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Victoria E Jackson

Showing results (11-20 of 36) with videos related to

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The Journal of Clinical Investigation|August 8, 2017
Phenotypic and pharmacogenetic evaluation of patients with thiazide-induced hyponatremiaJames S Ware, Louise V Wain, Sarath K Channavajjhala, et al.
Medrxiv : the Preprint Server for Health Sciences|June 9, 2023
Statistical haemoglobin thresholds to define anaemia across the lifecycleSabine Braat, Katherine Fielding, Jiru Han, et al.
The Lancet. Haematology|March 3, 2024
Haemoglobin thresholds to define anaemia from age 6 months to 65 years: estimates from international data sourcesSabine Braat, Katherine L Fielding, Jiru Han, et al.
Blood|March 17, 2023
Iron homeostasis governs erythroid phenotype in polycythemia veraCavan Bennett, Victoria E Jackson, Anne Pettikiriarachchi, et al.
Molecular Psychiatry|September 18, 2022
Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain developmentAntony Kaspi, Michael S Hildebrand, Victoria E Jackson, et al.
Molecular Psychiatry|January 19, 2023
Correction: Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain developmentAntony Kaspi, Michael S Hildebrand, Victoria E Jackson, et al.
Neurology|April 30, 2020
Severe childhood speech disorder: Gene discovery highlights transcriptional dysregulationMichael S Hildebrand, Victoria E Jackson, Thomas S Scerri, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 1, 2019
Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystoniaKamal Khan, Michael Zech, Angela T Morgan, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|April 28, 2021
A systematic analysis of protein-altering exonic variants in chronic obstructive pulmonary diseaseMatthew Moll, Victoria E Jackson, Bing Yu, et al.
Nature Communications|September 28, 2023
A common human MLKL polymorphism confers resistance to negative regulation by phosphorylationSarah E Garnish, Katherine R Martin, Maria Kauppi, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
The Journal of Clinical Investigation|August 8, 2017
Phenotypic and pharmacogenetic evaluation of patients with thiazide-induced hyponatremiaJames S Ware, Louise V Wain, Sarath K Channavajjhala, et al.
Medrxiv : the Preprint Server for Health Sciences|June 9, 2023
Statistical haemoglobin thresholds to define anaemia across the lifecycleSabine Braat, Katherine Fielding, Jiru Han, et al.
The Lancet. Haematology|March 3, 2024
Haemoglobin thresholds to define anaemia from age 6 months to 65 years: estimates from international data sourcesSabine Braat, Katherine L Fielding, Jiru Han, et al.
Blood|March 17, 2023
Iron homeostasis governs erythroid phenotype in polycythemia veraCavan Bennett, Victoria E Jackson, Anne Pettikiriarachchi, et al.
Molecular Psychiatry|September 18, 2022
Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain developmentAntony Kaspi, Michael S Hildebrand, Victoria E Jackson, et al.
Molecular Psychiatry|January 19, 2023
Correction: Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain developmentAntony Kaspi, Michael S Hildebrand, Victoria E Jackson, et al.
Neurology|April 30, 2020
Severe childhood speech disorder: Gene discovery highlights transcriptional dysregulationMichael S Hildebrand, Victoria E Jackson, Thomas S Scerri, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 1, 2019
Recessive variants in ZNF142 cause a complex neurodevelopmental disorder with intellectual disability, speech impairment, seizures, and dystoniaKamal Khan, Michael Zech, Angela T Morgan, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|April 28, 2021
A systematic analysis of protein-altering exonic variants in chronic obstructive pulmonary diseaseMatthew Moll, Victoria E Jackson, Bing Yu, et al.
Nature Communications|September 28, 2023
A common human MLKL polymorphism confers resistance to negative regulation by phosphorylationSarah E Garnish, Katherine R Martin, Maria Kauppi, et al.
Pageof 4