A citation-based method for searching scientific literature

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



D M McDonald-McGinn, M K Tonnesen, A Laufer-Cahana, B Finucane, D A Driscoll, B S Emanuel, E H Zackai. Genet Med 2001
Times Cited: 199




List of shared articles



Times cited

Congenital Heart Defects and Dysmorphic Facial Features in Patients Suspicious of 22q11.2 Deletion Syndrome in Southern Brazil.
Bruna Lixinski Diniz, Andressa Schneiders Santos, Andressa Barreto Glaeser, Bruna Baierle Guaraná, Cláudia Fernandes Lorea, Juliana Alves Josahkian, Janaína Huber, Rafael Fabiano Machado Rosa, Paulo Ricardo Gazzola Zen. J Pediatr Genet 2020
0

Microdeletion 22q11.2 syndrome: Does thymus incidental surgical resection affect its immunological profile?
E M Navarrete-Rodríguez, B E Del-Rio-Navarro, D E García-Fajardo, G J Baay-Guzmán, S E Espinosa-Padilla, E A Medina-Torres, N I Moguel-Molina, M Sánchez-Curiel-Loyo, N Nájera-Martínez, J Navarro-Munguía,[...]. Allergol Immunopathol (Madr) 2019
0

Primary immunodeficiency and autoimmunity: A comprehensive review.
Laura Amaya-Uribe, Manuel Rojas, Gholamreza Azizi, Juan-Manuel Anaya, M Eric Gershwin. J Autoimmun 2019
31

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

A Novel TBX1 Variant Causing Hypoparathyroidism and Deafness.
Malak Alghamdi, Reem Al Khalifah, Doua K Al Homyani, Waleed H Alkhamis, Stefan T Arold, Aishah Ekhzaimy, Mohammed El-Wetidy, Tarek Kashour, Rabih Halwani. J Endocr Soc 2019
1


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

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