Year |
Citation |
Score |
2020 |
Linton SR, Popa AM, Luck SJ, Bolden K, Carter CS, Niendam TA, Simon TJ. 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. American Journal of Medical Genetics. Part A. PMID 32319730 DOI: 10.1002/Ajmg.A.61596 |
0.665 |
|
2019 |
McCabe KL, Popa AM, Durdle C, Amato M, Cabaral MH, Cruz J, Wong LM, Harvey D, Tartaglia N, Simon TJ. Quantifying the resolution of spatial and temporal representation in children with 22q11.2 deletion syndrome. Journal of Neurodevelopmental Disorders. 11: 40. PMID 31861974 DOI: 10.1186/S11689-019-9301-1 |
0.696 |
|
2019 |
Popa AM, Cruz JR, Wong LM, Harvey DJ, Angkustsiri K, Leckliter IN, Perez-Edgar K, Simon TJ. Seeing Eye to Eye With Threat: Atypical Threat Bias in Children With 22q11.2 Deletion Syndrome. American Journal On Intellectual and Developmental Disabilities. 124: 549-567. PMID 31756146 DOI: 10.1352/1944-7558-124.6.549 |
0.688 |
|
2016 |
Popa A, Hunsaker N, Deng MY, Garner J, Cruz J, Cung N, Reyes D, Simon T. Cortical tissue volumes correlate to cavum septum pellucidum size in children with 22q11.2 ddeletion syndrome and typical controls F1000research. 5. DOI: 10.7490/F1000Research.1111954.1 |
0.669 |
|
2015 |
Popa A, Beaton E, Cruz J, Wong L, Cung N, Harvey D, Simon T. Adaptation to a mild stressor in initially anxious children as related to their attention to perceived threat in a dot probe experiment F1000research. 6. DOI: 10.7490/F1000Research.1098145.1 |
0.68 |
|
2014 |
Popa A, Cruz J, Angkustsiri K, Brahmbhatt K, Cung N, Leckliter I, Quintero A, Reyes D, Shapiro H, Simon T. Atypical adaptation responses to threat stimuli in children with chromosome 22q11.2 deletion syndrome F1000research. 5. DOI: 10.7490/F1000Research.1095553.1 |
0.532 |
|
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