OpenURL Connection Search

Select item for more details and to access through your institution.

A novel RNA-mediated mechanism causing down-regulation of insulating promoter interactions in human embryonic stem cells.
Published in:
Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-02373-1
By:
- Liu, Yingjuan;
- Williams, Simon G.;
- Jones, Hayden R.;
- Keavney, Bernard D.;
- Choy, Mun-Kit
Publication type:
Article
A review of causal discovery methods for molecular network analysis.
Published in:
Molecular Genetics & Genomic Medicine, 2022, v. 10, n. 10, p. 1, doi. 10.1002/mgg3.2055
By:
- Kelly, Jack;
- Berzuini, Carlo;
- Keavney, Bernard;
- Tomaszewski, Maciej;
- Guo, Hui
Publication type:
Article
Significantly increased risk of chronic obstructive pulmonary disease amongst adults with predominantly mild congenital heart disease.
Published in:
Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-21433-8
By:
- Byrne, Dominic J. F.;
- Williams, Simon G.;
- Nakev, Apostol;
- Frain, Simon;
- Baross, Stephanie L.;
- Vestbo, Jørgen;
- Keavney, Bernard D.;
- Talavera, David
Publication type:
Article
Ebstein anomaly associated with left ventricular noncompaction: An autosomal dominant condition that can be caused by mutations in MYH7.
Published in:
American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2013, v. 163C, n. 3, p. 178, doi. 10.1002/ajmg.c.31365
By:
- Vermeer, Alexa M.C.;
- van Engelen, Klaartje;
- Postma, Alex V.;
- Baars, Marieke J.H.;
- Christiaans, Imke;
- De Haij, Simone;
- Klaassen, Sabine;
- Mulder, Barbara J.M.;
- Keavney, Bernard
Publication type:
Article
Concise Review: Cardiac Disease Modeling Using Induced Pluripotent Stem Cells.
Published in:
Stem Cells, 2015, v. 33, n. 9, p. 2643, doi. 10.1002/stem.2070
By:
- Yang, Chunbo;
- Al-Aama, Jumana;
- Stojkovic, Miodrag;
- Keavney, Bernard;
- Trafford, Andrew;
- Lako, Majlinda;
- Armstrong, Lyle
Publication type:
Article
Fine-mapping of an ancestral recombination breakpoint in DCP1.
Published in:
Nature Genetics, 1999, v. 23, n. 3, p. 270, doi. 10.1038/15449
By:
- Farrall, Martin;
- Keavney, Bernard;
- McKenzie, Colin;
- Delépine, Marc;
- Matsuda, Fumihiko;
- Lathrop, G. Mark
Publication type:
Article
Global prevalence of congenital heart disease in school-age children: a meta-analysis and systematic review.
Published in:
2020
By:
- Liu, Yingjuan;
- Chen, Sen;
- Zühlke, Liesl;
- Babu-Narayan, Sonya V.;
- Black, Graeme C.;
- Choy, Mun-kit;
- Li, Ningxiu;
- Keavney, Bernard D.
Publication type:
journal article
Non-muscle myosin IIB (Myh10) is required for epicardial function and coronary vessel formation during mammalian development.
Published in:
PLoS Genetics, 2017, v. 13, n. 10, p. 1, doi. 10.1371/journal.pgen.1007068
By:
- 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.
Publication type:
Article
Functionally Significant, Rare Transcription Factor Variants in Tetralogy of Fallot.
Published in:
PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0095453
By:
- Töpf, Ana;
- Griffin, Helen R.;
- Glen, Elise;
- Soemedi, Rachel;
- Brown, Danielle L.;
- Hall, Darroch;
- Rahman, Thahira J.;
- Eloranta, Jyrki J.;
- Jüngst, Christoph;
- Stuart, A. Graham;
- O'Sullivan, John;
- Keavney, Bernard D.;
- Goodship, Judith A.
Publication type:
Article
Common Variation Neighbouring Micro-RNA 22 Is Associated with Increased Left Ventricular Mass.
