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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1997 1
2002 2
2003 1
2004 6
2005 8
2006 6
2007 7
2008 4
2009 2
2010 19
2011 15
2012 17
2013 24
2014 13
2015 15
2016 6
2017 12
2018 7
2019 5
2020 4
2021 2
2022 3
2024 1

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150 results

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Page 1
Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications.
Sterenborg RBTM, Steinbrenner I, Li Y, Bujnis MN, Naito T, Marouli E, Galesloot TE, Babajide O, Andreasen L, Astrup A, Åsvold BO, Bandinelli S, Beekman M, Beilby JP, Bork-Jensen J, Boutin T, Brody JA, Brown SJ, Brumpton B, Campbell PJ, Cappola AR, Ceresini G, Chaker L, Chasman DI, Concas MP, Coutinho de Almeida R, Cross SM, Cucca F, Deary IJ, Kjaergaard AD, Echouffo Tcheugui JB, Ellervik C, Eriksson JG, Ferrucci L, Freudenberg J; GHS DiscovEHR; Regeneron Genetics Center; Fuchsberger C, Gieger C, Giulianini F, Gögele M, Graham SE, Grarup N, Gunjača I, Hansen T, Harding BN, Harris SE, Haunsø S, Hayward C, Hui J, Ittermann T, Jukema JW, Kajantie E, Kanters JK, Kårhus LL, Kiemeney LALM, Kloppenburg M, Kühnel B, Lahti J, Langenberg C, Lapauw B, Leese G, Li S, Liewald DCM, Linneberg A, Lominchar JVT, Luan J, Martin NG, Matana A, Meima ME, Meitinger T, Meulenbelt I, Mitchell BD, Møllehave LT, Mora S, Naitza S, Nauck M, Netea-Maier RT, Noordam R, Nursyifa C, Okada Y, Onano S, Papadopoulou A, Palmer CNA, Pattaro C, Pedersen O, Peters A, Pietzner M, Polašek O, Pramstaller PP, Psaty BM, Punda A, Ray D, Redmond P, Richards JB, Ridker PM, Russ TC, Ryan KA, Olesen MS, Schultheiss UT, Sel… See abstract for full author list ➔ Sterenborg RBTM, et al. Among authors: haunso s. Nat Commun. 2024 Jan 30;15(1):888. doi: 10.1038/s41467-024-44701-9. Nat Commun. 2024. PMID: 38291025 Free PMC article.
Genetic Variants Close to TTN, NKX2-5, and MYH6 Associate With AVNRT.
Andreasen L, Ahlberg G, Ægisdottir HM, Sveinbjörnsson G, Lundegaard PR, Hartmann JP, Paludan-Müller C, Hadji-Turdeghal K, Ghouse J, Pehrson S, Jensen HK, Riahi S, Hansen J, Sandgaard N, Sørensen E, Banasik K, Sækmose SG, Bruun MT, Hjalgrim H, Erikstrup C, Pedersen OB, Wittig M, Haunsø S, Ostrowski SR; DBDS Genomic Consortium; Franke A, Brunak S, Kanters JK, Ellervik C, Bundgaard H, Ullum H, Gudbjartsson DF, Thorsteinsdottir U, Holm H, Arnar DO, Stefansson K, Svendsen JH, Olesen MS. Andreasen L, et al. Among authors: haunso s. Circ Res. 2022 Oct 28;131(10):862-865. doi: 10.1161/CIRCRESAHA.122.321556. Epub 2022 Oct 7. Circ Res. 2022. PMID: 36205134 No abstract available.
Whole-Exome Sequencing Implicates Neuronal Calcium Channel with Familial Atrial Fibrillation.
Vad OB, Yan Y, Denti F, Ahlberg G, Refsgaard L, Bomholtz SH, Santos JL, Rasmussen S, Haunsø S, Svendsen JH, Christophersen IE, Schmitt N, Olesen MS, Bentzen BH. Vad OB, et al. Among authors: haunso s. Front Genet. 2022 Jan 28;13:806429. doi: 10.3389/fgene.2022.806429. eCollection 2022. Front Genet. 2022. PMID: 35154276 Free PMC article.
Associations between common ECG abnormalities and out-of-hospital cardiac arrest.
Søndergaard MM, Nielsen JB, Mortensen RN, Gislason G, Køber L, Lippert F, Graff C, Haunsø S, Svendsen JH, Kragholm KH, Pietersen AH, Lind BS, Hjortshøj SP, Holst AG, Struijk JJ, Torp-Pedersen C, Hansen SM. Søndergaard MM, et al. Among authors: haunso s. Open Heart. 2019 May 21;6(1):e000905. doi: 10.1136/openhrt-2018-000905. eCollection 2019. Open Heart. 2019. PMID: 31217990 Free PMC article.
Genetic variants on chromosomes 7p31 and 12p12 are associated with abnormal atrial electrical activation in patients with early-onset lone atrial fibrillation.
Seifert MB, Olesen MS, Christophersen IE, Nielsen JB, Carlson J, Holmqvist F, Tveit A, Haunsø S, Svendsen JH, Platonov PG. Seifert MB, et al. Among authors: haunso s. Ann Noninvasive Electrocardiol. 2019 Nov;24(6):e12661. doi: 10.1111/anec.12661. Epub 2019 Jun 1. Ann Noninvasive Electrocardiol. 2019. PMID: 31152482 Free PMC article.
150 results