Resultaten visas 1 - 10 / 5355
resultat / per sida
Vilka publikationsuppgifter finns i tjänsten?
Publikationens namn
Upphovspersoner
Publikationskanal
År
Publicationer information ikon

Migraine with aura - genetic susceptibility variants

Öppen tillgång
Nuottamo, Marjo Eveliina
Dissertationes Scholae Doctoralis Ad Sanitatem Investigandam Universitatis Helsinkiensis2022Publicationer information ikon

Idiopathic Pulmonary Fibrosis Is Associated with Common Genetic Variants and Limited Rare Variants

Referentgranskad
Öppen tillgång
DOI
10.1164/rccm.202207-1331OC
NHLBI Trans-Omics Precision Med; Peljto, Anna L.; Blumhagen, Rachel Z.; Walts, Avram D.; Cardwell, J...
American journal of respiratory and critical care medicine2023Publicationer information ikon

Genetic variants predisposing to prognosis in pulmonary sarcoidosis

Lahtela, Elisa
Dissertationes Scholae Doctoralis Ad Sanitatem Investigandam Universitatis Helsinkiensis2018Publicationer information ikon

CRY2 Genetic Variants Associate with Dysthymia

Referentgranskad
Öppen tillgång
DOI
10.1371/journal.pone.0071450
Kovanen, Leena; Kaunisto, Mari; Donner, Kati; Saarikoski, Sirkku T.; Partonen, Timo
PLoS ONE2013Publicationer information ikon

Shared genetic variants suggest common pathways in allergy and autoimmune diseases

Referentgranskad
Öppen tillgång
DOI
10.1016/j.jaci.2016.10.055
Kreiner, Eskil;Waage, Johannes;Standl, Marie;Brix, Susanne;Pers, Tune H.;Alves, Alexessander Couto;W...
Journal of allergy and clinical immunology2017Publicationer information ikon

Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use

Referentgranskad
Öppen tillgång
DOI
10.1016/j.biopsych.2018.11.024
CHD Exome Consortium; Consortium Genetics Smoking; EPIC-CVD Consortium; Understanding Soc Sci Grp; B...
Biological psychiatry2019Publicationer information ikon

FINEMAP - a statistical software for identifying causal genetic variants

Öppen tillgång
Benner, Christian
Dissertationes Scholae Doctoralis Ad Sanitatem Investigandam Universitatis Helsinkiensis2019Publicationer information ikon

Genetic variants linked to education predict longevity

Referentgranskad
Öppen tillgång
DOI
10.1073/pnas.1605334113
Marioni RE, Ritchie SJ, Joshi PK, Hagenaars SP, Okbay A, Fischer K, Adams MJ, Hill WD, Davies G, Nag...
Proceedings of the National Academy of Sciences of the United States of America2016Publicationer information ikon

Genetic variants linked to education predict longevity

Referentgranskad
DOI
10.1073/pnas.1605334113
Marioni, RE;Ritchie, SJ;Joshi, PK;Hagenaars, SP;Okbay, A;Fischer, K;Adams, MJ;Hill, WD;Davies, G;Nag...
Proceedings of the National Academy of Sciences of the United States of America2016Publicationer information ikon

Genetic variants of ghrelin in metabolic disorders

Referentgranskad
DOI
10.1016/j.peptides.2011.04.013
Ukkola, Olavi
Peptides2011

Migraine with aura - genetic susceptibility variants

Öppen tillgång
2022

Idiopathic Pulmonary Fibrosis Is Associated with Common Genetic Variants and Limited Rare Variants

Referentgranskad
Öppen tillgång
DOI
10.1164/rccm.202207-1331OC
2023

Genetic variants predisposing to prognosis in pulmonary sarcoidosis

2018

CRY2 Genetic Variants Associate with Dysthymia

Referentgranskad
Öppen tillgång
DOI
10.1371/journal.pone.0071450
2013

Shared genetic variants suggest common pathways in allergy and autoimmune diseases

Referentgranskad
Öppen tillgång
DOI
10.1016/j.jaci.2016.10.055
2017

Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use

Referentgranskad
Öppen tillgång
DOI
10.1016/j.biopsych.2018.11.024
2019

FINEMAP - a statistical software for identifying causal genetic variants

Öppen tillgång
2019

Genetic variants linked to education predict longevity

Referentgranskad
Öppen tillgång
DOI
10.1073/pnas.1605334113
2016

Genetic variants linked to education predict longevity

Referentgranskad
DOI
10.1073/pnas.1605334113
2016

Genetic variants of ghrelin in metabolic disorders

Referentgranskad
DOI
10.1016/j.peptides.2011.04.013
2011