A citation-based method for searching scientific literature

Ivo F A C Fokkema, Peter E M Taschner, Gerard C P Schaafsma, J Celli, Jeroen F J Laros, Johan T den Dunnen. Hum Mutat 2011
Times Cited: 605



Pauline C Ng, Steven Henikoff. Nucleic Acids Res 2003
Times Cited: 3409




List of shared articles



Times cited

Novel phenotype and genotype spectrum of WDR62 in two patients with associated primary autosomal recessive microcephaly.
Hajar Aryan, Shaghayegh Zokaei, Dariush Farhud, Mohammad Keykhaei, Mahmoud Reza Ashrafi, Maryam Rasulinezhad, Seyyed Mohammad Mahdi Hosseini, Ehsan Razmara, Ali Reza Tavasoli. Ir J Med Sci 2022
0

BRCA1/2 variants of unknown significance in hereditary breast and ovarian cancer (HBOC) syndrome: Looking for the hidden meaning.
Daniele Fanale, Alessia Pivetti, Daniela Cancelliere, Antonio Spera, Marco Bono, Alessia Fiorino, Erika Pedone, Nadia Barraco, Chiara Brando, Alessandro Perez,[...]. Crit Rev Oncol Hematol 2022
1

Whole-genome sequencing identifies rare missense variants of WNT16 and ERVW-1 causing the systemic lupus erythematosus.
Jianhai Chen, Ping Zhang, Haidi Chen, Xin Wang, Xuefei He, Jie Zhong, HuaPing Zheng, Xiaoyu Li, Ivan Jakovlić, Yong Zhang,[...]. Genomics 2022
0

Prioritizing variants of uncertain significance for reclassification using a rule-based algorithm in inherited retinal dystrophies.
Ionut-Florin Iancu, Almudena Avila-Fernandez, Ana Arteche, Maria Jose Trujillo-Tiebas, Rosa Riveiro-Alvarez, Berta Almoguera, Inmaculada Martin-Merida, Marta Del Pozo-Valero, Irene Perea-Romero, Marta Corton,[...]. NPJ Genom Med 2021
3

A novel deletion variant in CLN3 with highly variable expressivity is responsible for juvenile neuronal ceroid lipofuscinoses.
Naser Gilani, Ehsan Razmara, Mehmet Ozaslan, Ihsan Kareem Abdulzahra, Saeid Arzhang, Ali Reza Tavasoli, Masoud Garshasbi. Acta Neurol Belg 2021
2