Ammar Zaghlool
Uppsala, C, Sweden
Last Updated: 09/26/2026
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Found 13 publications
Mosaic loss of chromosome Y in blood is associated with male susceptibility for idiopathic pulmonary fibrosis.
Journal: Communications medicine
Published: September 23, 2024
Hematopoietic loss of Y chromosome leads to cardiac fibrosis and heart failure mortality.
Journal: Science (New York, N.Y.)
Published: July 20, 2022
Characterization of the nuclear and cytosolic transcriptomes in human brain tissue reveals new insights into the subcellular distribution of RNA transcripts.
Journal: Scientific reports
Published: April 24, 2020
Expression profiling and in situ screening of circular RNAs in human tissues.
Journal: Scientific reports
Published: July 05, 2018
Novel Y-Chromosome Long Non-Coding RNAs Expressed in Human Male CNS During Early Development.
Journal: Frontiers in genetics
Published: June 13, 2018
Exome sequencing reveals NAA15 and PUF60 as candidate genes associated with intellectual disability.
Exome sequencing reveals NAA15 and PUF60 as candidate genes associated with intellectual disability.
Journal: American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics
Published: December 28, 2016
Mutations in HECW2 are associated with intellectual disability and epilepsy.
Journal: Journal of medical genetics
Published: February 02, 2016
A Role for the Chromatin-Remodeling Factor BAZ1A in Neurodevelopment.
Journal: Human mutation
Published: December 30, 2015
Last Updated: 09/26/2026