A citation-based method for searching scientific literature

Wai Lun Alan Fung, Nancy J Butcher, Gregory Costain, Danielle M Andrade, Erik Boot, Eva W C Chow, Brian Chung, Cheryl Cytrynbaum, Hanna Faghfoury, Leona Fishman, Sixto García-Miñaúr, Susan George, Anthony E Lang, Gabriela Repetto, Andrea Shugar, Candice Silversides, Ann Swillen, Therese van Amelsvoort, Donna M McDonald-McGinn, Anne S Bassett. Genet Med 2015
Times Cited: 114



A K Ryan, J A Goodship, D I Wilson, N Philip, A Levy, H Seidel, S Schuffenhauer, H Oechsler, B Belohradsky, M Prieur, A Aurias, F L Raymond, J Clayton-Smith, E Hatchwell, C McKeown, F A Beemer, B Dallapiccola, G Novelli, J A Hurst, J Ignatius, A J Green, R M Winter, L Brueton, K Brøndum-Nielsen, P J Scambler. J Med Genet 1997
Times Cited: 820




List of shared articles



Times cited

Inborn errors of thymic stromal cell development and function.
Alexandra Y Kreins, Stefano Maio, Fatima Dhalla. Semin Immunopathol 2021
2

A Rare Etiology of Hypocalcemic Seizures in Adulthood: Clues to Diagnosis from Facial Dysmorphism.
Nisha Batra, Ravi Kant, Kausik Mandal, Kriti Joshi. Neurol India 2021
0

Late diagnosed DiGeorge syndrome in a 44-year-old female: a rare cause for recurrent syncopes in adulthood-a case report.
Khuraman Isgandarova, Stephan Molatta, Philipp Sommer. Eur Heart J Case Rep 2021
0

Consensus document on optimal management of patients with common arterial trunk.
Mark G Hazekamp, David J Barron, Joanna Dangel, Tessa Homfray, Monique R M Jongbloed, Inga Voges. Cardiol Young 2021
0

Consensus document on optimal management of patients with common arterial trunk.
Mark G Hazekamp, David J Barron, Joanna Dangel, Tessa Homfray, Monique R M Jongbloed, Inga Voges. Eur J Cardiothorac Surg 2021
1

Epilepsy and seizures in young people with 22q11.2 deletion syndrome: Prevalence and links with other neurodevelopmental disorders.
Christopher B Eaton, Rhys H Thomas, Khalid Hamandi, Gareth C Payne, Michael P Kerr, David E J Linden, Michael J Owen, Adam C Cunningham, Ullrich Bartsch, Siske S Struik,[...]. Epilepsia 2019
14

Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well-established knowledge to new frontiers.
Marta Unolt, Paolo Versacci, Silvia Anaclerio, Caterina Lambiase, Giulio Calcagni, Matteo Trezzi, Adriano Carotti, Terrence Blaine Crowley, Elaine H Zackai, Elizabeth Goldmuntz,[...]. Am J Med Genet A 2018
17

Defective Vagal Innervation in Murine Tbx1 Mutant Hearts.
Amélie Calmont, Naomi Anderson, Jenifer P Suntharalingham, Richard Ang, Andrew Tinker, Peter J Scambler. J Cardiovasc Dev Dis 2018
3

Neuropsychiatric aspects of 22q11.2 deletion syndrome: considerations in the prenatal setting.
Anne S Bassett, Gregory Costain, Christian R Marshall. Prenat Diagn 2017
9

Neuroradiographic findings in 22q11.2 deletion syndrome.
Lauren A Bohm, Tom C Zhou, Tyler J Mingo, Sarah L Dugan, Richard J Patterson, James D Sidman, Brianne B Roby. Am J Med Genet A 2017
10