Colocalization of corneal resistance factor GWAS loci with GTEx e/sQTLs highlights plausible candidate causal genes for keratoconus postnatal corneal stroma weakening

por Jiang, Xinyi, Boutin, Thibaud, Vitart, Veronique
Publicado 2023

Fine-mapping and cell-specific enrichment at corneal resistance factor loci prioritize candidate causal regulatory variants

por Jiang, Xinyi, Dellepiane, Nefeli, Pairo-Castineira, Erola, Boutin, Thibaud, Kumar, Yatendra, Bickmore, Wendy A., Vitart, Veronique
Publicado 2020

Electronic health record and genome-wide genetic data in Generation Scotland participants

por Kerr, Shona M., Campbell, Archie, Marten, Jonathan, Vitart, Veronique, McIntosh, Andrew M, Porteous, David J., Hayward, Caroline
Publicado 2017

Bayesian methods for instrumental variable analysis with genetic instruments (‘Mendelian randomization’): example with urate transporter SLC2A9 as an instrumental variable for effe...

por McKeigue, Paul M, Campbell, Harry, Wild, Sarah, Vitart, Veronique, Hayward, Caroline, Rudan, Igor, Wright, Alan F, Wilson, James F
Publicado 2010

A mouse model of brittle cornea syndrome caused by mutation in Zfp469

por Stanton, Chloe M., Findlay, Amy S., Drake, Camilla, Mustafa, Mohammad Z., Gautier, Philippe, McKie, Lisa, Jackson, Ian J., Vitart, Veronique
Publicado 2021

Insights into the genetic basis of retinal detachment

por Boutin, Thibaud S, Charteris, David G, Chandra, Aman, Campbell, Susan, Hayward, Caroline, Campbell, Archie, Nandakumar, Priyanka, Hinds, David, Mitry, Danny, Vitart, Veronique
Publicado 2020

Recent genomic heritage in Scotland

por Amador, Carmen, Huffman, Jennifer, Trochet, Holly, Campbell, Archie, Porteous, David, Wilson, James F, Hastie, Nick, Vitart, Veronique, Hayward, Caroline, Navarro, Pau, Haley, Chris S
Publicado 2015

Pedigree- and SNP-Associated Genetics and Recent Environment are the Major Contributors to Anthropometric and Cardiometabolic Trait Variation

por Xia, Charley, Amador, Carmen, Huffman, Jennifer, Trochet, Holly, Campbell, Archie, Porteous, David, Hastie, Nicholas D., Hayward, Caroline, Vitart, Veronique, Navarro, Pau, Haley, Chris S.
Publicado 2016

Regional variation in health is predominantly driven by lifestyle rather than genetics

por Amador, Carmen, Xia, Charley, Nagy, Réka, Campbell, Archie, Porteous, David, Smith, Blair H., Hastie, Nick, Vitart, Veronique, Hayward, Caroline, Navarro, Pau, Haley, Chris S.
Publicado 2017

Correction: Pedigree- and SNP-Associated Genetics and Recent Environment are the Major Contributors to Anthropometric and Cardiometabolic Trait Variation

por Xia, Charley, Amador, Carmen, Huffman, Jennifer, Trochet, Holly, Campbell, Archie, Porteous, David, Scotland, Generation, Hastie, Nicholas D., Hayward, Caroline, Vitart, Veronique, Navarro, Pau, Haley, Chris S.
Publicado 2017

The power of regional heritability analysis for rare and common variant detection: simulations and application to eye biometrical traits

por Uemoto, Yoshinobu, Pong-Wong, Ricardo, Navarro, Pau, Vitart, Veronique, Hayward, Caroline, Wilson, James F., Rudan, Igor, Campbell, Harry, Hastie, Nicholas D., Wright, Alan F., Haley, Chris S.
Publicado 2013

Determinants of retinal microvascular features and their relationships in two European populations

por Kirin, Mirna, Nagy, Reka, MacGillivray, Thomas J., Polašek, Ozren, Hayward, Caroline, Rudan, Igor, Campbell, Harry, Wild, Sarah, Wright, Alan F., Wilson, James F., Vitart, Veronique
Publicado 2017

Uncovering Networks from Genome-Wide Association Studies via Circular Genomic Permutation

por Cabrera, Claudia P., Navarro, Pau, Huffman, Jennifer E., Wright, Alan F., Hayward, Caroline, Campbell, Harry, Wilson, James F., Rudan, Igor, Hastie, Nicholas D., Vitart, Veronique, Haley, Chris S.
Publicado 2012

Copy Number Variation across European Populations

por Chen, Wanting, Hayward, Caroline, Wright, Alan F., Hicks, Andrew A., Vitart, Veronique, Knott, Sara, Wild, Sarah H., Pramstaller, Peter P., Wilson, James F., Rudan, Igor, Porteous, David J.
Publicado 2011

Genetic Comparison of a Croatian Isolate and CEPH European Founders

por Navarro, Pau, Vitart, Véronique, Hayward, Caroline, Tenesa, Albert, Zgaga, Lina, Juricic, Danica, Polasek, Ozren, Hastie, Nicholas D, Rudan, Igor, Campbell, Harry, Wright, Alan F, Haley, Chris S, Knott, Sara A
Publicado 2010

Comparative assessment of methods for estimating individual genome-wide homozygosity-by-descent from human genomic data

por Polašek, Ozren, Hayward, Caroline, Bellenguez, Celine, Vitart, Veronique, Kolčić, Ivana, McQuillan, Ruth, Saftić, Vanja, Gyllensten, Ulf, Wilson, James F, Rudan, Igor, Wright, Alan F, Campbell, Harry, Leutenegger, Anne-Louise
Publicado 2010

Localising Loci underlying Complex Trait Variation Using Regional Genomic Relationship Mapping

por Nagamine, Yoshitaka, Pong-Wong, Ricardo, Navarro, Pau, Vitart, Veronique, Hayward, Caroline, Rudan, Igor, Campbell, Harry, Wilson, James, Wild, Sarah, Hicks, Andrew A., Pramstaller, Peter P., Hastie, Nicholas, Wright, Alan F., Haley, Chris S.
Publicado 2012

Genomic prediction of complex human traits: relatedness, trait architecture and predictive meta-models

por Spiliopoulou, Athina, Nagy, Reka, Bermingham, Mairead L., Huffman, Jennifer E., Hayward, Caroline, Vitart, Veronique, Rudan, Igor, Campbell, Harry, Wright, Alan F., Wilson, James F., Pong-Wong, Ricardo, Agakov, Felix, Navarro, Pau, Haley, Chris S.
Publicado 2015

Novel pathogenic mutations in C1QTNF5 support a dominant negative disease mechanism in late-onset retinal degeneration

por Stanton, Chloe M., Borooah, Shyamanga, Drake, Camilla, Marsh, Joseph A., Campbell, Susan, Lennon, Alan, Soares, Dinesh C., Vallabh, Neeru A., Sahni, Jayashree, Cideciyan, Artur V., Dhillon, Baljean, Vitart, Veronique, Jacobson, Samuel G., Wright, Alan F., Hayward, Caroline
Publicado 2017

Local Exome Sequences Facilitate Imputation of Less Common Variants and Increase Power of Genome Wide Association Studies

por Joshi, Peter K., Prendergast, James, Fraser, Ross M., Huffman, Jennifer E., Vitart, Veronique, Hayward, Caroline, McQuillan, Ruth, Glodzik, Dominik, Polašek, Ozren, Hastie, Nicholas D., Rudan, Igor, Campbell, Harry, Wright, Alan F., Haley, Chris S., Wilson, James F., Navarro, Pau
Publicado 2013