Caroline Hayward

Genome-wide association study identifies _FUT8_ and _ESR2_ as co-regulators of a bi-antennary N-linked glycan A2 (GlcNAc~2~Man~3~GlcNAc~2~) in human plasma proteins (2009)

Gordan Lauc, Jennifer Huffman, Caroline Hayward, Ana Knezevic, Ozren Polasek, Olga Gornik, ...

HPLC analysis of N-glycans quantified levels of the biantennary glycan (A2) in plasma proteins of 924 individuals. Subsequent genome-wide association study (GWAS) using 317,503 single nucleotide...

Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis (2009)

Johansson, Åsa, Marroni, Fabio, Hayward, Caroline, Franklin, Christopher S., Kirichenko, Anatoly V., Jonasson, Inger, ...

Genes for height have gained interest for decades, but only recently have candidate genes started to be identified. We have performed linkage analysis and genome-wide association for height in...

A genetic association analysis of cognitive ability and cognitive ageing using 325 markers for 109 genes associated with oxidative stress or cognition (2007)

Harris, Sarah E, Fox, Helen, Wright, Alan F, Hayward, Caroline, Starr, John M, Whalley, Lawrence J, ...

Abstract Background Non-pathological cognitive ageing is a distressing condition affecting an increasing number of people in our 'ageing society'. Oxidative stress is hypothesised to have a major...

Effects of genome-wide heterozygosity on a range of biomedically relevant human quantitative traits (2007)

Campbell, Harry, Carothers, Andrew D., Rudan, Igor, Hayward, Caroline, Biloglav, Zrinka, Barac, Lovorka, ...

The dramatic changes in human population structure over the last 200 years have resulted in significant levels of outbreeding, which, in turn, is predicted to lead to increased levels of individual...

Effects of genome-wide heterozygosity on a range of biomedically relevant human quantitative traits (2007)

Campbell, Harry, Carothers, Andrew D., Rudan, Igor, Hayward, Caroline, Biloglav, Zrinka, Barac, Lovorka, ...

The dramatic changes in human population structure over the last 200 years have resulted in significant levels of outbreeding which in turn is predicted to lead to increased levels of individual...

Historic Exposure to Plague and Present-day Frequency of CCR5del32 in Two Isolated Island Communities of Dalmatia, Croatia (2006)

Smoljanović, Mladen, Ristić, Smiljana, Hayward, Caroline

Aim: To assess the frequency of deletion of 32 base pairs in a CCR5 gene, shown to confer resistance to HIV infection, in two isolated island communities of Dalmatia, Croatia, with different...

Disease mechanisms in late-onset retinal macular degeneration associated with mutation in C1QTNF5 (2006)

Shu, Xinhua, Tulloch, Brian, Lennon, Alan, Vlachantoni, Dafni, Zhou, Xinzhi, Hayward, Caroline, ...

Late-onset retinal macular degeneration (L-ORMD) is an autosomal dominant condition resembling age-related macular degeneration (AMD) in which a key pathological feature is a thick extracellular...

Disease mechanisms in late-onset retinal macular degeneration associated with mutation in C1QTNF5 (2006)

Shu, Xinhua, Tulloch, Brian, Lennon, Alan, Vlachantoni, Dafni, Zhou, Xinzhi, Hayward, Caroline, ...

Late-onset retinal macular degeneration (L-ORMD) is an autosomal dominant condition resembling age-related macular degeneration (AMD) in which a key pathological feature is a thick extracellular...

Lost in Transition – The Island of Susak (1951–2001) (2004)

Rudan, Igor, Stevanović, Ranko, Vitart, Veronique, Vuletić, Gorka, Sibbett, Lorna, Vuletić, Silvije, ...

The isolated population of the Island of Susak was thoroughly studied by a multidisciplinary team of the Croatian Academy of Sciences and Arts in early 1950’s. Recently, a team of scientists...

Identification of SATB2 as the cleft palate gene on 2q32-q33 (2003)

FitzPatrick, David R., Carr, Ian M., McLaren, Lorna, Leek, Jack P., Wightman, Patrick, Williamson, Kathy, ...

Cytogenetic evidence, in the form of deletions and balanced translocations, points to the existence of a locus on 2q32-q33, for which haploinsufficiency results in isolated cleft palate (CPO). Here...

Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration - a genetic model for age-related macular degeneration (2003)

Hayward, Caroline, Shu, Xinhua, Cideciyan, Artur V, Lennon, Alan, Barran, Perdita, Zareparsi, Sepideh, ...

A primary feature of age-related macular degeneration (AMD) is the presence of extracellular deposits between the retinal pigment epithelium (RPE) and underlying Bruch's membrane, leading to RPE...

Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration - a genetic model for age-related macular degeneration (2003)

Hayward, Caroline, Shu, Xinhua, Cideciyan, Artur V, Lennon, Alan, Barran, Perdita, Zareparsi, Sepideh, ...

