Genomics of common diseases: approaching the tipping point

Por Wright, Alan F
Publicado em 2011

Complex genetic diseases: controversy over the Croesus code

Por Wright, Alan F, Hastie, Nicholas D
Publicado em 2001

PCR detection of existing and new polymorphism at the TIMP locus

Por Aldred, Micheala A., Wright, Alan F.
Publicado em 1991

RPGR: Its role in photoreceptor physiology, human disease, and future therapies

Por Megaw, Roly D., Soares, Dinesh C., Wright, Alan F.
Publicado no Exp Eye Res (2015)

Human population structure, genome autozygosity and human health

Por Campbell, Harry, Rudan, Igor, Bittles, Alan H, Wright, Alan F
Publicado em 2009

Strategy for Mapping Quantitative Trait Loci (QTL) by Using Human Metapopulations

Por Rudan, Igor, Biloglav, Zrinka, Carothers, Andrew D., Wright, Alan F., Campbell, Harry
Publicado em 2006

Identity-by-Descent-Based Phasing and Imputation in Founder Populations Using Graphical Models

Por Palin, Kimmo, Campbell, Harry, Wright, Alan F, Wilson, James F, Durbin, Richard
Publicado em 2011

Unilateral retinitis pigmentosa occurring in an individual with a mutation in the CLRN1 gene

Por Sim, Peng Yong, Jeganathan, V Swetha E, Wright, Alan F., Cackett, Peter
Publicado no BMJ Case Rep (2018)

Evolutionary Characterization of the Retinitis Pigmentosa GTPase Regulator Gene

Por Raghupathy, Rakesh Kotapati, Gautier, Philippe, Soares, Dinesh C., Wright, Alan F., Shu, Xinhua
Publicado no Invest Ophthalmol Vis Sci (2015)

Late-Onset Retinal Degeneration caused by C1QTNF5 Mutation: Sub-Retinal Pigment Epithelium Deposits and Visual Consequences

Por Jacobson, Samuel G., Cideciyan, Artur V., Sumaroka, Alexander, Roman, Alejandro J., Wright, Alan F.
Publicado no JAMA Ophthalmol (2014)

Mortality and Cancer Incidence in Carriers of Balanced Robertsonian Translocations: A National Cohort Study

Por Schoemaker, Minouk J, Jones, Michael E, Higgins, Craig D, Wright, Alan F, Swerdlow, Anthony J
Publicado no Am J Epidemiol (2019)

Mortality and cancer incidence in carriers of constitutional t(11;22)(q23;q11) translocations: A prospective study

Por Schoemaker, Minouk J, Jones, Michael E, Higgins, Craig D, Wright, Alan F, Swerdlow, Anthony J
Publicado no Int J Cancer (2019)

Increased Level of Linkage Disequilibrium in Rural Compared with Urban Communities: A Factor to Consider in Association-Study Design

Por Vitart, Veronique, Carothers, Andrew D., Hayward, Caroline, Teague, Peter, Hastie, Nicholas D., Campbell, Harry, Wright, Alan F.
Publicado em 2005

A genetic association analysis of cognitive ability and cognitive ageing using 325 markers for 109 genes associated with oxidative stress or cognition

Por Whalley Lawrence J, Starr John M, Hayward Caroline, Wright Alan F, Fox Helen, Harris Sarah E, Deary Ian J
Publicado em 2007-07-01

A genetic association analysis of cognitive ability and cognitive ageing using 325 markers for 109 genes associated with oxidative stress or cognition

Por Harris, Sarah E, Fox, Helen, Wright, Alan F, Hayward, Caroline, Starr, John M, Whalley, Lawrence J, Deary, Ian J
Publicado em 2007

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 em 2010

RPGR-ORF15, which is mutated in retinitis pigmentosa, associates with SMC1, SMC3, and microtubule transport proteins

Por Khanna, Hemant, Hurd, Toby W., Lillo, Concepcion, Shu, Xinhua, Parapuram, Sunil K., He, Shirley, Akimoto, Masayuki, Wright, Alan F., Margolis, Ben, Williams, David S., Swaroop, Anand
Publicado em 2005

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 em 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 no J Hypertens (2017)

Remapping of the RP15 Locus for X-Linked Cone-Rod Degeneration to Xp11.4-p21.1, and Identification of a De Novo Insertion in the RPGR Exon ORF15

Por Mears, Alan J., Hiriyanna, Suja, Vervoort, Raf, Yashar, Beverly, Gieser, Linn, Fahrner, Stacey, Daiger, Stephen P., Heckenlively, John R., Sieving, Paul A., Wright, Alan F., Swaroop, Anand
Publicado em 2000