W. Hofmann

发表

Analysis of Array-CGH Data Using the R and Bioconductor Software Suite

D. Steinemann, W. Hofmann, A. Weigmann, 2009, Comparative and functional genomics.

Comprehensive MALDI-TOF Biotyping of the Non-Redundant Harvard Pseudomonas aeruginosa PA14 Transposon Insertion Mutant Library

M. Kostrzewa, S. Häussler, W. Hofmann, 2015, PloS one.

Cryptic TCF3 fusions in childhood leukemia - detection by RNA-sequencing.

D. Steinemann, M. Schrappe, A. Möricke, 2021, Genes, chromosomes & cancer.

Routes of Clonal Evolution into Complex Karyotypes in Myelodysplastic Syndrome Patients with 5q Deletion

M. Heuser, F. Thol, A. Ganser, 2018, International journal of molecular sciences.

The identification of pathogenic variants in BRCA1/2 negative, high risk, hereditary breast and/or ovarian cancer patients: High frequency of FANCM pathogenic variants

D. Steinemann, E. Schröck, T. Illig, 2019, International journal of cancer.

Frequency and prognostic impact of PAX5 p.P80R in pediatric acute lymphoblastic leukemia patients treated on an AIEOP‐BFM acute lymphoblastic leukemia protocol

D. Steinemann, M. Schrappe, A. Möricke, 2020, Genes, chromosomes & cancer.

GT198 (PSMC3IP) germline variants in early-onset breast cancer patients from hereditary breast and ovarian cancer families

D. Steinemann, T. Illig, W. Hofmann, 2017, Genes & cancer.

Chromosomal Instability and Telomere Shortening in Long-Term Culture of Hematopoietic Stem Cells: Insights from a Cell Culture Model of RPS14 Haploinsufficiency

A. Schambach, U. Modlich, W. Hofmann, 2013, Cytogenetic and Genome Research.

Cytogenetic follow-up by karyotyping and fluorescence in situ hybridization: implications for monitoring patients with myelodysplastic syndrome and deletion 5q treated with lenalidomide

P. Fenaux, E. Hellström-Lindberg, H. Kreipe, 2011, Haematologica.

Pathological mutations in PNKP trigger defects in DNA single-strand break repair but not DNA double-strand break repair

A. Leal, K. Caldecott, H. Hanzlíková, 2020, Nucleic acids research.

Short Telomeres Before Lenalidomide Treatment Predict Leukemic Progression In Patients with Myelodysplastic Syndrome and Deletion 5q

K. Nielsen, E. Hellström-Lindberg, M. Morgan, 2010 .

Candidate genes and sequence variants for susceptibility to mycobacterial infection identified by whole-exome sequencing

T. Illig, G. H. Bruun, B. Andresen, 2022, Frontiers in Genetics.

Copy Number Analysis in a Large Cohort Suggestive of Inborn Errors of Immunity Indicates a Wide Spectrum of Relevant Chromosomal Losses and Gains

D. Steinemann, T. Illig, Anita Fernandez, 2022, Journal of Clinical Immunology.

Telomere shortening, TP53 mutations and deletions in chronic lymphocytic leukemia result in increased chromosomal instability and breakpoint clustering in heterochromatic regions

H. Kreipe, W. Hofmann, B. Schlegelberger, 2017, Annals of Hematology.

From a variant of unknown significance to pathogenic: Reclassification of a large novel duplication in BRCA2 by high‐throughput sequencing

D. Steinemann, W. Hofmann, B. Schlegelberger, 2019, Molecular genetics & genomic medicine.

CYP2E1 genotyping in renal cell/urothelial cancer patients in comparison with control populations.

W. Hofmann, V. Janitzky, K. Farker, 1998, International journal of clinical pharmacology and therapeutics.

Human BRCA1-Associated Breast Cancer: No Increase in Numerical Chromosomal Instability Compared to Sporadic Tumors

D. Steinemann, H. Kreipe, W. Hofmann, 2011, Cytogenetic and Genome Research.

MDS1 and EVI1 complex locus (MECOM): a novel candidate gene for hereditary hematological malignancies

D. Steinemann, T. Illig, G. Wulf, 2017, Haematologica.

Implementation of RNA sequencing and array CGH in the diagnostic workflow of the AIEOP-BFM ALL 2017 trial on acute lymphoblastic leukemia

D. Steinemann, M. Schrappe, A. Möricke, 2020, Annals of Hematology.

De novo missense variants in the RAP1B gene identified in two patients with syndromic thrombocytopenia

D. Steinemann, W. Hofmann, B. Schlegelberger, 2020, Clinical genetics.

Telomere shortening and chromosomal instability in myelodysplastic syndromes

H. Kreipe, K. Vang Nielsen, W. Hofmann, 2009, Genes, chromosomes & cancer.

Histone methyltransferase Suv39h1 deficiency prevents Myc‐induced chromosomal instability in murine myeloid leukemias

H. Kreipe, U. Modlich, C. Baum, 2013, Genes, chromosomes & cancer.

Clonal heterogeneity in childhood myelodysplastic syndromes—Challenge for the detection of chromosomal imbalances by array‐CGH

D. Steinemann, P. Lichter, C. Niemeyer, 2010, Genes, chromosomes & cancer.

Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity

D. Steinemann, H. Prokisch, T. Illig, 2018, Breast Cancer Research.

Rare compound heterozygous variants in PNKP identified by whole exome sequencing in a German patient with ataxia‐oculomotor apraxia 4 and pilocytic astrocytoma

D. Steinemann, T. Illig, M. Golas, 2018, Clinical genetics.

CTLA-4 Insufficiency due to a Novel CTLA-4 Deletion, Identified through Copy Number Variation Analysis

F. Atschekzei, T. Witte, W. Hofmann, 2022, International Archives of Allergy and Immunology.

Systematic genetic analysis of pediatric patients with autoinflammatory diseases

D. Viemann, C. Klemann, A. Bergmann, 2023, Frontiers in Genetics.

A Novel Alu Element Insertion in ATM Induces Exon Skipping in Suspected HBOC Patients

D. Steinemann, T. Dörk, W. Hofmann, 2023, Human Mutation.

Haploinsufficiency of ETV6 and CDKN1B in patients with acute myeloid leukemia and complex karyotype

D. Steinemann, L. Bullinger, K. Döhner, 2014, BMC Genomics.

Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity

D. Steinemann, H. Prokisch, T. Illig, 2018, Breast Cancer Research.

A ‘telomere-associated secretory phenotype’ cooperates with BCR-ABL to drive malignant proliferation of leukemic cells

D. Steinemann, A. Schuppert, C. Bokemeyer, 2014, Leukemia.

Telomere shortening, clonal evolution and disease progression in myelodysplastic syndrome patients with 5q deletion treated with lenalidomide

K. Nielsen, E. Hellström-Lindberg, M. Morgan, 2012, Leukemia.

Haploinsufficiency of ETV6 and CDKN1B in patients with acute myeloid leukemia and complex karyotype

D. Steinemann, L. Bullinger, K. Döhner, 2014, BMC Genomics.