Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Henry Wiersma"'
Autor:
Jochen Mierau, Pauline Lanting, Patrick Deelen, Robert Warmerdam, Floranne Boulogne, Annique Claringbould, Lude Franke, Yinjie Zhu, Ming-Jie Duan, Hermien H. Dijk, Roel D. Freriks, Louise H. Dekker, Jochen O. Mierau, Marike Boezen, Jackie Dekens, Judith Vonk, Ilja Nolte, Anil Ori, Marjolein Dijkema, Henry Wiersma, Soesma Medema Jankipersadsing
Publikováno v:
BMJ Open, Vol 11, Iss 3 (2021)
Objectives Studies in clinical settings showed a potential relationship between socioeconomic status (SES) and lifestyle factors with COVID-19, but it is still unknown whether this holds in the general population. In this study, we investigated the a
Externí odkaz:
https://doaj.org/article/d36c3be833c54a75948bd3937bfb012c
Autor:
Floranne Boulogne, Laura Claus, Henry Wiersma, Roy Oelen, Floor Schukking, Niek de Klein, Shuang Li, Harm-Jan Westra, Bert van der Zwaag, Franka van Reekum, Dana Sierks, Ria Schönauer, Zhigui Li, Emilia Bijlsma, Willem Jan Bos, Jan Halbritter, Nine Knoers, Whitney Besse, Patrick Deelen, Lude Franke, Albertien van Eerde
Genetic testing in patients with suspected hereditary kidney disease may not reveal the genetic cause for the disorder as potentially pathogenic variants can reside in genes that are not yet known to be involved in kidney disease. To help identify th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36c4362c139d6655acdc5a724d222027
https://doi.org/10.21203/rs.3.rs-1870632/v1
https://doi.org/10.21203/rs.3.rs-1870632/v1
Autor:
Richard Allman, Gillian Dite, Henry Wiersma, Robert Warmerdam, Irene Van Blokland, Pauline Lanting, Erika Spaeth, Nicholas Murphy
Publikováno v:
Epidemiology And Infection, 150:e91. Cambridge University Press
Using nested case–control data from the Lifelines COVID-19 cohort, we undertook a validation study of a clinical and genetic model to predict the risk of severe COVID-19 in people with confirmed COVID-19 and in people with confirmed or self-reporte
Autor:
Henry Wiersma, Patrick Deelen, Olivier B. Bakker, Annique Claringbould, Sophie Mulcahy Symmons, Iris Jonkers, Urmo Võsa, Floranne Boulogne, Harm-Jan Westra, Lude Franke
Genetic variants identified through genome-wide association studies (GWAS) are typically non-coding and exert small regulatory effects on downstream genes, but which downstream genes are ultimately impacted and how they confer risk remains mostly unc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aad801ae1da78e3206e37a4812d80fc6
https://doi.org/10.1101/2021.10.21.21265342
https://doi.org/10.1101/2021.10.21.21265342
Autor:
Henry Wiersma, Robert Warmerdam, Marike Boezen, Pauline Lanting, Patrick Deelen, J. M. Vonk, Lude Franke, Marjolein X.L. Dijkema
Physical and mental health are determined by an interplay between nature, i.e. genetics, and nurture, which encompasses experiences and exposures that can be short or long-lasting. Depressive episodes, for example, are partly the result of an interac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::569bcd2ef2595bd756154679183d7520
https://doi.org/10.31234/osf.io/uksxt
https://doi.org/10.31234/osf.io/uksxt
Autor:
Henry Wiersma, Lude Franke, Floor Schukking, Jan Halbritter, Floranne Boulogne, Shuang Li, Harm-Jan Westra, Nine V A M Knoers, Niek de Klein, Albertien M. van Eerde, Franka E. van Reekum, Roy Oelen, Bert van der Zwaag, Laura R. Claus, Patrick Deelen
Publikováno v:
Nephrology Dialysis Transplantation. 36
Background and Aims Genetic testing in patients with suspected hereditary kidney disease does not always reveal the genetic cause for the patient's disorder. Potentially pathogenic variants can reside in genes that are not known to be involved in kid
Autor:
Henry Wiersma, Dana Sierks, Niek de Klein, Patrick Deelen, Floranne Boulogne, Ria Schönauer, Bert van der Zwaag, Franka E. van Reekum, Jan Halbritter, Floor Schukking, Roy Oelen, Shuang Li, Harm-Jan Westra, Lude Franke, Albertien M. van Eerde, Laura R. Claus, Nine V A M Knoers
BackgroundGenetic testing in patients with suspected hereditary kidney disease may not reveal the genetic cause for the disorder as potentially pathogenic variants can reside in genes that are not yet known to be involved in kidney disease. To help i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba3a16be56d7df86e3467f8b49cb5784
https://doi.org/10.1101/2021.03.10.21253054
https://doi.org/10.1101/2021.03.10.21253054
Autor:
Raun van Ooijen, Henry Wiersma, Jackie A M Dekens, Patrick Deelen, Pauline Lanting, Sicco A. Scherjon, Esteban A Lopera Maya, Olivier B. Bakker, H. Marike Boezen, Marjolein X.L. Dijkema, Louise H. Dekker, Soesma A Jankipersadsing, Katherine Mc Intyre, Floranne Boulogne, Robert Warmerdam, Anil P.S. Ori, Sijmen A. Reijneveld, Judith M. Vonk, Alexandra Zhernakova, Viola Angelini, Irene V. van Blokland, Anna Sijtsma, Elianne Zijlstra, Annique Claringbould, Ute Bültmann, Cisca Wijmenga, Jochen O. Mierau, Lude Franke, Sandra Brouwer, Johanna C. Herkert, Morris A. Swertz
Publikováno v:
BMJ Open, 11(3):e044474. BMJ PUBLISHING GROUP
BMJ Open
BMJ Open, Vol 11, Iss 3 (2021)
BMJ Open
BMJ Open, Vol 11, Iss 3 (2021)
PurposeThe Lifelines COVID-19 cohort was set up to assess the psychological and societal impacts of the COVID-19 pandemic and investigate potential risk factors for COVID-19 within the Lifelines prospective population cohort.ParticipantsParticipants