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190 peer-reviewed articles • 30,197 peer-reviewed citations • Sorted by year • Download PDF (PDF by citations)
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1A genome-wide association study in 10,000 individuals links plasma N-glycome to liver disease and anti-inflammatory proteins
Nature Communications, 2025, 16,
11.06Citations (PDF)
2Fast and Simple Protocol for N-Glycome Analysis of Human Blood Plasma Proteome
Biomolecules, 2024, 14, 1551
3.12Citations (PDF)
3Noncoding rare variants in PANX3 are associated with chronic back pain
Pain, 2023, 164, 864-869
2.910Citations (PDF)
4Evidence of causal effects of blood pressure on back pain and back pain on type II diabetes provided by a bidirectional Mendelian randomization study
Spine Journal, 2023, 23, 1161-1171
2.319Citations (PDF)
5Genotype-by-environment interactions in chronic back pain
Spine Journal, 2023, 23, 1108-1114
2.31Citations (PDF)
6Twelve Years of Genome-Wide Association Studies of Human Protein N-Glycosylation
Engineering, 2023, 26, 17-31
5.910Citations (PDF)
7Development and Replication of a Genome-Wide Polygenic Risk Score for Chronic Back Pain
Journal of Personalized Medicine, 2023, 13, 977
1.915Citations (PDF)
8Bidirectional Mendelian Randomization Study of Personality Traits Reveals a Positive Feedback Loop Between Neuroticism and Back Pain
Journal of Pain, 2023, 24, 1875-1885
1.213Citations (PDF)
9GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification
Nature Genetics, 2023, 55, 1448-1461
14.198Citations (PDF)
10Investigation of the causal relationships between human IgG N-glycosylation and 12 common diseases associated with changes in the IgG N-glycome
Human Molecular Genetics, 2022, 31, 1545-1559
2.120Citations (PDF)
11Genetic regulation of post-translational modification of two distinct proteins
Nature Communications, 2022, 13,
11.042Citations (PDF)
12ANANASTRA: annotation and enrichment analysis of allele-specific transcription factor binding at SNPs
Nucleic Acids Research, 2022, 50, W51-W56
11.229Citations (PDF)
13Association Between Human Gut Microbiome and N-Glycan Composition of Total Plasma Proteome
Frontiers in Microbiology, 2022, 13,
2.96Citations (PDF)
14Causal effects of psychosocial factors on chronic back pain: a bidirectional Mendelian randomisation study
European Spine Journal, 2022, 31, 1906-1915
1.736Citations (PDF)
15Method for the Isolation of “RNA-seq-Quality” RNA from Human Intervertebral Discs after Mortar and Pestle Homogenization
Cells, 2022, 11, 3578
3.45Citations (PDF)
16Replication of 15 loci involved in human plasma protein N-glycosylation in 4802 samples from four cohorts
Glycobiology, 2021, 31, 82-88
1.824Citations (PDF)
17Nontrivial Replication of Loci Detected by Multi-Trait Methods
Frontiers in Genetics, 2021, 12,
1.68Citations (PDF)
18Genome-wide association studies of low back pain and lumbar spinal disorders using electronic health record data identify a locus associated with lumbar spinal stenosis
Pain, 2021, 162, 2263-2272
2.931Citations (PDF)
19The limits of normal approximation for adult height
European Journal of Human Genetics, 2021, 29, 1082-1091
2.111Citations (PDF)
20Multivariate genome-wide analysis of immunoglobulin G N-glycosylation identifies new loci pleiotropic with immune function
Human Molecular Genetics, 2021, 30, 1259-1270
2.121Citations (PDF)
21Genome-wide association study identifies RNF123 locus as associated with chronic widespread musculoskeletal pain
Annals of the Rheumatic Diseases, 2021, 80, 1227-1235
6.561Citations (PDF)
22Identification of tissue-specific and common methylation quantitative trait loci in healthy individuals using MAGAR
Epigenetics and Chromatin, 2021, 14,
2.24Citations (PDF)
23PheLiGe: an interactive database of billions of human genotype–phenotype associations
Nucleic Acids Research, 2021, 49, D1347-D1350
