Search details
1.
A genetics-first approach to understanding autism and schizophrenia spectrum disorders: the 22q11.2 deletion syndrome.
Mol Psychiatry
; 28(1): 341-353, 2023 01.
Article
in English
| MEDLINE | ID: mdl-36192458
2.
Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome.
Genet Med
; 25(3): 100344, 2023 03.
Article
in English
| MEDLINE | ID: mdl-36729052
3.
Updated clinical practice recommendations for managing children with 22q11.2 deletion syndrome.
Genet Med
; 25(3): 100338, 2023 03.
Article
in English
| MEDLINE | ID: mdl-36729053
4.
Within-family influences on dimensional neurobehavioral traits in a high-risk genetic model.
Psychol Med
; 52(14): 3184-3192, 2022 10.
Article
in English
| MEDLINE | ID: mdl-33443009
5.
Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins.
Hum Mol Genet
; 28(22): 3724-3733, 2019 11 15.
Article
in English
| MEDLINE | ID: mdl-31884517
6.
Altered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study.
Mol Psychiatry
; 25(11): 2818-2831, 2020 11.
Article
in English
| MEDLINE | ID: mdl-31358905
7.
Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome.
Curr Psychiatry Rep
; 23(3): 13, 2021 02 24.
Article
in English
| MEDLINE | ID: mdl-33625600
8.
Low prevalence of substance use in people with 22q11.2 deletion syndrome.
Br J Psychiatry
; 215(5): 661-667, 2019 11.
Article
in English
| MEDLINE | ID: mdl-30604657
9.
White matter abnormalities in 22q11.2 deletion syndrome patients showing cognitive decline.
Psychol Med
; 48(10): 1655-1663, 2018 07.
Article
in English
| MEDLINE | ID: mdl-29143717
10.
Understanding the pediatric psychiatric phenotype of 22q11.2 deletion syndrome.
Am J Med Genet A
; 176(10): 2182-2191, 2018 10.
Article
in English
| MEDLINE | ID: mdl-30194907
11.
Untargeted metabolic analysis in dried blood spots reveals metabolic signature in 22q11.2 deletion syndrome.
Transl Psychiatry
; 12(1): 97, 2022 03 09.
Article
in English
| MEDLINE | ID: mdl-35264571
12.
A normative chart for cognitive development in a genetically selected population.
Neuropsychopharmacology
; 47(7): 1379-1386, 2022 06.
Article
in English
| MEDLINE | ID: mdl-33782512
13.
A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants.
Am J Psychiatry
; 178(1): 77-86, 2021 01 01.
Article
in English
| MEDLINE | ID: mdl-33384013
14.
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome.
Nat Med
; 26(12): 1912-1918, 2020 12.
Article
in English
| MEDLINE | ID: mdl-33169016
15.
Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2.
Neurology
; 90(23): e2059-e2067, 2018 06 05.
Article
in English
| MEDLINE | ID: mdl-29752303
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