Works by Feenstra, Bjarke
Results: 48
Familial aggregation of tonsillectomy in early childhood and adolescence.
- Published in:
- Clinical Epidemiology, 2018, v. 10, p. 97, doi. 10.2147/CLEP.S148575
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- Article
Plasma Lipids, Genetic Variants Near APOA1, and the Risk of Infantile Hypertrophic Pyloric Stenosis.
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- JAMA: Journal of the American Medical Association, 2013, v. 310, n. 7, p. 714, doi. 10.1001/jama.2013.242978
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- Article
Cumulative Incidence of Thiazide-Induced Hyponatremia: A Population-Based Cohort Study.
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- Annals of Internal Medicine, 2024, v. 177, n. 1, p. 1, doi. 10.7326/M23-1989
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- Article
Genome-wide analyses of neonatal jaundice reveal a marked departure from adult bilirubin metabolism.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-51947-w
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- Article
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.
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- Human Molecular Genetics, 2012, v. 21, n. 24, p. 5344, doi. 10.1093/hmg/dds372
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- Article
Sequence variants at CYP1A1–CYP1A2 and AHR associate with coffee consumption.
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- Human Molecular Genetics, 2011, v. 20, n. 10, p. 2071, doi. 10.1093/hmg/ddr086
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- Article
Comprehensive genome-wide association study of different forms of hernia identifies more than 80 associated loci.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-30921-4
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- Article
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.
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- 2020
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- Publication type:
- journal article
The gene, environment association studies consortium (GENEVA): maximizing the knowledge obtained from GWAS by collaboration across studies of multiple conditions.
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- Genetic Epidemiology, 2010, v. 34, n. 4, p. 364, doi. 10.1002/gepi.20492
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- Article
Sequence variants in ARHGAP15, COLQ and FAM155A associate with diverticular disease and diverticulitis.
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- Nature Communications, 2017, v. 8, n. 6, p. 15789, doi. 10.1038/ncomms15789
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- Article
Common variants upstream of KDR encoding VEGFR2 and in TTC39B associate with endometriosis.
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- Nature Communications, 2016, v. 7, n. 7, p. 12350, doi. 10.1038/ncomms12350
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- Article
Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight.
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- 2016
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- journal article
Birth characteristics and risk of febrile seizures.
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- Acta Neurologica Scandinavica, 2021, v. 144, n. 1, p. 51, doi. 10.1111/ane.13420
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- Article
The Essence of Linkage-based Imprinting Detection: Comparing Power, Type 1 Error, and the Effects of Confounders in Two Different Analysis Approaches.
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- Annals of Human Genetics, 2010, v. 74, n. 3, p. 248, doi. 10.1111/j.1469-1809.2010.00568.x
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- Article
Genetic regulation of spermine oxidase activity and cancer risk: a Mendelian randomization study.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-97069-x
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- Article
Acute and persistent symptoms in non-hospitalized PCR-confirmed COVID-19 patients.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-92045-x
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- Article
Genome-Wide Association Study Identifies Four Loci Associated with Eruption of Permanent Teeth.
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- PLoS Genetics, 2011, v. 7, n. 9, p. 1, doi. 10.1371/journal.pgen.1002275
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- Article
Mapping Quantitative Trait Loci by an Extension of the Haley—Knott Regression Method Using Estimating Equations.
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- Genetics, 2006, v. 173, n. 4, p. 2269, doi. 10.1534/genetics.106.058537
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- Article
A Quantitative Trait Locus Mixture Model That Avoids Spurious LOD Score Peaks.
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- Genetics, 2004, v. 167, n. 2, p. 959, doi. 10.1534/genetics.103.025437
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- Article
Determination of NAT2 acetylation status in the Greenlandic population.
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- Archives of Toxicology, 2016, v. 90, n. 4, p. 883, doi. 10.1007/s00204-015-1501-1
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- Article
Seasonal Variation and Risk of Febrile Seizures: A Danish Nationwide Cohort Study.
