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):
Age of Hypertension Onset: Potential for Improving Risk Estimation and Hypertension Management?
Suvila K, Niiranen TJ.
Hypertension. 2021 Nov;78(5):1475-1477.
Polygenic risk provides biological validity for the ICHD-3 criteria among Finnish migraine families.
Häppölä P, Gormley P, Nuottamo ME, Artto V, Sumelahti ML, Nissilä M, Keski-Säntti P, Ilmavirta M, Kaunisto MA, Hämäläinen EI, Ripatti S, Pirinen M, Wessman M, Palotie A, Kallela M; International Headache Genetics Consortium (IHGC).
Cephalalgia. 2021 Oct 14:3331024211045651.
The role of family factors in the association between early adulthood BMI and risk of cardiovascular disease. An intergenerational study of BMI in early adulthood and cardiovascular mortality in parents, aunts and uncles.
Kjøllesdal MKR, Carslake D, Smith GD, Shaikh F, Næss Ø.
Int J Obes (Lond). 2021 Oct 14.
Association of severe childhood infections with depression and intentional self-harm in adolescents and young adults.
Leone M, Kuja-Halkola R, Leval A, D'Onofrio BM, Larsson H, Lichtenstein P, Bergen SE.
Brain Behav Immun. 2021 Oct 13:S0889-1591(21)00580-8.
Genome-wide association study of cardiac troponin I in the general population.
Moksnes MR, Røsjø H, Richmond A, Lyngbakken MN, Graham SE, Hansen AF, Wolford BN, Gagliano Taliun SA, LeFaive J, Rasheed H, Thomas LF, Zhou W, Aung N, Surakka I, Douville NJ, Campbell A, Porteous DJ, Petersen SE, Munroe PB, Welsh P, Sattar N, Smith GD, Fritsche LG, Nielsen JB, Åsvold BO, Hveem K, Hayward C, Willer CJ, Brumpton BM, Omland T.
Hum Mol Genet. 2021 Oct 13;30(21):2027-2039.
TIGER: The gene expression regulatory variation landscape of human pancreatic islets.
Alonso L, Piron A, Morán I, Guindo-Martínez M, Bonàs-Guarch S, Atla G, Miguel-Escalada I, Royo R, Puiggròs M, Garcia-Hurtado X, Suleiman M, Marselli L, Esguerra JLS, Turatsinze JV, Torres JM, Nylander V, Chen J, Eliasson L, Defrance M, Amela R; MAGIC, Mulder H, Gloyn AL, Groop L, Marchetti P, Eizirik DL, Ferrer J, Mercader JM, Cnop M, Torrents D.
Cell Rep. 2021 Oct 12;37(2):109807.
Gain-of-function variants in GABRD reveal a novel pathway for neurodevelopmental disorders and epilepsy.
Ahring PK, Liao VWY, Gardella E, Johannesen KM, Krey I, Selmer KK, Stadheim BF, Davis H, Peinhardt C, Koko M, Coorg RK, Syrbe S, Bertsche A, Santiago-Sim T, Diemer T, Fenger CD, Platzer K, Eichler EE, Lerche H, Lemke JR, Chebib M, Møller RS.
Brain. 2021 Oct 11:awab391.
Multivariate alterations in insula - Medial prefrontal cortex linked to genetics in 12q24 in schizophrenia.
Jiang W, Rootes-Murdy K, Chen J, Bizzozero NIP, Calhoun VD, van Erp TGM, Ehrlich S, Agartz I, Jönsson EG, Andreassen OA, Wang L, Pearlson GD, Glahn DC, Hong E, Liu J, Turner JA.
Psychiatry Res. 2021 Oct 10;306:114237.
Wavelet Screening: a novel approach to analyzing GWAS data.<
Denault WRP, Gjessing HK, Juodakis J, Jacobsson B, Jugessur A.
BMC Bioinformatics. 2021 Oct 7;22(1):484.
A genome-wide meta-analysis uncovers six sequence variants conferring risk of vertigo.
Skuladottir AT, Bjornsdottir G, Nawaz MS, Petersen H, Rognvaldsson S, Moore KHS, Olafsson PI, Magnusson SH, Bjornsdottir A, Sveinsson OA, Sigurdardottir GR, Saevarsdottir S, Ivarsdottir EV, Stefansdottir L, Gunnarsson B, Muhlestein JB, Knowlton KU, Jones DA, Nadauld LD, Hartmann AM, Rujescu D, Strupp M, Walters GB, Thorgeirsson TE, Jonsdottir I, Holm H, Thorleifsson G, Gudbjartsson DF, Sulem P, Stefansson H, Stefansson K.
