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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Featured Papers
Remove obstacles to sharing health data with researchers outside of the European Union.
Bentzen HB, Castro R, Fears R, Griffin G, Ter Meulen V, Ursin G.
Nat Med. 2021 Aug;27(8):1329-1333.
There are about 5,000 collaborative projects between the US National Institutes of Health (NIH) and EEA countries. At least 40 clinical and observational studies on risk factors and exposures for cancer have been suspended or delayed because of the current legal challenges. This article explains why it is so difficult to transfer privacy-protected personal data from the European Economic Area (EEA) to outside the EEA, and the serious implications for medical research, citizens and patients. For this data sharing to happen, the EU must now work with other countries to resolve statutory conflicts, but this will also require cooperation from those countries.
Image credit: Courtesy Springer Nature
Nordic Health Registry-Based Research: A Review of Health Care Systems and Key Registries.
Laugesen K, Ludvigsson JF, Schmidt M, Gissler M, Valdimarsdottir UA, Lunde A, Sørensen HT.
Clin Epidemiol. 2021 Jul 19;13:533-554.
Nordic registries and cohorts are the basis of a lot of what’s known about the epidemiology of human disease. They also provide a Nordic advantage in achieving genome-based precision medicine. This review provides an overview of five Nordic health care systems (Denmark, Finland, Iceland, Norway, and Sweden, but not Estonia), describes key registries, and offers guidance on how to navigate the practical and ethical aspects of setting up Nordic study collaborations.
Genetic insights into biological mechanisms governing human ovarian ageing.<
Ruth KS, Day FR, Hussain J, Martínez-Marchal A, […] Hoffmann ER, Murray A, Roig I, Perry JRB.
Nature. 2021 Aug 4. doi: 10.1038/s41586-021-03779-7.
An international research team combined genomics and functional data to shed light on the biology of reproductive aging in women. A genome-wide association study (GWAS) in more than 200,000 women of European ancestry (including Nordic cohorts) found 290 loci associated with the age of natural menopause, with effect sizes from 3.5 weeks to 1.5 years. The variants explain 10-12% of trait variance and were broadly replicated in 78,000 East Asians. The study found a polygenic component to menopause timing across the age range and implicated DNA damage repair processes from fetal to adult life in ovarian reserve and reproductive lifespan. Further analysis suggested a causal relationship between earlier menopause and increased risk of Type 2 diabetes and osteoporosis but reduced risk of hormone-sensitive cancers, such as breast and ovarian. (Tweetorial)
Image credit: KL Murphy/Courtesy Springer Nature
August Nordic Papers List (Most Recent First)
Genome-wide analysis reveals genetic overlap between alcohol use behaviors, schizophrenia and bipolar disorder and identifies novel shared risk loci.
Wiström ED, O'Connell KS, Karadag N, Bahrami S, Hindley GFL, Lin A, Cheng W, Steen NE, Shadrin A, Frei O, Djurovic S, Dale AM, Andreassen OA, Smeland OB.
Addiction. 2021 Sep 2.
Lymph node metastases in breast cancer: Investigating associations with tumor characteristics, molecular subtypes and polygenic risk score using a continuous growth model.
Isheden G, Grassmann F, Czene K, Humphreys K.
Int J Cancer. 2021 Sep 15;149(6):1348-1357.
Comparison of cardiovascular disease and cancer prevalence between Mediterranean and north European middle-aged populations (The Cilento on Ageing Outcomes Study and The Malmö Offspring Study).
Melander O, Antonini P, Ottosson F, Brunkwall L, Gallo W, Nilsson PM, Orho-Melander M, Pacente G, D'Arena G, Di Somma S.
Intern Emerg Med. 2021 Sep;16(6):1567-1572.
Predictive Accuracy of a Clinical and Genetic Risk Model for Atrial Fibrillation.
Khurshid S, Mars N, Haggerty CM, Huang Q, Weng LC, Hartzel DN, Lunetta KL, Ashburner JM, Anderson CD, Benjamin EJ, Salomaa V, Ellinor PT, Fornwalt BK, Ripatti S, Trinquart L, Lubitz SA; Regeneron Genetics Center.
