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by McRae, Jeremy F and Clayton, Stephen and Fitzgerald, Tomas W and Kaplanis, Joanna and Prigmore, Elena and Rajan, Diana and Sifrim, Alejandro and Aitken, Stuart and Akawi, Nadia and Alvi, Mohsan and Ambridge, Kirsty and Barrett, Daniel M and Bayzetinova, Tanya and Jones, Philip and Jones, Wendy D and King, Daniel and Krishnappa, Netravathi and Mason, Laura E and Singh, Tarjinder and Tivey, Adrian R and Ahmed, Munaza and Anjum, Uruj and Archer, Hayley and Armstrong, Ruth and Awada, Jana and Balasubramanian, Meena and Banka, Siddharth and Baralle, Diana and Barnicoat, Angela and Batstone, Paul and Baty, David and Bennett, Chris and Berg, Jonathan and Bernhard, Birgitta and Bevan, A. Paul and Bitner-Glindzicz, Maria and Blair, Edward and Blyth, Moira and Bohanna, David and Bourdon, Louise and Bourn, David and Bradley, Lisa and Brady, Angela and Brent, Simon and Brewer, Carole and Brunstrom, Kate and Bunyan, David J and Burn, John and Canham, Natalie and Castle, Bruce and Chandler, Kate and Chatzimichali, Elena and Cilliers, Deirdre and Clarke, Angus and Clasper, Susan and Clayton-Smith, Jill and Clowes, Virginia and Coates, Andrea and Cole, Trevor and Colgiu, Irina and Collins, Amanda and Collinson, Morag N and Connell, Fiona and Cooper, Nicola and Cox, Helen and Cresswell, Lara and Cross, Gareth and Crow, Yanick and D'Alessandro, Mariella and Dabir, Tabib and Davidson, Rosemarie and Davies, Sally and De Vries, Dylan and Dean, John and Deshpande, Charu and Devlin, Gemma and Dixit, Abhijit and Dobbie, Angus and Donaldson, Alan and Donnai, Dian and Donnelly, Deirdre and Donnelly, Carina and Douglas, Angela and Douzgou, Sofia and Duncan, Alexis and Eason, Jacqueline and Ellard, Sian and Ellis, Ian and Elmslie, Frances and Evans, Karenza and Everest, Sarah and Fendick, Tina and Fisher, Richard and Flinter, Frances and Foulds, Nicola and Fry, Andrew and Fryer, Alan and Gardiner, Carol and Gaunt, Lorraine and Ghali, Neeti and ... and Deciphering Developmental Disorders Study
Nature, ISSN 0028-0836, 02/2017, Volume 542, Issue 7642, pp. 433 - 438
The genomes of individuals with severe, undiagnosed developmental disorders are enriched in damaging de novo mutations (DNMs) in developmentally important... 
INTELLECTUAL DISABILITY | METAANALYSIS | VARIANTS | GENETICS | HEART-DEFECTS | MULTIDISCIPLINARY SCIENCES | GENES | SEQUENCE | FRAMEWORK | DISCOVERY | GENOME | Prevalence | Humans | Middle Aged | Parents | Male | Mi-2 Nucleosome Remodeling and Deacetylase Complex - genetics | Developmental Disabilities - genetics | Casein Kinase II - genetics | Autoantigens - genetics | Young Adult | ras GTPase-Activating Proteins - genetics | Adult | Female | Child | CDC2 Protein Kinase - genetics | Histone-Lysine N-Methyltransferase - genetics | Repressor Proteins - genetics | Sex Characteristics | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Mutation - genetics | Nerve Tissue Proteins - genetics | Sequence Analysis, DNA | Homeodomain Proteins - genetics | DEAD-box RNA Helicases - genetics | Exome - genetics | Phenotype | Myeloid-Lymphoid Leukemia Protein - genetics | Adolescent | Heredity - genetics | Protein Phosphatase 2C - genetics | Cohort Studies | Child development deviations | Genetic aspects | Genetic disorders | Developmental disabilities | Distribution | Genes | Families & family life | Births | Genomes | Mutation | Causality | Estimates | Age | TRIO | MYT1L | EHMT1 | HNRNPU | SUV420H1 | COL4A3BP | SYNGAP1 | PPP2R1A | POGZ | EP300 | KCNH1 | SCN1A | MEF2C | CDKL5 | CSNK2A1 | DYRK1A | CASK | ALG13 | FOXP1 | KAT6B | TBL1XR1 | KAT6A | SCN8A | KCNQ2 | EEF1A2 | KCNQ3 | ADNP | PhenIcons | SET | KMT2A | ANKRD11 | STXBP1 | FOXG1 | ZC4H2 | ITPR1 | De novo mutation | Seizures | ZBTB18 | CREBBP | SMAD4 | PDHA1 | IQSEC2 | AUTS2 | BCL11A | BRAF | SMARCA2 | GRIN2B | MED13L | GNAO1 | CNOT3 | TCF4 | SCN2A | CDK13 | GABRB3 | SETD5 | KDM5B | Developmental Disease | DDX3X | CHD8 | PTEN | CHD4 | TCF20 | CTCF | CHD2 | WDR45 | SLC6A1 | MECP2 | CHAMP1 | KIF1A | Average Faces | MSL3 | PPP2R5D | SMC1A | ARID1B | DNM1 | CNKSR2 | PACS1 | WAC | ZMYND11 | AHDC1 | NFIX | SATB2 | HDAC8 | PPM1D | GNAI1 | PURA | PUF60 | NSD1 | Intellectual Disability | SLC35A2 | DYNC1H1 | NAA10 | USP9X | PTPN11 | GATAD2B | ASXL1 | KANSL1 | ASXL3 | CTNNB1 | QRICH1
Journal Article
Heart, ISSN 1355-6037, 05/2019, Volume 105, Issue Suppl 6, p. A161
BackgroundHypothesis-free unbiased -omics approaches have started to revolutionise our understanding of adipose tissue (AT) biology providing an exciting... 
Cardiovascular disease | Nitric oxide | Endothelium
Journal Article
Nature Genetics, ISSN 1061-4036, 11/2015, Volume 47, Issue 11, pp. 1363 - 1369
Journal Article
Journal Article
Korean Circulation Journal, ISSN 1738-5520, 09/2017, Volume 47, Issue 5, pp. 670 - 685
Obesity is a clinical entity critically involved in the development and progression of cardiovascular disease (CVD), which is characterised by variable... 
Obesity | Oxidative stress | Cardiovascular disease | Adipose tissue | METABOLIC SYNDROME | CARDIAC & CARDIOVASCULAR SYSTEMS | INCREASED EXPRESSION | HEART-FAILURE | ANGIOTENSIN-ALDOSTERONE SYSTEM | BODY-FAT DISTRIBUTION | ENDOTHELIAL FUNCTION | RISK-FACTOR | INSULIN-RESISTANCE | OBESITY PARADOX | Review | 내과학
Journal Article
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 10, p. e26206
Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant genetic condition affecting the vascular system and is characterised by epistaxis,... 
TRANSMEMBRANE CONDUCTANCE REGULATOR | BETA-BINDING-PROTEIN | TGF-BETA | INTRACELLULAR-TRANSPORT | ENDOTHELIAL-CELLS | BIOLOGY | PROTEIN-MISFOLDING DISEASES | ROBINOW-SYNDROME | TRAFFIC JAMS | MUTATIONS | Protein Structure, Tertiary | Humans | Endoplasmic Reticulum - metabolism | Models, Molecular | Receptors, Cell Surface - metabolism | Mutant Proteins - metabolism | Telangiectasia, Hereditary Hemorrhagic - genetics | Antigens, CD - genetics | Subcellular Fractions - metabolism | Mutation, Missense - genetics | Antigens, CD - metabolism | Protein Transport | Endoglin | Mutant Proteins - chemistry | Receptors, Cell Surface - chemistry | Antigens, CD - chemistry | Cell Membrane - metabolism | Glycoside Hydrolases - metabolism | HeLa Cells | Receptors, Cell Surface - genetics | Telangiectasia, Hereditary Hemorrhagic - metabolism | Telangiectasis | Genetic aspects | Transforming growth factors | Analysis | Fluorescence microscopy | Quality control | Health sciences | Disease | Trafficking | Genes | Transforming growth factor-b | Fluorescence | Amino acids | Confocal | Kinases | Hemorrhage | Machinery | Proteins | Genotype & phenotype | Signal transduction | Missense mutation | Nose | Enzymes | Anemia | Missense mutant | Cystic fibrosis | Glycosylation | Vascular system | Zona pellucida | Morbidity | Mutants | Medicine | Pathology | Signaling | Cell lines | Genetic engineering | Mutation | Endoplasmic reticulum | Traffic congestion
Journal Article
Science, ISSN 0036-8075, 12/2018, Volume 362, Issue 6419, pp. 1161 - 1164
Journal Article
Journal Article
Birth Defects Research Part A: Clinical and Molecular Teratology, ISSN 1542-0752, 07/2013, Volume 97, Issue 7, pp. 456 - 462
Journal Article