Genomics

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Preeclampsia InterPregGen Consortium: GWAS meta-analysis summary statistics for European fetal preeclampsia cases versus controls and GWAS genotype data for European fetal preeclampsia cases


ABSTRACT: Preeclampsia (PE) is a syndrome affecting pregnant mothers and fetus/babies characterised by hypertension and proteinuria, and is a leading cause of maternal and fetal death and of premature births worldwide. The InterPregGen Consortium was funded by a European Framework 7 (FP7) grant and grew out of the WTCCC3 GWAS comparing ~2000 UK PE mothers with ~6000 common UK controls. The EGAS00001001048 study is a GWAS meta-analysis of UK and Icelandic PE fetal (baby) cases versus controls and is one component of the InterPregGen FP7 project.

PROVIDER: EGAS00001001048 | EGA |

REPOSITORIES: EGA

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Publications

Variants in the fetal genome near FLT1 are associated with risk of preeclampsia.

McGinnis Ralph R   Steinthorsdottir Valgerdur V   Williams Nicholas O NO   Thorleifsson Gudmar G   Shooter Scott S   Hjartardottir Sigrun S   Bumpstead Suzannah S   Stefansdottir Lilja L   Hildyard Lucy L   Sigurdsson Jon K JK   Kemp John P JP   Silva Gabriela B GB   Thomsen Liv Cecilie V LCV   Jääskeläinen Tiina T   Kajantie Eero E   Chappell Sally S   Kalsheker Noor N   Moffett Ashley A   Hiby Susan S   Lee Wai Kwong WK   Padmanabhan Sandosh S   Simpson Nigel A B NAB   Dolby Vivien A VA   Staines-Urias Eleonora E   Engel Stephanie M SM   Haugan Anita A   Trogstad Lill L   Svyatova Gulnara G   Zakhidova Nodira N   Najmutdinova Dilbar D   Dominiczak Anna F AF   Gjessing Håkon K HK   Casas Juan P JP   Dudbridge Frank F   Walker James J JJ   Pipkin Fiona Broughton FB   Thorsteinsdottir Unnur U   Geirsson Reynir T RT   Lawlor Debbie A DA   Iversen Ann-Charlotte AC   Magnus Per P   Laivuori Hannele H   Stefansson Kari K   Morgan Linda L  

Nature genetics 20170619 8


Preeclampsia, which affects approximately 5% of pregnancies, is a leading cause of maternal and perinatal death. The causes of preeclampsia remain unclear, but there is evidence for inherited susceptibility. Genome-wide association studies (GWAS) have not identified maternal sequence variants of genome-wide significance that replicate in independent data sets. We report the first GWAS of offspring from preeclamptic pregnancies and discovery of the first genome-wide significant susceptibility loc  ...[more]

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