Published in:
PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0055061
By:
- Harper, Andrew R.;
- Mayosi, Bongani M.;
- Rodriguez, Antony;
- Rahman, Thahira;
- Hall, Darroch;
- Mamasoula, Chrysovalanto;
- Avery, Peter J.;
- Keavney, Bernard D.
Publication type:
Article
High-Throughput 13-Parameter Immunophenotyping Identifies Shifts in the Circulating T-Cell Compartment Following Reperfusion in Patients with Acute Myocardial Infarction.
Published in:
PLoS ONE, 2012, v. 7, n. 10, p. 1, doi. 10.1371/journal.pone.0047155
By:
- Hoffmann, Jedrzej;
- Fiser, Karel;
- Weaver, Jolanta;
- Dimmick, Ian;
- Loeher, Monika;
- Pircher, Hanspeter;
- Martin-Ruiz, Carmen;
- Veerasamy, Murugapathy;
- Keavney, Bernard;
- von Zglinicki, Thomas;
- Spyridopoulos, Ioakim
Publication type:
Article
Functional Significance of SRJ Domain Mutations in CITED2.
Published in:
PLoS ONE, 2012, v. 7, n. 10, p. 1, doi. 10.1371/journal.pone.0046256
By:
- Chen, Chiann-mun;
- Bentham, Jamie;
- Cosgrove, Catherine;
- Braganca, Jose;
- Cuenda, Ana;
- Bamforth, Simon D.;
- Schneider, Jürgen E.;
- Watkins, Hugh;
- Keavney, Bernard;
- Davies, Benjamin;
- Bhattacharya, Shoumo
Publication type:
Article
Genotype at the P554L Variant of the Hexose-6 Phosphate Dehydrogenase Gene Is Associated with Carotid Intima-Medial Thickness.
Published in:
PLoS ONE, 2011, v. 6, n. 8, p. 1, doi. 10.1371/journal.pone.0023248
By:
- Rahman, Thahira J.;
- Walker, Elizabeth A.;
- Mayosi, Bongani M.;
- Hall, Darroch H.;
- Avery, Peter J.;
- Connell, John M. C.;
- Watkins, Hugh;
- Stewart, Paul M.;
- Keavney, Bernard
Publication type:
Article
Correction of Population Stratification in Large Multi-Ethnic Association Studies.
Published in:
PLoS ONE, 2008, v. 3, n. 1, p. 1, doi. 10.1371/journal.pone.0001382
By:
- Serre, David;
- Montpetit, Alexandre;
- Paré, Guillaume;
- Engert, James C.;
- Yusuf, Salim;
- Keavney, Bernard;
- Hudson, Thomas J.;
- Anand, Sonia
Publication type:
Article
Genetic Mechanisms Mediating Atherosclerosis Susceptibility at the Chromosome 9p21 Locus.
Published in:
Current Atherosclerosis Reports, 2011, v. 13, n. 3, p. 193, doi. 10.1007/s11883-011-0178-z
By:
- Cunnington, Michael;
- Keavney, Bernard
Publication type:
Article
Familial and phenotypic associations of the aldosterone Renin ratio.
Published in:
2009
By:
- Alvarez-Madrazo, Samantha;
- Padmanabhan, Sandosh;
- Mayosi, Bongani M;
- Watkins, Hugh;
- Avery, Peter;
- Wallace, A Michael;
- Fraser, Robert;
- Davies, Eleanor;
- Keavney, Bernard;
- Connell, John M
Publication type:
journal article
Association between aldosterone production and variation in the 11beta-hydroxylase (CYP11B1) gene.
Published in:
2006
By:
- Imrie, Helen;
- Freel, Marie;
- Mayosi, Bongani M;
- Davies, Eleanor;
- Fraser, Robert;
- Ingram, Mary;
- Cordell, Heather J;
- Farrall, Martin;
- Avery, Peter J;
- Watkins, Hugh;
- Keavney, Bernard;
- Connell, John M C
Publication type:
journal article
Genetic variation at the locus encompassing 11-beta hydroxylase and aldosterone synthase accounts for heritability in cortisol precursor (11-deoxycortisol) urinary metabolite excretion.
