| human | Q5 |
| P496 | ORCID iD | 0000-0003-1478-649X |
| P108 | employer | Statens Serum Institut | Q3378353 |
| P106 | occupation | researcher | Q1650915 |
| Q35661744 | A novel common variant in DCST2 is associated with length in early life and height in adulthood |
| Q42121685 | A quantitative trait locus mixture model that avoids spurious LOD score peaks |
| Q37276250 | Association of adiposity genetic variants with menarche timing in 92,105 women of European descent |
| Q37258646 | Association of maternal CNVs in GSTT1/GSTT2 with smoking, preterm delivery, and low birth weight. |
| Q91045562 | Associations of autozygosity with a broad range of human phenotypes |
| Q42367768 | CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits |
| Q38727086 | CPT1A Missense Mutation Associated With Fatty Acid Metabolism and Reduced Height in Greenlanders |
| Q24169697 | Characterization of large structural genetic mosaicism in human autosome |
| Q92311722 | Co-occurrence of infantile hypertrophic pyloric stenosis and congenital heart defects: a nationwide cohort study |
| Q34572775 | Common variants associated with general and MMR vaccine-related febrile seizures |
| Q37173595 | Common variants at 12q15 and 12q24 are associated with infant head circumference |
| Q36956625 | Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis |
| Q37129450 | Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis |
| Q112638055 | Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci |
| Q57285403 | Consortium genome-wide meta-analysis for childhood dental caries traits |
| Q57278041 | Consortium-based genome-wide meta-analysis for childhood dental caries traits |
| Q42502463 | Correction: The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study |
| Q34441746 | Defining the role of common variation in the genomic and biological architecture of adult human height |
| Q28385149 | Detectable clonal mosaicism from birth to old age and its relationship to cancer |
| Q47737479 | Detecting sample misidentifications in genetic association studies |
| Q42702218 | Determination of NAT2 acetylation status in the Greenlandic population |
| Q28646221 | Directional dominance on stature and cognition in diverse human populations |
| Q98719737 | Dissecting maternal and fetal genetic effects underlying the associations between maternal phenotypes, birth outcomes, and adult phenotypes: A mendelian-randomization and haplotype-based genetic score analysis in 10,734 mother-infant pairs |
| Q57105402 | Erratum: Common variants at 12q15 and 12q24 are associated with infant head circumference |
| Q49385571 | Familial aggregation of tonsillectomy in early childhood and adolescence. |
| Q91995911 | GWAS on longitudinal growth traits reveals different genetic factors influencing infant, child, and adult BMI |
| Q40055866 | Genetic Associations with Gestational Duration and Spontaneous Preterm Birth |
| Q36738318 | Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight |
| Q57285419 | Genetic architecture of early childhood growth phenotypes gives insights into their link with later obesity |
| Q102388878 | Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women |
| Q33622547 | Genetic regulation of gene expression in the epileptic human hippocampus |
| Q22305005 | Genetic studies of body mass index yield new insights for obesity biology |
| Q34182520 | Genetic variability in beta-defensins is not associated with susceptibility to Staphylococcus aureus bacteremia |
| Q36450086 | Genetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) interacts with maternal self-reported smoking status during pregnancy to influence birth weight |
| Q58618794 | Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders |
| Q34973837 | Genome partitioning of genetic variation for complex traits using common SNPs |
| Q46530826 | Genome-wide association analyses identify variants in developmental genes associated with hypospadias |
| Q36861322 | Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index |
| Q100316395 | Genome-wide association study identifies 48 common genetic variants associated with handedness |
| Q34023060 | Genome-wide association study identifies four loci associated with eruption of permanent teeth |
| Q34981439 | Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche |
| Q40414209 | Genome-wide association study identifies variants in HORMAD2 associated with tonsillectomy |
| Q48146651 | Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus |
| Q28943266 | Genome-wide association study of classical Hodgkin lymphoma and Epstein-Barr virus status-defined subgroups |
| Q57285441 | Genome-wide association study of offspring birth weight in 86,577 women highlights maternal genetic effects that are independent of fetal genetics |
| Q47172157 | Genome-wide association study of offspring birth weight in 86,577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics |
| Q37111977 | Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances |
| Q36045132 | Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes |
| Q34678968 | Genome-wide associations for birth weight and correlations with adult disease |
| Q57046290 | Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis |
| Q30303149 | Genome-wide meta-analysis identifies six novel loci associated with habitual coffee consumption |
| Q42562768 | Improving vaccine safety through a better understanding of vaccine adverse events |
| Q35038370 | Mapping quantitative trait loci by an extension of the Haley-Knott regression method using estimating equations |
| Q61852669 | Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors |
| Q64109834 | Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors |
| Q33566637 | Maternal contributions to preterm delivery |
| Q24596087 | Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis |
| Q36580238 | Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis |
| Q47218106 | Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks. |
| Q36708957 | New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism |
| Q57285488 | No association between age at menarche and sex of offspring |
| Q36959694 | No observed association for mitochondrial SNPs with preterm delivery and related outcomes |
| Q100523202 | Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits |
| Q34289136 | Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche |
| Q28943512 | Plasma lipids, genetic variants near APOA1, and the risk of infantile hypertrophic pyloric stenosis |
| Q35613131 | Replication of a genome-wide association study of birth weight in preterm neonates |
| Q34829535 | Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption |
| Q33786392 | Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis |
| Q34868144 | Sequence variants in oxytocin pathway genes and preterm birth: a candidate gene association study |
| Q63353083 | Study of correlation between the NAT2 phenotype and genotype status among Greenlandic Inuit |
| Q28752426 | The Gene, Environment Association Studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions |
| Q34673513 | The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study |
| Q92914682 | The derived allele of a novel intergenic variant at chromosome 11 associates with lower body mass index and a favorable metabolic phenotype in Greenlanders |
| Q34389357 | The essence of linkage-based imprinting detection: comparing power, type 1 error, and the effects of confounders in two different analysis approaches |
| Q34151528 | Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies |
| Q34409547 | Use of macrolides in mother and child and risk of infantile hypertrophic pyloric stenosis: nationwide cohort study |
| Q34310095 | Using family data as a verification standard to evaluate copy number variation calling strategies for genetic association studies |
| Q57285390 | Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 are associated with gestational duration |
| Q93064046 | Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration |
| Q34685114 | X-chromosomal maternal and fetal SNPs and the risk of spontaneous preterm delivery in a Danish/Norwegian genome-wide association study |
| Q63762373 | [Genome-wide association studies] |
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