Balancing the local and the universal in maintaining ethical access to a genomics biobank

por Heeney, Catherine, Kerr, Shona M.
Publicado 2017

VIKING II, a worldwide observational cohort of volunteers with northern isles ancestry

por Kerr, Shona M., Edwards, Rachel, Buchanan, David, Dean, John, Miedzybrodzka, Zosia, Wilson, James F.
Publicado 2023

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

Generation Scotland: Donor DNA Databank; A control DNA resource

por Kerr, Shona M, Liewald, David CM, Campbell, Archie, Taylor, Kerrie, Wild, Sarah H, Newby, David, Turner, Marc, Porteous, David J
Publicado 2010

Common Genetic Variants Explain the Majority of the Correlation Between Height and Intelligence: The Generation Scotland Study

por Marioni, Riccardo E., Batty, G. David, Hayward, Caroline, Kerr, Shona M., Campbell, Archie, Hocking, Lynne J., Porteous, David J., Visscher, Peter M., Deary, Ian J.
Publicado 2014

Pedigree and genotyping quality analyses of over 10,000 DNA samples from the Generation Scotland: Scottish Family Health Study

por Kerr, Shona M, Campbell, Archie, Murphy, Lee, Hayward, Caroline, Jackson, Cathy, Wain, Louise V, Tobin, Martin D, Dominiczak, Anna, Morris, Andrew, Smith, Blair H, Porteous, David J
Publicado 2013

Clinical case study meets population cohort: identification of a BRCA1 pathogenic founder variant in Orcadians

por Kerr, Shona M., Cowan, Emma, Klaric, Lucija, Bell, Christine, O’Sullivan, Dawn, Buchanan, David, Grzymski, Joseph J., van Hout, Cristopher V., Tzoneva, Gannie, Shuldiner, Alan R., Wilson, James F., Miedzybrodzka, Zosia
Publicado 2023

Assessment of dried blood spots for DNA methylation profiling

por Walker, Rosie M., MacGillivray, Louise, McCafferty, Sarah, Wrobel, Nicola, Murphy, Lee, Kerr, Shona M., Morris, Stewart W., Campbell, Archie, McIntosh, Andrew M., Porteous, David J., Evans, Kathryn L.
Publicado 2019

Novel Urinary Peptidomic Classifier Predicts Incident Heart Failure

por Zhang, Zhen‐Yu, Ravassa, Susana, Nkuipou‐Kenfack, Esther, Yang, Wen‐Yi, Kerr, Shona M., Koeck, Thomas, Campbell, Archie, Kuznetsova, Tatiana, Mischak, Harald, Padmanabhan, Sandosh, Dominiczak, Anna F., Delles, Christian, Staessen, Jan A.
Publicado 2017

A practical checklist for return of results from genomic research in the European context

por Vears, Danya F., Hallowell, Nina, Bentzen, Heidi Beate, Ellul, Bridget, Nøst, Therese Haugdahl, Kerasidou, Angeliki, Kerr, Shona M., Th. Mayrhofer, Michaela, Mežinska, Signe, Ormondroyd, Elizabeth, Solberg, Berge, Sand, Birgitte Wirum, Budin-Ljøsne, Isabelle
Publicado 2023

Targeted genetic testing for familial hypercholesterolaemia using next generation sequencing: a population-based study

por Norsworthy, Penny J, Vandrovcova, Jana, Thomas, Ellen RA, Campbell, Archie, Kerr, Shona M, Biggs, Jennifer, Game, Laurence, Soutar, Anne K, Smith, Blair H, Dominiczak, Anna F, Porteous, David J, Morris, Andrew D, Scotland, Generation, Aitman, Timothy J
Publicado 2014

Molecular genetic contributions to socioeconomic status and intelligence

por Marioni, Riccardo E., Davies, Gail, Hayward, Caroline, Liewald, Dave, Kerr, Shona M., Campbell, Archie, Luciano, Michelle, Smith, Blair H., Padmanabhan, Sandosh, Hocking, Lynne J., Hastie, Nicholas D., Wright, Alan F., Porteous, David J., Visscher, Peter M., Deary, Ian J.
Publicado 2014

An actionable KCNH2 Long QT Syndrome variant detected by sequence and haplotype analysis in a population research cohort

por Kerr, Shona M., Klaric, Lucija, Halachev, Mihail, Hayward, Caroline, Boutin, Thibaud S., Meynert, Alison M., Semple, Colin A., Tuiskula, Annukka M., Swan, Heikki, Santoyo-Lopez, Javier, Vitart, Veronique, Haley, Chris, Dean, John, Miedzybrodzka, Zosia, Aitman, Timothy J., Wilson, James F.
Publicado 2019

