Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Jonatan, Halvardson"'
Autor:
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
Publikováno v:
BMC Genomics, Vol 25, Iss 1, Pp 1-11 (2024)
Abstract Background Mosaic loss of chromosome Y (LOY) in leukocytes is the most prevalent somatic aneuploidy in aging humans. Men with LOY have increased risks of all-cause mortality and the major causes of death, including many forms of cancer. It h
Externí odkaz:
https://doaj.org/article/3fb79618f8b24d1694b937e0dfc03697
Autor:
Moeen Riaz, Jonas Mattisson, Galina Polekhina, Andrew Bakshi, Jonatan Halvardson, Marcus Danielsson, Adam Ameur, John McNeil, Lars A. Forsberg, Paul Lacaze
Publikováno v:
Cell & Bioscience, Vol 11, Iss 1, Pp 1-8 (2021)
Abstract Background Mosaic loss of Y chromosome (LOY) is the most common somatic change that occurs in circulating white blood cells of older men. LOY in leukocytes is associated with increased risk for all-cause mortality and a range of common disea
Externí odkaz:
https://doaj.org/article/6c13a30b4ab04fb99c76deb137dfceec
Autor:
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
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Abstract Mosaic loss of chromosome Y (LOY) in immune cells is a male-specific mutation associated with increased risk for morbidity and mortality. The CD99 gene, positioned in the pseudoautosomal regions of chromosomes X and Y, encodes a cell surface
Externí odkaz:
https://doaj.org/article/59f0cb315b52492d8a02d3b3ffbc2609
Autor:
Eva Lindholm Carlström, Jonatan Halvardson, Mitra Etemadikhah, Lennart Wetterberg, Karl-Henrik Gustavson, Lars Feuk
Publikováno v:
BMC Medical Genomics, Vol 12, Iss 1, Pp 1-9 (2019)
Abstract Background Non-syndromic intellectual disability is genetically heterogeneous with dominant, recessive and complex forms of inheritance. We have performed detailed genetic studies in a large multi-generational Swedish family, including sever
Externí odkaz:
https://doaj.org/article/7722400c1fef40928b252530b1a420ea
Autor:
Martin M. Johansson, Philipp Pottmeier, Pascalina Suciu, Tauseef Ahmad, Ammar Zaghlool, Jonatan Halvardson, Elisabeth Darj, Lars Feuk, Christiane Peuckert, Elena Jazin
Publikováno v:
Frontiers in Genetics, Vol 10 (2019)
Global microarray gene expression analyses previously demonstrated differences in female and male embryos during neurodevelopment. In particular, before sexual maturation of the gonads, the differences seem to concentrate on the expression of genes e
Externí odkaz:
https://doaj.org/article/a5e2fb89068844bc81cf1644ab815bce
Autor:
Ragnar P. Kristjansson, Steven A. McCarroll, Florian Zink, Malcolm G. Dunlop, Nicholas J. Wareham, Yoichiro Kamatani, Daniel F. Gudbjartsson, Giulio Genovese, Rong Li, Stephen J. Chanock, Unnur Thorsteinsdottir, Ben Kinnersley, Kari Stefansson, Philip J. Law, Martin Ingelsson, Lars Forsberg, Joe Dennis, Richard S. Houlston, Jonatan Halvardson, Nicola D. Kerrison, Chikashi Terao, Douglas F. Easton, Anna Murray, Yunxuan Jiang, Jan P. Dumanski, Chey Loveday, Steve P Jackson, Robert A. Scott, Edyta Rychlicka-Buniowska, Ian Tomlinson, Daniel J Wright, Deborah J. Thompson, Victoria A Fisher, Yoshinori Murakami, John R. B. Perry, Paweł Olszewski, Felix R. Day, Eva Hoffmann, Hanna Davies, Po-Ru Loh, Adam Auton, Siddhartha Kar, Behrooz Torabi Moghadam, Clare Turnbull, Ken K. Ong, Marcus Danielsson, Jacob C. Ulirsch, Jonas Mattisson, Patrick Sulem, Olafur B. Davidsson, Mitchell J. Machiela
Publikováno v:
Thompson, D J, Genovese, G, Kar, S, Perry, J RB & et al. 2019, ' Genetic predisposition to mosaic Y chromosome loss in blood ', Nature, vol. 575, pp. 652–657 . https://doi.org/10.1038/s41586-019-1765-3
Nature, 575(7784), 652-657. Nature Publishing Group
Thompson, D J, Genovese, G, Forsberg, L A, Perry, J R B, International Lung Cancer Consortium (INTEGRAL-ILCCO), Boomsma, D, Nivard, M, van Dongen, J, Pool, R & Hottenga, J J 2019, ' Genetic predisposition to mosaic Y chromosome loss in blood ', Nature, vol. 575, no. 7784, pp. 652-657 . https://doi.org/10.1038/s41586-019-1765-3
Nature
2019, ' Genetic predisposition to mosaic Y chromosome loss in blood ', Nature, vol. 575, no. 7784, pp. 652-657 . https://doi.org/10.1038/s41586-019-1765-3
