نتائج البحث - "Nardone A."

المساهمون: Medicum, Institute for Molecular Medicine Finland, Complex Disease Genetics, Samuli Olli Ripatti / Principal Investigator, HUSLAB, Epigenetics of Complex Diseases and Traits, Department of Medicine, Helsinki University Hospital Area, Centre of Excellence in Complex Disease Genetics, Department of Public Health, Faculty Common Matters (Faculty of Social Sciences), Elisabeth Ingrid Maria Widen / Principal Investigator, Genomic Discoveries and Clinical Translation

مصطلحات موضوعية: Cholesterol, Genetics, Genome-wide association study, GWAS, Lipids, 1184 Genetics, developmental biology, physiology, 3142 Public health care science, environmental and occupational health, 3141 Health care science, 112 Statistics and probability

وصف الملف: application/pdf

العلاقة: GMP, PN, and CW are supported by NHLBI R01HL127564. GMP and PN are supported by R01HL142711. AG acknowledge support from the Wellcome Trust (201543/B/16/Z), European Union Seventh Framework Programme FP7/2007–2013 under grant agreement no. HEALTH-F2-2013–601456 (CVGenes@Target) & the TriPartite Immunometabolism Consortium [TrIC]-Novo Nordisk Foundation’s Grant number NNF15CC0018486. JMM is supported by American Diabetes Association Innovative and Clinical Translational Award 1–19-ICTS-068. SR was supported by the Academy of Finland Center of Excellence in Complex Disease Genetics (Grant No 312062), the Finnish Foundation for Cardiovascular Research, the Sigrid Juselius Foundation, and University of Helsinki HiLIFE Fellow and Grand Challenge grants. EW was supported by the Finnish innovation fund Sitra (EW) and Finska Läkaresällskapet. CNS was supported by American Heart Association Postdoctoral Fellowships 15POST24470131 and 17POST33650016. Charles N Rotimi is supported by Z01HG200362. Zhe Wang, Michael H Preuss, and Ruth JF Loos are supported by R01HL142302. NJT is a Wellcome Trust Investigator (202802/Z/16/Z), is the PI of the Avon Longitudinal Study of Parents and Children (MRC & WT 217065/Z/19/Z), is supported by the University of Bristol NIHR Biomedical Research Centre (BRC-1215–2001) and the MRC Integrative Epidemiology Unit (MC_UU_00011), and works within the CRUK Integrative Cancer Epidemiology Programme (C18281/A19169). Ruth E Mitchell is a member of the MRC Integrative Epidemiology Unit at the University of Bristol funded by the MRC (MC_UU_00011/1). Simon Haworth is supported by the UK National Institute for Health Research Academic Clinical Fellowship. Paul S. de Vries was supported by American Heart Association grant number 18CDA34110116. Julia Ramierz acknowledges support by the People Programme of the European Union’s Seventh Framework Programme grant n° 608765 and Marie Sklodowska-Curie grant n° 786833. Maria Sabater-Lleal is supported by a Miguel Servet contract from the ISCIII Spanish Health Institute (CP17/00142) and co-financed by the European Social Fund. Jian Yang is funded by the Westlake Education Foundation. Olga Giannakopoulou has received funding from the British Heart Foundation (BHF) (FS/14/66/3129). CHARGE Consortium cohorts were supported by R01HL105756. Study-specific acknowledgements are available in the Additional file : Supplementary Note. 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A P , Boehnke , M , Brown , C D , Natarajan , P , Deloukas , P , Willer , C J , Assimes , T L & Peloso , G M 2022 , ' Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis ' , Genome Biology , vol. 23 , no. 1 , 268 . https://doi.org/10.1186/s13059-022-02837-1Test; ORCID: /0000-0001-7870-070X/work/130600781; ORCID: /0000-0003-0542-5967/work/130601174; ORCID: /0000-0002-8773-7149/work/130605566; 85144774123; 73609295-cdc2-4438-a33f-d480ed37cb6d; http://hdl.handle.net/10138/355889Test

الإتاحة: http://hdl.handle.net/10138/355889Test

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7

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Identifying missing pieces in color vision defects: a genome-wide association study in Silk Road populations

المؤلفون: Nardone, Giuseppe Giovanni, Spedicati, Beatrice, Concas, Maria Pina, Santin, Aurora, Morgan, Anna, Mazzetto, Lorenzo, Battaglia-Parodi, Maurizio, Girotto, Giorgia

المساهمون: Ministero dell'Università e della Ricerca

المصدر: Frontiers in Genetics ; volume 14 ; ISSN 1664-8021

مصطلحات موضوعية: Genetics (clinical), Genetics, Molecular Medicine

الإتاحة: https://doi.org/10.3389/fgene.2023.1161696Test

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Female-Specific Association Between Variants on Chromosome 9 and Self-Reported Diagnosis of Irritable Bowel Syndrome

المصدر: Gastroenterology. 155(1)

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/625706n2Test

View record in eScholarship

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Sarcopenia and bone health: new acquisitions for a firm liaison

المؤلفون: Tarantino, Umberto, Greggi, Chiara, Visconti, Virginia Veronica, Cariati, Ida, Bonanni, Roberto, Gasperini, Beatrice, Nardone, Italo, Gasbarra, Elena, Iundusi, Riccardo

المساهمون: Tarantino, U, Greggi, C, Visconti, Vv, Cariati, I, Bonanni, R, Gasperini, B, Nardone, I, Gasbarra, E, Iundusi, R

مصطلحات موضوعية: bone–muscle crosstalk, genetics, osteoporosis, osteosarcopenia, sarcopenia, Settore MED/33 - MALATTIE APPARATO LOCOMOTORE

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/36465879; info:eu-repo/semantics/altIdentifier/wos/WOS:000928021600001; volume:14; firstpage:1; lastpage:14; numberofpages:14; journal:THERAPEUTIC ADVANCES IN MUSCULOSKELETAL DISEASE; https://hdl.handle.net/2108/329624Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85143291015

الإتاحة: https://doi.org/10.1177/1759720X221138354Test
https://hdl.handle.net/2108/329624Test

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Challenging Occam’s Razor: Dual Molecular Diagnoses Explain Entangled Clinical Pictures

المؤلفون: Beatrice Spedicati, Anna Morgan, Giulia Pianigiani, Luciana Musante, Elisa Rubinato, Aurora Santin, Giuseppe Giovanni Nardone, Flavio Faletra, Giorgia Girotto

المصدر: Genes, Vol 13, Iss 11, p 2023 (2022)

مصطلحات موضوعية: dual molecular diagnosis, multilocus genomic variation, whole exome sequencing, Genetics, QH426-470

وصف الملف: electronic resource

العلاقة: https://www.mdpi.com/2073-4425/13/11/2023Test; https://doaj.org/toc/2073-4425Test

الوصول الحر: https://doaj.org/article/bb855db63c164a25862519c3958679a0Test

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