نتائج البحث - Jonas Mengel‐From
- يعرض 1 - 12 نتائج من 12
-
1
-
2
-
3
-
4
-
5
-
6
-
7
-
8
-
9
Genetics of monozygotic twins reveals the impact of environmental sensitivity on psychiatric and neurodevelopmental phenotypes حسب Elham Assary, Jonathan R. I. Coleman, Gibran Hemani, Margot P. van de Weijer, Laurence J Howe, Teemu Palviainen, Katrina L. Grasby, Rafael Ahlskog, Marianne Nygaard, Rosa Cheesman, Kai Lim, Chandra A. Reynolds, Juan R. Ordoñana, Lucía Colodro‐Conde, Scott D. Gordon, Juan J. Madrid‐Valero, Anbupalam Thalamuthu, Jouke‐Jan Hottenga, Jonas Mengel‐From, Nicola J. Armstrong, Perminder S. Sachdev, Teresa Lee, Henry Brodaty, Julian N. Trollor, Margaret J. Wright, David Ames, Vibeke S. Catts, Antti Latvala, Eero Vuoksimaa, Travis T. Mallard, K. Paige Harden, Elliot M. Tucker‐Drob, Sven Oskarsson, Christopher J. Hammond, Kaare Christensen, Mark J. Taylor, Sebastian Lundström, Henrik Larsson, Robert Karlsson, Nancy L. Pedersen, Karen A. Mather, Sarah E. Medland, Dorret I. Boomsma, Nicholas G. Martin, Robert Plomin, Meike Bartels, Paul Lichtenstein, Jaakko Kaprio, Thalia C. Eley, Neil M Davies, Patricia B. Munroe, Robert Keers
منشور في 2025Artigo -
10
Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing loss حسب Natalia Trpchevska, Maxim B. Freidin, Linda Broer, Berthe C. Oosterloo, Shuyang Yao, Yitian Zhou, Barbara Vona, Charles E. Bishop, Argyro Bizaki-Vallaskangas, Barbara Canlon, Fabio Castellana, Daniel I. Chasman, Stacey S. Cherny, Kaare Christensen, Maria Pina Concas, Adolfo Correa, Ran Elkon, Jonas Mengel‐From, Yan Gao, Anne B.S. Giersch, Giorgia Girotto, Alexander Guðjónsson, Vilmundur Guðnason, Nancy L. Heard‐Costa, Ronna Hertzano, Jacob Hjelmborg, Jens Hjerling‐Leffler, Howard J. Hoffman, Jaakko Kaprio, Johannes Kettunen, Kristi Krebs, Anna K. Kähler, François Lallemend, Lenore J. Launer, I‐Min Lee, Hampton L. Leonard, Chuan-Ming Li, Hubert Löwenheim, Patrik K. E. Magnusson, Joyce B. J. van Meurs, Lili Milani, Cynthia C. Morton, Antti Mäkitie, Mike A. Nalls, Giuseppe Giovanni Nardone, Marianne Nygaard, Teemu Palviainen, Sheila R. Pratt, Nicola Quaranta, Joel Rämö, Elmo Saarentaus, Rodolfo Sardone, Claudia L. Satizábal, John M. Schweinfurth, Sudha Seshadri, Eric J. Shiroma, Eldad D. Shulman, Eleanor M. Simonsick, Christopher Spankovich, Anke Tropitzsch, Volker M. Lauschke, Patrick F. Sullivan, André Goedegebure, Christopher R. Cederroth, Frances M. K. Williams, A. Paul Nagtegaal, Andres Metspalu, Mari Nelis, Reedik Mägi, Tõnu Esko
منشور في 2022Revisão -
11
Genome-wide association studies identify 137 genetic loci for DNA methylation biomarkers of aging حسب Daniel L. McCartney, Josine L. Min, Rebecca C. Richmond, Ake T. Lu, Maria Sobczyk, Gail Davies, Linda Broer, Xiuqing Guo, Ayoung Jeong, Jeesun Jung, Silva Kasela, Şeyma Katrinli, Pei‐Lun Kuo, Pamela R. Matías‐García, Pashupati P. Mishra, Marianne Nygaard, Teemu Palviainen, Amit Patki, Laura M. Raffield, Scott M. Ratliff, Tom G. Richardson, Oliver Robinson, Mette Soerensen, Dianjianyi Sun, Pei-Chien Tsai, Matthijs D. van der Zee, Rosie M. Walker, Xiaochuan Wang, Yunzhang Wang, Rui Xia, Zongli Xu, Jie Yao, Wei Zhao, Adolfo Correa, Eric Boerwinkle, Pierre‐Antoine Dugué, Peter Durda, Hannah R. Elliott, Christian Gieger, Eco J. C. de Geus, Sarah E. Harris, Gibran Hemani, Medea Imboden, Mika