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

Year Number of Results
1995 1
1996 1
1997 1
1998 2
1999 1
2000 1
2001 2
2002 4
2003 4
2004 3
2005 1
2006 4
2008 4
2009 7
2010 2
2011 3
2012 3
2014 1
2017 2
2018 1
2020 1
2021 2
2022 0
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46 results
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Page 1
Genetic background of ataxia in children younger than 5 years in Finland.
Ignatius E, Isohanni P, Pohjanpelto M, Lahermo P, Ojanen S, Brilhante V, Palin E, Suomalainen A, Lönnqvist T, Carroll CJ. Ignatius E, et al. Among authors: lahermo p. Neurol Genet. 2020 Jun 5;6(4):e444. doi: 10.1212/NXG.0000000000000444. eCollection 2020 Aug. Neurol Genet. 2020. PMID: 32637629 Free PMC article.
Missense mutations in small muscle protein X-linked (SMPX) cause distal myopathy with protein inclusions.
Johari M, Sarparanta J, Vihola A, Jonson PH, Savarese M, Jokela M, Torella A, Piluso G, Said E, Vella N, Cauchi M, Magot A, Magri F, Mauri E, Kornblum C, Reimann J, Stojkovic T, Romero NB, Luque H, Huovinen S, Lahermo P, Donner K, Comi GP, Nigro V, Hackman P, Udd B. Johari M, et al. Among authors: lahermo p. Acta Neuropathol. 2021 Aug;142(2):375-393. doi: 10.1007/s00401-021-02319-x. Epub 2021 May 11. Acta Neuropathol. 2021. PMID: 33974137 Free PMC article.
Dominant Distal Myopathy 3 (MPD3) Caused by a Deletion in the HNRNPA1 Gene.
Hackman P, Rusanen SM, Johari M, Vihola A, Jonson PH, Sarparanta J, Donner K, Lahermo P, Koivunen S, Luque H, Soininen M, Mahjneh I, Auranen M, Arumilli M, Savarese M, Udd B. Hackman P, et al. Among authors: lahermo p. Neurol Genet. 2021 Oct 27;7(6):e632. doi: 10.1212/NXG.0000000000000632. eCollection 2021 Dec. Neurol Genet. 2021. PMID: 34722876 Free PMC article.
Association between genes of Disrupted in schizophrenia 1 (DISC1) interactors and schizophrenia supports the role of the DISC1 pathway in the etiology of major mental illnesses.
Tomppo L, Hennah W, Lahermo P, Loukola A, Tuulio-Henriksson A, Suvisaari J, Partonen T, Ekelund J, Lönnqvist J, Peltonen L. Tomppo L, et al. Among authors: lahermo p. Biol Psychiatry. 2009 Jun 15;65(12):1055-62. doi: 10.1016/j.biopsych.2009.01.014. Epub 2009 Feb 28. Biol Psychiatry. 2009. PMID: 19251251 Free PMC article.
Migration waves to the Baltic Sea region.
Lappalainen T, Laitinen V, Salmela E, Andersen P, Huoponen K, Savontaus ML, Lahermo P. Lappalainen T, et al. Among authors: lahermo p. Ann Hum Genet. 2008 May;72(Pt 3):337-48. doi: 10.1111/j.1469-1809.2007.00429.x. Epub 2008 Feb 19. Ann Hum Genet. 2008. PMID: 18294359 Free article.
Regional differences among the Finns: a Y-chromosomal perspective.
Lappalainen T, Koivumäki S, Salmela E, Huoponen K, Sistonen P, Savontaus ML, Lahermo P. Lappalainen T, et al. Among authors: lahermo p. Gene. 2006 Jul 19;376(2):207-15. doi: 10.1016/j.gene.2006.03.004. Epub 2006 Mar 18. Gene. 2006. PMID: 16644145
Methylation of H19 and its imprinted control region (H19 ICR1) in Müllerian aplasia.
Sandbacka M, Bruce S, Halttunen M, Puhakka M, Lahermo P, Hannula-Jouppi K, Lipsanen-Nyman M, Kere J, Aittomäki K, Laivuori H. Sandbacka M, et al. Among authors: lahermo p. Fertil Steril. 2011 Jun 30;95(8):2703-6. doi: 10.1016/j.fertnstert.2011.03.019. Epub 2011 Apr 2. Fertil Steril. 2011. PMID: 21458801
A quality assessment survey of SNP genotyping laboratories.
Lahermo P, Liljedahl U, Alnaes G, Axelsson T, Brookes AJ, Ellonen P, Groop PH, Halldén C, Holmberg D, Holmberg K, Keinänen M, Kepp K, Kere J, Kiviluoma P, Kristensen V, Lindgren C, Odeberg J, Osterman P, Parkkonen M, Saarela J, Sterner M, Strömqvist L, Talas U, Wessman M, Palotie A, Syvänen AC. Lahermo P, et al. Hum Mutat. 2006 Jul;27(7):711-4. doi: 10.1002/humu.20346. Hum Mutat. 2006. PMID: 16786507
46 results