Zobrazeno 1 - 10
of 1 332
pro vyhledávání: '"Hocking LJ"'
Autor:
Hocking, LJ
No description available
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80393df14e0992877da8f90bab8ef334
Autor:
Hocking, LJ
While systems development projects have become associated with increasingly sophisticated technologies and organisational changes, the models underlying the process have not kept pace. The Legislation Systems Project (LSP) is an example of a recent p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a329222e7098dd3c60b37b1f9621cec
Autor:
Hocking LJ; Institute of Medical Sciences, University of Aberdeen, Aberdeen, Scotland, UK., Andrews C; East of Scotland Regional Genetics Service, NHS Tayside, Ninewells Hospital, Dundee, Scotland, UK., Armstrong C; North of Scotland Medical Genetic Service, NHS Grampian, Polwarth Building, Foresterhill, Aberdeen, Scotland, UK., Ansari M; South East Scotland Genetic Service, NHS Lothian, Western General Hospital, Edinburgh, Scotland, UK., Baty D; East of Scotland Regional Genetics Service, NHS Tayside, Ninewells Hospital, Dundee, Scotland, UK., Berg J; East of Scotland Regional Genetics Service, NHS Tayside, Ninewells Hospital, Dundee, Scotland, UK.; School of Medicine, University of Dundee, Dundee, Scotland, UK., Bradley T; West of Scotland Centre for Genomic Medicine, NHS Greater Glasgow & Clyde, Queen Elizabeth University Hospital, Glasgow, Scotland, UK., Clark C; North of Scotland Medical Genetic Service, NHS Grampian, Polwarth Building, Foresterhill, Aberdeen, Scotland, UK., Diamond A; South East Scotland Genetic Service, NHS Lothian, Western General Hospital, Edinburgh, Scotland, UK., Doherty J; West of Scotland Centre for Genomic Medicine, NHS Greater Glasgow & Clyde, Queen Elizabeth University Hospital, Glasgow, Scotland, UK., Lampe A; South East Scotland Genetic Service, NHS Lothian, Western General Hospital, Edinburgh, Scotland, UK., McGowan R; West of Scotland Centre for Genomic Medicine, NHS Greater Glasgow & Clyde, Queen Elizabeth University Hospital, Glasgow, Scotland, UK.; School of Medicine, Dentistry & Nursing, University of Glasgow, Glasgow, Scotland, UK., Moore DJ; South East Scotland Genetic Service, NHS Lothian, Western General Hospital, Edinburgh, Scotland, UK., O'Sullivan D; North of Scotland Medical Genetic Service, NHS Grampian, Polwarth Building, Foresterhill, Aberdeen, Scotland, UK., Purvis A; West of Scotland Centre for Genomic Medicine, NHS Greater Glasgow & Clyde, Queen Elizabeth University Hospital, Glasgow, Scotland, UK., Santoyo-Lopez J; Edinburgh Genomics, University of Edinburgh, Edinburgh, Scotland, UK., Westwood P; West of Scotland Centre for Genomic Medicine, NHS Greater Glasgow & Clyde, Queen Elizabeth University Hospital, Glasgow, Scotland, UK., Abbott M; Health Economics Research Unit, University of Aberdeen, Aberdeen, Scotland, UK., Williams N; West of Scotland Centre for Genomic Medicine, NHS Greater Glasgow & Clyde, Queen Elizabeth University Hospital, Glasgow, Scotland, UK., Aitman TJ; Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, Scotland, UK. tim.aitman@ed.ac.uk., Miedzybrodzka Z; Institute of Medical Sciences, University of Aberdeen, Aberdeen, Scotland, UK. zosia@abdn.ac.uk.; North of Scotland Medical Genetic Service, NHS Grampian, Polwarth Building, Foresterhill, Aberdeen, Scotland, UK. zosia@abdn.ac.uk.; North of Scotland Regional Genetic Service, NHS Grampian, Ashgrove House, Foresterhill, Aberdeen, Scotland, UK. zosia@abdn.ac.uk.
Publikováno v:
European journal of human genetics : EJHG [Eur J Hum Genet] 2023 Feb; Vol. 31 (2), pp. 231-238. Date of Electronic Publication: 2022 Dec 06.
