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10/2018, Routledge Media and Cultural Studies Companions, ISBN 9780367580506, 492
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Nature communications, ISSN 2041-1723, 05/2018, Volume 9, Issue 1, pp. 1864 - 11
Central corneal thickness (CCT) is a highly heritable trait associated with complex eye diseases such as keratoconus and glaucoma. We perform a genome-wide... 
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Lumican - metabolism | Glaucoma, Open-Angle - genetics | Humans | Corneal Diseases - metabolism | Corneal Dystrophies, Hereditary - ethnology | Corneal Diseases - genetics | Ehlers-Danlos Syndrome - genetics | Corneal Dystrophies, Hereditary - pathology | Loeys-Dietz Syndrome - metabolism | Mendelian Randomization Analysis | Fibrillin-1 - metabolism | Cornea - pathology | Keratoconus - pathology | Corneal Diseases - pathology | Decorin - genetics | Gene Expression | Eye Diseases, Hereditary - pathology | Lumican - genetics | ADAMTS Proteins - metabolism | Proteoglycans - metabolism | Ehlers-Danlos Syndrome - ethnology | European Continental Ancestry Group | Myopia - pathology | Cornea - metabolism | Myopia - ethnology | Loeys-Dietz Syndrome - pathology | Corneal Diseases - ethnology | Marfan Syndrome - metabolism | Marfan Syndrome - pathology | Cornea - abnormalities | Quantitative Trait Loci | Proteoglycans - genetics | ADAMTS Proteins - genetics | Transforming Growth Factor beta2 - metabolism | Corneal Dystrophies, Hereditary - genetics | Glaucoma, Open-Angle - pathology | Keratoconus - metabolism | Loeys-Dietz Syndrome - ethnology | Glaucoma, Open-Angle - ethnology | Myopia - metabolism | Ehlers-Danlos Syndrome - pathology | Marfan Syndrome - ethnology | Keratoconus - genetics | Glaucoma, Open-Angle - metabolism | Fibrillin-1 - genetics | Eye Diseases, Hereditary - ethnology | Genome-Wide Association Study | Quantitative Trait, Heritable | Corneal Dystrophies, Hereditary - metabolism | Marfan Syndrome - genetics | Eye Diseases, Hereditary - genetics | Myopia - genetics | Asian Continental Ancestry Group | Keratoconus - ethnology | Ehlers-Danlos Syndrome - metabolism | Loeys-Dietz Syndrome - genetics | Polymorphism, Single Nucleotide | Transforming Growth Factor beta2 - genetics | Genome, Human | Decorin - metabolism | Eye Diseases, Hereditary - metabolism | Glaucoma | Cornea | Genes | Myopia | Association analysis | Genomes | Gene expression | Tissues | Connective tissues | Keratoconus | Collagen | Eye diseases | Extracellular matrix | Index Medicus
Journal Article
by Su, Zhan and Gay, Laura J and Strange, Amy and Palles, Claire and Band, Gavin and Whiteman, David C and Lescai, Francesco and Langford, Cordelia and Nanji, Manoj and Edkins, Sarah and van der Winkel, Anouk and Levine, David and Sasieni, Peter and Bellenguez, Céline and Howarth, Kimberley and Freeman, Colin and Trudgill, Nigel and Tucker, Art T and Pirinen, Matti and Peppelenbosch, Maikel P and van der Laan, Luc J W and Kuipers, Ernst J and Drenth, Joost P H and Peters, Wilbert H and Reynolds, John V and Kelleher, Dermot P and McManus, Ross and Grabsch, Heike and Prenen, Hans and Bisschops, Raf and Krishnadath, Kausila and Siersema, Peter D and van Baal, Jantine W P M and Middleton, Mark and Petty, Russell