Systematic evaluation of environmental factors: Persistent pollutants and nutrients correlated with serum lipid levels

Autor: Butte, Atul, Patel, CJ, Cullen, MR, Ioannidis, JP, Butte, AJ

Publikováno v: Butte, Atul; Patel, CJ; Cullen, MR; Ioannidis, JP; & Butte, AJ. (2012). Systematic evaluation of environmental factors: Persistent pollutants and nutrients correlated with serum lipid levels. UC San Francisco: Retrieved from: http://www.escholarship.org/uc/item/69c6b27h

Background Both genetic and environmental factors contribute to triglyceride, low-density lipoprotein-cholesterol (LDL-C), and high-density lipoprotein-cholesterol (HDL-C) levels. Although genome-wide association studies are currently testing the gen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_______325::c16a92eebb46baedec6a911a7a713e32
http://www.escholarship.org/uc/item/69c6b27h

Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease

Autor: Sharma M, Maraganore DM, Ioannidis JP, Riess O, Aasly JO, Annesi G, Abahuni N, Bentivoglio AR, Brice A, Van Broeckhoven C, Chartier-Harlin MC, Destée A, Djarmati A, Elbaz A, Farrer M, Ferrarese C, Gibson JM, Gispert S, Hattori N, Jasinska-Myga B, Klein C

Publikováno v: Neurobiology of aging (2011).
info:cnr-pdr/source/autori:Sharma M, Maraganore DM, Ioannidis JP, Riess O, Aasly JO, Annesi G, Abahuni N, Bentivoglio AR, Brice A, Van Broeckhoven C, Chartier-Harlin MC, Destée A, Djarmati A, Elbaz A, Farrer M, Ferrarese C, Gibson JM, Gispert S, Hattori N, Jasinska-Myga B, Klein C,/titolo:Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease./doi:/rivista:Neurobiology of aging/anno:2011/pagina_da:/pagina_a:/intervallo_pagine:/volume

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::4696fa91ed3927ccf489b919483d5604
https://publications.cnr.it/doc/50352

EULAR recommendations for the management of Systemic Lupus Erytematosus (SLE) Report of a Task Force of the European Standing Committee for International Clinical Studies Including Therapeutics (ESCISIT)*

Autor: Bertsias, Gk, Ioannidis, Jp, Boletis, J, Bombardieri, Stefano, Cervera, R, Dostal, C, Font, J, Gilboe, Im, Houssiau, F, Huizinga, T, Isenberg, D, Kallenberg, Cg, Khamashta, M, Piette, Jc, Schneider, M, Smolen, J, Sturfelt, G, Tincani, A, VAN VOLLENHOVEN, R, Gordon, C, Boumpas, Dt

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od______3728::25b9a601f3640c9027ba43cc254a4013
http://hdl.handle.net/11568/117328

Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study

Autor: Elbaz A, Nelson LM, Payami H, Ioannidis JP, Fiske BK, Annesi G, Carmine Belin A, Factor SA, Ferrarese C, Hadjigeorgiou GM, Higgins DS, Kawakami H, Kruger R, Marder KS, Mayeux RP, Mellick GD, Nutt JG, Ritz B, Samii A, Tanner CM, Van Broeckhoven C, Van

Publikováno v: Lancet neurology
5 (2006): 917–923.
info:cnr-pdr/source/autori:Elbaz A, Nelson LM, Payami H, Ioannidis JP, Fiske BK, Annesi G, Carmine Belin A, Factor SA, Ferrarese C, Hadjigeorgiou GM, Higgins DS, Kawakami H, Kruger R, Marder KS, Mayeux RP, Mellick GD, Nutt JG, Ritz B, Samii A, Tanner CM, Van Broeckhoven C, Van/titolo:Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study/doi:/rivista:Lancet neurology (Print)/anno:2006/pagina_da:917/pagina_a:923/intervallo_pagine:917–923/volume:5

BACKGROUND: A genome-wide association study identified 13 single-nucleotide polymorphisms (SNPs) significantly associated with Parkinson's disease. Small-scale replication studies were largely non-confirmatory, but a meta-analysis that included data

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::ecc2957335a9b6d6a476d3d6a15b43e0
https://publications.cnr.it/doc/49998

Differential genetic effects of ESR1 gene polymorphisms on osteoporosis outcomes

Autor: Ioannidis, JP, Ralston, SH, Bennett, ST, Brandi, ML, Grinberg, D, Karassa, FB, Langdahl, B, van Meurs, Joyce, Mosekilde, L, Scollen, S, Albagha, OM, Bustamante, M, Carey, AH, Dunning, AM, Enjuanes, A, van Leeuwen, Hans, Mavilia, C, Masi, L, McGuigan, FEA, Nogues, X, Pols, Huib, Reid, DM, Schuit, Stephanie, Sherlock, RE, Uitterlinden, André

Publikováno v: JAMA-Journal of the American Medical Association, 292(17), 2105-2114. American Medical Association

CONTEXT: Both bone mineral density (BMD) and fracture risk have a strong genetic component. Estrogen receptor alpha (ESR1) is a candidate gene for osteoporosis, but previous studies of ESR1 polymorphisms in this field were hampered by small sample si

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::1e560447f7be182460908b607176acd8
https://pubmed.ncbi.nlm.nih.gov/15523071