受强制性开放获取政策约束的文章 - Pål Rasmus Njølstad了解详情
整体RCNEuropean CommissionNIHMRCWellcomeBMBFNIHRSwedish Research CouncilBHFNHMRCDNRFESRCZonMwInnovation Fund DenmarkARCCIHRFRQSDFFNWOBBSRCCancer Research UKDiabetes UKDoris Duke Charitable FoundationGovernment of SpainUK Research & InnovationDFGAcademy of FinlandRoyal Society UKGatesFNRSINSERMFORTEGovernment of ItalyCarlsberg Foundation DKVAAHANSERCKnut and Alice Wallenberg FoundationKNAWDHFBusiness FinlandJDRFSNSFHHMIGenome CanadaHelmholtzDBTAcademy of Medical Sciences, UKCSOEPSRCANRResearch Grants Council, Hong KongLeducq Foundation, USAHealth Data Research, UKNordforsk
无法在其他位置公开访问的文章:5 篇
The number of tandem repeats in the carboxyl-ester lipase (CEL) gene as a risk factor in alcoholic and idiopathic chronic pancreatitis
A Ragvin, K Fjeld, FU Weiss, J Torsvik, A Aghdassi, J Mayerle, P Simon, ...
Pancreatology 13 (1), 29-32, 2013
强制性开放获取政策: German Research Foundation
CIITA gene variants are associated with rheumatoid arthritis in Scandinavian populations
MC Eike, B Skinningsrud, M Ronninger, A Stormyr, TK Kvien, G Joner, ...
Genes & Immunity 13 (5), 431-436, 2012
强制性开放获取政策: US National Institutes of Health, Forskningsrådet för arbetsliv, hälsa och …
The homeobox factor Irx3 maintains adipogenic identity
JI Bjune, L Lawrence-Archer, GV Røsland, KJ Tronstad, PR Njølstad, ...
Metabolism 103, 154014, 2020
强制性开放获取政策: European Commission, Research Council of Norway
Nuclear import of glucokinase in pancreatic beta-cells is mediated by a nuclear localization signal and modulated by SUMOylation
BB Johansson, K Fjeld, MH Solheim, J Shirakawa, E Zhang, M Keindl, ...
Molecular and Cellular Endocrinology 454, 146-157, 2017
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Characterization of CEL-DUP2: Complete duplication of the carboxyl ester lipase gene is unlikely to influence risk of chronic pancreatitis
K Fjeld, E Masson, JH Lin, P Michl, T Stokowy, A Gravdal, K El Jellas, ...
Pancreatology 20 (3), 377-384, 2020
强制性开放获取政策: German Research Foundation, National Institute of Health and Medical …
可在其他位置公开访问的文章:162 篇
The genetic architecture of type 2 diabetes
C Fuchsberger, J Flannick, TM Teslovich, A Mahajan, V Agarwala, ...
Nature 536 (7614), 41-47, 2016
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Physical activity attenuates the influence of FTO variants on obesity risk: a meta-analysis of 218,166 adults and 19,268 children
TO Kilpeläinen, L Qi, S Brage, SJ Sharp, E Sonestedt, E Demerath, ...
PLoS medicine 8 (11), e1001116, 2011
强制性开放获取政策: US National Institutes of Health, British Heart Foundation, Cancer Research UK
Rare and low-frequency coding variants alter human adult height
E Marouli, M Graff, C Medina-Gomez, KS Lo, AR Wood, TR Kjaer, RS Fine, ...
Nature 542 (7640), 186-190, 2017
强制性开放获取政策: US National Institutes of Health, UK Biotechnology and Biological Sciences …
Loss-of-function mutations in SLC30A8 protect against type 2 diabetes
J Flannick, G Thorleifsson, NL Beer, SBR Jacobs, N Grarup, NP Burtt, ...
Nature genetics 46 (4), 357-363, 2014
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Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
NM Warrington, RN Beaumont, M Horikoshi, FR Day, Ø Helgeland, ...
Nature genetics 51 (5), 804-814, 2019
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Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
V Turcot, Y Lu, HM Highland, C Schurmann, AE Justice, RS Fine, ...
Nature genetics 50 (1), 26-41, 2018
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Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population
K Estrada, I Aukrust, L Bjørkhaug, NP Burtt, JM Mercader, H García-Ortiz, ...
Jama 311 (22), 2305-2314, 2014
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Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects
LJ Howe, MG Nivard, TT Morris, AF Hansen, H Rasheed, Y Cho, ...
Nature genetics 54 (5), 581-592, 2022
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Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes
A Molven, M Ringdal, AM Nordbø, H Ræder, J Støy, GM Lipkind, ...
Diabetes 57 (4), 1131-1135, 2008
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A recombined allele of the lipase gene CEL and its pseudogene CELP confers susceptibility to chronic pancreatitis
K Fjeld, FU Weiss, D Lasher, J Rosendahl, JM Chen, BB Johansson, ...
Nature genetics 47 (5), 518-522, 2015
强制性开放获取政策: National Fund for Scientific Research, Belgium, German Research Foundation …
Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes
AR Majithia, J Flannick, P Shahinian, M Guo, MA Bray, P Fontanillas, ...
Proceedings of the National Academy of Sciences 111 (36), 13127-13132, 2014
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Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study
P Bowman, Å Sulen, F Barbetti, J Beltrand, P Svalastoga, E Codner, ...
The lancet Diabetes & endocrinology 6 (8), 637-646, 2018
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Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics
RN Beaumont, NM Warrington, A Cavadino, J Tyrrell, M Nodzenski, ...
Human molecular genetics 27 (4), 742-756, 2018
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Common and rare forms of diabetes mellitus: towards a continuum of diabetes subtypes
J Flannick, S Johansson, PR Njølstad
Nature Reviews Endocrinology 12 (7), 394-406, 2016
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Assessing the causal relationship of maternal height on birth size and gestational age at birth: a mendelian randomization analysis
G Zhang, J Bacelis, C Lengyel, K Teramo, M Hallman, Ø Helgeland, ...
PLoS medicine 12 (8), e1001865, 2015
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