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by Cheng, Ching-Yu and Schache, Maria and Ikram, M. Kamran and Young, Terri L and Guggenheim, Jeremy A and Vitart, Veronique and MacGregor, Stuart and Verhoeven, Virginie J.M and Barathi, Veluchamy A and Liao, Jiemin and Hysi, Pirro G and Bailey-Wilson, Joan E and St. Pourcain, Beate and Kemp, John P and Timpson, Nicholas J and Evans, David M and Montgomery, Grant W and Mishra, Aniket and Wang, Ya Xing and Rochtchina, Elena and Polasek, Ozren and Amin, Najaf and van Leeuwen, Elisabeth M and Wilson, James F and de Jong, Paulus T.V.M and Vingerling, Johannes R and Tay, Wan-Ting and Zheng, Yingfeng and Chew, Merwyn and Rahi, Jugnoo S and Yamashiro, Kenji and Miyake, Masahiro and Delcourt, Cécile and Williams, Cathy and Guggenheim, Jeremy A and Northstone, Kate and Ring, Susan M and Burdon, Kathryn P and Fogarty, Rhys D and Igo, Robert P and Chew, Emily and Janmahasathian, Sarayut and Wilson, Joan E. Bailey and MacGregor, Stuart and Lu, Yi and Xu, Liang and Baird, Paul N and Rochtchina, Elena and Mitchell, Paul and Wang, Jie Jin and Nangia, Vinay and Hayward, Caroline and Polasek, Ozren and Campbell, Harry and Rudan, Igor and Vatavuk, Zoran and Paterson, Andrew D and Young, Terri L and Verhoeven, Virginie J.M and Klaver, Caroline C and van Duijn, Cornelia M and Metspalu, Andres and Haller, Toomas and Mihailov, Evelin and Pärssinen, Olavi and Wojciechowski, Robert and Schache, Maria and Pfeiffer, Norbert and Höhn, René and Pang, Chi Pui and Chen, Peng and Wegner, Aharon and Yip, Shea Ping and Ho, Daniel W.H and Murgia, Federico and Portas, Laura and Wilson, James F and Hewitt, Alex W and Ang, Wei and Wong, Tien-Yin and Fan, Qiao and Cheng, Ching-Yu and Zhou, Xin and Tai, E-Shyong and Mackey, David A and Hammond, Christopher J and Morrison, Margaux and Zhou, Xiangtian and Chen, Wei and Lehtimäki, Terho and Mäkelä, Kari-Matti and Raitakari, Olli and Kähönen, Mika and Burdon, Kathryn P and Craig, Jamie E and Iyengar, Sudha K and Igo, Robert P and Reinhart, William and Belin, Michael W and Schultze, Robert L and ... and Molecular Risk Factors Program Project and BMES and CROATIA-Vis and Duke Myopia Study and DNA, Genotyping, Data QC and Informatics Group and Epigenetics and Central ECG Reading Unit and GEMT and Consortium for Refractive Error and Myopia and AREDS1c and FITSA and Computed Tomography Reading Center and Estonian Genome Project / EGCUT and WESDR and Central Fundus Photograph Reading Center and Utah Timorese and Penn Family Studies and ALIENOR and Beijing Eye Study and Data and Analysis Group and TwinsUK and Wenzhou and EDIC Publications and Erasmus Rucphen Family Study and DCCT and Yokohama Study and ANZRAG and Members and CROATIA-Split and CIEMS and SCES and LIKI and External Evaluation Committee and 1958 British Birth Cohort and TEST and Gutenberg Health Study and Central Carotid Ultrasound Unit and SCORM and The Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions, and Complications Research Group and Central Biochemistry Laboratory and Myopia Genomics Study (Hong Kong HTI) and Central Neuropsychological Coding Unit and Framingham Eye Study and National Institute of Diabetes and Digestive and Kidney Disease Program Office and Genetic Studies Group and Ogliastra Genetic Park Study and CROATIA-Korčula and AREDS1a and BATS and Young Finns Study and Management