نتائج البحث - Halvardson, Jonatan

Exome RNA sequencing reveals rare and novel alternative transcripts حسب Halvardson, Jonatan, Zaghlool, Ammar, Feuk, Lars

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Reply to Veitia حسب Danielsson, Marcus, Halvardson, Jonatan, Mattisson, Jonas, Forsberg, Lars A.

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Efficient cellular fractionation improves RNA sequencing analysis of mature and nascent transcripts from human tissues حسب Zaghlool, Ammar, Ameur, Adam, Nyberg, Linnea, Halvardson, Jonatan, Grabherr, Manfred, Cavelier, Lucia, Feuk, Lars

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Linkage and exome analysis implicate multiple genes in non-syndromic intellectual disability in a large Swedish family حسب Lindholm Carlström, Eva, Halvardson, Jonatan, Etemadikhah, Mitra, Wetterberg, Lennart, Gustavson, Karl-Henrik, Feuk, Lars

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Reduced cell surface levels of GPI‐linked markers in a new case with PIGG loss of function حسب Zhao, Jin James, Halvardson, Jonatan, Knaus, Alexej, Georgii‐Hemming, Patrik, Baeck, Peter, Krawitz, Peter M., Thuresson, Ann‐Charlotte, Feuk, Lars

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Transcriptome Analysis of Post-Mortem Brain Tissue Reveals Up-Regulation of the Complement Cascade in a Subgroup of Schizophrenia Patients حسب Lindholm Carlström, Eva, Niazi, Adnan, Etemadikhah, Mitra, Halvardson, Jonatan, Enroth, Stefan, Stockmeier, Craig A., Rajkowska, Grazyna, Nilsson, Bo, Feuk, Lars

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A Role for the Chromatin‐Remodeling Factor BAZ1A in Neurodevelopment حسب Zaghlool, Ammar, Halvardson, Jonatan, Zhao, Jin J., Etemadikhah, Mitra, Kalushkova, Antonia, Konska, Katarzyna, Jernberg‐Wiklund, Helena, Thuresson, Ann‐Charlotte, Feuk, Lars

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Novel Y-Chromosome Long Non-Coding RNAs Expressed in Human Male CNS During Early Development حسب Johansson, Martin M., Pottmeier, Philipp, Suciu, Pascalina, Ahmad, Tauseef, Zaghlool, Ammar, Halvardson, Jonatan, Darj, Elisabeth, Feuk, Lars, Peuckert, Christiane, Jazin, Elena

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A polygenic risk score predicts mosaic loss of chromosome Y in circulating blood cells حسب Riaz, Moeen, Mattisson, Jonas, Polekhina, Galina, Bakshi, Andrew, Halvardson, Jonatan, Danielsson, Marcus, Ameur, Adam, McNeil, John, Forsberg, Lars A., Lacaze, Paul

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Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathy حسب Spiegel, Ronen, Saada, Ann, Halvardson, Jonatan, Soiferman, Devorah, Shaag, Avraham, Edvardson, Simon, Horovitz, Yoseph, Khayat, Morad, Shalev, Stavit A, Feuk, Lars, Elpeleg, Orly

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Whole genome sequencing of consanguineous families reveals novel pathogenic variants in intellectual disability حسب Thuresson, Ann‐Charlotte, Soussi Zander, Cecilia, Zhao, Jin J., Halvardson, Jonatan, Maqbool, Khurram, Månsson, Else, Stenninger, Eric, Holmlund, Ulrika, Öhrner, Ylva, Feuk, Lars

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Identification and rescue of a tRNA wobble inosine deficiency causing intellectual disability disorder حسب Ramos, Jillian, Proven, Melissa, Halvardson, Jonatan, Hagelskamp, Felix, Kuchinskaya, Ekaterina, Phelan, Benjamin, Bell, Ryan, Kellner, Stefanie M., Feuk, Lars, Thuresson, Ann-Charlotte, Fu, Dragony

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Infantile Cerebellar-Retinal Degeneration Associated with a Mutation in Mitochondrial Aconitase, ACO2 حسب Spiegel, Ronen, Pines, Ophry, Ta-Shma, Asaf, Burak, Efrat, Shaag, Avraham, Halvardson, Jonatan, Edvardson, Shimon, Mahajna, Muhammad, Zenvirt, Shamir, Saada, Ann, Shalev, Stavit, Feuk, Lars, Elpeleg, Orly

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Mutations in HECW2 are associated with intellectual disability and epilepsy حسب Halvardson, Jonatan, Zhao, Jin J, Zaghlool, Ammar, Wentzel, Christian, Georgii-Hemming, Patrik, Månsson, Else, Ederth Sävmarker, Helena, Brandberg, Göran, Soussi Zander, Cecilia, Thuresson, Ann-Charlotte, Feuk, Lars

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Loss of Y and clonal hematopoiesis in blood—two sides of the same coin? حسب Ljungström, Viktor, Mattisson, Jonas, Halvardson, Jonatan, Pandzic, Tatjana, Davies, Hanna, Rychlicka-Buniowska, Edyta, Danielsson, Marcus, Lacaze, Paul, Cavelier, Lucia, Dumanski, Jan P., Baliakas, Panagiotis, Forsberg, Lars A.