Circ Genom Precis Med. 2021 Aug 31:CIRCGEN121003355.
Sequence variants in malignant hyperthermia genes in Iceland: classification and actionable findings in a population database.
Fridriksdottir R, Jonsson AJ, Jensson BO, Sverrisson KO, Arnadottir GA, Skarphedinsdottir SJ, Katrinardottir H, Snaebjornsdottir S, Jonsson H, Eiriksson O, Oskarsson GR, Oddsson A, Jonasdottir A, Jonasdottir A, Sigurdsson GH, Indridason EP, Sigurdsson SB, Bjornsdottir G, Saemundsdottir J, Magnusson OT, Bjornsson HT, Thorsteinsdottir U, Sigurdsson TS, Sulem P, Sigurdsson MI, Stefansson K.
Eur J Hum Genet. 2021 Aug 31.
A validated generally applicable approach using the systematic assessment of disease modules by GWAS reveals a multi-omic module strongly associated with risk factors in multiple sclerosis.
Badam TVS, de Weerd HA, Martínez-Enguita D, Olsson T, Alfredsson L, Kockum I, Jagodic M, Lubovac-Pilav Z, Gustafsson M.
BMC Genomics. 2021 Aug 30;22(1):631.
Genome-wide association study identifies first locus associated with susceptibility to cerebral venous thrombosis.
Ken-Dror G, Cotlarciuc I, Martinelli I, Grandone E, Hiltunen S, Lindgren E, Margaglione M, Duchez VLC, Triquenot AB, Zedde M, Mancuso M, Ruigrok YM, Marjot T, Worrall B, Majersik JJ, Metso TM, Putaala J, Haapaniemi E, Zuurbier SM, Brouwer MC, Passamonti SM, Abbattista M, Bucciarelli P, Mitchell BD, Kittner SJ, Lemmens R, Jern C, Pappalardo E, Costa P, Colombi M, de Sousa DA, Rodrigues S, Canhão P, Tkach A, Santacroce R, Favuzzi G, Arauz A, Colaizzo D, Spengos K, Hodge A, Ditta R, Pezzini A, Debette S, Coutinho JM, Thijs V, Jood K, Pare G, Tatlisumak T, Ferro JM, Sharma P; International Stroke Genetics Consortium (ISGC) & Bio-Repository to Establish the Aetiology of Sinovenous Thrombosis (BEAST) collaborators.
Ann Neurol. 2021 Aug 30.
Estimating the Population Benefits of Blood Pressure Lowering: A Wide-Angled Mendelian Randomization Study in UK Biobank.
Higgins H, Mason AM, Larsson SC, Gill D, Langenberg C, Burgess S.
J Am Heart Assoc. 2021 Aug 28:e021098.
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications.
Johannesen KM, Liu Y, Koko M, Gjerulfsen CE, Sonnenberg L, Schubert J, Fenger CD, Eltokhi A, Rannap M, Koch NA, Lauxmann S, Krüger J, Kegele J, Canafoglia L, Franceschetti S, Mayer T, Rebstock J, Zacher P, Ruf S, Alber M, Sterbova K, Lassuthová P, Vlckova M, Lemke JR, Platzer K, Krey I, Heine C, Wieczorek D, Kroell-Seger J, Lund C, Klein KM, Billie Au PY, Rho JM, Ho AW, Masnada S, Veggiotti P, Giordano L, Accorsi P, Hoei-Hansen CE, Striano P, Zara F, Verhelst H, Verhoeven JS, van der Zwaag B, Harder AVE, Brilstra E, Pendziwiat M, Lebon S, Vaccarezza M, Minh Le N, Christensen J, Grønborg S, Scherer SW, Howe J, Fazeli W, Howell KB, Leventer R, Stutterd C, Walsh S, Gerard M, Gerard B, Matricardi S, Bonardi CM, Sartori S, Berger A, Hoffman-Zacharska D, Mastrangelo M, Darra F, Vøllo A, Motazacker MM, Lakeman P, Nizon M, Betzler C, Altuzarra C, Caume R, Roubertie A, Gélisse P, Marini C, Guerrini R, Bilan F, Tibussek D, Koch-Hogrebe M, Perry MS, Ichikawa S, Dadali E, Sharkov A, Mishina I, Abramov M, Kanivets I, Korostelev S, Kutsev S, Wain KE, Eisenhauer N, Wagner M, Savatt JM, Müller-Schlüter K, Bassan H, Borovikov A, Nassogne MC, Destrée A, Schoonjans AS, Meuwissen M, Buzatu M, Jansen A, Scalais E, Srivastava S, Tan WH, Olson HE, Loddenkemper T, Poduri A, Helbig KL, Helbig I, Fitzgerald MP, Goldberg EM, Roser T, Borggraefe I, Brünger T, May P, Lal D, Lederer D, Rubboli G, Heyne HO, Lesca G, Hedrich UBS, Benda J, Gardella E, Lerche H, Møller RS.
