Результати пошуку - Jessica van Setten
- Показ 1 - 20 результатів із 39
- На наступну сторінку
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Twenty-Five Novel Loci for Carotid Intima-Media Thickness: A Genome-Wide Association Study in >45 000 Individuals and Meta-Analysis of >100 000 Individuals за авторством Ming Wai Yeung, Siqi Wang, Yordi J. van de Vegte, Oleg Borisov, Jessica van Setten, Harold Snieder, Niek Verweij, M. Abdullah Said, Pim van der Harst
Опубліковано 2021Revisão -
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A Mendelian randomization analysis of cardiac MRI measurements as surrogate outcomes for heart failure and atrial fibrillation за авторством Amand F. Schmidt, Chris Finan, Jessica van Setten, Esther Puyol‐Antón, Bram Ruijsink, Mimount Bourfiss, Abdulrahman Alasiri, B. K. Velthuis, Folkert W. Asselbergs, Anneline S.J.M. te Riele
Опубліковано 2025Artigo -
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Loss of Y Chromosome in Blood Is Associated With Major Cardiovascular Events During Follow-Up in Men After Carotid Endarterectomy за авторством Saskia Haitjema, Daniel Kofink, Jessica van Setten, Sander W. van der Laan, Arjan H. Schoneveld, James Eales, Maciej Tomaszewski, Saskia C.A. de Jager, Gerard Pasterkamp, Folkert W. Asselbergs, Hester M. den Ruijter
Опубліковано 2017Artigo -
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Tacrolimus troughs and genetic determinants of metabolism in kidney transplant recipients: A comparison of four ancestry groups за авторством Moataz E. Mohamed, David P. Schladt, Weihua Guan, Baolin Wu, Jessica van Setten, Brendan J. Keating, David Iklé, Rory P. Remmel, Casey R. Dorr, Roslyn B. Mannon, Arthur J. Matas, Ajay K. Israni, William S. Oetting, Pamala A. Jacobson
Опубліковано 2019Artigo -
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Prevalence and Disease Expression of Pathogenic and Likely Pathogenic Variants Associated With Inherited Cardiomyopathies in the General Population за авторством Mimount Bourfiss, Marion van Vugt, Abdulrahman Alasiri, Bram Ruijsink, Jessica van Setten, Amand F. Schmidt, Dennis Dooijes, Esther Puyol‐Antón, Birgitta K. Velthuis, J. Peter van Tintelen, Anneline S.J.M. te Riele, Annette F. Baas, Folkert W. Asselbergs
Опубліковано 2022Artigo -
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Integrative Functional Annotation of 52 Genetic Loci Influencing Myocardial Mass Identifies Candidate Regulatory Variants and Target Genes за авторством Daiane Hemerich, Jiayi Pei, Magdaléna Harakaľová, Jessica van Setten, Sander Boymans, Bastiaan J. Boukens, Igor R. Efimov, Michelle Michels, Jolanda van der Velden, Aryan Vink, Caroline Cheng, Pim van der Harst, Jason H. Moore, Michal Mokrý, Vinicius Tragante, Folkert W. Asselbergs
Опубліковано 2019Artigo -
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Composition of Carotid Atherosclerotic Plaque Is Associated With Cardiovascular Outcome за авторством Willem E. Hellings, Wouter Peeters, Frans L. Moll, Sebastiaan R.D. Piers, Jessica van Setten, Peter J. van der Spek, Jean‐Paul P.M. de Vries, Kees A. Seldenrijk, Peter C. de Bruin, Aryan Vink, Evelyn Velema, Dominique P.V. de Kleijn, Gerard Pasterkamp
Опубліковано 2010Artigo -
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Genome-wide association study of coronary and aortic calcification implicates risk loci for coronary artery disease and myocardial infarction за авторством Jessica van Setten, Ivana Išgum, Joanna Smolonska, Stephan Ripke, Pim A. de Jong, Matthijs Oudkerk, Harry J. de Koning, Jan‐Willem J. Lammers, Pieter Zanen, Harry J.M. Groen, H. Marike Boezen, Dirkje S. Postma, Cisca Wijmenga, Max A. Viergever, Willem P.Th.M. Mali, Paul I. W. de Bakker
Опубліковано 2013Artigo -
