Cornelia M. Van Duijn

Cornelia M. Van Duijn's AcademicInfluence.com Rankings

Biology

#14291

World Rank

#18004

Historical Rank

Genetics

#1624

World Rank

#1732

Historical Rank

biology Degrees

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Biology

Cornelia M. Van Duijn's Degrees

PhD Genetics University of Amsterdam
Masters Biomedical Sciences University of Amsterdam
Bachelors Biomedical Sciences University of Amsterdam

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Cornelia M. Van Duijn's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Genetic studies of body mass index yield new insights for obesity biology (2015) (3549)
Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease (2013) (3484)
Effects of Age, Sex, and Ethnicity on the Association Between Apolipoprotein E Genotype and Alzheimer Disease: A Meta-analysis (1997) (3245)
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index (2010) (2011)
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2010) (1801)
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21 (2006) (1377)
Genome-wide association study of blood pressure and hypertension (2009) (1371)
Genome-wide meta-analyses identify multiple loci associated with smoking behavior (2010) (1107)
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (2014) (933)
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2010) (897)
Identification of seven loci affecting mean telomere length and their association with disease (2013) (761)
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance (2012) (756)
New loci associated with kidney function and chronic kidney disease (2010) (754)
Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the β–amyloid precursor protein gene (1992) (752)
Variants in MTNR1B influence fasting glucose levels (2009) (742)
Common genetic variants influence human subcortical brain structures (2015) (731)
Sequence variants at CHRNB3–CHRNA6 and CYP2A6 affect smoking behavior (2010) (688)
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations (2012) (678)
Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study (2008) (661)
Whole-genome sequence variation, population structure and demographic history of the Dutch population (2014) (650)
Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function (2010) (605)
Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility (2019) (589)
Multiple loci associated with indices of renal function and chronic kidney disease (2009) (583)
Alcohol consumption and risk of dementia: the Rotterdam Study (2002) (570)
Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma (2011) (526)
A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis (2001) (515)
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies (2010) (477)
Apolipoprotein E4 allele in a population–based study of early–onset Alzheimer's disease (1994) (455)
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) (421)
DJ-1( PARK7), a novel gene for autosomal recessive, early onset parkinsonism (2003) (419)
FTO genotype is associated with phenotypic variability of body mass index (2012) (407)
Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture (2015) (399)
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia (2013) (379)
Meta-analysis of telomere length in 19 713 subjects reveals high heritability, stronger maternal inheritance and a paternal age effect (2013) (375)
Sequence variants at CHRNB 3 – CHRNA 6 and CYP 2 A 6 affect smoking behavior (2010) (312)
Large-scale genomic analyses link reproductive ageing to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair (2015) (308)
Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders (2013) (299)
Variant of TREM 2 Associated with the Risk of Alzheimer ’ s Disease (2012) (296)
Genome-wide association analysis identifies susceptibility loci for migraine without aura (2012) (286)
Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies (2006) (284)
Susceptibility loci for intracranial aneurysm in European and Japanese populations (2008) (283)
Metabolic network failures in Alzheimer's disease: A biochemical road map (2017) (280)
Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus (2013) (279)
Consanguineous marriages, pearls and perils: Geneva International Consanguinity Workshop Report (2011) (271)
The Neuronal Transporter Gene SLC6A15 Confers Risk to Major Depression (2009) (211)
A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14 (2010) (208)
A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25 (2010) (207)
Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis (2008) (203)
Estimating human age from T-cell DNA rearrangements (2010) (173)
Convergent genetic and expression data implicate immunity in Alzheimer's disease (2014) (172)
The vast complexity of primary open angle glaucoma: Disease genes, risks, molecular mechanisms and pathobiology (2013) (162)
The dopamine D4 receptor gene 48-base-pair-repeat polymorphism and mood disorders: A meta-analysis (2005) (159)
Glucocorticoid Receptor Gene-Based SNP Analysis in Patients with Recurrent Major Depression (2006) (156)
Altered bile acid profile in mild cognitive impairment and Alzheimer's disease: Relationship to neuroimaging and CSF biomarkers (2018) (151)
Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways (2012) (150)
Linkage disequilibrium in young genetically isolated Dutch population (2004) (146)
A genome-wide association study of aging (2011) (146)
The effect of APOE and other common genetic variants on the onset of Alzheimer's disease and dementia: a community-based cohort study (2018) (139)