Flexible and scalable diagnostic filtering of genomic variants using G2P with Ensembl VEP

por Thormann, Anja, Halachev, Mihail, McLaren, William, Moore, David J., Svinti, Victoria, Campbell, Archie, Kerr, Shona M., Tischkowitz, Marc, Hunt, Sarah E., Dunlop, Malcolm G., Hurles, Matthew E., Wright, Caroline F., Firth, Helen V., Cunningham, Fiona, FitzPatrick, David R.
Publicado 2019

Increased ultra-rare variant load in an isolated Scottish population impacts exonic and regulatory regions

por Halachev, Mihail, Meynert, Alison, Taylor, Martin S., Vitart, Veronique, Kerr, Shona M., Klaric, Lucija, Aitman, Timothy J., Haley, Chris S., Prendergast, James G., Pugh, Carys, Hume, David A., Harris, Sarah E., Liewald, David C., Deary, Ian J., Semple, Colin A., Wilson, James F.
Publicado 2019

The genetic landscape of Scotland and the Isles

por Gilbert, Edmund, O’Reilly, Seamus, Merrigan, Michael, McGettigan, Darren, Vitart, Veronique, Joshi, Peter K., Clark, David W., Campbell, Harry, Hayward, Caroline, Ring, Susan M., Golding, Jean, Goodfellow, Stephanie, Navarro, Pau, Kerr, Shona M., Amador, Carmen, Campbell, Archie, Haley, Chris S., Porteous, David J., Cavalleri, Gianpiero L., Wilson, James F.
Publicado 2019

Typing myalgic encephalomyelitis by infection at onset: A DecodeME study

por Bretherick, Andrew D., McGrath, Simon J., Devereux-Cooke, Andy, Leary, Sian, Northwood, Emma, Redshaw, Anna, Stacey, Pippa, Tripp, Claire, Wilson, Jim, Chowdhury, Sonya, Lewis, Isabel, Almelid, Øyvind, Baby, Sumy V., Baker, Tom, Becher, Hannes, Boutin, Thibaud, Clyde, Malgorzata, Garcia, Diana, Ireland, John, Kerr, Shona M., McDowall, Ewan, Perry, David, Samms, Gemma L., Vitart, Veronique, Wolfe, Jareth C., Ponting, Chris P.
Publicado 2023

Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants

por Nagy, Reka, Boutin, Thibaud S., Marten, Jonathan, Huffman, Jennifer E., Kerr, Shona M., Campbell, Archie, Evenden, Louise, Gibson, Jude, Amador, Carmen, Howard, David M., Navarro, Pau, Morris, Andrew, Deary, Ian J., Hocking, Lynne J., Padmanabhan, Sandosh, Smith, Blair H., Joshi, Peter, Wilson, James F., Hastie, Nicholas D., Wright, Alan F., McIntosh, Andrew M., Porteous, David J., Haley, Chris S., Vitart, Veronique, Hayward, Caroline
Publicado 2017

DecodeME: community recruitment for a large genetics study of myalgic encephalomyelitis / chronic fatigue syndrome

por Devereux-Cooke, Andy, Leary, Sian, McGrath, Simon J., Northwood, Emma, Redshaw, Anna, Shepherd, Charles, Stacey, Pippa, Tripp, Claire, Wilson, Jim, Mar, Margaret, Boobyer, Danielle, Bromiley, Sam, Chowdhury, Sonya, Dransfield, Claire, Almas, Mohammed, Almelid, Øyvind, Buchanan, David, Garcia, Diana, Ireland, John, Kerr, Shona M., Lewis, Isabel, McDowall, Ewan, Migdal, Malgorzata, Murray, Phil, Perry, David, Ponting, Chris P., Vitart, Veronique, Wolfe, Jareth C.
Publicado 2022

Urinary peptides in heart failure: a link to molecular pathophysiology

por He, Tianlin, Mischak, Michaela, Clark, Andrew L., Campbell, Ross T., Delles, Christian, Díez, Javier, Filippatos, Gerasimos, Mebazaa, Alexandre, McMurray, John J.V., González, Arantxa, Raad, Julia, Stroggilos, Rafael, Bosselmann, Helle S., Campbell, Archie, Kerr, Shona M., Jackson, Colette E., Cannon, Jane A., Schou, Morten, Girerd, Nicolas, Rossignol, Patrick, McConnachie, Alex, Rossing, Kasper, Schanstra, Joost P., Zannad, Faiez, Vlahou, Antonia, Mullen, William, Jankowski, Vera, Mischak, Harald, Zhang, Zhenyu, Staessen, Jan A., Latosinska, Agnieszka
Publicado 2021