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Author Details

Johanna Jakobsdottir
2005
42
25
PMIDPaper TitleJournal TitlePublished Year
37953992Elevated symptoms of depression and anxiety among family members and friends of critically ill COVID-19 patients - an observational study of five cohorts across four countries.Lancet Reg Health Eur2023
37850429Adverse childhood experiences and psychological functioning among women with schizophrenia or bipolar disorder: population-based study.2023
37726573Association between adverse childhood experiences and perinatal depressive symptoms: a cross-sectional analysis of 16,831 women in Iceland.2023
35101173Adverse childhood experiences and resilience among adult women: A population-based study.eLife2022
35697829Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.Commun Biol2022
36269046Cardiovascular disease and subsequent risk of psychiatric disorders: a nationwide sibling-controlled study.Elife2022
36057275Risk factors for workplace sexual harassment and violence among a national cohort of women in Iceland: a cross-sectional study.Lancet Public Health, The2022
36421883Association between Adverse Childhood Experiences and Multiple Sclerosis in Icelandic Women-A Population-Based Cohort Study.Brain Sciences2022
35532192Sleep disturbances among women in a Subarctic region: a nationwide study.Sleep2022
35184745Association between adverse childhood experiences and premenstrual disorders: a cross-sectional analysis of 11,973 women.BMC Medicine2022
35020900Cohort Profile: COVIDMENT: COVID-19 cohorts on mental health across six nations.Int J Epidemiol2022
34132423Cesarean birth, obstetric emergencies, and adverse neonatal outcomes in Iceland during a period of increasing labor induction.Birth2021
34301663Illness severity and risk of mental morbidities among patients recovering from COVID-19: a cross-sectional study in the Icelandic population.BMJ Open2021
31356640The impact of APOE genotype on survival: Results of 38,537 participants from six population-based cohorts (E2-CHARGE).PLoS One2019
31645637Genome-wide association meta-analysis identifies five novel loci for age-related hearing impairment.Sci Rep2019
30820047Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing.Nat Genet2019
31152163A catalog of genetic loci associated with kidney function from analyses of a million individuals.Nat Genet2019
30072576Co-regulatory networks of human serum proteins link genetics to disease.Science2018
29083408Exome-wide association study of plasma lipids in >300,000 individuals.Nat Genet2017
28714976Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.Nat Genet2017
27764101Rare Functional Variant in TM2D3 is Associated with Late-Onset Alzheimer's Disease.PLoS Genet2016
25778476A novel Alzheimer disease locus located near the gene encoding tau protein.Mol Psychiatry2016
27340842Evaluation of a Genetic Risk Score to Improve Risk Prediction for Alzheimer's Disease.J Alzheimers Dis2016
27256766G-STRATEGY: Optimal Selection of Individuals for Sequencing in Genetic Association Studies.Genet Epidemiol2016
27476799Novel Genetic Variants Associated With Increased Vertebral Volumetric BMD, Reduced Vertebral Fracture Risk, and Increased Expression of SLC1A3 and EPHB2.J Bone Miner Res2016
26567291Novel Genetic Loci Associated With Retinal Microvascular Diameter.Circ Cardiovasc Genet2016
27618448Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci.Nat Genet2016
25832410PLD3 variants in population studies.Nature2015
25631608Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.Nat Commun2015
24507775Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol.Am J Hum Genet2014
24430505Genetic determinants of heel bone properties: genome-wide association meta-analysis and replication in the GEFOS/GENOMOS consortium.Hum Mol Genet2014
24507774Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks.Am J Hum Genet2014
23643379MASTOR: mixed-model association mapping of quantitative traits in samples with related individuals.American Journal of Human Genetics2013
22253316Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype.Int J Epidemiol2012
21169531Dissection of chromosome 16p12 linkage peak suggests a possible role for CACNG3 variants in age-related macular degeneration susceptibility.Invest Ophthalmol Vis Sci2011
20385819Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration.Proc Natl Acad Sci U S A2010
19197355Interpretation of genetic association studies: markers with replicated highly significant odds ratios may be poor classifiers.PLoS Genet2009
18493315C2 and CFB genes in age-related maculopathy and joint action with CFH and LOC387715 genes.PLoS One2008
17924351Estimating prevalence, false-positive rate, and false-negative rate with use of repeated testing when true responses are unknown.American Journal of Human Genetics2007
17000705CFH, ELOVL4, PLEKHA1 and LOC387715 genes and susceptibility to age-related maculopathy: AREDS and CHS cohorts and meta-analyses.Hum Mol Genet2006
16080115Susceptibility genes for age-related maculopathy on chromosome 10q26.Am J Hum Genet2005
15930014Candidate gene analysis suggests a role for fatty acid biosynthesis and regulation of the complement system in the etiology of age-related maculopathy.Hum Mol Genet2005
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