Amyloid precursor protein gene mutation in early-onset Alzheimer's disease (1991) (132)
Genetic risk of primary open angle glaucoma (1998) (121)
Sex-specific genetic effects influence variation in body composition (2008) (118)
The Multiple Sclerosis Genomic Map: Role of peripheral immune cells and resident microglia in susceptibility (2017) (113)
Circulating metabolites and general cognitive ability and dementia: Evidence from 11 cohort studies (2018) (113)
Refining genetic associations in multiple sclerosis (2008) (108)
Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval (2002) (107)
A major SNP haplotype of the arginine vasopressin 1B receptor protects against recurrent major depression (2003) (104)
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution (2011) (104)
Genetics of cortisol secretion and depressive symptoms: A candidate gene and genome wide association approach (2011) (103)
Alzheimer's Disease Genes and Cognition in the Nondemented General Population (2013) (91)
An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype (2017) (89)
Mutations in the hemochromatosis gene (HFE), Parkinson's disease and parkinsonism (2003) (88)
Genetic risk of neurodegenerative diseases is associated with mild cognitive impairment and conversion to dementia (2015) (81)
EVI5 is a risk gene for multiple sclerosis (2008) (80)
Association of Alzheimer's disease GWAS loci with MRI markers of brain aging (2015) (79)
Serum levels of interleukin-6 are not elevated in patients with Alzheimer's disease (1990) (77)
Genome-wide Studies of Verbal Declarative Memory in Nondemented Older People: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium (2015) (75)
Epidemiology of the dementias: recent developments and new approaches. (1996) (73)
Genetic polymorphisms and heart failure (2004) (66)
Serum apolipoprotein E level is not increased in Alzheimer's disease: the Rotterdam study (1998) (66)
ACE gene is associated with Alzheimer's disease and atrophy of hippocampus and amygdala (2005) (65)
The apolipoprotein E gene and its age-specific effects on cognitive function (2010) (65)
A population-based study of the effect of the HFE C282Y and H63D mutations on iron metabolism (2003) (59)
Transferrin and HFE genes interact in Alzheimer's disease risk: the Epistasis Project (2012) (58)
The Consortium on Health and Ageing: Network of Cohorts in Europe and the United States (CHANCES) project—design, population and data harmonization of a large-scale, international study (2014) (56)
Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia (2013) (55)
Epistatic effect of genes from the dopamine and serotonin systems on the temperament traits of Novelty Seeking and Harm Avoidance (2002) (51)
Erratum: Genome-wide association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence (2017) (50)
The impact of apolipoprotein E on dementia in persons with Down's syndrome (2008) (50)
Influence of the prion protein and the apolipoprotein E genotype on the Creutzfeldt–Jakob Disease phenotype (2001) (50)
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families (2018) (50)
Genetic association of the presenilin-1 regulatory region with early-onset Alzheimer's disease in a population-based sample (1999) (49)
PLD3 variants in population studies (2015) (49)
Common DNA variants predict tall stature in Europeans (2014) (48)
PARK 7 , a Novel Locus for Autosomal Recessive Early-Onset Parkinsonism , on Chromosome 1 p 36 (2001) (47)
Mutation screening of the tau gene in patients with early-onset Alzheimer's disease (1999) (47)
The expression of type III hyperlipoproteinemia: involvement of lipolysis genes (2009) (45)
Heritability of fasting glucose levels in a young genetically isolated population (2006) (44)
Cathepsin D gene and the risk of Alzheimer's disease: A population-based study and meta-analysis (2011) (44)
Amyloid β secretase gene (BACE) is neither mutated in nor associated with early-onset Alzheimer's disease (2001) (44)
The −491 A/T polymorphism in the regulatory region of the Apolipoprotein E gene and early-onset Alzheimer's disease (1998) (42)
Hormone replacement therapy and Alzheimer's disease. (1999) (42)
Polymorphisms in the prion protein gene and in the doppel gene increase susceptibility for Creutzfeldt–Jakob disease (2004) (41)
Distinguishing true from false positives in genomic studies: p values (2013) (39)
Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction (2019) (38)
Genes, pathways, and animal models in primary open-angle glaucoma (2015) (37)
Genetic epidemiology of Creutzfeldt-Jakob disease in Europe. (2001) (36)
The GAB2 Gene and the Risk of Alzheimer's Disease: Replication and Meta-Analysis (2009) (36)
Comparison of participant information and informed consent forms of five European studies in genetic isolated populations (2010) (35)
Epidemiology of neurological diseases in elderly people: what did we learn from the Rotterdam Study? (2006) (35)
Disentangling the biological pathways involved in early features of Alzheimer's disease in the Rotterdam Study (2018) (35)
Association of cyclin-dependent kinase 5 and neuronal activators p35 and p39 complex in early-onset Alzheimer's disease (2005) (33)
APOE genotyping in differential diagnosis of Alzheimer's disease (1996) (33)
Epigenome-wide Association Study of Attention-Deficit/Hyperactivity Disorder Symptoms in Adults (2019) (32)
Strong linkage on 2q33.3 to familial early-onset generalized osteoarthritis and a consideration of two positional candidate genes (2006) (32)
Common variants in Alzheimer’s disease: Novel association of six genetic variants with AD and risk stratification by polygenic risk scores (2019) (30)
Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies (2015) (29)
Discovery by the Epistasis Project of an epistatic interaction between the GSTM3 gene and the HHEX/IDE/KIF11 locus in the risk of Alzheimer's disease (2013) (29)
Cerebrovascular risk factors do not contribute to genetic variance of cognitive function The ERF study (2007) (29)
A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15 q 25 (2010) (29)
Genetic variants in RBFOX3 are associated with sleep latency (2016) (29)
Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study (2020) (29)
HFE variants, APOE and Alzheimer's disease: Findings from the population-based Rotterdam Study (2009) (28)
A transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration (2020) (28)
The UBQLN1 polymorphism, UBQ-8i, at 9q22 is not associated with Alzheimer's disease with onset before 70 years (2006) (28)
Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia (vol 99, pg 13675, 2002) (2002) (28)
Genes predict village of origin in rural Europe (2010) (28)
Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide (2017) (28)
Mutation analysis of candidate genes within the 2q33.3 linkage area for familial early-onset generalised osteoarthritis (2007) (27)
Genetic Determinants of Cortical Structure (Thickness, Surface Area and Volumes) among Disease Free Adults in the CHARGE Consortium (2018) (26)
Lack of evidence for a role of genetic variation in TMEM230 in the risk for Parkinson's disease in the Caucasian population (2017) (25)
Serum apolipoprotein E is associated with long-term risk of Alzheimer’s disease: The Rotterdam Study (2016) (25)
Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine (2016) (25)
Fine-mapping the effects of Alzheimer's disease risk loci on brain morphology (2016) (25)
Apolipoprotein E genotype does not affect the age of onset of dementia in families with defined tau mutations (1999) (23)
Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions (2012) (23)
TMEM106B Influences Volume of Left-Sided Temporal Lobe and Interhemispheric Structures in the General Population (2014) (23)
Association of adiponectin and leptin with relative telomere length in seven independent cohorts including 11,448 participants (2014) (23)
Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses (2016) (22)
Age-related maculopathy: Its genetic basis (2001) (22)
Suggestive linkage of ADHD to chromosome 18q22 in a young genetically isolated Dutch population (2009) (22)
The molecular genetics of early-onset Alzheimer's disease (2004) (22)
Nonsynonymous Variation in NKPD1 Increases Depressive Symptoms in European Populations (2017) (21)
Linkage analysis of adult height in a large pedigree from a Dutch genetically isolated population (2009) (20)
Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (Nature Genetics (2010) 42 (105-116)) (2010) (20)
A rare missense variant of CASP7 is associated with familial late-onset Alzheimer's disease (2018) (20)
A Genome-Wide Association Study in isolated populations reveals new genes associated to common food likings (2016) (18)
Relationship of the Ubiquilin 1 gene with Alzheimer's and Parkinson's disease and cognitive function (2007) (18)
VEGF Polymorphisms Are Associated With Endocardial Cushion Defects: A Family-Based Case-Control Study (2010) (17)
315 Estrogen, apolipoprotein E and the risk of Alzheimer's Disease (1996) (16)
Menopause and the Brain (1997) (16)
Familial aggregation of preeclampsia and intrauterine growth restriction in a genetically isolated population in The Netherlands (2008) (16)
The impact of genetic testing on complex diseases (2005) (16)
Is Parental Age Related to the Risk of Alzheimer's Disease? (1990) (16)
UvA-DARE ( Digital Academic Repository ) Four Novel Loci ( 19 q 13 , 6 q 24 , 12 q 24 , and 5 q 14 ) Influence the Microcirculation In Vivo (2010) (15)
Decreased DNA repair capacity in familial, but not in sporadic Alzheimer's disease (1991) (15)
Corrigendum: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis (2011) (15)
Sequencing of high-complexity DNA pools for identification of nucleotide and structural variants in regions associated with complex traits (2011) (15)
Towards predictive genetic testing of complex diseases (2006) (14)
Neopterin and the risk of dementia in persons with Down syndrome (2009) (14)
How to kickstart a national biobanking infrastructure – experiences and prospects of BBMRI-NL (2012) (13)
Erratum: Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia (Proceedings of the National Academy of Sciences of the United States of America (October 15, 2002) 99:21 (13675-13680)) (2002) (13)
Genome-wide association analysis on five isolated populations identifies variants of the HLA-DOA gene associated with white wine liking (2015) (13)
Association of 5 0 estrogen receptor alpha gene polymorphisms with bone mineral density, vertebral bone area and fracture risk (2003) (13)
Plasma β amyloid and impaired CO2-induced cerebral vasomotor reactivity (2007) (12)
Ninety-nine independent genetic loci influencing general cognitive function include genes associated with brain health and structure (N = 280,360) (2017) (12)
Low-density lipoprotein receptor mutations generate synthetic genome-wide associations (2012) (12)
CDH6 and HAGH protein levels in plasma associate with Alzheimer’s disease in APOE ε4 carriers (2019) (12)
Multi-trait genome-wide association study identifies new loci associated with optic disc parameters (2019) (12)
IS ALZHEIMER'S DISEASE DISTINCT FROM NORMAL AGEING? (1988) (12)
Does bilirubin protect against hemochromatosis gene (HFE) related mortality? (2004) (11)