Thompson, D J, Genovese, G, Halvardson, J, Ulirsch, J C, Wright, D J, Terao, C, Davidsson, O B, Day, F R, Sulem, P, Jiang, Y, Danielsson, M, Davies, H, Dennis, J, Dunlop, M G, Easton, D F, Fisher, V A, Zink, F, Houlston, R S, Ingelsson, M, Kar, S, Kerrison, N D, Kinnersley, B, Kristjansson, R P, Law, P J, Li, R, Loveday, C, Mattisson, J, McCarroll, S A, Murakami, Y, Murray, A, Olszewski, P, Rychlicka-Buniowska, E, Scott, R A, Thorsteinsdottir, U, Tomlinson, I, Moghadam, B T, Turnbull, C, Wareham, N J, Gudbjartsson, D F, Kamatani, Y, Hoffmann, E R, Jackson, S P, Stefansson, K, Auton, A, Ong, K K, Machiela, M J, Loh, P-R, Dumanski, J P, Chanock, S J, Forsberg, L A, International Lung Cancer Consortium (INTEGRAL-ILCCO) & The PRACTICAL Consortium 2019, ' Genetic predisposition to mosaic Y chromosome loss in blood ', Nature, vol. 575, no. 7784, pp. 652-657 . https://doi.org/10.1038/s41586-019-1765-3
Nature, 575(7784), 652-657. Nature Publishing Group
Thompson, D J, Genovese, G, Forsberg, L A, Perry, J R B, International Lung Cancer Consortium (INTEGRAL-ILCCO), Boomsma, D, Nivard, M, van Dongen, J, Pool, R & Hottenga, J J 2019, ' Genetic predisposition to mosaic Y chromosome loss in blood ', Nature, vol. 575, no. 7784, pp. 652-657 . https://doi.org/10.1038/s41586-019-1765-3
Nature
2019, ' Genetic predisposition to mosaic Y chromosome loss in blood ', Nature, vol. 575, no. 7784, pp. 652-657 . https://doi.org/10.1038/s41586-019-1765-3
Thompson, D J, Genovese, G, Halvardson, J, Ulirsch, J C, Wright, D J, Terao, C, Davidsson, O B, Day, F R, Sulem, P, Jiang, Y, Danielsson, M, Davies, H, Dennis, J, Dunlop, M G, Easton, D F, Fisher, V A, Zink, F, Houlston, R S, Ingelsson, M, Kar, S, Kerrison, N D, Kinnersley, B, Kristjansson, R P, Law, P J, Li, R, Loveday, C, Mattisson, J, McCarroll, S A, Murakami, Y, Murray, A, Olszewski, P, Rychlicka-Buniowska, E, Scott, R A, Thorsteinsdottir, U, Tomlinson, I, Moghadam, B T, Turnbull, C, Wareham, N J, Gudbjartsson, D F, Kamatani, Y, Hoffmann, E R, Jackson, S P, Stefansson, K, Auton, A, Ong, K K, Machiela, M J, Loh, P-R, Dumanski, J P, Chanock, S J, Forsberg, L A, International Lung Cancer Consortium (INTEGRAL-ILCCO) & The PRACTICAL Consortium 2019, ' Genetic predisposition to mosaic Y chromosome loss in blood ', Nature, vol. 575, no. 7784, pp. 652-657 . https://doi.org/10.1038/s41586-019-1765-3
Mosaic loss of chromosome Y (LOY) in circulating white blood cells is the most common form of clonal mosaicism1–5, yet our knowledge of the causes and consequences of this is limited. Here, using a computational approach, we estimate that 20% of th
Autor:
Jonatan Halvardson, Lars Feuk, Mitra Etemadikhah, Eva Lindholm Carlström, Lennart Wetterberg, Karl-Henrik Gustavson
Publikováno v:
BMC Medical Genomics, Vol 12, Iss 1, Pp 1-9 (2019)
BMC Medical Genomics
BMC Medical Genomics
Background Non-syndromic intellectual disability is genetically heterogeneous with dominant, recessive and complex forms of inheritance. We have performed detailed genetic studies in a large multi-generational Swedish family, including several member
Autor:
Mitra Etemadikhah, Grazyna Rajkowska, Craig A. Stockmeier, Lars Feuk, Adnan Niazi, Eva Lindholm Carlström, Bo Nilsson, Jonatan Halvardson, Stefan Enroth
Publikováno v:
Genes
Volume 12
Issue 8
Genes, Vol 12, Iss 1242, p 1242 (2021)
Volume 12
Issue 8
Genes, Vol 12, Iss 1242, p 1242 (2021)
Schizophrenia is a genetically complex neuropsychiatric disorder with largely unresolved mechanisms of pathology. Identification of genes and pathways associated with schizophrenia is important for understanding the development, progression and treat
Autor:
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
Publikováno v:
Leukemia. 36(3)
Autor:
Malin Edén, Maria Hammond, Hanna Davies, Amanda Raine, Jonatan Halvardson, Jonas Mattisson, Martin Ingelsson, Marcus Danielsson, Jan P. Dumanski, Lars Forsberg, Jessica Nordlund, Caroline J. Gallant, Lena Kilander
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-9 (2021)
Mosaic loss of chromosome Y (LOY) in immune cells is a male-specific mutation associated with increased risk for morbidity and mortality. TheCD99gene, positioned in the pseudoautosomal regions of chromosomes X and Y, encodes a cell surface protein es