A primary feature of age-related macular degeneration (AMD) is the presence of extracellular deposits between the retinal pigment epithelium (RPE) and underlying Bruch's membrane, leading to RPE...

Identification of SATB2 as the cleft palate gene on 2q32-q33 (2003)

FitzPatrick, David R., Carr, Ian M., McLaren, Lorna, Leek, Jack P., Wightman, Patrick, Williamson, Kathy, ...

Cytogenetic evidence, in the form of deletions and balanced translocations, points to the existence of a locus on 2q32–q33, for which haploinsufficiency results in isolated cleft palate (CPO). Here...

Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degeneration (2003)

Hayward, Caroline, Shu, Xinhua, Cideciyan, Artur V., Lennon, Alan, Barran, Perdita, Zareparsi, Sepideh, ...

A primary feature of age-related macular degeneration (AMD) is the presence of extracellular deposits between the retinal pigment epithelium (RPE) and underlying Bruch's membrane, leading to RPE...

Identification of SATB2 as the cleft palate gene on 2q32-q33 (2003)

FitzPatrick, David R., Carr, Ian M., McLaren, Lorna, Leek, Jack P., Wightman, Patrick, Williamson, Kathy, ...

Cytogenetic evidence, in the form of deletions and balanced translocations, points to the existence of a locus on 2q32-q33, for which haploinsufficiency results in isolated cleft palate (CPO). Here...

Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration - a genetic model for age-related macular degeneration (2003)

Hayward, Caroline, Shu, Xinhua, Cideciyan, Artur V, Lennon, Alan, Barran, Perdita, Zareparsi, Sepideh, ...

A primary feature of age-related macular degeneration (AMD) is the presence of extracellular deposits between the retinal pigment epithelium (RPE) and underlying Bruch's membrane, leading to RPE...

Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration - a genetic model for age-related macular degeneration (2003)

Hayward, Caroline, Shu, Xinhua, Cideciyan, Artur V, Lennon, Alan, Barran, Perdita, Zareparsi, Sepideh, ...

A primary feature of age-related macular degeneration (AMD) is the presence of extracellular deposits between the retinal pigment epithelium (RPE) and underlying Bruch's membrane, leading to RPE...

Ageing: Cognitive change and the APOEe4 allele (2002)

Deary, Ian J, Whiteman, Martha C, Pattie, Alison, Starr, John M, Hayward, Caroline, Wright, Alan F, ...

There is a marked variation in whether people retain sufficient cognitive function to maintain their quality of life and independence in old age, even among those without dementia, so it would be...

Ageing: Cognitive change and the APOEe4 allele (2002)

Deary, Ian J, Whiteman, Martha C, Pattie, Alison, Starr, John M, Hayward, Caroline, Wright, Alan F, ...

There is a marked variation in whether people retain sufficient cognitive function to maintain their quality of life and independence in old age, even among those without dementia, so it would be...

Linkage analysis of maturity-onset diabetes of the young (MODY): Genetic heterogeneity and nonpenetrance

Bowden, Donald W., Akots, Gita, Rothschild, Cynthia B., Falls, Kathleen F., Sheehy, Michael J., Hayward, Caroline, ...

We have analyzed the inheritance of maturity-onset diabetes of the young (MODY) on chromosome 20 in a large multigeneration family, the R.-W. family, and in two other MODY families. Of the four...

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

Vitart, Veronique, Carothers, Andrew D., Hayward, Caroline, Teague, Peter, Hastie, Nicholas D., Campbell, Harry, ...

Few studies have investigated genetic differentiation within nonisolate European populations, despite the initiation of large national sample collections such as U.K. Biobank. Here, we used short...

Linkage analysis of maturity-onset diabetes of the young (MODY): Genetic heterogeneity and nonpenetrance

Bowden, Donald W., Akots, Gita, Rothschild, Cynthia B., Falls, Kathleen F., Sheehy, Michael J., Hayward, Caroline, ...

We have analyzed the inheritance of maturity-onset diabetes of the young (MODY) on chromosome 20 in a large multigeneration family, the R.-W. family, and in two other MODY families. Of the four...

Runs of Homozygosity in European Populations

McQuillan, Ruth, Leutenegger, Anne-Louise, Abdel-Rahman, Rehab, Franklin, Christopher S., Pericic, Marijana, Barac-Lauc, Lovorka, ...

Estimating individual genome-wide autozygosity is important both in the identification of recessive disease variants via homozygosity mapping and in the investigation of the effects of genome-wide...

Genetic Determinants of Circulating Sphingolipid Concentrations in European Populations

Hicks, Andrew A., Pramstaller, Peter P., Johansson, Åsa, Vitart, Veronique, Rudan, Igor, Ugocsai, Peter, ...

Sphingolipids have essential roles as structural components of cell membranes and in cell signalling, and disruption of their metabolism causes several diseases, with diverse neurological,...