Publications by authors named "Dirk Prawitt"

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Molecular mechanisms of human overgrowth and use of in its diagnostics: chances and challenges.
Dirk Prawitt, Thomas Eggermann

Front Genet· June 2024

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Interindividual variability in cold-pressor pain sensitivity is not explained by peripheral vascular responding and generalizes to a C-nociceptor-specific pain phenotype.
Richard D Martel, Georgios Papafragou, Sylvia Weigand, Roman Rolke, Dirk Prawitt

Pain· March 2024

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Comprehensive genetic testing approaches as the basis for personalized management of growth disturbances: current status and perspectives.
Danielle Christine Maria van der Kaay, Anne Rochtus, Gerhard Binder, Ingo Kurth, Dirk Prawitt

Endocr Connect· November 2022

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Further understanding of paternal uniparental disomy in Beckwith-Wiedemann syndrome.
Thomas Eggermann, Dirk Prawitt

Expert Rev Endocrinol Metab· November 2022

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Molecular Basis of Beckwith-Wiedemann Syndrome Spectrum with Associated Tumors and Consequences for Clinical Practice.
Thomas Eggermann, Eamonn R Maher, Christian P Kratz, Dirk Prawitt

Cancers (Basel)· June 2022

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Hypermethylation of intron 2 in childhood cancer patients, leukemia and tumor cell lines suggest a role for oncogenic transformation.
Danuta Galetzka, Julia Böck, Lukas Wagner, Marcus Dittrich, Olesja Sinizyn, Dirk Prawitt

EXCLI J· January 2022

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Correction to: Molecular karyotyping and gene expression analysis in childhood cancer patients.
Danuta Galetzka, Tobias Müller, Marcus Dittrich, Miriam Endres, Nergiz Kartal, Dirk Prawitt

J Mol Med (Berl)· November 2020

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Cancer incidence and spectrum among children with genetically confirmed Beckwith-Wiedemann spectrum in Germany: a retrospective cohort study.
Sümeyye Cöktü, Claudia Spix, Melanie Kaiser, Jasmin Beygo, Stephanie Kleinle, Dirk Prawitt

Br J Cancer· August 2020

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Molecular karyotyping and gene expression analysis in childhood cancer patients.
Galetzka Danuta, Müller Tobias, Dittrich Marcus, Endres Miriam, Kartal Nergiz, Prawitt Dirk

J Mol Med (Berl)· August 2020

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Genetic testing in inherited endocrine disorders: joint position paper of the European reference network on rare endocrine conditions (Endo-ERN).
Thomas Eggermann, Miriam Elbracht, Ingo Kurth, Anders Juul, Trine Holm Johannsen, Dirk Prawitt

Orphanet J Rare Dis· June 2020

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Recommendations for a nomenclature system for reporting methylation aberrations in imprinted domains.
David Monk, Joannella Morales, Johan T den Dunnen, Silvia Russo, Franck Court, Dirk Prawitt

Epigenetics· December 2018

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In renal cell carcinoma the PTEN splice variant PTEN-Δ shows similar function as the tumor suppressor PTEN itself.
Ines Breuksch, Jonas Welter, Heide-Katharina Bauer, Thorsten Enklaar, Sebastian Frees, Dirk Prawitt

Cell Commun Signal· June 2018

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Expert consensus document: Clinical and molecular diagnosis, screening and management of Beckwith-Wiedemann syndrome: an international consensus statement.
Frédéric Brioude, Jennifer M Kalish, Alessandro Mussa, Alison C Foster, Jet Bliek, Dirk Prawitt

Nat Rev Endocrinol· April 2018

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[Beckwith-Wiedemann Syndrome (BWS) Current Status of Diagnosis and Clinical Management: Summary of the First International Consensus Statement].
Miriam Elbracht, Dirk Prawitt, Rebekka Nemetschek, Christian Kratz, Thomas Eggermann

Klin Padiatr· April 2018

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Calcium-sensing receptor (CaSR) promotes development of bone metastasis in renal cell carcinoma.
Sebastian Frees, Ines Breuksch, Tobias Haber, Heide-Katharina Bauer, Claudia Chavez-Munoz, Dirk Prawitt

Oncotarget· March 2018

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Integrin α5 triggers the metastatic potential in renal cell carcinoma.
Ines Breuksch, Franz Prosinger, Fabian Baehr, Franz-Peter Engelhardt, Heide-Katharina Bauer, Dirk Prawitt

Oncotarget· December 2017

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Personalized therapy: CNS HGNET-BCOR responsiveness to arsenic trioxide combined with radiotherapy.
Claudia Paret, Alexandra Russo, Henrike Otto, Arnulf Mayer, Sebastian Zahnreich, Dirk Prawitt

Oncotarget· December 2017

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Overriding TKI resistance of renal cell carcinoma by combination therapy with IL-6 receptor blockade.
Kei Ishibashi, Tobias Haber, Ines Breuksch, Susanne Gebhard, Takashi Sugino, Dirk Prawitt

Oncotarget· August 2017

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Novel deletion in 11p15.5 imprinting center region 1 in a patient with Beckwith-Wiedemann syndrome provides insight into distal enhancer regulation and tumorigenesis.
Nadine Bachmann, Roman Crazzolara, Florian Bohne, Dieter Kotzot, Kathrin Maurer, Dirk Prawitt

Pediatr Blood Cancer· March 2017

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Kaiso mediates human ICR1 methylation maintenance and H19 transcriptional fine regulation.
Florian Bohne, David Langer, Ursula Martiné, Claudia S Eider, Regina Cencic, Dirk Prawitt

Clin Epigenetics· December 2016

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EMQN best practice guidelines for the molecular genetic testing and reporting of chromosome 11p15 imprinting disorders: Silver-Russell and Beckwith-Wiedemann syndrome.
Katja Eggermann, Jet Bliek, Frédéric Brioude, Elizabeth Algar, Karin Buiting, Dirk Prawitt

Eur J Hum Genet· October 2016

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Prenatal molecular testing for Beckwith-Wiedemann and Silver-Russell syndromes: a challenge for molecular analysis and genetic counseling.
Thomas Eggermann, Frédéric Brioude, Silvia Russo, Maria P Lombardi, Jet Bliek, Dirk Prawitt

Eur J Hum Genet· June 2016

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Phenotypic spectrum and extent of DNA methylation defects associated with multilocus imprinting disturbances.
Susanne Bens, Julia Kolarova, Jasmin Beygo, Karin Buiting, Almuth Caliebe, Dirk Prawitt

Epigenomics· June 2016

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Next-generation sequencing reveals germline mutations in an infant with synchronous occurrence of nephro- and neuroblastoma.
Johanna Theruvath, Alexandra Russo, Bettina Kron, Claudia Paret, Arthur Wingerter, Dirk Prawitt

Pediatr Hematol Oncol· May 2016

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Bone Metastasis in Renal Cell Carcinoma is Preprogrammed in the Primary Tumor and Caused by AKT and Integrin α5 Signaling.
Tobias Haber, Elke Jöckel, Frederik C Roos, Kerstin Junker, Dirk Prawitt

J Urol· August 2015

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