A curated list of scholarly publications relevant to research, policy and health care from the Nordic human genetics and precision medicine community and their collaborators.
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Nordic Papers List (Most Recent First):
Large-Scale Screening for Monogenic and Clinically Defined Familial Hypercholesterolemia in Iceland.
Björnsson E, Thorgeirsson G, Helgadóttir A, Thorleifsson G, Sveinbjörnsson G, Kristmundsdóttir S, Jónsson H, Jónasdóttir A, Jónasdóttir Á, Sigurðsson Á, Guðnason T, Ólafsson Í, Sigurðsson EL, Sigurðardóttir Ó, Viðarsson B, Baldvinsson M, Bjarnason R, Danielsen R, Matthíasson SE, Thórarinsson BL, Grétarsdóttir S, Steinthórsdóttir V, Halldórsson BV, Andersen K, Arnar DO, Jónsdóttir I, Guðbjartsson DF, Hólm H, Thorsteinsdóttir U, Sulem P, Stefánsson K.
Arterioscler Thromb Vasc Biol. 2021 Oct;41(10):2616-2628.
Adult-onset inflammatory bowel disease and rate of serious infections compared to the general population: a nationwide register-based cohort study 2002-2017.
Ludvigsson JF, Holmgren J, Grip O, Halfvarson J, Askling J, Sachs MC, Olén O.
Scand J Gastroenterol. 2021 Oct;56(10):1152-1162.
Risk and protective factors for mental disorders beyond genetics: an evidence-based atlas.
Arango C, Dragioti E, Solmi M, Cortese S, Domschke K, Murray RM, Jones PB, Uher R, Carvalho AF, Reichenberg A, Shin JI, Andreassen OA, Correll CU, Fusar-Poli P.
World Psychiatry. 2021 Oct;20(3):417-436.
Selection criteria for assembling a pediatric cancer predisposition syndrome gene panel.
Byrjalsen A, Diets IJ, Bakhuizen J, Hansen TVO, Schmiegelow K, Gerdes AM, Stoltze U, Kuiper RP, Merks JHM, Wadt K, Jongmans M.
Fam Cancer. 2021 Oct;20(4):279-287.
Sleep-disordered breathing-related symptoms and risk of stroke: cohort study and Mendelian randomization analysis.
Titova OE, Yuan S, Baron JA, Lindberg E, Michaëlsson K, Larsson SC.
J Neurol. 2021 Oct 1.
Insomnia symptoms and subclinical myocardial injury: Data from the Nord-Trøndelag Health (HUNT) study.
Sigurdardottir FD, Lyngbakken MN, Hveem K, Hrubos Strøm H, Røsjø H, Redline S, Omland T.
J Sleep Res. 2021 Oct;30(5):e13299.
A cross-population atlas of genetic associations for 220 human phenotypes.
Sakaue S, Kanai M, Tanigawa Y, Karjalainen J, Kurki M, Koshiba S, Narita A, Konuma T, Yamamoto K, Akiyama M, Ishigaki K, Suzuki A, Suzuki K, Obara W, Yamaji K, Takahashi K, Asai S, Takahashi Y, Suzuki T, Shinozaki N, Yamaguchi H, Minami S, Murayama S, Yoshimori K, Nagayama S, Obata D, Higashiyama M, Masumoto A, Koretsune Y; FinnGen, Ito K, Terao C, Yamauchi T, Komuro I, Kadowaki T, Tamiya G, Yamamoto M, Nakamura Y, Kubo M, Murakami Y, Yamamoto K, Kamatani Y, Palotie A, Rivas MA, Daly MJ, Matsuda K, Okada Y.
Nat Genet. 2021 Sep 30.
Diabetes status-related differences in risk factors and mediators of heart failure in the general population: results from the MORGAM/BiomarCaRE consortium.
Vuori MA, Reinikainen J, Söderberg S, Bergdahl E, Jousilahti P, Tunstall-Pedoe H, Zeller T, Westermann D, Sans S, Linneberg A, Iacoviello L, Costanzo S, Salomaa V, Blankenberg S, Kuulasmaa K, Niiranen TJ.