Published in:
2005
By:
- Keavney, Bernard;
- Mayosi, Bongani;
- Gaukrodger, Nicole;
- Imrie, Helen;
- Baker, Michelle;
- Fraser, Robert;
- Ingram, Mary;
- Watkins, Hugh;
- Farrall, Martin;
- Davies, Eleanor;
- Connell, John
Publication type:
journal article
Utility of NT-proBNP as a rule-out test for left ventricular dysfunction in very old people with limiting dyspnoea: the Newcastle 85+ Study.
Published in:
BMC Cardiovascular Disorders, 2014, v. 14, n. 1, p. 128, doi. 10.1186/1471-2261-14-128
By:
- Collerton, Joanna;
- Kingston, Andrew;
- Yousaf, Fahad;
- Davies, Karen;
- Kenny, Antoinette;
- Neely, Dermot;
- Martin-Ruiz, Carmen;
- MacGowan, Guy;
- Robinson, Louise;
- Kirkwood, Thomas B. L.;
- Keavney, Bernard
Publication type:
Article
Utility of NT-proBNP as a rule-out test for left ventricular dysfunction in very old people with limiting dyspnoea: the Newcastle 85+ Study.
Published in:
2014
By:
- Collerton, Joanna;
- Kingston, Andrew;
- Yousaf, Fahad;
- Davies, Karen;
- Kenny, Antoinette;
- Neely, Dermot;
- Martin-Ruiz, Carmen;
- MacGowan, Guy;
- Robinson, Louise;
- Kirkwood, Thomas Bl;
- Keavney, Bernard;
- Kirkwood, Thomas B L
Publication type:
journal article
An Induced Pluripotent Stem Cell Model of Hypoplastic Left Heart Syndrome (HLHS) Reveals Multiple Expression and Functional Differences in HLHS-Derived Cardiac Myocytes.
Published in:
Stem Cells Translational Medicine, 2014, v. 3, n. 4, p. 416, doi. 10.5966/sctm.2013-0105
By:
- YAN JIANG;
- HABIBOLLAH, SABA;
- TILGNER, KATARZYNA;
- COLLIN, JOSEPH;
- BARTA, TOMAS;
- AL-AAMA, JUMANA YOUSUF;
- TESAROV, LENKA;
- HUSSAIN, RAFIQUL;
- TRAFFORD, ANDREW W.;
- KIRKWOOD, GRAHAM;
- SERNAGOR, EVELYNE;
- ELEFTHERIOU, CYRIL G.;
- PRZYBORSKI, STEFAN;
- STOJKOVIĆ, MIODRAG;
- LAKO, MAJLINDA;
- KEAVNEY, BERNARD;
- ARMSTRONG, LYLE
Publication type:
Article
Author Correction: Promoter interactome of human embryonic stem cell-derived cardiomyocytes connects GWAS regions to cardiac gene networks.
Published in:
Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-07399-0
By:
- Choy, Mun-Kit;
- Javierre, Biola M.;
- Williams, Simon G.;
- Baross, Stephanie L.;
- Liu, Yingjuan;
- Wingett, Steven W.;
- Akbarov, Artur;
- Wallace, Chris;
- Freire-Pritchett, Paula;
- Rugg-Gunn, Peter J.;
- Spivakov, Mikhail;
- Fraser, Peter;
- Keavney, Bernard D.
Publication type:
Article
Measured haplotype analysis of the aldosterone synthase gene and heart size.
Published in:
2005
By:
- Mayosi, Bongani M.;
- Keavney, Bernard;
- Watkins, Hugh;
- Farrall, Martin
Publication type:
Correction Notice
Measured haplotype analysis of the aldosterone synthase gene and heart size.