Refining Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder Genetic Loci by Integrating Summary Data From Genome-wide Association, Gene Expression, and DNA Methylation Studies (2020) (11)
Role of APOE in dementia: A critical reappraisal. (1998) (11)
PLASMA AMYLOID BETA LEVELS, CEREBRAL SMALL-VESSEL DISEASES AND COGNITION: THE ROTTERDAM STUDY (2017) (10)
The GAB2 gene and the risk of Alzheimer's disease: Replication and meta-analysis (2009) (10)
Mutation analysis of the chromosome 14q24.3 dihydrolipoyl succinyltransferase (DLST) gene in patients with early-onset Alzheimer disease (1995) (10)
Associations between the deletion polymorphism of the angiotensin 1-converting enzyme gene and ocular signs of primary open-angle glaucoma (2005) (9)
GENESTAT: an information portal for design and analysis of genetic association studies (2009) (9)
Erratum: Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families (Neuron (2018) 98(4) (743–753.e4), (S0896627318303222) (10.1016/j.neuron.2018.04.014)) (2018) (9)
A deletion in DJ-1 and the risk of dementia—a population-based survey (2004) (9)
Tissue-Specific Alteration of Metabolic Pathways Influences Glycemic Regulation (2019) (9)
The dystrophin gene and cognitive function in the general population (2014) (9)
Erratum: Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis (American Journal of Human Genetics (2016) 99(2) (481–488)(S0002929716302208)(10.1016/j.ajhg.2016.06.016)) (2016) (8)
Apolipoprotein E ϵ4 allele is associated with left ventricular systolic dysfunction (2004) (8)
miLD and booLD Programs for Calculation and Analysis of Corrected Linkage Disequilibrium (2003) (8)
Evidence for major gene inheritance of Alzheimer disease in families of patients with and without APOE Îµ4 (1996) (8)
Apolipoprotein E genotype and concomitant clinical features in early-onset Alzheimer's disease (2004) (8)
COMPREHENSIVE GENE-GENE INTERACTION META-ANALYSIS OF IGAP GWA STUDIES (2014) (7)
3 Population-specific genotype imputations using minimac or IMPUTE 2 (2018) (7)
Genetic Factors in Early- and Late-Onset Alzheimer’s Disease (1999) (7)
Increased High Density Lipoprotein-levels associated with Age-related Macular degeneration. Evidence from the EYE-RISK and E3 Consortia (2018) (7)
The ERCC 6 Gene and Age-related Macular Degeneration (2010) (6)
Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (Proceedings of the National Academy Sciences of the United States of America (2011) 108, 17, (7119-7124)) (2011) (6)
No evidence for prion protein gene locus multiplication in Creutzfeldt-Jakob disease (2010) (6)
Prospects of genetic research of mild cognitive impairment (2004) (6)
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) (6)
Association of the IGF1 gene with fasting insulin levels (2016) (5)
Anticipation in familial amyotrophic lateral sclerosis with SOD 1G 93 S mutation (2002) (5)
Exome sequencing identifies rare damaging variants in the ATP8B4 and ABCA1 genes as novel risk factors for Alzheimer’s Disease (2020) (5)
METABOLITES ASSOCIATED WITH COGNITIVE FUNCTION IN THE ROTTERDAM STUDY AND ERASMUS RUCPHEN FAMILY STUDY (2016) (4)
Genome-wide association study of plasma triglycerides, phospholipids and relation to cardio-metabolic risk factors (2019) (4)
ASSOCIATION OF ALZHEIMER DISEASE GWAS LOCI WITH MRI-MARKERS OF BRAIN AGING (2014) (4)
EXOME CHIP META-ANALYSIS OF ALZHEIMER'S DISEASE IN THE IGAP CONSORTIUM (2014) (4)
Erratum: Common genetic variants associated with cognitive performance identified using the proxy-phenotype method (Proc Natl Acad Sci USA (2014) 111 (13790-13794) DOI: 10.1073/pnas.1404623111) (2015) (4)
749 Evidence for major gene inheritance of Alzheimer disease in families of patients with and without APOE ε4. VS Rao (1996) (4)
Association study between a promoter polymorphism in the presenilin 1 gene and late-onset Alzheimer's disease (2000) (3)
Telomere length variation reduces with age: evidence of survivor effect (2014) (3)
Supplementary Material 5 (2014) (3)
Gut microbiome-wide association study of depression (2021) (3)
Effects of Age and Ethnicity on the Link Between APOE ∊4 and Alzheimer Disease—Reply (1998) (3)
Supplementary Material 3 (2015) (3)
Correction for Schumann et al., Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (2011) (3)
Supplementary Material 6 (2014) (3)
Supplementary Material 7 (2014) (3)
Apolipoprotein E genotype modifies the association between smoking and early-onset Alzheimer's disease (1995) (3)
PLD3 ASSOCIATES TO PROLINE A PROPOSED BIOMARKER IN MAPSTONE ET AL (2014) (3)
Reply to “Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis” (2010) (2)
Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis Reply (2010) (2)
University of Groningen Physical Activity Attenuates the Influence of FTO Variants on Obesity Risk (2011) (2)
Behavioral and psychological signs and symptoms in patients with dementia of the Alzheimer type (DAT) and frontotemporal dementia (FTD): No effect of APOE genotype (2002) (2)
P4-154 Genomic sequencing of MAPT provides an extended SNP map and identifies >30 H1 subhaplotypes (2004) (2)
The alpha-2 macroglobulin gene in Alzheimer's disease: A population-based study and meta-analysis (2000) (2)
Risk factors for Alzheimer's disease : a genetic-epidemiologic study (1992) (2)
The apolipoprotein E gene and the risk of early-onset Alzheimer's disease (1995) (2)
CYP 1 A 2 and coffee intake and the modifying effect of sex , age , and smoking 1 – 3 (2012) (2)
Reply to — Alzheimer's disease and the family effect (1994) (2)
EIF 2 AK 3 variants in Dutch patients with Alzheimer ' s disease (2018) (2)