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Allele-specific NKX2-5 binding underlies multiple genetic associations with human electrocardiographic traits за авторством Paola Benaglio, Agnieszka D’Antonio‐Chronowska, Wubin Ma, Feng Yang, William W. Greenwald, Margaret K. R. Donovan, Christopher DeBoever, He Li, Frauke Drees, Sanghamitra Singhal, Hiroko Matsui, Jessica van Setten, Nona Sotoodehnia, Kyle J. Gaulton, Erin N. Smith, Matteo D’Antonio, Michael G. Rosenfeld, Kelly A. Frazer
Опубліковано 2019Artigo -
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Sequence variants with large effects on cardiac electrophysiology and disease за авторством Kristján Norland, Garðar Sveinbjörnsson, Rósa B. Þórólfsdóttir, Olafur B. Davidsson, Vinicius Tragante, Sridharan Rajamani, Anna Helgadóttir, Sólveig Grétarsdóttir, Jessica van Setten, Folkert W. Asselbergs, Jon T. Sverrisson, Sigurdur S. Stephensen, Gylfi Óskarsson, Engilbert Sigurðsson, Karl Andersen, Ragnar Daníelsen, Guðmundur Þorgeirsson, Unnur Þorsteinsdóttir, Davíð O. Arnar, Patrick Sulem, Hilma Hólm, Daníel F. Guðbjartsson, Kāri Stefánsson
Опубліковано 2019Artigo -
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Human Validation of Genes Associated With a Murine Atherosclerotic Phenotype за авторством Gerard Pasterkamp, Sander W. van der Laan, Saskia Haitjema, Hassan Foroughi Asl, Marten A. Siemelink, Tim Bezemer, Jessica van Setten, Martin Dichgans, Rainer Malik, Bradford B. Worrall, Heribert Schunkert, Nilesh J. Samani, Dominique P.V. de Kleijn, Hugh S. Markus, Imo E. Hoefer, Tom Michoel, Saskia C.A. de Jager, Johan Björkegren, Hester M. den Ruijter, Folkert W. Asselbergs
Опубліковано 2016Revisão -
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Druggable proteins influencing cardiac structure and function: Implications for heart failure therapies and cancer cardiotoxicity за авторством Amand F. Schmidt, Mimount Bourfiss, Abdulrahman Alasiri, Esther Puyol‐Antón, Sandesh Chopade, Marion van Vugt, Sander W. van der Laan, Christian Groß, Chris Clarkson, Albert Henry, Tom Lumbers, Pim van der Harst, Nora Franceschini, Joshua C. Bis, Birgitta K. Velthuis, Anneline S.J.M. te Riele, Aroon D. Hingorani, Bram Ruijsink, Folkert W. Asselbergs, Jessica van Setten, Chris Finan
Опубліковано 2023Artigo -
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Improved imputation quality of low-frequency and rare variants in European samples using the ‘Genome of The Netherlands’ за авторством Patrick Deelen, Androniki Menelaou, Jin‐Moo Lee, Alexandros Kanterakis, Freerk van Dijk, Carolina Medina‐Gómez, Laurent C. Francioli, Jouke‐Jan Hottenga, Lennart C. Karssen, Karol Estrada, Eskil Kreiner‐Møller, Fernando Rivadeneira, Jessica van Setten, Javier Gutierrez‐Achury, Harm-Jan Westra, Lude Franke, David van Enckevort, Martijn Dijkstra, Heorhiy Byelas, Cornelia M. van Duijn, Paul I. W. de Bakker, Cisca Wijmenga, Morris A. Swertz
Опубліковано 2014Artigo -
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Functionally distinct ERAP1 and ERAP2 are a hallmark of HLA-A29-(Birdshot) Uveitis за авторством Jonas J. W. Kuiper, Jessica van Setten, Matthew Devall, Mircea Cretu-Stancu, Sanne Hiddingh, Roel A. Ophoff, Tom Missotten, Michelle Helena van Velthoven, Anneke I. den Hollander, Carel B. Hoyng, Edward James, Emma Reeves, Miguel Cordero‐Coma, Alejandro Fonollosa, Alfredo Adán, Javier Martı́n, Bobby P. C. Koeleman, Joke H. de Boer, Sara L. Pulit, Ana Márquez, Timothy R. D. J. Radstake
Опубліковано 2018Revisão -
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NPHP1 (Nephrocystin-1) Gene Deletions Cause Adult-Onset ESRD за авторством Rozemarijn Snoek, Jessica van Setten, Brendan J. Keating, Ajay K. Israni, Pamala A. Jacobson, William S. Oetting, Arthur J. Matas, Roslyn B. Mannon, Zhongyang Zhang, Weijia Zhang, Ke Hao, Barbara Murphy, Roman Reindl‐Schwaighofer, Andreas Heinzl, Rainer Oberbauer, Ondřej Viklický, Peter J. Conlon, Caragh P. Stapleton, Stephan J. L. Bakker, Harold Snieder, Edith Peters, Bert van der Zwaag, Nine Knoers, Martin H. de Borst, Albertien M. van Eerde