Published in:
European Journal of Human Genetics, 2003, v. 11, n. 5, p. 395, doi. 10.1038/sj.ejhg.5200967
By:
- Mayosi, Bongani M;
- Keavney, Bernard;
- Watkins, Hugh;
- Farrall, Martin
Publication type:
Article
Telomere length is associated with left ventricular function in the oldest old: the Newcastle 85+ study.
Published in:
European Heart Journal, 2007, v. 28, n. 2, p. 172
By:
- Collerton, Joanna;
- Martin-Ruiz, Carmen;
- Kenny, Antoinette;
- Barrass, Karen;
- von Zglinicki, Thomas;
- Kirkwood, Tom;
- Keavney, Bernard
Publication type:
Article
Toll the bell for another genetic association?
Published in:
European Heart Journal, 2006, v. 27, n. 21, p. 2489, doi. 10.1093/eurheartj/ehl299
By:
- Keavney, Bernard
Publication type:
Article
Genotype at a promoter polymorphism of the interleukin-6 gene is associated with baseline levels of plasma C-reactive protein
Published in:
Cardiovascular Research, 2002, v. 53, n. 4, p. 1029, doi. 10.1016/S0008-6363(01)00534-X
By:
- Vickers, Mark A.;
- Green, Fiona R.;
- Terry, Catherine;
- Mayosi, Bongani M.;
- Julier, Cecile;
- Lathrop, Mark;
- Ratcliffe, Peter J.;
- Watkins, Hugh C.;
- Keavney, Bernard
Publication type:
Article
Structural modelling of the cardiovascular system.
Published in:
Biomechanics & Modeling in Mechanobiology, 2018, v. 17, n. 5, p. 1217, doi. 10.1007/s10237-018-1024-9
By:
- Owen, Benjamin;
- Bojdo, Nicholas;
- Jivkov, Andrey;
- Keavney, Bernard;
- Revell, Alistair
Publication type:
Article
Activation of telomerase by TA-65 enhances immunity and reduces inflammation post myocardial infarction.
Published in:
GeroScience, 2023, v. 45, n. 4, p. 2689, doi. 10.1007/s11357-023-00794-6
By:
- Bawamia, Bilal;
- Spray, Luke;
- Wangsaputra, Vincent K.;
- Bennaceur, Karim;
- Vahabi, Sharareh;
- Stellos, Konstantinos;
- Kharatikoopaei, Ehsan;
- Ogundimu, Emmanuel;
- Gale, Chris P.;
- Keavney, Bernard;
- Maier, Rebecca;
- Hancock, Helen;
- Richardson, Gavin;
- Austin, David;
- Spyridopoulos, Ioakim
Publication type:
Article
Marked variation in heritability estimates of left ventricular mass depending on modality of measurement.
Published in:
Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-49961-w
By:
- Nethononda, Richard M.;
- McGurk, Kathryn A.;
- Whitworth, Polly;
- Francis, Jane;
- Mamasoula, Chysovalanto;
- Cordell, Heather J.;
- Neubauer, Stefan;
- Keavney, Bernard D.;
- Mayosi, Bongani M.;
- Farrall, Martin;
- Watkins, Hugh
Publication type:
Article
Association of Cholesteryl Ester Transfer Protein Genotypes With CETP Mass and Activity, Lipid Levels, and Coronary Risk.
Published in:
JAMA: Journal of the American Medical Association, 2008, v. 299, n. 23, p. 2777, doi. 10.1001/jama.299.23.2777
By:
- Thompson, Alexander;
- Di Angelantonio, Emanuele;
- Sarwar, Nadeem;
- Erqou, Sebhat;
- Saleheen, Danish;
- Dullaart, Robin P. F.;
- Keavney, Bernard;
- Zheng Ye;
- Danesh, John
Publication type:
Article
Association of Apolipoprotein E Genotypes With Lipid Levels and Coronary Risk.
