Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Femke N. G. van 't Hof"'
Autor:
Femke N. G. van ’t Hof, Ynte M. Ruigrok, Cue Hyunkyu Lee, Stephan Ripke, Graig Anderson, Mariza de Andrade, Annette F. Baas, Jan D. Blankensteijn, Erwin P. Böttinger, Matthew J. Bown, Joseph Broderick, Philippe Bijlenga, David S. Carrell, Dana C. Crawford, David R. Crosslin, Christian Ebeling, Johan G. Eriksson, Myriam Fornage, Tatiana Foroud, Mikael von und zu Fraunberg, Christoph M. Friedrich, Emília I. Gaál, Omri Gottesman, Dong‐Chuan Guo, Seamus C. Harrison, Juha Hernesniemi, Albert Hofman, Ituro Inoue, Juha E. Jääskeläinen, Gregory T. Jones, Lambertus A. L. M. Kiemeney, Riku Kivisaari, Nerissa Ko, Seppo Koskinen, Michiaki Kubo, Iftikhar J. Kullo, Helena Kuivaniemi, Mitja I. Kurki, Aki Laakso, Dongbing Lai, Suzanne M. Leal, Hanna Lehto, Scott A. LeMaire, Siew‐Kee Low, Jennifer Malinowski, Catherine A. McCarty, Dianna M. Milewicz, Thomas H. Mosley, Yusuke Nakamura, Hirofumi Nakaoka, Mika Niemelä, Jennifer Pacheco, Peggy L. Peissig, Joanna Pera, Laura Rasmussen‐Torvik, Marylyn D. Ritchie, Fernando Rivadeneira, Andre M. van Rij, Regie Lyn P. Santos‐Cortez, Athanasios Saratzis, Agnieszka Slowik, Atsushi Takahashi, Gerard Tromp, André G. Uitterlinden, Shefali S. Verma, Sita H. Vermeulen, Gao T. Wang, Buhm Han, Gabriël J. E. Rinkel, Paul I. W. de Bakker, Ana Verissimo, Benjamin J. Wright, Suzannah Bumpstead, Solveig Gretarsdottir, Stephen A. Badger, Anne H. Child, Rachel E. Clough, Gillian Cockerill, Hany Hafez, D. Julian A. Scott, Simon Futers, Soroush Sohrabi, Alberto Smith, Matthew M. Thompson, Frank M. van Bockxmeer, Stefan E. Matthiasson, Gudmar Thorleifsson, Unnur Thorsteinsdottir, Joep A. W. Teijink, Cisca Wijmenga, Jacqueline de Graaf, Lambertus A. Kiemeney, Jutta Palmen, Andrew J. Smith, Jes S. Lindholt, Declan T. Bradley, Matthew Waltham, Sarah Edkins, Rhian Gwilliam, Sarah E. Hunt, Simon Potter, Jonathan Golledge, Per Eriksson, Paul E. Norman, Janet T. Powell, Kari Stefansson, John R. Thompson, Steve E. Humphries, Robert D. Sayers, Panos Deloukas, Nilesh J. Samani, L. Victoria Phillip, Geraldine B. Hill, Michael J. A. Williams, Ian A. Thomson, Jo Krysa, Gerard T. Wilkins, Tony R. Merriman, Thodor M. Vasudevan, David R. Lewis, Ross D. Blair, Andrew A. Hill
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 5, Iss 7 (2016)
BackgroundIntracranial aneurysms (IAs), abdominal aortic aneurysms (AAAs), and thoracic aortic aneurysms (TAAs) all have a familial predisposition. Given that aneurysm types are known to co‐occur, we hypothesized that there may be shared genetic ri
Externí odkaz:
https://doaj.org/article/2acb672bf4a74a25b54ac4cd784f7c16
Autor:
John A L Meeuwsen, Femke N G van T Hof, Wouter van Rheenen, Gabriel J E Rinkel, Jan H Veldink, Ynte M Ruigrok
Publikováno v:
PLoS ONE, Vol 12, Iss 5, p e0176558 (2017)
INTRODUCTION:We compared circulating microRNA (miRNA) levels in plasma of patients with intracranial aneurysms (IA) to those of controls as a first step towards finding potential biomarkers for individuals at high risk of IA development and its subse
Externí odkaz:
https://doaj.org/article/213ca71088f34e9e9342b890a04e0da2
Autor:
Mitja I Kurki, Emília Ilona Gaál, Johannes Kettunen, Tuuli Lappalainen, Androniki Menelaou, Verneri Anttila, Femke N G van 't Hof, Mikael von Und Zu Fraunberg, Seppo Helisalmi, Mikko Hiltunen, Hanna Lehto, Aki Laakso, Riku Kivisaari, Timo Koivisto, Antti Ronkainen, Jaakko Rinne, Lambertus A L Kiemeney, Sita H Vermeulen, Mari A Kaunisto, Johan G Eriksson, Arpo Aromaa, Markus Perola, Terho Lehtimäki, Olli T Raitakari, Veikko Salomaa, Murat Gunel, Emmanouil T Dermitzakis, Ynte M Ruigrok, Gabriel J E Rinkel, Mika Niemelä, Juha Hernesniemi, Samuli Ripatti, Paul I W de Bakker, Aarno Palotie, Juha E Jääskeläinen
