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

Year Number of Results
1996 1
1998 2
1999 1
2000 1
2002 3
2003 3
2004 3
2008 3
2009 3
2010 8
2011 6
2012 3
2013 4
2014 4
2015 6
2016 2
2017 3
2018 5
2019 6
2020 4
2021 2
2022 2
2023 1
2024 0

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PubMed for id: 27445

67 results

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Page 1
Genome-Wide Significance for PCLO as a Gene for Major Depressive Disorder.
Mbarek H, Milaneschi Y, Hottenga JJ, Ligthart L, de Geus EJC, Ehli EA, Willemsen G, Davies GE, Smit JH, Boomsma DI, Penninx BWJH. Mbarek H, et al. Twin Res Hum Genet. 2017 Aug;20(4):267-270. doi: 10.1017/thg.2017.30. Epub 2017 May 25. Twin Res Hum Genet. 2017. PMID: 28540843
Loss of PCLO function underlies pontocerebellar hypoplasia type III.
Ahmed MY, Chioza BA, Rajab A, Schmitz-Abe K, Al-Khayat A, Al-Turki S, Baple EL, Patton MA, Al-Memar AY, Hurles ME, Partlow JN, Hill RS, Evrony GD, Servattalab S, Markianos K, Walsh CA, Crosby AH, Mochida GH. Ahmed MY, et al. Neurology. 2015 Apr 28;84(17):1745-50. doi: 10.1212/WNL.0000000000001523. Epub 2015 Apr 1. Neurology. 2015. PMID: 25832664 Free PMC article.
The Piccolo Intronic Single Nucleotide Polymorphism rs13438494 Regulates Dopamine and Serotonin Uptake and Shows Associations with Dependence-Like Behavior in Genomic Association Study.
Uno K, Nishizawa D, Seo S, Takayama K, Matsumura S, Sakai N, Ohi K, Nabeshima T, Hashimoto R, Ozaki N, Hasegawa J, Sato N, Tanioka F, Sugimura H, Fukuda KI, Higuchi S, Ujike H, Inada T, Iwata N, Sora I, Iyo M, Kondo N, Won MJ, Naruse N, Uehara-Aoyama K, Itokawa M, Yamada M, Ikeda K, Miyamoto Y, Nitta A. Uno K, et al. Curr Mol Med. 2015;15(3):265-74. doi: 10.2174/1566524015666150330145722. Curr Mol Med. 2015. PMID: 25817861
67 results