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Priit Palta

Showing results (61-70 of 73) with videos related to

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Nature|January 28, 2014
De novo mutations in schizophrenia implicate synaptic networksMenachem Fromer, Andrew J Pocklington, David H Kavanagh, et al.
Neuron|May 8, 2018
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 FamiliesPadhraig Gormley, Mitja I Kurki, Marjo Eveliina Hiekkala, et al.
The Lancet Regional Health. Europe|July 17, 2025
External exposome and incident asthma across the life course in 14 European cohorts: a prospective analysis within the EXPANSE projectZhebin Yu, Sara Kress, Natalia Blay, et al.
Plos Genetics|August 1, 2014
Distribution and medical impact of loss-of-function variants in the Finnish founder populationElaine T Lim, Peter Würtz, Aki S Havulinna, et al.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2026
The Biobank Rare Variant consortium powers the discovery of rare genetic associations through global collaborationDuncan S Palmer, Barney Hill, Sam Hodgson, et al.
Nature Communications|April 5, 2025
The Estonian Biobank's journey from biobanking to personalized medicineLili Milani, Maris Alver, Sven Laur, et al.
Neurology. Genetics|April 12, 2016
Genetic analysis for a shared biological basis between migraine and coronary artery diseaseBendik S Winsvold, Christopher P Nelson, Rainer Malik, et al.
Gut|July 9, 2026
Cross-definition GWAS of IBS in 2.8 million individuals reveals cardiometabolic and triglyceride-linked mechanismsBiagio Di Lorenzo, Leticia Camargo Tavares, Cristian Díaz-Muñoz, et al.
Nature Genetics|June 25, 2013
Genome-wide meta-analysis identifies new susceptibility loci for migraineVerneri Anttila, Bendik S Winsvold, Padhraig Gormley, et al.
Nature Genetics|June 21, 2016
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migrainePadhraig Gormley, Verneri Anttila, Bendik S Winsvold, et al.
Pageof 8

Showing results (61-70 of 73) with videos related to

Sort By:
Pageof 8
Nature|January 28, 2014
De novo mutations in schizophrenia implicate synaptic networksMenachem Fromer, Andrew J Pocklington, David H Kavanagh, et al.
Neuron|May 8, 2018
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 FamiliesPadhraig Gormley, Mitja I Kurki, Marjo Eveliina Hiekkala, et al.
The Lancet Regional Health. Europe|July 17, 2025
External exposome and incident asthma across the life course in 14 European cohorts: a prospective analysis within the EXPANSE projectZhebin Yu, Sara Kress, Natalia Blay, et al.
Plos Genetics|August 1, 2014
Distribution and medical impact of loss-of-function variants in the Finnish founder populationElaine T Lim, Peter Würtz, Aki S Havulinna, et al.
Medrxiv : the Preprint Server for Health Sciences|June 4, 2026
The Biobank Rare Variant consortium powers the discovery of rare genetic associations through global collaborationDuncan S Palmer, Barney Hill, Sam Hodgson, et al.
Nature Communications|April 5, 2025
The Estonian Biobank's journey from biobanking to personalized medicineLili Milani, Maris Alver, Sven Laur, et al.
Neurology. Genetics|April 12, 2016
Genetic analysis for a shared biological basis between migraine and coronary artery diseaseBendik S Winsvold, Christopher P Nelson, Rainer Malik, et al.
Gut|July 9, 2026
Cross-definition GWAS of IBS in 2.8 million individuals reveals cardiometabolic and triglyceride-linked mechanismsBiagio Di Lorenzo, Leticia Camargo Tavares, Cristian Díaz-Muñoz, et al.
Nature Genetics|June 25, 2013
Genome-wide meta-analysis identifies new susceptibility loci for migraineVerneri Anttila, Bendik S Winsvold, Padhraig Gormley, et al.
Nature Genetics|June 21, 2016
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migrainePadhraig Gormley, Verneri Anttila, Bendik S Winsvold, et al.
Pageof 8