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



Michael H Gollob, Douglas L Jones, Andrew D Krahn, Lynne Danis, Xiang-Qun Gong, Qing Shao, Xiaoqin Liu, John P Veinot, Anthony S L Tang, Alexandre F R Stewart, Frederique Tesson, George J Klein, Raymond Yee, Allan C Skanes, Gerard M Guiraudon, Lisa Ebihara, Donglin Bai. N Engl J Med 2006
Times Cited: 350




List of shared articles



Times cited

Molecular insight into heart development and congenital heart disease: An update review from the Arab countries.
Elhadi H Aburawi, Hanan E Aburawi, Keith M Bagnall, Zahurul A Bhuiyan. Trends Cardiovasc Med 2015
10

Impact of copy number variation on human neurocognitive deficits and congenital heart defects: A systematic review.
Katrina Savory, Susruta Manivannan, Malik Zaben, Orhan Uzun, Yasir Ahmed Syed. Neurosci Biobehav Rev 2020
1

Brain Disorders and Chemical Pollutants: A Gap Junction Link?
Marc Mesnil, Norah Defamie, Christian Naus, Denis Sarrouilhe. Biomolecules 2020
1

A variant in the carboxyl-terminus of connexin 40 alters GAP junctions and increases risk for tetralogy of Fallot.
Valentina Guida, Rosangela Ferese, Marcella Rocchetti, Monica Bonetti, Anna Sarkozy, Serena Cecchetti, Vania Gelmetti, Francesca Lepri, Massimiliano Copetti, Giuseppe Lamorte,[...]. Eur J Hum Genet 2013
24

Mutations in cardiovascular connexin genes.
Filippo Molica, Merlijn J P Meens, Sandrine Morel, Brenda R Kwak. Biol Cell 2014
23

Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways.
Candice K Silversides, Anath C Lionel, Gregory Costain, Daniele Merico, Ohsuke Migita, Ben Liu, Tracy Yuen, Jessica Rickaby, Bhooma Thiruvahindrapuram, Christian R Marshall,[...]. PLoS Genet 2012
106

Phenotypic Variability Associated with a Large Recurrent 1q21.1 Microduplication in a Three-Generation Family.
Judith M A Verhagen, Nicole de Leeuw, Dimitri N M Papatsonis, Els W M Grijseels, Ronald R de Krijger, Marja W Wessels. Mol Syndromol 2015
11