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1.	Pedersen, TR, et al. (author) Cholesterol lowering and the use of healthcare resources. Results of the Scandinavian Simvastatin Survival Study 1996 In: Circulation. - 0009-7322. ; 93:10, s. 1796-1802 Journal article (peer-reviewed)
2.	Grip, L, et al. (author) A low molecular weight, selective thrombin inhibitor, inogatran, vs heparin, in unstable coronary artery disease in 1209 patients. A double-blind, randomized, dose-finding study. Thrombin inhibition in Myocardial Ischaemia (TRIM) study group 1997 In: European heart journal. - : Oxford University Press (OUP). - 0195-668X .- 1522-9645. ; 18:9, s. 1416-1425 Journal article (peer-reviewed)
3.	Bancroft, EK, et al. (author) Targeted prostate cancer screening in BRCA1 and BRCA2 mutation carriers: results from the initial screening round of the IMPACT study 2014 In: European urology. - : Elsevier BV. - 1873-7560 .- 0302-2838. ; 66:3, s. 489-499 Journal article (peer-reviewed)
4.	Bancroft, EK, et al. (author) Psychosocial impact of undergoing prostate cancer screening for men with BRCA1 or BRCA2 mutations 2019 In: BJU international. - : Wiley. - 1464-410X .- 1464-4096. ; 123:2, s. 284-292 Journal article (peer-reviewed)
5.	Nicolas, Aude, et al. (author) Genome-wide Analyses Identify KIF5A as a Novel ALS Gene 2018 In: Neuron. - : Cell Press. - 0896-6273 .- 1097-4199. ; 97:6, s. 1268-1283.e6 Journal article (peer-reviewed)abstract To identify novel genes associated with ALS, we undertook two lines of investigation. We carried out a genome-wide association study comparing 20,806 ALS cases and 59,804 controls. Independently, we performed a rare variant burden analysis comparing 1,138 index familial ALS cases and 19,494 controls. Through both approaches, we identified kinesin family member 5A (KIF5A) as a novel gene associated with ALS. Interestingly, mutations predominantly in the N-terminal motor domain of KIF5A are causative for two neurodegenerative diseases: hereditary spastic paraplegia (SPG10) and Charcot-Marie-Tooth type 2 (CMT2). In contrast, ALS-associated mutations are primarily located at the C-terminal cargo-binding tail domain and patients harboring loss-of-function mutations displayed an extended survival relative to typical ALS cases. Taken together, these results broaden the phenotype spectrum resulting from mutations in KIF5A and strengthen the role of cytoskeletal defects in the pathogenesis of ALS.
6.	Gehlen, J., et al. (author) First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B 2022 In: Human Genetics and Genomics Advances. - : Elsevier BV. - 2666-2477. ; 3:2 Journal article (peer-reviewed)abstract Esophageal atresia with or without tracheoesophageal fistula (EA/TEF) is the most common congenital malformation of the upper digestive tract. This study represents the first genome-wide association study (GWAS) to identify risk loci for EA/TEF. We used a European case-control sample comprising 764 EA/TEF patients and 5,778 controls and observed genome-wide significant associations at three loci. On chromosome 10q21 within the gene CTNNA3 (p = 2.11 × 10−8; odds ratio [OR] = 3.94; 95% confidence interval [CI], 3.10–5.00), on chromosome 16q24 next to the FOX gene cluster (p = 2.25 × 10−10; OR = 1.47; 95% CI, 1.38–1.55) and on chromosome 17q12 next to the gene HNF1B (p = 3.35 × 10−16; OR = 1.75; 95% CI, 1.64–1.87). We next carried out an esophageal/tracheal transcriptome profiling in rat embryos at four selected embryonic time points. Based on these data and on already published data, the implicated genes at all three GWAS loci are promising candidates for EA/TEF development. We also analyzed the genetic EA/TEF architecture beyond the single marker level, which revealed an estimated single-nucleotide polymorphism (SNP)-based heritability of around 37% ± 14% standard deviation. In addition, we examined the polygenicity of EA/TEF and found that EA/TEF is less polygenic than other complex genetic diseases. In conclusion, the results of our study contribute to a better understanding on the underlying genetic architecture of ET/TEF with the identification of three risk loci and candidate genes. © 2022 The Authors
7.	Adam, A, et al. (author) Abstracts from Hydrocephalus 2016. 2017 In: Fluids and Barriers of the CNS. - : Springer Science and Business Media LLC. - 2045-8118. ; 14:Suppl 1 Journal article (peer-reviewed)
8.	Gustafson, Stefan, et al. (author) Studies on receptors for hyaluronan and the turnover of radioactively-labelled hyaluronan in mice and rats 1995 In: Second international workshop on hyaluronan in drug delivery. - 1853152536 - 9781853152535 ; , s. 5-7 Conference paper (other academic/artistic)
9.	Eiermann, B, et al. (author) Knowledge databases for clinical decision support in drug prescribing-development, quality assurance, management, integration, implementation and evaluation of clinical value 2010 In: Clinical Decision Support. - Vienna. Book chapter (other academic/artistic)
10.	Gräsner, J. -T, et al. (author) Epidemiology of cardiac arrest in Europe : European Resuscitation Council Guidelines 2021 2021 In: Notfall & Rettungsmedizin. - : Springer Medizin. - 1434-6222 .- 1436-0578. ; 24:4, s. 346-366 Journal article (peer-reviewed)abstract In this section of the European Resuscitation Council Guidelines 2021, key information on the epidemiology and outcome of in- and out-of-hospital cardiac arrest are presented. Key contributions from the European Registry of Cardiac Arrest (EuReCa) collaboration are highlighted. Recommendations are presented to enable health systems to develop registries as a platform for quality improvement and to provide support for health system planning and responses to cardiac arrest.

