Understanding rare genetic variants within the terminal pathway of complement system in preeclampsia.

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Bibliographic Details
Title: Understanding rare genetic variants within the terminal pathway of complement system in preeclampsia.
Authors: Lokki AI; Translational Immunology Research Program, Research Programs Unit and Bacteriology and Immunology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland. inkeri.lokki@helsinki.fi.; Heart and Lung Center, Helsinki University Central Hospital and University of Helsinki, Helsinki, Finland. inkeri.lokki@helsinki.fi., Triebwasser M; Department of Pediatrics, Division of Pediatric Hematology and Oncology, University of Michigan, Ann Arbor, MI, USA., Daly E; Hospital and Harvard Medical School, Boston, MA, USA., Kurki MI; Institute for Molecular Medicine Finland, Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland.; Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA., Perola M; Department of Public Health and Welfare, National Institute for Health and Welfare, Helsinki, Finland., Auro K; Department of Public Health and Welfare, National Institute for Health and Welfare, Helsinki, Finland., Salmon JE; Hospital for Special Surgery; Weill Medical College of Cornell University, New York, NY, USA., Anuja J; Division of Nephrology, Department of Medicine, Washington University School of Medicine in St. Louis, St. Louis, MO, USA., Daly M; Institute for Molecular Medicine Finland, Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland.; Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA., Atkinson JP; Division of Rheumatology, Department of Medicine, Washington University School of Medicine, St. Louis, MO, USA., Laivuori H; Institute for Molecular Medicine Finland, Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland.; Medical and Clinical Genetics, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.; Department of Obstetrics and Gynecology, Tampere University Hospital and the Wellbeing Services County of Pirkanmaa, Tampere, Finland.; Center for Child, Adolescent, and Maternal Health Research, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland., Meri S; Translational Immunology Research Program, Research Programs Unit and Bacteriology and Immunology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland. seppo.meri@helsinki.fi.; HUSLAB Diagnostic Center, Helsinki University Central Hospital, Helsinki, Finland. seppo.meri@helsinki.fi.
Corporate Authors: FINNPEC Core Investigator Group
Source: Genes and immunity [Genes Immun] 2025 Feb; Vol. 26 (1), pp. 22-26. Date of Electronic Publication: 2024 Dec 17.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural
Journal Info: Publisher: Nature Pub. Group Country of Publication: England NLM ID: 100953417 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1476-5470 (Electronic) Linking ISSN: 14664879 NLM ISO Abbreviation: Genes Immun Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1476-5470
DOI:10.1038/s41435-024-00310-6