Author Correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis
| Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Nature Portfolio
2022-09-01
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| Series: | Nature Communications |
| Online Access: | https://doi.org/10.1038/s41467-022-33222-y |
| _version_ | 1811264868202840064 |
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| author | C. S. Gallagher N. Mäkinen H. R. Harris N. Rahmioglu O. Uimari J. P. Cook N. Shigesi T. Ferreira D. R. Velez-Edwards T. L. Edwards S. Mortlock Z. Ruhioglu F. Day C. M. Becker V. Karhunen H. Martikainen M.-R. Järvelin R. M. Cantor P. M. Ridker K. L. Terry J. E. Buring S. D. Gordon S. E. Medland G. W. Montgomery D. R. Nyholt D. A. Hinds J. Y. Tung the 23andMe Research Team J. R. B. Perry P. A. Lind J. N. Painter N. G. Martin A. P. Morris D. I. Chasman S. A. Missmer K. T. Zondervan C. C. Morton |
| author_facet | C. S. Gallagher N. Mäkinen H. R. Harris N. Rahmioglu O. Uimari J. P. Cook N. Shigesi T. Ferreira D. R. Velez-Edwards T. L. Edwards S. Mortlock Z. Ruhioglu F. Day C. M. Becker V. Karhunen H. Martikainen M.-R. Järvelin R. M. Cantor P. M. Ridker K. L. Terry J. E. Buring S. D. Gordon S. E. Medland G. W. Montgomery D. R. Nyholt D. A. Hinds J. Y. Tung the 23andMe Research Team J. R. B. Perry P. A. Lind J. N. Painter N. G. Martin A. P. Morris D. I. Chasman S. A. Missmer K. T. Zondervan C. C. Morton |
| author_sort | C. S. Gallagher |
| collection | DOAJ |
| first_indexed | 2024-04-12T20:12:06Z |
| format | Article |
| id | doaj.art-0c4b62618c4b49c594faae5d08fef721 |
| institution | Directory Open Access Journal |
| issn | 2041-1723 |
| language | English |
| last_indexed | 2024-04-12T20:12:06Z |
| publishDate | 2022-09-01 |
| publisher | Nature Portfolio |
| record_format | Article |
| series | Nature Communications |
| spelling | doaj.art-0c4b62618c4b49c594faae5d08fef7212022-12-22T03:18:13ZengNature PortfolioNature Communications2041-17232022-09-011311210.1038/s41467-022-33222-yAuthor Correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosisC. S. Gallagher0N. Mäkinen1H. R. Harris2N. Rahmioglu3O. Uimari4J. P. Cook5N. Shigesi6T. Ferreira7D. R. Velez-Edwards8T. L. Edwards9S. Mortlock10Z. Ruhioglu11F. Day12C. M. Becker13V. Karhunen14H. Martikainen15M.-R. Järvelin16R. M. Cantor17P. M. Ridker18K. L. Terry19J. E. Buring20S. D. Gordon21S. E. Medland22G. W. Montgomery23D. R. Nyholt24D. A. Hinds25J. Y. Tung26the 23andMe Research TeamJ. R. B. Perry27P. A. Lind28J. N. Painter29N. G. Martin30A. P. Morris31D. I. Chasman32S. A. Missmer33K. T. Zondervan34C. C. Morton35Department of Genetics, Harvard Medical SchoolDepartment of Obstetrics and Gynecology, Brigham and Women’s Hospital, Harvard Medical SchoolProgram in Epidemiology, Division of Public Health Sciences, Fred Hutchinson Cancer Research CenterWellcome Centre for Human Genetics, University of OxfordEndometriosis CaRe Centre, Nuffield Department of Women’s and Reproductive Health, University of Oxford, John Radcliffe HospitalDepartment of Biostatistics, University of LiverpoolEndometriosis CaRe Centre, Nuffield Department of Women’s and Reproductive Health, University of Oxford, John Radcliffe HospitalWellcome Centre for Human Genetics, University of OxfordVanderbilt Genetics Institute, Vanderbilt Epidemiology Center, Institute for Medicine and Public Health, Department of Obstetrics and Gynecology, Vanderbilt University Medical CenterDivision of Epidemiology, Department of Medicine, Institute for Medicine and Public Health, Vanderbilt Genetics Institute, Vanderbilt University Medical CenterInstitute for Molecular Bioscience, University of QueenslandDepartment of Obstetrics and Gynecology, Brigham and Women’s Hospital, Harvard Medical SchoolMRC Epidemiology Unit, University of Cambridge School of Clinical Medicine, Institute of Metabolic Science, Cambridge Biomedical CampusEndometriosis CaRe Centre, Nuffield Department of Women’s and Reproductive Health, University of Oxford, John Radcliffe HospitalCenter for Life Course Health Research, Faculty of Medicine, University of OuluDepartment of Obstetrics and Gynecology, Oulu University Hospital and PEDEGO Research Unit & Medical Research Center Oulu, University of Oulu and Oulu University HospitalCenter for Life Course Health Research, Faculty of Medicine, University of OuluDepartment of Human Genetics, David Geffen School of Medicine, University of California at Los AngelesDivision of Preventative Medicine, Brigham and Women’s Hospital, Harvard Medical SchoolObstetrics and Gynecology Epidemiology Center, Brigham and Women’s Hospital and Harvard Medical SchoolDivision of Preventative Medicine, Brigham and Women’s Hospital, Harvard Medical SchoolGenetic Epidemiology, QIMR Berghofer Medical Research InstitutePsychiatric Genetics, QIMR Berghofer Medical Research InstituteInstitute for Molecular Bioscience, University of QueenslandGenetic Epidemiology, QIMR Berghofer Medical Research Institute23andMe23andMeMRC Epidemiology Unit, University of Cambridge School of Clinical Medicine, Institute of Metabolic Science, Cambridge Biomedical CampusPsychiatric Genetics, QIMR Berghofer Medical Research InstitutePsychiatric Genetics, QIMR Berghofer Medical Research InstituteGenetic Epidemiology, QIMR Berghofer Medical Research InstituteWellcome Centre for Human Genetics, University of OxfordDivision of Preventative Medicine, Brigham and Women’s Hospital, Harvard Medical SchoolDepartment of Epidemiology, Harvard T.H. Chan School of Public HealthWellcome Centre for Human Genetics, University of OxfordDepartment of Obstetrics and Gynecology, Brigham and Women’s Hospital, Harvard Medical Schoolhttps://doi.org/10.1038/s41467-022-33222-y |
| spellingShingle | C. S. Gallagher N. Mäkinen H. R. Harris N. Rahmioglu O. Uimari J. P. Cook N. Shigesi T. Ferreira D. R. Velez-Edwards T. L. Edwards S. Mortlock Z. Ruhioglu F. Day C. M. Becker V. Karhunen H. Martikainen M.-R. Järvelin R. M. Cantor P. M. Ridker K. L. Terry J. E. Buring S. D. Gordon S. E. Medland G. W. Montgomery D. R. Nyholt D. A. Hinds J. Y. Tung the 23andMe Research Team J. R. B. Perry P. A. Lind J. N. Painter N. G. Martin A. P. Morris D. I. Chasman S. A. Missmer K. T. Zondervan C. C. Morton Author Correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis Nature Communications |
| title | Author Correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis |
| title_full | Author Correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis |
| title_fullStr | Author Correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis |
| title_full_unstemmed | Author Correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis |
| title_short | Author Correction: Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis |
| title_sort | author correction genome wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis |
| url | https://doi.org/10.1038/s41467-022-33222-y |
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