A citation-based method for searching scientific literature

Nayef Jarrous, Dhivakar Mani, Aravind Ramanathan. FEBS J 2021
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Bi-allelic POLR3A Loss-of-Function Variants Cause Autosomal-Recessive Wiedemann-Rautenstrauch Syndrome.
Jennifer A Wambach, Daniel J Wegner, Nivedita Patni, Martin Kircher, Marcia C Willing, Dustin Baldridge, Chao Xing, Anil K Agarwal, Samantha A Schrier Vergano, Chirag Patel,[...]. Am J Hum Genet 2018
24
100



Phenotype and genotype in patients with Larsen syndrome: clinical homogeneity and allelic heterogeneity in seven patients.
Katta Mohan Girisha, Abdul Mueed Bidchol, Luitgard Graul-Neumann, Ashish Gupta, Ute Hehr, Davor Lessel, Sean Nader, Hitesh Shah, Julia Wickert, Kerstin Kutsche. BMC Med Genet 2016
11
100

Clinical spectrum of 4H leukodystrophy caused by POLR3A and POLR3B mutations.
Nicole I Wolf, Adeline Vanderver, Rosalina M L van Spaendonk, Raphael Schiffmann, Bernard Brais, Marianna Bugiani, Erik Sistermans, Coriene Catsman-Berrevoets, Johan M Kros, Pedro Soares Pinto,[...]. Neurology 2014
101
100

Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia.
Martina Minnerop, Delia Kurzwelly, Holger Wagner, Anne S Soehn, Jennifer Reichbauer, Feifei Tao, Tim W Rattay, Michael Peitz, Kristina Rehbach, Alejandro Giorgetti,[...]. Brain 2017
50
100


RNA polymerase III transcription as a disease factor.
Meghdad Yeganeh, Nouria Hernandez. Genes Dev 2020
13
100

Specific combinations of biallelic POLR3A variants cause Wiedemann-Rautenstrauch syndrome.
Stefano Paolacci, Yun Li, Emanuele Agolini, Emanuele Bellacchio, Carlos E Arboleda-Bustos, Dido Carrero, Debora Bertola, Lihadh Al-Gazali, Mariel Alders, Janine Altmüller,[...]. J Med Genet 2018
24
100

Mutations of POLR3A encoding a catalytic subunit of RNA polymerase Pol III cause a recessive hypomyelinating leukodystrophy.
Geneviève Bernard, Eliane Chouery, Maria Lisa Putorti, Martine Tétreault, Asako Takanohashi, Giovanni Carosso, Isabelle Clément, Odile Boespflug-Tanguy, Diana Rodriguez, Valérie Delague,[...]. Am J Hum Genet 2011
149
100

Hereditary Syndromes with Signs of Premature Aging.
Davor Lessel, Christian Kubisch. Dtsch Arztebl Int 2019
10
100

Inborn errors in RNA polymerase III underlie severe varicella zoster virus infections.
Benson Ogunjimi, Shen-Ying Zhang, Katrine B Sørensen, Kristian A Skipper, Madalina Carter-Timofte, Gaspard Kerner, Stefanie Luecke, Thaneas Prabakaran, Yujia Cai, Josephina Meester,[...]. J Clin Invest 2017
72
100

Wiedemann-Rautenstrauch syndrome: A phenotype analysis.
Stefano Paolacci, Debora Bertola, José Franco, Shehla Mohammed, Marco Tartaglia, Bernd Wollnik, Raoul C Hennekam. Am J Med Genet A 2017
19
100

Analyses of LMNA-negative juvenile progeroid cases confirms biallelic POLR3A mutations in Wiedemann-Rautenstrauch-like syndrome and expands the phenotypic spectrum of PYCR1 mutations.
Davor Lessel, Ayse Bilge Ozel, Susan E Campbell, Abdelkrim Saadi, Martin F Arlt, Keisha Melodi McSweeney, Vasilica Plaiasu, Katalin Szakszon, Anna Szőllős, Cristina Rusu,[...]. Hum Genet 2018
14
100

Neonatal progeriod syndrome associated with biallelic truncating variants in POLR3A.
Allison M Jay, Robert L Conway, Isabelle Thiffault, Carol Saunders, Emily Farrow, John Adams, Helga V Toriello. Am J Med Genet A 2016
21
100


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.