Detalhe da pesquisa
1.
CFH Y402H confers similar risk of soft drusen and both forms of advanced AMD.
PLoS Med
; 3(1): e5, 2006 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-16300415
2.
A whole genome association study in Icelandic multiple sclerosis patients with 4804 markers.
J Neuroimmunol
; 143(1-2): 88-92, 2003 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-14575921
3.
A whole genome association study in multiple sclerosis patients from north Portugal.
J Neuroimmunol
; 143(1-2): 116-9, 2003 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-14575927
4.
A sequence variant on 17q21 is associated with age at onset and severity of asthma.
Eur J Hum Genet
; 18(8): 902-8, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20372189
5.
Variant in the sequence of the LINGO1 gene confers risk of essential tremor.
Nat Genet
; 41(3): 277-9, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19182806
6.
Sequence variants in the RNF212 gene associate with genome-wide recombination rate.
Science
; 319(5868): 1398-401, 2008 Mar 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-18239089
7.
Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits.
Nat Genet
; 40(11): 1313-8, 2008 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-18849993