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Jonatan Halvardson

Showing results (11-20 of 31) with videos related to

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Cell & Bioscience|December 13, 2021
A polygenic risk score predicts mosaic loss of chromosome Y in circulating blood cellsMoeen Riaz, Jonas Mattisson, Galina Polekhina, et al.
Frontiers in Genetics|October 15, 2019
Novel Y-Chromosome Long Non-Coding RNAs Expressed in Human Male CNS During Early DevelopmentMartin M Johansson, Philipp Pottmeier, Pascalina Suciu, et al.
Genes|August 27, 2021
Transcriptome Analysis of Post-Mortem Brain Tissue Reveals Up-Regulation of the Complement Cascade in a Subgroup of Schizophrenia PatientsEva Lindholm Carlström, Adnan Niazi, Mitra Etemadikhah, et al.
Human Mutation|June 23, 2016
A Role for the Chromatin-Remodeling Factor BAZ1A in NeurodevelopmentAmmar Zaghlool, Jonatan Halvardson, Jin J Zhao, et al.
Clinical Genetics|December 8, 2018
Whole genome sequencing of consanguineous families reveals novel pathogenic variants in intellectual disabilityAnn-Charlotte Thuresson, Cecilia Soussi Zander, Jin J Zhao, et al.
European Journal of Human Genetics : EJHG|November 28, 2013
Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathyRonen Spiegel, Ann Saada, Jonatan Halvardson, et al.
RNA (New York, N.Y.)|August 9, 2020
Identification and rescue of a tRNA wobble inosine deficiency causing intellectual disability disorderJillian Ramos, Melissa Proven, Jonatan Halvardson, et al.
American Journal of Human Genetics|March 13, 2012
Infantile cerebellar-retinal degeneration associated with a mutation in mitochondrial aconitase, ACO2Ronen Spiegel, Ophry Pines, Asaf Ta-Shma, et al.
Journal of Medical Genetics|June 24, 2016
Mutations in HECW2 are associated with intellectual disability and epilepsyJonatan Halvardson, Jin J Zhao, Ammar Zaghlool, et al.
BMC Genomics|March 5, 2024
Loss of chromosome Y in regulatory T cellsJonas Mattisson, Jonatan Halvardson, Hanna Davies, et al.
Pageof 4

Showing results (11-20 of 31) with videos related to

Sort By:
Pageof 4
Cell & Bioscience|December 13, 2021
A polygenic risk score predicts mosaic loss of chromosome Y in circulating blood cellsMoeen Riaz, Jonas Mattisson, Galina Polekhina, et al.
Frontiers in Genetics|October 15, 2019
Novel Y-Chromosome Long Non-Coding RNAs Expressed in Human Male CNS During Early DevelopmentMartin M Johansson, Philipp Pottmeier, Pascalina Suciu, et al.
Genes|August 27, 2021
Transcriptome Analysis of Post-Mortem Brain Tissue Reveals Up-Regulation of the Complement Cascade in a Subgroup of Schizophrenia PatientsEva Lindholm Carlström, Adnan Niazi, Mitra Etemadikhah, et al.
Human Mutation|June 23, 2016
A Role for the Chromatin-Remodeling Factor BAZ1A in NeurodevelopmentAmmar Zaghlool, Jonatan Halvardson, Jin J Zhao, et al.
Clinical Genetics|December 8, 2018
Whole genome sequencing of consanguineous families reveals novel pathogenic variants in intellectual disabilityAnn-Charlotte Thuresson, Cecilia Soussi Zander, Jin J Zhao, et al.
European Journal of Human Genetics : EJHG|November 28, 2013
Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathyRonen Spiegel, Ann Saada, Jonatan Halvardson, et al.
RNA (New York, N.Y.)|August 9, 2020
Identification and rescue of a tRNA wobble inosine deficiency causing intellectual disability disorderJillian Ramos, Melissa Proven, Jonatan Halvardson, et al.
American Journal of Human Genetics|March 13, 2012
Infantile cerebellar-retinal degeneration associated with a mutation in mitochondrial aconitase, ACO2Ronen Spiegel, Ophry Pines, Asaf Ta-Shma, et al.
Journal of Medical Genetics|June 24, 2016
Mutations in HECW2 are associated with intellectual disability and epilepsyJonatan Halvardson, Jin J Zhao, Ammar Zaghlool, et al.
BMC Genomics|March 5, 2024
Loss of chromosome Y in regulatory T cellsJonas Mattisson, Jonatan Halvardson, Hanna Davies, et al.
Pageof 4