Lista de obras - Mette Klarskov Andersen - Dominio Público Uruguay

A common Greenlandic Inuit BRCA1 RING domain founder mutation

artículo científico publicado en 2008

Allelic methylation levels of the noncoding VTRNA2-1 located on chromosome 5q31.1 predict outcome in AML

artículo científico publicado en 2011

Antimicrobial use before chronic lymphocytic leukemia: a retrospective cohort study

artículo científico publicado en 2020

CLLU1 expression analysis adds prognostic information to risk prediction in chronic lymphocytic leukemia.

artículo científico publicado en 2007

CLLU1 expression levels predict time to initiation of therapy and overall survival in chronic lymphocytic leukemia.

artículo científico publicado en 2006

Children with low-risk acute lymphoblastic leukemia are at highest risk of second cancers.

artículo científico publicado en 2017

Clinical Outcomes in Patients with Multi-Hit <i>TP53</i> Chronic Lymphocytic Leukemia Treated with Ibrutinib

publication published on 07 May 2021

Clinical and cytogenetic features of a population-based consecutive series of 285 pediatric T-cell acute lymphoblastic leukemias: rare T-cell receptor gene rearrangements are associated with poor outcome

artículo científico publicado en 2009

Clinical and cytogenetic features of pediatric dic(9;20)(p13.2;q11.2)-positive B-cell precursor acute lymphoblastic leukemias: a Nordic series of 24 cases and review of the literature

artículo científico publicado en 2008

Clinical and genetic features of pediatric acute lymphoblastic leukemia in Down syndrome in the Nordic countries

artículo científico publicado en 2014

Combining epigenetic therapy with venetoclax overcomes alemtuzumab resistance in T-cell prolymphocytic leukemia. A case report of a 26-year-old man with a prior history of T-cell acute lymphoblastic leukemia and GI-T lymphoma

scientific article published on 24 September 2020

Cytogenetic abnormalities in childhood acute myeloid leukaemia: a Nordic series comprising all children enrolled in the NOPHO-93-AML trial between 1993 and 2001.

artículo científico publicado en 2003

Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literature

artículo científico publicado en 2007

Early relapsed disease of multiple myeloma following up-front HDM-ASCT: a study based on the Danish Multiple Myeloma Registry in the period 2005 to 2014.

artículo científico publicado en 2018

Epidemiology and Clinical Significance of Secondary and Therapy-Related Acute Myeloid Leukemia: A National Population-Based Cohort Study

artículo científico publicado en 2015

Epstein-Barr virus reactivation is a potentially severe complication in chronic lymphocytic leukemia patients with poor prognostic biological markers and fludarabine refractory disease

artículo científico publicado en 2008

Evidence of residual disease in cryopreserved ovarian cortex from female patients with leukemia

artículo científico publicado en 2010

Genome-wide analysis of cytogenetic aberrations in ETV6/RUNX1-positive childhood acute lymphoblastic leukaemia

article

Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

artículo científico publicado en 2013

High incidence of the ETV6/RUNX1 fusion gene in paediatric precursor B-cell acute lymphoblastic leukaemias with trisomy 21 as the sole cytogenetic change: a Nordic series of cases diagnosed 1989-2005.

artículo científico publicado en 2006

High modal number and triple trisomies are highly correlated favorable factors in childhood B-cell precursor high hyperdiploid acute lymphoblastic leukemia treated according to the NOPHO ALL 1992/2000 protocols

artículo científico publicado en 2013

Hypermethylation of the VTRNA1-3 Promoter is Associated with Poor Outcome in Lower Risk Myelodysplastic Syndrome Patients

artículo científico publicado en 2015

Hypogammaglobulinemia in newly diagnosed chronic lymphocytic leukemia is a predictor of early death

artículo científico publicado en 2016

Identification of novel high-impact recessively inherited type 2 diabetes risk variants in the Greenlandic population

