Detalhe da pesquisa
1.
Pharmacogenetics of methylphenidate response and tolerability in attention-deficit/hyperactivity disorder.
Pharmacogenomics J
; 17(1): 98-104, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26810137
2.
Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations.
Mol Psychiatry
; 19(7): 784-90, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-23999528
3.
Candidate-gene association study searching for genetic factors involved in migraine chronification.
Cephalalgia
; 35(6): 500-7, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25169732
4.
The genetics of attention deficit/hyperactivity disorder in adults, a review.
Mol Psychiatry
; 17(10): 960-87, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22105624
5.
Genetic architecture of ADHD and overlap with other psychiatric disorders and cognition-related phenotypes.
Neurosci Biobehav Rev
; 153: 105313, 2023 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-37451654
6.
A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication.
Mol Psychiatry
; 15(11): 1053-66, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-20157310
7.
Exploration of 19 serotoninergic candidate genes in adults and children with attention-deficit/hyperactivity disorder identifies association for 5HT2A, DDC and MAOB.
Mol Psychiatry
; 14(1): 71-85, 2009 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-17938636
8.
Association study of the serotoninergic system in migraine in the Spanish population.
Am J Med Genet B Neuropsychiatr Genet
; 153B(1): 177-84, 2010 Jan 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-19455600
9.
Meta-analysis of brain-derived neurotrophic factor p.Val66Met in adult ADHD in four European populations.
Am J Med Genet B Neuropsychiatr Genet
; 153B(2): 512-523, 2010 Mar 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-19603419
10.
Lack of association of hormone receptor polymorphisms with migraine.
Eur J Neurol
; 16(3): 413-5, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19175383
11.
Genetic analysis of 27 Spanish patients with hemiplegic migraine, basilar-type migraine and childhood periodic syndromes.
Cephalalgia
; 28(10): 1039-47, 2008 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-18644040
12.
Preliminary evidence for association of genetic variants in pri-miR-34b/c and abnormal miR-34c expression with attention deficit and hyperactivity disorder.
Transl Psychiatry
; 6(8): e879, 2016 08 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-27576168
13.
Exome chip analyses in adult attention deficit hyperactivity disorder.
Transl Psychiatry
; 6(10): e923, 2016 10 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-27754487
14.
Transcriptomic and genetic studies identify NFAT5 as a candidate gene for cocaine dependence.
Transl Psychiatry
; 5: e667, 2015 Oct 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-26506053
15.
Splicing mutations, mainly IVS6-1(G>T), account for 70% of fumarylacetoacetate hydrolase (FAH) gene alterations, including 7 novel mutations, in a survey of 29 tyrosinemia type I patients.
Hum Mutat
; 20(3): 180-8, 2002 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-12203990
16.
Adult-onset autosomal recessive ataxia with thalamic lesions in a Finnish family.
Neurology
; 57(6): 1043-9, 2001 Sep 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-11571332
17.
Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain disease.
Neurology
; 56(8): 1059-69, 2001 Apr 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-11320179
18.
Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts unlinked to the LAMA2, FCMD and MEB loci.
Neuromuscul Disord
; 10(8): 548-52, 2000 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-11053680
19.
Two new mild homozygous mutations in Gaucher disease patients: clinical signs and biochemical analyses.
Am J Med Genet
; 70(4): 437-43, 1997 Jun 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-9182788
20.
Mutation analysis of Gaucher disease patients from Argentina: high prevalence of the RecNciI mutation.
Am J Med Genet
; 80(4): 343-51, 1998 Dec 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-9856561