GENOME-WIDE META-ANALYSIS OF LATE-ONSET ALZHEIMER’S DISEASE USING RARE VARIANT IMPUTATION IN 64,859 SUBJECTS IDENTIFIES RISK LOCI WITH ROLES IN INNATE IMMUNITY AND CARDIOVASCULAR TRAITS: THE INTERNATIONAL GENOMICS OF ALZHEIMER’S PROJECT (IGAP) (2019) (1)
polymorphisms with bone mineral density, vertebral bone area and fracture risk (2003) (1)
In vitro analysis of Alzheimer's disease-related presenilin 1 and 2 mutations: effect on beta-amyloid processing (2002) (1)
Genetic Diagnosis of Age-RMacular Degeneration: The Role of Molecular Genetics in the Identification of High Risk Eyes (2008) (1)
Can Dietary Antioxidants Reduce the Genetic Risk of Early Age-Related Macular Degeneration? (2009) (1)
Identification of novel rare genetic variants associated with COPD in the general population (2018) (1)
ALDH2 and Head and Neck Cancer: a Meta-analysis implementing a Mendelian Randomization approach (2009) (1)
Supplementary Material 4 (2015) (1)
A study of ADHD in a genetic isolate (2000) (1)
GENETIC RISK OF NEURODEGENERATIVE DISEASES IS ASSOCIATED WITH MILD COGNITIVE IMPAIRMENT AND CONVERSION TO DEMENTIA: THE ROTTERDAM STUDY (2014) (1)
WHOLE-GENOME SEQUENCING IN FAMILIAL LATE-ONSET ALZHEIMER’S DISEASE IDENTIFIES RARE VARIATION IN AD CANDIDATE GENES (2017) (1)
EVALUATION OF THE ABSOLUTE GENETIC RISK OF ALZHEIMER'S DISEASE IN THE AGING POPULATION (2016) (1)
Supplementary Material 15 (2013) (1)
Genome-wide Association Studies From Four Cohorts Reveal Multiple Novel Loci Related To Pulmonary Function (2010) (1)
Alzheimer's disease, genetic and environmental factors (1998) (1)
A genome-wide SNP-by-NO2 interaction study on lung function in the LifeLines study (2017) (1)
Nicastrin significantly modifies risk for familial early-onset Alzheimer's disease in a Dutch population based sample (2002) (1)
Abstract 1967: Genome-wide Association Analysis of 25,330 Individuals Identifies Multiple Loci Associated With Resting Heart Rate (2009) (1)
Erratum: Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology (The American Journal of Human Genetics (2019) 105(1) (15–28), (S0002929719301880), (10.1016/j.ajhg.2019.05.002)) (2019) (1)
Supplementary Material 9 (2013) (1)
A genome-wide search for novel early-onset Alzheimer disease genes (2000) (1)
Multi-ancestry analysis of gene-sleep interactions in 126,926 individuals identifies multiple novel blood lipid loci that contribute to our understanding of sleep-associated adverse blood lipid profile (2019) (1)
An International Genome-Wide Association Study of Glaucoma-Related Optic Disc Parameters in 18,000 Caucasians: the International Glaucoma Genetics Consortium (2013) (1)
Polygenic overlap between C-reactive protein , plasma lipids and Alzheimer ’ s disease 1 2 (2017) (1)
Low-frequency variant imputation identifies rare variant candidate loci in a gwas of late-onset Alzheimer’s disease in the igap consortium (2015) (1)
Two-octapeptide repeat deletion of the prion protein gene associated with a rapidly progressive dementia (2001) (1)
Heritability and genetics of personality in healthy families and families with affective disorders from Sweden (2002) (1)
Heritability and Determinants of Intraocular Pressure in an Isolated Population in the Netherlands (2006) (1)
DNA methylation mediates the association between occupational exposures and lung function (2017) (1)
A genome-wide association study identifies a susceptibility 1 locus for refractive errors and myopia at 15 q 14 2 3 (2010) (1)
Identification of Biomarkers for the Prevention of Chronic Disease (2020) (1)
Exome-chip meta-analysis identifies novel loci, including ADAMTS6 associated with cardiac conduction (2018) (1)
Phosphosphingolipid levels are associated with cognitive function and level of education in healthy subjects (2012) (1)
The First Genome-Wide Association Meta-Analysis of Borderline Personality Disorder Features (2017) (1)
Complement factor H polymorphism, complement activators, and risk of age-related macular degeneration (2006) (1)
Discovery and Refinement Supplementary (2015) (1)
Whole exome sequence analysis of white matter hyperintensities on cranial MRI (2015) (1)
A genome-wide linkage study for COPD in a Dutch genetic isolate (2017) (0)
PATHWAY-SPECIFIC GENETIC RISK SCORE ASSOCIATED WITH ALZHEIMER’S DISEASE AND WHITE MATTER LESIONS IN COGNITIVELY NORMAL SUBJECTS (2017) (0)
Metabolomics Prediction of Future Type 2 Diabetes (2016) (0)
Development of algorithms and software for high-performance computing in genetic analysis of complex human traits (2004) (0)
Abstract 2074: Association of Hypertension Drug Target Genes With Blood Pressure and Hypertension: Results From a Genome-wide Association Study in 29,136 Individuals (2009) (0)
Contents Vol. 61, 2006 (2006) (0)
Delft University of Technology EIF2AK3 variants in Dutch patients with Alzheimer's disease (2018) (0)
THE INFLUENCE OF GENETIC AND ENVIRONMENTAL FACTORS ON BLOOD PRESSURE VARIANCE IN A GENETICALLY ISOLATED POPULATION: P2.224 (2004) (0)
University of Groningen Measurement and genetic architecture of lifetime depression in the Netherlands as assessed by LIDAS (Lifetime Depression Assessment Self-report) Fedko, (2020) (0)
variant at 19 q 13 . 2 in relation with DNA methylation and gene expression (2018) (0)
HIGH-DIMENSIONAL ANALYSIS OF RNA EXPRESSION WITH CORTICAL THICKNESS (2018) (0)
Abstract 2073: Genome-wide Association Studies of the Ankle-brachial Index: A Meta-analysis of 12 Cohorts Including 28083: Participants (2009) (0)
Prediction of Age-related Macular Degeneration based on Genotype and Phenotype in the Population-based Rotterdam Study (2012) (0)
