Suchergebnisse - Jonatan Halvardson
- Treffer 1 - 14 von 14
-
1
Exome RNA sequencing reveals rare and novel alternative transcripts von Jonatan Halvardson, Ammar Zaghlool, Lars Feuk
Veröffentlicht 2012Artigo -
2
-
3
Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathy von Ronen Spiegel, Ann Saada, Jonatan Halvardson, Devorah Soiferman, Avraham Shaag, Simon Edvardson, Yoseph Horovitz, Morad Khayat, Stavit A. Shalev, Lars Feuk, Orly Elpeleg
Veröffentlicht 2013Artigo -
4
Mutations in<i>HECW2</i>are associated with intellectual disability and epilepsy von Jonatan Halvardson, Jin Zhao, Ammar Zaghlool, Christian Wentzel, Patrik Georgii‐Hemming, Else Månsson, Helena Ederth Sävmarker, Göran Brandberg, Cecilia Zander, Ann‐Charlotte Thuresson, Lars Feuk
Veröffentlicht 2016Artigo -
5
Exome sequencing reveals <i>NAA15</i> and <i>PUF60</i> as candidate genes associated with intellectual disability von Jin Zhao, Jonatan Halvardson, Cecilia Zander, Ammar Zaghlool, Patrik Georgii‐Hemming, Else Månsson, Göran Brandberg, Helena Ederth Sävmarker, Carina Frykholm, Ekaterina Kuchinskaya, Ann‐Charlotte Thuresson, Lars Feuk
Veröffentlicht 2017Artigo -
6
Loss of Y and clonal hematopoiesis in blood—two sides of the same coin? von Viktor Ljungström, Jonas Mattisson, Jonatan Halvardson, Tatjana Pandzic, Hanna Davies, Edyta Rychlicka-Buniowska, Marcus Danielsson, Paul Lacaze, Lucia Cavelier, Jan P. Dumanski, Panagiotis Baliakas, Lars A. Forsberg
Veröffentlicht 2021Carta -
7
Infantile Cerebellar-Retinal Degeneration Associated with a Mutation in Mitochondrial Aconitase, ACO2 von Ronen Spiegel, Ophry Pines, Asaf Ta‐Shma, Efrat Burak, Avraham Shaag, Jonatan Halvardson, Simon Edvardson, Muhammad Mahajna, Shamir Zenvirt, Ann Saada, Stavit A. Shalev, Lars Feuk, Orly Elpeleg
Veröffentlicht 2012Artigo -
8
Loss of chromosome Y in regulatory T cells von Jonas Mattisson, Jonatan Halvardson, Hanna Davies, Bożena Bruhn‐Olszewska, Paweł Olszewski, Marcus Danielsson, Josefin Bjurling, Amanda Lindberg, Ammar Zaghlool, Edyta Rychlicka-Buniowska, Jan P. Dumanski, Lars A. Forsberg
Veröffentlicht 2024Artigo -
9
Leukocytes with chromosome Y loss have reduced abundance of the cell surface immunoprotein CD99 von Jonas Mattisson, Marcus Danielsson, Maria Hammond, Hanna Davies, Caroline J. Gallant, Jessica Nordlund, Amanda Raine, Malin Edén, Lena Kilander, Martin Ingelsson, Jan P. Dumanski, Jonatan Halvardson, Lars A. Forsberg
Veröffentlicht 2021Artigo -
10
Longitudinal changes in the frequency of mosaic chromosome Y loss in peripheral blood cells of aging men varies profoundly between individuals von Marcus Danielsson, Jonatan Halvardson, Hanna Davies, Behrooz Torabi Moghadam, Jonas Mattisson, Edyta Rychlicka-Buniowska, Janusz Jaszczyński, Julia Heintz, Lars Lannfelt, Vilmantas Giedraitis, Martin Ingelsson, Jan P. Dumanski, Lars A. Forsberg
Veröffentlicht 2019Artigo -
11
