Výsledky vyhledávání - Linda Broer
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Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis Autor Ilse A Hoppenbrouwers, Yurii S. Aulchenko, A. Cecile J.W. Janssens, Sreeram V. Ramagopalan, Linda Broer, Manfred Kayser, George C. Ebers, Ben A. Oostra, Cornelia M. van Duijn, Rogier Q. Hintzen
Vydáno 2009Artigo -
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A bioinformatics pipeline for estimating mitochondrial DNA copy number and heteroplasmy levels from whole genome sequencing data Autor Stephanie L. Battle, Daniela Puiu, Joost Verlouw, Linda Broer, Eric Boerwinkle, Kent D. Taylor, Jerome I. Rotter, S.S Rich, Megan L. Grove, Nathan Pankratz, Jessica L. Fetterman, Chunyu Liu, Dan E. Arking
Vydáno 2022Artigo -
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Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify<i>WNT9A</i>as novel osteoarthritis gene Autor Cindy G. Boer, Michelle S. Yau, Sarah J. Rice, Rodrigo Coutinho de Almeida, Kathleen Cheung, Unnur Styrkársdóttir, Lorraine Southam, Linda Broer, J. Mark Wilkinson, André G. Uitterlinden, Eleftheria Zeggini, David T. Felson, John Loughlin, Mariel Young, Terence D. Capellini, Ingrid Meulenbelt, Joyce B. J. van Meurs
Vydáno 2020Artigo -
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A comparison of genotyping arrays Autor Joost Verlouw, Eva Clemens, Jard H. de Vries, Oliver Zolk, Annemieke J.M.H. Verkerk, Antoinette am Zehnhoff‐Dinnesen, Carolina Medina‐Gómez, Claudia Lanvers‐Kaminsky, Fernando Rivadeneira, Thorsten Langer, Joyce B. J. van Meurs, Marry M. van den Heuvel‐Eibrink, André G. Uitterlinden, Linda Broer
Vydáno 2021Artigo -
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Leukocyte telomere length associates with prospective mortality independent of immune-related parameters and known genetic markers Autor Joris Deelen, Marian Beekman, Veryan Codd, Stella Trompet, Linda Broer, Sara Hägg, Krista Fischer, Peter Thijssen, H. Eka D. Suchiman, Iris Postmus, André G. Uitterlinden, Albert Hofman, Anton J. M. de Craen, Andres Metspalu, Nancy L. Pedersen, Cornelia M. van Duijn, J. Wouter Jukema, Jeanine J. Houwing‐Duistermaat, Nilesh J. Samani, P. Eline Slagboom
Vydáno 2014Artigo -
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Genome-wide association and functional studies identify a role for matrix Gla protein in osteoarthritis of the hand Autor Wouter den Hollander, Cindy G. Boer, Deborah Hart, Michelle S. Yau, Y.F. Ramos, Sarah Metrustry, Linda Broer, Joris Deelen, L. Adrienne Cupples, Fernando Rivadeneira, M. Kloppenburg, Marjolein J. Peters, Tim D. Spector, Albert Hofman, P. Eline Slagboom, Rob G. H. H. Nelissen, André G. Uitterlinden, David T. Felson, Ana M. Valdes, Ingrid Meulenbelt, Joyce B. J. van Meurs
Vydáno 2017Artigo -