Biological validation of statistical epistasis signals. (2015) (0)
Is the Shape of the Optic Disc Heritable (2006) (0)
CIRCULATING METABOLITES’ ASSOCIATION WITH ALZHEIMER’S DISEASE–ASSOCIATED GENETIC VARIANTS (2018) (0)
P.1.020 A whole gene based SNP study of the AVP 1B receptor gene: A possible protective effect in the etiology of major depression (2003) (0)
Abstract 56: Genome-wide Association Studies of Incident Stroke: The Charge Consortium (2014) (0)
Title : Six new loci associated with body mass index highlight a neuronal influence on body weight regulation (0)
Variants In The Nicotine Acetylcholine Receptor (CHRNA 3/5) Locus May Play A Role In COPD Development Via Smoking Status (2016) (0)
Identification of novel genes related to airway obstruction in never-smokers (2015) (0)
1a. Full Title: Analysis of gene-environment interactions: Genome-wide association interaction analysis of SNPs and sex on obesity traits in CHARGE b. Abbreviated Title: G-E GWAS SNPs and sex 2. Writing Group: (2009) (0)
Whole genome sequencing of late-onset Alzheimer's disease patients from genetic isolate (2015) (0)
Hintzen et al. reply (2010) (0)
Integration techniques for modern bioinformatics workflows (2018) (0)
Disease Associations: Human Leukocyte Antigen (HLA) and Apolipoprotein E (APOE) Gene (2006) (0)
Case-control studies of environmental influences in diseases with genetic determinants, (Letter) (1992) (0)
DT‐01‐06: Withdrwan (2015) (0)
Analyses of whole genome sequencing and imputed datasets identify a rare variant associated with intraocular pressure within the TMCO1 gene (2015) (0)
Heritability of carotid artery plaque in an isolated population (2004) (0)
Investigating Neurological Disease: Prion diseases (2001) (0)
Post-GWAS analysis approaches uncover dozens of novel genes associated with myopic refractive error (2017) (0)
Preparing forpresymptomatic DNA testing for early onsetAlzheimer's disease/cerebral haemorrhage andhereditary Pickdisease (1997) (0)
Subject Index Vol. 61, 2006 (2006) (0)
Supplementary Material (nature09270-s1) (2012) (0)
Common mechanisms underlying intraocular pressure identified in functional analysis of gene lists from genome-wide association study results in IGGC cohorts (2014) (0)
METABOLIC BLOOD-BASED BIOMARKERS RELATE TO BRAIN ATROPHY AND WHITE MATTER HYPERINTENSITIES IN ALZHEIMER’S DISEASE (2018) (0)
W48 GENETIC VARIATION WITHIN ADIPONUTRIN IS ASSOCIATED WITH LIPOPROTEIN METABOLISM AND LIVER FUNCTION (2010) (0)
O2-02-03 Linkage-based full genome scan for late onset Alzheimer’s disease in a genetically isolated population (2006) (0)
International meta-analysis of genetic factors influencing intraocular pressure: the International Glaucoma Genetics Consortium Study (2013) (0)
A straightforward approach to evaluate false positive associations in studies of gene interaction (2003) (0)
Prospective Cohort Studies Control and - Multilocus Genetic Risk Score Associates With Ischemic Stroke in Case (2014) (0)
Systematic analysis of the effect of novel Alzheimer disease PS1/2 mutations on A beta secretion (2002) (0)
A Genome-wide Association Study Identifies A Novel Locus Influencing Optic Disc Size On Chromosome 22q13.1 (2011) (0)
Vascular endothelial growth factor polymorphisms are associated with congenital heart defects. (2008) (0)
arthralgia, chondrocalcinosis and osteoarthritis gene predisposes to HFE The H63D variant in the (2007) (0)
Whole-exome sequencing in dutch families with Alzheimer’s disease (2015) (0)
Is ‘good’ cholesterol bad for Age-related Macular Degeneration? Evidence from the EYE-RISK and E3 Consortia (2018) (0)
Multi-omics approach to assess genetic susceptibility of COPD in never-smokers (2018) (0)
Risk Ratio Of Incident Late Age-related Macular Degeneration For Cfh And Arms2 In The Population-based Rotterdam Study (2011) (0)
Correction (2019) (0)
16GENOME-WIDE META-ANALYSES REVEAL NOVEL LOCI FOR VERBAL SHORT-TERM MEMORY AND LEARNING AND SHOW GENETIC CORRELATION WITH SCHIZOPHRENIA, ALZHEIMER'S DISEASE, AND TYPE 2 DIABETES (2019) (0)
WHOLE GENOME SEQUENCING IN FAMILIAL LATE-ONSET ALZHEIMER’S DISEASE IDENTIFIES VARIATIONS IN TTC3 AND FSIP2 (2016) (0)
Homozygosity of the prion Met129Val polymorphism increases risk of developing clinical early-onset but not late-onset Alzheimer's disease (2001) (0)
GENETIC DETERMINANTS OF MRI SUBCORTICAL BRAIN STRUCTURES: 24 NOVEL LOCI IDENTIFIED THROUGH GWAS IN 26,000 PERSONS (2016) (0)
Polymorphisms in the 5 ' regulatory region of presenilin 1 associated with an increased risk for early-onset Alzheimers Disease (1999) (0)
FREQUENCY AND HERITABILITY OF THE METABOLIC SYNDROME IN A GENETICALLY ISOLATED POPULATION: 5A.2 (2004) (0)
carpometacarpal joint of the hand disc degeneration and osteoarthritis of the first Association of matrilin-3 polymorphisms with spinal (2006) (0)
Familial aggregation of ischemic stroke in a genetically isolated population (2004) (0)
Analyses of low-frequency and rare variants associated with intraocular pressure (2016) (0)
Genetics in Glaucoma patients of African descent study (GIGA): Genetic African ancestry is associated with central corneal thickness and intraocular pressure in primary open-angle glaucoma patients. (2017) (0)
Grading the Credibility of Genetic Associations in Alzheimer’s Disease Using the Interim Venice Criteria (2011) (0)
CIRCULATING METABOLITES ARE ASSOCIATED WITH WHITE MATTER HYPERINTENSITIES (2018) (0)
vCJD: a single non adaptive strain (2011) (0)
A study of the genetics of hypertension (2000) (0)
Reply to Corder and Roses (1996) (0)
A common strain of agent is present in variant CJD cases from five different countries (2010) (0)
