Listar por autor "AMIN, N."
Mostrando ítems 1-13 de 13
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Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation
(Molecular Psychiatry. vol. 25, n° 8, pp. 1859-1875, 2020-08)Article de revueLibre acceso
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Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Abeta, tau, immunity and lipid processing
(Nature genetics. vol. 51, n° 9, pp. 1423-1424, 2019-09)Article de revue -
Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
(Nature Communications. vol. 9, n° 1, pp. 2098, 2018-05-29)Article de revueLibre acceso
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Genetic correlations and genome-wide associations of cortical structure in general population samples of 22,824 adults
(Nature Communications. vol. 11, n° 1, pp. 4796, 2020)Article de revueLibre acceso
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Author Correction: Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function
(Nat Commun. vol. 10, n° 1, pp. 2068, 2019-05-01)Article de revueLibre acceso
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A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure
(American Journal of Human Genetics. vol. 102, n° 3, pp. 375-400, 2018-03-01)Article de revue -
Genetic architecture of subcortical brain structures in 38,851 individuals
(Nature Genetics. vol. 51, n° 11, pp. 1624-1636, 2019-11)Article de revue -
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
(Nature Genetics. vol. 50, n° 10, pp. 1412-1425, 2018-10)Article de revue -
Publisher Correction: Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
(Nature Genetics. vol. 50, n° 12, pp. 1755, 2018-12)Article de revue -
Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Abeta, tau, immunity and lipid processing
(Nature Genetics. vol. 51, n° 3, pp. 414-430, 2019-03)Article de revue -
Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities
ARMSTRONG, N. J.; MATHER, K. A.; SARGURUPREMRAJ, Muralidharan
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(Stroke. vol. 51, n° 7, pp. 2111-2121, 2020)Article de revue -
A genome-wide association study identifies genetic loci associated with specific lobar brain volumes
(Communications biology. vol. 2, pp. 285, 2019-08-02)Article de revueLibre acceso
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Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error
(Nature Genetics. vol. 50, n° 6, pp. 834-848, 2018-06)Article de revue