Autor:
McAllister, K, Yarwood, A, Bowes, J, Orozco, G, Viatte, S, Diogo, D, Hocking, LJ, Steer, S, Wordsworth, P, Wilson, AG, Morgan, AW, Kremer, JM, Pappas, D, Gregersen, P, Klareskog, L, Plenge, R, Barton, A, Greenberg, J, Worthington, J, Eyre, S
OBJECTIVE: A recent high-density fine-mapping (ImmunoChip) study of genetic associations in rheumatoid arthritis (RA) identified 14 risk loci with validated genome-wide significance, as well as a number of loci showing associations suggestive of sign
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::92e4565181d9cccf217bb3bc5bcc4af9
https://doi.org/10.1002/art.38183
https://doi.org/10.1002/art.38183
Autor:
McClure, A, Lunt, M, Eyre, S, Ke, X, Thomson, W, Hinks, A, Bowes, J, Gibbons, L, Plant, D, Wilson, AG, Marinou, I, Morgan, AW, Emery, P, Steer, S, Hocking, LJ, Reid, DM, Wordsworth, P, Harrison, P, Worthington, J, Barton, A, Consortium, BIRAC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::81158b29dec2ac82fe6d6e6908ad690e
https://ora.ox.ac.uk/objects/uuid:0c185526-255b-4408-9204-a551088744bd
https://ora.ox.ac.uk/objects/uuid:0c185526-255b-4408-9204-a551088744bd
Autor:
Ibrahim-Verbaas, CA, Bressler, J, Debette, S, Schuur, M, Smith, AV, Bis, JC, Davies, G, Trompet, S, Smith, JA, Wolf, C, Chibnik, LB, Liu, Y, Vitart, V, Kirin, M, Petrovic, K, Polasek, O, Zgaga, L, Fawns-Ritchie, C, Hoffmann, P, Karjalainen, J, Lahti, J, Llewellyn, DJ, Schmidt, CO, Mather, KA, Chouraki, V, Sun, Q, Resnick, SM, Rose, LM, Oldmeadow, C, Stewart, M, Smith, BH, Gudnason, V, Yang, Q, Mirza, SS, Jukema, JW, deJager, PL, Harris, TB, Liewald, DC, Amin, N, Coker, LH, Stegle, O, Lopez, OL, Schmidt, R, Teumer, A, Ford, I, Karbalai, N, Becker, JT, Jonsdottir, MK, Au, R, Fehrmann, Rsn, Herms, S, Nalls, M, Zhao, W, Turner, ST, Yaffe, K, Lohman, K, van Swieten, JC, Kardia, Slr, Knopman, DS, Meeks, WM, Heiss, G, Holliday, EG, Schofield, PW, Tanaka, T, Stott, DJ, Wang, J, Ridker, P, Gow, AJ, Pattie, A, Starr, JM, Hocking, LJ, Armstrong, NJ, McLachlan, S, Shulman, JM, Pilling, LC, Eiriksdottir, G, Scott, RJ, Kochan, NA, Palotie, A, Hsieh, Y-C, Eriksson, JG, Penman, A, Gottesman, RF, Oostra, BA, Yu, L, DeStefano, AL, Beiser, A, Garcia, M, Rotter, JI, Nöthen, MM, Hofman, A, Slagboom, PE, Westendorp, Rgj, Buckley, BM, Wolf, PA, Uitterlinden, AG, Psaty, BM, Grabe, HJ, Bandinelli, S, Chasman, DI
Publikováno v:
Molecular psychiatry, vol 21, iss 2
To identify common variants contributing to normal variation in two specific domains of cognitive functioning, we conducted a genome-wide association study (GWAS) of executive functioning and information processing speed in non-demented older adults
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::52c0df7312cccfcd4035cf69242b2802
https://escholarship.org/uc/item/7d8152n1
https://escholarship.org/uc/item/7d8152n1
Autor:
Reppe, S, Wang, Y, Thompson, WK, McEvoy, LK, Schork, AJ, Zuber, V, LeBlanc, M, Bettella, F, Mills, IG, Desikan, RS, Djurovic, S, Gautvik, KM, Dale, AM, Andreassen, OA, Estrada, K, Styrkarsdottir, U, Evangelou, E, Hsu, YH, Duncan, EL, Ntzani, EE, Oei, L, Albagha, OME, Amin, N, Kemp, JP, Koller, DL, Li, G, Liu, CT, Minster, RL, Moayyeri, A, Vandenput, L, Willner, D, Xiao, SM, Yerges-Armstrong, LM, Zheng, HF, Alonso, N, Eriksson, J, Kammerer, CM, Kaptoge, SK, Leo, PJ, Thorleifsson, G, Wilson, SG, Wilson, JF, Aalto, V, Alen, M, Aragaki, AK, Aspelund, T, Center, JR, Dailiana, Z, Duggan, DJ, Garcia, M, Garcia-Giralt, N, Giroux, S, Hallmans, G, Hocking, LJ, Husted, LB, Jameson, KA, Khusainova, R, Kim, GS, Kooperberg, C, Koromila, T, Kruk, M, Laaksonen, M, Lacroix, AZ
Publikováno v:
Reppe, S; Wang, Y; Thompson, WK; McEvoy, LK; Schork, AJ; Zuber, V; et al.(2015). Genetic sharing with cardiovascular disease risk factors and diabetes reveals novel bone mineral density loci. PLoS ONE, 10(12). doi: 10.1371/journal.pone.0144531. UC San Diego: Retrieved from: http://www.escholarship.org/uc/item/1dx1t1xx
© 2015 Reppe et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are cre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6e8a1a438fe15a4ec3d353f19b5c2042
http://hdl.handle.net/10044/1/32666
http://hdl.handle.net/10044/1/32666
Publikováno v:
Chinese Journal of Tissue Engineering Research / Zhongguo Zuzhi Gongcheng Yanjiu. 10/8/2024, Vol. 28 Issue 28, p4572-4577. 6p.
