Genome-wide association study of bronchopulmonary dysplasia: a potential role for variants near the CRP gene.

Autor: Mahlman M; PEDEGO Research Unit, Medical Research Center Oulu, University of Oulu, Oulu, Finland. mari.mahlman@gmail.com.; Department of Children and Adolescents, Oulu University Hospital, Oulu, Finland. mari.mahlman@gmail.com., Karjalainen MK; PEDEGO Research Unit, Medical Research Center Oulu, University of Oulu, Oulu, Finland.; Department of Children and Adolescents, Oulu University Hospital, Oulu, Finland., Huusko JM; PEDEGO Research Unit, Medical Research Center Oulu, University of Oulu, Oulu, Finland.; Department of Children and Adolescents, Oulu University Hospital, Oulu, Finland.; Perinatal Institute, Cincinnati Children's Hospital Medical Center and Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA., Andersson S; Children's Hospital, University of Helsinki, and Helsinki University Hospital, Helsinki, Finland., Kari MA; Children's Hospital, University of Helsinki, and Helsinki University Hospital, Helsinki, Finland., Tammela OKT; Tampere University Hospital, Tampere University, and Center of Pediatric Child Health, Tampere, Finland., Sankilampi U; Department of Pediatrics, Kuopio University Hospital, Kuopio, Finland., Lehtonen L; Turku University Hospital, and the University of Turku, Turku, Finland., Marttila RH; PEDEGO Research Unit, Medical Research Center Oulu, University of Oulu, Oulu, Finland.; Department of Children and Adolescents, Oulu University Hospital, Oulu, Finland., Bassler D; Department of Neonatology, University Hospital Zurich, and University of Zurich, Zurich, Switzerland., Poets CF; Department of Neonatology, Tuebingen University Hospital, Tuebingen, Germany., Lacaze-Masmonteil T; Department of Paediatrics, Cumming School of Medicine, University of Calgary, Alberta, Canada., Danan C; Inserm, U955, Créteil, France.; CRB, CHI-Creteil, France.; Department of neonatology, CHI-Creteil, Creteil, France., Delacourt C; Inserm, U955, Créteil, France.; AP-HP, Hôpital Necker-Enfants Malades, Service de Pneumologie Pédiatrique, Paris, France.; Université Paris-Descartes, Paris, France., Palotie A; Analytic and Translational Genetics Unit, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.; Program in Medical and Population Genetics, The Broad Institute of MIT and Harvard, Cambridge, MA, USA.; The Stanley Center for Psychiatric Research, The Broad Institute of MIT and Harvard, Cambridge, MA, USA.; Institute for Molecular Medicine Finland, University of Helsinki, Helsinki, Finland.; Psychiatric & Neurodevelopmental Genetics Unit, Department of Psychiatry, Massachusetts General Hospital, Boston, MA, USA.; Department of Neurology, Massachusetts General Hospital, Boston, MA, USA., Muglia LJ; Perinatal Institute, Cincinnati Children's Hospital Medical Center and Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA., Lavoie PM; BC Children's Hospital Research Institute, Vancouver Canada, Vancouver, Canada., Hadchouel A; Inserm, U955, Créteil, France.; AP-HP, Hôpital Necker-Enfants Malades, Service de Pneumologie Pédiatrique, Paris, France.; Université Paris-Descartes, Paris, France., Rämet M; PEDEGO Research Unit, Medical Research Center Oulu, University of Oulu, Oulu, Finland.; Department of Children and Adolescents, Oulu University Hospital, Oulu, Finland.; BioMediTech Institute and Faculty of Medical and Life Sciences, University of Tampere, Tampere, Finland., Hallman M; PEDEGO Research Unit, Medical Research Center Oulu, University of Oulu, Oulu, Finland.; Department of Children and Adolescents, Oulu University Hospital, Oulu, Finland.

Publikováno v: Scientific reports [Sci Rep] 2017 Aug 24; Vol. 7 (1), pp. 9271. Date of Electronic Publication: 2017 Aug 24.

Prospective epigenome and transcriptome analyses of cord and peripheral blood from preterm infants at risk of bronchopulmonary dysplasia.

Autor: Cho, Hye-Youn¹ (AUTHOR), Wang, Xuting^1,2 (AUTHOR), Campbell, Michelle R.¹ (AUTHOR), Panduri, Vijayalakshmi³ (AUTHOR), Coviello, Silvina⁴ (AUTHOR), Caballero, Mauricio T.^4,5 (AUTHOR), Bennett, Brian D.² (AUTHOR), Kleeberger, Steven R.¹ (AUTHOR), Polack, Fernando P.^4,6 (AUTHOR), Ofman, Gaston^4,7 (AUTHOR), Bell, Douglas A.⁸ (AUTHOR) bell1@niehs.nih.gov

Publikováno v: Scientific Reports. 7/28/2023, Vol. 13 Issue 1, p1-21. 21p.

Epigenome-wide association study of bronchopulmonary dysplasia in preterm infants: results from the discovery-BPD program.

Autor: Wang, Xuting¹ (AUTHOR), Cho, Hye-Youn¹ (AUTHOR), Campbell, Michelle R.¹ (AUTHOR), Panduri, Vijayalakshmi² (AUTHOR), Coviello, Silvina³ (AUTHOR), Caballero, Mauricio T.^3,4 (AUTHOR), Sambandan, Deepa^1,5 (AUTHOR), Kleeberger, Steven R.¹ (AUTHOR), Polack, Fernando P.^3,6 (AUTHOR), Ofman, Gaston^3,7 (AUTHOR), Bell, Douglas A.¹ (AUTHOR) bell1@niehs.nih.gov

Publikováno v: Clinical Epigenetics. 4/28/2022, Vol. 14 Issue 1, p1-20. 20p.

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