Detalhe da pesquisa
1.
Deep psychophysiological phenotyping of adolescents and adults with 22q11.2 deletion syndrome: a multilevel approach to defining core disease processes.
BMC Psychiatry
; 23(1): 425, 2023 06 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-37312091
2.
Deep phenotyping in 3q29 deletion syndrome: recommendations for clinical care.
Genet Med
; 23(5): 872-880, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33564151
3.
Comprehensive phenotyping of neuropsychiatric traits in a multiplex 3q29 deletion family: a case report.
BMC Psychiatry
; 20(1): 184, 2020 04 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-32321479
4.
Study protocol for The Emory 3q29 Project: evaluation of neurodevelopmental, psychiatric, and medical symptoms in 3q29 deletion syndrome.
BMC Psychiatry
; 18(1): 183, 2018 06 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29884173
5.
Common polymorphism in the oxytocin receptor gene (OXTR) is associated with human social recognition skills.
Proc Natl Acad Sci U S A
; 111(5): 1987-92, 2014 Feb 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-24367110
6.
Regulatory polymorphisms in human DBH affect peripheral gene expression and sympathetic activity.
Circ Res
; 115(12): 1017-25, 2014 Dec 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-25326128
7.
The effect of hypocalcemia in early childhood on autism-related social and communication skills in patients with 22q11 deletion syndrome.
Eur Arch Psychiatry Clin Neurosci
; 265(6): 519-24, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25267002
8.
Reduced amplitude and slowed latency of the acoustic startle response in adolescents and adults with 22q11.2 deletion syndrome.
Schizophr Res
; 269: 9-17, 2024 May 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-38703519
9.
Psychosis spectrum symptoms among individuals with schizophrenia-associated copy number variants and evidence of cerebellar correlates of symptom severity.
Psychiatry Res
; 335: 115867, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38537595
10.
Alcohol and alcohol-related harm in China: policy changes needed.
Bull World Health Organ
; 91(4): 270-6, 2013 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23599550
11.
The gut microbiome: a new frontier in autism research.
Curr Psychiatry Rep
; 15(2): 337, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23307560
12.
Sex dependent influence of a functional polymorphism in steroid 5-α-reductase type 2 (SRD5A2) on post-traumatic stress symptoms.
Am J Med Genet B Neuropsychiatr Genet
; 162B(3): 283-292, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23505265
13.
Adaptive behavior deficits in individuals with 3q29 deletion syndrome.
medRxiv
; 2023 Apr 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37066139
14.
Visual-Motor Integration Deficits in 3q29 Deletion Syndrome.
J Autism Dev Disord
; 2023 Jun 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-37354284
15.
Depression and anxiety symptoms among women who carry the FMR1 premutation: impact of raising a child with fragile X syndrome is moderated by CRHR1 polymorphisms.
Am J Med Genet B Neuropsychiatr Genet
; 159B(5): 549-59, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22573456
16.
Autism spectrum disorder symptom expression in individuals with 3q29 deletion syndrome.
Mol Autism
; 13(1): 50, 2022 12 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-36566217
17.
Linkage analysis of plasma dopamine ß-hydroxylase activity in families of patients with schizophrenia.
Hum Genet
; 130(5): 635-43, 2011 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-21509519
18.
Predictors of neonatal hypothalamic-pituitary-adrenal axis activity at delivery.
Clin Endocrinol (Oxf)
; 75(1): 90-5, 2011 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-21521269
19.
Pharmaco-genetically guided treatment of recurrent rage outbursts in an adult male with 15q13.3 deletion syndrome.
Am J Med Genet A
; 155A(4): 805-10, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21594999
20.
Copy number variants: a new molecular frontier in clinical psychiatry.
Curr Psychiatry Rep
; 13(2): 129-37, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21253883