Autor:
Pratiwi, Rita Dwi1 ritadwipratiwi@wdh.ac.id, Andriati, Riris1, Ayuningtyas, Gita1, Aulia, Gina2, Arimurti, Ikada Septi3, Puspita, Ratumas Ratih1, Poddar, Sandeep4
Publikováno v:
Malaysian Journal of Medicine & Health Sciences. 2024 Supplement, Vol. 20, p145-150. 6p.
Autor:
Van Leeuwen, EM, Karssen, LC, Deelen, J, Isaacs, A, Medina-Gomez, C, Mbarek, H, Kanterakis, A, Trompet, S, Postmus, I, Verweij, N, Van Enckevort, DJ, Huffman, JE, White, CC, Feitosa, MF, Bartz, TM, Manichaikul, A, Joshi, PK, Peloso, GM, Deelen, P, Van Dijk, F, Willemsen, G, De Geus, EJ, Milaneschi, Y, Penninx, BWJH, Francioli, LC, Menelaou, A, Pulit, SL, Rivadeneira, F, Hofman, A, Oostra, BA, Franco, OH, Leach, IM, Beekman, M, De Craen, AJM, Uh, HW, Trochet, H, Hocking, LJ, Porteous, DJ, Sattar, N, Packard, CJ, Buckley, BM, Brody, JA, Bis, JC, Rotter, JI, Mychaleckyj, JC, Campbell, H, Duan, Q, Lange, LA, Wilson, JF, Hayward, C, Polasek, O, Vitart, V, Rudan, I, Wright, AF, Rich, SS, Psaty, BM, Borecki, IB, Kearney, PM, Stott, DJ, Cupples, LA, Jukema, JW, Van Der Harst, P, Sijbrands, EJ, Hottenga, JJ, Uitterlinden, AG, Swertz, MA, Van Ommen, GJB, De Bakker, PIW, Eline Slagboom, P, Boomsma, DI, Wijmenga, C, Van Duijn, CM, Neerincx, PBT, Elbers, CC, Palamara, PF, Peer, I, Abdellaoui, A, Kloosterman, WP, Van Oven, M, Vermaat, M, Li, M, Laros, JFJ, Stoneking, M, De Knijff, P, Kayser, M, Veldink, JH, Van Den Berg, LH, Byelas, H, Den Dunnen, JT, Dijkstra, M, Amin, N, Van Der Velde, KJ, Van Setten, J
Publikováno v:
Van Leeuwen, EM; Karssen, LC; Deelen, J; Isaacs, A; Medina-Gomez, C; Mbarek, H; et al.(2015). Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels. Nature Communications, 6. doi: 10.1038/ncomms7065. UCLA: Retrieved from: http://www.escholarship.org/uc/item/0pf7030w
© 2015 Macmillan Publishers Limited. All rights reserved. Variants associated with blood lipid levels may be population-specific. To identify low-frequency variants associated with this phenotype, population-specific reference panels may be used. He
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______325::40fe9f479300706910e75022cbf7bdca
http://www.escholarship.org/uc/item/0pf7030w
http://www.escholarship.org/uc/item/0pf7030w