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Search: WFRF:(Salazar Claudia) > (2016)

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  • Bentham, James, et al. (author)
  • A century of trends in adult human height
  • 2016
  • In: eLIFE. - : eLife Sciences Publications Ltd. - 2050-084X. ; 5
  • Journal article (peer-reviewed)abstract
    • Being taller is associated with enhanced longevity, and higher education and earnings. We reanalysed 1472 population-based studies, with measurement of height on more than 18.6 million participants to estimate mean height for people born between 1896 and 1996 in 200 countries. The largest gain in adult height over the past century has occurred in South Korean women and Iranian men, who became 20.2 cm (95% credible interval 17.5–22.7) and 16.5 cm (13.3– 19.7) taller, respectively. In contrast, there was little change in adult height in some sub-Saharan African countries and in South Asia over the century of analysis. The tallest people over these 100 years are men born in the Netherlands in the last quarter of 20th century, whose average heights surpassed 182.5 cm, and the shortest were women born in Guatemala in 1896 (140.3 cm; 135.8– 144.8). The height differential between the tallest and shortest populations was 19-20 cm a century ago, and has remained the same for women and increased for men a century later despite substantial changes in the ranking of countries.
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  • Jakobsdottir, Johanna, et al. (author)
  • Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease
  • 2016
  • In: PLOS Genetics. - : Public Library of Science (PLoS). - 1553-7390 .- 1553-7404. ; 12:10
  • Journal article (peer-reviewed)abstract
    • We performed an exome-wide association analysis in 1393 late-onset Alzheimer's disease (LOAD) cases and 8141 controls from the CHARGE consortium. We found that a rare variant (P155L) in TM2D3 was enriched in Icelanders (similar to 0.5% versus < 0.05% in other European populations). In 433 LOAD cases and 3903 controls from the Icelandic AGES substudy, P155L was associated with increased risk and earlier onset of LOAD [odds ratio (95% CI) = 7.5 (3.5-15.9), p = 6.6x10(-9)]. Mutation in the Drosophila TM2D3 homolog, almondex, causes a phenotype similar to loss of Notch/Presenilin signaling. Human TM2D3 is capable of rescuing these phenotypes, but this activity is abolished by P155L, establishing it as a functionally damaging allele. Our results establish a rare TM2D3 variant in association with LOAD susceptibility, and together with prior work suggests possible links to the beta-amyloid cascade.
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  • Result 1-4 of 4
Type of publication
journal article (4)
Type of content
peer-reviewed (4)
Author/Editor
Salomaa, Veikko (3)
Peeters, Petra H (2)
Overvad, Kim (2)
Kaaks, Rudolf (2)
Boeing, Heiner (2)
Trichopoulou, Antoni ... (2)
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Bueno-de-Mesquita, H ... (2)
Norat, Teresa (2)
Riboli, Elio (2)
Joffres, Michel (2)
McKee, Martin (2)
Lundqvist, Annamari (2)
Van Minh, Hoang (2)
Giwercman, Aleksande ... (2)
Wade, Alisha N. (2)
Cooper, Cyrus (2)
Hardy, Rebecca (2)
Sunyer, Jordi (2)
Brenner, Hermann (2)
Claessens, Frank (2)
Craig, Cora L. (2)
Sjostrom, Michael (2)
Adams, Robert (2)
Thijs, Lutgarde (2)
Staessen, Jan A (2)
Schutte, Aletta E. (2)
Björkelund, Cecilia, ... (2)
Farzadfar, Farshad (2)
Geleijnse, Johanna M ... (2)
Guessous, Idris (2)
Jonas, Jost B. (2)
Kasaeian, Amir (2)
Khader, Yousef Saleh (2)
Khang, Young-Ho (2)
Lotufo, Paulo A. (2)
Malekzadeh, Reza (2)
Mensink, Gert B. M. (2)
Mohan, Viswanathan (2)
Nagel, Gabriele (2)
Qorbani, Mostafa (2)
Rivera, Juan A. (2)
Sepanlou, Sadaf G. (2)
Szponar, Lucjan (2)
Alkerwi, Ala'a (2)
Bjertness, Espen (2)
Kengne, Andre P. (2)
McGarvey, Stephen T. (2)
Shiri, Rahman (2)
Topor-Madry, Roman (2)
Branca, Francesco (2)
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University
Umeå University (3)
Lund University (3)
University of Gothenburg (2)
Luleå University of Technology (2)
Uppsala University (1)
Stockholm University (1)
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Linköping University (1)
Karolinska Institutet (1)
Swedish University of Agricultural Sciences (1)
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Language
English (4)
Research subject (UKÄ/SCB)
Medical and Health Sciences (4)
Natural sciences (1)
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