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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2013 | 2 |
2014 | 2 |
2017 | 2 |
2018 | 2 |
2019 | 1 |
2020 | 1 |
2024 | 0 |
PubMed for id: 1677501750
7 results
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Page 1
Dysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndrome.
J Clin Invest. 2020 Aug 3;130(8):4423-4439. doi: 10.1172/JCI131656.
J Clin Invest. 2020.
PMID: 32453716
Free PMC article.
Association Study of ARMC9 Gene Variants with Vogt-Koyanagi-Harada Disease in Japanese Patients.
Ohno T, Meguro A, Takeuchi M, Yamane T, Teshigawara T, Kitaichi N, Horie Y, Namba K, Ohno S, Nakao K, Sakamoto T, Sakai T, Nakano T, Keino H, Okada AA, Takeda A, Fukuhara T, Mashimo H, Ohguro N, Oono S, Enaida H, Okinami S, Mizuki N.
Ohno T, et al.
Ocul Immunol Inflamm. 2019;27(5):699-705. doi: 10.1080/09273948.2018.1523438. Epub 2018 Nov 5.
Ocul Immunol Inflamm. 2019.
PMID: 30395750
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Whole exome sequencing reveals a mutation in ARMC9 as a cause of mental retardation, ptosis, and polydactyly.
Kar A, Phadke SR, Das Bhowmik A, Dalal A.
Kar A, et al.
Am J Med Genet A. 2018 Jan;176(1):34-40. doi: 10.1002/ajmg.a.38537. Epub 2017 Nov 21.
Am J Med Genet A. 2018.
PMID: 29159890
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Mutations in ARMC9, which Encodes a Basal Body Protein, Cause Joubert Syndrome in Humans and Ciliopathy Phenotypes in Zebrafish.
Van De Weghe JC, Rusterholz TDS, Latour B, Grout ME, Aldinger KA, Shaheen R, Dempsey JC, Maddirevula S, Cheng YH, Phelps IG, Gesemann M, Goel H, Birk OS, Alanzi T, Rawashdeh R, Khan AO; University of Washington Center for Mendelian Genomics; Bamshad MJ, Nickerson DA, Neuhauss SCF, Dobyns WB, Alkuraya FS, Roepman R, Bachmann-Gagescu R, Doherty D.
Van De Weghe JC, et al.
Am J Hum Genet. 2017 Jul 6;101(1):23-36. doi: 10.1016/j.ajhg.2017.05.010. Epub 2017 Jun 15.
Am J Hum Genet. 2017.
PMID: 28625504
Free PMC article.
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Genome-wide genetic and transcriptomic investigation of variation in antibody response to dietary antigens.
Rubicz R, Yolken R, Alaedini A, Drigalenko E, Charlesworth JC, Carless MA, Severance EG, Krivogorsky B, Dyer TD, Kent JW Jr, Curran JE, Johnson MP, Cole SA, Almasy L, Moses EK, Blangero J, Göring HH.
Rubicz R, et al.
Genet Epidemiol. 2014 Jul;38(5):439-46. doi: 10.1002/gepi.21817.
Genet Epidemiol. 2014.
PMID: 24962563
Free PMC article.
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Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk.
Chubb D, Weinhold N, Broderick P, Chen B, Johnson DC, Försti A, Vijayakrishnan J, Migliorini G, Dobbins SE, Holroyd A, Hose D, Walker BA, Davies FE, Gregory WA, Jackson GH, Irving JA, Pratt G, Fegan C, Fenton JA, Neben K, Hoffmann P, Nöthen MM, Mühleisen TW, Eisele L, Ross FM, Straka C, Einsele H, Langer C, Dörner E, Allan JM, Jauch A, Morgan GJ, Hemminki K, Houlston RS, Goldschmidt H.
Chubb D, et al.
Nat Genet. 2013 Oct;45(10):1221-1225. doi: 10.1038/ng.2733. Epub 2013 Aug 18.
Nat Genet. 2013.
PMID: 23955597
Free PMC article.
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Genome-wide association analyses suggest NELL1 influences adverse metabolic response to HCTZ in African Americans.
Del-Aguila JL, Beitelshees AL, Cooper-Dehoff RM, Chapman AB, Gums JG, Bailey K, Gong Y, Turner ST, Johnson JA, Boerwinkle E.
Del-Aguila JL, et al.
Pharmacogenomics J. 2014 Feb;14(1):35-40. doi: 10.1038/tpj.2013.3. Epub 2013 Feb 12.
Pharmacogenomics J. 2014.
PMID: 23400010
Free PMC article.
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