Works by Kerr, Shona M.

Results: 16

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

Published in:

PLoS Genetics, 2019, v. 15, n. 11, p. 1, doi. 10.1371/journal.pgen.1008480

By:

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.

Publication type:

Article

Novel Urinary Peptidomic Classifier Predicts Incident Heart Failure.

Published in:

2017

By:

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.;
Zhang, Zhen-Yu;
Nkuipou-Kenfack, Esther;
Yang, Wen-Yi

Publication type:

journal article

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

Published in:

BMC Neurology, 2022, v. 22, n. 1, p. 1, doi. 10.1186/s12883-022-02763-6

By:

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.

Publication type:

Article

Cohort Profile: Generation Scotland: Scottish Family Health Study (GS:SFHS). The study, its participants and their potential for genetic research on health and illness.

Published in:

International Journal of Epidemiology, 2013, v. 42, n. 3, p. 689, doi. 10.1093/ije/dys084

By:

Smith, Blair H;
Campbell, Archie;
Linksted, Pamela;
Fitzpatrick, Bridie;
Jackson, Cathy;
Kerr, Shona M;
Deary, Ian J;
MacIntyre, Donald J;
Campbell, Harry;
McGilchrist, Mark;
Hocking, Lynne J;
Wisely, Lucy;
Ford, Ian;
Lindsay, Robert S;
Morton, Robin;
Palmer, Colin N A;
Dominiczak, Anna F;
Porteous, David J;
Morris, Andrew D

Publication type:

Article

Ott, a Mouse X-Linked Multigene Family Expressed Specifically During Meiosis.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 8, p. 1139, doi. 10.1093/hmg/5.8.1139

By:

Kerr, Shona M.;
Taggart, Mary H.;
Lee, Muriel;
Cooke, Howard J.

Publication type:

Article

An RBM Homologue Maps to the Mouse Y Chromosome and is Expressed in Germ Cells.

Published in:

Human Molecular Genetics, 1996, v. 5, n. 7, p. 869, doi. 10.1093/hmg/5.7.869

By:

Elliott, David J.;
Ma, Kun;
Kerr, Shona M.;
Thakrar, Rekben;
Speed, Robert;
Chandley, Ann C.;
Cooke, Howard

Publication type:

Article

Effect of Five Genetic Variants Associated with Lung Function on the Risk of Chronic Obstructive Lung Disease, and Their Joint Effects on Lung Function.

Published in:

American Journal of Respiratory & Critical Care Medicine, 2011, v. 184, n. 7, p. 786, doi. 10.1164/rccm.201102-0192OC

By:

Artigas, María Soler;
Wain, Louise V.;
Repapi, Emmanouela;
Obeidat, Ma'en;
Sayers, Ian;
Burton, Paul R.;
Johnson, Toby;
Jing Hua Zhao;
Albrecht, Eva;
Dominiczak, Anna F.;
Kerr, Shona M.;
Smith, Blair H.;
Cadby, Gemma;
Hui, Jennie;
Palmer, Lyle J.;
Hingorani, Aroon D.;
Wannamethee, S. Goya;
Whincup, Peter H.;
Ebrahim, Shah;
Smith, George Davey

Publication type:

Article

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

Published in:

Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-47436-6

By:

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.

Publication type:

Article

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

Published in:

2017

By:

Heeney, Catherine;
Kerr, Shona M.

Publication type:

journal article

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

Published in:

Genome Medicine, 2017, v. 9, p. 1, doi. 10.1186/s13073-017-0414-4

By:

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.

Publication type:

Article

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

Published in:

BMC Medical Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2350-14-38

By:

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.

Publication type:

Article

Generation Scotland: Donor DNA Databank; A control DNA resource.

Published in:

BMC Medical Genetics, 2010, v. 11, p. 166, doi. 10.1186/1471-2350-11-166

By:

Kerr, Shona M.;
Liewald, David C. M.;
Campbell, Archie;
Taylor, Kerrie;
Wild, Sarah H.;
Newby, David;
Turner, Marc;
Porteous, David J.

Publication type:

Article

Urinary peptides in heart failure: a link to molecular pathophysiology.

Published in:

European Journal of Heart Failure, 2021, v. 23, n. 11, p. 1875, doi. 10.1002/ejhf.2195

By:

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

Publication type:

Article

Participant engagement and involvement in longitudinal cohort studies: qualitative insights from a selection of pregnancy and birth, twin, and family-based population cohort studies.

Published in:

BMC Medical Research Methodology, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12874-024-02419-8

By:

Budin-Ljøsne, Isabelle;
Fredheim, Nanna A. G.;
Jevne, Charlotte Alison;
Kleven, Bojana Milanovic;
Charles, Marie Aline;
Felix, Janine F.;
Flaig, Robin;
García, María Paz;
Havdahl, Alexandra;
Islam, Shahid;
Kerr, Shona M.;
Meder, Inger Kristine;
Molloy, Lynn;
Morton, Susan M. B.;
Pizzi, Costanza;
Rahman, Aamnah;
Willemsen, Gonneke;
Wood, Diane;
Harris, Jennifer R.

Publication type:

Article

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

Published in:

Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-10016-3

By:

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.

Publication type:

Article

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

Published in:

BMC Medical Genetics, 2014, v. 15, n. 1, p. 1, doi. 10.1186/1471-2350-15-70

By:

Norsworthy, Penny J.;
Vandrovcova, Jana;
Thomas, Ellen R. A.;
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.

Publication type:

Article