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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
by Strange, Amy and Capon, Francesca and Spencer, Chris C.A and Knight, Jo and Weale, Michael E and Allen, Michael H and Barton, Ane and Band, Gavin and Bellenguez, Céline and Bergboer, Judith G.M and BlackweL, Jenefer M and Bramon, Elvira and Bumpstead, Suzanah J and Casas, Juan P and Cork, Michael J and Corvin, Aiden and Deloukas, Panos and Dilthey, Alexander and Duncanson, Audrey and Edkins, Sarah and EstiviL, Xavier and Fitzgerald, Oliver and FrEman, Colin and Giardina, Emiliano and Gray, Ema and Hofer, Angelika and Hüffmeier, Ulrike and Hunt, Sarah E and Irvine, Alan D and Jankowski, Janusz and Kirby, Brian and Langford, Cordelia and Lascorz, Jesés and Leman, Joyce and Leslie, Stephen and MaLbris, Lotus and Markus, Hugh S and Mathew, Christopher G and McLean, W H Irwin and McManus, Ros and MöSner, Rotraut and Moutsianas, Loukas and Naluai, Asa T and Nestle, Frank O and NoveLi, Giuseppe and Onoufriadis, Alexandros and Palmer, Colin N.A and Perricone, Carlo and Pirinen, Mati and Plomin, Robert and PoTer, Simon C and Pujol, Ramon M and Rautanen, Ana and Riveira-Munoz, Eva and Ryan, Anthony W and Salmhofer, Wolfgang and SamuelSon, Lena and Sawcer, Stephen J and Schalkwijk, Jost and Smith, Catherine H and Ståhle, Mona and Su, Zhan and Tazi-Ahnini, Rachid and Traupe, Heiko and Viswanathan, Ananth C and Warren, Richard B and Weger, Wolfgang and Wolk, Katarina and WOd, Nicholas and Worthington, Jane and Young, Helen S and Zeeuwen, Patrick L J.M and Hayday, Adrian and Burden, A David and Griffiths, Christopher E.M and Kere, Juha and Reis, André and McVean, Gilean and Evans, David M and Brown, Mathew A and Barker, Jonathan N and Peltonen, Lena and Donely, Peter and Trembath, Richard C
Nature genetics, ISSN 1061-4036, 11/2010, Volume 42, Issue 11, pp. 985 - 990
Journal Article
PloS one, ISSN 1932-6203, 2013, Volume 8, Issue 8, pp. e71690 - e71690
Journal Article
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 Ruderfer, Douglas M and Ripke, Stephan and McQuillin, Andrew and Boocock, James and Stahl, Eli A and Pavlides, Jennifer M. Whitehead and Charney, Alexander W and Loohuis, Loes M. Olde and Domenici, Enrico and Di Florio, Arianna and Papiol, Sergi and Kalman, Janos L and Trubetskoy, Vassily and Adolfsson, Rolf and Agartz, Ingrid and Agerbo, Esben and Akil, Huda and Albani, Diego and Albus, Margot and Alda, Martin and Alexander, Madeline and Alliey-Rodriguez, Ney and Als, Thomas D and Amin, Farooq and Anjorin, Adebayo and Arranz, Maria J and Awasthi, Swapnil and Bacanu, Silviu A and Badner, Judith A and Baekvad-Hansen, Marie and Bakker, Steven and Band, Gavin and Barchas, Jack D and Bass, Nicholas and Bauer, Michael and Baune, Bernhard T and Begemann, Martin and Bellenguez, Celine and Belliveau, Richard A and Bellivier, Frank and Bender, Stephan and Berrettini, Wade H and Bevilacqua, Elizabeth and Biernacka, Joanna M and Bigdeli, Tim B and Blackwell, Jenefer M and Blackwood, Douglas H.R and Pedersen, Carsten Bocker and Boehnke, Michael and Boks, Marco and Borglum, Anders D and Bramon, Elvira and Breen, Gerome and Brown, Matthew A and Bruggeman, Richard and Buccola, Nancy G and Buckner, Randy L and Budde, Monika and Bulik-Sullivan, Brendan and Bumpstead, Suzannah J and Bunney, William and Burmeister, Margit and Buxbaum, Joseph D and Bybjerg-Grauholm, Jonas and Byerley, William and Cahn, Wiepke and Cai, Guiqing and Campion, Dominique and Cantor, Rita M and Carr, Vaughan J and Carrera, Noa and Casas, Juan P and Casas, Miquel and Catts, Stanley V and Cervantes, Pablo and Chambert, Kimberley D and Chan, Raymond C.K and Chen, Eric Y.H and Chen, Ronald Y.L and Cheng, Wei and Cheung, Eric F.C and Chong, Siow Ann and Clarke, Toni-Kim and Cloninger, C. Robert and Cohen, David and Cohen, Nadine and Coleman, Jonathan R.I and Cormican, Paul and Coryell, William and Craddock, Nicholas and Craig, David W and Crowley, James J and Cruceanu, Cristiana and Curtis, David and Czerski, Piotr M and Dale, Anders M and Daly, Mark J and Dannlowski, Udo and Darvasi, Ariel and Davidson, Michael and ... and Bipolar Disorder and Schizophrenia Working Group of the Psychiatric Genomics Consortium and Wellcome Trust Case-Control Consortium and Psychosis Endophenotypes International Consortium and Psychosis Endophenotypes Inter and Psychiat Genomics Consortium and Wellcome Trust Case-Control and Bipolar Disorder and Schizophrenia Working Group of the Psychiatric Genomics Consortium. Electronic address: douglas.ruderfer@vanderbilt.edu
Cell (Cambridge), ISSN 0092-8674, 06/2018, Volume 173, Issue 7, pp. 1705 - 1715.e16
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
Journal Article
Nature communications, ISSN 2041-1723, 07/2014, Volume 5, Issue 1, pp. 4204 - 4204
..., Richard Pearson3, Damjan Vukcevic3, Cordelia Langford8, Panos Deloukas8, Sarah Hunt8, Emma Gray8, Serge Dronov8, Simon C. Potter8, Avazeh Tashakkori-Ghanbaria8, Sarah... 
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