Detalhe da pesquisa
1.
Antigen presentation profiling reveals recognition of lymphoma immunoglobulin neoantigens.
Nature
; 543(7647): 723-727, 2017 03 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-28329770
2.
Next-generation sequencing-based detection of circulating tumour DNA After allogeneic stem cell transplantation for lymphoma.
Br J Haematol
; 175(5): 841-850, 2016 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-27711974
3.
Diverse somatic mutation patterns and pathway alterations in human cancers.
Nature
; 466(7308): 869-73, 2010 Aug 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-20668451
4.
Deep-sequencing approach for minimal residual disease detection in acute lymphoblastic leukemia.
Blood
; 120(26): 5173-80, 2012 Dec 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-23074282
5.
Massive evolution of the immunoglobulin heavy chain locus in children with B precursor acute lymphoblastic leukemia.
Blood
; 120(22): 4407-17, 2012 Nov 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-22932801
6.
A comparison of minimal residual disease detection in autografts among ASO-qPCR, droplet digital PCR, and next-generation sequencing in patients with multiple myeloma who underwent autologous stem cell transplantation.
Br J Haematol
; 183(4): 664-668, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29270982
7.
High-throughput method for analyzing methylation of CpGs in targeted genomic regions.
Proc Natl Acad Sci U S A
; 107(28): 12587-92, 2010 Jul 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-20616066
8.
Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT.
Nat Genet
; 34(1): 91-6, 2003 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-12704386
9.
A Systematic Method for Detecting Abnormal mRNA Splicing and Assessing Its Clinical Impact in Individuals Undergoing Genetic Testing for Hereditary Cancer Syndromes.
J Mol Diagn
; 25(3): 156-167, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36563937
10.
High-throughput, high-accuracy array-based resequencing.
Proc Natl Acad Sci U S A
; 106(16): 6712-7, 2009 Apr 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-19342489
11.
Prediction of epigenetically regulated genes in breast cancer cell lines.
BMC Bioinformatics
; 11: 305, 2010 Jun 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-20525369
12.
Rapid identification of somatic mutations in colorectal and breast cancer tissues using mismatch repair detection (MRD).
Hum Mutat
; 29(3): 441-50, 2008 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-18186519
13.
Functional single nucleotide polymorphism-based association studies.
Hum Genomics
; 2(6): 391-402, 2006 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-16848977
14.
The prognostic value of clonal heterogeneity and quantitative assessment of plasma circulating clonal IG-VDJ sequences at diagnosis in patients with follicular lymphoma.
Oncotarget
; 8(5): 8765-8774, 2017 Jan 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-28060738
15.
High quality copy number and genotype data from FFPE samples using Molecular Inversion Probe (MIP) microarrays.
BMC Med Genomics
; 2: 8, 2009 Feb 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-19228381
16.
Highly efficient somatic-mutation identification using Escherichia coli mismatch-repair detection.
Nat Methods
; 4(9): 713-5, 2007 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-17704782
17.
Large-scale characterization of public database SNPs causing non-synonymous changes in three ethnic groups.
Hum Genet
; 119(1-2): 75-83, 2006 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-16391945
18.
Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes.
Am J Hum Genet
; 76(4): 561-71, 2005 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-15719322
19.
PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis.
Am J Hum Genet
; 77(4): 567-81, 2005 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-16175503
20.
Molecular basis of intrahepatic cholestasis.
Ann Med
; 36(8): 606-17, 2004.
Artigo
em Inglês
| MEDLINE | ID: mdl-15768832