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44 ta ish

Ish: 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

    Maqola20127 iqtibos
    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

    MaqolaOchiq kirish20075 iqtibos
    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

    Maqola20014 iqtibos
    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

    Maqola20043 iqtibos
    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

    Sharh maqolaOchiq kirish20013 iqtibos
    ABI

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

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

    MaqolaOchiq kirish19983 iqtibos
    ABI

  7. The Future of Genetic Studies of Complex Human Diseases

    Neil Risch, Kathleen R. Merikangas

    Maqola19962 iqtibos
    ABI

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

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

    Maqola20042 iqtibos
    ABI

  9. Genotype imputation for genome-wide association studies

    Jonathan Marchini, Bryan Howie

    Sharh maqola20102 iqtibos
    ABI

  10. 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

    MaqolaOchiq kirish20032 iqtibos
    ABI

  11. The Global Impact of Pre-eclampsia and Eclampsia

    Lelia Duley

    Sharh maqola20092 iqtibos
    ABI

  12. Parental origin of sequence variants associated with complex diseases

    Augustine Kong, Valgerður Steinthórsdóttir, Gísli Másson +26

    MaqolaOchiq kirish20092 iqtibos
    ABI

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

    T. G. Consortium

    Maqola20072 iqtibos
    ABI

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

    David M Altshuler, David Altshuler, Leena Peltonen +80

    MaqolaOchiq kirish20102 iqtibos
    ABI

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

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

    Maqola20112 iqtibos
    ABI

  16. Finding the missing heritability of complex diseases

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

    Sharh maqola20092 iqtibos
    ABI

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  19. Sarlavhasiz

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  20. 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

    Maqola20032 iqtibos
    ABI

  21. Sarlavhasiz

    Boshqa1 iqtibos
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  22. Sarlavhasiz

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  23. Sarlavhasiz

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  24. Sarlavhasiz

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  25. Sarlavhasiz

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