Leukemia

Publications

ISSN	1476-5551
ISSN-L	0887-6924
IUID	55b3c5d894124a02b8085783f533fa5d
Modified	2020-11-27T13:14:04.009Z
Created	2017-05-09T09:12:20.073Z

Year 2022

PubMed DOI Crossref

Single base substitution and insertion/deletion mutational signatures in adult core binding factor acute myeloid leukemia.

Gunnarsson R, Yang M, Biloglav A, ..., Paulsson K, Johansson B

Leukemia 36 (6) 1681-1684 [2022-06-00; online 2022-04-01]

NGI Short read [Service] NGI Uppsala (SNP&SEQ Technology Platform) [Service] National Genomics Infrastructure [Service]

PubMed DOI Crossref

Loss of Y and clonal hematopoiesis in blood-two sides of the same coin?

Ljungström V, Mattisson J, Halvardson J, ..., Baliakas P, Forsberg LA

Leukemia 36 (3) 889-891 [2022-03-00; online 2021-11-01]

Bioinformatics Compute and Storage [Service] Clinical Genomics Uppsala [Service] NGI SNP genotyping [Service] NGI Uppsala (SNP&SEQ Technology Platform) [Service] National Genomics Infrastructure [Service]

Year 2021

PubMed DOI Crossref

Covid-19 in patients with chronic lymphocytic leukemia: clinical outcome and B- and T-cell immunity during 13 months in consecutive patients.

Blixt L, Bogdanovic G, Buggert M, ..., Hansson L, Österborg A

Leukemia - (-) - [2021-09-25; online 2021-09-25]

Autoimmunity and Serology Profiling [Service]

PubMed DOI Crossref

Co-mutation pattern, clonal hierarchy, and clone size concur to determine disease phenotype of SRSF2P95-mutated neoplasms.

Todisco G, Creignou M, Gallì A, ..., Cazzola M, Malcovati L

Leukemia 35 (8) 2371-2381 [2021-08-00; online 2020-12-21]

Clinical Genomics Uppsala [Service]

Year 2019

PubMed DOI Crossref

FLT3N676K drives acute myeloid leukemia in a xenograft model of KMT2A-MLLT3 leukemogenesis.

Hyrenius-Wittsten A, Pilheden M, Falqués-Costa A, ..., Järås M, Hagström-Andersson AK

Leukemia 33 (9) 2310-2314 [2019-09-00; online 2019-04-05]

Clinical Genomics Lund [Service]

Year 2018

PubMed DOI Crossref

PRR14L mutations are associated with chromosome 22 acquired uniparental disomy, age-related clonal hematopoiesis and myeloid neoplasia.

Chase A, Pellagatti A, Singh S, ..., Boultwood J, Cross NCP

Leukemia - (-) - [2018-12-20; online 2018-12-20]

NGI Stockholm (Genomics Applications) [Service] NGI Stockholm (Genomics Production) [Service] National Genomics Infrastructure [Service]

PubMed DOI Crossref

Mutation, methylation, and gene expression profiles in dup(1q)-positive pediatric B-cell precursor acute lymphoblastic leukemia.

Gunnarsson R, Dilorenzo S, Lundin-Ström KB, ..., Isaksson A, Johansson B

Leukemia 32 (10) 2117-2125 [2018-10-00; online 2018-03-12]

Bioinformatics Compute and Storage [Service] Bioinformatics Support and Infrastructure [Collaborative] Bioinformatics Support, Infrastructure and Training [Collaborative] NGI Uppsala (SNP&SEQ Technology Platform) [Service] National Genomics Infrastructure [Service]

PubMed DOI Crossref

Male sex and the pattern of recurrent myeloid mutations are strong independent predictors of blood transfusion intensity in patients with myelodysplastic syndromes

Rydén J, Edgren G, Karimi M, ..., Hellström-Lindberg E, Höglund P

Leukemia - (-) - [2018-09-28; online 2018-09-28]

Clinical Genomics Uppsala [Service]

Year 2017

PubMed DOI Crossref

Validation of risk stratification models in acute myeloid leukemia using sequencing-based molecular profiling.

