Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Linda Tømmerdal Roten"'
Publikováno v:
BMC Medical Ethics, Vol 23, Iss 1, Pp 1-8 (2022)
Abstract Background The aim of the present survey was to investigate newly discharged hospital patients’ opinions on secondary use of their hospital data and biospecimens within the context of health research in general and, more specifically, on g
Externí odkaz:
https://doaj.org/article/f78e9327cade4625a5515afa14aa2347
Publikováno v:
BMC Medical Ethics
Background The aim of the present survey was to investigate newly discharged hospital patients’ opinions on secondary use of their hospital data and biospecimens within the context of health research in general and, more specifically, on genetic re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24ad9363e48e4a464623d363a05908f4
https://hdl.handle.net/11250/3056093
https://hdl.handle.net/11250/3056093
Autor:
Philip E. Melton, Ann-Charlotte Iversen, Liv Cecilie Vestrheim Thomsen, Eric K. Moses, Maria Lisa Odland, Linda Tømmerdal Roten, Ottar Nygård, Ingvill Lyslo, Kjersti Tollaksen, Line Bjørge, Chen Sun, Kristin Melheim Strand, Rigmor Austgulen
Publikováno v:
Journal of Hypertension
Supplemental Digital Content is available in the text
Objective: Preeclampsia is a complex genetic disease of pregnancy with a heterogenous presentation, unknown cause and potential severe outcomes for both mother and child. Preeclamptic women h
Objective: Preeclampsia is a complex genetic disease of pregnancy with a heterogenous presentation, unknown cause and potential severe outcomes for both mother and child. Preeclamptic women h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3943b738817be5aea5fdacbceaee216
https://doi.org/10.1097/hjh.0000000000000696
https://doi.org/10.1097/hjh.0000000000000696
Autor:
Pål Richard Romundstad, Bernhard Lämmle, Anne Sophie von Krogh, Anders Waage, Linda Tømmerdal Roten, Johanna A. Kremer Hovinga, Petter Quist-Paulsen
Publikováno v:
Thrombosis Research. 136:282-288
Introduction Known genetic variants with reference to preeclampsia only explain a proportion of the heritable contribution to the development of this condition. The association between preeclampsia and the risk of cardiovascular disease later in life
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8371fa1b41b6d9d96d92c06d7ccabfa
https://doi.org/10.1016/j.thromres.2015.06.022
https://doi.org/10.1016/j.thromres.2015.06.022
Autor:
Kjersti Tollaksen, Kari Klungsøyr, Line Bjørge, Rigmor Austgulen, Mona H. Fenstad, Gunhild Bærheim, Christian Tappert, Liv Cecilie Vestrheim Thomsen, Ferenc Macsali, Linda Tømmerdal Roten, Elisabeth Araya
Publikováno v:
Acta Obstetricia et Gynecologica Scandinavica. 92:943-950
Objective Evaluating the validity of pre-eclampsia registration in the Medical Birth Registry of Norway (MBRN) according to both broader and restricted disease definitions. Design Retrospective nested cohort study. Setting Multicenter study. Populati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1ce3fd712b892a9cc5d06629966b087
https://doi.org/10.1111/aogs.12159
https://doi.org/10.1111/aogs.12159
Autor:
Rigmor Austgulen, Eric K. Moses, Siri Forsmo, F. Skorpen, Matthew P. Johnson, Linda Tømmerdal Roten, Mona H. Fenstad
Publikováno v:
Molecular Human Reproduction
The etiology of preeclampsia is complex, with susceptibility being attributable to multiple environmental factors and a large genetic component. Although many candidate genes for preeclampsia have been suggested and studied, the specific causative ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::abc263b54e424248306da55a80558584
https://doi.org/10.1093/molehr/gar014
https://doi.org/10.1093/molehr/gar014
Autor:
Åsa Johansson, Matthew P. Johnson, Eric K. Moses, Mari Løset, Mona H. Fenstad, Irina P. Eide, Siv Boon Mundal, Linda Tømmerdal Roten, R. K. Sande, Rigmor Austgulen, John Blangero, Line Bjørge, Thomas D. Dyer, Siri Forsmo
Publikováno v:
Molecular Human Reproduction
Variation in the Storkhead box-1 (STOX1) gene has previously been associated with pre-eclampsia. In this study, we assess candidate single nucleotide polymorphisms (SNPs) in STOX1 in an independent population cohort of pre-eclamptic (n = 1.139) and n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8eddc963664da3b0da73ee20db6c260
http://europepmc.org/articles/PMC2989830
http://europepmc.org/articles/PMC2989830
Autor:
Siri Forsmo, Thomas D. Dyer, Christine East, Rigmor Austgulen, Linda Tømmerdal Roten, Shaun P. Brennecke, Matthew P. Johnson, Eric K. Moses, John Blangero
Publikováno v:
Human Genetics. 126:655-666
Preeclampsia is a heritable pregnancy disorder that presents new onset hypertension and proteinuria. We have previously reported genetic linkage to preeclampsia on chromosomes 2q, 5q and 13q in an Australian/New Zealand (Aust/NZ) familial cohort. Thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::951cd63c6eab5ae91195c647bd3ee7e0
https://doi.org/10.1007/s00439-009-0714-x
https://doi.org/10.1007/s00439-009-0714-x
Autor:
Matthew P. Johnson, Rigmor Austgulen, Eric K. Moses, Linda Tømmerdal Roten, John Blangero, Elizabeth B Fitzpatrick, Siri Forsmo, Shaun P. Brennecke, Thomas D. Dyer
Publikováno v:
European Journal of Human Genetics. 17:250-257
Genome-wide scans in Icelandic, Australian/New Zealand and Finnish pedigrees have provided evidence for maternal susceptibility loci for pre-eclampsia on chromosome 2, although at different positions (Iceland: 2p13 and 2q23, Australia/New Zealand: 2p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89be98fecedfc3cb453141250480e14d
https://doi.org/10.1038/ejhg.2008.158
https://doi.org/10.1038/ejhg.2008.158
Autor:
Mona H. Fenstad, Linda Tømmerdal Roten, Rigmor Austgulen, Juha Kere, Shaun P. Brennecke, J. M. Proffitt, Tia Aalto-Viljakainen, Hannele Laivuori, Eero Kajantie, John Blangero, Christine East, Eric K. Moses, Seppo Heinonen, Matthew P. Johnson, K. Mäkikallio, Thomas D. Dyer
Publikováno v:
Pregnancy hypertension. 2(3)
Introduction We have previously localized a preeclampsia susceptibility locus on chromosome 2q22 in 34 Australian and New Zealand (AUS/NZL) families. Using an extended number of AUS/NZL families ( n =74) we have now performed a comprehensive molecula
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71d8d00c953379839451473a91f02e8c
https://pubmed.ncbi.nlm.nih.gov/26105291
https://pubmed.ncbi.nlm.nih.gov/26105291