Detalhe da pesquisa
1.
Pathogenic variants in HGF give rise to childhood-to-late onset primary lymphoedema by loss of function.
Hum Mol Genet
; 2024 Apr 26.
Artigo
Inglês
| MEDLINE | ID: mdl-38676400
2.
Validation of Recently Proposed Colorectal Cancer Susceptibility Gene Variants in an Analysis of Families and Patients-a Systematic Review.
Gastroenterology
; 152(1): 75-77.e4, 2017 01.
Artigo
Inglês
| MEDLINE | ID: mdl-27713038
3.
Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis.
Hum Mol Genet
; 23(17): 4729-37, 2014 Sep 01.
Artigo
Inglês
| MEDLINE | ID: mdl-24737748
4.
Developmental timing of mutations revealed by whole-genome sequencing of twins with acute lymphoblastic leukemia.
Proc Natl Acad Sci U S A
; 110(18): 7429-33, 2013 Apr 30.
Artigo
Inglês
| MEDLINE | ID: mdl-23569245
5.
Prioritizing rare variants with conditional likelihood ratios.
Hum Hered
; 79(1): 5-13, 2015.
Artigo
Inglês
| MEDLINE | ID: mdl-25659987
6.
Deciphering the genetic architecture of low-penetrance susceptibility to colorectal cancer.
Hum Mol Genet
; 22(24): 5075-82, 2013 Dec 15.
Artigo
Inglês
| MEDLINE | ID: mdl-23904454
7.
Deciphering the 8q24.21 association for glioma.
Hum Mol Genet
; 22(11): 2293-302, 2013 Jun 01.
Artigo
Inglês
| MEDLINE | ID: mdl-23399484
8.
Association analysis using next-generation sequence data from publicly available control groups: the robust variance score statistic.
Bioinformatics
; 30(15): 2179-88, 2014 Aug 01.
Artigo
Inglês
| MEDLINE | ID: mdl-24733292
9.
Multiple common susceptibility variants near BMP pathway loci GREM1, BMP4, and BMP2 explain part of the missing heritability of colorectal cancer.
PLoS Genet
; 7(6): e1002105, 2011 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-21655089
10.
The silent mutational landscape of infant MLL-AF4 pro-B acute lymphoblastic leukemia.
Genes Chromosomes Cancer
; 52(10): 954-60, 2013 Oct.
Artigo
Inglês
| MEDLINE | ID: mdl-23893660
11.
Fine-mapping of colorectal cancer susceptibility loci at 8q23.3, 16q22.1 and 19q13.11: refinement of association signals and use of in silico analysis to suggest functional variation and unexpected candidate target genes.
Hum Mol Genet
; 20(14): 2879-88, 2011 Jul 15.
Artigo
Inglês
| MEDLINE | ID: mdl-21531788
12.
Chromosome 7p11.2 (EGFR) variation influences glioma risk.
Hum Mol Genet
; 20(14): 2897-904, 2011 Jul 15.
Artigo
Inglês
| MEDLINE | ID: mdl-21531791
13.
MHC variation and risk of childhood B-cell precursor acute lymphoblastic leukemia.
Blood
; 117(5): 1633-40, 2011 Feb 03.
Artigo
Inglês
| MEDLINE | ID: mdl-21059899
14.
Investigation of clinical characteristics and genome associations in the 'UK Lipoedema' cohort.
PLoS One
; 17(10): e0274867, 2022.
Artigo
Inglês
| MEDLINE | ID: mdl-36227936
15.
Allergy and glioma risk: test of association by genotype.
Int J Cancer
; 128(7): 1736-40, 2011 Apr 01.
Artigo
Inglês
| MEDLINE | ID: mdl-20503266
16.
Genome-wide association studies for detecting cancer susceptibility.
Br Med Bull
; 97: 27-46, 2011.
Artigo
Inglês
| MEDLINE | ID: mdl-21247937
17.
Insights into protein flexibility: The relationship between normal modes and conformational change upon protein-protein docking.
Proc Natl Acad Sci U S A
; 105(30): 10390-5, 2008 Jul 29.
Artigo
Inglês
| MEDLINE | ID: mdl-18641126
18.
Mutational processes contributing to the development of multiple myeloma.
Blood Cancer J
; 9(8): 60, 2019 08 06.
Artigo
Inglês
| MEDLINE | ID: mdl-31387987
19.
Identification of recurrent noncoding mutations in B-cell lymphoma using capture Hi-C.
Blood Adv
; 3(1): 21-32, 2019 01 08.
Artigo
Inglês
| MEDLINE | ID: mdl-30606723
20.
Whole-genome sequencing of multiple myeloma reveals oncogenic pathways are targeted somatically through multiple mechanisms.
Leukemia
; 32(11): 2459-2470, 2018 11.
Artigo
Inglês
| MEDLINE | ID: mdl-29654271