Published in:
JAMA: Journal of the American Medical Association, 2007, v. 298, n. 11, p. 1300, doi. 10.1001/jama.298.11.1300
By:
- Bennet, Anna M.;
- Di Angelantonio, Emanuele;
- Zheng Ye;
- Wensley, Frances;
- Dahlin, Anette;
- Ahlbom, Anders;
- Keavney, Bernard;
- Collins, Rory;
- Wiman, Björn;
- de Faire, Ulf;
- Danesh, John
Publication type:
Article
Quantitative Variation in Plasma Angiotensin-I Converting Enzyme Activity Shows Allelic Heterogeneity in the ABO Blood Group Locus.
Published in:
Annals of Human Genetics, 2013, v. 77, n. 6, p. 465, doi. 10.1111/ahg.12034
By:
- Terao, Chikashi;
- Bayoumi, Nervana;
- McKenzie, Colin A.;
- Zelenika, Diana;
- Muro, Shigeo;
- Mishima, Michiaki;
- Connell, John M C;
- Vickers, Mark A.;
- Lathrop, G. Mark;
- Farrall, Martin;
- Matsuda, Fumihiko;
- Keavney, Bernard D.
Publication type:
Article
Definition and delivery of an aortopathy bundle of care (ABC): a tool for improving diagnosis and management of Marfan syndrome and related conditions.
Published in:
Clinical Medicine, 2016, v. 16, p. s30, doi. 10.7861/clinmedicine.16-3-s30
By:
- Wright, Emma Burkitt;
- Henriques, Sasha;
- Houghton, Catherine;
- Clarke, Bernard;
- Keavney, Bernard;
- Venetucci, Luigi
Publication type:
Article
FLT4 causes developmental disorders of the cardiovascular and lymphovascular systems via pleiotropic molecular mechanisms.
Published in:
Cardiovascular Research, 2024, v. 120, n. 10, p. 1164, doi. 10.1093/cvr/cvae104
By:
- Monaghan, Richard M;
- Naylor, Richard W;
- Flatman, Daisy;
- Kasher, Paul R;
- Williams, Simon G;
- Keavney, Bernard D
Publication type:
Article
The physiological and pathological functions of VEGFR3 in cardiac and lymphatic development and related diseases.
Published in:
Cardiovascular Research, 2021, v. 117, n. 8, p. 1877, doi. 10.1093/cvr/cvaa291
By:
- Monaghan, Richard M;
- Page, Donna J;
- Ostergaard, Pia;
- Keavney, Bernard D
Publication type:
Article
Chromosome 16q22 variants in a region associated with cardiovascular phenotypes correlate with ZFHX3 expression in a transcript-specific manner.
Published in:
BMC Genetics, 2014, v. 15, n. 1, p. 178, doi. 10.1186/s12863-014-0136-1
By:
- Martin, Ruairidh I. R.;
- Owens, W Andrew;
- Cunnington, Michael S.;
- Mayosi, Bongani M.;
- Koref, Mauro Santibáñez;
- Keavney, Bernard D.
Publication type:
Article
Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to Tetralogy of Fallot.
Published in:
BMC Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2156-14-57
By:
- Doza, Julian Palomino;
- Topf, Ana;
- Bentham, Jamie;
- Bhattacharya, Shoumo;
- Cosgrove, Catherine;
- Brook, J. David;
- Granados-Riveron, Javier;
- Bu'Lock, Frances A.;
- O'Sullivan, John;
- Stuart, A. Graham;
- Parsons, Jonathan;
- Relton, Caroline;
- Goodship, Judith;
- Henderson, Deborah J.;
- Keavney, Bernard
Publication type:
Article
Congenital heart disease risk loci identified by genome-wide association study in European patients.