and Gillies, Richard and Burch, Nicola and Bhandari, Pradeep and Paterson, Stuart and Edwards, Cathryn and Penman, Ian and Vaidya, Kishor and Ang, Yeng and Murray, Iain and Patel, Praful and Ye, Weimin and Mullins, Paul and Wu, Anna H and Bird, Nigel C and Dallal, Helen and Shaheen, Nicholas J and Murray, Liam J and Koss, Konrad and Bernstein, Leslie and Romero, Yvonne and Hardie, Laura J and Zhang, Rui and Winter, Helen and Corley, Douglas A and Panter, Simon and Risch, Harvey A and Reid, Brian J and Sargeant, Ian and Gammon, Marilie D and Smart, Howard and Dhar, Anjan and McMurtry, Hugh and Ali, Haythem and Liu, Geoffrey and Casson, Alan G and Chow, Wong-Ho and Rutter, Matt and Tawil, Ashref and Morris, Danielle and Nwokolo, Chuka and Isaacs, Peter and Rodgers, Colin and Ragunath, Krish and MacDonald, Chris and Haigh, Chris and Monk, David and Davies, Gareth and Wajed, Saj and Johnston, David and Gibbons, Michael and Cullen, Sue and Church, Nicholas and Langley, Ruth and Griffin, Michael and Alderson, Derek and Deloukas, Panos and Hunt, Sarah E and Gray, Emma and Dronov, Serge and Potter, Simon C and Tashakkori-Ghanbaria, Avazeh and Anderson, Mark and Brooks, Claire and Blackwell, Jenefer M and Bramon, Elvira and ... and Wellcome Trust Case Control Consor and Esophageal Adenocarcinoma Genetics and Wellcome Trust Case Control Consortium 2 and Esophageal Adenocarcinoma Genetics Consortium and The Wellcome Trust Case Control Consortium 2 and The Esophageal Adenocarcinoma Genetics Consortium
Nature genetics, ISSN 1061-4036, 09/2012, Volume 44, Issue 10, pp. 1131 - 1136
Journal Article
Nature genetics, ISSN 1546-1718, 01/2013, Volume 45, Issue 2, pp. 208 - 213
Journal Article
Nature communications, ISSN 2041-1723, 07/2014, Volume 5, Issue 1, pp. 4204 - 4204
...,Nicole Harlaar7, Sophia J. Docherty2, Ken B. Hanscombe2, Maciej Trzaskowski2, Charles J.C. Curtis2, Amy Strange3, Colin Freeman3, Cline Bellenguez3, Zhan Su3... 
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Genetics, Population | Twins - genetics | Genome-Wide Association Study | Quantitative Trait, Heritable | Humans | Male | United Kingdom | Mathematics | Dyslexia - genetics | Learning | Twins - psychology | Reading | Dyslexia - psychology | Female | Polymorphism, Single Nucleotide | Child | Index Medicus
Journal Article
by Evans, David M and Spencer, Chris C A and Pointon, Jennifer J and Su, Zhan and Harvey, David and Kochan, Grazyna and Oppermann, Udo and Dilthey, Alexander and Pirinen, Matti and Stone, Millicent A and Appleton, Louise and Moutsianas, Loukas and Leslie, Stephen and Wordsworth, Tom and Kenna, Tony J and Karaderi, Tugce and Thomas, Gethin P and Ward, Michael M and Weisman, Michael H and Farrar, Claire and Bradbury, Linda A and Danoy, Patrick and Inman, Robert D and Maksymowych, Walter and Gladman, Dafna and Rahman, Proton and Morgan, Ann and Marzo-Ortega, Helena and Bowness, Paul and Gaffney, Karl and Gaston, J S Hill and Smith, Malcolm and Bruges-Armas, Jacome and Couto, Ana-Rita and Sorrentino, Rosa and Paladini, Fabiana and Ferreira, Manuel A and Xu, Huji and Liu, Yu and Jiang, Lei and Lopez-Larrea, Carlos and Díaz-Peña, Roberto and López-Vázquez, Antonio and Zayats, Tetyana and Band, Gavin and Bellenguez, Céline and Blackburn, Hannah and Blackwell, Jenefer M and