A citation-based method for searching scientific literature

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



Lisa J Kobrynski, Kathleen E Sullivan. Lancet 2007
Times Cited: 347




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

Downregulation of genes outside the deleted region in individuals with 22q11.2 deletion syndrome.
Anelisa Gollo Dantas, Marcos Leite Santoro, Natalia Nunes, Claudia Berlim de Mello, Larissa Salustiano Evangelista Pimenta, Vera Ayres Meloni, Diogo Cordeiro Queiroz Soares, Sintia Nogueira Belangero, Gianna Carvalheira, Chong Ae Kim,[...]. Hum Genet 2019
2

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

A case report of T-box 1 mutation causing phenotypic features of chromosome 22q11.2 deletion syndrome.
Raad A Haddad, Gregory A Clines, Jennifer A Wyckoff. Clin Diabetes Endocrinol 2019
1

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

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