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

Year Number of Results
1999 2
2002 1
2004 2
2005 2
2006 1
2007 2
2008 1
2009 2
2010 1
2011 5
2012 5
2013 2
2014 3
2015 5
2016 2
2017 2
2018 2
2019 1
2020 1
2023 1
2024 0

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36 results

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Page 1
Multiple epiphyseal dysplasia.
Dahlqvist J, Orlén H, Matsson H, Dahl N, Lönnerholm T, Gustavson KH. Dahlqvist J, et al. Among authors: matsson h. Acta Orthop. 2009 Dec;80(6):711-5. doi: 10.3109/17453670903473032. Acta Orthop. 2009. PMID: 19995321 Free PMC article.
Human ROBO1 regulates white matter structure in corpus callosum.
Darki F, Massinen S, Salmela E, Matsson H, Peyrard-Janvid M, Klingberg T, Kere J. Darki F, et al. Among authors: matsson h. Brain Struct Funct. 2017 Mar;222(2):707-716. doi: 10.1007/s00429-016-1240-y. Epub 2016 May 30. Brain Struct Funct. 2017. PMID: 27240594 Free PMC article.
Identification of NCAN as a candidate gene for developmental dyslexia.
Einarsdottir E, Peyrard-Janvid M, Darki F, Tuulari JJ, Merisaari H, Karlsson L, Scheinin NM, Saunavaara J, Parkkola R, Kantojärvi K, Ämmälä AJ, Yiu-Lin Yu N, Matsson H, Nopola-Hemmi J, Karlsson H, Paunio T, Klingberg T, Leinonen E, Kere J. Einarsdottir E, et al. Among authors: matsson h. Sci Rep. 2017 Aug 24;7(1):9294. doi: 10.1038/s41598-017-10175-7. Sci Rep. 2017. PMID: 28839234 Free PMC article.
Polymorphisms in DCDC2 and S100B associate with developmental dyslexia.
Matsson H, Huss M, Persson H, Einarsdottir E, Tiraboschi E, Nopola-Hemmi J, Schumacher J, Neuhoff N, Warnke A, Lyytinen H, Schulte-Körne G, Nöthen MM, Leppänen PH, Peyrard-Janvid M, Kere J. Matsson H, et al. J Hum Genet. 2015 Jul;60(7):399-401. doi: 10.1038/jhg.2015.37. Epub 2015 Apr 16. J Hum Genet. 2015. PMID: 25877001 Free PMC article.
Alpha-cardiac actin mutations produce atrial septal defects.
Matsson H, Eason J, Bookwalter CS, Klar J, Gustavsson P, Sunnegårdh J, Enell H, Jonzon A, Vikkula M, Gutierrez I, Granados-Riveron J, Pope M, Bu'Lock F, Cox J, Robinson TE, Song F, Brook DJ, Marston S, Trybus KM, Dahl N. Matsson H, et al. Hum Mol Genet. 2008 Jan 15;17(2):256-65. doi: 10.1093/hmg/ddm302. Epub 2007 Oct 18. Hum Mol Genet. 2008. PMID: 17947298
Variant Profiling of Candidate Genes in Pancreatic Ductal Adenocarcinoma.
Huang J, Löhr JM, Nilsson M, Segersvärd R, Matsson H, Verbeke C, Heuchel R, Kere J, Iafrate AJ, Zheng Z, Ye W. Huang J, et al. Among authors: matsson h. Clin Chem. 2015 Nov;61(11):1408-16. doi: 10.1373/clinchem.2015.238543. Epub 2015 Sep 16. Clin Chem. 2015. PMID: 26378065
Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis.
Fadista J, Skotte L, Geller F, Bybjerg-Grauholm J, Gørtz S, Romitti PA, Caggana M, Kay DM, Matsson H, Boyd HA, Hougaard DM, Nordenskjöld A, Mills JL, Melbye M, Feenstra B. Fadista J, et al. Among authors: matsson h. Hum Mol Genet. 2019 Jan 15;28(2):332-340. doi: 10.1093/hmg/ddy347. Hum Mol Genet. 2019. PMID: 30281099 Free PMC article.
Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus.
Fadista J, Lund M, Skotte L, Geller F, Nandakumar P, Chatterjee S, Matsson H, Granström AL, Wester T, Salo P, Virtanen V, Carstensen L, Bybjerg-Grauholm J, Hougaard DM, Pakarinen M, Perola M, Nordenskjöld A, Chakravarti A, Melbye M, Feenstra B. Fadista J, et al. Among authors: matsson h. Eur J Hum Genet. 2018 Apr;26(4):561-569. doi: 10.1038/s41431-017-0053-7. Epub 2018 Jan 29. Eur J Hum Genet. 2018. PMID: 29379196 Free PMC article.
36 results