Detalhe da pesquisa
1.
Discovery of novel predisposing coding and noncoding variants in familial Hodgkin lymphoma.
Blood
; 141(11): 1293-1307, 2023 03 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-35977101
2.
Association of polygenic risk score with the risk of chronic lymphocytic leukemia and monoclonal B-cell lymphocytosis.
Blood
; 131(23): 2541-2551, 2018 06 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29674426
3.
Parental longevity and survival among patients with multiple myeloma and monoclonal gammopathy of undetermined significance: a population-based study.
Br J Haematol
; 186(1): 37-44, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30906990
4.
Combined somatic mutation and copy number analysis in the survival of familial CLL.
Br J Haematol
; 181(5): 604-613, 2018 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-29687880
5.
Germline mutations in Protection of Telomeres 1 in two families with Hodgkin lymphoma.
Br J Haematol
; 181(3): 372-377, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29693246
6.
History of autoimmune disease is associated with impaired survival in multiple myeloma and monoclonal gammopathy of undetermined significance: a population-based study.
Ann Hematol
; 96(2): 261-269, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-27807648
7.
Mosaic 13q14 deletions in peripheral leukocytes of non-hematologic cancer cases and healthy controls.
J Hum Genet
; 61(5): 411-8, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-26763882
8.
Monoclonal gammopathy of undetermined significance and risk of lymphoid and myeloid malignancies: 728 cases followed up to 30 years in Sweden.
Blood
; 123(3): 338-45, 2014 Jan 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-24222331
9.
Whole exome sequencing in families at high risk for Hodgkin lymphoma: identification of a predisposing mutation in the KDR gene.
Haematologica
; 101(7): 853-60, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27365461
10.
Whole exome sequencing reveals a C-terminal germline variant in CEBPA-associated acute myeloid leukemia: 45-year follow up of a large family.
Haematologica
; 101(7): 846-52, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-26721895
11.
Juvenile myelomonocytic leukemia due to a germline CBL Y371C mutation: 35-year follow-up of a large family.
Hum Genet
; 134(7): 775-87, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25939664
12.
Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.
Blood
; 120(4): 843-6, 2012 Jul 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-22700719
13.
Infection in infancy and subsequent risk of developing lymphoma in children and young adults.
Blood
; 117(5): 1670-2, 2011 Feb 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-21127175
14.
Risk of acute myeloid leukemia and myelodysplastic syndromes after multiple myeloma and its precursor disease (MGUS).
Blood
; 118(15): 4086-92, 2011 Oct 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-21795746
15.
Personal and family history of immune-related conditions increase the risk of plasma cell disorders: a population-based study.
Blood
; 118(24): 6284-91, 2011 Dec 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-21998210
16.
Whole exome sequencing in families with CLL detects a variant in Integrin ß 2 associated with disease susceptibility.
Blood
; 128(18): 2261-2263, 2016 11 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-27629550
17.
Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL.
Blood
; 117(6): 1911-6, 2011 Feb 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-21131588
18.
A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma.
Am J Hum Genet
; 85(5): 679-91, 2009 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-19836008
19.
Survival in patients with familial and sporadic myeloproliferative neoplasms.
Blood
; 125(23): 3665-6, 2015 Jun 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-26045595
20.
Population-based study on the impact of the familial form of Waldenström macroglobulinemia on overall survival.
Blood
; 125(13): 2174-5, 2015 Mar 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-25814489