Per Bakke - Related publications

1988-1992 Department of clinical medicine K2 University of Bergen, Bergen, Hordaland, Norway 
NOTE: We are testing a new system for identifying relevant work based on semantic analysis that identifies similarities between recently published papers and the current author's publications. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches.
50 most relevant papers in past 60 days:
Year Citation  Score
2021 Sikdar S, Wyss AB, Lee MK, Hoang TT, Richards M, Beane Freeman LE, Parks C, Thorne PS, Hankinson JL, Umbach DM, Motsinger-Reif A, London SJ. Interaction between Genetic Risk Scores for reduced pulmonary function and smoking, asthma and endotoxin. Thorax. PMID 33963087 DOI: 10.1136/thoraxjnl-2020-215624   
2021 Aguado-Barrera ME, Martínez-Calvo L, Fernández-Tajes J, Calvo-Crespo P, Taboada-Valladares B, Lobato-Busto R, Gómez-Caamaño A, Vega A. Validation of Polymorphisms Associated with the Risk of Radiation-Induced Oesophagitis in an Independent Cohort of Non-Small-Cell Lung Cancer Patients. Cancers. 13. PMID 33810047 DOI: 10.3390/cancers13061447   
2021 Moll M, Jackson VE, Yu B, Grove ML, London SJ, Gharib SA, Bartz TM, Sitlani CM, Dupuis J, O'Connor GT, Xu H, Cassano PA, Patchen BK, Kim WJ, Park J, et al. A Systematic Analysis of Protein-altering Exonic Variants in Chronic Obstructive Pulmonary Disease. American Journal of Physiology. Lung Cellular and Molecular Physiology. PMID 33909500 DOI: 10.1152/ajplung.00009.2021   
2021 Nogee LM, Ryan RM. Genetic Testing for Neonatal Respiratory Disease. Children (Basel, Switzerland). 8. PMID 33799761 DOI: 10.3390/children8030216   
2021 Nogee LM, Ryan RM. Genetic Testing for Neonatal Respiratory Disease. Children (Basel, Switzerland). 8. PMID 33799761 DOI: 10.3390/children8030216   
2021 Gao Z, Dosman JA, Rennie DC, Schwartz DA, Yang IV, Beach J, Senthilselvan A. Effects of tumor necrosis factor (TNF) gene polymorphisms on the association between smoking and lung function among workers in swine operations. Journal of Toxicology and Environmental Health. Part A. 1-17. PMID 33715603 DOI: 10.1080/15287394.2021.1896404   
2021 Hausmann LD, de Almeida BS, de Souza IR, Drehmer MN, Fernandes BL, Wilkens RS, Vieira DSC, Lofgren SE, Lindenau JD, de Toledo E Silva G, Muniz YCN. Association of TNFRSF1A and IFNLR1 Gene Polymorphisms with the Risk of Developing Breast Cancer and Clinical Pathologic Features. Biochemical Genetics. PMID 33751344 DOI: 10.1007/s10528-021-10060-z   
2021 Chen L, Abel HJ, Das I, Larson DE, Ganel L, Kanchi KL, Regier AA, Young EP, Kang CJ, Scott AJ, Chiang C, Wang X, Lu S, Christ R, Service SK, et al. Association of structural variation with cardiometabolic traits in Finns. American Journal of Human Genetics. 108: 583-596. PMID 33798444 DOI: 10.1016/j.ajhg.2021.03.008   
2021 Zhu Z, Li J, Si J, Ma B, Shi H, Lv J, Cao W, Guo Y, Millwood IY, Walters RG, Lin K, Yang L, Chen Y, Du H, Yu B, et al. A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic etiology with obesity. The European Respiratory Journal. PMID 33766948 DOI: 10.1183/13993003.00199-2021   