Mosaic loss of chromosome Y in blood is associated with male susceptibility for idiopathic pulmonary fibrosis von Josefin Bjurling, Nicholas W. Chavkin, Jonatan Halvardson, Mark C. Thel, Jonas Mattisson, John S. Kim, Ammar Zaghlool, Shwu‐Fan Ma, Fernando J. Martínez, Kevin J. Anstrom, Imre Noth, Kenneth Walsh, Lars A. Forsberg
Veröffentlicht 2025Artigo -
12
Hematopoietic loss of Y chromosome leads to cardiac fibrosis and heart failure mortality von Soichi Sano, Keita Horitani, Hayato Ogawa, Jonatan Halvardson, Nicholas W. Chavkin, Ying Wang, Miho Sano, Jonas Mattisson, Atsushi Hata, Marcus Danielsson, Emiri Miura‐Yura, Ammar Zaghlool, Megan A. Evans, Tove Fall, Henry N. De Hoyos, Johan Sundström, Yoshimitsu Yura, Anupreet Kour, Yohei Arai, Mark C. Thel, Yuka Arai, Josyf C. Mychaleckyj, Karen K. Hirschi, Lars A. Forsberg, Kenneth Walsh
Veröffentlicht 2022Artigo -
13
Immune cells lacking Y chromosome show dysregulation of autosomal gene expression von Jan P. Dumanski, Jonatan Halvardson, Hanna Davies, Edyta Rychlicka-Buniowska, Jonas Mattisson, Behrooz Torabi Moghadam, Noémi Nagy, Kazimierz Węglarczyk, Karolina Bukowska-Straková, Marcus Danielsson, Paweł Olszewski, Arkadiusz Piotrowski, Erin Oerton, Aleksandra Ambicka, Marcin Przewoźnik, Łukasz Bełch, Tomasz Grodzicki, Piotr Chłosta, Stefan Imreh, Vilmantas Giedraitis, Lena Kilander, Jessica Nordlund, Adam Ameur, Ulf Gyllensten, Åsa Johansson, Alicja Józkowicz, Maciej Siedlar, Alicja Klich‐Rączka, Janusz Jaszczyński, Stefan Enroth, Jarosław Baran, Martin Ingelsson, John R. B. Perry, Janusz Ryś, Lars A. Forsberg
Veröffentlicht 2021Artigo -
14
Genetic predisposition to mosaic Y chromosome loss in blood von Deborah J. Thompson, Giulio Genovese, Jonatan Halvardson, Jacob C. Ulirsch, Daniel J. Wright, Chikashi Terao, Olafur B. Davidsson, Felix R. Day, Patrick Sulem, Yunxuan Jiang, Marcus Danielsson, Hanna Davies, Joe Dennis, Malcolm G. Dunlop, Douglas F. Easton, Victoria A. Fisher, Florian Zink, Richard S. Houlston, Martin Ingelsson, Siddhartha Kar, Nicola D. Kerrison, Ben Kinnersley, Ragnar P. Kristjansson, Philip Law, Rong Li, Chey Loveday, Jonas Mattisson, Steven A. McCarroll, Yoshinori Murakami, Anna Murray, Paweł Olszewski, Edyta Rychlicka-Buniowska, Robert A. Scott, Unnur Þorsteinsdóttir, Ian Tomlinson, Behrooz Torabi Moghadam, Clare Turnbull, Nicholas J. Wareham, Daníel F. Guðbjartsson, Yoichiro Kamatani, Eva R. Hoffmann, Stephen P. Jackson, Kāri Stefánsson, Adam Auton, Ken K. Ong, Mitchell J. Machiela, Po‐Ru Loh, Jan P. Dumanski, Stephen J. Chanock, Lars A. Forsberg, John R. B. Perry
Veröffentlicht 2019Artigo
Suchwerkzeuge:
Ähnliche Schlagworte
Biology
Genetics
Gene
Medicine
Immunology
Mutation
Chromosome
Exome sequencing
Internal medicine
Computational biology
DNA sequencing
Disease
Exome
Genome
Immune system
Phenotype
Stem cell
Y chromosome
Aconitase
Candidate gene
Cell biology
Copy-number variation
Endocrinology
Gene expression
Haematopoiesis
History
Intellectual disability
Mitochondrion
Molecular biology
Mosaic