Detalhe da pesquisa
1.
[Genetic risk factors and their influence on neural development in autism spectrum disorders]. / Genetische Risikofaktoren und ihre Auswirkungen auf die neurale Entwicklung bei Autismus-Spektrum-Störungen.
Z Kinder Jugendpsychiatr Psychother
; 50(3): 187-202, 2021 May.
Artigo
em Alemão
| MEDLINE | ID: mdl-34128703
2.
Impact of autism-associated genetic variants in interaction with environmental factors on ADHD comorbidities: an exploratory pilot study.
J Neural Transm (Vienna)
; 126(12): 1679-1693, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31707462
3.
Common functional variants of the glutamatergic system in Autism spectrum disorder with high and low intellectual abilities.
J Neural Transm (Vienna)
; 125(2): 259-271, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29147782
4.
The neurobiological basis of human aggression: A review on genetic and epigenetic mechanisms.
Am J Med Genet B Neuropsychiatr Genet
; 171(5): 650-75, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-26494515
5.
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.
PLoS Genet
; 8(2): e1002521, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22346768
6.
Common variants in genes of the postsynaptic FMRP signalling pathway are risk factors for autism spectrum disorders.
Hum Genet
; 133(6): 781-92, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24442360
7.
Common EIF4E variants modulate risk for autism spectrum disorders in the high-functioning range.
J Neural Transm (Vienna)
; 121(9): 1107-16, 2014 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-24818597
8.
ATM protein-dependent phosphorylation of Rad50 protein regulates DNA repair and cell cycle control.
J Biol Chem
; 286(36): 31542-56, 2011 Sep 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-21757780
9.
Human RAD50 deficiency in a Nijmegen breakage syndrome-like disorder.
Am J Hum Genet
; 84(5): 605-16, 2009 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19409520
10.
The methylome in females with adolescent Conduct Disorder: Neural pathomechanisms and environmental risk factors.
PLoS One
; 17(1): e0261691, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35089926
11.
Anxiety Is Associated With DPPIV Alterations in Children With Selective Mutism and Social Anxiety Disorder: A Pilot Study.
Front Psychiatry
; 12: 644553, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34267682
12.
Genetics of autistic disorders: review and clinical implications.
Eur Child Adolesc Psychiatry
; 19(3): 169-78, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19941018
13.
Quantitative genome-wide association study of six phenotypic subdomains identifies novel genome-wide significant variants in autism spectrum disorder.
Transl Psychiatry
; 10(1): 215, 2020 07 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32624584
14.
Nijmegen Breakage Syndrome mutations and risk of breast cancer.
Int J Cancer
; 122(4): 802-6, 2008 Feb 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17957789
15.
Loss of the Chr16p11.2 ASD candidate gene QPRT leads to aberrant neuronal differentiation in the SH-SY5Y neuronal cell model.
Mol Autism
; 9: 56, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-30443311
16.
Meta-analysis and association of two common polymorphisms of the human oxytocin receptor gene in autism spectrum disorder.
Autism Res
; 9(10): 1036-1045, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-26788924
17.
Clinical radiosensitivity in breast cancer patients carrying pathogenic ATM gene mutations: no observation of increased radiation-induced acute or late effects.
Radiother Oncol
; 69(2): 155-60, 2003 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-14643952
18.
Missense variants in ATM in 26,101 breast cancer cases and 29,842 controls.
Cancer Epidemiol Biomarkers Prev
; 19(9): 2143-51, 2010 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-20826828
19.
NBS1 variant I171V and breast cancer risk.
Breast Cancer Res Treat
; 112(1): 75-9, 2008 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-18049891
20.
Slow progression of ataxia-telangiectasia with double missense and in frame splice mutations.
Am J Med Genet A
; 126A(3): 272-7, 2004 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-15054841