11.220Citations (PDF)
24Sex- and age-specific genetic analysis of chronic back pain
Pain, 2021, 162, 1176-1187
2.941Citations (PDF)
25Prioritization of causal genes for coronary artery disease based on cumulative evidence from experimental and in silico studies
Scientific Reports, 2020, 10,
2.735Citations (PDF)
26Analysis of genetically independent phenotypes identifies shared genetic factors associated with chronic musculoskeletal pain conditions
Communications Biology, 2020, 3,
3.162Citations (PDF)
27Glycosylation of immunoglobulin G is regulated by a large network of genes pleiotropic with inflammatory diseases
Science Advances, 2020, 6,
8.2130Citations (PDF)
28Sequence variation at 8q24.21 and risk of back pain
F1000Research, 2020, 9, 424
0.31Citations (PDF)
29Identification of 12 genetic loci associated with human healthspan
Communications Biology, 2019, 2,
3.1161Citations (PDF)
30Insight into the genetic architecture of back pain and its risk factors from a study of 509,000 individuals
Pain, 2019, 160, 1361-1373
2.9119Citations (PDF)
31ISSLS Prize in Clinical Science 2020. Examining causal effects of body mass index on back pain: a Mendelian randomization study
European Spine Journal, 2019, 29, 686-691
1.749Citations (PDF)
32Glycosylation of Immunoglobulin G Associates With Clinical Features of Inflammatory Bowel Diseases
Gastroenterology, 2018, 154, 1320-1333.e10
0.9156Citations (PDF)
33A network-based conditional genetic association analysis of the human metabolome
GigaScience, 2018, 7,
2.514Citations (PDF)
34Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain
PLoS Genetics, 2018, 14, e1007601
2.2145Citations (PDF)
35Plasma N-Glycan Signatures Are Associated With Features of Inflammatory Bowel Diseases
Gastroenterology, 2018, 155, 829-843
0.9108Citations (PDF)
36Plasma N-glycome composition associates with chronic low back pain
Biochimica Et Biophysica Acta - General Subjects, 2018, 1862, 2124-2133
1.726Citations (PDF)
37Causal Effect of Plasminogen Activator Inhibitor Type 1 on Coronary Heart Disease
Journal of the American Heart Association, 2017, 6,
3.1113Citations (PDF)
38Multivariate discovery and replication of five novel loci associated with Immunoglobulin G N-glycosylation
Nature Communications, 2017, 8,
11.0122Citations (PDF)
39Validation of standard operating procedures in a multicenter retrospective study to identify -omics biomarkers for chronic low back pain
PLoS ONE, 2017, 12, e0176372
1.517Citations (PDF)
40The Association Between Glycosylation of Immunoglobulin G and Hypertension
Medicine (United States), 2016, 95, e3379
1.094Citations (PDF)
41‘Omics’ biomarkers associated with chronic low back pain: protocol of a retrospective longitudinal study
BMJ Open, 2016, 6, e012070
1.221Citations (PDF)
42IgG Glycome in Colorectal Cancer
Clinical Cancer Research, 2016, 22, 3078-3086
4.5136Citations (PDF)
43Genetic variants in RBFOX3 are associated with sleep latency
European Journal of Human Genetics, 2016, 24, 1488-1495
2.136Citations (PDF)
44The Menkes and Wilson disease genes counteract in copper toxicosis in Labrador retrievers: a new canine model for copper-metabolism disorders
DMM Disease Models and Mechanisms, 2016, 9, 25-38
1.382Citations (PDF)
45Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
Nature Communications, 2016, 7,
11.0515Citations (PDF)
46The GenABEL Project for statistical genomics
F1000Research, 2016, 5, 914
0.366Citations (PDF)
47A Genome Wide Association Study Links Glutamate Receptor Pathway to Sporadic Creutzfeldt-Jakob Disease Risk
PLoS ONE, 2015, 10, e0123654
1.533Citations (PDF)
48Inflammatory Bowel Disease Associates with Proinflammatory Potential of the Immunoglobulin G Glycome
Inflammatory Bowel Diseases, 2015, , 1
2.3170Citations (PDF)
49Nonadditive Effects of Genes in Human Metabolomics
Genetics, 2015, 200, 707-718
3.330Citations (PDF)
