A citation-based method for searching scientific literature

Rachel Soemedi, Ana Topf, Ian J Wilson, Rebecca Darlay, Thahira Rahman, Elise Glen, Darroch Hall, Ni Huang, Jamie Bentham, Shoumo Bhattacharya, Catherine Cosgrove, J David Brook, Javier Granados-Riveron, Kerry Setchfield, Frances Bu'lock, Chris Thornborough, Koenraad Devriendt, Jeroen Breckpot, Michael Hofbeck, Mark Lathrop, Anita Rauch, Gillian M Blue, David S Winlaw, Matthew Hurles, Mauro Santibanez-Koref, Heather J Cordell, Judith A Goodship, Bernard D Keavney. Hum Mol Genet 2012
Times Cited: 72

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

Times Cited
  Times     Co-cited

Heart defects and ocular anomalies in children with Down's syndrome.
N R Bromham, J M Woodhouse, M Cregg, E Webb, W I Fraser. Br J Ophthalmol 2002

Copy number variations and clinical cytogenetic diagnosis of constitutional disorders.
Charles Lee, A John Iafrate, Arthur R Brothman. Nat Genet 2007

The first missense mutation of NHS gene in a Tunisian family with clinical features of NHS syndrome including cardiac anomaly.
Manèl Chograni, Imen Rejeb, Lamia Ben Jemaa, Myriam Châabouni, Habiba Chaabouni Bouhamed. Eur J Hum Genet 2011

Oculo-Facio-Cardio-Dental Syndrome: A Case Report about a Rare Pathological Condition.
José Martinho, Hugo Ferreira, Siri Paulo, Anabela Paula, Carlos-Miguel Marto, Eunice Carrilho, Manuel Marques-Ferreira. Int J Environ Res Public Health 2019

Congenital Heart Defects and the Risk of Spontaneous Preterm Birth.
Niels B Matthiesen, John R Østergaard, Vibeke E Hjortdal, Tine B Henriksen. J Pediatr 2021

Clinical Features of Congenital and Developmental Cataract in East China: A Five-year Retrospective Review.
Xiangjia Zhu, Yu Du, Wenwen He, Ting Sun, Yinglei Zhang, Ruiqi Chang, Keke Zhang, Yi Lu. Sci Rep 2017

Whole-genome copy number variation analysis in anophthalmia and microphthalmia.
K F Schilter, L M Reis, A Schneider, T M Bardakjian, O Abdul-Rahman, B A Kozel, H H Zimmerman, U Broeckel, E V Semina. Clin Genet 2013

Aetiology of congenital and paediatric cataract in an Australian population.
M G Wirth, I M Russell-Eggitt, J E Craig, J E Elder, D A Mackey. Br J Ophthalmol 2002

Sclerocornea in a patient with van den Ende-Gupta syndrome homozygous for a SCARF2 microdeletion.
Michele P Migliavacca, Nara L M Sobreira, Graziela P M Antonialli, Mariana M Oliveira, Maria Isabel S A Melaragno, Ingele Casteels, Thomy de Ravel, Decio Brunoni, David Valle, Ana Beatriz A Perez. Am J Med Genet A 2014

YIF1B mutations cause a post-natal neurodevelopmental syndrome associated with Golgi and primary cilium alterations.
Jorge Diaz, Xavier Gérard, Michel-Boris Emerit, Julie Areias, David Geny, Julie Dégardin, Manuel Simonutti, Marie-Justine Guerquin, Thibault Collin, Cécile Viollet,[...]. Brain 2020

Truncating mutations in YIF1B cause a progressive encephalopathy with various degrees of mixed movement disorder, microcephaly, and epilepsy.
Mohammed AlMuhaizea, Rawan AlMass, Aljouhra AlHargan, Anoud AlBader, Eva Medico Salsench, Jude Howaidi, Jacie Ihinger, Peter Karachunski, Amber Begtrup, Monica Segura Castell,[...]. Acta Neuropathol 2020

Lens connexins alpha3Cx46 and alpha8Cx50 interact with zonula occludens protein-1 (ZO-1).
Peter A Nielsen, Amos Baruch, Valery I Shestopalov, Ben N G Giepmans, Irene Dunia, E Lucio Benedetti, Nalin M Kumar. Mol Biol Cell 2003

An evaluation of copy number variation detection tools from whole-exome sequencing data.
Renjie Tan, Yadong Wang, Sarah E Kleinstein, Yongzhuang Liu, Xiaolin Zhu, Hongzhe Guo, Qinghua Jiang, Andrew S Allen, Mingfu Zhu. Hum Mutat 2014

The 50th anniversary of the discovery of trisomy 21: the past, present, and future of research and treatment of Down syndrome.
André Mégarbané, Aimé Ravel, Clotilde Mircher, Franck Sturtz, Yann Grattau, Marie-Odile Rethoré, Jean-Maurice Delabar, William C Mobley. Genet Med 2009

Genetic characterisation of 22q11.2 variations and prevalence in patients with congenital heart disease.
Hai-Tao Hou, Huan-Xin Chen, Xiu-Li Wang, Chao Yuan, Qin Yang, Zhi-Gang Liu, Guo-Wei He. Arch Dis Child 2020

Genetics of Congenital Heart Disease.
Kylia Williams, Jason Carson, Cecilia Lo. Biomolecules 2019

Molecular genetics of congenital cataracts.
Jinyu Li, Xiangjun Chen, Yongbin Yan, Ke Yao. Exp Eye Res 2020

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.