A citation-based method for searching scientific literature

Anne S Bassett, Eva W C Chow, Janice Husted, Rosanna Weksberg, Oana Caluseriu, Gary D Webb, Michael A Gatzoulis. Am J Med Genet A 2005
Times Cited: 285



D M McDonald-McGinn, R Kirschner, E Goldmuntz, K Sullivan, P Eicher, M Gerdes, E Moss, C Solot, P Wang, I Jacobs, S Handler, C Knightly, K Heher, M Wilson, J E Ming, K Grace, D Driscoll, P Pasquariello, P Randall, D Larossa, B S Emanuel, E H Zackai. Genet Couns 1999
Times Cited: 311




List of shared articles



Times cited

The Genetics and Epigenetics of 22q11.2 Deletion Syndrome.
Qiumei Du, M Teresa de la Morena, Nicolai S C van Oers. Front Genet 2020
19


Clinical and immunophenotypic characteristics of patients with chromosome 22q11.2 deletion syndrome: a single institution's experience.
Serdar Nepesov, Fatma Deniz Aygün, Umut Küçüksezer, Emre Taşdemir, Haluk Çokuğraş, Yıldız Camcıoğlu. Turk Pediatri Ars 2019
0

Variable immune deficiency related to deletion size in chromosome 22q11.2 deletion syndrome.
Blaine Crowley, Melanie Ruffner, Donna M McDonald McGinn, Kathleen E Sullivan. Am J Med Genet A 2018
22

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

Otolaryngological features in a cohort of patients affected with 22q11.2 deletion syndrome: A monocentric survey.
Fiorentino Grasso, Emilia Cirillo, Giuseppe Quaremba, Vincenzo Graziano, Vera Gallo, Letizia Cruoglio, Carmine Botta, Claudio Pignata, Sergio Motta. Am J Med Genet A 2018
3

Signs of dysarthria in adults with 22q11.2 deletion syndrome.
Christina Persson, Katja Laakso, Hannah Edwardsson, Johanna Lindblom, Lena Hartelius. Am J Med Genet A 2017
7