50Identification of Novel Genetic Loci Associated with Thyroid Peroxidase Antibodies and Clinical Thyroid Disease
PLoS Genetics, 2014, 10, e1004123
2.2184Citations (PDF)
51Comparative Performance of Four Methods for High-throughput Glycosylation Analysis of Immunoglobulin G in Genetic and Epidemiological Research
Molecular and Cellular Proteomics, 2014, 13, 1598-1610
3.5196Citations (PDF)
52Glycans Are a Novel Biomarker of Chronological and Biological Ages
Journals of Gerontology - Series A Biological Sciences and Medical Sciences, 2014, 69, 779-789
2.5415Citations (PDF)
53Solving sequences of generalized least-squares problems on multi-threaded architectures
Applied Mathematics and Computation, 2014, 234, 606-617
1.16Citations (PDF)
54Identifying genetic risk variants for coronary heart disease in familial hypercholesterolemia: an extreme genetics approach
European Journal of Human Genetics, 2014, 23, 381-387
2.117Citations (PDF)
55High-Performance Mixed Models Based Genome-Wide Association Analysis with omicABEL software
F1000Research, 2014, 3, 200
0.317Citations (PDF)
56Common Variants in Mendelian Kidney Disease Genes and Their Association with Renal Function
Journal of the American Society of Nephrology: JASN, 2013, 24, 2105-2117
0.338Citations (PDF)
57Loci Associated with N-Glycosylation of Human Immunoglobulin G Show Pleiotropy with Autoimmune Diseases and Haematological Cancers
PLoS Genetics, 2013, 9, e1003225
2.2367Citations (PDF)
58Migraine is not associated with enhanced atherosclerosis
Cephalalgia, 2013, 33, 228-235
2.868Citations (PDF)
59Development and Application of Genomic Control Methods for Genome-Wide Association Studies Using Non-Additive Models
PLoS ONE, 2013, 8, e81431
1.519Citations (PDF)
60Region-Based Association Analysis of Human Quantitative Traits in Related Individuals
PLoS ONE, 2013, 8, e65395
1.530Citations (PDF)
61Common Genetic Determinants of Intraocular Pressure and Primary Open-Angle Glaucoma
PLoS Genetics, 2012, 8, e1002611
2.2189Citations (PDF)
62Evidence of Inbreeding Depression on Human Height
PLoS Genetics, 2012, 8, e1002655
2.298Citations (PDF)
63Genome-Wide Association Study Identifies Novel Loci Associated with Circulating Phospho- and Sphingolipid Concentrations
PLoS Genetics, 2012, 8, e1002490
2.2203Citations (PDF)
64Genome-Wide Association and Functional Follow-Up Reveals New Loci for Kidney Function
PLoS Genetics, 2012, 8, e1002584
2.2187Citations (PDF)
65The Empirical Power of Rare Variant Association Methods: Results from Sanger Sequencing in 1,998 Individuals
PLoS Genetics, 2012, 8, e1002496
2.2102Citations (PDF)
66Stratifying Type 2 Diabetes Cases by BMI Identifies Genetic Risk Variants in LAMA1 and Enrichment for Risk Variants in Lean Compared to Obese Cases
PLoS Genetics, 2012, 8, e1002741
2.2206Citations (PDF)
67Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals
PLoS Genetics, 2012, 8, e1002607
2.2458Citations (PDF)
68A Genetic Epidemiologic Study of Candidate Genes Involved in the Optic Nerve Head Morphology
2012, 53, 1485
10Citations (PDF)
69Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function
Human Molecular Genetics, 2012, 21, 5329-5343
2.167Citations (PDF)
70Eight genetic loci associated with variation in lipoprotein-associated phospholipase A2 mass and activity and coronary heart disease: meta-analysis of genome-wide association studies from five community-based studies
European Heart Journal, 2012, 33, 238-251
2.694Citations (PDF)
71Linkage analysis for plasma amyloid beta levels in persons with hypertension implicates Aβ-40 levels to presenilin 2
Human Genetics, 2012, 131, 1869-1876
1.97Citations (PDF)
72Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture
Nature Genetics, 2012, 44, 491-501
14.11,211Citations (PDF)
73Transferrin and HFE genes interact in Alzheimer's disease risk: the Epistasis Project
Neurobiology of Aging, 2012, 33, 202.e1-202.e13
2.458Citations (PDF)
74Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk
Neurobiology of Aging, 2012, 33, 1487.e21-1487.e28
2.442Citations (PDF)
75Association Between Chromosome 9p21 Variants and the Ankle-Brachial Index Identified by a Meta-Analysis of 21 Genome-Wide Association Studies
Circulation: Cardiovascular Genetics, 2012, 5, 100-112
3.7112Citations (PDF)
76A Genome-Wide Association Search for Type 2 Diabetes Genes in African Americans
PLoS ONE, 2012, 7, e29202
1.5205Citations (PDF)
77A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance
Nature Genetics, 2012, 44, 659-669
14.1838Citations (PDF)
78Refining genome-wide linkage intervals using a meta-analysis of genome-wide association studies identifies loci influencing personality dimensions
European Journal of Human Genetics, 2012, 21, 876-882
2.125Citations (PDF)
79Low-density lipoprotein receptor mutations generate synthetic genome-wide associations
European Journal of Human Genetics, 2012, 21, 563-566
2.18Citations (PDF)
80Heritability Estimates of Body Size in Fetal Life and Early Childhood
PLoS ONE, 2012, 7, e39901
1.554Citations (PDF)
81Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile
Nature Genetics, 2011, 43, 753-760
14.1316Citations (PDF)
82Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Nature, 2011, 478, 103-109
31.32,017Citations (PDF)
83Association of HSP70 and its Co-Chaperones with Alzheimer's Disease
Journal of Alzheimer's Disease, 2011, 25, 93-102
1.725Citations (PDF)
84Genetic architecture of circulating lipid levels
European Journal of Human Genetics, 2011, 19, 813-819
2.123Citations (PDF)
85Meta-analysis of genome-wide association for migraine in six population-based European cohorts
European Journal of Human Genetics, 2011, 19, 901-907
2.195Citations (PDF)
86PredictABEL: an R package for the assessment of risk prediction models
European Journal of Epidemiology, 2011, 26, 261-264
3.4262Citations (PDF)
87Linkage and association analyses of glaucoma related traits in a large pedigree from a Dutch genetically isolated population
Journal of Medical Genetics, 2011, 48, 802-809
2.238Citations (PDF)
88Genetic architecture of open angle glaucoma and related determinants
Journal of Medical Genetics, 2011, 48, 190-196
2.225Citations (PDF)
89Association of genetic variation with systolic and diastolic blood pressure among African Americans: the Candidate Gene Association Resource study
Human Molecular Genetics, 2011, 20, 2273-2284
2.1170Citations (PDF)
90Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene ( AUTS2 ) in the regulation of alcohol consumption
Proceedings of the National Academy of Sciences of the United States of America, 2011, 108, 7119-7124
5.3261Citations (PDF)
91Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
Nature Genetics, 2011, 43, 1005-1011
14.1427Citations (PDF)
92A Genome-Wide Screen for Interactions Reveals a New Locus on 4p15 Modifying the Effect of Waist-to-Hip Ratio on Total Cholesterol
PLoS Genetics, 2011, 7, e1002333
2.231Citations (PDF)
93Interaction of insulin and PPAR-α genes in Alzheimer’s disease: the Epistasis Project
Journal of Neural Transmission, 2011, 119, 473-479
2.320Citations (PDF)
94Detecting Low Frequent Loss-of-Function Alleles in Genome Wide Association Studies with Red Hair Color as Example
PLoS ONE, 2011, 6, e28145
1.519Citations (PDF)
95Genome-Wide Association Studies of MRI-Defined Brain Infarcts
Stroke, 2010, 41, 210-217
4.485Citations (PDF)
96Shared genetic factors in the co-occurrence of symptoms of depression and cardiovascular risk factors
Journal of Affective Disorders, 2010, 122, 247-252
3.222Citations (PDF)
97Ped_Outlier software for automatic identification of within-family outliers
Computational Biology and Chemistry, 2010, 34, 242-243
2.30Citations (PDF)
98The dopamine β-hydroxylase -1021C/T polymorphism is associated with the risk of Alzheimer's disease in the Epistasis Project