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The influence of genetic variation on late toxicities in childhood cancer survivors: A review Autor Eva Clemens, Anne-Lotte van der Kooi, Linda Broer, Eline van Dulmen‐den Broeder, Henk Visscher, Leontien C.M. Kremer, Wim J. E. Tissing, Jacqueline J. Loonen, Cécile M. Ronckers, Saskia M. F. Pluijm, Sebastian Neggers, Oliver Zolk, Thorsten Langer, Antoinette am Zehnhoff‐Dinnesen, Carmen L. Wilson, Melissa M. Hudson, Bruce Carleton, Joop S.E. Laven, André G. Uitterlinden, Marry M. van den Heuvel‐Eibrink
Vydáno 2018Revisão -
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Meta-analysis of telomere length in 19 713 subjects reveals high heritability, stronger maternal inheritance and a paternal age effect Autor Linda Broer, Veryan Codd, Dale R. Nyholt, Joris Deelen, Massimo Mangino, Gonneke Willemsen, Eva Albrecht, Najaf Amin, Marian Beekman, Eco J. C. de Geus, Anjali K. Henders, Christopher P. Nelson, Claire J. Steves, Margaret J. Wright, Anton J.M. de Craen, Aaron Isaacs, Mary Matthews, Alireza Moayyeri, Grant W. Montgomery, Ben A. Oostra, Jacqueline M. Vink, Tim D. Spector, P. Eline Slagboom, Nicholas G. Martin, Nilesh J. Samani, Cornelia M. van Duijn, Dorret I. Boomsma
Vydáno 2013Revisão -
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Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome Autor Felix R. Day, David A. Hinds, Joyce Y. Tung, Lisette Stolk, Unnur Styrkársdóttir, Richa Saxena, Andrew Bjonnes, Linda Broer, David B. Dunger, Bjarni V. Halldórsson, Debbie A. Lawlor, Guillaume Laval, Iain Mathieson, Wendy L. McCardle, Yvonne V. Louwers, Cindy Meun, Susan M. Ring, Robert A. Scott, Patrick Sulem, André G. Uitterlinden, Nicholas J. Wareham, Unnur Þorsteinsdóttir, Corrine K. Welt, Kāri Stefánsson, Joop S.E. Laven, Ken K. Ong, John R. B. Perry
Vydáno 2015Artigo -
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Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment Autor A. Paul Nagtegaal, Linda Broer, Nuno R. Zilhão, Jóhanna Jakobsdóttir, Charles E. Bishop, Marco Brumat, Mark Christiansen, Massimiliano Cocca, Yan Gao, Nancy L. Heard‐Costa, Daniel S. Evans, Nathan Pankratz, Sheila R. Pratt, T. Ryan Price, Christopher Spankovich, Mary Rachel Stimson, Karen Valle, Dragana Vuckovic, Helena RR. Wells, Guðný Eiríksdóttir, Erik Fransén, M. Arfan Ikram, Chuang-Ming Li, W. T. Longstreth, Claire J. Steves, Guy Van Camp, Adolfo Correa, Karen J. Cruickshanks, Paolo Gasparini, Giorgia Girotto, Robert C. Kaplan, Michael A. Nalls, John M. Schweinfurth, Sudha Seshadri, Nona Sotoodehnia, Gregory J. Tranah, André G. Uitterlinden, James G. Wilson, Vilmundur Guðnason, Howard J. Hoffman, Frances M. K. Williams, André Goedegebure
Vydáno 2019Revisão -
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Short telomere length is associated with impaired cognitive performance in European ancestry cohorts Autor Sara Hägg, Yiqiang Zhan, Robert Karlsson, Lotte Gerritsen, Alexander Ploner, S J van der Lee, Linda Broer, Joris Deelen, Riccardo E. Marioni, Andrew Wong, Anders Lundquist, Gu Zhu, Narelle K. Hansell, Elina Sillanpää, Iryna O. Fedko, Najaf Amin, Marian Beekman, Anton J.M. de Craen, Sofie Degerman, Sarah E. Harris, K-J Kan, Carmen Martin‐Ruiz, Grant W. Montgomery, Annelie Nordin Adolfsson, Chandra A. Reynolds, Nilesh J. Samani, H. Eka D. Suchiman, Anne Viljanen, Thomas von Zglinicki, Margaret J. Wright, J-J Hottenga, Dorret I. Boomsma, Taina Rantanen, Jaakko Kaprio, Dale R. Nyholt, Nicholas G. Martin, Lars Nyberg, Rolf Adolfsson, Diana Kuh, John M. Starr, Ian J. Deary, P. Eline Slagboom, Cornelia M. van Duijn, Veryan Codd, Nancy L. Pedersen
