Lista de obras -

Clearance of Somatic Mutations at Remission and the Risk of Relapse in Acute Myeloid Leukemia

artículo científico publicado en 2018

Clinical implications of TP53 mutations in myelodysplastic syndromes treated with hypomethylating agents

artículo científico publicado en 2016

Clinical implications of cancer gene mutations in patients with chronic lymphocytic leukemia treated with lenalidomide

artículo científico publicado en 2018

Clonal evolution of acute myeloid leukemia revealed by high-throughput single-cell genomics

artículo científico publicado en 2020

Common genetic variation and the control of HIV-1 in humans

artículo científico publicado en 2009

Comprehensive T cell repertoire characterization of non-small cell lung cancer

artículo científico publicado en 2020

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

artículo científico publicado en 2012

Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy

artículo científico publicado en 2012

Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia

artículo científico publicado en 2012

Genomic and immune heterogeneity are associated with differential responses to therapy in melanoma.

artículo científico publicado en 2017

Host determinants of HIV-1 control in African Americans

artículo científico publicado en 2010

Integrated molecular analysis of tumor biopsies on sequential CTLA-4 and PD-1 blockade reveals markers of response and resistance.

artículo científico publicado en 2017

Integrative genomic analysis of adult mixed phenotype acute leukemia delineates lineage associated molecular subtypes

artículo científico publicado en 2018

Late relapse in acute myeloid leukemia (AML): clonal evolution or therapy-related leukemia?

scholarly article by Musa Yilmaz et al published 16 January 2019 in Blood Cancer Journal

Leukemia stemness and co-occurring mutations drive resistance to IDH inhibitors in acute myeloid leukemia

artículo científico publicado en 2021

Preleukaemic clonal haemopoiesis and risk of therapy-related myeloid neoplasms: a case-control study

artículo científico

Publisher Correction: Clonal evolution of acute myeloid leukemia revealed by high-throughput single-cell genomics

artículo científico publicado en 2020

Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes

artículo científico publicado en 2010

Spatially resolved analyses link genomic and immune diversity and reveal unfavorable neutrophil activation in melanoma

artículo científico publicado en 2020

The characterization of twenty sequenced human genomes

artículo científico publicado en 2010

Using ERDS to infer copy-number variants in high-coverage genomes

artículo científico publicado en 2012

Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene

artículo científico publicado en 2010

Lista de obras de

Clearance of Somatic Mutations at Remission and the Risk of Relapse in Acute Myeloid Leukemia

Clinical implications of TP53 mutations in myelodysplastic syndromes treated with hypomethylating agents

Clinical implications of cancer gene mutations in patients with chronic lymphocytic leukemia treated with lenalidomide

Clonal evolution of acute myeloid leukemia revealed by high-throughput single-cell genomics

Common genetic variation and the control of HIV-1 in humans

Comprehensive T cell repertoire characterization of non-small cell lung cancer

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy

Exome sequencing followed by large-scale genotyping suggests a limited role for moderately rare risk factors of strong effect in schizophrenia

Genomic and immune heterogeneity are associated with differential responses to therapy in melanoma.

Host determinants of HIV-1 control in African Americans

Integrated molecular analysis of tumor biopsies on sequential CTLA-4 and PD-1 blockade reveals markers of response and resistance.

Integrative genomic analysis of adult mixed phenotype acute leukemia delineates lineage associated molecular subtypes

Late relapse in acute myeloid leukemia (AML): clonal evolution or therapy-related leukemia?

Leukemia stemness and co-occurring mutations drive resistance to IDH inhibitors in acute myeloid leukemia

Preleukaemic clonal haemopoiesis and risk of therapy-related myeloid neoplasms: a case-control study

Publisher Correction: Clonal evolution of acute myeloid leukemia revealed by high-throughput single-cell genomics

Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes

Spatially resolved analyses link genomic and immune diversity and reveal unfavorable neutrophil activation in melanoma

The characterization of twenty sequenced human genomes

Using ERDS to infer copy-number variants in high-coverage genomes

Whole-genome sequencing of a single proband together with linkage analysis identifies a Mendelian disease gene