Cardiovasc Diabetol. 2021 Sep 28;20(1):195.
Genetic variants associated with platelet count are predictive of human disease and physiological markers.
Mikaelsdottir E, Thorleifsson G, Stefansdottir L, Halldorsson G, Sigurdsson JK, Lund SH, Tragante V, Melsted P, Rognvaldsson S, Norland K, Helgadottir A, Magnusson MK, Ragnarsson GB, Kristinsson SY, Reykdal S, Vidarsson B, Gudmundsdottir IJ, Olafsson I, Onundarson PT, Sigurdardottir O, Sigurdsson EL, Grondal G, Geirsson AJ, Geirsson G, Gudmundsson J, Holm H, Saevarsdottir S, Jonsdottir I, Thorgeirsson G, Gudbjartsson DF, Thorsteinsdottir U, Rafnar T, Stefansson K.
Commun Biol. 2021 Sep 27;4(1):1132.
Prediction of Type 1 Diabetes at Birth: Cord Blood Metabolites vs Genetic Risk Score in the Norwegian Mother, Father, and Child Cohort.
Tapia G, Suvitaival T, Ahonen L, Lund-Blix NA, Njølstad PR, Joner G, Skrivarhaug T, Legido-Quigley C, Størdal K, Stene LC.
J Clin Endocrinol Metab. 2021 Sep 27;106(10):e4062-e4071.
Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome.
Porcu E, Sadler MC, Lepik K, Auwerx C, Wood AR, Weihs A, Sleiman MSB, Ribeiro DM, Bandinelli S, Tanaka T, Nauck M, Völker U, Delaneau O, Metspalu A, Teumer A, Frayling T, Santoni FA, Reymond A, Kutalik Z.
Nat Commun. 2021 Sep 24;12(1):5647.
Early life adversity due to bereavement and inflammatory diseases in the next generation - a population study in transgenerational stress exposure.
Brew BK, Lundholm C, Osvald EC, Chambers G, Öberg AS, Fang F, Almqvist C.
Am J Epidemiol. 2021 Sep 22:kwab236.
Anti-inflammatory diet and venous thromboembolism: Two prospective cohort studies.
Yuan S, Bruzelius M, Damrauer SM, Håkansson N, Wolk A, Åkesson A, Larsson SC.
Nutr Metab Cardiovasc Dis. 2021 Sep 22;31(10):2831-2838.
Identifying dominant-negative actions of a dopamine transporter variant in patients with parkinsonism and neuropsychiatric disease.
Herborg F, Jensen KL, Tolstoy S, Arends NV, Posselt LP, Shekar A, Aguilar JI, Lund VK, Erreger K, Rickhag M, Lycas MD, Lonsdale MN, Rahbek-Clemmensen T, Sørensen AT, Newman AH, Løkkegaard A, Kjærulff O, Werge T; iPSYCH researchers, Møller LB, Matthies HJ, Galli A, Hjermind LE, Gether U.
JCI Insight. 2021 Sep 22;6(18):e151496.
Vertex-wise multivariate genome-wide association study identifies 780 unique genetic loci associated with cortical morphology.
Shadrin AA, Kaufmann T, van der Meer D, Palmer CE, Makowski C, Loughnan R, Jernigan TL, Seibert TM, Hagler DJ, Smeland OB, Motazedi E, Chu Y, Lin A, Cheng W, Hindley G, Thompson WK, Fan CC, Holland D, Westlye LT, Frei O, Andreassen OA, Dale AM.
Neuroimage. 2021 Sep 21;244:118603.
Polygenic Score for Physical Activity Is Associated with Multiple Common Diseases.
Sillanpää E, Palviainen T, Ripatti S, Kujala UM, Kaprio J.
Med Sci Sports Exerc. 2021 Sep 20.
Methylome-wide association study of early life stressors and adult mental health.
Howard DM, Pain O, Arathimos R, Barbu MC, Amador C, Walker RM, Jermy B, Adams MJ, Deary IJ, Porteous D, Campbell A, Sullivan PF, Evans KL, Arseneault L, Wray NR, Meaney M, McIntosh AM, Lewis CM.
Hum Mol Genet. 2021 Sep 15:ddab274.