BMC Medical Genetics, 2010, 11,
1.854Citations (PDF)
99A meta-analysis of genome-wide data from five European isolates reveals an association of COL22A1, SYT1, and GABRR2with serum creatinine level
BMC Medical Genetics, 2010, 11,
1.853Citations (PDF)
100MQScore_SNP Software for Multipoint Parametric Linkage Analysis of Quantitative Traits in Large Pedigrees
Annals of Human Genetics, 2010, 74, 286-289
1.04Citations (PDF)
101The TCF7L2 Diabetes Risk Variant is Associated with HbA1C Levels: a Genome‐Wide Association Meta‐Analysis
Annals of Human Genetics, 2010, 74, 471-478
1.034Citations (PDF)
102Biological, clinical and population relevance of 95 loci for blood lipids
Nature, 2010, 466, 707-713
31.33,486Citations (PDF)
103Hundreds of variants clustered in genomic loci and biological pathways affect human height
Nature, 2010, 467, 832-838
31.31,893Citations (PDF)
104Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge
Nature Genetics, 2010, 42, 142-148
14.1625Citations (PDF)
105Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight
Nature Genetics, 2010, 42, 430-435
14.1235Citations (PDF)
106New loci associated with kidney function and chronic kidney disease
Nature Genetics, 2010, 42, 376-384
14.1778Citations (PDF)
107Sequence variants at CHRNB3–CHRNA6 and CYP2A6 affect smoking behavior
Nature Genetics, 2010, 42, 448-453
14.1678Citations (PDF)
108Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
Nature Genetics, 2010, 42, 579-589
14.11,714Citations (PDF)
109Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1
Nature Genetics, 2010, 42, 869-873
14.1364Citations (PDF)
110A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14
Nature Genetics, 2010, 42, 897-901
14.1210Citations (PDF)
111Reply to “Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis”
Nature Genetics, 2010, 42, 470-471
14.19Citations (PDF)
112Association between Type 2 Diabetes Loci and Measures of Fatness
PLoS ONE, 2010, 5, e8541
1.518Citations (PDF)
113Genome-wide Analysis of Genetic Loci Associated With Alzheimer Disease
JAMA - Journal of the American Medical Association, 2010, 303, 1832
15.81,155Citations (PDF)
114Association of Genome-Wide Variation With the Risk of Incident Heart Failure in Adults of European and African Ancestry
Circulation: Cardiovascular Genetics, 2010, 3, 256-266
3.7192Citations (PDF)
115Genetic Architecture of Plasma Adiponectin Overlaps With the Genetics of Metabolic Syndrome–Related Traits
Diabetes Care, 2010, 33, 908-913
6.573Citations (PDF)
116Genetic Variants Influencing Circulating Lipid Levels and Risk of Coronary Artery Disease
Arteriosclerosis, Thrombosis, and Vascular Biology, 2010, 30, 2264-2276
4.3400Citations (PDF)
117Genomic Variation Associated With Mortality Among Adults of European and African Ancestry With Heart Failure
Circulation: Cardiovascular Genetics, 2010, 3, 248-255
3.786Citations (PDF)
118A Genome-Wide Association Study of Optic Disc Parameters
PLoS Genetics, 2010, 6, e1000978
2.2198Citations (PDF)
119A Meta-analysis of Four Genome-Wide Association Studies of Survival to Age 90 Years or Older: The Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Journals of Gerontology - Series A Biological Sciences and Medical Sciences, 2010, 65A, 478-487
2.5126Citations (PDF)
120Genome-wide association analysis identifies multiple loci related to resting heart rate
Human Molecular Genetics, 2010, 19, 3885-3894
2.1144Citations (PDF)
121The apolipoprotein E gene and its age-specific effects on cognitive function
Neurobiology of Aging, 2010, 31, 1831-1833
2.461Citations (PDF)
122New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
Nature Genetics, 2010, 42, 105-116
14.12,127Citations (PDF)
123Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: Results of genome-wide association analyses including 4659 European individuals
Atherosclerosis, 2010, 208, 412-420
1.9149Citations (PDF)
