Detalhe da pesquisa
1.
Transcriptional Dysregulation Underlies Both Monogenic Arrhythmia Syndrome and Common Modifiers of Cardiac Repolarization.
Circulation
; 147(10): 824-840, 2023 03 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36524479
2.
High-Throughput Reclassification of SCN5A Variants.
Am J Hum Genet
; 107(1): 111-123, 2020 07 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32533946
3.
Genome-wide association and pathway analysis of left ventricular function after anthracycline exposure in adults.
Pharmacogenet Genomics
; 27(7): 247-254, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28542097
4.
A KCNJ8 mutation associated with early repolarization and atrial fibrillation.
Europace
; 14(10): 1428-32, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22562657
5.
A new locus for autosomal dominant generalized epilepsy associated with mild mental retardation on chromosome 3p.
Epilepsia
; 52(5): 993-9, 2011 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-21480884
6.
Reappraisal of the role of the DRD3 gene in essential tremor.
Parkinsonism Relat Disord
; 14(6): 471-5, 2008 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-18316228
7.
Infantile onset of hereditary spastic paraplegia poorly predicts the genotype.
Pediatr Neurol
; 36(6): 382-6, 2007 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-17560499
8.
Mutations in GABRA1, GABRA5, GABRG2 and GABRD receptor genes are not a major factor in the pathogenesis of familial focal epilepsy preceded by febrile seizures.
Neurosci Lett
; 394(1): 74-8, 2006 Feb 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-16256272
9.
Mutations in the GABRA1 and EFHC1 genes are rare in familial juvenile myoclonic epilepsy.
Epilepsy Res
; 71(2-3): 129-34, 2006 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-16839746
10.
Genetic and clinical risk prediction model for postoperative atrial fibrillation.
Circ Arrhythm Electrophysiol
; 8(1): 25-31, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25567478
11.
A genome-wide association study to identify genomic modulators of rate control therapy in patients with atrial fibrillation.
Am J Cardiol
; 114(4): 593-600, 2014 Aug 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-25015694
12.
A common variant on chromosome 4q25 is associated with prolonged PR interval in subjects with and without atrial fibrillation.
Am J Cardiol
; 113(2): 309-13, 2014 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24161141
13.
Common genetic polymorphism at 4q25 locus predicts atrial fibrillation recurrence after successful cardioversion.
Heart Rhythm
; 10(6): 849-55, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23428961
14.
Mutation in KIF5A can also cause adult-onset hereditary spastic paraplegia.
Neurogenetics
; 7(1): 47-50, 2006 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-16489470
15.
Identification of a novel locus for febrile seizures and epilepsy on chromosome 21q22.
Epilepsia
; 47(10): 1622-8, 2006 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-17054683
16.
Familial essential tremor with apparent autosomal dominant inheritance: should we also consider other inheritance modes?
Mov Disord
; 21(9): 1368-74, 2006 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-16721753