Genomic prediction of relapse in recipients of allogeneic haematopoietic stem cell transplantation

ranger: A Fast Implementation of Random Forests for High Dimensional Data in C++ and R

(2017) Marvin N. Wright et al.   Journal of Statistical Software

miR-194-5p/BCLAF1 deregulation in AML tumorigenesis

(2017) C Dell'Aversana et al.   LEUKEMIA

Genetic polymorphism related to monocyte-macrophage function is associated with graft-versus-host disease

(2017) Kati Hyvärinen et al.   Scientific Reports

Contrasting the Genetic Architecture of 30 Complex Traits from Summary Association Data

(2016) Huwenbo Shi et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Immunoseq: the identification of functionally relevant variants through targeted capture and sequencing of active regulatory regions in human immune cells

(2016) Andréanne Morin et al.   BMC Medical Genomics

Empirical estimation of genome-wide significance thresholds based on the 1000 Genomes Project data set

(2016) Masahiro Kanai et al.   JOURNAL OF HUMAN GENETICS

PANTHER version 11: expanded annotation data from Gene Ontology and Reactome pathways, and data analysis tool enhancements

(2016) Huaiyu Mi et al.   NUCLEIC ACIDS RESEARCH

Effect of genetic profiling on prediction of therapeutic resistance and survival in adult acute myeloid leukemia

(2015) R B Walter et al.   LEUKEMIA

Junk DNA and the long non-coding RNA twist in cancer genetics

(2015) H Ling et al.   ONCOGENE

Combining gene mutation with gene expression data improves outcome prediction in myelodysplastic syndromes

(2015) Moritz Gerstung et al.   Nature Communications

Somatic MED12 mutations are associated with poor prognosis markers in chronic lymphocytic leukemia

(2015) Kati Kämpjärvi et al.   Oncotarget

Identification and Utilization of Donor and Recipient Genetic Variants to Predict Survival After HCT: Are We Ready for Primetime?

(2015) Lara E. Sucheston-Campbell et al.   Current Hematologic Malignancy Reports

Second-generation PLINK: rising to the challenge of larger and richer datasets

(2015) Christopher C Chang et al.   GigaScience

Epigenetic alterations in acute myeloid leukemias

(2014) Parinaz Mehdipour et al.   FEBS Journal

Regularized Machine Learning in the Genetic Prediction of Complex Traits

(2014) Sebastian Okser et al.   PLoS Genetics

Donor Haplotype B of NK KIR Receptor Reduces the Relapse Risk in HLA-Identical Sibling Hematopoietic Stem Cell Transplantation of AML Patients

(2014) Ulla Impola et al.   Frontiers in Immunology

Multicenter Analyses Demonstrate Significant Clinical Effects of Minor Histocompatibility Antigens on GvHD and GvL after HLA-Matched Related and Unrelated Hematopoietic Stem Cell Transplantation

(2013) Eric Spierings et al.   BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION

High-resolution HLA matching in hematopoietic stem cell transplantation: a retrospective collaborative analysis

(2013) D. Furst et al.   BLOOD

Clinical Role of microRNAs in Cytogenetically Normal Acute Myeloid Leukemia:miR-155Upregulation Independently Identifies High-Risk Patients

(2013) Guido Marcucci et al.   JOURNAL OF CLINICAL ONCOLOGY

Epigenetics Meets Genetics in Acute Myeloid Leukemia: Clinical Impact of a Novel Seven-Gene Score

(2013) Guido Marcucci et al.   JOURNAL OF CLINICAL ONCOLOGY

Bringing genome-wide association findings into clinical use

(2013) Teri A. Manolio   NATURE REVIEWS GENETICS

High Trans-ethnic Replicability of GWAS Results Implies Common Causal Variants

(2013) Urko M. Marigorta et al.   PLoS Genetics

Comparison of Outcomes after HLA-Matched Sibling and Unrelated Donor Transplantation for Children with High-Risk Acute Lymphoblastic Leukemia

(2012) Mei-Jie Zhang et al.   BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION

Association of Disparities in Known Minor Histocompatibility Antigens with Relapse-Free Survival and Graft-versus-Host Disease after Allogeneic Stem Cell Transplantation

(2012) Willemijn Hobo et al.   BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION

Single nucleotide polymorphisms and outcome risk in unrelated mismatched hematopoietic stem cell transplantation: an exploration study

(2012) C. Harkensee et al.   BLOOD

Evaluation of published single nucleotide polymorphisms associated with acute GVHD

(2012) J. W. Chien et al.   BLOOD

The myth of the second remission of acute leukemia in the adult

(2012) S. J. Forman et al.   BLOOD

Chronic lymphocytic leukemia: A tale of one or two signals?

(2012) Nicholas Chiorazzi et al.   CELL RESEARCH

Random forests for genomic data analysis

(2012) Xi Chen et al.   GENOMICS

Association screening of common and rare genetic variants by penalized regression

(2010) H. Zhou et al.   BIOINFORMATICS

EGR-1 activation by EGF inhibits MMP-9 expression and lymphoma growth

(2010) F. Bouchard et al.   BLOOD

Genetic Variants and Their Interactions in the Prediction of Increased Pre-Clinical Carotid Atherosclerosis: The Cardiovascular Risk in Young Finns Study

(2010) Sebastian Okser et al.   PLoS Genetics

Genome-wide association analysis by lasso penalized logistic regression

(2009) Tong Tong Wu et al.   BIOINFORMATICS

Finding the missing heritability of complex diseases

(2009) Teri A. Manolio et al.   NATURE

Donor-recipient mismatch for common gene deletion polymorphisms in graft-versus-host disease

(2009) Steven A McCarroll et al.   NATURE GENETICS

ToppGene Suite for gene list enrichment analysis and candidate gene prioritization

(2009) J. Chen et al.   NUCLEIC ACIDS RESEARCH

Donors with group B KIR haplotypes improve relapse-free survival after unrelated hematopoietic cell transplantation for acute myelogenous leukemia

(2008) S. Cooley et al.   BLOOD