Wang M, Lindberg J, Klevebring D, ..., Lehmann S, Grönberg H

Leukemia 31 (10) 2029-2036 [2017-10-00; online 2017-02-07]

Clinical Genomics Stockholm [Service]

PubMed DOI Crossref

EGR2 mutations define a new clinically aggressive subgroup of chronic lymphocytic leukemia

Young E, Noerenberg D, Mansouri L, ..., Rosenquist R, Damm F

Leukemia 31 (7) 1547-1554 [2017-07-00; online 2017-01-03]

Bioinformatics Compute and Storage [Service] NGI Uppsala (SNP&SEQ Technology Platform) [Service] National Genomics Infrastructure [Service]

Year 2015

PubMed DOI Crossref

Profound parental bias associated with chromosome 14 acquired uniparental disomy indicates targeting of an imprinted locus.

Chase A, Leung W, Tapper W, ..., Dumanski JP, Cross NC

Leukemia 29 (10) 2069-2074 [2015-10-00; online 2015-06-27]

NGI Stockholm (Genomics Applications) NGI Stockholm (Genomics Production) National Genomics Infrastructure

PubMed DOI Crossref

Detection of leukemia-associated mutations in peripheral blood DNA of hematologically normal elderly individuals.

Score J, Chase A, Forsberg LA, ..., Gale RE, Cross NC

Leukemia 29 (7) 1600-1602 [2015-07-00; online 2015-01-30]

NGI Uppsala (SNP&SEQ Technology Platform) National Genomics Infrastructure

Year 2014

PubMed DOI Crossref

Feasibility of targeted next-generation sequencing of the TP53 and ATM genes in chronic lymphocytic leukemia.

Mansouri L, Sutton LA, Ljungström V, ..., Nilsson M, Rosenquist R

Leukemia 28 (3) 694-696 [2014-03-00; online 2013-10-31]

NGI Uppsala (SNP&SEQ Technology Platform) National Genomics Infrastructure

Year 2013

PubMed DOI Crossref

The transporter ABCB7 is a mediator of the phenotype of acquired refractory anemia with ring sideroblasts.

Nikpour M, Scharenberg C, Liu A, ..., Grandien A, Hellström-Lindberg E

Leukemia 27 (4) 889-896 [2013-04-00; online 2012-10-17]

NGI Stockholm (Genomics Applications) NGI Stockholm (Genomics Production) National Genomics Infrastructure

PubMed DOI Crossref

450K-array analysis of chronic lymphocytic leukemia cells reveals global DNA methylation to be relatively stable over time and similar in resting and proliferative compartments.

Cahill N, Bergh AC, Kanduri M, ..., Rosén A, Rosenquist R

Leukemia 27 (1) 150-158 [2013-01-00; online 2012-08-28]

Array and Analysis Facility NGI Uppsala (SNP&SEQ Technology Platform) National Genomics Infrastructure

Year 2012

PubMed DOI Crossref

Digital gene expression profiling of primary acute lymphoblastic leukemia cells.

Nordlund J, Kiialainen A, Karlberg O, ..., Lönnerholm G, Syvänen AC

Leukemia 26 (6) 1218-1227 [2012-06-00; online 2011-12-16]

Array and Analysis Facility NGI Uppsala (SNP&SEQ Technology Platform) National Genomics Infrastructure

Year 2010

PubMed DOI Crossref

Gene-specific and global methylation patterns predict outcome in patients with acute myeloid leukemia.

Deneberg S, Grövdal M, Karimi M, ..., Hellström-Lindberg E, Lehmann S

Leukemia 24 (5) 932-941 [2010-05-00; online 2010-03-20]

Bioinformatics and Expression Analysis (BEA)

PubMed DOI Crossref

Large but not small copy-number alterations correlate to high-risk genomic aberrations and survival in chronic lymphocytic leukemia: a high-resolution genomic screening of newly diagnosed patients.

Gunnarsson R, Isaksson A, Mansouri M, ..., Juliusson G, Rosenquist R

Leukemia 24 (1) 211-215 [2010-01-00; online 2009-09-11]

Array and Analysis Facility