Published in:
2021
By:
- Lahm, Harald;
- Jia, Meiwen;
- Dreßen, Martina;
- Wirth, Felix;
- Puluca, Nazan;
- Gilsbach, Ralf;
- Keavney, Bernard D.;
- Cleuziou, Julie;
- Beck, Nicole;
- Bondareva, Olga;
- Dzilic, Elda;
- Burri, Melchior;
- König, Karl C.;
- Ziegelmüller, Johannes A.;
- Abou-Ajram, Claudia;
- Neb, Irina;
- Zhong Zhang;
- Doppler, Stefanie A.;
- Mastantuono, Elisa;
- Lichtner, Peter
Publication type:
journal article
T lymphocytes and fractalkine contribute to myocardial ischemia/reperfusion injury in patients.
Published in:
Journal of Clinical Investigation, 2015, v. 125, n. 8, p. 3063, doi. 10.1172/JCI80055
By:
- Boag, Stephen E.;
- Das, Rajiv;
- Shmeleva, Evgeniya V.;
- Bagnall, Alan;
- Egred, Mohaned;
- Howard, Nicholas;
- Bennaceur, Karim;
- Zaman, Azfar;
- Keavney, Bernard;
- Spyridopoulos, Ioakim
Publication type:
Article
Association analysis identifies new risk loci for congenital heart disease in Chinese populations.
Published in:
Nature Communications, 2015, v. 6, n. 8, p. 8082, doi. 10.1038/ncomms9082
By:
- Lin, Yuan;
- Guo, Xuejiang;
- Zhao, Bijun;
- Liu, Juanjuan;
- Da, Min;
- Wen, Yang;
- Hu, Yuanli;
- Ni, Bixian;
- Zhang, Kai;
- Yang, Shiwei;
- Xu, Jing;
- Dai, Juncheng;
- Wang, Xiaowei;
- Xia, Yankai;
- Ma, Hongxia;
- Jin, Guangfu;
- Yu, Shiqiang;
- Liu, Jiayin;
- Keavney, Bernard D.;
- Goodship, Judith A.
Publication type:
Article
Human Tra2 proteins jointly control a CHEK1 splicing switch among alternative and constitutive target exons.
Published in:
Nature Communications, 2014, v. 5, n. 9, p. 4760, doi. 10.1038/ncomms5760
By:
- Best, Andrew;
- James, Katherine;
- Dalgliesh, Caroline;
- Hong, Elaine;
- Kheirolahi-Kouhestani, Mahsa;
- Curk, Tomaz;
- Xu, Yaobo;
- Danilenko, Marina;
- Hussain, Rafiq;
- Keavney, Bernard;
- Wipat, Anil;
- Klinck, Roscoe;
- Cowell, Ian G.;
- Cheong Lee, Ka;
- Austin, Caroline A.;
- Venables, Julian P.;
- Chabot, Benoit;
- Santibanez Koref, Mauro;
- Tyson-Capper, Alison;
- Elliott, David J.
Publication type:
Article
Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome.
Published in:
2021
By:
- Trevino, Cristina E.;
- Holleman, Aaron M.;
- Corbitt, Holly;
- Maslen, Cheryl L.;
- Rosser, Tracie C.;
- Cutler, David J.;
- Johnston, H. Richard;
- Rambo-Martin, Benjamin L.;
- Oberoi, Jai;
- Dooley, Kenneth J.;
- Capone, George T.;
- Reeves, Roger H.;
- Cordell, Heather J.;
- Keavney, Bernard D.;
- Agopian, A. J.;
- Goldmuntz, Elizabeth;
- Gruber, Peter J.;
- O'Brien, James E.;
- Bittel, Douglas C.;
- Wadhwa, Lalita
Publication type:
Correction Notice
Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome.
Published in:
Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-74650-4
By:
- Trevino, Cristina E.;
- Holleman, Aaron M.;
- Corbitt, Holly;
- Maslen, Cheryl L.;
- Rosser, Tracie C.;
- Cutler, David J.;
- Johnston, H. Richard;
- Rambo-Martin, Benjamin L.;
- Oberoi, Jai;
- Dooley, Kenneth J.;
- Capone, George T.;
- Reeves, Roger H.;
- Cordell, Heather J.;
- Keavney, Bernard D.;
- Agopian, A.J.;
- Goldmuntz, Elizabeth;
- Gruber, Peter J.;
- O’Brien, James E. Jr.;
- Bittel, Douglas C.;
- Wadhwa, Lalita
Publication type:
Article
Heritability of haemodynamics in the ascending aorta.