124Linkage and Genome‐wide Association Analysis of Obesity‐related Phenotypes: Association of Weight With the MGAT1 Gene
Obesity, 2010, 18, 803-808
2.960Citations (PDF)
125Prevalence of the variant allele rs61764370 T>G in the 3′UTR of KRAS among Dutch BRCA1, BRCA2 and non-BRCA1/BRCA2 breast cancer families
Breast Cancer Research and Treatment, 2010, 128, 79-84
1.836Citations (PDF)
126Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution
PLoS Genetics, 2009, 5, e1000508
2.2469Citations (PDF)
127Genetic evidence for a role of adiponutrin in the metabolism of apolipoprotein B-containing lipoproteins
Human Molecular Genetics, 2009, 18, 4669-4676
2.151Citations (PDF)
128Genomewide Association Studies of Stroke
New England Journal of Medicine, 2009, 360, 1718-1728
19.4434Citations (PDF)
129Genetic Variants Associated With Cardiac Structure and Function
JAMA - Journal of the American Medical Association, 2009, 302, 168
15.8216Citations (PDF)
130NRXN3 Is a Novel Locus for Waist Circumference: A Genome-Wide Association Study from the CHARGE Consortium
PLoS Genetics, 2009, 5, e1000539
2.2245Citations (PDF)
131Meta-Analysis of 28,141 Individuals Identifies Common Variants within Five New Loci That Influence Uric Acid Concentrations
PLoS Genetics, 2009, 5, e1000504
2.2617Citations (PDF)
132A Genome-Wide Association Study Reveals Variants in ARL15 that Influence Adiponectin Levels
PLoS Genetics, 2009, 5, e1000768
2.2156Citations (PDF)
133Genetic Determinants of Circulating Sphingolipid Concentrations in European Populations
PLoS Genetics, 2009, 5, e1000672
2.2206Citations (PDF)
134Association of Novel Genetic Loci With Circulating Fibrinogen Levels
Circulation: Cardiovascular Genetics, 2009, 2, 125-133
3.790Citations (PDF)
135Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis
Human Molecular Genetics, 2009, 18, 373-380
2.191Citations (PDF)
136A Genome-Wide Association Scan of RR and QT Interval Duration in 3 European Genetically Isolated Populations
Circulation: Cardiovascular Genetics, 2009, 2, 322-328
3.767Citations (PDF)
137Predicting human height by Victorian and genomic methods
European Journal of Human Genetics, 2009, 17, 1070-1075
2.1115Citations (PDF)
138Multiple loci associated with indices of renal function and chronic kidney disease
Nature Genetics, 2009, 41, 712-717
14.1613Citations (PDF)
139Genome-wide association study of blood pressure and hypertension
Nature Genetics, 2009, 41, 677-687
14.11,303Citations (PDF)
140Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies
Nature Genetics, 2009, 41, 1199-1206
14.1696Citations (PDF)
141PedStr Software for Cutting Large Pedigrees for Haplotyping, IBD Computation and Multipoint Linkage Analysis
Annals of Human Genetics, 2009, 73, 527-531
1.013Citations (PDF)
142Genome-wide Association Study of Smoking Initiation and Current Smoking
American Journal of Human Genetics, 2009, 84, 367-379
4.5134Citations (PDF)
143A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation
Human Molecular Genetics, 2009, 18, 3516-3524
2.178Citations (PDF)
144Replication by the Epistasis Project of the interaction between the genes for IL-6 and IL-10 in the risk of Alzheimer's disease
Journal of Neuroinflammation, 2009, 6, 22
6.146Citations (PDF)
145Genome-wide linkage analysis of serum creatinine in three isolated European populations
Kidney International, 2009, 76, 297-306
4.672Citations (PDF)
146Collaborative Meta-analysis: Associations of 150 Candidate Genes With Osteoporosis and Osteoporotic Fracture
Annals of Internal Medicine, 2009, 151, 528-537
7.3263Citations (PDF)
147Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis
Journal of Human Genetics, 2009, 54, 676-680
1.368Citations (PDF)
148A Study of the SORL1 Gene in Alzheimer's Disease and Cognitive Function
Journal of Alzheimer's Disease, 2009, 18, 51-64
1.738Citations (PDF)
149Role of shared genetic and environmental factors in symptoms of depression and body composition
