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

Year Number of Results
2007 1
2009 2
2010 5
2011 4
2012 3
2013 1
2014 2
2015 5
2016 5
2019 1
2020 2
2021 4
2023 1
2024 0

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PubMed (GeneRIF) for id: 57153

28 results

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Page 1
Lack of the human choline transporter-like protein SLC44A2 causes hearing impairment and a rare red blood phenotype.
Koehl B, Vrignaud C, Mikdar M, Nair TS, Yang L, Landry S, Laiguillon G, Giroux-Lathuile C, Anselme-Martin S, El Kenz H, Hermine O, Mohandas N, Cartron JP, Colin Y, Detante O, Marlu R, Le Van Kim C, Carey TE, Azouzi S, Peyrard T. Koehl B, et al. EMBO Mol Med. 2023 Mar 8;15(3):e16320. doi: 10.15252/emmm.202216320. Epub 2023 Jan 25. EMBO Mol Med. 2023. PMID: 36695047 Free PMC article.
Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis.
Hinds DA, Buil A, Ziemek D, Martinez-Perez A, Malik R, Folkersen L, Germain M, Mälarstig A, Brown A, Soria JM, Dichgans M, Bing N, Franco-Cereceda A, Souto JC, Dermitzakis ET, Hamsten A, Worrall BB, Tung JY; METASTROKE Consortium, INVENT Consortium; Sabater-Lleal M. Hinds DA, et al. Hum Mol Genet. 2016 May 1;25(9):1867-74. doi: 10.1093/hmg/ddw037. Epub 2016 Feb 9. Hum Mol Genet. 2016. PMID: 26908601 Free PMC article.
28 results