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Journal of family therapy, ISSN 0163-4445, 02/2018, Volume 40, Issue 1, pp. 142 - 143
Journal Article
by Sabater-Lleal, M and Huang, J and Chasman, D and Naitza, S and Dehghan, A and Johnson, A.D and Teumer, A and Reiner, A.P and Folkersen, L and Basu, S and Rudnicka, A.R and Trompet, S and Malarstig, A and Baumert, J and Bis, J.C and Guo, X and Hottenga, J.J and Shin, S.Y and Lopez, L.M and Lahti, J and Tanaka, T and Yanek, L.R and Oudot-Mellakh, T and Wilson, J.F and Navarro, P and Huffman, J.E and Zemunik, T and Redline, S and Mehra, R and Pulanic, D and Rudan, I and Wright, A.F and Kolcic, I and Polasek, O and Wild, S.H and Campbell, H and Curb, J.D and Wallace, R and Liu, S and Eaton, C.B and Becker, D.M and Becker, L.C and Bandinelli, S and Raikkonen, K and Widen, E and Palotie, A and Fornage, M and Green, D and Gross, M and Davies, G and Harris, S.E and Liewald, D.C and Starr, J.M and Williams, F.M and Grant, P.J and Spector, T.D and Strawbridge, R.J and Silveira, A and Sennblad, B and Rivadeneira, F and Uitterlinden, A.G and Franco, O.H and Hofman, A and Dongen, J. Van and Willemsen, G and Boomsma, D.I and Yao, J and Jenny, N. Swords and Haritunians, T and McKnight, B and Lumley, T and Taylor, K.D and Rotter, J.I and Psaty, B.M and Peters, A and Gieger, C and Illig, T and Grotevendt, A and Homuth, G and Volzke, H and Kocher, T and Goel, A and Franzosi, M.G and Seedorf, U and Clarke, R and Steri, M and Tarasov, K.V and Sanna, S and Schlessinger, D and Stott, D.J and Sattar, N and Buckley, B.M and Rumley, A and Lowe, G.D and McArdle, W.L and Chen, M.H and Tofler, G.H and Song, J and Boerwinkle, E and Folsom, A.R and ... and VTE Consortium and C4D Consortium and STROKE Consortium and Wellcome Trust Case Control Consortium 2 (WTCCC2) and CARDIoGRAM Consortium
Circulation (New York, N.Y.), ISSN 0009-7322, 2013, Volume 128, Issue 12, pp. 1310 - 1324
BACKGROUND: Estimates of the heritability of plasma fibrinogen concentration, an established predictor of cardiovascular disease, range from 34% to 50%.... 
Myocardial Infarction - genetics | Cardiovascular Diseases - ethnology | Venous Thromboembolism - ethnology | Humans | Middle Aged | Genetic Loci - genetics | Hispanic Americans - statistics & numerical data | Male | Cardiovascular Diseases - genetics | Stroke - genetics | Young Adult | Aged, 80 and over | Adult | Female | African Continental Ancestry Group - genetics | Venous Thromboembolism - metabolism | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Hispanic Americans - genetics | Cardiovascular Diseases - metabolism | Coronary Artery Disease - metabolism | Risk Factors | European Continental Ancestry Group - statistics & numerical data | Myocardial Infarction - metabolism | Fibrinogen - genetics | Coronary Artery Disease - ethnology | African Continental Ancestry Group - statistics & numerical data | Stroke - metabolism | Venous Thromboembolism - genetics | Adolescent | Coronary Artery Disease - genetics | Fibrinogen - metabolism | Polymorphism, Single Nucleotide - genetics | Stroke - ethnology | Genetic Predisposition to Disease - ethnology | Aged | Myocardial Infarction - ethnology | Physiological aspects | Genetic aspects | Research | Cardiovascular diseases | Fibrinogen | Kardiologi | Medicinsk genetik | Klinisk medicin | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
Journal Article
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
1991, ISBN 9780521330800, xvi, 684
Only a few centuries ago the English language consisted of a collection of dialects spoken mainly by monolinguals and only within the shores of a small island.... 
Dialects | English language | Sociolinguistics | Variation | Social aspects
Book
2009, ISBN 0230542522, viii, 209
This groundbreaking and truly interdisciplinary collection of essays examines how digital media technologies require us to rethink established... 