Psychiatric Genetics, 2009, 19, 32-38
0.616Citations (PDF)
150A powerful genome-wide feasible approach to detect parent-of-origin effects in studies of quantitative traits
European Journal of Human Genetics, 2009, 18, 379-384
2.19Citations (PDF)
151Genetic Factors Influence the Clustering of Depression among Individuals with Lower Socioeconomic Status
PLoS ONE, 2009, 4, e5069
1.512Citations (PDF)
152Cyclin-dependent kinase 5 is associated with risk for Alzheimer’s disease in a Dutch population-based study
Journal of Neurology, 2008, 255, 655-662
2.714Citations (PDF)
153Three Genome-wide Association Studies and a Linkage Analysis Identify HERC2 as a Human Iris Color Gene
American Journal of Human Genetics, 2008, 82, 411-423
4.5238Citations (PDF)
154Detection, Imputation, and Association Analysis of Small Deletions and Null Alleles on Oligonucleotide Arrays
American Journal of Human Genetics, 2008, 82, 1316-1333
4.542Citations (PDF)
155An approach for cutting large and complex pedigrees for linkage analysis
European Journal of Human Genetics, 2008, 16, 854-860
2.159Citations (PDF)
156Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis
Nature Genetics, 2008, 40, 1402-1403
14.1182Citations (PDF)
157Association of the gene encoding neurogranin with schizophrenia in males
Journal of Psychiatric Research, 2008, 42, 125-133
1.951Citations (PDF)
158Maternal Transmission of Multiple Sclerosis in a Dutch Population
Archives of Neurology, 2008, 65,
6.962Citations (PDF)
159Angiotensinogen M235T polymorphism and symptoms of depression in a population-based study and a family-based study
Psychiatric Genetics, 2008, 18, 162-166
0.617Citations (PDF)
160Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts
Nature Genetics, 2008, 41, 47-55
14.1795Citations (PDF)
161Variants in MTNR1B influence fasting glucose levels
Nature Genetics, 2008, 41, 77-81
14.1703Citations (PDF)
162Epistatic Effect of Cholesteryl Ester Transfer Protein and Hepatic Lipase on Serum High-Density Lipoprotein Cholesterol Levels
Journal of Clinical Endocrinology and Metabolism, 2007, 92, 2680-2687
3.325Citations (PDF)
163LPIN2 Is Associated With Type 2 Diabetes, Glucose Metabolism, and Body Composition
Diabetes, 2007, 56, 3020-3026
3.555Citations (PDF)
164Genetic Contributions to Glaucoma: Heritability of Intraocular Pressure, Retinal Nerve Fiber Layer Thickness, and Optic Disc Morphology
2007, 48, 3669
115Citations (PDF)
165Genomewide Rapid Association Using Mixed Model and Regression: A Fast and Simple Method For Genomewide Pedigree-Based Quantitative Trait Loci Association Analysis
Genetics, 2007, 177, 577-585
3.3430Citations (PDF)
166Heritability of blood pressure traits and the genetic contribution to blood pressure variance explained by four blood-pressure-related genes
Journal of Hypertension, 2007, 25, 565-570
1.484Citations (PDF)
167Relationship of the Ubiquilin 1 gene with Alzheimer's and Parkinson's disease and cognitive function
Neuroscience Letters, 2007, 424, 1-5
1.316Citations (PDF)
168A Genomewide Screen for Late-Onset Alzheimer Disease in a Genetically Isolated Dutch Population
American Journal of Human Genetics, 2007, 81, 17-31
4.5155Citations (PDF)
169GenABEL: an R library for genome-wide association analysis
Bioinformatics, 2007, 23, 1294-1296
3.21,816Citations (PDF)
170Heritabilities, apolipoprotein E, and effects of inbreeding on plasma lipids in a genetically isolated population: The Erasmus Rucphen Family Study
European Journal of Epidemiology, 2007, 22, 99-105
3.426Citations (PDF)
171The cholesteryl ester transfer protein (CETP) gene and the risk of Alzheimer’s disease
Neurogenetics, 2007, 8, 189-193
0.940Citations (PDF)
172A Genomic Background Based Method for Association Analysis in Related Individuals
PLoS ONE, 2007, 2, e1274
1.5243Citations (PDF)
173Predictive testing for complex diseases using multiple genes: Fact or fiction?
