Detalhe da pesquisa
1.
CNVs conferring risk of autism or schizophrenia affect cognition in controls.
Nature
; 505(7483): 361-6, 2014 Jan 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-24352232
2.
A variant associated with nicotine dependence, lung cancer and peripheral arterial disease.
Nature
; 452(7187): 638-642, 2008 Apr 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-18385739
3.
Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology.
Nat Commun
; 13(1): 634, 2022 02 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35110524
4.
A genetic risk factor for periodic limb movements in sleep.
N Engl J Med
; 357(7): 639-47, 2007 Aug 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-17634447
5.
Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients.
Neurology
; 90(4): e332-e341, 2018 01 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-29288229
6.
PDE4D and ALOX5AP genetic variants and risk for Ischemic Cerebrovascular Disease in Sweden.
J Neurol Sci
; 263(1-2): 113-7, 2007 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-17655870
7.
Author Correction: Rare SLC13A1 variants associate with intervertebral disc disorder highlighting role of sulfate in disc pathology.
Nat Commun
; 13(1): 2419, 2022 Apr 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-35477715
8.
HLA class II sequence variants influence tuberculosis risk in populations of European ancestry.
Nat Genet
; 48(3): 318-22, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26829749