2021 Cai R, Dong Y, Fang M, Fan Y, Cheng Z, Zhou Y, Gao J, Han F, Guo C, Ma X. Genome-Wide Association Identifies Risk Pathways for SAPHO Syndrome. Frontiers in Cell and Developmental Biology. 9: 643644. PMID 33816493 DOI: 10.3389/fcell.2021.643644   
2021 Malato J, Sotzny F, Bauer S, Freitag H, Fonseca A, Grabowska AD, Graça L, Cordeiro C, Nacul L, Lacerda EM, Castro-Marrero J, Scheibenbogen C, Westermeier F, Sepúlveda N. The SARS-CoV-2 receptor angiotensin-converting enzyme 2 (ACE2) in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: analysis of high-throughput genetic, epigenetic, and gene expression studies. Medrxiv : the Preprint Server For Health Sciences. PMID 33791744 DOI: 10.1101/2021.03.23.21254175   
2021 Deng F, Zhu P, Liao C, Li S, Hu X, Wang Y, Wu Z, Huang S, Zhong W, Zhao B, Ma G, Li Y. Genetic Variants of Contribute to Susceptibility of Ischemic Stroke among Southern Chinese Population. Biomed Research International. 2021: 6634253. PMID 33937403 DOI: 10.1155/2021/6634253   
2021 Arai H, Cao S, Battaglin F, Wang J, Kawanishi N, Tokunaga R, Loupakis F, Stintzing S, Soni S, Zhang W, Mancao C, Salhia B, Mumenthaler SM, Cremolini C, Heinemann V, et al. RNA-binding protein polymorphisms as novel biomarkers to predict outcomes of metastatic colorectal cancer: A meta-analysis from TRIBE, FIRE-3 and MAVERICC. Molecular Cancer Therapeutics. PMID 33785650 DOI: 10.1158/1535-7163.MCT-20-0649   
2021 Dhindsa RS, Mattsson J, Nag A, Wang Q, Wain LV, Allen R, Wigmore EM, Ibanez K, Vitsios D, Deevi SVV, Wasilewski S, Karlsson M, Lassi G, Olsson H, Muthas D, ... , et al. Identification of a missense variant in SPDL1 associated with idiopathic pulmonary fibrosis. Communications Biology. 4: 392. PMID 33758299 DOI: 10.1038/s42003-021-01910-y   
2021 Prizment AE, McSweeney S, Pankratz N, Joshu CE, Hwang JH, Platz EA, Ryan CJ. Prostate Cancer Mortality Associated with Aggregate Polymorphisms in Androgen-Regulating Genes: The Atherosclerosis Risk in the Communities (ARIC) Study. Cancers. 13. PMID 33921650 DOI: 10.3390/cancers13081958   
2021 Benway CJ, Liu J, Guo F, Du F, Randell SH, Cho MH, Silverman EK, Zhou X, . Chromatin Landscapes of Human Lung Cells Predict Potentially Functional COPD GWAS Variants. American Journal of Respiratory Cell and Molecular Biology. PMID 33788674 DOI: 10.1165/rcmb.2020-0475OC   
2021 Yidan S, Zizhao T, Wei Z, Mo L, Cong H, Lin H, Shengying Q. Genome-wide association study on liver function tests in Chinese. Yi Chuan = Hereditas. 43: 249-260. PMID 33724209 DOI: 10.16288/j.yczz.20-435   
2021 Zihlif M, Imraish A, Al-Rawashdeh B, Qteish A, Husami R, Husami R, Tahboub F, Jarrar Y, Lee SJ. The Association of IgE Levels with Genetic Polymorphisms among Asthmatic Patients. Journal of Personalized Medicine. 11. PMID 33922216 DOI: 10.3390/jpm11050329   
2021 Monasky MM, Micaglio E, Ciconte G, Rivolta I, Borrelli V, Ghiroldi A, D'Imperio S, Binda A, Melgari D, Benedetti S, Mitrovic P, Anastasia L, Mecarocci V, Ćalović Ž, Casari G, et al. Novel p.Val1667Asp Missense Variant Segregation and Characterization in a Family with Severe Brugada Syndrome and Multiple Sudden Deaths. International Journal of Molecular Sciences. 22. PMID 33946750 DOI: 10.3390/ijms22094700   
