1. A common classification framework for histone sequence alterations in tumours: an expert consensus proposal. Issue 2 (7th May 2021) Authors: Leske, Henning; Dalgleish, Raymond; Lazar, Alexander J; Reifenberger, Guido; Cree, Ian A Journal: Journal of pathology Issue: Volume 254:Issue 2(2021) Page Start: 109 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Cafe Variome: General‐Purpose Software for Making Genotype–Phenotype Data Discoverable in Restricted or Open Access Contexts. Issue 10 (25th August 2015) Authors: Lancaster, Owen; Beck, Tim; Atlan, David; Swertz, Morris; Thangavelu, Dhiwagaran; Veal, Colin; Dalgleish, Raymond; Brookes, Anthony J Journal: Human mutation Issue: Volume 36:Issue 10(2015:Oct.) Page Start: 957 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. HGVS Recommendations for the Description of Sequence Variants: 2016 Update. Issue 6 (25th March 2016) Authors: den Dunnen, Johan T.; Dalgleish, Raymond; Maglott, Donna R.; Hart, Reece K.; Greenblatt, Marc S.; McGowan‐Jordan, Jean; Roux, Anne‐Francoise; Smith, Timothy; Antonarakis, Stylianos E.; Taschner, Peter E.M. Journal: Human mutation Issue: Volume 37:Issue 6(2016) Page Start: 564 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Hgvs: A Python package for manipulating sequence variants using HGVS nomenclature: 2018 Update. Issue 12 (5th September 2018) Authors: Wang, Meng; Callenberg, Keith M.; Dalgleish, Raymond; Fedtsov, Alexandre; Fox, Naomi K.; Freeman, Peter J.; Jacobs, Kevin B.; Kaleta, Piotr; McMurry, Andrew J.; Prlić, Andreas; Rajaraman, Veena; Hart, Reece K. Journal: Human mutation Issue: Volume 39:Issue 12(2018) Page Start: 1803 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. LSDBs and How They Have Evolved. Issue 6 (14th March 2016) Authors: Dalgleish, Raymond Journal: Human mutation Issue: Volume 37:Issue 6(2016) Page Start: 532 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Mutations in COL1A1 Gene Change Dentin Nanostructure: A Response. Issue 8 (26th April 2018) Authors: Dalgleish, Raymond Journal: Anatomical record Issue: Volume 301:Issue 8(2018) Page Start: 1307 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. VariantValidator: Accurate validation, mapping, and formatting of sequence variation descriptions. Issue 1 (17th October 2017) Authors: Freeman, Peter J.; Hart, Reece K.; Gretton, Liam J.; Brookes, Anthony J.; Dalgleish, Raymond Journal: Human mutation Issue: Volume 39:Issue 1(2018) Page Start: 61 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Variobox: Automatic Detection and Annotation of Human Genetic Variants. Issue 2 (21st November 2013) Authors: Gaspar, Paulo; Lopes, Pedro; Oliveira, Jorge; Santos, Rosário; Dalgleish, Raymond; Oliveira, José Luís Journal: Human mutation Issue: Volume 35:Issue 2(2014:Feb.) Page Start: 202 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Verifying nomenclature of DNA variants in submitted manuscripts: Guidance for journals. Issue 1 (10th December 2020) Authors: Higgins, Jan; Dalgleish, Raymond; den Dunnen, Johan T.; Barsh, Greg; Freeman, Peter J.; Cooper, David N.; Cullinan, Sara; Davies, Kay E.; Dorkins, Huw; Gong, Li; Imoto, Issei; Klein, Teri E.; Korf, Bruce; Misra, Adya; Paalman, Mark H.; Ratzel, Sarah; Reichardt, Juergen K. V.; Rehm, Heidi L.; Toku... Journal: Human mutation Issue: Volume 42:Issue 1(2021) Page Start: 3 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