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Exome sequencing reveals NAA15 and PUF60 as candidate genes associated with intellectual disability حسب Zhao, Jin J., Halvardson, Jonatan, Zander, Cecilia S., Zaghlool, Ammar, Georgii‐Hemming, Patrik, Månsson, Else, Brandberg, Göran, Sävmarker, Helena E., Frykholm, Carina, Kuchinskaya, Ekaterina, Thuresson, Ann‐Charlotte, Feuk, Lars

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Leukocytes with chromosome Y loss have reduced abundance of the cell surface immunoprotein CD99 حسب Mattisson, Jonas, Danielsson, Marcus, Hammond, Maria, Davies, Hanna, Gallant, Caroline J., Nordlund, Jessica, Raine, Amanda, Edén, Malin, Kilander, Lena, Ingelsson, Martin, Dumanski, Jan P., Halvardson, Jonatan, Forsberg, Lars A.

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Longitudinal changes in the frequency of mosaic chromosome Y loss in peripheral blood cells of aging men varies profoundly between individuals حسب Danielsson, Marcus, Halvardson, Jonatan, Davies, Hanna, Torabi Moghadam, Behrooz, Mattisson, Jonas, Rychlicka-Buniowska, Edyta, Jaszczyński, Janusz, Heintz, Julia, Lannfelt, Lars, Giedraitis, Vilmantas, Ingelsson, Martin, Dumanski, Jan P., Forsberg, Lars A.

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Immune cells lacking Y chromosome show dysregulation of autosomal gene expression حسب Dumanski, Jan P., Halvardson, Jonatan, Davies, Hanna, Rychlicka-Buniowska, Edyta, Mattisson, Jonas, Moghadam, Behrooz Torabi, Nagy, Noemi, Węglarczyk, Kazimierz, Bukowska-Strakova, Karolina, Danielsson, Marcus, Olszewski, Paweł, Piotrowski, Arkadiusz, Oerton, Erin, Ambicka, Aleksandra, Przewoźnik, Marcin, Bełch, Łukasz, Grodzicki, Tomasz, Chłosta, Piotr L., Imreh, Stefan, Giedraitis, Vilmantas, Kilander, Lena, Nordlund, Jessica, Ameur, Adam, Gyllensten, Ulf, Johansson, Åsa, Józkowicz, Alicja, Siedlar, Maciej, Klich-Rączka, Alicja, Jaszczyński, Janusz, Enroth, Stefan, Baran, Jarosław, Ingelsson, Martin, Perry, John R. B., Ryś, Janusz, Forsberg, Lars A.

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Genetic predisposition to mosaic Y chromosome loss in blood حسب Thompson, Deborah J., Genovese, Giulio, Halvardson, Jonatan, Ulirsch, Jacob C., Wright, Daniel J., Terao, Chikashi, Davidsson, Olafur B., Day, Felix R., Sulem, Patrick, Jiang, Yunxuan, Danielsson, Marcus, Davies, Hanna, Dennis, Joe, Dunlop, Malcolm G., Easton, Douglas F., Fisher, Victoria A., Zink, Florian, Houlston, Richard S., Ingelsson, Martin, Kar, Siddhartha, Kerrison, Nicola D., Kinnersley, Ben, Kristjansson, Ragnar P., Law, Philip J., Li, Rong, Loveday, Chey, Mattisson, Jonas, McCarroll, Steven A., Murakami, Yoshinori, Murray, Anna, Olszewski, Pawel, Rychlicka-Buniowska, Edyta, Scott, Robert A., Thorsteinsdottir, Unnur, Tomlinson, Ian, Torabi Moghadam, Behrooz, Turnbull, Clare, Wareham, Nicholas J., Gudbjartsson, Daniel F., Kamatani, Yoichiro, Hoffmann, Eva R., Jackson, Steve P., Stefansson, Kari, Auton, Adam, Ong, Ken K., Machiela, Mitchell J., Loh, Po-Ru, Dumanski, Jan P., Chanock, Stephen J., Forsberg, Lars A., Perry, John R. B.

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