Search

Author/Creator Haferlach, Torsten

2. A robust molecular pattern for myelodysplastic syndromes in two independent cohorts investigated by next‐generation sequencing can be revealed by comparative bioinformatic analyses. (12th June 2014)

Authors:
Rose, Dominic; Kohlmann, Alexander; Nagata, Yasunobu; Ogawa, Seishi; Haferlach, Claudia; Kern, Wolfgang; Schnittger, Susanne; Haferlach, Torsten
Journal:
British journal of haematology
Issue:
Volume 167:Number 2(2014:Oct.)
Page Start:
278
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. A sex-informed approach to improve the personalised decision making process in myelodysplastic syndromes: a multicentre, observational cohort study. Issue 2 (February 2023)

Authors:
Maggioni, Giulia; Bersanelli, Matteo; Travaglino, Erica; Alfonso Piérola, Ana; Kasprzak, Annika; Sangerman Montserrat, Arnan; Sauta, Elisabetta; Sala, Claudia; Matteuzzi, Tommaso; Meggendorfer, Manja; Gnocchi, Matteo; Zhao, Lin-Pierre; Tentori, Cristina Astrid; Nachtkamp, Kathrin; Dall'Olio, Dani...
Journal:
Lancet
Issue:
Volume 10:Issue 2(2023)
Page Start:
e117
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

6. Acute lymphoblastic leukemia with low hypodiploid/near triploid karyotype is a specific clinical entity and exhibits a very high TP53 mutation frequency of 93%. Issue 6 (11th March 2014)

Authors:
Mühlbacher, Verena; Zenger, Melanie; Schnittger, Susanne; Weissmann, Sandra; Kunze, Franziska; Kohlmann, Alexander; Bellos, Frauke; Kern, Wolfgang; Haferlach, Torsten; Haferlach, Claudia
Journal:
Genes, chromosomes & cancer
Issue:
Volume 53:Issue 6(2014:Jun.)
Page Start:
524
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

8. Adverse prognostic impact of complex karyotype (≥3 cytogenetic alterations) in adult T-cell acute lymphoblastic leukemia (T-ALL). (October 2021)

Authors:
Genescà, Eulàlia; Morgades, Mireia; González-Gil, Celia; Fuster-Tormo, Francisco; Haferlach, Claudia; Meggendorfer, Manja; Montesinos, Pau; Barba, Pere; Gil, Cristina; Coll, Rosa; Moreno, María-José; Martínez-Carballeira, Daniel; García-Cadenas, Irene; Vives, Susana; Ribera, Jordi; González-Campo...
Journal:
Leukemia research
Issue:
Volume 109(2021)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

9. AML with gain of chromosome 8 as the sole chromosomal abnormality (+8sole) is associated with a specific molecular mutation pattern including ASXL1 mutations in 46.8% of the patients. Issue 3 (March 2015)

Authors:
Alpermann, Tamara; Haferlach, Claudia; Eder, Christiane; Nadarajah, Niroshan; Meggendorfer, Manja; Kern, Wolfgang; Haferlach, Torsten; Schnittger, Susanne
Journal:
Leukemia research
Issue:
Volume 39:Issue 3(2015:Mar.)
Page Start:
265
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

10. Analysis for loss of heterozygosity on chromosome arm 13q by STR analysis or SNP sequencing can replace analysis of FLT3‐ITD to detect patients with prognostically adverse AML. Issue 12 (3rd September 2014)

Authors:
Schnittger, Susanne; Haferlach, Claudia; Kern, Wolfgang; Haferlach, Torsten
Journal:
Genes, chromosomes & cancer
Issue:
Volume 53:Issue 12(2014:Dec.)
Page Start:
1008
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