相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Familial aggregation of early-onset cancers
Sanna M. M. Heikkinen et al.
INTERNATIONAL JOURNAL OF CANCER (2020)
The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants
Ana Rio-Machin et al.
NATURE COMMUNICATIONS (2020)
Germline genetic factors in the pathogenesis of myeloproliferative neoplasms
Christine Bellanne-Chantelot et al.
BLOOD REVIEWS (2020)
Hereditary Predisposition to Hematopoietic Neoplasms: When Bloodline Matters for Blood Cancers
Abhishek A. Mangaonkar et al.
MAYO CLINIC PROCEEDINGS (2020)
Characterization of an X-chromosome-linked telomere biology disorder in females with DKC1 mutation
Elina A. M. Hirvonen et al.
LEUKEMIA (2019)
The association of germline variants with chronic lymphocytic leukemia outcome suggests the implication of novel genes and pathways in clinical evolution
Adrian Mosquera Orgueira et al.
BMC CANCER (2019)
Completeness of pediatric cancer registration in the Finnish Cancer Registry
M. Jokela et al.
ACTA ONCOLOGICA (2019)
Analysis of 153 115 patients with hematological malignancies refines the spectrum of familial risk
Amit Sud et al.
BLOOD (2019)
Identifying breast cancer susceptibility genes - a review of the genetic background in familial breast cancer
Camilla Wendt et al.
ACTA ONCOLOGICA (2019)
Familial risks of acute myeloid leukemia, myelodysplastic syndromes, and myeloproliferative neoplasms
Amit Sud et al.
BLOOD (2018)
Recent progress in Lynch syndrome and other familial colorectal cancer syndromes
Patrick M. Boland et al.
CA-A CANCER JOURNAL FOR CLINICIANS (2018)
Germline alterations in a consecutive series of acute myeloid leukemia
Ulla Wartiovaara-Kautto et al.
LEUKEMIA (2018)
Diagnostics of rare disorders: whole-exome sequencing deciphering locus heterogeneity in telomere biology disorders
Luca Trotta et al.
ORPHANET JOURNAL OF RARE DISEASES (2018)
Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma
Molly Went et al.
NATURE COMMUNICATIONS (2018)
Prognostic tumor sequencing panels frequently identify germ line variants associated with hereditary hematopoietic malignancies
Michael W. Drazer et al.
BLOOD ADVANCES (2018)
Quality measures of the population-based Finnish Cancer Registry indicate sound data quality for solid malignant tumours
Maarit K. Leinonen et al.
EUROPEAN JOURNAL OF CANCER (2017)
Concordant and discordant familial cancer: Familial risks, proportions and population impact
Christoph Frank et al.
INTERNATIONAL JOURNAL OF CANCER (2017)
Prognostic Mutations in Myelodysplastic Syndrome after Stem-Cell Transplantation
R. C. Lindsley et al.
NEW ENGLAND JOURNAL OF MEDICINE (2017)
Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia
Phillip J. Law et al.
NATURE COMMUNICATIONS (2017)
The genomic landscape of pediatric myelodysplastic syndromes
Jason R. Schwartz et al.
NATURE COMMUNICATIONS (2017)
Familial risk of non-Hodgkin lymphoma by sex, relationship, age at diagnosis and histology: a joint study from five Nordic countries
M. Fallah et al.
LEUKEMIA (2016)
Search for familial clustering of multiple myeloma with any cancer
C. Frank et al.
LEUKEMIA (2016)
Coverage and accuracy of myeloproliferative and myelodysplastic neoplasms in the Finnish Cancer Registry
Maarit K. Leinonen et al.
ACTA ONCOLOGICA (2016)
How I diagnose and manage individuals at risk for inherited myeloid malignancies
Michael W. Drazer et al.
BLOOD (2016)
The 2016 revision of the World Health Organization classification of lymphoid neoplasms
Steven H. Swerdlow et al.
BLOOD (2016)
Genomic analysis of germ line and somatic variants in familial myelodysplasia/acute myeloid leukemia
Jane E. Churpek et al.
