Analysis of 200,000 Exome-Sequenced UK Biobank Subjects Implicates Genes Involved in Increased and Decreased Risk of Hypertension

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: Analysis of 200,000 Exome-Sequenced UK Biobank Subjects Implicates Genes Involved in Increased and Decreased Risk of Hypertension ; volume:9 ; number:1-2 ; year:2021 ; pages:17-29 ; extent:13
Pulse ; 9, Heft 1-2 (2021), 17-29 (gesamt 13)

Creator: Curtis, David

DOI: 10.1159/000517419

URN: urn:nbn:de:101:1-2021093000144393028174

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:36 AM CEST

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Curtis, David

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Analysis of 200,000 Exome-Sequenced UK Biobank Subjects Implicates Genes Involved in Increased and Decreased Risk of Hypertension

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Other Objects (12)

Analysis of Rare Variants in 470,000 Exome-Sequenced UK Biobank Participants Implicates Novel Genes Affecting Risk of Hypertension

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Secondary findings in 421 whole exome-sequenced Chinese children

Exome-wide analysis implicates rare protein-altering variants in human handedness

Family specific genetic predisposition to breast cancer: results from Tunisian whole exome sequenced breast cancer cases

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Whole-exome sequencing of individuals from an isolated population under extreme conditions implicates rare risk variants of schizophrenia

Correction: Whole-exome sequencing of individuals from an isolated population under extreme conditions implicates rare risk variants of schizophrenia

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Comparisons between sequenced and re-sequenced genomes of historical subterranean clover mottle virus isolates

Linkage analysis using whole exome sequencing data implicates SLC17A1, SLC17A3, TATDN2 and TMEM131L in type 1 diabetes in Kuwaiti families

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Weighted Burden Analysis of Exome-Sequenced Case-Control Sample Implicates Synaptic Genes in Schizophrenia Aetiology

Investigation of Recessive Effects of Coding Variants on Common Clinical Phenotypes in Exome-Sequenced UK Biobank Participants

Secondary findings in 421 whole exome-sequenced Chinese children

Exome-wide analysis implicates rare protein-altering variants in human handedness

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Whole-exome sequencing of individuals from an isolated population under extreme conditions implicates rare risk variants of schizophrenia

Correction: Whole-exome sequencing of individuals from an isolated population under extreme conditions implicates rare risk variants of schizophrenia

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Comparisons between sequenced and re-sequenced genomes of historical subterranean clover mottle virus isolates

Linkage analysis using whole exome sequencing data implicates SLC17A1, SLC17A3, TATDN2 and TMEM131L in type 1 diabetes in Kuwaiti families

Analysis of Rare Variants in 470,000 Exome-Sequenced UK Biobank Participants Implicates Novel Genes Affecting Risk of Hypertension

Weighted Burden Analysis of Exome-Sequenced Case-Control Sample Implicates Synaptic Genes in Schizophrenia Aetiology

Investigation of Recessive Effects of Coding Variants on Common Clinical Phenotypes in Exome-Sequenced UK Biobank Participants

Secondary findings in 421 whole exome-sequenced Chinese children

Exome-wide analysis implicates rare protein-altering variants in human handedness

Family specific genetic predisposition to breast cancer: results from Tunisian whole exome sequenced breast cancer cases

Whole-exome sequencing in UK Biobank reveals rare genetic architecture for depression

Whole-exome sequencing of individuals from an isolated population under extreme conditions implicates rare risk variants of schizophrenia

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Diversity of CFTR variants across ancestries characterized using 454,727 UK biobank whole exome sequences

Comparisons between sequenced and re-sequenced genomes of historical subterranean clover mottle virus isolates

Linkage analysis using whole exome sequencing data implicates SLC17A1, SLC17A3, TATDN2 and TMEM131L in type 1 diabetes in Kuwaiti families

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