Опубліковано 2018Artigo -
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Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid за авторством Jurjen J. Luykx, S C Bakker, Eef G.W.M. Lentjes, M Neeleman, E Strengman, Lara J. Mentink, Joseph DeYoung, Simone de Jong, Jae Hoon Sul, Eleazar Eskin, Kristel van Eijk, Jessica van Setten, Jacobine E. Buizer‐Voskamp, Rita M. Cantor, Ake T. Lu, M van Amerongen, Eric P.A. van Dongen, Peter Keijzers, Teus H. Kappen, Paul Borgdorff, Peter Bruins, Eske M. Derks, René S. Kahn, Roel A. Ophoff
Опубліковано 2013Artigo -
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A genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathy за авторством Jonas J. W. Kuiper, Jessica van Setten, Stephan Ripke, Ruben van ‘t Slot, Flip Mulder, Tom Missotten, G. S. Baarsma, Laurent C. Francioli, Sara L. Pulit, Carolien G. F. de Kovel, Ninette ten Dam‐van Loon, Anneke I. den Hollander, Paulien Huis in het Veld, Carel B. Hoyng, Miguel Cordero‐Coma, Javier Martı́n, Víctor Llorenç, Bharti Arya, Dhanes Thomas, Steven C. Bakker, Roel A. Ophoff, Aniki Rothová, Paul I. W. de Bakker, Tuna Mutis, Bobby P. C. Koeleman
Опубліковано 2014Artigo -
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Elevated Plasma Complement Factors in <i>CRB1</i>-Associated Inherited Retinal Dystrophies за авторством Lude Moekotte, Joke de Boer, Sanne Hiddingh, Aafke de Ligt, Xuan‐Thanh‐An Nguyen, Carel B. Hoyng, Chris F. Inglehearn, Martin McKibbin, Tina M. Lamey, Jennifer A. Thompson, Fred K. Chen, Terri L. McLaren, Alaa AlTalbishi, Daan M. Panneman, Erica G. M. Boonen, Sandro Banfi, Béatrice Bocquet, Isabelle Meunier, Elfride De Baere, Robert K. Koenekoop, Monika Ołdak, Carlo Rivolta, Lisa Roberts, Raj Ramesar, R. Strupaite-Sileikiene, Susanne Kohl, G. Jane Farrar, Marion van Vugt, Jessica van Setten, Susanne Roosing, L. Ingeborgh van den Born, Camiel J.F. Boon, Maria M. van Genderen, Jonas J. W. Kuiper
Опубліковано 2025Artigo -
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The Genome of the Netherlands: design, and project goals за авторством Dorret I. Boomsma, Cisca Wijmenga, P. Eline Slagboom, Morris A. Swertz, Lennart C. Karssen, Abdel Abdellaoui, Kai Ye, Victor Guryev, Martijn Vermaat, Freerk van Dijk, Laurent C. Francioli, Jouke‐Jan Hottenga, Jeroen F. J. Laros, Qibin Li, Yingrui Li, Hongzhi Cao, Ruoyan Chen, Yuanping Du, Ning Li, Sujie Cao, Jessica van Setten, Androniki Menelaou, Sara L. Pulit, Jayne Y. Hehir‐Kwa, Marian Beekman, Clara C. Elbers, Heorhiy Byelas, Anton J. M. de Craen, Patrick Deelen, Martijn Dijkstra, Johan T. den Dunnen, Peter de Knijff, Jeanine J. Houwing‐Duistermaat, Vyacheslav Koval, Karol Estrada, Albert Hofman, Alexandros Kanterakis, David van Enckevort, Hailiang Mai, Mathijs Kattenberg, Jin‐Moo Lee, Pieter B. Neerincx, Ben A. Oostra, Fernanodo Rivadeneira, H. Eka D. Suchiman, André G. Uitterlinden, Gonneke Willemsen, Bruce H. R. Wolffenbuttel, Jun Wang, Paul I. W. de Bakker, Gert-Jan van Ommen, Cornelia M. van Duijn
Опубліковано 2013Artigo
Інструменти для пошуку:
Пов'язані теми
Biology
Medicine
Gene
Genetics
Internal medicine
Genotype
Single-nucleotide polymorphism
Genome-wide association study
Cardiology
Genetic association
Computational biology
Phenotype
Population
Allele
Bioinformatics
Genome
Coronary artery disease
Environmental health
Quantitative trait locus
Atrial fibrillation
Candidate gene
Disease
Haplotype
Odds ratio
Cardiomyopathy
Dilated cardiomyopathy
Endocrinology
Heart failure
Blood pressure
Computer science