A citation-based method for searching scientific literature

Wai Lun Alan Fung, Nancy J Butcher, Gregory Costain, Danielle M Andrade, Erik Boot, Eva W C Chow, Brian Chung, Cheryl Cytrynbaum, Hanna Faghfoury, Leona Fishman, Sixto García-Miñaúr, Susan George, Anthony E Lang, Gabriela Repetto, Andrea Shugar, Candice Silversides, Ann Swillen, Therese van Amelsvoort, Donna M McDonald-McGinn, Anne S Bassett. Genet Med 2015
Times Cited: 114

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

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

Neurobiological perspective of 22q11.2 deletion syndrome.
Janneke R Zinkstok, Erik Boot, Anne S Bassett, Noboru Hiroi, Nancy J Butcher, Claudia Vingerhoets, Jacob A S Vorstman, Therese A M J van Amelsvoort. Lancet Psychiatry 2019

Glutamatergic function in a genetic high-risk group for psychosis: A proton magnetic resonance spectroscopy study in individuals with 22q11.2 deletion.
Maria Rogdaki, Pamela Hathway, Maria Gudbrandsen, Robert A McCutcheon, Sameer Jauhar, Eileen Daly, Oliver Howes. Eur Neuropsychopharmacol 2019

Accurate diagnosis of spinal muscular atrophy and 22q11.2 deletion syndrome using limited deoxynucleotide triphosphates and high-resolution melting.
Xiaoqing Zhang, Bo Wang, Lichen Zhang, Guoling You, Robert A Palais, Luming Zhou, Qihua Fu. BMC Genomics 2018

Whole-genome sequencing suggests mechanisms for 22q11.2 deletion-associated Parkinson's disease.
Nancy J Butcher, Daniele Merico, Mehdi Zarrei, Lucas Ogura, Christian R Marshall, Eva W C Chow, Anthony E Lang, Stephen W Scherer, Anne S Bassett. PLoS One 2017

Pediatric healthcare costs for patients with 22q11.2 deletion syndrome.
Peter Benn, Sushma Iyengar, Terrence Blaine Crowley, Elaine H Zackai, Evanette K Burrows, Solomon Moshkevich, Donna M McDonald-McGinn, Kathleen E Sullivan, Zachary Demko. Mol Genet Genomic Med 2017

Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data.
Kin Y Mok, Una Sheerin, Javier Simón-Sánchez, Afnan Salaka, Lucy Chester, Valentina Escott-Price, Kiran Mantripragada, Karen M Doherty, Alastair J Noyce, Niccolo E Mencacci,[...]. Lancet Neurol 2016