48

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
296

Mouse models for mitochondrial disease.
D C Wallace. Am J Med Genet 2001
125