Jasmin Lisfeld

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A recurrent 11q aberration pattern characterizes a subset of MYC-negative high-grade B-cell lymphomas resembling Burkitt lymphoma.

R. Spang, W. Klapper, R. Siebert, 2014, Blood.

Next-generation phenotyping integrated in a national framework for patients with ultra-rare disorders improves genetic diagnostics and yields new molecular findings

Heinen, Heiko, Kehrer, 2023, medRxiv.

The neurodevelopmental and facial phenotype in individuals with a TRIP12 variant

Q. Waisfisz, S. Julia, D. Wieczorek, 2023, European Journal of Human Genetics.

Prevalence and clinical prediction of mitochondrial disorders in a large neuropediatric cohort

H. Prokisch, F. Kortüm, S. Wortmann, 2021, Clinical genetics.

Whole-Exome Sequencing in Critically Ill Neonates and Infants: Diagnostic Yield and Predictability of Monogenic Diagnosis

F. Kortüm, D. Lessel, J. Denecke, 2021, Neonatology.

Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencing

R. Spang, P. Stadler, A. Rosenwald, 2012, Nature Genetics.

conditional expression of Myd 88 ( p . L 252 P ) leads to the development of diffuse large B cell lymphoma in mice

A. Rosenwald, R. Eils, W. Klapper, 2017 .

Impact of Fc gamma-receptor polymorphisms on the response to rituximab treatment in children and adolescents with mature B cell lymphoma/leukemia

B. Burkhardt, A. Attarbaschi, A. Reiter, 2016, Annals of Hematology.

Non‐anaplastic peripheral T‐cell lymphoma in children and adolescents – a retrospective analysis of the NHL‐BFM study group

W. Klapper, B. Burkhardt, A. Attarbaschi, 2015, British journal of haematology.

ALK-positive anaplastic large cell lymphoma limited to the skin: clinical, histopathological and molecular analysis of 6 pediatric cases. A report from the ALCL99 study

W. Klapper, R. Siebert, M. Tinguely, 2013, Haematologica.

The landscape of genomic alterations across childhood cancers

Michael C. Heinold, Jules N. A. Kerssemakers, David C. Jones, 2018, Nature.

Autosomal dominantly inherited myopathy likely caused by the TNNT1 variant p.(Asp65Ala)

K. Kutsche, J. Matschke, J. Lisfeld, 2022, Human mutation.

MYC/MIZ1-dependent gene repression inversely coordinates the circadian clock with cell cycle and proliferation

P. Stadler, A. Rosenwald, R. Eils, 2016, Nature Communications.

Recurrent loss of heterozygosity in 1p36 associated with TNFRSF14 mutations in IRF4 translocation negative pediatric follicular lymphomas

S. Bens, W. Klapper, R. Siebert, 2013, Haematologica.

A deep intronic variant in DNM1 in a patient with developmental and epileptic encephalopathy creates a splice acceptor site and affects only transcript variants including exon 10a

K. Kutsche, M. Alawi, J. Lisfeld, 2023, neurogenetics.

Subcutaneous panniculitis‐like T‐cell lymphoma in children: a detailed clinicopathological description of 11 multifocal cases with a high frequency of haemophagocytic syndrome

W. Klapper, A. Attarbaschi, U. Kontny, 2015, The British journal of dermatology.

Recurrent loss of heterozygosity in 1p36 associated with TNFRSF14 mutations in IRF4 translocation negative pediatric follicular lymphomas

S. Bens, W. Klapper, R. Siebert, 2013, Haematologica.

Non‐anaplastic peripheral T‐cell lymphoma in children and adolescents – a retrospective analysis of the NHL‐BFM study group

W. Klapper, B. Burkhardt, A. Attarbaschi, 2015, British journal of haematology.

High resolution copy number analysis of IRF4 translocation‐positive diffuse large B‐cell and follicular lymphomas

S. Bens, W. Klapper, R. Siebert, 2013, Genes, chromosomes & cancer.