Kähönen, Sharon L. R. Kardia, Jacob K. Kresovich, Shengxu Li, Kathryn L. Lunetta, Massimo Mangino, Dan Mason, Andrew M. McIntosh, Jonas Mengel‐From, Ann Zenobia Moore, Joanne M. Murabito, Miina Ollikainen, James S. Pankow, Nancy L. Pedersen, Annette Peters, Silvia Polidoro, David J. Porteous, Olli T. Raitakari, Stephen S. Rich, Dale P. Sandler, Elina Sillanpää, Alicia K. Smith, Melissa C. Southey, Konstantin Strauch, Hemant K. Tiwari, Toshiko Tanaka, Therese Tillin, André G. Uitterlinden, David Van Den Berg, Jenny van Dongen, James G. Wilson, John Wright, İdil Yet, Donna K. Arnett, Stefania Bandinelli, Jordana T. Bell, Alexandra M. Binder, Dorret I. Boomsma, Wei Chen, Kaare Christensen, Karen N. Conneely, Paul Elliott, Luigi Ferrucci, Myriam Fornage, Sara Hägg, Caroline Hayward, Marguerite M Irvin, Jaakko Kaprio, Debbie A. Lawlor, Terho Lehtimäki, Falk W. Lohoff, Lili Milani, Roger L. Milne, Nicole Probst‐Hensch, Alex P. Reiner, Beate Ritz, Jerome I. Rotter
منشور في 2021Artigo -
12
A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity حسب Sven J. van der Lee, Olivia J. Conway, Iris E. Jansen, Minerva M. Carrasquillo, Luca Kleineidam, Erik B. van den Akker, Isabel Hernández, Kristel R. van Eijk, Najada Stringa, Jason Chen, Anna Zettergren, Till F. M. Andlauer, Mónica Díez-Fairén, Javier Simón‐Sánchez, Alberto Lleó, Henrik Zetterberg, Marianne Nygaard, Cornelis Blauwendraat, Jeanne E. Savage, Jonas Mengel‐From, Sonia Moreno‐Grau, Michael Wagner, Juan Fortea, Michael J. Keogh, Kaj Blennow, Ingmar Skoog, Manuel A. Friese, Olga Pletnikova, Miren Zulaica, Carmen Lage, Itziar de Rojas, Steffi G. Riedel‐Heller, Ignacio Illán‐Gala, Wei Wei, Bernard Jeune, Adelina Orellana, Florian Then Bergh, Xue Wang, Marc Hulsman, Nina Beker, Niccoló Tesi, Christopher M. Morris, Begoña Indakoetxea, Lyduine E. Collij, Martin Scherer, Estrella Morenas‐Rodríguez, James W. Ironside, Bart N.M. van Berckel, Daniel Alcolea, Heinz Wiendl, Samantha L. Strickland, Pau Pástor, Eloy Rodríguez‐Rodríguez, Bradley F. Boeve, Ronald C. Petersen, Tanis J. Ferman, Jay A. van Gerpen, Marcel J. T. Reinders, Ryan J. Uitti, Lluís Tárraga, Wolfgang Maier, Oriol Dols‐Icardo, Amit Kawalia, Carolina Dalmasso, Merçé Boada, Uwe K. Zettl, Natasja M. van Schoor, Marian Beekman, Mariet Allen, Eliezer Masliah, Adolfo López de Munain, Alexander Pantelyat, Zbigniew K. Wszołek, Owen A. Ross, Dennis W. Dickson, Caroline Graff, David S. Knopman, Rosa Rademakers, Afina W. Lemstra, Yolande A.L. Pijnenburg, Philip Scheltens, Thomas Gasser, Patrick F. Chinnery, Bernhard Hemmer, Martijn Huisman, Juan C. Troncoso, Fermín Moreno, Ellen A. Nøhr, Thorkild I. A. Sørensen, Peter Heutink, Pascual Sánchez‐Juan, Daniëlle Posthuma, Jordi Clarimón, Kaare Christensen, Nilüfer Ertekin‐Taner, Sonja W. Scholz, Alfredo Ramı́rez, Agustı́n Ruiz, P. Eline Slagboom, Wiesje M. van der Flier
منشور في 2019Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Genetics
Gene
Medicine
Genotype
Single-nucleotide polymorphism
Cognition
Evolutionary biology
Genome-wide association study
Internal medicine
Population
Candidate gene
Chemistry
Computational biology
Danish
Dementia
Disease
Environmental health
Genetic association
Gerontology
Heritability
Linguistics
Neuroscience
Oncology
Organic chemistry
Philosophy
Psychiatry
Psychology
Twin study
Acrylonitrile