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44 та иш

Иш: InterPregGen:genetic studies of pre-eclampsia in three continents

  1. An integrated map of genetic variation from 1,092 human genomes

    Zamin Iqbal, Zamin Iqbal, Andy Rimmer +95

    Мақола20127 иқтибос
    ABI

  2. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

    Paul R. Burton, David G. Clayton, Lon R. Cardon +95

    Мақола20075 иқтибос
    ABI

  3. The Classification and Diagnosis of the Hypertensive Disorders of Pregnancy: Statement from the International Society for the Study of Hypertension in Pregnancy (ISSHP)

    Mark Brown, Marshall D. Lindheimer, Michael de Swiet +2

    Мақола20014 иқтибос
    ABI

  4. Maternal and fetal genetic factors account for most of familial aggregation of preeclampsia: A population‐based Swedish cohort study

    Sven Cnattingius, Marie Reilly, Yudi Pawitan +1

    Мақола20043 иқтибос
    ABI

  5. THE CLASSIFICATION AND DIAGNOSIS OF THE HYPERTENSIVE DISORDERS OF PREGNANCY: STATEMENT FROM THE INTERNATIONAL SOCIETY FOR THE STUDY OF HYPERTENSION IN PREGNANCY (ISSHP)

    Mark Brown, Marshall D. Lindheimer, Michael de Swiet +2

    Шарҳ мақола20013 иқтибос
    ABI

  6. The Future of Genetic Studies of Complex Human Diseases

    Neil Risch, Kathleen R. Merikangas

    Мақола19962 иқтибос
    ABI

  7. Paternity Change and the Recurrence Risk in Familial Hypertensive Disorder in Pregnancy

    Sigrun Hjartardottir, Björn Geir Leifsson, Reynir Tómas Geirsson +1

    Мақола20042 иқтибос
    ABI

  8. Genotype imputation for genome-wide association studies

    Jonathan Marchini, Bryan Howie

    Шарҳ мақола20102 иқтибос
    ABI

  9. Excess placental soluble fms-like tyrosine kinase 1 (sFlt1) may contribute to endothelial dysfunction, hypertension, and proteinuria in preeclampsia

    Sharon E. Maynard, Jiang-Yong Min, Jaime R. Merchan +10

    Мақола20032 иқтибос
    ABI

  10. Fetal and maternal contributions to risk of pre-eclampsia: population based study

    R. T. Lie, Svein Rasmussen, Helge Brunborg +3

    Мақола19982 иқтибос
    ABI

  11. The Global Impact of Pre-eclampsia and Eclampsia

    Lelia Duley

    Шарҳ мақола20092 иқтибос
    ABI

  12. Parental origin of sequence variants associated with complex diseases

    Augustine Kong, Valgerður Steinthórsdóttir, Gísli Másson +26

    Мақола20092 иқтибос
    ABI

  13. Babies, pre-eclamptic mothers and grandparents: a three-generation phenotyping study

    T. G. Consortium

    Мақола20072 иқтибос
    ABI

  14. Integrating common and rare genetic variation in diverse human populations

    David M Altshuler, David Altshuler, Leena Peltonen +80

    Мақола20102 иқтибос
    ABI

  15. Saving Mothers’ Lives: Reviewing maternal deaths to make motherhood safer: 2006–2008

    Roch Cantwell, T. H. Clutton-Brock, Griselda Cooper +23

    Мақола20112 иқтибос
    ABI

  16. Finding the missing heritability of complex diseases

    Teri A. Manolio, Francis S. Collins, Nancy J. Cox +24

    Шарҳ мақола20092 иқтибос
    ABI

  17. Excess placental soluble fms-like tyrosine kinase 1 (sFlt1) may contribute to endothelial dysfunction, hypertension, and proteinuria in preeclampsia

    Sharon E. Maynard, Jiangyong Min, Jaime R. Merchan +10

    Мақола20032 иқтибос
    ABI

  18. Сарлавҳасиз

    Бошқа1 иқтибос
    ABI

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    Бошқа1 иқтибос
    ABI

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    Бошқа1 иқтибос
    ABI

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    Бошқа1 иқтибос
    ABI

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    Бошқа1 иқтибос
    ABI

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    Бошқа1 иқтибос
    ABI

  24. Сарлавҳасиз

    Бошқа1 иқтибос
    ABI

  25. Сарлавҳасиз

    Бошқа1 иқтибос
    ABI