A citation-based method for searching scientific literature

Anne S Bassett, Donna M McDonald-McGinn, Koen Devriendt, Maria Cristina Digilio, Paula Goldenberg, Alex Habel, Bruno Marino, Solveig Oskarsdottir, Nicole Philip, Kathleen Sullivan, Ann Swillen, Jacob Vorstman. J Pediatr 2011
Times Cited: 291



T H Shaikh, H Kurahashi, S C Saitta, A M O'Hare, P Hu, B A Roe, D A Driscoll, D M McDonald-McGinn, E H Zackai, M L Budarf, B S Emanuel. Hum Mol Genet 2000
Times Cited: 376




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
1

Prenatal sonographic and cytogenetic/molecular findings of 22q11.2 microdeletion syndrome in 48 confirmed cases in a single tertiary center.
Tugba Sarac Sivrikoz, Seher Basaran, Recep Has, Birsen Karaman, Ibrahim Halil Kalelioglu, Melike Kirgiz, Umut Altunoglu, Atil Yuksel. Arch Gynecol Obstet 2021
0

Magnitude and heterogeneity of brain structural abnormalities in 22q11.2 deletion syndrome: a meta-analysis.
Maria Rogdaki, Maria Gudbrandsen, Robert A McCutcheon, Charlotte E Blackmore, Stefan Brugger, Christine Ecker, Michael C Craig, Eileen Daly, Declan G M Murphy, Oliver Howes. Mol Psychiatry 2020
13

22q11.2 deletion syndrome and congenital heart disease.
Elizabeth Goldmuntz. Am J Med Genet C Semin Med Genet 2020
6

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


Prenatal Screening for 22q11.2 Deletion Using a Targeted Microarray-Based Cell-Free DNA Test.
Maximilian Schmid, Eric Wang, Patrick E Bogard, Elisa Bevilacqua, Coleen Hacker, Susie Wang, Jigna Doshi, Karen White, Jennifer Kaplan, Andrew Sparks,[...]. Fetal Diagn Ther 2018
8