Publikováno v:
PLoS Genetics, Vol 10, Iss 1, p e1004134 (2014)
3% of the population develops saccular intracranial aneurysms (sIAs), a complex trait, with a sporadic and a familial form. Subarachnoid hemorrhage from sIA (sIA-SAH) is a devastating form of stroke. Certain rare genetic variants are enriched in the
Externí odkaz:
https://doaj.org/article/32f285a882bc4a268bef0faa8f726fc3
Autor:
Kenneth A, Myers, Femke N G, van 't Hof, Lynette G, Sadleir, Geneviève, Legault, Elisabeth, Simard-Tremblay, David J, Amor, Ingrid E, Scheffer
Publikováno v:
Pediatrics. 144(3)
Girls with pathogenic variants in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a811190f02721dba5a241105985c48d3
https://pubmed.ncbi.nlm.nih.gov/31439621
https://pubmed.ncbi.nlm.nih.gov/31439621
Autor:
Jan H. Veldink, Wouter van Rheenen, John A. L. Meeuwsen, Femke N G van 't Hof, Ynte M. Ruigrok, Gabriel J.E. Rinkel
Publikováno v:
PLoS ONE [E], 12(5). Public Library of Science
PLoS ONE
PLoS ONE, Vol 12, Iss 5, p e0176558 (2017)
PLoS ONE
PLoS ONE, Vol 12, Iss 5, p e0176558 (2017)
INTRODUCTION:We compared circulating microRNA (miRNA) levels in plasma of patients with intracranial aneurysms (IA) to those of controls as a first step towards finding potential biomarkers for individuals at high risk of IA development and its subse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54732a126db980199d435536f782bf4d
https://dspace.library.uu.nl/handle/1874/350437
https://dspace.library.uu.nl/handle/1874/350437
Autor:
Arno de Wilde, Ynte M. Ruigrok, Albert Hofman, André G. Uitterlinden, Julien Vaucher, Femke N G van 't Hof, Paul I.W. de Bakker, Lambertus A. Kiemeney, Michael V. Holmes, Gabriel J.E. Rinkel, Jan D. Blankensteijn, Fernando Rivadeneira, Sita H. Vermeulen, Annette F. Baas
Publikováno v:
European Journal of Human Genetics, 25(6), 758-762. Nature Publishing Group
van 't Hof, F NG, Vaucher, J, Holmes, M V, de Wilde, A, Baas, A F, Blankensteijn, J D, Hofman, A, Kiemeney, L ALM, Rivadeneira, F, Uitterlinden, A G, Vermeulen, S H, Rinkel, G JE, de Bakker, P IW & Ruigrok, Y M 2017, ' Genetic variants associated with type 2 diabetes and adiposity and risk of intracranial and abdominal aortic aneurysms ', European Journal of Human Genetics, vol. 25, no. 6, pp. 758-762 . https://doi.org/10.1038/ejhg.2017.48
European Journal of Human Genetics, 25, 758-762
European Journal of Human Genetics, 25(6), 758. Nature Publishing Group
European Journal of Human Genetics, 25, 6, pp. 758-762
van 't Hof, F NG, Vaucher, J, Holmes, M V, de Wilde, A, Baas, A F, Blankensteijn, J D, Hofman, A, Kiemeney, L ALM, Rivadeneira, F, Uitterlinden, A G, Vermeulen, S H, Rinkel, G JE, de Bakker, P IW & Ruigrok, Y M 2017, ' Genetic variants associated with type 2 diabetes and adiposity and risk of intracranial and abdominal aortic aneurysms ', European Journal of Human Genetics, vol. 25, no. 6, pp. 758-762 . https://doi.org/10.1038/ejhg.2017.48
European Journal of Human Genetics, 25, 758-762
European Journal of Human Genetics, 25(6), 758. Nature Publishing Group
European Journal of Human Genetics, 25, 6, pp. 758-762
Epidemiological studies show that type 2 diabetes (T2D) is inversely associated with intracranial aneurysms (IA) and abdominal aortic aneurysms (AAA). Although adiposity has not been considered a risk factor for IA, there have been inconsistent repor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9e4736aa2107f9178080afb60a6f009
https://doi.org/10.1038/ejhg.2017.48
https://doi.org/10.1038/ejhg.2017.48
Autor:
Irene C. van der Schaaf, Franciscus J. Wolters, Ynte M. Ruigrok, Femke N G van 't Hof, Ingeborg Rasing, Gabriel J.E. Rinkel, Rachel Kleinloog
Publikováno v:
Neurosurgery. 73:705-708
