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



Anne-Claire Noël, Fanny Pelluard, Anne-Lise Delezoide, Louise Devisme, Laurence Loeuillet, Brigitte Leroy, Alain Martin, Raymonde Bouvier, Annie Laquerriere, Corinne Jeanne-Pasquier, Betty Bessieres-Grattagliano, Charlotte Mechler, Elisabeth Alanio, Camille Leroy, Dominique Gaillard. Am J Med Genet A 2014
Times Cited: 24




List of shared articles



Times cited

Camptodactyly and DiGeorge syndrome: A rare hand anomaly.
C M Hurley, N McHugh, S Carr, J L Kelly. JPRAS Open 2021
0

Prenatal screening of DiGeorge (22q11.2 deletion) syndrome by abnormalities of the great arteries among Thai pregnant women.
Kuntharee Traisrisilp, Fuanglada Tongprasert, Kasemsri Srisupundit, Suchaya Luewan, Theera Tongsong. Obstet Gynecol Sci 2020
2

How diseases became "genetic".
Ilana Löwy. Cien Saude Colet 2019
0

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

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

Camptodactyly and the 22q11.2 deletion syndrome.
Natario L Couser, Chetna K Pande, Jonathan M Walsh, James Tepperberg, Arthur S Aylsworth. Am J Med Genet A 2017
2

[22q11.2 microdeletion syndrome: Analysis of the care pathway before the genetic diagnosis].
T Ingrao, L Lambert, M Valduga, G Bosser, E Albuisson, B Leheup. Arch Pediatr 2017
2