1. Comprehensive genetic testing approaches as the basis for personalized management of growth disturbances: current status and perspectives. Issue 11 (10th October 2022) Authors: van der Kaay, Danielle Christine Maria; Rochtus, Anne; Binder, Gerhard; Kurth, Ingo; Prawitt, Dirk; Netchine, Irène; Johannsson, Gudmundur; Hokken-Koelega, Anita C S; Elbracht, Miriam; Eggermann, Thomas Journal: Endocrine connections Issue: Volume 11:Issue 11(2023) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Further understanding of paternal uniparental disomy in Beckwith-Wiedemann syndrome. Issue 6 (2nd November 2022) Authors: Eggermann, Thomas; Prawitt, Dirk Journal: Expert review of endocrinology & metabolism Issue: Volume 17:Issue 6(2022) Page Start: 513 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Kaiso mediates human ICR1 methylation maintenance and H19 transcriptional fine regulation. Issue 1 (December 2016) Authors: Bohne, Florian; Langer, David; Martiné, Ursula; Eider, Claudia; Cencic, Regina; Begemann, Matthias; Elbracht, Miriam; Bülow, Luzie; Eggermann, Thomas; Zechner, Ulrich; Pelletier, Jerry; Zabel, Bernhard; Enklaar, Thorsten; Prawitt, Dirk Journal: Clinical epigenetics Issue: Volume 8:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Next-generation sequencing reveals germline mutations in an infant with synchronous occurrence of nephro- and neuroblastoma. (18th May 2016) Authors: Theruvath, Johanna; Russo, Alexandra; Kron, Bettina; Paret, Claudia; Wingerter, Arthur; El Malki, Khalifa; Neu, Marie A.; Alt, Francesca; Staatz, Gundula; Stein, Raimund; Seidmann, Larissa; Prawitt, Dirk; Faber, Jörg Journal: Pediatric hematology and oncology Issue: Volume 33:Number 4(2016) Page Start: 264 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Novel deletion in 11p15.5 imprinting center region 1 in a patient with Beckwith–Wiedemann syndrome provides insight into distal enhancer regulation and tumorigenesis. Issue 3 (21st September 2016) Authors: Bachmann, Nadine; Crazzolara, Roman; Bohne, Florian; Kotzot, Dieter; Maurer, Kathrin; Enklaar, Thorsten; Prawitt, Dirk; Bergmann, Carsten Journal: Pediatric blood & cancer Issue: Volume 64:Issue 3(2017) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Phenotypic spectrum and extent of DNA methylation defects associated with multilocus imprinting disturbances. (June 2016) Authors: Bens, Susanne; Kolarova, Julia; Beygo, Jasmin; Buiting, Karin; Caliebe, Almuth; Eggermann, Thomas; Gillessen-Kaesbach, Gabriele; Prawitt, Dirk; Thiele-Schmitz, Susanne; Begemann, Matthias; Enklaar, Thorsten; Gutwein, Jana; Haake, Andrea; Paul, Ulrike; Richter, Julia; Soellner, Lukas; Vater, Inga;... Journal: Epigenomics Issue: Volume 8:Number 6(2016) Page Start: 801 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Recommendations for a nomenclature system for reporting methylation aberrations in imprinted domains. Issue 2 (1st February 2018) Authors: Monk, David; Morales, Joannella; den Dunnen, Johan T.; Russo, Silvia; Court, Franck; Prawitt, Dirk; Eggermann, Thomas; Beygo, Jasmin; Buiting, Karin; Tümer, Zeynep Journal: Epigenetics Issue: Volume 13:Issue 2(2018) Page Start: 117 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