Committee and Kyoto high myopia and Central ANS Reading Unit and SP2 and Publications Committee and Wellcome Trust Case Control Consortium 2 and Rotterdam Study and Aichi cohort and Data Coordinating Center and SIMES and ORCADES and SINDI and The Fuchs’ Genetics Multi-Center Study Group and Study Chairmen and RAINE and STARS and Clinical Coordinating Center and Hong Kong cohort study and AREDS1b and Duke FECD Fuchs Dystrophy GWAS and ALSPAC and KORA and Consortium Refractive Error Myopia and Fuchs Genetics Multictr Study Grp and Diabet Control Complications Trial and Wellcome Trust Case Control Consor and Fuchs' Genetics Multi-Center Study Group and Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions, and Complications Research Group
The American Journal of Human Genetics, ISSN 0002-9297, 08/2013, Volume 93, Issue 2, pp. 264 - 277
Journal Article
Journal Article
Environmental Science & Technology, ISSN 0013-936X, 06/2013, Volume 47, Issue 12, pp. 6349 - 6357
Journal Article
PLoS ONE, ISSN 1932-6203, 10/2012, Volume 7, Issue 10, p. e46742
Journal Article
Micron, ISSN 0968-4328, 12/2012, Volume 43, Issue 12, pp. 1293 - 1298
► We have obtained elastic modulus values for Bowman's layer and the anterior stroma. ► Atomic force microscopy was used to determine the elastic modulus. ►... 
Atomic force microscopy | Corneal biomechanics | ELASTIC PROPERTIES | MOLECULE | VERSATILE TOOL | CROSS-LINKING | AFM | BASEMENT-MEMBRANES | MICROSCOPY | MECHANICAL-PROPERTIES | BIOMECHANICAL PROPERTIES | EPITHELIAL-CELLS | BIOLOGY | Biomechanical Phenomena | Elastic Modulus | Microscopy, Atomic Force - methods | Compliance | Humans | Cornea - physiology | Microscope and microscopy
Journal Article
PloS one, ISSN 1932-6203, 2016, Volume 11, Issue 6, p. e0157418
...About the Authors: Benjamin R. Lin Affiliation: Stein Eye Institute, David Geffen School of Medicine at UCLA, Los Angeles, California, United States of America... 
EXCLUSION | COLLAGEN | GENE | MULTIDISCIPLINARY SCIENCES | XVII | BEHNKE CORNEAL-DYSTROPHY | INDIVIDUAL PHENOTYPIC VARIANCES | CDB2 | PREDICTION | FAMILY | Autoantigens - metabolism | Epithelial Cells - metabolism | Alternative Splicing | Cytoskeletal Proteins - genetics | Humans | Corneal Dystrophies, Hereditary - genetics | Male | Epithelium, Corneal - pathology | Autoantigens - genetics | Case-Control Studies | Exome | Corneal Dystrophies, Hereditary - pathology | Genes, Dominant | Female | Gene Expression | Genome-Wide Association Study | Chromosomes, Human, Pair 10 - chemistry | Gene Frequency | Non-Fibrillar Collagens - genetics | Epithelial Cells - pathology | Chromosome Mapping | Corneal Dystrophies, Hereditary - diagnosis | Corneal Dystrophies, Hereditary - metabolism | Sequence Analysis, DNA | Non-Fibrillar Collagens - metabolism | Phenotype | Pedigree | Alleles | Epithelium, Corneal - metabolism | Heterozygote | Aged | Polymorphism, Single Nucleotide | Mutation | Phenotypes | Cornea | Filtration | Splicing | Epithelial cells | Genes | Genomes | Gene sequencing | Proteins | Medicine | Gene frequency | Corneal dystrophy | Collagen | Chromosome 10 | Dynamin | Genetics | Dystrophy | Genetic testing | Growth factors | Chromosomes | Deoxyribonucleic acid--DNA | DNA sequencing | Deoxyribonucleic acid | DNA
Journal Article
JAMA ophthalmology, ISSN 2168-6165, 02/2019, Volume 137, Issue 2, pp. 185 - 193
Journal Article