Abstract 150: Trans-ethnic GWAS of Mri-defined Brain Infarcts: Charge Consortium (2015) (0)
Glu318gly in presenilin-1 is a neutral mutation in relation to dementia: the Rotterdam study (1999) (0)
Edinburgh Explorer No evidence for association between tau gene haplotypic variants and susceptibility to Creutzfeldt-Jakob disease (2018) (0)
A transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration (2020) (0)
Genetics Identification of a Candidate Gene for Astigmatism (2013) (0)
GENOMEWIDE LINKAGE ANALYSIS IDENTIFIES NOVEL CANDIDATE GENES FOR ALZHEIMER’S DISEASE (2016) (0)
UvA-DARE ( Digital Academic Repository ) The ERCC 6 Gene and Age-Related Macular Degeneration (2010) (0)
Risk factors for Alzheimer's disease: Prologue (1991) (0)
case-control study frontotemporal dementia: a retrospective Medical and environmental risk factors for sporadic (2006) (0)
Abstract 3195: The APOA5 Gene is Associated with Familial Combined Hyperlipidemia and Dyslipidemia (2006) (0)
A study of the genetic susceptibility to cerebral white matter lesions in patients with hypertension (2001) (0)
ALZHEIMER'S DISEASE SEQUENCING PROJECT: CASE-CONTROL ANALYSES (2017) (0)
Bis, J. C. et al. (2014) Associations of NINJ2 sequence variants with incident ischemic stroke in the Cohorts for Heart and Aging in Genomic (2014) (0)
Genetics in Glaucoma patients of African descent study (GIGA): Clinical characteristics of Primary Open-Angle Glaucoma (POAG) in patients from Tanzania and South Africa (2016) (0)
WHOLE-GENOME SEQUENCING IN NON-HISPANIC WHITE FAMILIES IMPLICATES RARE VARIATION IN LATE-ONSET ALZHEIMER’S DISEASE RISK (2018) (0)
Title Genome-Wide Association Study of Retinopathy in Individualswithout Diabetes (2013) (0)
Genome-wide linkage screen of cognitive function identifies susceptible chromosomal regions (2010) (0)
A Genome-Wide Association Study of Glaucomatous Optic Neuropathy (2010) (0)
IDENTIFICATION OF WHOLE EXOME SEQUENCING VARIANTS ASSOCIATED WITH LATE-ONSET ALZHEIMER'S DISEASE IN THE COHORTS FOR HEART AND AGING RESEARCH IN GENOMIC EPIDEMIOLOGY (CHARGE) CONSORTIUM (2016) (0)
KIF1B, the First Neuronally Expressed Gene Associated with Multiple Sclerosis (2009) (0)
Genetic studies of dementia and related traits (2009) (0)
PROFILING PERIPHERAL METABOLIC DYSREGULATION IN ALZHEIMER’S DISEASE: THE ADDED VALUE OF MULTIPLE SIGNATURES (2017) (0)
Association of plasma amyloid beta peptide and anti-amyloid antibodies with risk of dementia in individuals with down syndrome (2011) (0)
Genome-wide association and functional follow-up reveals new loci for kidney function | NOVA. The University of Newcastle's Digital Repository (2012) (0)
VKučinskas-2001-2016 (2016) (0)
Drugs 2004; 64 (16): 1801-1816 (2004) (0)
Genome-wide significant evidence for linkage on chromosome 10q in 10 multiplex BP families (2006) (0)
Edinburgh Explorer Cerebrospinal fluid biomarker supported diagnosis of Creutzfeldt-Jakob disease and rapid dementias (2018) (0)
Genetics In Glaucoma patients of African descent study (GIGA): Known genetic risk factors for Primary Open Angle Glaucoma in a South African population (2016) (0)
Genome-wide association study of lobar brain volumes (2015) (0)
222 A genetic-epidemiological study of frontal lobe dementia in The Netherlands (1996) (0)
Shared genetic effects between diabetes-related traits and glaucoma-related traits (2018) (0)
Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years (2017) (0)
Parent of origin effect in multiple sclerosis in a genetic isolate in the Netherlands (2007) (0)
Whole-exome sequencing in age-related macular degeneration identifies rare protein-altering variants in COL8A1, a component of Bruch’s membrane (2018) (0)
Epigenome-wide association reveals extensive perturbations in DNA methylation associated with adiposity and its adverse metabolic consequences. Authors (2015) (0)
Investigation of genome-wide association genotype data to identify potential pathways and components of variant CJD susceptibility (2012) (0)
Genome-wide association study of memory performance (2011) (0)
DNA methylation is associated with lung function levels in never-smokers (2017) (0)
Evaluation of the myocilin mutation Gln368Stop (rs74315329) 1 demonstrates reduced penetrance in European populations 2 (2017) (0)
Genome-Wide Association Study Identifies a Locus and Candidate Gene for Refractive Errors and Myopia in the General Population (2010) (0)
P1-309 Evidence for interaction between the Cholesteryl ester transfer protein (CETP) gene and APOE in late onset Alzheimer’s disease (2006) (0)
Central cornea thickness Genome Wide Association Meta Analyses - Summary statistics (2018) (0)
EFFECTS OF AGE AND ETHNICITY ON THE LINK BETWEEN APOE EPSILON 4 AND ALZHEIMER DISEASE. AUTHORS' REPLY (1998) (0)
Assessing the genetic overlap between myopia and primary open-angle glaucoma (2018) (0)
Genetic epidemiological studies of MRI pathology: the CHARGE consortium (2011) (0)
Genome-wide association studies of hippocampal volume: The CHARGE consortium (2011) (0)
Identification Of Novel Genes Related To Two Definitions Of Airway Obstruction In Never-Smokers (2016) (0)
STOP-GAIN VARIANT IN MICROGLIA-EXPRESSED GENE GMIP IS ASSOCIATED WITH EARLY-ONSET ALZHEIMER’S DISEASE (2018) (0)
O2-02-08 Duplication of the APP locus in a Dutch family with early-onset Alzheimer dementia (2006) (0)
S0033291720000100jra 1..10 (2020) (0)
Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error (2014) (0)
S202 A GENOME WIDE ASSOCIATION STUDY ON CHRONIC WIDESPREAD PAIN: EVIDENCE FOR INVOLVEMENT OF THE 5P15.2 REGION (2011) (0)
