A citation-based method for searching scientific literature

Robert J Shprintzen. Dev Disabil Res Rev 2008
Times Cited: 274

Tamar Green, Doron Gothelf, Bronwyn Glaser, Martin Debbane, Amos Frisch, Moshe Kotler, Abraham Weizman, Stephan Eliez. J Am Acad Child Adolesc Psychiatry 2009
Times Cited: 195

List of shared articles

Times cited

Developmental trajectories and brain correlates of directed forgetting in 22q11.2 deletion syndrome.
Céline Souchay, Maria Padula, Maude Schneider, Martin Debbané, Stéphan Eliez. Brain Res 2021

Atypical attentional filtering of visual information in youth with chromosome 22q11.2 deletion syndrome as indexed by event-related potentials.
S R Linton, A M Popa, S J Luck, K Bolden, K Angkustsiri, C S Carter, T A Niendam, T J Simon. Neuroimage Clin 2021

Effectiveness and side effects of psychopharmacotherapy in individuals with 22q11.2 deletion syndrome with comorbid psychiatric disorders: a systematic review.
Mariela Mosheva, Liran Korotkin, Raquel E Gur, Abraham Weizman, Doron Gothelf. Eur Child Adolesc Psychiatry 2020

Neural and behavioral measures suggest that cognitive and affective functioning interactions mediate risk for psychosis-proneness symptoms in youth with chromosome 22q11.2 deletion syndrome.
Samantha R Linton, Abbie M Popa, Steven J Luck, Khalima Bolden, Cameron S Carter, Tara A Niendam, Tony J Simon. Am J Med Genet A 2020

Identification of relevant International Classification of Functioning Disability and Health (ICF) categories in patients with 22q11.2 Deletion Syndrome: a Delphi exercise.
Ana Paula Carvalho Corrêa, Carla Trevisan Martins Ribeiro, Dafne Dain Gandelman Horovitz, Luciana Castaneda Ribeiro. Codas 2020

Education and employment trajectories from childhood to adulthood in individuals with 22q11.2 deletion syndrome.
Mariela Mosheva, Virginie Pouillard, Yael Fishman, Lydia Dubourg, Dafna Sofrin-Frumer, Yaffa Serur, Abraham Weizman, Stephan Eliez, Doron Gothelf, Maude Schneider. Eur Child Adolesc Psychiatry 2019

An implicit and reliable neural measure quantifying impaired visual coding of facial expression: evidence from the 22q11.2 deletion syndrome.
Arnaud Leleu, Emilie Favre, Alexandre Yailian, Hugo Fumat, Juliette Klamm, Isabelle Amado, Jean-Yves Baudouin, Nicolas Franck, Caroline Demily. Transl Psychiatry 2019

Hypogyrification and its association with cognitive impairment in children with 22q11.2 deletion Syndrome: A preliminary report.
Olivia Lutz, Paulo Lizano, Suraj Sarvode Mothi, Adam Joseph, Neeraj Tandon, Leighanne Ormston, Stephen Hooper, Matcheri Keshavan, Vandana Shashi. Psychiatry Res Neuroimaging 2019

Lower cortisol levels and attenuated cortisol reactivity to daily-life stressors in adults with 22q11.2 deletion syndrome.
Esther D A van Duin, Thomas Vaessen, Zuzana Kasanova, Wolfgang Viechtbauer, Ulrich Reininghaus, Peter Saalbrink, Claudia Vingerhoets, Dennis Hernaus, Jan Booij, Ann Swillen,[...]. Psychoneuroendocrinology 2019

Speech-Language Disorders in 22q11.2 Deletion Syndrome: Best Practices for Diagnosis and Management.
Cynthia B Solot, Debbie Sell, Anne Mayne, Adriane L Baylis, Christina Persson, Oksana Jackson, Donna M McDonald-McGinn. Am J Speech Lang Pathol 2019

Seeing Eye to Eye With Threat: Atypical Threat Bias in Children With 22q11.2 Deletion Syndrome.
Abbie M Popa, Joshua R Cruz, Ling M Wong, Danielle J Harvey, Kathleen Angkustsiri, Ingrid N Leckliter, Koraly Perez-Edgar, Tony J Simon. Am J Intellect Dev Disabil 2019

Baseline connectome modular abnormalities in the childhood phase of a longitudinal study on individuals with chromosome 22q11.2 deletion syndrome.
Liang Zhan, Lisanne M Jenkins, Aifeng Zhang, Giorgio Conte, Angus Forbes, Danielle Harvey, Kathleen Angkustsiri, Naomi J Goodrich-Hunsaker, Courtney Durdle, Aaron Lee,[...]. Hum Brain Mapp 2018

Age-dependent expression pattern in the mammalian brain of a novel, small peptide encoded in the 22q11.2 deletion syndrome region.
Sabrina Kragness, Mark A A Harrison, Joby J Westmoreland, Adam Burstain, Laurie R Earls. Gene Expr Patterns 2018

No evidence for the presence of genetic variants predisposing to psychotic disorders on the non-deleted 22q11.2 allele of VCFS patients.
M Guipponi, F Santoni, M Schneider, C Gehrig, X B Bustillo, W R Kates, B Morrow, M Armando, S Vicari, F Sloan-Béna,[...]. Transl Psychiatry 2017

Quantifying indices of short- and long-range white matter connectivity at each cortical vertex.
Maria Carmela Padula, Marie Schaer, Elisa Scariati, A Kadir Mutlu, Daniela Zöller, Maude Schneider, Stephan Eliez. PLoS One 2017

Facial emotion perception by intensity in children and adolescents with 22q11.2 deletion syndrome.
Arnaud Leleu, Guillaume Saucourt, Caroline Rigard, Gabrielle Chesnoy, Jean-Yves Baudouin, Massimiliano Rossi, Patrick Edery, Nicolas Franck, Caroline Demily. Eur Child Adolesc Psychiatry 2016

The hippocampi of children with chromosome 22q11.2 deletion syndrome have localized anterior alterations that predict severity of anxiety.
Julia A Scott, Naomi Goodrich-Hunsaker, Kristopher Kalish, Aaron Lee, Michael R Hunsaker, Cynthia M Schumann, Owen T Carmichael, Tony J Simon. J Psychiatry Neurosci 2016