BACKGROUND Genetic risk factors for intracranial aneurysms may influence the size of aneurysms. OBJECTIVE To assess the association between genetic risk factors and the size of aneurysms at the time of rupture. METHODS Genotypes of 7 independent sing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01fd5ef3c5184697159107a47b0a3236
https://doi.org/10.1227/neu.0000000000000078
https://doi.org/10.1227/neu.0000000000000078
Autor:
Riku Kivisaari, Mikael von und zu Fraunberg, Emilia I. Gaal, Aki Laakso, Hanna Lehto, Juha Hernesniemi, Diederik van de Beek, Mitja I. Kurki, Paul I.W. de Bakker, Femke N G van 't Hof, Ynte M. Ruigrok, Matthijs C. Brouwer, Gabriël J.E. Rinkel, Mika Niemelä, Rachel Kleinloog, Juha E. Jääskeläinen
Publikováno v:
Neurology
Neurology, 83(1), 34-39. Lippincott Williams and Wilkins
ResearcherID
Neurology, 83(1), 34-39. Lippincott Williams and Wilkins
ResearcherID
Objective: We investigated whether risk alleles of single nucleotide polymorphisms associated with intracranial aneurysm (IA) are enriched in patients with familial IA, IA located at the middle cerebral artery (MCA), or IA rupture at a younger age. M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7293c43bd44dbe61a80f9e045ccd5224
https://pubmed.ncbi.nlm.nih.gov/24934137
https://pubmed.ncbi.nlm.nih.gov/24934137
Autor:
Mikael von und zu Fraunberg, Aki Laakso, Juha E. Jääskeläinen, Laura Sauerbeck, Mitja I. Kurki, Riku Kivisaari, Ynte M. Ruigrok, Aarno Palotie, Matthew L. Flaherty, Stephan Ripke, John H. Huston, Robert D. Brown, Charles J Moomaw, Daniel Woo, Craig S. Anderson, Irene Meissner, Thomas H. Mosley, Daniel L. Koller, Dawn Kleindorfer, Nerissa U. Ko, Gabriël J.E. Rinkel, Jason Mackey, Femke N G van 't Hof, Agnieszka Slowik, Mika Niemelä, Myriam Fornage, Tatiana Foroud, Sita H. Vermeulen, Hanna Lehto, Emilia I. Gaal, Lambertus A. Kiemeney, Juha Hernesniemi, Dongbing Lai, Guy A. Rouleau, Johan G. Eriksson, Edward Sander Connolly, Marek Moskała, Bradford B. Worrall, Joseph Broderick, Joanna Pera
Publikováno v:
Stroke, 45, 3194-9
Stroke, 45, 11, pp. 3194-9
Stroke, 45, 11, pp. 3194-9
Background and Purpose— Common variants have been identified using genome-wide association studies which contribute to intracranial aneurysms (IA) susceptibility. However, it is clear that the variants identified to date do not account for the esti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9963e8a93c81a7d65bfdcf34fff8c19e
https://doi.org/10.1161/STROKEAHA.114.006096
https://doi.org/10.1161/STROKEAHA.114.006096
Autor:
Seppo Helisalmi, Timo Koivisto, Hanna Lehto, Mikael von und zu Fraunberg, Emilia I. Gaal, Emmanouil T. Dermitzakis, Juha Hernesniemi, Antti Ronkainen, Veikko Salomaa, Johannes Kettunen, Gabriël J.E. Rinkel, Arpo Aromaa, Murat Gunel, Mika Niemelä, Paul I.W. de Bakker, Johan G. Eriksson, Lambertus A. Kiemeney, Sita H. Vermeulen, Aki Laakso, Androniki Menelaou, Olli T. Raitakari, Juha E. Jääskeläinen, Mari A. Kaunisto, Mikko Hiltunen, Femke N G van 't Hof, Terho Lehtimäki, Mitja I. Kurki, Samuli Ripatti, Aarno Palotie, Tuuli Lappalainen, Jaakko Rinne, Markus Perola, Verneri Anttila, Riku Kivisaari, Ynte M. Ruigrok
Publikováno v:
PLOS Genetics, Vol. 10, No 1 (2014) P. e1004134
PLoS Genetics, Vol 10, Iss 1, p e1004134 (2014)
Plos Genetics, 10, e1004134
PLoS Genetics
Plos Genetics, 10, 1, pp. e1004134
PLoS Genetics, Vol 10, Iss 1, p e1004134 (2014)
Plos Genetics, 10, e1004134
PLoS Genetics
Plos Genetics, 10, 1, pp. e1004134
3% of the population develops saccular intracranial aneurysms (sIAs), a complex trait, with a sporadic and a familial form. Subarachnoid hemorrhage from sIA (sIA-SAH) is a devastating form of stroke. Certain rare genetic variants are enriched in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6244321f9fcd36cf8a75291a1fa4ef0e
https://archive-ouverte.unige.ch/unige:90276
https://archive-ouverte.unige.ch/unige:90276