Brain. 2021 Aug 25:awab321.
Integrative genetic, genomic and transcriptomic analysis of heat shock protein and nuclear hormone receptor gene associations with spontaneous preterm birth.
Huusko JM, Tiensuu H, Haapalainen AM, Pasanen A, Tissarinen P, Karjalainen MK, Zhang G, Christensen K, Ryckman KK, Jacobsson B, Murray JC, Kingsmore SF, Hallman M, Muglia LJ, Rämet M.
Sci Rep. 2021 Aug 24;11(1):17115.
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations.
Boer CG, Hatzikotoulas K, Southam L, Stefánsdóttir L, Zhang Y, Coutinho de Almeida R, Wu TT, Zheng J, Hartley A, Teder-Laving M, Skogholt AH, Terao C, Zengini E, Alexiadis G, Barysenka A, Bjornsdottir G, Gabrielsen ME, Gilly A, Ingvarsson T, Johnsen MB, Jonsson H, Kloppenburg M, Luetge A, Lund SH, Mägi R, Mangino M, Nelissen RRGHH, Shivakumar M, Steinberg J, Takuwa H, Thomas LF, Tuerlings M; arcOGEN Consortium; HUNT All-In Pain; ARGO Consortium; Regeneron Genetics Center, Babis GC, Cheung JPY, Kang JH, Kraft P, Lietman SA, Samartzis D, Slagboom PE, Stefansson K, Thorsteinsdottir U, Tobias JH, Uitterlinden AG, Winsvold B, Zwart JA, Davey Smith G, Sham PC, Thorleifsson G, Gaunt TR, Morris AP, Valdes AM, Tsezou A, Cheah KSE, Ikegawa S, Hveem K, Esko T, Wilkinson JM, Meulenbelt I, Lee MTM, van Meurs JBJ, Styrkársdóttir U, Zeggini E.
Cell. 2021 Aug 24:S0092-8674(21)00941-7.
Genetically Predicted Milk Intake and Risk of Neurodegenerative Diseases.
Zhang Z, Wang M, Yuan S, Larsson SC, Liu X.
Nutrients. 2021 Aug 23;13(8):2893.
Familial and genetic associations between autism spectrum disorder and other neurodevelopmental and psychiatric disorders.
Ghirardi L, Kuja-Halkola R, Butwicka A, Martin J, Larsson H, D'Onofrio BM, Lichtenstein P, Taylor MJ.
J Child Psychol Psychiatry. 2021 Aug 20.
A Danish Hospital Outbreak of SARS-CoV-2. Combining WGS with epidemiological links offers surprising new information.
Olesen B, Hansen TA, Hansen VM, Gyrup HB, Marloth T, Nielsen L.
J Hosp Infect. 2021 Aug 20:S0195-6701(21)00295-4.
Cerebrospinal fluid test results and associations with subsequent mental disorders, neurological diseases, and CNS infections: A population-based cohort study.
Orlovska-Waast S, Petersen LV, Gasse C, Nordentoft M, Mortensen PB, Kondziella D, Benros ME.
Brain Behav Immun. 2021 Aug 12;98:210-218.