Image processing | Multimedia systems | Social aspects | Memory | Digital techniques | Communication
Book
by Lane, Athene and Metcalfe, Chris and Young, Grace J and Peters, Tim J and Blazeby, Jane and Avery, Kerry N. L and Dedman, Daniel and Down, Liz and Mason, Malcolm D and Neal, David E and Hamdy, Freddie C and Donovan, Jenny L and Bonnington, Sue and Bradshaw, Lynne and Cooper, Debbie and Elliott, Emma and Herbert, Pippa and Holding, Peter and Howson, Joanne and Jones, Mandy and Lennon, Teresa and Lyons, Norma and Moody, Hilary and Plumb, Claire and O'Sullivan, Tricia and Salter, Liz and Tidball, Sarah and Thompson, Pauline and Adam, Tonia and Askew, Sarah and Atkinson, Sharon and Baynes, Tim and Blaikie, Jan and Brain, Carole and Breen, Viv and Brunt, Sarah and Bryne, Sean and Bythem, Jo and Clarke, Jenny and Cloete, Jenny and Dark, Susan and Davis, Gill and La Rue, Rachael and Denizot, Jane and Dewhurst, Elspeth and Dimes, Anna and Dixon, Nicola and Ebbs, Penny and Emmerson, Ingrid and Ferguson, Jill and Gadd, Ali and Geoghegan, Lisa and Grant, Alison and Grant, Collette and Gray, Catherine and Godfrey, Rosemary and Goodwin, Louise and Hall, Susie and Hart, Liz and Harvey, Andrew and Hoult, Chloe and Hawkins, Sarah and Holling, Sharon and Innes, Alastair and Kilner, Sue and Marshall, Fiona and Mellen, Louise and Moore, Andrea and Napier, Sally and Needham, Julie and Pearse, Kevin and Pisa, Anna and Rees, Mark and Richards, Elliw and Robson, Lindsay and Roxburgh, Janet and Samuel, Nikki and Sharkey, Irene and Slater, Michael and Smith, Donna and Taggart, Pippa and Taylor, Helen and Taylor, Vicky and Thomas, Ayesha and Tomkies, Briony and Trewick, Nicola and Ward, Claire and Walker, Christy and Williams, Ayesha and Woodhouse, Colin and Wyber, Elizabeth and Aning, Jonathan and Bollina, Prasad and Catto, Jim and Doble, Andrew and Doherty, Alan and Durkan, Garett and Gillatt, David and Hughes, Owen and Kocklebergh, Roger and ... and ProtecT Study Grp and ProtecT Study group and the ProtecT Study group
BJU International, ISSN 1464-4096, 12/2016, Volume 118, Issue 6, pp. 869 - 879
Journal Article
PLOS ONE, ISSN 1932-6203, 11/2019, Volume 14, Issue 11, p. e0224402
...Author(s): Jenny C. A. Read 1,*, Sheima Rafiq 1, Jess Hugill 1, Therese Casanova 1, Carla Black 1, Adam O'Neill 1, Vicente Puyat 1, Helen Haggerty 2, Kathryn... 
STEREOPSIS | VISION | FRISBY | INTERPUPILLARY DISTANCE | BIAS | MULTIDISCIPLINARY SCIENCES | CONSENT | STEREOACUITY | ACUITY | AMBLYOPIA | REFRACTION | Vision disorders in children | Neurosciences | Sensitivity analysis | Testability | Norms | Visual acuity | Medical screening | Acuity | Children & youth | Studies | Visual thresholds | Vision | Eye (anatomy) | Binocular vision | Children | Reliability | Age
Journal Article
Journal Article
by Sabater-Lleal, M and Huang, J and Chasman, D and Naitza, S and Dehghan, A and Johnson, AD and Teumer, A and Reiner, AP and Folkersen, L and Basu, S and Rudnicka, AR and Trompet, S and Malarstig, A and Baumert, J and Bis, JC and Guo, XQ and Hottenga, JJ and Shin, SY and Lopez, LM and Lahti, J and Tanaka, T and Yanek, LR and Oudot-Mellakh, T and Wilson, JF and Navarro, P and Huffman, JE and Zemunik, T and Redline, S and Mehra, R and Pulanic, D and Rudan, I and Wright, AF and Kolcic, I and Polasek, O and Wild, SH and Campbell, H and Curb, JD and Wallace, R and Liu, SM and Eaton, CB and Becker, DM and Becker, LC and Bandinelli, S and Raikkonen, K and Widen, E and Palotie, A and Fornage, M and Green, D and Gross, M and Davies, G and Harris, SE and Liewald, DC and Starr, JM and Williams, FMK and Grant, PJ and Spector, TD and Strawbridge, RJ and Silveira, A and Sennblad, B and Rivadeneira, F and Uitterlinden, AG and Franco, OH and Hofman, A and van Dongen, J and Willemsen, G and Boomsma, DI and Yao, J and Jenny, NS and Haritunians, T and McKnight, B and Lumley, T and Taylor, KD and Rotter, JI and Psaty, BM and Peters, A and Gieger, C and Illig, T and Grotevendt, A and Homuth, G and Volzke, H and Kocher, T and Goel, A and Franzosi, MG and Seedorf, U and Clarke, R and Steri, M and Tarasov, KV and Sanna, S and Schlessinger, D and Stott, DJ and Sattar, N and Buckley, BM and Rumley, A and Lowe, GD and McArdle, WL and Chen, MH and Tofler, GH and Song, J and Boerwinkle, E and Folsom, AR and ... and VTE Consortium and CD4 Consortium and STROKE Consortium and CARDIoGRAM Consortium and WTCCC2
CIRCULATION, ISSN 0009-7322, 09/2013, Volume 128, Issue 12, pp. 1310 - 1324
Background Estimates of the heritability of plasma fibrinogen concentration, an established predictor of cardiovascular disease, range from 34% to 50%. Genetic... 
CARDIAC & CARDIOVASCULAR SYSTEMS | RISK-FACTORS | fibrinogen | VARIANTS | genome-wide association study | GENE-EXPRESSION | PERIPHERAL VASCULAR DISEASE | cardiovascular diseases | CORONARY-HEART-DISEASE | HEMOSTASIS | gene expression
Journal Article
Investigative Ophthalmology and Visual Science, ISSN 0146-0404, 04/2011, Volume 52, Issue 5, pp. 2352 - 2364
PURPOSE. To investigate the cortical mechanisms that prevent diplopia in intermittent exotropia (X(T)) during binocular alignment (orthotropia). METHODS. The... 
EYE | SURGERY | MAXIMUM-LIKELIHOOD | THRESHOLD METHOD | STRABISMIC SUPPRESSION | RETINAL CORRESPONDENCE | OPHTHALMOLOGY | DISTANCE STEREOACUITY | Humans | Child, Preschool | Male | Vision, Binocular - physiology | Visual Cortex - physiology | Young Adult | Exotropia - physiopathology | Adolescent | Depth Perception - physiology | Adult | Female |