Identification of residual leukemic cells by flow cytometry in childhood B-cell precursor acute lymphoblastic leukemia: verification of leukemic state by flow-sorting and molecular/cytogenetic methods

artículo científico publicado en 2011

Large BRCA1 and BRCA2 genomic rearrangements in Danish high risk breast-ovarian cancer families

artículo científico publicado en 2008

Latent autoimmune diabetes in adults differs genetically from classical type 1 diabetes diagnosed after the age of 35 years

artículo científico publicado en 2010

Leukemic blasts are present at low levels in spinal fluid in one-third of childhood acute lymphoblastic leukemia cases

artículo científico publicado en 2016

Loss-of-function variants in ADCY3 increase risk of obesity and type 2 diabetes

artículo científico publicado en 2018

Machine learning can identify newly diagnosed patients with CLL at high risk of infection

scientific article published on 17 January 2020

Methotrexate/6-mercaptopurine maintenance therapy influences the risk of a second malignant neoplasm after childhood acute lymphoblastic leukemia: results from the NOPHO ALL-92 study

scientific article published on 17 February 2009

MicroRNA-130a-mediated down-regulation of Smad4 contributes to reduced sensitivity to TGF-β1 stimulation in granulocytic precursors

artículo científico publicado en 2011

Mutations in idiopathic cytopenia of undetermined significance assist diagnostics and correlate to dysplastic changes

artículo científico publicado en 2016

Novel germline c-MET mutation in a family with hereditary papillary renal carcinoma.

artículo científico publicado en 2012

Paediatric B-cell precursor acute lymphoblastic leukaemia with t(1;19)(q23;p13): clinical and cytogenetic characteristics of 47 cases from the Nordic countries treated according to NOPHO protocols

artículo científico publicado en 2011

Postphlebitic Syndrome and General Surgery: An Epidemiologic Investigation

article published in 1991

RNA profiling reveals familial aggregation of molecular subtypes in non-BRCA1/2 breast cancer families

artículo científico publicado en 2014

Screening of 1331 Danish breast and/or ovarian cancer families identified 40 novel BRCA1 and BRCA2 mutations

artículo científico publicado en 2011

Studies of the common DIO2 Thr92Ala polymorphism and metabolic phenotypes in 7342 Danish white subjects

artículo científico publicado en 2006

The -250G>A promoter variant in hepatic lipase associates with elevated fasting serum high-density lipoprotein cholesterol modulated by interaction with physical activity in a study of 16,156 Danish subjects.

artículo científico publicado en 2008

The Number of Signaling Pathways Altered by Driver Mutations in Chronic Lymphocytic Leukemia Impacts Disease Outcome

artículo científico publicado en 2020

The functional Pro129Thr variant of the FAAH gene is not associated with various fat accumulation phenotypes in a population-based cohort of 5,801 whites

article

The idic(X)(q13) in myeloid malignancies: breakpoint clustering in segmental duplications and association with TET2 mutations.

artículo científico publicado en 2010

Type 2 diabetes susceptibility gene variants predispose to adult-onset autoimmune diabetes

article

Zinc transporter type 8 autoantibodies (ZnT8A): prevalence and phenotypic associations in latent autoimmune diabetes patients and patients with adult onset type 1 diabetes

article published in 2013

[A new genetic diagnosis of familiar gastrointestinal stromal tumour].

artículo científico publicado en 2012

Lista de obras de Mette Klarskov Andersen

A common Greenlandic Inuit BRCA1 RING domain founder mutation

Allelic methylation levels of the noncoding VTRNA2-1 located on chromosome 5q31.1 predict outcome in AML

Antimicrobial use before chronic lymphocytic leukemia: a retrospective cohort study

CLLU1 expression analysis adds prognostic information to risk prediction in chronic lymphocytic leukemia.

CLLU1 expression levels predict time to initiation of therapy and overall survival in chronic lymphocytic leukemia.

Children with low-risk acute lymphoblastic leukemia are at highest risk of second cancers.

Clinical Outcomes in Patients with Multi-Hit <i>TP53</i> Chronic Lymphocytic Leukemia Treated with Ibrutinib

Clinical and cytogenetic features of a population-based consecutive series of 285 pediatric T-cell acute lymphoblastic leukemias: rare T-cell receptor gene rearrangements are associated with poor outcome

Clinical and cytogenetic features of pediatric dic(9;20)(p13.2;q11.2)-positive B-cell precursor acute lymphoblastic leukemias: a Nordic series of 24 cases and review of the literature

Clinical and genetic features of pediatric acute lymphoblastic leukemia in Down syndrome in the Nordic countries

Combining epigenetic therapy with venetoclax overcomes alemtuzumab resistance in T-cell prolymphocytic leukemia. A case report of a 26-year-old man with a prior history of T-cell acute lymphoblastic leukemia and GI-T lymphoma

Cytogenetic abnormalities in childhood acute myeloid leukaemia: a Nordic series comprising all children enrolled in the NOPHO-93-AML trial between 1993 and 2001.

Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literature

Early relapsed disease of multiple myeloma following up-front HDM-ASCT: a study based on the Danish Multiple Myeloma Registry in the period 2005 to 2014.

Epidemiology and Clinical Significance of Secondary and Therapy-Related Acute Myeloid Leukemia: A National Population-Based Cohort Study

Epstein-Barr virus reactivation is a potentially severe complication in chronic lymphocytic leukemia patients with poor prognostic biological markers and fludarabine refractory disease

Evidence of residual disease in cryopreserved ovarian cortex from female patients with leukemia

Genome-wide analysis of cytogenetic aberrations in ETV6/RUNX1-positive childhood acute lymphoblastic leukaemia

Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

High incidence of the ETV6/RUNX1 fusion gene in paediatric precursor B-cell acute lymphoblastic leukaemias with trisomy 21 as the sole cytogenetic change: a Nordic series of cases diagnosed 1989-2005.

High modal number and triple trisomies are highly correlated favorable factors in childhood B-cell precursor high hyperdiploid acute lymphoblastic leukemia treated according to the NOPHO ALL 1992/2000 protocols

Hypermethylation of the VTRNA1-3 Promoter is Associated with Poor Outcome in Lower Risk Myelodysplastic Syndrome Patients

Hypogammaglobulinemia in newly diagnosed chronic lymphocytic leukemia is a predictor of early death

Identification of novel high-impact recessively inherited type 2 diabetes risk variants in the Greenlandic population

Identification of residual leukemic cells by flow cytometry in childhood B-cell precursor acute lymphoblastic leukemia: verification of leukemic state by flow-sorting and molecular/cytogenetic methods

Large BRCA1 and BRCA2 genomic rearrangements in Danish high risk breast-ovarian cancer families

Latent autoimmune diabetes in adults differs genetically from classical type 1 diabetes diagnosed after the age of 35 years

Leukemic blasts are present at low levels in spinal fluid in one-third of childhood acute lymphoblastic leukemia cases

Loss-of-function variants in ADCY3 increase risk of obesity and type 2 diabetes

Machine learning can identify newly diagnosed patients with CLL at high risk of infection

Methotrexate/6-mercaptopurine maintenance therapy influences the risk of a second malignant neoplasm after childhood acute lymphoblastic leukemia: results from the NOPHO ALL-92 study

MicroRNA-130a-mediated down-regulation of Smad4 contributes to reduced sensitivity to TGF-β1 stimulation in granulocytic precursors

Mutations in idiopathic cytopenia of undetermined significance assist diagnostics and correlate to dysplastic changes

Novel germline c-MET mutation in a family with hereditary papillary renal carcinoma.

Paediatric B-cell precursor acute lymphoblastic leukaemia with t(1;19)(q23;p13): clinical and cytogenetic characteristics of 47 cases from the Nordic countries treated according to NOPHO protocols

Postphlebitic Syndrome and General Surgery: An Epidemiologic Investigation

RNA profiling reveals familial aggregation of molecular subtypes in non-BRCA1/2 breast cancer families

Screening of 1331 Danish breast and/or ovarian cancer families identified 40 novel BRCA1 and BRCA2 mutations

Studies of the common DIO2 Thr92Ala polymorphism and metabolic phenotypes in 7342 Danish white subjects

The -250G>A promoter variant in hepatic lipase associates with elevated fasting serum high-density lipoprotein cholesterol modulated by interaction with physical activity in a study of 16,156 Danish subjects.

The Number of Signaling Pathways Altered by Driver Mutations in Chronic Lymphocytic Leukemia Impacts Disease Outcome

The functional Pro129Thr variant of the FAAH gene is not associated with various fat accumulation phenotypes in a population-based cohort of 5,801 whites

The idic(X)(q13) in myeloid malignancies: breakpoint clustering in segmental duplications and association with TET2 mutations.

Type 2 diabetes susceptibility gene variants predispose to adult-onset autoimmune diabetes

Zinc transporter type 8 autoantibodies (ZnT8A): prevalence and phenotypic associations in latent autoimmune diabetes patients and patients with adult onset type 1 diabetes

[A new genetic diagnosis of familiar gastrointestinal stromal tumour].