Clinical and molecular delineation of PUS3-associated neurodevelopmental disorders.
Nøstvik M, Kateta SM, Schönewolf-Greulich B, Afenjar A, Barth M, Boschann F, Doummar D, Haack TB, Keren B, Livshits LA, Mei D, Park J, Pisano T, Prouteau C, Umair M, Waqas A, Ziegler A, Guerrini R, Møller RS, Tümer Z.
Clin Genet. 2021 Aug 20.
Joint associations of depression, genetic susceptibility and the area of residence for coronary heart disease incidence.
Silventoinen K, Korhonen K, Lahtinen H, Jelenkovic A, Havulinna AS, Ripatti S, Salomaa V, Davey Smith G, Martikainen P.
J Epidemiol Community Health. 2021 Aug 18:jech-2021-216451.
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 Aug 19:ATVBAHA120315904.
Cohort Profile: The Copenhagen Baby Heart Study (CBHS).
Vøgg ROB, Basit S, Raja AA, Sillesen AS, Pihl C, Vejlstrup N, Jonsen EH, Larsen OW, Zingenberg H, Boyd HA, Iversen KK, Bundgaard H.
Int J Epidemiol. 2021 Aug 17:dyab147.
Association of Variants Near the Bradykinin Receptor B2 Gene With Angioedema in Patients Taking ACE Inhibitors.
Ghouse J, Ahlberg G, Andreasen L, Banasik K, Brunak S, Schwinn M, Larsen IH, Petersen O, Sørensen E, Ullum H, Rasmussen ER, Eriksson N, Hallberg P, Wadelius M, Bundgaard H, Olesen MS.
J Am Coll Cardiol. 2021 Aug 17;78(7):696-709.
Genotype-phenotype correlation in arrhythmogenic right ventricular cardiomyopathy-risk of arrhythmias and heart failure.
Christensen AH, Platonov PG, Jensen HK, Chivulescu M, Svensson A, Dahlberg P, Madsen T, Frederiksen TC, Heliö T, Lie ØH, Haugaa KH, Hastrup Svendsen J, Bundgaard H.
J Med Genet. 2021 Aug 16:jmedgenet-2021-107911.
Sex Differences in Genetic Risk for Hypertension.
Kauko A, Aittokallio J, Vaura F, Ji H, Ebinger JE, Niiranen T, Cheng S.
Hypertension. 2021 Aug 15:HYPERTENSIONAHA12117796.
Familial co-aggregation of attention-deficit/hyperactivity disorder and autoimmune diseases: a cohort study based on Swedish population-wide registers.
Hegvik TA, Chen Q, Kuja-Halkola R, Klungsøyr K, Butwicka A, Lichtenstein P, Almqvist C, Faraone SV, Haavik J, Larsson H.
Int J Epidemiol. 2021 Aug 11:dyab151.
Cohort profile: Epigenetics in Pregnancy (EPIPREG) - population-based sample of European and South Asian pregnant women with epigenome-wide DNA methylation (850k) in peripheral blood leukocytes.
Fragoso-Bargas N, Opsahl JO, Kiryushchenko N, Böttcher Y, Lee-Ødegård S, Qvigstad E, Richardsen KR, Waage CW, Sletner L, Jenum AK, Prasad RB, Groop LC, Moen GH, Birkeland KI, Sommer C.
PLoS One. 2021 Aug 13;16(8):e0256158.
RSPO3 is important for trabecular bone and fracture risk in mice and humans.
Nilsson KH, Henning P, Shahawy ME, Nethander M, Andersen TL, Ejersted C, Wu J, Gustafsson KL, Koskela A, Tuukkanen J, Souza PPC, Tuckermann J, Lorentzon M, Ruud LE, Lehtimäki T, Tobias JH, Zhou S, Lerner UH, Richards JB, Movérare-Skrtic S, Ohlsson C.
Nat Commun. 2021 Aug 13;12(1):4923.
Distinct Molecular Signatures of Clinical Clusters in People with Type 2 Diabetes: an IMIRHAPSODY Study.
