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9 result(s) for 'author#Veronique Vitart' within BMC

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  1. Myalgic encephalomyelitis / chronic fatigue syndrome (ME/CFS) is a common, long-term condition characterised by post-exertional malaise, often with fatigue that is not significantly relieved by rest. ME/CFS ha...

    Authors: Andy Devereux-Cooke, Sian Leary, Simon J. McGrath, Emma Northwood, Anna Redshaw, Charles Shepherd, Pippa Stacey, Claire Tripp, Jim Wilson, Margaret Mar, Danielle Boobyer, Sam Bromiley, Sonya Chowdhury, Claire Dransfield, Mohammed Almas, Øyvind Almelid…
    Citation: BMC Neurology 2022 22:269
    Content type: Study protocol Published on:

  2. Genome-wide homozygosity estimation from genomic data is becoming an increasingly interesting research topic. The aim of this study was to compare different methods for estimating individual homozygosity-by-de...

    Authors: Ozren Polašek, Caroline Hayward, Celine Bellenguez, Veronique Vitart, Ivana Kolčić, Ruth McQuillan, Vanja Saftić, Ulf Gyllensten, James F Wilson, Igor Rudan, Alan F Wright, Harry Campbell and Anne-Louise Leutenegger
    Citation: BMC Genomics 2010 11:139
    Content type: Research article Published on:

  3. The Generation Scotland: Scottish Family Health Study (GS:SFHS) is a family-based population cohort with DNA, biological samples, socio-demographic, psychological and clinical data from approximately 24,000 ad...

    Authors: Reka Nagy, Thibaud S. Boutin, Jonathan Marten, Jennifer E. Huffman, Shona M. Kerr, Archie Campbell, Louise Evenden, Jude Gibson, Carmen Amador, David M. Howard, Pau Navarro, Andrew Morris, Ian J. Deary, Lynne J. Hocking, Sandosh Padmanabhan, Blair H. Smith…
    Citation: Genome Medicine 2017 9:23
    Content type: Research Published on:

  4. The Generation Scotland Scottish Family Health Study (GS:SFHS) includes 23,960 participants from across Scotland with records for many health-related traits and environmental covariates. Genotypes at ~700 K SN...

    Authors: Carmen Amador, Jennifer Huffman, Holly Trochet, Archie Campbell, David Porteous, James F Wilson, Nick Hastie, Veronique Vitart, Caroline Hayward, Pau Navarro and Chris S Haley
    Citation: BMC Genomics 2015 16:437
    Content type: Research article Published on:

  5. Genetic variants within nearly 1000 loci are known to contribute to modulation of blood lipid levels. However, the biological pathways underlying these associations are frequently unknown, limiting understandi...

    Authors: Stavroula Kanoni, Sarah E. Graham, Yuxuan Wang, Ida Surakka, Shweta Ramdas, Xiang Zhu, Shoa L. Clarke, Konain Fatima Bhatti, Sailaja Vedantam, Thomas W. Winkler, Adam E. Locke, Eirini Marouli, Greg J. M. Zajac, Kuan-Han H. Wu, Ioanna Ntalla, Qin Hui…
    Citation: Genome Biology 2022 23:268
    Content type: Research Published on:

  6. Serum creatinine (SCR) is the most important biomarker for a quick and non-invasive assessment of kidney function in population-based surveys. A substantial proportion of the inter-individual variability in SCR l...

    Authors: Cristian Pattaro, Alessandro De Grandi, Veronique Vitart, Caroline Hayward, Andre Franke, Yurii S Aulchenko, Asa Johansson, Sarah H Wild, Scott A Melville, Aaron Isaacs, Ozren Polasek, David Ellinghaus, Ivana Kolcic, Ute Nöthlings, Lina Zgaga, Tatijana Zemunik…
    Citation: BMC Medical Genetics 2010 11:41
    Content type: Research article Published on:

  7. Associations between microvascular variation and chronic kidney disease (CKD) have been reported previously. Non-invasive retinal fundus imaging enables evaluation of the microvascular network and may offer in...

    Authors: Euan N. Paterson, Chris Cardwell, Thomas J. MacGillivray, Emanuele Trucco, Alexander S. Doney, Paul Foster, Alexander P. Maxwell and Gareth J. McKay
    Citation: BMC Nephrology 2021 22:72
    Content type: Research article Published on:

  8. Eye and hair colour is highly variable in the European population, and is largely genetically determined. Both linkage and association studies have previously been used to identify candidate genes underlying t...

    Authors: Jonas Mengel-From, Terence H Wong, Niels Morling, Jonathan L Rees and Ian J Jackson
    Citation: BMC Genetics 2009 10:88
    Content type: Research article Published on:

  9. Genome-wide association studies (GWAS) have identified many common single nucleotide polymorphisms (SNPs) that associate with clinical phenotypes, but these SNPs usually explain just a small part of the herita...

    Authors: Harish Dharuri, Peter Henneman, Ayse Demirkan, Jan Bert van Klinken, Dennis Owen Mook-Kanamori, Rui Wang-Sattler, Christian Gieger, Jerzy Adamski, Kristina Hettne, Marco Roos, Karsten Suhre, Cornelia M Van Duijn, Ko Willems van Dijk and Peter AC 't Hoen
    Citation: BMC Genomics 2013 14:865
    Content type: Research article Published on: