| Systematic identification of genetic influences on methylation across the human life course TR Gaunt, HA Shihab, G Hemani, JL Min, G Woodward, O Lyttleton, ... Genome biology 17, 1-14, 2016 | 615 | 2016 |
| Prenatal exposure to maternal smoking and offspring DNA methylation across the lifecourse: findings from the Avon Longitudinal Study of Parents and Children (ALSPAC) RC Richmond, AJ Simpkin, G Woodward, TR Gaunt, O Lyttleton, ... Human molecular genetics 24 (8), 2201-2217, 2015 | 413 | 2015 |
| Data resource profile: accessible resource for integrated epigenomic studies (ARIES) CL Relton, T Gaunt, W McArdle, K Ho, A Duggirala, H Shihab, ... International journal of epidemiology 44 (4), 1181-1190, 2015 | 293 | 2015 |
| Prenatal exposure to maternal cigarette smoking and DNA methylation: epigenome-wide association in a discovery sample of adolescents and replication in an independent cohort at … KWK Lee, R Richmond, P Hu, L French, J Shin, C Bourdon, E Reischl, ... Environmental health perspectives 123 (2), 193-199, 2015 | 237 | 2015 |
| Clinical genetic testing using a custom-designed steroid-resistant nephrotic syndrome gene panel: analysis and recommendations ES Sen, P Dean, L Yarram-Smith, A Bierzynska, G Woodward, C Buxton, ... Journal of medical genetics 54 (12), 795-804, 2017 | 76 | 2017 |
| Expanding the clinical spectrum of recessive truncating mutations of KLHL7 to a Bohring-Opitz-like phenotype AL Bruel, S Bigoni, J Kennedy, M Whiteford, C Buxton, G Parmeggiani, ... Journal of medical genetics 54 (12), 830-835, 2017 | 19 | 2017 |
| The West Midland Familial Hypercholesterolaemia (FH) screening programme: Evaluating the utility of the 12 SNP polygenic risk score (PRS) across ethnic groupings E George, J Bellaby, S Day, R Dhillon, S Horton, K Dyer, R Cramb, ... Atherosclerosis Plus 43, S5-S6, 2021 | 1 | 2021 |
| Genetic testing for Familial Hypercholesterolaemia in the genomic era. The utility of an NGS test for monogenic and polygenic hypercholesterolaemia E Watson, J Honeychurch, A Hills, P Dean, L Yarram-Smith, G Woodward, ... Atherosclerosis Supplements 28, e4, 2017 | 1 | 2017 |
| Modernising workflows for high throughput testing for Familial Hypercholesterolaemia: How to deliver a cost effective genetic testing service J Honeychurch, A Hills, P Dean, M Greenslade, C Buxton, G Woodward, ... Atherosclerosis 245, e250, 2016 | 1 | 2016 |
| Clinical validation of the Galeas Hereditary Cancer NGS panel, a comprehensive sample-to-report platform for clinical cancer risk profiling P Paganopoulou, G Woodward, L Delfino, K Cook, Y Wallis, S Butler, ... EUROPEAN JOURNAL OF HUMAN GENETICS 32, 628-628, 2024 | | 2024 |
| HEART UK 34th Annual Medical & Scientific Virtual Conference July 2021-Oral abstracts Abstracts C Duff-Farrier, M Pennock, E Watson, N Forrester, S Marsh, A Waite, ... ATHEROSCLEROSIS PLUS 43, S2-S9, 2021 | | 2021 |
| APOE gene testing in FH referrals–the story so far C Duff-Farrier, M Pennock, E Watson, N Forrester, S Marsh, A Waite, ... Atherosclerosis Plus 43, S2, 2021 | | 2021 |
| Novel truncating recessive mutations in KLHL7 gene causing Bohring-Opitz like syndrome A Bruel, S Bigoni, J Kennedy, M Whiteford, C Buxton, G Parmeggiani, ... EUROPEAN JOURNAL OF HUMAN GENETICS 26, 479-479, 2018 | | 2018 |
| Familial hypercholesterolaemia in the genomic era: improving the clinical utility of current genetic testing C Knowles, A Hills, E Watson, M Pennock, C Dent, J Evans, C Robinson, ... Atherosclerosis Supplements 34, e4, 2018 | | 2018 |
| Autosomal recessive hypercholesterolaemia due to homozygous ldlrap1 variants: a bristol case review J Honeychurch, A Hills, E Watson, M Pennock, C Dent, J Evans, ... Atherosclerosis Supplements 34, e3, 2018 | | 2018 |
| Development of a multigene panel screening test for hypertriglyceridaemia using next generation sequencing P Downie, J Honeychurch, P Dean, R Whittington, G Woodward, R Moore, ... Atherosclerosis 275, e59, 2018 | | 2018 |
| Standardising genetic variant classification for FH–application of the ACMG guidelines C Dent, A Hills, J Honeychurch, E Watson, P Dean, G Woodward, ... Atherosclerosis Supplements 28, e7, 2017 | | 2017 |
| Development of a multigene panel screening test for hypertriglyceridaemia using next generation sequencing P Downie, J Honeychurch, P Dean, R Whittington, G Woodward, R Moore, ... Atherosclerosis Supplements 28, e7-e8, 2017 | | 2017 |
| CLINICAL GENETIC TESTING USING NEXT GENERATION SEQUENCING IN STEROID-RESISTANT NEPHROTIC SYNDROME AND ALPORT SYNDROME E Sen, P Dean, L Yarram-smith, A Bierzynska, G Woodward, C Buxton, ... PEDIATRIC NEPHROLOGY 32 (9), 1653-1654, 2017 | | 2017 |
| Validation and utility of a new NGS assay for familial hypercholesterolaemia incorporating 12 LDL-C-raising SNPs J Honeychurch, E Watson, A Hills, P Dean, G Woodward, M Wadsley, ... Atherosclerosis 255, 6-7, 2016 | | 2016 |