Slieker RC, Donnelly LA, Fitipaldi H, Bouland GA, Giordano GN, Åkerlund M, Gerl MJ, Ahlqvist E, Ali A, Dragan I, Elders P, Festa A, Hansen MK, van der Heijden AA, Aly DM, Kim M, Kuznetsov D, Mehl F, Klose C, Simons K, Pavo I, Pullen TJ, Suvitaival T, Wretlind A, Rossing P, Lyssenko V, Quigley CL, Groop L, Thorens B, Franks PW, Ibberson M, Rutter GA, Beulens JW, 't Hart LM, Pearson ER.
Diabetes. 2021 Aug 10:db201281.
Dominant-negative actions of a dopamine transporter variant identified 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, Kjaerulff O, Werge T, Møller LB, Matthies HJ, Galli A, Hjermind LE, Gether U.
JCI Insight. 2021 Aug 10:151496.
Gut microbial biomarkers for the treatment response in first-episode, drug-naïve schizophrenia: a 24-week follow-up study.
Yuan X, Wang Y, Li X, Jiang J, Kang Y, Pang L, Zhang P, Li A, Lv L, Andreassen OA, Fan X, Hu S, Song X.
Transl Psychiatry. 2021 Aug 10;11(1):422.
Towards prevention of autoimmune diseases: The example of rheumatoid arthritis.
Hensvold A, Klareskog L.
Eur J Immunol. 2021 Aug;51(8):1921-1933.
Derivation and Molecular Characterization of a Morphological Subpopulation of Human iPSC Astrocytes Reveal a Potential Role in Schizophrenia and Clozapine Response.
Akkouh IA, Hribkova H, Grabiec M, Budinska E, Szabo A, Kasparek T, Andreassen OA, Sun YM, Djurovic S.
Schizophr Bull. 2021 Aug 5:sbab092.
Prominent health problems, socioeconomic deprivation, and higher brain age in lonely and isolated individuals: A population-based study.
de Lange AG, Kaufmann T, Quintana DS, Winterton A, Andreassen OA, Westlye LT, Ebmeier KP.
Behav Brain Res. 2021 Aug 4;414:113510.
Lifetime risk of rheumatoid arthritis-associated interstitial lung disease in MUC5Bmutation carriers.
Palomäki A; FinnGen Rheumatology Clinical Expert Group, Palotie A, Koskela J, Eklund KK, Pirinen M; FinnGen, Ripatti S, Laitinen T, Mars N.
Ann Rheum Dis. 2021 Aug 3:annrheumdis-2021-220698. (Editorial)
Single-cell multimodal analysis in a case with reduced penetrance of Progranulin-Frontotemporal Dementia.
Natarajan K, Eisfeldt J, Hammond M, Laffita-Mesa JM, Patra K, Khoshnood B, Öijerstedt L, Graff C.
Acta Neuropathol Commun. 2021 Aug 3;9(1):132.
Mendelian randomisation study of smoking exposure in relation to breast cancer risk.
