Whole exome sequencing reveals HSPA1L as a genetic risk factor for spontaneous preterm birth.

Journal: PLOS Genetics

Published: 2018-07-01

DOI: 10.1371/journal.pgen.1007394

Affiliations: 19

Authors: 27

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Institutions FC
23andMe, Inc., United States of America (USA) 0.19
Stead Family Department of Pediatrics, UI, United States of America (USA) 0.11
Department of Public Health, SDU, Denmark 0.07
Department of Population and Quantitative Health Sciences, CWRU, United States of America (USA) 0.07
Children's Mercy Center for Pediatric Genomic Medicine, United States of America (USA) 0.07
Department of Biological Sciences, VU, United States of America (USA) 0.07
Department of Children and Adolescents, Oulu University Hospital, Finland 0.06
Medical Research Center Oulu (MRC Oulu), Finland 0.06
Helsinki University Central Hospital (HUCH), Finland 0.04
Department of Epidemiology (EPI), UI, United States of America (USA) 0.04
Department of Biostatistics, UI, United States of America (USA) 0.04
Rady Children's Institute for Genomic Medicine, Rady Children's Hospital-San Diego, United States of America (USA) 0.04
March of Dimes Prematurity Research Center Ohio Collaborative, United States of America (USA) 0.02
UC Center for Prevention of Preterm Birth, United States of America (USA) 0.02
UC Department of Pediatrics, United States of America (USA) 0.02
UC Division of Human Genetics, United States of America (USA) 0.02
Sahlgrenska Academy, GU, Sweden 0.02
Department of Genetics and Bioinformatics, NIPH, Norway 0.02

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