Published in:
Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-71354-7
By:
- McGurk, Kathryn A.;
- Owen, Benjamin;
- Watson, William D.;
- Nethononda, Richard M.;
- Cordell, Heather J.;
- Farrall, Martin;
- Rider, Oliver J.;
- Watkins, Hugh;
- Revell, Alistair;
- Keavney, Bernard D.
Publication type:
Article
Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome.
Published in:
Human Molecular Genetics, 2021, v. 30, n. 6, p. 500, doi. 10.1093/hmg/ddab002
By:
- McGurk, Kathryn A;
- Williams, Simon G;
- Guo, Hui;
- Watkins, Hugh;
- Farrall, Martin;
- Cordell, Heather J;
- Nicolaou, Anna;
- Keavney, Bernard D
Publication type:
Article
Induced pluripotent stem cell modelling of HLHS underlines the contribution of dysfunctional NOTCH signalling to impaired cardiogenesis.
Published in:
Human Molecular Genetics, 2017, v. 26, n. 16, p. 3031, doi. 10.1093/hmg/ddx140
By:
- Chunbo Yang;
- Yaobo Xu;
- Min Yu;
- Lee, David;
- Alharti, Sameer;
- Hellen, Nicola;
- Shaik, Noor Ahmad;
- Banaganapalli, Babajan;
- Ali Mohamoud, Hussein Sheikh;
- Elango, Ramu;
- Przyborski, Stefan;
- Tenin, Gennadiy;
- Williams, Simon;
- O'Sullivan, John;
- Al-Radi, Osman O.;
- Atta, Jameel;
- Harding, Sian E.;
- Keavney, Bernard;
- Lako, Majlinda;
- Armstrong, Lyle
Publication type:
Article
Concentric hypertrophic remodelling and subendocardial dysfunction in mitochondrial DNA point mutation carriers†.
Published in:
2013
By:
- Bates, Matthew G.D.;
- Hollingsworth, Kieren G.;
- Newman, Jane H.;
- Jakovljevic, Djordje G.;
- Blamire, Andrew M.;
- MacGowan, Guy A.;
- Keavney, Bernard D.;
- Chinnery, Patrick F.;
- Turnbull, Douglass M.;
- Taylor, Robert W.;
- Trenell, Michael I.;
- Gorman, Grainne S.
Publication type:
Journal Article
Concentric hypertrophic remodelling and subendocardial dysfunction in mitochondrial DNA point mutation carriers†.
Published in:
European Heart Journal - Cardiovascular Imaging, 2013, v. 14, n. 7, p. 650, doi. 10.1093/ehjci/jes226
By:
- Bates, Matthew G.D.;
- Hollingsworth, Kieren G.;
- Newman, Jane H.;
- Jakovljevic, Djordje G.;
- Blamire, Andrew M.;
- MacGowan, Guy A.;
- Keavney, Bernard D.;
- Chinnery, Patrick F.;
- Turnbull, Douglass M.;
- Taylor, Robert W.;
- Trenell, Michael I.;
- Gorman, Grainne S.
Publication type:
Article
Association between common polymorphisms of the proopiomelanocortin gene and body fat distribution: a family study.
Published in:
2005
By:
- Baker M;
- Gaukrodger N;
- Mayosi BM;
- Imrie H;
- Farrall M;
- Watkins H;
- Connell JMC;
- Avery PJ;
- Keavney B;
- Baker, Michelle;
- Gaukrodger, Nicole;
- Mayosi, Bongani M;
- Imrie, Helen;
- Farrall, Martin;
- Watkins, Hugh;
- Connell, John M C;
- Avery, Peter J;
- Keavney, Bernard
Publication type:
journal article

Found: 83