Vydáno 2017Revisão -
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GWAS of Longevity in CHARGE Consortium Confirms APOE and FOXO3 Candidacy Autor Linda Broer, Aron S. Buchman, Joris Deelen, Daniel S. Evans, Jessica D. Faul, Kathryn L. Lunetta, Paola Sebastiani, Jennifer A. Smith, Albert V. Smith, Toshiko Tanaka, Lei Yu, Alice M. Arnold, Thor Aspelund, Emelia J. Benjamin, Philip L. De Jager, Gudny Eirkisdottir, Denis A. Evans, Melissa E. Garcia, Albert Hofman, Robert C. Kaplan, Sharon L. R. Kardia, Douglas P. Kiel, Ben A. Oostra, Eric Orwoll, Neeta Parimi, Bruce M. Psaty, Fernando Rivadeneira, Jerome I. Rotter, Sudha Seshadri, Andrew B. Singleton, Henning Tiemeier, André G. Uitterlinden, Wei Zhao, Stefania Bandinelli, David A. Bennett, Luigi Ferrucci, Vilmundur Guðnason, Tamara B. Harris, David Karasik, Lenore J. Launer, Thomas T. Perls, P. Eline Slagboom, Gregory J. Tranah, David R. Weir, Anne B. Newman, Cornelia M. van Duijn, Joanne M. Murabito
Vydáno 2014Revisão -
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Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria Autor Felix R. Day, Tugce Karaderi, Michelle R. Jones, Cindy Meun, Chunyan He, Alex Drong, Peter Kraft, Nan Lin, Hongyan Huang, Linda Broer, Reedik Mägi, Richa Saxena, Triin Laisk, Margrit Urbanek, M. Geoffrey Hayes, Guðmar Þorleifsson, Juan Fernández‐Tajes, Anubha Mahajan, Benjamin H. Mullin, Bronwyn Stuckey, Timothy D. Spector, Scott G. Wilson, Mark O. Goodarzi, Lea K. Davis, Barbara Obermayer‐Pietsch, André G. Uitterlinden, Verneri Anttila, Benjamin M. Neale, Marjo‐Riitta Järvelin, Bart C.J.M. Fauser, Irina Kowalska, Jenny A. Visser, Marianne Andersen, Ken K. Ong, Elisabet Stener‐Victorin, David A. Ehrmann, Richard S. Legro, Andres Salumets, Mark I. McCarthy, Laure Morin‐Papunen, Unnur Þorsteinsdóttir, Kāri Stefánsson, Unnur Styrkársdóttir, John R. B. Perry, Andrea Dunaif, Joop S.E. Laven, Steve Franks, Cecilia M. Lindgren, Corrine K. Welt
Vydáno 2018Revisão -
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Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region Autor Marjolein J. Peters, Linda Broer, Hanneke L.D.M. Willemen, Guðný Eiríksdóttir, Lynne J. Hocking, Kate L. Holliday, Michael A. Horan, Ingrid Meulenbelt, Tuhina Neogi, Maria Popham, Carsten Oliver Schmidt, Anushka Soni, Ana M. Valdes, Najaf Amin, Elaine Dennison, Niels Eijkelkamp, Tamara B. Harris, Deborah Hart, Albert Hofman, Frank Huygen, Anthony James, Gareth T. Jones, Lenore J. Launer, H. Kerkhof, Marjolein de Kruijf, John McBeth, M. Kloppenburg, William Ollier, Ben A. Oostra, Antony Payton, Fernando Rivadeneira, Blair H. Smith, Albert V. Smith, Lisette Stolk, Alexander Teumer, Wendy Thomson, André G. Uitterlinden, Ke Wang, Sophie H van Wingerden, Nigel Arden, Cyrus Cooper, David T. Felson, Vilmundur Guðnason, Gary J. Macfarlane, Neil Pendleton, P. Eline Slagboom, Tim D. Spector, Henry Völzke, Annemieke Kavelaars, Cornelia M. van Duijn, Frances M. K. Williams, Joyce B. J. van Meurs