2021 Dugué PA, Yu C, McKay T, Wong EM, Joo JE, Tsimiklis H, Hammet F, Mahmoodi M, Theys D, kConFab, Hopper JL, Giles GG, Milne RL, Steen JA, Dowty JG, et al. : Genetic Variation, Heritable Methylation and Disease Association. International Journal of Molecular Sciences. 22. PMID 33802562 DOI: 10.3390/ijms22052535   
2021 Read RW, Schlauch KA, Lombardi VC, Cirulli ET, Washington NL, Lu JT, Grzymski JJ. Genome-Wide Identification of Rare and Common Variants Driving Triglyceride Levels in a Nevada Population. Frontiers in Genetics. 12: 639418. PMID 33763119 DOI: 10.3389/fgene.2021.639418   
2021 Kosnik MB, Enroth S, Karlsson O. Distinct genetic regions are associated with differential population susceptibility to chemical exposures. Environment International. 152: 106488. PMID 33714141 DOI: 10.1016/j.envint.2021.106488   
2021 Andolfo I, Russo R, Lasorsa VA, Cantalupo S, Rosato BE, Bonfiglio F, Frisso G, Abete P, Cassese GM, Servillo G, Esposito G, Gentile I, Piscopo C, Villani R, Fiorentino G, et al. Common variants at 21q22.3 locus influence and gene expression and susceptibility to severe COVID-19. Iscience. 24: 102322. PMID 33748697 DOI: 10.1016/j.isci.2021.102322   
2021 Liu J, Deng Y, Yu B, Mo B, Luo L, Yang J, Zhang X, Wang Z, Wang Y, Zhu J, Yang H, Fang S, Cheng Z, Li J, Shu Y, et al. Targeted resequencing showing novel common and rare genetic variants increases the risk of asthma in the Chinese Han population. Journal of Clinical Laboratory Analysis. e23813. PMID 33969541 DOI: 10.1002/jcla.23813   
2021 Rasool S, Dar R, Khan MS, Ayoub SG, Rashid S, Rehman MU, Jan T, Qureshi MA, Andrabi KI. MYP2 locus genes: Sequence variations, genetic association studies and haplotypic association in patients with High Myopia. International Journal of Biochemistry and Molecular Biology. 12: 35-48. PMID 33824778   
2021 Andlauer TFM, Mühleisen TW, Hoffstaedter F, Teumer A, Wittfeld K, Teuber A, Reinbold CS, Grotegerd D, Bülow R, Caspers S, Dannlowski U, Herms S, Hoffmann P, Kircher T, Minnerup H, et al. Genetic factors influencing a neurobiological substrate for psychiatric disorders. Translational Psychiatry. 11: 192. PMID 33782385 DOI: 10.1038/s41398-021-01317-7   
2021 Wegermann K, Garrett ME, Zheng J, Coviello A, Moylan CA, Abdelmalek MF, Chow SC, Guy CD, Diehl AM, Ashley-Koch A, Suzuki A. Sex and Menopause Modify the Effect of Single Nucleotide Polymorphism Genotypes on Fibrosis in NAFLD. Hepatology Communications. 5: 598-607. PMID 33860118 DOI: 10.1002/hep4.1668   
2021 Castro I, Sampaio-Marques B, C Areias A, Sousa H, Fernandes Â, Sanchez-Maldonado JM, Cunha C, Carvalho A, Sainz J, Ludovico P. Functional Genetic Variants in Are Associated with Acute Myeloid Leukemia. Cancers. 13. PMID 33809750 DOI: 10.3390/cancers13061344   
2021 Suri P, Stanaway IB, Zhang Y, Freidin MB, Tsepilov YA, Carrell DS, Williams FMK, Aulchenko YS, Hakonarson H, Namjou B, Crosslin DR, Jarvik GP, Lee MT. Genome-wide association studies of low back pain and lumbar spinal disorders using electronic health record data identify a locus associated with lumbar spinal stenosis. Pain. PMID 33729212 DOI: 10.1097/j.pain.0000000000002221   
