Detalhe da pesquisa
1.
Parental influence on human germline de novo mutations in 1,548 trios from Iceland.
Nature
; 549(7673): 519-522, 2017 09 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-28959963
2.
Genome-wide association study identifies 74 loci associated with educational attainment.
Nature
; 533(7604): 539-42, 2016 05 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-27225129
3.
Selection against variants in the genome associated with educational attainment.
Proc Natl Acad Sci U S A
; 114(5): E727-E732, 2017 01 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-28096410
4.
Clonal hematopoiesis, with and without candidate driver mutations, is common in the elderly.
Blood
; 130(6): 742-752, 2017 08 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28483762
5.
Nonsense mutation in the LGR4 gene is associated with several human diseases and other traits.
Nature
; 497(7450): 517-20, 2013 May 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-23644456
6.
Multi-nucleotide de novo Mutations in Humans.
PLoS Genet
; 12(11): e1006315, 2016 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-27846220
7.
Insertion of an SVA-E retrotransposon into the CASP8 gene is associated with protection against prostate cancer.
Hum Mol Genet
; 25(5): 1008-18, 2016 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26740556
8.
Rate of de novo mutations and the importance of father's age to disease risk.
Nature
; 488(7412): 471-5, 2012 Aug 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-22914163
9.
A mutation in APP protects against Alzheimer's disease and age-related cognitive decline.
Nature
; 488(7409): 96-9, 2012 Aug 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-22801501
10.
A frameshift deletion in the sarcomere gene MYL4 causes early-onset familial atrial fibrillation.
Eur Heart J
; 38(1): 27-34, 2017 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27742809
11.
Detection of sharing by descent, long-range phasing and haplotype imputation.
Nat Genet
; 40(9): 1068-75, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19165921
12.
Rare mutations associating with serum creatinine and chronic kidney disease.
Hum Mol Genet
; 23(25): 6935-43, 2014 Dec 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-25082825
13.
Germline sequence variants in TGM3 and RGS22 confer risk of basal cell carcinoma.
Hum Mol Genet
; 23(11): 3045-53, 2014 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24403052
14.
Variant of TREM2 associated with the risk of Alzheimer's disease.
N Engl J Med
; 368(2): 107-16, 2013 Jan 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-23150908
15.
Missing heritability and strategies for finding the underlying causes of complex disease.
Nat Rev Genet
; 11(6): 446-50, 2010 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-20479774
16.
Fine-scale recombination rate differences between sexes, populations and individuals.
Nature
; 467(7319): 1099-103, 2010 Oct 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-20981099
17.
Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets.
PLoS Genet
; 9(6): e1003530, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23754956
18.
Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution.
Nat Genet
; 39(2): 218-25, 2007 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-17206141
19.
A variant in CDKAL1 influences insulin response and risk of type 2 diabetes.
Nat Genet
; 39(6): 770-5, 2007 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-17460697
20.
Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.
Nat Genet
; 39(5): 631-7, 2007 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-17401366