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Numrering	Referens	Omslagsbild	Hitta
1.	2021 swepub:Mat__t
2.	Ahmad, T, et al. (författare) Global patient outcomes after elective surgery: prospective cohort study in 27 low-, middle- and high-income countries 2016 Ingår i: British journal of anaesthesia. - : Elsevier BV. - 1471-6771 .- 0007-0912. ; 117:5, s. 601- Tidskriftsartikel (refereegranskat)
3.	Ahmad, T, et al. (författare) In-hospital clinical outcomes after upper gastrointestinal surgery: Data from an international observational study 2017 Ingår i: European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology. - : Elsevier BV. - 1532-2157 .- 0748-7983. ; 43:12, s. 2324-2332 Tidskriftsartikel (refereegranskat)
4.	Ahmad, T, et al. (författare) Use of failure-to-rescue to identify international variation in postoperative care in low-, middle- and high-income countries: a 7-day cohort study of elective surgery 2017 Ingår i: British journal of anaesthesia. - : Elsevier BV. - 1471-6771 .- 0007-0912. ; 119:2, s. 258-266 Tidskriftsartikel (refereegranskat)
5.	Sawcer, Stephen, et al. (författare) Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis 2011 Ingår i: Nature. - : Springer Science and Business Media LLC. - 0028-0836 .- 1476-4687. ; 476:7359, s. 214-219 Tidskriftsartikel (refereegranskat)abstract Multiple sclerosis is a common disease of the central nervous system in which the interplay between inflammatory and neurodegenerative processes typically results in intermittent neurological disturbance followed by progressive accumulation of disability. Epidemiological studies have shown that genetic factors are primarily responsible for the substantially increased frequency of the disease seen in the relatives of affected individuals, and systematic attempts to identify linkage in multiplex families have confirmed that variation within the major histocompatibility complex (MHC) exerts the greatest individual effect on risk. Modestly powered genome-wide association studies (GWAS) have enabled more than 20 additional risk loci to be identified and have shown that multiple variants exerting modest individual effects have a key role in disease susceptibility. Most of the genetic architecture underlying susceptibility to the disease remains to be defined and is anticipated to require the analysis of sample sizes that are beyond the numbers currently available to individual research groups. In a collaborative GWAS involving 9,772 cases of European descent collected by 23 research groups working in 15 different countries, we have replicated almost all of the previously suggested associations and identified at least a further 29 novel susceptibility loci. Within the MHC we have refined the identity of the HLA-DRB1 risk alleles and confirmed that variation in the HLA-A gene underlies the independent protective effect attributable to the class I region. Immunologically relevant genes are significantly overrepresented among those mapping close to the identified loci and particularly implicate T-helper-cell differentiation in the pathogenesis of multiple sclerosis.
6.	Aad, G., et al. (författare) Measurement of the W boson polarization in top quark decays with the ATLAS detector 2012 Ingår i: Journal of High Energy Physics. - 1029-8479 .- 1126-6708. ; :6 Tidskriftsartikel (refereegranskat)
7.	Alkner, Sara, et al. (författare) Contralateral breast cancer can represent a metastatic spread of the first primary tumor: determination of clonal relationship between contralateral breast cancers using next-generation whole genome sequencing. 2015 Ingår i: Breast Cancer Research. - : Springer Science and Business Media LLC. - 1465-5411 .- 1465-542X. ; 17:1 Tidskriftsartikel (refereegranskat)abstract By convention, a contralateral breast cancer (CBC) is treated as a new primary tumor, independent of the first cancer (BC1). Although there have been indications that the second tumor (BC2) sometimes may represent a metastatic spread of BC1, this has never been conclusively shown. We sought to apply next-generation sequencing to determine a "genetic barcode" for each tumor and reveal the clonal relationship of CBCs.
8.	Ferrari, Raffaele, et al. (författare) Frontotemporal dementia and its subtypes: a genome-wide association study. 2014 Ingår i: Lancet Neurology. - 1474-4465. ; 13:7, s. 686-699 Tidskriftsartikel (refereegranskat)abstract Frontotemporal dementia (FTD) is a complex disorder characterised by a broad range of clinical manifestations, differential pathological signatures, and genetic variability. Mutations in three genes-MAPT, GRN, and C9orf72-have been associated with FTD. We sought to identify novel genetic risk loci associated with the disorder.
9.	Aad, G., et al. (författare) 2013 Ingår i: The European Physical Journal C. - : Springer Science and Business Media LLC. - 1434-6052. ; 73:3 Tidskriftsartikel (refereegranskat)
10.	Aad, G, et al. (författare) ATLAS Run 1 searches for direct pair production of third-generation squarks at the Large Hadron Collider. 2015 Ingår i: European Physical Journal C. Particles and Fields. - : Springer Science and Business Media LLC. - 1434-6044 .- 1434-6052. ; 75:10 Tidskriftsartikel (refereegranskat)

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Författare/redaktör: Walker, R. (42); Jones, G. (39); Price, D. (39); Spagnolo, S. (39); Young, C. (39); Esposito, B. (38); visa fler...; Li, L. (37); Yao, L. (35); Gao, Y. (31); Williams, M (27); Buchanan, J. (25); Thomas, P. (25); Baker, A. (25); Lee, S (25); Pereira, A (25); Young, R. (25); Sinha, A. (25); Thomas, J. (25); Murphy, S. (25); Liu, Y. (24); Kaufman, M (24); Taylor, D (24); Clark, M. (24); Martin, A. (24); Robinson, S. (24); Day, C. (24); Page, A. (24); Zhang, W. (24); West, A. (24); Smith, P. (24); Morris, J. (24); Williams, J (24); Wood, R (24); Bowden, M. (24); Davis, W. (24); Afzal, M (24); Rodrigues, P (24); Duran, I (24); Kundu, A. (24); Lopez, J. M. (24); Martin, Y. (24); Cox, M (24); Wang, N. (24); Belli, F. (24); Godwin, J (24); Airila, M (24); Albanese, R (24); Ambrosino, G (24); Amosov, V (24); Angelone, M (24); visa färre...

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