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Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss.
Am J Hum Genet. 2022 Jun 2;109(6):1077-1091. doi: 10.1016/j.ajhg.2022.04.010. Epub 2022 May 16.
Am J Hum Genet. 2022.
PMID: 35580588
Free PMC article.
Challenging Occam's Razor: Dual Molecular Diagnoses Explain Entangled Clinical Pictures.
Spedicati B, Morgan A, Pianigiani G, Musante L, Rubinato E, Santin A, Nardone GG, Faletra F, Girotto G.
Spedicati B, et al. Among authors: nardone gg.
Genes (Basel). 2022 Nov 3;13(11):2023. doi: 10.3390/genes13112023.
Genes (Basel). 2022.
PMID: 36360260
Free PMC article.
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Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis.
Kanoni S, Graham SE, Wang Y, Surakka I, Ramdas S, Zhu X, Clarke SL, Bhatti KF, Vedantam S, Winkler TW, Locke AE, Marouli E, Zajac GJM, Wu KH, Ntalla I, Hui Q, Klarin D, Hilliard AT, Wang Z, Xue C, Thorleifsson G, Helgadottir A, Gudbjartsson DF, Holm H, Olafsson I, Hwang MY, Han S, Akiyama M, Sakaue S, Terao C, Kanai M, Zhou W, Brumpton BM, Rasheed H, Havulinna AS, Veturi Y, Pacheco JA, Rosenthal EA, Lingren T, Feng Q, Kullo IJ, Narita A, Takayama J, Martin HC, Hunt KA, Trivedi B, Haessler J, Giulianini F, Bradford Y, Miller JE, Campbell A, Lin K, Millwood IY, Rasheed A, Hindy G, Faul JD, Zhao W, Weir DR, Turman C, Huang H, Graff M, Choudhury A, Sengupta D, Mahajan A, Brown MR, Zhang W, Yu K, Schmidt EM, Pandit A, Gustafsson S, Yin X, Luan J, Zhao JH, Matsuda F, Jang HM, Yoon K, Medina-Gomez C, Pitsillides A, Hottenga JJ, Wood AR, Ji Y, Gao Z, Haworth S, Yousri NA, Mitchell RE, Chai JF, Aadahl M, Bjerregaard AA, Yao J, Manichaikul A, Hwu CM, Hung YJ, Warren HR, Ramirez J, Bork-Jensen J, Kårhus LL, Goel A, Sabater-Lleal M, Noordam R, Mauro P, Matteo F, McDaid AF, Marques-Vidal P, Wielscher M, Trompet S, Sattar N, Møllehave LT, Munz M, Zeng L, Huang J, Yang B, Poveda A, Kurbasic A, L…
See abstract for full author list ➔
Kanoni S, et al. Among authors: nardone gg.
Genome Biol. 2022 Dec 27;23(1):268. doi: 10.1186/s13059-022-02837-1.
Genome Biol. 2022.
PMID: 36575460
Free PMC article.
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The Enigmatic Genetic Landscape of Hereditary Hearing Loss: A Multistep Diagnostic Strategy in the Italian Population.
Spedicati B, Santin A, Nardone GG, Rubinato E, Lenarduzzi S, Graziano C, Garavelli L, Miccoli S, Bigoni S, Morgan A, Girotto G.
Spedicati B, et al. Among authors: nardone gg.
Biomedicines. 2023 Feb 24;11(3):703. doi: 10.3390/biomedicines11030703.
Biomedicines. 2023.
PMID: 36979683
Free PMC article.
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Identifying missing pieces in color vision defects: a genome-wide association study in Silk Road populations.
Nardone GG, Spedicati B, Concas MP, Santin A, Morgan A, Mazzetto L, Battaglia-Parodi M, Girotto G.
Nardone GG, et al.
Front Genet. 2023 Jun 9;14:1161696. doi: 10.3389/fgene.2023.1161696. eCollection 2023.
Front Genet. 2023.
PMID: 37359372
Free PMC article.
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Puzzling Out the Genetic Architecture of Endometriosis: Whole-Exome Sequencing and Novel Candidate Gene Identification in a Deeply Clinically Characterised Cohort.
Santin A, Spedicati B, Morgan A, Lenarduzzi S, Tesolin P, Nardone GG, Mazzà D, Di Lorenzo G, Romano F, Buonomo F, Mangogna A, Concas MP, Zito G, Ricci G, Girotto G.
Santin A, et al. Among authors: nardone gg.
Biomedicines. 2023 Jul 27;11(8):2122. doi: 10.3390/biomedicines11082122.
Biomedicines. 2023.
PMID: 37626618
Free PMC article.
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The Bittersweet Symphony of COVID-19: Associations between TAS1Rs and TAS2R38 Genetic Variations and COVID-19 Symptoms.
Santin A, Spedicati B, Pecori A, Nardone GG, Concas MP, Piatti G, Menini A, Tirelli G, Boscolo-Rizzo P, Girotto G.
Santin A, et al. Among authors: nardone gg.
Life (Basel). 2024 Feb 3;14(2):219. doi: 10.3390/life14020219.
Life (Basel). 2024.
PMID: 38398728
Free PMC article.
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