Detalhe da pesquisa
1.
Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations.
Cell;
182(5): 1198-1213.e14, 2020 09 03.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32888493
2.
The power of genetic diversity in genome-wide association studies of lipids.
Nature;
600(7890): 675-679, 2021 12.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34887591
3.
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids.
Am J Hum Genet;
109(8): 1366-1387, 2022 08 04.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35931049
4.
Author Correction: The power of genetic diversity in genome-wide association studies of lipids.
Nature;
618(7965): E19-E20, 2023 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37237109
5.
Negligible impact of rare autoimmune-locus coding-region variants on missing heritability.
Nature;
498(7453): 232-5, 2013 Jun 13.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23698362
6.
A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.
Nat Genet;
39(7): 827-9, 2007 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17558408
7.
Genome-wide analysis of allelic expression imbalance in human primary cells by high-throughput transcriptome resequencing.
Hum Mol Genet;
19(1): 122-34, 2010 Jan 01.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19825846
8.
Transferability of genetic loci and polygenic scores for cardiometabolic traits in British Pakistani and Bangladeshi individuals.
Nat Commun;
13(1): 4664, 2022 08 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35945198
9.
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis.
Genome Biol;
23(1): 268, 2022 12 27.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36575460
10.
Detection, imputation, and association analysis of small deletions and null alleles on oligonucleotide arrays.
Am J Hum Genet;
82(6): 1316-33, 2008 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18519066
11.
Shared and distinct genetic variants in type 1 diabetes and celiac disease.
N Engl J Med;
359(26): 2767-77, 2008 Dec 25.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19073967
12.
Fine-scale population structure and demographic history of British Pakistanis.
Nat Commun;
12(1): 7189, 2021 12 10.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34893604
13.
Characterising a healthy adult with a rare HAO1 knockout to support a therapeutic strategy for primary hyperoxaluria.
Elife;
92020 03 24.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32207686
14.
Suspicious breast lesions: assessment of 3D Doppler US indexes for classification in a test population and fourfold cross-validation scheme.
Radiology;
249(2): 463-70, 2008 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-18936310
15.
Recurrent cancer after breast-conserving surgery with radiation therapy for ductal carcinoma in situ: mammographic features, method of detection, and stage of recurrence.
AJR Am J Roentgenol;
189(1): 140-4, 2007 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17579163
16.
Muramyl dipeptide and toll-like receptor sensitivity in NOD2-associated Crohn's disease.
Lancet;
365(9473): 1794-6, 2005.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15910952
17.
Detection of muramyl dipeptide-sensing pathway defects in patients with Crohn's disease.
Inflamm Bowel Dis;
12(7): 598-605, 2006 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-16804397
18.
Health and population effects of rare gene knockouts in adult humans with related parents.
Science;
352(6284): 474-7, 2016 Apr 22.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26940866
19.
A common CTLA4 haplotype associated with coeliac disease.
Eur J Hum Genet;
13(4): 440-4, 2005 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-15657618
20.
Recent advances in coeliac disease genetics.
Gut;
58(4): 473-6, 2009 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19299378