A citation-based method for searching scientific literature

Miri Carmel, Omer Zarchi, Elena Michaelovsky, Amos Frisch, Miriam Patya, Tamar Green, Doron Gothelf, Abraham Weizman. J Psychiatr Res 2014
Times Cited: 16



K C Murphy, L A Jones, M J Owen. Arch Gen Psychiatry 1999
Times Cited: 757




List of shared articles



Times cited

Molecular genetics of 22q11.2 deletion syndrome.
Bernice E Morrow, Donna M McDonald-McGinn, Beverly S Emanuel, Joris R Vermeesch, Peter J Scambler. Am J Med Genet A 2018
48

PRODH rs450046 and proline x COMT Val¹⁵⁸ Met interaction effects on intelligence and startle in adults with 22q11 deletion syndrome.
Mariken B de Koning, Esther D A van Duin, Erik Boot, Oswald J N Bloemen, Jaap A Bakker, Kathryn M Abel, Thérèse A M J van Amelsvoort. Psychopharmacology (Berl) 2015
9

Lower [18F]fallypride binding to dopamine D2/3 receptors in frontal brain areas in adults with 22q11.2 deletion syndrome: a positron emission tomography study.
Esther D A van Duin, Jenny Ceccarini, Jan Booij, Zuzana Kasanova, Claudia Vingerhoets, Jytte van Huijstee, Alexander Heinzel, Siamak Mohammadkhani-Shali, Oliver Winz, Felix Mottaghy,[...]. Psychol Med 2020
2


A cross-comparison of cognitive ability across 8 genomic disorders.
Michael Mortillo, Jennifer G Mulle. Curr Opin Genet Dev 2021
1

The role of COMT and plasma proline in the variable penetrance of autistic spectrum symptoms in 22q11.2 deletion syndrome.
E Hidding, H Swaab, L M J de Sonneville, H van Engeland, J A S Vorstman. Clin Genet 2016
11