Multi-trait genome-wide association study identifies new loci associated with optic disc parameters. (2019) (0)
Dna Methylation Mediates The Effect Of Cigarette Smoke Exposure On Lung Function Levels (2017) (0)
Chromosome 17 linked dementia in the absence of tau mutations (2001) (0)
A Genome-Wide Association Scan for Episodic Memory Decline in Aging (2011) (0)
Mutation analysis of candidate genes for chromosome 17-linked tau-negative FTD (2004) (0)
Review: Principles of neuroepidemiology (2003) (0)
frontotemporal dementia Apolipoprotein E 4 in the temporal variant of (2002) (0)
Estrogen and early-onset Alzheimer's disease (1999) (0)
The Personalized PREvention of Chronic Diseases (PRECeDI) recommendations on Personalized Medicine (2018) (0)
A genomewide association meta-analysis of plasma beta-amyloid peptide concentrations in the elderly (2013) (0)
Identification of plasma metabolites associated with intraocular pressure in a Dutch family-based study (2015) (0)
DO THE VARIANTS IDENTIFIED IN IGAP IMPROVE RISK PREDICTION OF ALZHEIMER'S DISEASE? (2014) (0)
1a. Full Title: Analysis of gene-environment interactions: Genome-wide association interaction analysis of SNPs and age on obesity traits in CHARGe (2009) (0)
12 GENOME-WIDE ASSOCIATION META-ANALYSIS IDENTIFIES NEW LOCI AND GENES INFLUENCING HUMAN INTELLIGENCE (2019) (0)
Genome-Wide Association Study of Executive Function (2011) (0)
Multi-ancestry genome-wide association study accounting for gene-psychosocial factor interactions identifies novel loci for blood pressure traits (2020) (0)
Functional characterization of GWAS loci associated with fracture risk (2013) (0)
Follow-Up in Myocardial Infarction Genome-Wide Association Study for Coronary Artery Calcification With (2011) (0)
Atypical clinical phenotype in a 2 octapeptide repeat insert mutation in the prion protein gene (2002) (0)
Reply to Okhubo et al.: Absence of association between codon 129/219 polymorphisms of the prion protein gene and Alzheimer's disease in Japan (2003) (0)
GENE-BASED ANALYSES IN WHOLE GENOME SEQUENCING OF FAMILIAL LATE-ONSET ALZHEIMER’S DISEASE (2018) (0)
Identification of microRNAs associated with glaucoma using GWAS data. (2017) (0)
The metabolic profile associated with head and neck cancer genetic variation and dietary intake (2020) (0)
Novel genes associated with the level of FEV1 in never-smokers in the context of occupational exposure (2015) (0)
782 Estimation of the mutation frequency of presenilin-1 in a population-based sample of early-onset Alzheimer disease (1996) (0)
A genome-wide scan in extended families with bipolar disorder from an isolated region in North Sweden reveals candidate loci on chromosomes 2q and 9q (2002) (0)
Multi-ancestry genome-wide association study accounting for gene-psychosocial factor interactions identifies novel loci for blood pressure traits (2020) (0)
use of human growth hormone Creutzfeldt-Jakob disease 38 years after diagnostic (2006) (0)
Homozygosity of valine at PRNP codon 129 is associated with early onset Alzheimer's disease in a Dutch population based sample (2002) (0)
Novel Dutch FFI family with heterogeneous course and newly described histology (2012) (0)
The Effect of the Apolipoprotein E Gene on Optic Disc Parameters (2009) (0)
Gene by gene interaction analyses identifies evidence of epistasis and new candidate genes that influence intraocular pressure in the general population (2015) (0)
The role of functional genetic variation in Alzheimer's disease: The CHARGE consortium (2013) (0)
Defining strain characteristics for variant CJD cases from five different countries (2011) (0)
Poster #S4 TWO CANDIDATE GENE-BASED ASSOCIATION STUDIES OF ANTIPSYCHOTIC-INDUCED MOVEMENT DISORDERS IN LONG-STAY PSYCHIATRIC PATIENTS: PROSPECTIVE STUDIES (2014) (0)
Gene-based replication strategy and meta-analysis in the context of epistasis: application for Alzheimer’s disease. (2015) (0)
The genetic basis of cross-phenotype correlation with bone fracture risk: the GEFOS consortium (2013) (0)
Identification of a gene involved in multiple sclerosis in a genetically isolated population (2005) (0)
Study of Inbreeding of Age–Related Macular Degeneration in a Genetically Isolated Population (2005) (0)
University of Groningen Transmission of human mtDNA heteroplasmy in the Genome of the Netherlands families (2016) (0)
Molecular basis of complex diseases (2001) (0)
Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation (vol 25, pg 1859, 2018) (2020) (0)
SERUM LIPOCALIN-2: MONITORING THE NEUROPATHOLOGICAL PROGRESSION OF AD IN DOWN SYNDROME? (2014) (0)
The impact of partial and complete loss of function mutations in endothelial lipase on hdl levels and functionality in humans (2018) (0)
Is Retinal Nerve Fiber Layer Thickness Related to Cognitive Function in Healthy Individuals (2007) (0)
Exome-wide analyses of glaucoma-related endophenotypes in 19,700 individuals (2017) (0)
Genetic Risk of Parkinson Disease in the General Population (P6.373) (2016) (0)
THE ASSOCIATION BETWEEN PRION PROTEIN CODON 129 AND THE RISK OF MILD COGNITIVE IMPAIRMENT AND DEMENTIA: A POPULATION-BASED COHORT STUDY (2019) (0)
Identification Of Novel Genes Related To Obstruction Of The Small Airways In Adult Never-Smokers (2016) (0)
Epigenome-wide association study of body mass index, and the adverse outcomes of adiposity Authors (2016) (0)
CEREBROSPINAL FLUID AND PLASMA LEVELS OF LYSOPHOSPHATIDIC ACIDS (LPAS) ASSOCIATE WITH CEREBROSPINAL FLUID Aβ-42 AND P-TAU (2006) (0)
Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA Kettunen (0)

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