1. A comprehensive bioinformatic analysis of 126 patients with an inherited platelet disorder to identify both sequence and copy number genetic variants. Issue 11 (8th October 2020) Authors: Almazni, Ibrahim; Stapley, Rachel J.; Khan, Abdullah O.; Morgan, Neil V. Journal: Human mutation Issue: Volume 41:Issue 11(2020) Page Start: 1848 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A comprehensive targeted next‐generation sequencing panel for genetic diagnosis of patients with suspected inherited thrombocytopenia. Issue 4 (8th October 2018) Authors: Johnson, Ben; Doak, Rachel; Allsup, David; Astwood, Emma; Evans, Gillian; Grimley, Charlotte; James, Beki; Myers, Bethan; Stokley, Simone; Thachil, Jecko; Wilde, Jonathan; Williams, Mike; Makris, Mike; Lowe, Gillian C.; Wallis, Yvonne; Daly, Martina E.; Morgan, Neil V. Journal: Research and practice in thrombosis and haemostasis Issue: Volume 2:Issue 4(2018) Page Start: 640 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. An adaptable analysis workflow for characterization of platelet spreading and morphology. (2nd January 2021) Authors: Pike, Jeremy A.; Simms, Victoria A.; Smith, Christopher W.; Morgan, Neil V.; Khan, Abdullah O.; Poulter, Natalie S.; Styles, Iain B.; Thomas, Steven G. Journal: Platelets Issue: Volume 32:Number 1(2021) Page Start: 54 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Evaluation of the Total Thrombus-Formation System (T-TAS): application to human and mouse blood analysis. (3rd October 2019) Authors: Al Ghaithi, Rashid; Mori, Jun; Nagy, Zoltan; Maclachlan, Annabel; Hardy, Lewis; Philippou, Helen; Hethershaw, Emma; Morgan, Neil V.; Senis, Yotis A.; Harrison, Paul Journal: Platelets Issue: Volume 30:Number 7(2019) Page Start: 893 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Gene of the issue: RUNX1 mutations and inherited bleeding. (17th February 2017) Authors: Morgan, Neil V.; Daly, Martina E. Journal: Platelets Issue: Volume 28:Number 2(2017) Page Start: 208 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. GoldVariants, a resource for sharing rare genetic variants detected in bleeding, thrombotic, and platelet disorders: Communication from the ISTH SSC Subcommittee on Genomics in Thrombosis and Hemostasis. (5th August 2021) Authors: Megy, Karyn; Downes, Kate; Morel‐Kopp, Marie‐Christine; Bastida, José M.; Brooks, Shannon; Bury, Loredana; Leinoe, Eva; Gomez, Keith; Morgan, Neil V.; Othman, Maha; Ouwehand, Willem H.; Perez Botero, Juliana; Rivera, José; Schulze, Harald; Trégouët, David‐Alexandre; Freson, Kathleen Journal: Journal of thrombosis and haemostasis Issue: Volume 19:Number 10(2021) Page Start: 2612 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Inherited ADAMTS13 mutations associated with Thrombotic Thrombocytopenic Purpura: a short review and update. (1st January 2023) Authors: Markham-Lee, Zoe; Morgan, Neil V.; Emsley, Jonas Journal: Platelets Issue: Volume 34:Number 1(2023) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Inherited platelet disorders: Insight from platelet genomics using next-generation sequencing. (2nd January 2017) Authors: Maclachlan, Annabel; Watson, Steve P.; Morgan, Neil V. Journal: Platelets Issue: Volume 28:Number 1(2017) Page Start: 14 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Inherited thrombocytopenia: novel insights into megakaryocyte maturation, proplatelet formation and platelet lifespan. (17th August 2016) Authors: Johnson, Ben; Fletcher, Sarah J.; Morgan, Neil V. Journal: Platelets Issue: Volume 27:Number 6(2016) Page Start: 519 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Investigation of the contribution of an underlying platelet defect in women with unexplained heavy menstrual bleeding. (2nd January 2019) Authors: Lowe, Gillian C.; Fickowska, Roksana; Al Ghaithi, Rashid; Maclachlan, Annabel; Harrison, Paul; Lester, Will; Watson, Steve P.; Myers, Bethan; Clark, Justin; Morgan, Neil V. Journal: Platelets Issue: Volume 30:Number 1(2019) Page Start: 56 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