Ammar Zaghlool

Mosaic loss of chromosome Y in blood is associated with male susceptibility for idiopathic pulmonary fibrosis

Bjurling, Josefin; Chavkin, Nicholas W.; Halvardson, Jonatan; Thel, Mark C. et al.

Ingår i Communications Medicine, 2025

• DOI för Mosaic loss of chromosome Y in blood is associated with male susceptibility for idiopathic pulmonary fibrosis
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Loss of chromosome Y in regulatory T cells

Mattisson, Jonas; Halvardson, Jonatan; Davies, Hanna; Bruhn-Olszewska, Bozena et al.

Ingår i BMC Genomics, 2024

• DOI för Loss of chromosome Y in regulatory T cells
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Hematopoietic loss of Y chromosome leads to cardiac fibrosis and heart failure mortality

Sano, Soichi; Horitani, Keita; Ogawa, Hayato; Halvardson, Jonatan et al.

Ingår i Science, s. 292-297, 2022

• DOI för Hematopoietic loss of Y chromosome leads to cardiac fibrosis and heart failure mortality

Characterization of the nuclear and cytosolic transcriptomes in human brain tissue reveals new insights into the subcellular distribution of RNA transcripts

Zaghlool, Ammar; Niazi, Adnan; Björklund, Åsa K.; Orzechowski Westholm, Jakub et al.

Ingår i Scientific Reports, 2021

• DOI för Characterization of the nuclear and cytosolic transcriptomes in human brain tissue reveals new insights into the subcellular distribution of RNA transcripts
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Novel Y-Chromosome Long Non-Coding RNAs Expressed in Human Male CNS During Early Development

Johansson, Martin M.; Pottmeier, Philipp; Suciu, Pascalina; Ahmed, Tauseef et al.

Ingår i Frontiers in Genetics, 2019

• DOI för Novel Y-Chromosome Long Non-Coding RNAs Expressed in Human Male CNS During Early Development
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Mosaic loss of chromosome Y in blood is associated with male susceptibility for idiopathic pulmonary fibrosis

Bjurling, Josefin; Chavkin, Nicholas W.; Halvardson, Jonatan; Thel, Mark C. et al.

Ingår i Communications Medicine, 2025

• DOI för Mosaic loss of chromosome Y in blood is associated with male susceptibility for idiopathic pulmonary fibrosis
• Ladda ner fulltext (pdf) av Mosaic loss of chromosome Y in blood is associated with male susceptibility for idiopathic pulmonary fibrosis

Loss of chromosome Y in regulatory T cells

Mattisson, Jonas; Halvardson, Jonatan; Davies, Hanna; Bruhn-Olszewska, Bozena et al.

Ingår i BMC Genomics, 2024

• DOI för Loss of chromosome Y in regulatory T cells
• Ladda ner fulltext (pdf) av Loss of chromosome Y in regulatory T cells

Hematopoietic loss of Y chromosome leads to cardiac fibrosis and heart failure mortality

Sano, Soichi; Horitani, Keita; Ogawa, Hayato; Halvardson, Jonatan et al.

Ingår i Science, s. 292-297, 2022

• DOI för Hematopoietic loss of Y chromosome leads to cardiac fibrosis and heart failure mortality

Characterization of the nuclear and cytosolic transcriptomes in human brain tissue reveals new insights into the subcellular distribution of RNA transcripts

Zaghlool, Ammar; Niazi, Adnan; Björklund, Åsa K.; Orzechowski Westholm, Jakub et al.

Ingår i Scientific Reports, 2021

• DOI för Characterization of the nuclear and cytosolic transcriptomes in human brain tissue reveals new insights into the subcellular distribution of RNA transcripts
• Ladda ner fulltext (pdf) av Characterization of the nuclear and cytosolic transcriptomes in human brain tissue reveals new insights into the subcellular distribution of RNA transcripts

Novel Y-Chromosome Long Non-Coding RNAs Expressed in Human Male CNS During Early Development

Johansson, Martin M.; Pottmeier, Philipp; Suciu, Pascalina; Ahmed, Tauseef et al.

Ingår i Frontiers in Genetics, 2019

• DOI för Novel Y-Chromosome Long Non-Coding RNAs Expressed in Human Male CNS During Early Development
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Expression profiling and in situ screening of circular RNAs in human tissues

Zaghlool, Ammar; Ameur, Adam; Wu, Chenglin; Westholm, Jakub Orzechowski et al.

Ingår i Scientific Reports, 2018

• DOI för Expression profiling and in situ screening of circular RNAs in human tissues
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Exome sequencing reveals NAA15 and PUF60 as candidate genes associated with intellectual disability

Zhao, Jin James; Halvardson, Jonatan; Zander, Cecilia; Zaghlool, Ammar et al.

Ingår i American Journal of Medical Genetics Part B, s. 10-20, 2018

• DOI för Exome sequencing reveals NAA15 and PUF60 as candidate genes associated with intellectual disability
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Mutations in HECW2 are associated with intellectual disability and epilepsy

Halvardson, Jonatan; Zhao, Jin J.; Zaghlool, Ammar; Wentzel, Christian et al.

Ingår i Journal of Medical Genetics, s. 697-704, 2016

• DOI för Mutations in HECW2 are associated with intellectual disability and epilepsy
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A Role for the Chromatin-Remodeling Factor BAZ1A in Neurodevelopment

Zaghlool, Ammar; Halvardson, Jonatan; Zhao, Jin J.; Etemadikhah, Mitra et al.

Ingår i Human Mutation, s. 964-975, 2016

• DOI för A Role for the Chromatin-Remodeling Factor BAZ1A in Neurodevelopment
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Mosaic loss of chromosome Y in peripheral blood is associated with shorter survival and higher risk of cancer

Forsberg, Lars A.; Rasi, Chiara; Malmqvist, Niklas; Davies, Hanna et al.

Ingår i Nature Genetics, s. 624-628, 2014

• DOI för Mosaic loss of chromosome Y in peripheral blood is associated with shorter survival and higher risk of cancer

Efficient cellular fractionation improves RNA sequencing analysis of mature and nascent transcripts from human tissues

Zaghlool, Ammar; Ameur, Adam; Nyberg, Linnea; Halvardson, Jonatan et al.

Ingår i BMC Biotechnology, s. 99, 2013

• DOI för Efficient cellular fractionation improves RNA sequencing analysis of mature and nascent transcripts from human tissues
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Exome RNA sequencing reveals rare and novel alternative transcripts

Halvardson, Jonatan; Zaghlool, Ammar; Feuk, Lars

Ingår i Nucleic Acids Research, 2013

• DOI för Exome RNA sequencing reveals rare and novel alternative transcripts

Total RNA sequencing reveals nascent transcription and widespread co-transcriptional splicing in the human brain

Ameur, Adam; Zaghlool, Ammar; Halvardson, Jonatan; Wetterbom, Anna et al.

Ingår i Nature Structural & Molecular Biology, s. 1435-1440, 2011

• DOI för Total RNA sequencing reveals nascent transcription and widespread co-transcriptional splicing in the human brain

Genome-wide Characterization of RNA Expression and Processing

Zaghlool, Ammar

2013

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Splicing in the Human Brain

Zaghlool, Ammar; Ameur, Adam; Cavelier, Lucia; Feuk, Lars

Ingår i Brain Transcriptome, s. 95-125, Elsevier, 2014

• DOI för Splicing in the Human Brain

Mutation in the chromatin-remodeling factor BAZ1A is associated with intellectual disability

Zaghlool, Ammar; Halvardson, Jonatan; Zhao, Jin; Kalushkova, Antonia et al.