2021 Wang Q, Jin B, Liu F, Li Z, Tan Y, Liang W, Huang F. DNA-based eyelid trait prediction in Chinese Han population. International Journal of Legal Medicine. PMID 33969445 DOI: 10.1007/s00414-021-02570-7   
2021 Ming J, Wei X, Han M, Adi D, Abuzhalihan J, Wang YT, Yang YN, Li XM, Xie X, Fu ZY, Gai MT, Ma YT. Genetic variation of RNF145 gene and blood lipid levels in Xinjiang population, China. Scientific Reports. 11: 5969. PMID 33727652 DOI: 10.1038/s41598-021-85503-z   
2021 Zhang YM, Liu XZ, Zhou XJ, Liu LJ, Shi SF, Hou P, Lv JC, Zhang H. A Functional Variant rs3093023 in Is Associated With IgA Nephropathy by Regulating Th17 Cells in a North Han Chinese Population. Frontiers in Immunology. 12: 600598. PMID 33717080 DOI: 10.3389/fimmu.2021.600598   
2021 Reay WR, El Shair SI, Geaghan MP, Riveros C, Holliday EG, McEvoy MA, Hancock S, Peel R, Scott RJ, Attia JR, Cairns MJ. Genetic association and causal inference converge on hyperglycaemia as a modifiable factor to improve lung function. Elife. 10. PMID 33720009 DOI: 10.7554/eLife.63115   
2021 Imraish A, Abu-Thiab T, Zihlif M. IL-13 and FOXO3 genes polymorphisms regulate IgE levels in asthmatic patients. Biomedical Reports. 14: 55. PMID 33884198 DOI: 10.3892/br.2021.1431   
2021 Hishida A, Nakatochi M, Tamura T, Nagayoshi M, Okada R, Kubo Y, Tsukamoto M, Kadomatsu Y, Suzuki S, Nishiyama T, Kuriyama N, Watanabe I, Takezaki T, Nishimoto D, Kuriki K, ... , et al. Genome-wide association study of serum prostate-specific antigen levels based on 1000 Genomes imputed data in Japanese: the Japan Multi-Institutional Collaborative Cohort Study. Nagoya Journal of Medical Science. 83: 183-194. PMID 33727749 DOI: 10.18999/nagjms.83.1.183   
2021 Jiang Z, Zhao L, Zhang X, Zhang W, Feng Y, Li T. Common variants in KCNK5 and FHL5 genes contributed to the susceptibility of migraine without aura in Han Chinese population. Scientific Reports. 11: 6807. PMID 33762637 DOI: 10.1038/s41598-021-86374-0   
2021 Hormozdiari F, Jung J, Eskin E, J Joo JW. MARS: leveraging allelic heterogeneity to increase power of association testing. Genome Biology. 22: 128. PMID 33931127 DOI: 10.1186/s13059-021-02353-8   
2021 Carrera C, Cárcel-Márquez J, Cullell N, Torres-Águila N, Muiño E, Castillo J, Sobrino T, Campos F, Rodríguez-Castro E, Llucia-Carol L, Millán M, Muñoz-Narbona L, López-Cancio E, Bustamante A, Ribó M, ... , et al. Single nucleotide variations in ZBTB46 are associated with post-thrombolytic parenchymal haematoma. Brain : a Journal of Neurology. PMID 33723576 DOI: 10.1093/brain/awab090   
2021 Zhang M, Xi Z, Saez-Atienzar S, Chia R, Moreno D, Sato C, Montazer Haghighi M, Traynor BJ, Zinman L, Rogaeva E. Combined epigenetic/genetic study identified an ALS age of onset modifier. Acta Neuropathologica Communications. 9: 75. PMID 33892821 DOI: 10.1186/s40478-021-01183-w   