BLOOD (2015)
Risk of familial classical Hodgkin lymphoma by relationship, histology, age, and sex: a joint study from five Nordic countries
Elham Kharazmi et al.
BLOOD (2015)
Acute lymphoblastic leukemia: an assessment of international incidence, survival, and disease burden
Aaron J. Katz et al.
CANCER CAUSES & CONTROL (2015)
Acute Lymphoblastic Leukemia in Children
Stephen P. Hunger et al.
NEW ENGLAND JOURNAL OF MEDICINE (2015)
Age at Birth of First Child and Fecundity of Women Survivors of Childhood Acute Lymphoblastic Leukemia (1987-2007): A Study of the Childhood Cancer Registry of the Rhone-Alpes Region in France (ARCERRA)
Fernand Freycon et al.
PEDIATRIC HEMATOLOGY AND ONCOLOGY (2015)
Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms
William Tapper et al.
NATURE COMMUNICATIONS (2015)
Perinatal and Familial Risk Factors for Acute Lymphoblastic Leukemia in a Swedish National Cohort
Casey Crump et al.
CANCER (2015)
Treatment of Hodgkin Lymphoma: A 50-Year Perspective
George P. Canellos et al.
JOURNAL OF CLINICAL ONCOLOGY (2014)
High Familial Risk in Nodular Lymphocyte-Predominant Hodgkin Lymphoma
Silva Saarinen et al.
JOURNAL OF CLINICAL ONCOLOGY (2013)
Familial risks for childhood acute lymphocytic leukaemia in Sweden and Finland: far exceeding the effects of known germline variants
Elham Kharazmi et al.
BRITISH JOURNAL OF HAEMATOLOGY (2012)
Familial Aggregation of Acute Myeloid Leukemia and Myelodysplastic Syndromes
Lynn R. Goldin et al.
JOURNAL OF CLINICAL ONCOLOGY (2012)
Malignant hematologic diseases in adolescents and young adults
William A. Wood et al.
BLOOD (2011)
Evidence for a common genetic aetiology in high-risk families with multiple haematological malignancy subtypes
Elizabeth M. Tegg et al.
BRITISH JOURNAL OF HAEMATOLOGY (2010)
Heritability of Hematologic Malignancies: From Pedigrees to Genomics
Jane E. Churpek et al.
HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA (2010)
Risk of cancer among children of cancer patients-a nationwide study in Finland
Laura-Maria S. Madanat-Harjuoja et al.
INTERNATIONAL JOURNAL OF CANCER (2010)
Increased risks of polycythemia vera, essential thrombocythemia, and myelofibrosis among 24 577 first-degree relatives of 11 039 patients with myeloproliferative neoplasms in Sweden
Ola Landgren et al.
BLOOD (2008)
Probability of parenthood after early onset cancer: A population-based study
Laura-Maria S. Madanat et al.
INTERNATIONAL JOURNAL OF CANCER (2008)
Sex- and kindred-specific familial risk of non-Hodgkin's lymphoma
Kamila Czene et al.
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION (2007)
The familial risk of Hodgkin's lymphoma ranks among the highest in the Swedish Family-Cancer Database
A. Altieri et al.
LEUKEMIA (2006)
Family history of hematopoietic malignancy and risk of lymphoma
ET Chang et al.
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE (2005)
Familial risk for non-Hodgkin lymphoma and other lymphoproliferative malignancies by histopathologic subtype: the Swedish Family-Cancer Database
A Altieri et al.
BLOOD (2005)
A cohort study of cancer risk in relation to family histories of cancer in the Utah Population Database
RA Kerber et al.
CANCER (2005)
Familial aggregation of Hodgkin lymphoma and related tumors
LR Goldin et al.
CANCER (2004)
Familial risk of lymphoproliferative tumors in families of patients with chronic lymphocytic leukemia: results from the Swedish Family-Cancer Database
LR Goldin et al.
BLOOD (2004)
Cancer as a complex phenotype: Pattern of cancer distribution within and beyond the nuclear family
LT Amundadottir et al.
PLOS MEDICINE (2004)
分享论文
