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

Ralph McGinnis; Valgerður Steinthórsdóttir; Nicholas Williams; Guðmar Þorleifsson; Scott Shooter; Sigrun Hjartardottir; Suzannah Bumpstead; Lilja Stefánsdóttir; Lucy Hildyard; Jon K. Sigurdsson; John P. Kemp; Gabriela B. Silva; Liv Cecilie Vestrheim Thomsen; Tiina Jääskeläinen; Eero Kajantie; Sally Chappell; Noor Kalsheker; Ashley Moffett; Susan E. Hiby; Wai Lee; Sandosh Padmanabhan; Nigel Simpson; Vivien A. Dolby; Eleonora Staines-Urias; Stephanie M. Engel; A. Haugan; Lill Trogstad; Gulnara Svyatova; Nodira Zakhidova; Dilbar Najmutdinova; Anna F. Dominiczak; Håkon K. Gjessing; Juan P. Casas; Frank Dudbridge; James J. Walker; Fiona Broughton Pipkin; Unnur Þorsteinsdóttir; Reynir Tómas Geirsson; Debbie A. Lawlor; Ann‐Charlotte Iversen; Per Magnus; Hannele Laivuori; Kāri Stefánsson; Linda Morgan

doi:10.1038/ng.3895

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

Ralph McGinnis(Wellcome Sanger Institute), Valgerður Steinthórsdóttir(deCODE Genetics (Iceland)), Nicholas Williams(Wellcome Sanger Institute), Guðmar Þorleifsson(deCODE Genetics (Iceland)), Scott Shooter(Wellcome Sanger Institute), Sigrun Hjartardottir(Reykjavík University), Suzannah Bumpstead(Wellcome Sanger Institute), Lilja Stefánsdóttir(deCODE Genetics (Iceland)), Lucy Hildyard(Wellcome Sanger Institute), Jon K. Sigurdsson(deCODE Genetics (Iceland)), John P. Kemp(Translational Research Institute), Gabriela B. Silva(Norwegian University of Science and Technology), Liv Cecilie Vestrheim Thomsen(Norwegian University of Science and Technology), Tiina Jääskeläinen(University of Helsinki), Eero Kajantie(University of Helsinki), Sally Chappell(University of Nottingham), Noor Kalsheker(University of Nottingham), Ashley Moffett(University of Cambridge), Susan E. Hiby(University of Cambridge), Wai Lee(University of Glasgow), Sandosh Padmanabhan(University of Glasgow), Nigel Simpson(University of Leeds), Vivien A. Dolby(University of Leeds), Eleonora Staines-Urias(Nuffield Orthopaedic Centre), Stephanie M. Engel(University of North Carolina at Chapel Hill), A. Haugan(Norwegian Institute of Public Health), Lill Trogstad(Norwegian Institute of Public Health), Gulnara Svyatova(Kazakh Institute of Oncology and Radiology), Nodira Zakhidova(Academy of Sciences Republic of Uzbekistan), Dilbar Najmutdinova(Tashkent Pediatric Medical Institute), Anna F. Dominiczak(University of Glasgow), Håkon K. Gjessing(Norwegian Institute of Public Health), Juan P. Casas(Farr Institute), Frank Dudbridge(London School of Hygiene & Tropical Medicine), James J. Walker(University of Leeds), Fiona Broughton Pipkin(University of Nottingham), Unnur Þorsteinsdóttir(deCODE Genetics (Iceland)), Reynir Tómas Geirsson(Reykjavík University), Debbie A. Lawlor(University of Bristol), Ann‐Charlotte Iversen(Norwegian University of Science and Technology), Per Magnus(Norwegian Institute of Public Health), Hannele Laivuori(University of Helsinki), Kāri Stefánsson(deCODE Genetics (Iceland)), Linda Morgan(University of Nottingham)

Nature Genetics

June 19, 2017

10.1038/ng.3895

Cited by 261Open Access

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