Publications by Raf Hussain - ePrints

Browsing publications by Raf Hussain.

Newcastle Authors	Title	Year
Dr Joseph Collin Dr Agata Rozanska Dr Veronika Boczonadi Marina Moya Molina Adrienne Unsworth et al.	Deciphering the spatio-temporal transcriptional and chromatin accessibility of human retinal organoid development at the single cell level	2024
Dr Joseph Collin Dr Agata Rozanska Zerti Zerti Adrienne Unsworth Moira Crosier et al.	Single-cell analyses reveal transient retinal progenitor cells in the ciliary margin of developing human retina	2024
Dr Ken Baker Dr David McDonald Dr Gill Hulme Raf Hussain Dr Jonathan Coxhead et al.	Single-cell insights into immune dysregulation in rheumatoid arthritis flare versus drug-free remission	2024
Dr Joseph Collin Dr Megan Hasoon Zerti Zerti Sarah Hammadi Professor David Steel et al.	Single-cell RNA sequencing reveals transcriptional changes of human choroidal and retinal pigment epithelium cells during fetal development, in healthy adult and intermediate age-related macular degeneration	2023
Robert Jackson Catherine Hatton Dr Jarmila Spegarova Dr Maria Georgiou Dr Joseph Collin et al.	Conjunctival epithelial cells resist productive SARS-CoV-2 infection	2022
Dr Angela Pyle Dr Helen Griffin Dr Jonathan Coxhead Raf Hussain Professor Gavin Hudson et al.	Heteroplasmic mitochondrial DNA variants in cardiovascular diseases	2022
Dr Agata Rozanska Rodrigo Cerna Chavez Dr Rachel Queen Dr Joseph Collin Dr Darin Zerti et al.	pRB-depleted pluripotent stem cell retinal organoids recapitulate cell state transitions of retinoblastoma development and suggest an important role for pRB in retinal cell differentiation	2022
Dr Marina Danilenko Dr Claire Keeling Dr Stephen Crosier Dr Martina Finetti Dr Daniel Williamson et al.	Single-cell DNA sequencing identifies risk-associated clonal complexity and evolutionary trajectories in childhood medulloblastoma development	2022
Ramada Khasawneh Dr Ralf Kist Dr Rachel Queen Raf Hussain Dr Jonathan Coxhead et al.	Msx1 haploinsufficiency modifies the Pax9-deficient cardiovascular phenotype	2021
Dr Joseph Collin Dr Rachel Queen Dr Darin Zerti Dr Sanja Bojic Nicky Moyse et al.	A single cell atlas of human cornea that defines its development, limbal progenitor cells and their interactions with the immune cells	2021
Dr Laura Jardine Dr Simone Webb Issac Goh Dr Gary Reynolds Dr Michael Mather et al.	Blood and immune development in human fetal bone marrow and Down syndrome	2021
Catherine Hatton Dr Rachel Botting Dr Maria Duenas Fadic Dr Iram Haq Dr Bernard Verdon et al.	Delayed induction of type I and III interferons mediates nasal epithelial cell permissiveness to SARS-CoV-2	2021
Dr Joseph Collin Dr Rachel Queen Dr Darin Zerti Dr Birthe Hilgen Maria Georgiou et al.	Co-expression of SARS-CoV-2 entry genes in the superficial adult human conjunctival, limbal and corneal epithelium suggests an additional route of entry via the ocular surface	2020
Dr Hannah Lowes Dr Fiona Robertson Dr Angela Pyle Raf Hussain Dr Jonathan Coxhead et al.	The Human Coronavirus Receptor ANPEP (CD13) Is Overexpressed in Parkinson's Disease	2020
Dr Joseph Collin Dr Darin Zerti Dr Rachel Queen Dr Roman Bauer Dr Jonathan Coxhead et al.	CRX Expression in Pluripotent Stem Cell‐Derived Photoreceptors Marks a Transplantable Subpopulation of Early Cones	2019
Raf Hussain Professor David Steel Dr Teresa Sandinha	Cutting the Internal Limiting Membrane With Zero Aspiration Technique: A Clinical Audit	2019
Dr Joseph Collin Dr Rachel Queen Dr Darin Zerti Dr Birthe Hilgen Raf Hussain et al.	Deconstructing Retinal Organoids: Single cell RNA-Seq reveals the cellular components of human pluripotent stem cell-derived retina	2019
Dr Christopher Duncan Angela Grainger Andrew Skelton Raf Hussain Dr Joe Willet et al.	Early-onset autoimmune disease due to a heterozygous loss-of-function mutation in TNFAIP3 (A20)	2018
Dr Jonathan Coxhead Dr Marzena Kurzawa-Akanbi Raf Hussain Dr Angela Pyle Professor Patrick Chinnery et al.	Somatic mtDNA variation is an important component of Parkinson's disease	2016
Dr Michael Keogh Dr Hannah Steele Dr Konstantinos Douroudis Dr Angela Pyle Dr Jennifer Duff et al.	Frequency of rare recessive mutations in unexplained late onset cerebellar ataxia	2015
Dr Saba Habibollah Dr Katarzyna Tilgner Dr Joseph Collin Dr Tomas Barta Raf Hussain et al.	An Induced Pluripotent Stem Cell Model of Hypoplastic Left Heart Syndrome (HLHS) Reveals Multiple Expression and Functional Differences in HLHS-Derived Cardiac Myocytes	2014
Matthieu Miossec Raf Hussain Professor Judith Goodship Professor Bernard Keavney	Investigating the cause of transposition of great arteries	2014
Matthieu Miossec Raf Hussain Dr Thahira Rahman Dr Ana Topf Dr Mauro Santibanez Koref et al.	Investigating the cause of transposition of great arteries; exome sequencing analysis	2014
Dr Helen Griffin Dr David McDonald Dr Rachel Dickinson Angela Grainger Dr Louise Reynard et al.	Whole exome sequencing as a diagnostic tool in primary immunodeficiency	2012
Dr Rachel Dickinson Dr Helen Griffin Dr Venetia Bigley Dr Louise Reynard Raf Hussain et al.	Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency	2011
Angeline Tan Dr Ana Topf Dr Helen Griffin Raf Hussain James Eden et al.	Role of Genetic Variation in the Transcriptional Inhibitor Protein SMAD6 in the Predispoition to Congenital Cardiovascular Malformation	2009
Professor Bernard Keavney Dr Thahira Rahman James Eden Raf Hussain	Association between the purinergic receptors P2X4, P2X6 and P2X7 genetic variation and blood pressure in a British population	2007
Raf Hussain Dr Alberto Lopes Professor Richard Edmondson	The feasibility of storing ovarian tumor cells on databasing paper: establishing a library of ovarian cancer DNA	2007
Raf Hussain Dr Clive Ballard Professor Jim Edwardson Dr Christopher Morris	Transferrin gene polymorphism in Alzheimer's disease and dementia with Lewy bodies in humans	2002