| DNA base repair–recognition and initiation of catalysis B Dalhus, JK Laerdahl, PH Backe, M Bjørås FEMS microbiology reviews 33 (6), 1044-1078, 2009 | 179 | 2009 |
| PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasia A Stray-Pedersen, PH Backe, HS Sorte, L Mørkrid, NY Chokshi, ... The American Journal of Human Genetics 95 (1), 96-107, 2014 | 161 | 2014 |
| X-ray crystallographic and NMR studies of the third KH domain of hnRNP K in complex with single-stranded nucleic acids PH Backe, AC Messias, RBG Ravelli, M Sattler, S Cusack Structure 13 (7), 1055-1067, 2005 | 139 | 2005 |
| Hallmarks of processivity in glycoside hydrolases from crystallographic and computational studies of the Serratia marcescens chitinases CM Payne, J Baban, SJ Horn, PH Backe, AS Arvai, B Dalhus, M Bjørås, ... Journal of Biological Chemistry 287 (43), 36322-36330, 2012 | 106 | 2012 |
| Structures of endonuclease V with DNA reveal initiation of deaminated adenine repair B Dalhus, AS Arvai, I Rosnes, ØE Olsen, PH Backe, I Alseth, H Gao, ... Nature structural & molecular biology 16 (2), 138-143, 2009 | 99 | 2009 |
| Separation-of-function mutants unravel the dual-reaction mode of human 8-oxoguanine DNA glycosylase B Dalhus, M Forsbring, IH Helle, ES Vik, RJ Forstrøm, PH Backe, I Alseth, ... Structure 19 (1), 117-127, 2011 | 96 | 2011 |
| Human OXR1 maintains mitochondrial DNA integrity and counteracts hydrogen peroxide-induced oxidative stress by regulating antioxidant pathways involving p21 M Yang, L Luna, JG Sørbø, I Alseth, RF Johansen, PH Backe, NC Danbolt, ... Free Radical Biology and Medicine 77, 41-48, 2014 | 81 | 2014 |
| A potential founder variant in CARMIL2/RLTPR in three Norwegian families with warts, molluscum contagiosum, and T‐cell dysfunction HS Sorte, LT Osnes, B Fevang, P Aukrust, HC Erichsen, PH Backe, ... Molecular Genetics & Genomic Medicine 4 (6), 604-616, 2016 | 68 | 2016 |
| Biallelic variants in KIF14 cause intellectual disability with microcephaly P Makrythanasis, R Maroofian, A Stray-Pedersen, D Musaev, MS Zaki, ... European journal of human genetics 26 (3), 330-339, 2018 | 67 | 2018 |
| Novel UCHL1 mutations reveal new insights into ubiquitin processing SL Rydning, PH Backe, MML Sousa, Z Iqbal, AM Øye, Y Sheng, M Yang, ... Human molecular genetics 26 (6), 1031-1040, 2017 | 45 | 2017 |
| Structural insight into repair of alkylated DNA by a new superfamily of DNA glycosylases comprising HEAT-like repeats B Dalhus, IH Helle, PH Backe, I Alseth, T Rognes, M Bjørås, JK Laerdahl Nucleic acids research 35 (7), 2451-2459, 2007 | 36 | 2007 |
| Impaired oxidative stress response characterizes HUWE1-promoted X-linked intellectual disability M Bosshard, R Aprigliano, C Gattiker, V Palibrk, E Markkanen, PH Backe, ... Scientific reports 7 (1), 15050, 2017 | 32 | 2017 |
| In situ cofactor regeneration enables selective CO2 reduction in a stable and efficient enzymatic photoelectrochemical cell K Xu, A Chatzitakis, PH Backe, Q Ruan, J Tang, F Rise, M Bjørås, T Norby Applied Catalysis B: Environmental 296, 120349, 2021 | 29 | 2021 |
| Susceptibility to infections, without concomitant hyper-IgE, reported in 1976, is caused by hypomorphic mutation in the phosphoglucomutase 3 (PGM3) gene KE Lundin, A Hamasy, PH Backe, LN Moens, E Falk-Sörqvist, ... Clinical Immunology 161 (2), 366-372, 2015 | 29 | 2015 |
| Hereditary tyrosinaemia type I in Norway: incidence and three novel small deletions in the fumarylacetoacetase gene YT Bliksrud, E Brodtkorb, PH Backe, B Woldseth, H Rootwelt Scandinavian journal of clinical and laboratory investigation 72 (5), 369-373, 2012 | 27 | 2012 |
| Generalized epilepsy in a family with basal ganglia calcifications and mutations in SLC20A2 and CHRNB2 R Fjaer, E Brodtkorb, AM Øye, Y Sheng, MD Vigeland, KA Kvistad, ... European Journal of Medical Genetics 58 (11), 624-628, 2015 | 26 | 2015 |
| Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis SL Rydning, J Koht, Y Sheng, P Sowa, HS Hjorthaug, IM Wedding, ... Brain 142 (4), e12-e12, 2019 | 25 | 2019 |
| A novel somatic mutation in GNB2 provides new insights to the pathogenesis of Sturge–Weber syndrome R Fjær, K Marciniak, O Sundnes, H Hjorthaug, Y Sheng, C Hammarström, ... Human molecular genetics 30 (21), 1919-1931, 2021 | 23 | 2021 |
| Novel deletion mutation identified in a patient with late-onset combined methylmalonic acidemia and homocystinuria, cblC Type PH Backe, M Ytre-Arne, ÅK Røhr, E Brodtkorb, B Fowler, H Rootwelt, ... JIMD Reports-Volume 11, 79-85, 2013 | 22 | 2013 |
| Four novel mutations identified in Norwegian patients result in intermittent maple syrup urine disease when combined with the R301C mutation E Brodtkorb, J Strand, PH Backe, AM Lund, M Bjørås, T Rootwelt, ... Molecular genetics and metabolism 100 (4), 324-332, 2010 | 19 | 2010 |
Magnar BjøråsProfessor in molecular medicine在 ntnu.no 的电子邮件经过验证