Commun Biol. 2021 Oct 7;4(1):1148.
Genetic Stratification of Age-Dependent Parkinson's Disease Risk by Polygenic Hazard Score.
Pihlstrøm L, Fan CC, Frei O, Tan M, Karunamuni RA, Blauwendraat C, Bandres-Ciga S, Gan-Or Z, Grosset DG; International Parkinson's Disease Genomics Consortium (IPDGC), Dale AM, Seibert TM, Andreassen OA.
Mov Disord. 2021 Oct 6.
The Angelman Syndrome Online Registry - A multilingual approach to support global research.
Krey I, Heine C, Frömming M, Herrmann J, Møller RS, Weckhuysen S, Courage C, Beblo S, Syrbe S, Lemke JR.
Eur J Med Genet. 2021 Oct 4;64(12):104349.
CD4+ T-cell DNA methylation changes during pregnancy significantly correlate with disease-associated methylation changes in autoimmune diseases.
Badam TV, Hellberg S, Mehta RB, Lechner-Scott J, Lea RA, Tost J, Mariette X, Svensson-Arvelund J, Nestor CE, Benson M, Berg G, Jenmalm MC, Gustafsson M, Ernerudh J.
Epigenetics. 2021 Oct 4:1-16.
A life course approach to understanding associations between natural environments and mental well-being for the Danish blood donor cohort.
Engemann K, Svenning JC, Arge L, Brandt J, Bruun MT, Didriksen M, Erikstrup C, Geels C, Hertel O, Horsdal HT, Kaspersen KA, Mikkelsen S, Mortensen PB, Nielsen KR, Ostrowski SR, Pedersen OB, Tsirogiannis C, Sabel CE, Sigsgaard T, Ullum H, Pedersen CB.
Health Place. 2021 Oct 2;72:102678.
Early manifestations of genetic risk for neurodevelopmental disorders.
Askeland RB, Hannigan LJ, Ask H, Ayorech Z, Tesli M, Corfield E, Magnus P, Njølstad PR, Andreassen OA, Davey Smith G, Reichborn-Kjennerud T, Havdahl A.
J Child Psychol Psychiatry. 2021 Oct 4.
Genome-Wide Association Study of Peripheral Artery Disease.
van Zuydam NR, Stiby A, Abdalla M, Austin E, Dahlström EH, McLachlan S, Vlachopoulou E, Ahlqvist E, Di Liao C, Sandholm N, Forsblom C, Mahajan A, Robertson NR, Rayner NW, Lindholm E, Sinisalo J, Perola M, Kallio M, Weiss E, Price J, Paterson A, Klein B, Salomaa V, Palmer CNA, Groop PH, Groop L, McCarthy MI, de Andrade M, Morris AP, Hopewell JC, Colhoun HM, Kullo IJ; GoLEAD Consortium, SUMMIT Consortium†.
Circ Genom Precis Med. 2021 Oct;14(5):e002862. Epub 2021 Oct 4.
Use of incretin-based drugs and risk of cholangiocarcinoma: Scandinavian cohort study.
Ueda P, Wintzell V, Melbye M, Eliasson B, Svensson AM, Franzén S, Gudbjörnsdottir S, Hveem K, Jonasson C, Svanström H, Pasternak B.
Diabetologia. 2021 Oct;64(10):2204-2214.
Bidirectional associations between treatment-resistant depression and general medical conditions.
Madsen KB, Momen NC, Petersen LV, Plana-Ripoll O, Haarman BCM, Drexhage H, Mortensen PB, McGrath JJ, Munk-Olsen T.
Eur Neuropsychopharmacol. 2021 Oct;51:7-19.
A registry-based randomised trial comparing an SGLT2 inhibitor and metformin as standard treatment of early stage type 2 diabetes (SMARTEST): Rationale, design and protocol.
Sundström J, Kristófi R, Östlund O, Bennet L, Eliasson B, Jansson S, Leksell J, Almby K, Lundqvist M, Eriksson JW; SMARTEST study group (see list in Appendix).
J Diabetes Complications. 2021 Oct;35(10):107996.
Hyperglycaemia-associated Caspase-3 predicts diabetes and coronary artery disease events.
Sun J, Singh P, Österlund J, Orho-Melander M, Melander O, Engström G, Edsfeldt A.
J Intern Med. 2021 Oct;290(4):855-865.