Gene of the issue: RUNX1 mutations and inherited bleeding

od Morgan, Neil V., Daly, Martina E.
Izdano u Platelets (2017)

Inherited Thrombocytopenia: Update on Genes and Genetic Variants Which may be Associated With Bleeding

od Almazni, Ibrahim, Stapley, Rachel, Morgan, Neil V.
Izdano u Front Cardiovasc Med (2019)

New insights into glycoprotein Ibα desialylation-mediated platelet clearance

od Yule, Jack, Morgan, Neil V., Poulter, Natalie S.
Izdano u Platelets (2020)

Inherited thrombocytopenia: novel insights into megakaryocyte maturation, proplatelet formation and platelet lifespan

od Johnson, Ben, Fletcher, Sarah J., Morgan, Neil V.
Izdano u Platelets (2016)

Inherited platelet disorders: Insight from platelet genomics using next-generation sequencing

od Maclachlan, Annabel, Watson, Steve P., Morgan, Neil V.
Izdano u Platelets (2017)

High Frequency of Large Intragenic Deletions in the Fanconi Anemia Group A Gene

od Morgan, Neil V., Tipping, Alex J., Joenje, Hans, Mathew, Christopher G.
Izdano 1999

SLFN14 gene mutations associated with bleeding

od Stapley, Rachel J., Pisareva, Vera P., Pisarev, Andrey V., Morgan, Neil V.
Izdano u Platelets (2019)

CRISPR-Cas9 Mediated Labelling Allows for Single Molecule Imaging and Resolution

od Khan, Abdullah O., Simms, Victoria A., Pike, Jeremy A., Thomas, Steven G., Morgan, Neil V.
Izdano u Sci Rep (2017)

Whole exome sequencing identifies a mutation in thrombomodulin as the genetic cause of a suspected platelet disorder in a family with normal platelet function

od Maclachlan, Annabel, Dolan, Gerry, Grimley, Charlotte, Watson, Steve P., Morgan, Neil V., on behalf of the UK GAPP Study Group
Izdano u Platelets (2017)

Role of the novel endoribonuclease SLFN14 and its disease-causing mutations in ribosomal degradation

od Fletcher, Sarah J., Pisareva, Vera P., Khan, Abdullah O., Tcherepanov, Andrew, Morgan, Neil V., Pisarev, Andrey V.
Izdano u RNA (2018)

Cell-Free DNA in the Investigation of Miscarriage

od Colley, Emily, Devall, Adam J., Williams, Helen, Hamilton, Susan, Smith, Paul, Morgan, Neil V., Quenby, Siobhan, Coomarasamy, Arri, Allen, Stephanie
Izdano u J Clin Med (2020)

Initiation codon mutation in βB1-crystallin (CRYBB1) associated with autosomal recessive nuclear pulverulent cataract

od Meyer, Esther, Rahman, Fatimah, Owens, Jessica, Pasha, Shanaz, Morgan, Neil V., Trembath, Richard C., Stone, Edwin M., Moore, Anthony T., Maher, Eamonn R.
Izdano 2009

Microsatellite markers as a rapid approach for autozygosity mapping in Hermansky-Pudlak syndrome: Identification of the second HPS7 mutation in a patient presenting late in life

od Lowe, Gillian C., Guiu, Isabel Sánchez, Chapman, Oliver, Rivera, José, Lordkipanidzé, Marie, Dovlatova, Natalia, Wilde, Jonathan, Watson, Steve P., Morgan, Neil V.
Izdano 2013

Mutation in GNE is associated with severe congenital thrombocytopenia

od Futterer, Jane, Dalby, Amanda, Lowe, Gillian C., Johnson, Ben, Simpson, Michael A., Motwani, Jayashree, Williams, Mike, Watson, Steve P., Morgan, Neil V.
Izdano u Blood (2018)

Mutation Analysis of CHRNA1, CHRNB1, CHRND, and RAPSN Genes in Multiple Pterygium Syndrome/Fetal Akinesia Patients

od Vogt, Julie, Harrison, Benjamin J., Spearman, Hayley, Cossins, Judy, Vermeer, Sascha, ten Cate, Lambert Naudin, Morgan, Neil V., Beeson, David, Maher, Eamonn R.
Izdano 2008

Schlafen 14 (SLFN14) is a novel antiviral factor involved in the control of viral replication

od Seong, Rak-Kyun, Seo, Seong-wook, Kim, Ji-Ae, Fletcher, Sarah J., Morgan, Neil V., Kumar, Mukesh, Choi, Young-Ki, Shin, Ok Sarah
Izdano u Immunobiology (2017)

Investigation of the contribution of an underlying platelet defect in women with unexplained heavy menstrual bleeding

od Lowe, Gillian C., Fickowska, Roksana, Al Ghaithi, Rashid, Maclachlan, Annabel, Harrison, Paul, Lester, Will, Watson, Steve P., Myers, Bethan, Clark, Justin, Morgan, Neil V.
Izdano u Platelets (2018)

Optimised insert design for improved single-molecule imaging and quantification through CRISPR-Cas9 mediated knock-in

od Khan, Abdullah O., White, Carl W., Pike, Jeremy A., Yule, Jack, Slater, Alexandre, Hill, Stephen J., Poulter, Natalie S., Thomas, Steven G., Morgan, Neil V.
Izdano u Sci Rep (2019)

Evidence that autosomal recessive spastic cerebral palsy-1 (CPSQ1) is caused by a missense variant in HPDL

od Morgan, Neil V, Yngvadottir, Bryndis, O’Driscoll, Mary, Clark, Graeme R, Walsh, Diana, Martin, Ezequiel, Tee, Louise, Reid, Evan, Titheradge, Hannah L, Maher, Eamonn R
Izdano u Brain Commun (2021)

High-throughput platelet spreading analysis: a tool for the diagnosis of platelet-based bleeding disorders

od Khan, Abdullah O., Maclachlan, Annabel, Lowe, Gillian C., Nicolson, Phillip L.R., Ghaithi, Rashid Al, Thomas, Steven G., Watson, Steve P., Pike, Jeremy A., Morgan, Neil V.
Izdano u Haematologica (2020)