Vydáno 2012Revisão -
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MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis Autor Christina M. Lill, Brit‐Maren M. Schjeide, Christiane Graetz, Maria Ban, Antonio Alcina, Miguel A. Ortiz, Jennifer Pérez‐Boza, Vincent Damotte, David R. Booth, Aitzkoa Lopez de Lapuente, Linda Broer, Marcel Schilling, Denis A. Akkad, Orhan Aktaş, Iraide Alloza, Alfredo Rodríguez Antigüedad, Rafa Arroyo, Paul Blaschke, Mathias Buttmann, Andrew Chan, Alastair Compston, Isabelle Cournu‐Rebeix, Thomas Dörner, Jörg T. Epplen, Óscar Fernández, Lisa-Ann Gerdes, Léna Guillot‐Noël, Hans-Peter Hartung, Sabine Hoffjan, Guillermo Izquierdo, Anu Kemppinen, Antje Kroner, Christian Kubisch, Tania Kümpfel, Shu Li, Ulman Lindenberger, Peter Lohse, Catherine Lubetzki, Felix Luessi, Sunny Malhotra, Julia Mescheriakova, Xavier Montalbán, Caroline Papeix, Lidia Fernández-Paredes, Peter Rieckmann, Elisabeth Steinhagen‐Thiessen, Alexander Winkelmann, Uwe K. Zettl, Rogier Hintzen, Koen Vandenbroeck, G. A. Stewart, Bertrand Fontaine, Manuel Comabella, Elena Urcelay, Fuencisla Matesanz, Stephen Sawcer, Lars Bertram, Frauke Zipp
Vydáno 2013Artigo -
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Genome-Wide Association Study Identifies Novel Loci Associated with Circulating Phospho- and Sphingolipid Concentrations Autor Ayşe Demirkan, Cornelia M. van Duijn, Péter Ugocsai, Aaron Isaacs, Peter P. Pramstaller, Gerhard Liebisch, James F. Wilson, Åsa Johansson, Igor Rudan, Yurii S. Aulchenko, Anatoly V. Kirichenko, A. Cecile J.W. Janssens, Ritsert C. Jansen, Carsten Gnewuch, Francisco S. Domingues, Cristian Pattaro, Sarah H. Wild, Inger Jonasson, Ozren Polašek, Irina V. Zorkoltseva, Albert Hofman, Lennart C. Karssen, Maksim Struchalin, James Floyd, Wilmar Igl, Zrinka Biloglav, Linda Broer, Arne Pfeufer, Irene Pichler, Susan Campbell, Ghazal Zaboli, Ivana Kolčić, Fernando Rivadeneira, Jennifer E. Huffman, Nicholas D. Hastie, André G. Uitterlinden, Lude Franke, Christopher Franklin, Véronique Vitart, Christopher P. Nelson, Michael Preuß, Joshua C. Bis, Christopher J. O’Donnell, Nora Franceschini, Jacqueline C.M. Witteman, Tatiana I. Axenovich, Ben A. Oostra, Thomas Meitinger, Andrew A. Hicks, Caroline Hayward, Alan F. Wright, Ulf Gyllensten, Harry Campbell, Gerd Schmitz
Vydáno 2012Revisão -
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Telomere length in circulating leukocytes is associated with lung function and disease Autor Eva Albrecht, Elina Sillanpää, Stefan Karrasch, Alexessander Couto Alves, Veryan Codd, Iiris Hovatta, Jessica L. Buxton, Christopher P. Nelson, Linda Broer, Sara Hägg, Massimo Mangino, Gonneke Willemsen, Ida Surakka, Manuel A. R. Ferreira, Najaf Amin, Ben A. Oostra, Heli Bäckmand, Markku Peltonen, Seppo Sarna, Taina Rantanen, Sarianna Sipilä, Tellervo Korhonen, Pamela A. F. Madden, Christian Gieger, Rudolf A. Jörres, Joachim Heinrich, Jürgen Behr, Rudolf M. Huber, Annette Peters, Konstantin Strauch, H.