1. Comprehensive analysis of the MLH1 promoter region in 480 patients with colorectal cancer and 1150 controls reveals new variants including one with a heritable constitutional MLH1 epimutation. Issue 4 (22nd February 2018) Authors: Morak, Monika; Ibisler, Ayseguel; Keller, Gisela; Jessen, Ellen; Laner, Andreas; Gonzales-Fassrainer, Daniela; Locher, Melanie; Massdorf, Trisari; Nissen, Anke M; Benet-Pagès, Anna; Holinski-Feder, Elke Journal: Journal of medical genetics Issue: Volume 55:Issue 4(2018) Page Start: 240 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Constitutional chromothripsis of the APC locus as a cause of genetic predisposition to colon cancer. Issue 10 (14th December 2021) Authors: Scharf, Florentine; Leal Silva, Rafaela Magalhaes; Morak, Monika; Hastie, Alex; Pickl, Julia M A; Sendelbach, Kai; Gebhard, Christian; Locher, Melanie; Laner, Andreas; Steinke-Lange, Verena; Koehler, Udo; Holinski-Feder, Elke; Wolf, Dieter A Journal: Journal of medical genetics Issue: Volume 59:Issue 10(2022) Page Start: 976 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Critical assessment of secondary findings in genes linked to primary arrhythmia syndromes. Issue 5 (18th February 2020) Authors: Diebold, Isabel; Schön, Ulrike; Scharf, Florentine; Benet‐Pagès, Anna; Laner, Andreas; Holinski‐Feder, Elke; Abicht, Angela Journal: Human mutation Issue: Volume 41:Issue 5(2020) Page Start: 1025 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Extending the critical regions for mutations in the non‐coding gene RNU4ATAC in another patient with Roifman Syndrome. Issue 11 (11th October 2018) Authors: Hallermayr, Ariane; Graf, Janine; Koehler, Udo; Laner, Andreas; Schönfeld, Brigitte; Benet‐Pagès, Anna; Holinski‐Feder, Elke Journal: Clinical case reports Issue: Volume 6:Issue 11(2018) Page Start: 2224 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Front Cover, Volume 43, Issue 8. Issue 8 (15th July 2022) Authors: Laner, Andreas; Maver, Ales; den Dunnen, Johan T. Other Names: Laner Andreas guestEditor.; Maver Ales guestEditor.; den Dunnen Johan T. guestEditor. Journal: Human mutation Issue: Volume 43:Issue 8(2022) Page Start: i Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genome‐wide CNV analysis in 221 unrelated patients and targeted high‐throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis. Issue 6 (30th September 2014) Authors: Horpaopan, Sukanya; Spier, Isabel; Zink, Alexander M.; Altmüller, Janine; Holzapfel, Stefanie; Laner, Andreas; Vogt, Stefanie; Uhlhaas, Siegfried; Heilmann, Stefanie; Stienen, Dietlinde; Pasternack, Sandra M.; Keppler, Kathleen; Adam, Ronja; Kayser, Katrin; Moebus, Susanne; Draaken, Markus; Degen... Journal: International journal of cancer Issue: Volume 136:Issue 6(2015:Mar. 15) Page Start: E578 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Human Mutation special issue on "Variant Effect Prediction". Issue 8 (15th July 2022) Authors: Laner, Andreas; Maver, Ales; den Dunnen, Johan T. Other Names: Laner Andreas guestEditor.; Maver Ales guestEditor.; den Dunnen Johan T. guestEditor. Journal: Human mutation Issue: Volume 43:Issue 8(2022) Page Start: 973 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. LAMA2 gene mutation update: Toward a more comprehensive picture of the laminin‐α2 variome and its related phenotypes. Issue 10 (10th August 2018) Authors: Oliveira, Jorge; Gruber, Angela; Cardoso, Márcio; Taipa, Ricardo; Fineza, Isabel; Gonçalves, Ana; Laner, Andreas; Winder, Thomas L.; Schroeder, Jocelyn; Rath, Julie; Oliveira, Márcia E.; Vieira, Emília; Sousa, Ana Paula; Vieira, José Pedro; Lourenço, Teresa; Almendra, Luciano; Negrão, Luís; Santo... Journal: Human mutation Issue: Volume 39:Issue 10(2018) Page Start: 1314 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases. Issue 3 (27th November 2015) Authors: Spier, Isabel; Drichel, Dmitriy; Kerick, Martin; Kirfel, Jutta; Horpaopan, Sukanya; Laner, Andreas; Holzapfel, Stefanie; Peters, Sophia; Adam, Ronja; Zhao, Bixiao; Becker, Tim; Lifton, Richard P; Perner, Sven; Hoffmann, Per; Kristiansen, Glen; Timmermann, Bernd; Nöthen, Markus M; Holinski-Feder, ... Journal: Journal of medical genetics Issue: Volume 53:Issue 3(2016) Page Start: 172 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Phosphatidylinositol 3-kinase (PI3K) signalling regulates insulin-like-growth factor binding protein-2 (IGFBP-2) production in human adipocytes. Issue 3 (June 2015) Authors: Wilhelm, Franziska; Kässner, Franziska; Schmid, Gordian; Kratzsch, Jürgen; Laner, Andreas; Wabitsch, Martin; Körner, Antje; Kiess, Wieland; Garten, Antje Journal: Growth hormone & IGF research Issue: Volume 25:Issue 3(2015:Jun.) Page Start: 115 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