Park HA, Neumeyer S, Michailidou K, Bolla MK, Wang Q, Dennis J, Ahearn TU, Andrulis IL, Anton-Culver H, Antonenkova NN, Arndt V, Aronson KJ, Augustinsson A, Baten A, Beane Freeman LE, Becher H, Beckmann MW, Behrens S, Benitez J, Bermisheva M, Bogdanova NV, Bojesen SE, Brauch H, Brenner H, Brucker SY, Burwinkel B, Campa D, Canzian F, Castelao JE, Chanock SJ, Chenevix-Trench G, Clarke CL; NBCS Collaborators, Conroy DM, Couch FJ, Cox A, Cross SS, Czene K, Daly MB, Devilee P, Dörk T, Dos-Santos-Silva I, Dwek M, Eccles DM, Eliassen AH, Engel C, Eriksson M, Evans DG, Fasching PA, Flyger H, Fritschi L, García-Closas M, García-Sáenz JA, Gaudet MM, Giles GG, Glendon G, Goldberg MS, Goldgar DE, González-Neira A, Grip M, Guénel P, Hahnen E, Haiman CA, Håkansson N, Hall P, Hamann U, Han S, Harkness EF, Hart SN, He W, Heemskerk-Gerritsen BAM, Hopper JL, Hunter DJ; ABCTB Investigators; kConFab Investigators, Jager A, Jakubowska A, John EM, Jung A, Kaaks R, Kapoor PM, Keeman R, Khusnutdinova E, Kitahara CM, Koppert LB, Koutros S, Kristensen VN, Kurian AW, Lacey J, Lambrechts D, Le Marchand L, Lo WY, Lubiński J, Mannermaa A, Manoochehri M, Margolin S, Martinez ME, Mavroudis D, Meindl A, Menon U, Milne RL, Muranen TA, Nevanlinna H, Newman WG, Nordestgaard BG, Offit K, Olshan AF, Olsson H, Park-Simon TW, Peterlongo P, Peto J, Plaseska-Karanfilska D, Presneau N, Radice P, Rennert G, Rennert HS, Romero A, Saloustros E, Sawyer EJ, Schmidt MK, Schmutzler RK, Schoemaker MJ, Schwentner L, Scott C, Shah M, Shu XO, Simard J, Smeets A, Southey MC, Spinelli JJ, Stevens V, Swerdlow AJ, Tamimi RM, Tapper WJ, Taylor JA, Terry MB, Tomlinson I, Troester MA, Truong T, Vachon CM, van Veen EM, Vijai J, Wang S, Wendt C, Winqvist R, Wolk A, Ziogas A, Dunning AM, Pharoah PDP, Easton DF, Zheng W, Kraft P, Chang-Claude J.
Br J Cancer. 2021 Aug 2.
Mammographic features are associated with cardiometabolic disease risk and mortality.
Grassmann F, Yang H, Eriksson M, Azam S, Hall P, Czene K.
Eur Heart J. 2021 Aug 2:ehab502.
Swedish Covid-19 Investigation for Future Insights - A Population Epidemiology Approach Using Register Linkage (SCIFI-PEARL).
Nyberg F, Franzén S, Lindh M, Vanfleteren L, Hammar N, Wettermark B, Sundström J, Santosa A, Björck S, Gisslén M.
Clin Epidemiol. 2021 Jul 30;13:649-659.
Personalized Medicine Through GPCR Pharmacogenomics
Hauser, AS.
Reference Module in Biomedical Sciences, Elsevier, 2021 July 29. ISBN 9780128012383.
DNA Methylation-Based Interferon Scores Associate With Sub-Phenotypes in Primary Sjögren's Syndrome.
Imgenberg-Kreuz J, Sandling JK, Norheim KB, Johnsen SJA, Omdal R, Syvänen AC, Svenungsson E, Rönnblom L, Eloranta ML, Nordmark G.
Front Immunol. 2021 Jul 16;12:702037.
Association of Protective HLA-A With HLA-B∗27 Positive Ankylosing Spondylitis.
Nordin J, Pettersson M, Rosenberg LH, Mathioudaki A, Karlsson Å, Murén E, Tandre K, Rönnblom L, Kastbom A, Cedergren J, Eriksson P, Söderkvist P, Lindblad-Toh K, Meadows JRS.
Front Genet. 2021 Jul 15;12:659042.
The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research.
Salgado D, Armean IM, Baudis M, Beltran S, Capella-Gutierrez S, Carvalho-Silva D, Dominguez Del Angel V, Dopazo J, Furlong LI, Gao B, Garcia L, Gerloff D, Gut I, Gyenesei A, Habermann N, Hancock JM, Hanauer M, Hovig E, Johansson LF, Keane T, Korbel J, Lauer KB, Laurie S, Leskošek B, Lloyd D, Marques-Bonet T, Mei H, Monostory K, Piñero J, Poterlowicz K, Rath A, Samarakoon P, Sanz F, Saunders G, Sie D, Swertz MA, Tsukanov K, Valencia A, Vidak M, Yenyxe González C, Ylstra B, Béroud C.
F1000Res. 2020 Oct 13;9:ELIXIR-1229.