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British journal of psychiatry, ISSN 0007-1250, 01/2009, Volume 194, Issue 1, pp. 25 - 33
Journal Article
Nature genetics, ISSN 1546-1718, 01/2013, Volume 45, Issue 2, pp. 208 - 213
Journal Article
Nature genetics, ISSN 1546-1718, 06/2017, Volume 49, Issue 8, pp. 1167 - 1173
Journal Article
British journal of psychiatry, ISSN 0007-1250, 06/2009, Volume 194, Issue 6, pp. 527 - 534
Background Subtle abnormalities in frontal white matter have been reported in bipolar disorder. Aims To assess whether impaired integrity of white matter... 
Papers | Life Sciences & Biomedicine | Psychiatry | Science & Technology | Genetic Predisposition to Disease | Humans | Middle Aged | Male | Bipolar Disorder - genetics | Case-Control Studies | Neuropsychological Tests | Anisotropy | Pedigree | Bipolar Disorder - pathology | Brain - pathology | Adult | Female | Diffusion Magnetic Resonance Imaging - methods | 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 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
Nature communications, ISSN 2041-1723, 07/2014, Volume 5, Issue 1, pp. 4204 - 4204
... Edkins8,Suzannah J. Bumpstead8, Jenefer M. Blackwell9,10, Elvira Bramon11,12, Matthew A. Brown13, Juan P. Casas14,15, Aiden Corvin16, Audrey Duncanson17, Janusz A.Z... 
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