‐Erich Wichmann, Mélanie Waldenberger, Alexandra I. F. Blakemore, Eco J. C. de Geus, Dale R. Nyholt, Anjali K. Henders, Päivi Piirilä, Aila Rissanen, Patrik K. E. Magnusson, Ana Viñuela, Kirsi H. Pietiläinen, Nicholas G. Martin, Nancy L. Pedersen, Dorret I. Boomsma, Tim D. Spector, Cornelia M. van Duijn, Jaakko Kaprio, Nilesh J. Samani, Marjo‐Riitta Järvelin, Holger Schulz
Vydáno 2013Revisão -
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Genome-wide analysis of mitochondrial DNA copy number reveals loci implicated in nucleotide metabolism, platelet activation, and megakaryocyte proliferation Autor RJ Longchamps, Stephanie Yang, Christina A. Castellani, Wen Shi, Jon D. Lane, Megan L. Grove, T.M. Bartz, Chloé Sarnowski, C. Liu, Kimberley Burrows, Anna L. Guyatt, Tom R. Gaunt, Tim Kacprowski, Jingyun Yang, Philip L. De Jager, Lei Yu, Aviv Bergman, Rui Xia, Myriam Fornage, M.F. Feitosa, MK Wojczynski, Aldi T. Kraja, M. A. Province, Najaf Amin, Fernando Rivadeneira, Henning Tiemeier, André G. Uitterlinden, Linda Broer, Joyce B. J. van Meurs, Cornelia M. van Duijn, Laura M. Raffield, Leslie A. Lange, Stephen S. Rich, Rozenn N. Lemaître, Mark O. Goodarzi, C. M. Sitlani, Angel C. Y. Mak, David A. Bennett, Santiago Rodrı́guez, Joanne M. Murabito, Kathryn L. Lunetta, N Sotoodehnia, Gil Atzmon, Kenny Ye, Nir Barzilai, J. A. Brody, Bruce M. Psaty, Kent D. Taylor, Jerome I. Rotter, Eric Boerwinkle, Nathan Pankratz, Dan E. Arking
Vydáno 2021Artigo -
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Genome-wide association analysis of coffee drinking suggests association with CYP1A1/CYP1A2 and NRCAM Autor Najaf Amin, Enda M. Byrne, J Johnson, Georgia Chenevix‐Trench, Stefan Walter, Ilja M. Nolte, J M Vink, R Rawal, Massimo Mangino, Alexander Teumer, J C Keers, G Verwoert, S Baumeister, Reiner Biffar, Astrid Petersmann, Norbert Dahmen, Angela Doering, Aaron Isaacs, Linda Broer, Naomi R. Wray, Grant W. Montgomery, Daniel Levy, B M Psaty, Vilmundur Guðnason, A Chakravarti, P Sulem, Daníel F. Guðbjartsson, Lambertus A. Kiemeney, U Thorsteinsdottir, K Stefansson, Frank J.A. van Rooij, Yurii S. Aulchenko, Jouke‐Jan Hottenga, Fernando Rivadeneira, A Hofman, André G. Uitterlinden, Christopher J. Hammond, Seung‐Yun Shin, M. Arfan Ikram, Jacqueline C.M. Witteman, A. Cecile J.W. Janssens, H Snieder, Henning Tiemeier, B H R Wolfenbuttel, B A Oostra, Andrew C Heath, E. Wichmann, Tim D. Spector, H J Grabe, D I Boomsma, Nicholas G. Martin, Cornelia M. van Duijn
Vydáno 2011Revisão
Vyhledávací nástroje:
Související témata
Biology
Genetics
Gene
Medicine
Genotype
Single-nucleotide polymorphism
Genome-wide association study
Internal medicine
Genetic association
Computational biology
Endocrinology
Genome
Allele
Bioinformatics
Disease
Evolutionary biology
Meta-analysis
Psychology
Genetic architecture
Demography
Obesity
Population
Quantitative trait locus
Sociology
Allele frequency
Association (psychology)
DNA
Oncology
Pathology
Phenotype