Bramon, Elvira and Bumpstead, Suzannah J and Casas, Juan P and Corvin, Aiden and Craddock, Nicholas and Deloukas, Panos and Dronov, Serge and Duncanson, Audrey and Edkins, Sarah and Freeman, Colin and Gillman, Matthew and Gray, Emma and Gwilliam, Rhian and Hammond, Naomi and Hunt, Sarah E and Jankowski, Janusz and Jayakumar, Alagurevathi and Langford, Cordelia and Liddle, Jennifer and Markus, Hugh S and Mathew, Christopher G and McCann, Owen T and McCarthy, Mark I and Palmer, Colin N A and Peltonen, Leena and Plomin, Robert and Potter, Simon C and Rautanen, Anna and Ravindrarajah, Radhi and Ricketts, Michelle and Samani, Nilesh and Sawcer, Stephen J and Strange, Amy and Trembath, Richard C and Viswanathan, Ananth C and Waller, Matthew and Weston, Paul and Whittaker, Pamela and Widaa, Sara and Wood, Nicholas W and McVean, Gilean and Reveille, John D and Wordsworth, B Paul and Brown, Matthew A and Donnelly, Peter and The Australo-Anglo-American Spondyloarthritis Consortium (TASC) and the Wellcome Trust Case Control Consortium 2 (WTCCC2) and Spondyloarthritis Research Consortium of Canada (SPARCC) and Australo-Anglo-Amer Spondyloarthri and Wellcome Trust Case Control Consor and Spondyloarthrit Res Consortium Can and Wellcome Trust Case Control Consortium 2 (WTCCC2) and Australo-Anglo-American Spondyloarthritis Consortium (TASC)
Nature genetics, ISSN 1546-1718, 07/2011, Volume 43, Issue 8, pp. 761 - 767
Journal Article
by Strange, A and Capon, F and Spencer, C.C and Knight, J and Weale, M.E and Allen, M.H and Barton, A and Band, G and Bellenguez, C and Bergboer, J.G.M and Blackwell, J.M and Bramon, E and Bumpstead, S.J and Casas, J.P and Cork, M.J and Corvin, A and Deloukas, P and Dilthey, A and Duncanson, A and Edkins, S and Estivill, X and Fitzgerald, O and Freeman, C and Giardina, E and Gray, E and Hofer, A and Huffmeier, U and Hunt, S.E and Irvine, A.D and Jankowski, J and Kirby, B and Langford, C and Lascorz, J and Leman, J and Leslie, S and Mallbris, L and Markus, H.S and Mathew, C.G and McLean, W.H.I and McManus, R and Mossner, R and Moutsianas, L and Naluai, A.T and Nestle, F.O and Novelli, G and Onoufriadis, A and Palmer, C.N and Perricone, C and Pirinen, M and Plomin, R and Potter, S.C and Pujol, R.M and Rautanen, A and Riveira-Munoz, E and Ryan, A.W and Salmhofer, W and Samuelsson, L and Sawcer, S.J and Schalkwijk, J and Smith, C.H and Stahle, M and Su, Z and Tazi-Ahnini, R and Traupe, H and Viswanathan, A.C and Warren, R.B and Weger, W and Wolk, K and Wood, N and Worthington, J and Young, H.S and Zeeuwen, P.L.J.M and Hayday, A and Burden, A.D and Griffiths, C.E and Kere, J and Reis, A and McVean, G and Evans, D.M and Brown, M.A and Barker, J.N and Peltonen, L and Donnelly, P and Trembath, R.C and Genetic Analysis of Psoriasis Consortium & the Wellcome Trust Case Control Consortium 2 and Wellcome Trust Case Control and Genetic Anal Psoriasis Consortium and Sahlgrenska akademin and Institutionen för biomedicin, avdelningen för medicinsk genetik och klinisk genetik and Göteborgs universitet and Gothenburg University and Institute of Biomedicine, Department of Medical and Clinical Genetics and Sahlgrenska Academy
Nature genetics, ISSN 1546-1718, 10/2010, Volume 42, Issue 11, pp. 985 - 990
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