Defining the role of essential genes in human disease
Dickerson, Jonathan E, Zhu, Ana, Robertson, David L, Hentges, Kathryn E
Published in PloS one (11.11.2011)
Published in PloS one (11.11.2011)
Get full text
Journal Article
Properties of genes essential for mouse development
Kabir, Mitra, Barradas, Ana, Tzotzos, George T, Hentges, Kathryn E, Doig, Andrew J
Published in PloS one (31.05.2017)
Published in PloS one (31.05.2017)
Get full text
Journal Article
Functions of cilia in cardiac development and disease
Shaikh Qureshi, Wasay Mohiuddin, Hentges, Kathryn E.
Published in Annals of human genetics (01.01.2024)
Published in Annals of human genetics (01.01.2024)
Get full text
Journal Article
The role of splicing factors in retinitis pigmentosa: links to cilia
Maxwell, Dale W, O'Keefe, Raymond T, Roy, Sudipto, Hentges, Kathryn E
Published in Biochemical Society transactions (30.06.2021)
Published in Biochemical Society transactions (30.06.2021)
Get more information
Journal Article
Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot
Page, Donna J, Miossec, Matthieu J, Williams, Simon G, Monaghan, Richard M, Fotiou, Elisavet, Cordell, Heather J, Sutcliffe, Louise, Topf, Ana, Bourgey, Mathieu, Bourque, Guillaume, Eveleigh, Robert, Dunwoodie, Sally L, Winlaw, David S, Bhattacharya, Shoumo, Breckpot, Jeroen, Devriendt, Koenraad, Gewillig, Marc, Brook, J David, Setchfield, Kerry J, Bu’Lock, Frances A, O’Sullivan, John, Stuart, Graham, Bezzina, Connie R, Mulder, Barbara J.M, Postma, Alex V, Bentham, James R, Baron, Martin, Bhaskar, Sanjeev S, Black, Graeme C, Newman, William G, Hentges, Kathryn E, Lathrop, G Mark, Santibanez-Koref, Mauro, Keavney, Bernard D
Published in Circulation research (15.02.2019)
Published in Circulation research (15.02.2019)
Get full text
Journal Article
Predicting congenital renal tract malformation genes using machine learning
Kabir, Mitra, Stuart, Helen M., Lopes, Filipa M., Fotiou, Elisavet, Keavney, Bernard, Doig, Andrew J., Woolf, Adrian S., Hentges, Kathryn E.
Published in Scientific reports (14.08.2023)
Published in Scientific reports (14.08.2023)
Get full text
Journal Article
A missense mutation of ErbB2 produces a novel mouse model of stillbirth associated with a cardiac abnormality but lacking abnormalities of placental structure
Shawer, Heba, Aiyelaagbe, Esther, Clowes, Christopher, Lean, Samantha C, Lu, Yinhui, Kadler, Karl E, Kerby, Alan, Dilworth, Mark R, Hentges, Kathryn E, Heazell, Alexander E P
Published in PloS one (03.06.2020)
Published in PloS one (03.06.2020)
Get full text
Journal Article
Non-muscle myosin IIB (Myh10) is required for epicardial function and coronary vessel formation during mammalian development
Ridge, Liam A, Mitchell, Karen, Al-Anbaki, Ali, Shaikh Qureshi, Wasay Mohiuddin, Stephen, Louise A, Tenin, Gennadiy, Lu, Yinhui, Lupu, Irina-Elena, Clowes, Christopher, Robertson, Abigail, Barnes, Emma, Wright, Jayne A, Keavney, Bernard, Ehler, Elisabeth, Lovell, Simon C, Kadler, Karl E, Hentges, Kathryn E
Published in PLoS genetics (01.10.2017)
Published in PLoS genetics (01.10.2017)
Get full text
Journal Article
Filamentous nestin and nonmuscle myosin IIB are associated with a migratory phenotype in neonatal rat cardiomyocytes
Bergeron, Alexandre, Brezai, Andra, Shukr, Rami, Villeneuve, Louis, Allen, Bruce G., Qureshi, Wasay M. S., Hentges, Kathryn E., Calderone, Angelino
Published in Journal of cellular physiology (01.02.2021)
Published in Journal of cellular physiology (01.02.2021)
Get full text
Journal Article
Disease modeling of core pre-mRNA splicing factor haploinsufficiency
Wood, Katherine A, Rowlands, Charlie F, Qureshi, Wasay Mohiuddin Shaikh, Thomas, Huw B, Buczek, Weronika A, Briggs, Tracy A, Hubbard, Simon J, Hentges, Kathryn E, Newman, William G, O’Keefe, Raymond T
Published in Human molecular genetics (15.11.2019)
Published in Human molecular genetics (15.11.2019)
Get full text
Journal Article
EFTUD2 missense variants disrupt protein function and splicing in mandibulofacial dysostosis Guion‐Almeida type
Thomas, Huw B., Wood, Katherine A., Buczek, Weronika A., Gordon, Christopher T., Pingault, Véronique, Attié‐Bitach, Tania, Hentges, Kathryn E., Varghese, Vinod C., Amiel, Jeanne, Newman, William G., O'Keefe, Raymond T.
Published in Human mutation (01.08.2020)
Published in Human mutation (01.08.2020)
Get full text
Journal Article
Identifying mouse developmental essential genes using machine learning
Tian, David, Wenlock, Stephanie, Kabir, Mitra, Tzotzos, George, Doig, Andrew J, Hentges, Kathryn E
Published in Disease models & mechanisms (01.12.2018)
Published in Disease models & mechanisms (01.12.2018)
Get full text
Journal Article
Association of congenital cardiovascular malformation and neuropsychiatric phenotypes with 15q11.2 (BP1-BP2) deletion in the UK Biobank
Williams, Simon G, Nakev, Apostol, Guo, Hui, Frain, Simon, Tenin, Gennadiy, Liakhovitskaia, Anna, Saha, Priyanka, Priest, James R, Hentges, Kathryn E, Keavney, Bernard D
Published in European journal of human genetics : EJHG (01.09.2020)
Published in European journal of human genetics : EJHG (01.09.2020)
Get full text
Journal Article
Erbb2 is required for cardiac atrial electrical activity during development
Tenin, Gennadiy, Clowes, Christopher, Wolton, Kathryn, Krejci, Eliska, Wright, Jayne A, Lovell, Simon C, Sedmera, David, Hentges, Kathryn E
Published in PloS one (30.09.2014)
Published in PloS one (30.09.2014)
Get full text
Journal Article