A citation-based method for searching scientific literature

L A Jerome, V E Papaioannou. Nat Genet 2001
Times Cited: 721



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

Congenital Athymia: Genetic Etiologies, Clinical Manifestations, Diagnosis, and Treatment.
Cathleen Collins, Emily Sharpe, Abigail Silber, Sarah Kulke, Elena W Y Hsieh. J Clin Immunol 2021
1

T-Cell Immunodeficiencies With Congenital Alterations of Thymic Development: Genes Implicated and Differential Immunological and Clinical Features.
Giuliana Giardino, Carla Borzacchiello, Martina De Luca, Roberta Romano, Rosaria Prencipe, Emilia Cirillo, Claudio Pignata. Front Immunol 2020
5


Vestibular dysfunction is a manifestation of 22q11.2 deletion syndrome.
Annelore Willaert, Charlotte Van Eynde, Nicolas Verhaert, Christian Desloovere, Vincent Vander Poorten, Koenraad Devriendt, Ann Swillen, Greet Hens. Am J Med Genet A 2019
3

Ontogeny of the facial phenotypic variability in Mexican patients with 22q11.2 deletion syndrome.
Arodi Farrera, María Villanueva, Alfredo Vizcaíno, Patricia Medina-Bravo, Norma Balderrábano-Saucedo, Mariana Rives, David Cruz, Elizabeth Hernández-Carbajal, Javier Granados-Riveron, Rocío Sánchez-Urbina. Head Face Med 2019
0


Congenital respiratory tract disorders in 22q11.2 deletion syndrome.
Emmy Verheij, Lucienne Speleman, Aebele B Mink van der Molen, Henricus G X M Thomeer. Int J Pediatr Otorhinolaryngol 2018
4

Dysregulation of TBX1 dosage in the anterior heart field results in congenital heart disease resembling the 22q11.2 duplication syndrome.
Erica Hasten, Donna M McDonald-McGinn, Terrence B Crowley, Elaine Zackai, Beverly S Emanuel, Bernice E Morrow, Silvia E Racedo. Hum Mol Genet 2018
10

A pilot study on immuno-psychiatry in the 22q11.2 deletion syndrome: A role for Th17 cells in psychosis?
Elfi Vergaelen, Carmen Schiweck, Kristof Van Steeland, Jacqueline Counotte, Wim Veling, Ann Swillen, Hemmo Drexhage, Stephan Claes. Brain Behav Immun 2018
12

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

Gene expression profiling in the developing secondary palate in the absence of Tbx1 function.
Maria Zoupa, Guilherme Machado Xavier, Stephanie Bryan, Ioannis Theologidis, Matthew Arno, Martyn T Cobourne. BMC Genomics 2018
2

Genetic Imbalances in Argentinean Patients with Congenital Conotruncal Heart Defects.
Marisol Delea, Lucía D Espeche, Carlos D Bruque, María Paz Bidondo, Lucía S Massara, Jaen Oliveri, Paloma Brun, Viviana R Cosentino, Celeste Martinoli, Norma Tolaba,[...]. Genes (Basel) 2018
2