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Type of publication: journal article (125); conference paper (20); reports (10); research review (5); book chapter (3); review (1); show more...; show less...

Type of content: peer-reviewed (130); other academic/artistic (34)

Author/Editor: Lilja, A (28); Lilja, B (26); Lilja, Hans (16); Lilja, G (16); Langstrom, B (15); Lilja, Gisela (15); show more...; Lilja, H. (13); Cronberg, Tobias (10); Andersson, J (9); Friberg, Hans (9); Lilja, Mikael (7); Meister, B (6); Valind, S (6); Lilja, L (6); Bark, C (6); Berggren, PO (5); Hartvig, P (5); Kirk, J. (4); Cook, J. (4); Friedman, E. (4); Herlitz, Johan, 1949 (4); Pettersson, K (4); Nilsson, C (4); Andersson, JLR (4); Teo, SH (4); Lubinski, J (4); Wickman, M (4); Liljegren, A (4); Persson, L (4); Evans, DG (4); Falconer, A (4); Gronberg, H (4); Kote-Jarai, Z (4); Cybulski, C (4); Eeles, RA (4); Nicolai, N (4); Nielsen, Niklas (4); Strom, S (4); Gordh, T (4); Johannsson, O (4); Rennert, G. (4); Domchek, S. (4); Walker, L. (4); Brewer, C (4); Donaldson, A (4); Buys, S (4); Flodmark, O. (4); Bancroft, EK (4); Page, EC (4); Maehle, L (4); show less...

University: Lund University (58); Karolinska Institutet (56); Uppsala University (39); Umeå University (10); VTI - The Swedish National Road and Transport Research Institute (9); University of Gothenburg (8); show more...; Linnaeus University (6); Linköping University (5); University of Borås (5); University of Gävle (3); Örebro University (3); Luleå University of Technology (1); Stockholm University (1); Mälardalen University (1); Jönköping University (1); Mid Sweden University (1); Chalmers University of Technology (1); Högskolan Dalarna (1); Marie Cederschiöld högskola (1); show less...

Language: English (152); Swedish (10); German (2)

Research subject (UKÄ/SCB): Medical and Health Sciences (77); Natural sciences (6); Engineering and Technology (2); Social Sciences (1); Humanities (1)

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