Genetics in Medicine, 2006, 8, 395-400
3.4210Citations (PDF)
174Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies
Nature Genetics, 2006, 38, 556-560
14.1230Citations (PDF)
175Solution for underflow problem in linkage and segregation analysis
Computational Biology and Chemistry, 2006, 30, 382-385
2.33Citations (PDF)
176Chromosome-Wise Dissection of the Genome of the Extremely Big Mouse Line DU6i
Genetics, 2006, 172, 401-410
3.317Citations (PDF)
177The Effect of Genetic Drift in a Young Genetically Isolated Population
Annals of Human Genetics, 2005, 69, 288-295
1.0132Citations (PDF)
178Hearing impairment in Dutch patients with connexin 26 (GJB2) and connexin 30 (GJB6) mutations
International Journal of Pediatric Otorhinolaryngology, 2005, 69, 165-174
0.938Citations (PDF)
179Evidence for novel loci for late-onset Parkinson’s disease in a genetic isolate from the Netherlands
Human Genetics, 2005, 119, 51-60
1.94Citations (PDF)
180Angiotensinogen Promoter B-Haplotype Associated With Cerebral Small Vessel Disease Enhances Basal Transcriptional Activity
Stroke, 2004, 35, 2592-2597
4.433Citations (PDF)
181Linkage disequilibrium in young genetically isolated Dutch population
European Journal of Human Genetics, 2004, 12, 527-534
2.1107Citations (PDF)
182A major SNP haplotype of the arginine vasopressin 1B receptor protects against recurrent major depression
Molecular Psychiatry, 2004, 9, 287-292
5.3110Citations (PDF)
183A deletion in DJ-1 and the risk of dementia—a population-based survey
Neuroscience Letters, 2004, 372, 196-199
1.37Citations (PDF)
184Chromosomal segregation and fertility in Robertsonian chromosomal heterozygotes of the house musk shrew (Suncus murinus, Insectivora, Soricidae)
Heredity, 1998, 81, 335-341
1.415Citations (PDF)
185Chromosomal segregation and fertility in Robertsonian chromosomal heterozygotes of the house musk shrew (Suncus murinus, Insectivora, Soricidae)
Heredity, 1998, 81, 335-341
1.41Citations (PDF)
186Segregation analysis of animal pedigree data from inter-population crosses.
Genes and Genetic Systems, 1997, 72, 291-296
0.40Citations (PDF)
187Defining the genetic control of human blood plasma N-glycome using genome-wide association study
Human Molecular Genetics, 0, ,
2.144Citations (PDF)
188Title is missing!
0
1Citations (PDF)
189Quantitative Modeling of IgG N-Glycosylation Profiles from Population Data
International Journal of Molecular Sciences, 0, 26, 11495
3.21Citations (PDF)
190Evaluating transportability of in vitro cellular models to in vivo human phenotypes using gene perturbation data
Nature Communications, 0, 17,
11.01Citations (PDF)