2021 Li B, Wang Z, Chen Q, Li K, Wang X, Wang Y, Zeng Q, Han Y, Lu B, Zhao Y, Zhang R, Jiang L, Pan H, Luo T, Zhang Y, et al. GPCards: An integrated database of genotype-phenotype correlations in human genetic diseases. Computational and Structural Biotechnology Journal. 19: 1603-1611. PMID 33868597 DOI: 10.1016/j.csbj.2021.03.011   
2021 Belanger MJ, Kelly EM, Tahir UA, Benson MD. Genetic Risk Assessment for Atherosclerotic Cardiovascular Disease: A Guide for the General Cardiologist. Cardiology in Review. PMID 33758125 DOI: 10.1097/CRD.0000000000000384   
2021 Sun SY, Huang RZ, Huang H, Zhang MQ, Sun HL. Lack of association between single nucleotide polymorphisms in TCF7L2 and T2DM in the Chinese Yao population: A case-control study. Medicine. 100: e25326. PMID 33761736 DOI: 10.1097/MD.0000000000025326   
2021 Hayashi T, Shibata T, Nakamura M, Sakurai N, Takano H, Ota M, Nomura-Horita T, Hayashi R, Shimasaki T, Ostuka T, Tahara T, Arisawa T. Polymorphisms Located in 3'-UTR are Associated with Severity of Atrophy and Methylation Status in the Gastric Mucosa. Genetic Testing and Molecular Biomarkers. 25: 255-262. PMID 33877894 DOI: 10.1089/gtmb.2020.0299   
2021 Chakraborty S, Sharma A, Sharma A, Sihota R, Bhattacharjee S, Acharya M. Haplotype-based genomic analysis reveals novel association of genic region with primary angle closure glaucoma. Journal of Biosciences. 46. PMID 33737499   
2021 Inshaw JRJ, Sidore C, Cucca F, Stefana MI, Crouch DJM, McCarthy MI, Mahajan A, Todd JA. Analysis of overlapping genetic association in type 1 and type 2 diabetes. Diabetologia. PMID 33830302 DOI: 10.1007/s00125-021-05428-0   
2021 Takiguchi H, Yang CX, Yang CWT, Sahin B, Whalen BA, Milne S, Akata K, Yamasaki K, Yang JSW, Cheung CY, Vander Werff R, McNagny KM, Leitao Filho FS, Shaipanich T, van Eeden SF, et al. Macrophages with reduced expressions of classical M1 and M2 surface markers in human bronchoalveolar lavage fluid exhibit pro-inflammatory gene signatures. Scientific Reports. 11: 8282. PMID 33859282 DOI: 10.1038/s41598-021-87720-y   
2021 Li X, Liu D, Sun Y, Yang J, Yu Y. Association of genetic variants in enamel-formation genes with dental caries: A meta- and gene-cluster analysis. Saudi Journal of Biological Sciences. 28: 1645-1653. PMID 33732050 DOI: 10.1016/j.sjbs.2020.11.071   
2021 Wang Z, Liu Y, Wang W, Qu H, Han Y, Hou Y. Association of dipeptidyl peptidase IV polymorphism, serum lipid profile, and coronary artery stenosis in patients with coronary artery disease and type 2 diabetes. Medicine. 100: e25209. PMID 33787603 DOI: 10.1097/MD.0000000000025209   
2021 Restuadi R, Garton FC, Benyamin B, Lin T, Williams KL, Vinkhuyzen A, van Rheenen W, Zhu Z, Laing NG, Mather KA, Sachdev PS, Ngo ST, Steyn FJ, Wallace L, Henders AK, et al. Polygenic risk score analysis for amyotrophic lateral sclerosis leveraging cognitive performance, educational attainment and schizophrenia. European Journal of Human Genetics : Ejhg. PMID 33907316 DOI: 10.1038/s41431-021-00885-y   
2021 Wei Y, Wang X, Chew EY, Ding Y. Confident identification of subgroups from SNP testing in RCTs with binary outcomes. Biometrical Journal. Biometrische Zeitschrift. PMID 33751636 DOI: 10.1002/bimj.202000170