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- Neuroepidemiology, 2022, v. 56, n. 2, p. 138, doi. 10.1159/000522065
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- Article
Common variants associated with general and MMR vaccine-related febrile seizures.
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- Nature Genetics, 2014, v. 46, n. 12, p. 1274, doi. 10.1038/ng.3129
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- Article
Genome-wide association analyses identify variants in developmental genes associated with hypospadias.
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- Nature Genetics, 2014, v. 46, n. 9, p. 957, doi. 10.1038/ng.3063
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- Article
New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism.
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- Nature Genetics, 2013, v. 45, n. 1, p. 76, doi. 10.1038/ng.2477
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- Publication type:
- Article
Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis.
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- Nature Genetics, 2012, v. 44, n. 3, p. 334, doi. 10.1038/ng.1067
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- Article
Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis.
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- Nature Genetics, 2012, v. 44, n. 2, p. 187, doi. 10.1038/ng.1017
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- Article
Genome partitioning of genetic variation for complex traits using common SNPs.
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- Nature Genetics, 2011, v. 43, n. 6, p. 519, doi. 10.1038/ng.823
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- Article
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.
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- Nature Genetics, 2010, v. 42, n. 12, p. 1077, doi. 10.1038/ng.714
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- Article
Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche.
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- Nature Genetics, 2009, v. 41, n. 6, p. 734, doi. 10.1038/ng.383
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- Article
The derived allele of a novel intergenic variant at chromosome 11 associates with lower body mass index and a favorable metabolic phenotype in Greenlanders.
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- PLoS Genetics, 2020, v. 16, n. 1, p. 1, doi. 10.1371/journal.pgen.1008544
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- Article
Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis.
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- Human Molecular Genetics, 2019, v. 28, n. 2, p. 332, doi. 10.1093/hmg/ddy347
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- Article
Consortium-based genome-wide meta-analysis for childhood dental caries traits.
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- Human Molecular Genetics, 2018, v. 27, n. 17, p. 3113, doi. 10.1093/hmg/ddy237
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- Article
Genetic regulation of gene expression in the epileptic human hippocampus.
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- Human Molecular Genetics, 2017, v. 26, n. 9, p. 1759, doi. 10.1093/hmg/ddx061
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- Article
Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index.
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- Human Molecular Genetics, 2016, v. 25, n. 2, p. 389, doi. 10.1093/hmg/ddv472
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- Article
Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.
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- Human Molecular Genetics, 2013, v. 22, n. 18, p. 3807, doi. 10.1093/hmg/ddt231
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- Article
STUDY OF CORRELATION BETWEEN THE NAT2 PHENOTYPE AND GENOTYPE STATUS AMONG GREENLANDIC INUIT.
- Published in:
- EXCLI Journal, 2018, v. 17, p. 1043, doi. 10.17179/excli2018-1671
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- Article
Association of Adiposity Genetic Variants With Menarche Timing in 92,105 Women of European Descent.
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- 2013
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- Journal Article
Association of Adiposity Genetic Variants With Menarche Timing in 92,105 Women of European Descent.
- Published in:
- American Journal of Epidemiology, 2013, v. 178, n. 3, p. 451, doi. 10.1093/aje/kws473
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- Article
Maternal Contributions to Preterm Delivery.
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- American Journal of Epidemiology, 2009, v. 170, n. 11, p. 1358, doi. 10.1093/aje/kwp324
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- Article
Meta-analysis of genome-wide association studies of gestational duration and spontaneous preterm birth identifies new maternal risk loci.
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- PLoS Genetics, 2023, v. 19, n. 10, p. 1, doi. 10.1371/journal.pgen.1010982
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- Article
Detecting Sample Misidentifications in Genetic Association Studies.
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- Statistical Applications in Genetics & Molecular Biology, 2012, v. 11, n. 3, p. 1
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- Article
Improving Vaccine Safety Through a Better Understanding of Vaccine Adverse Events.
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- Clinical Infectious Diseases, 2015, v. 60, n. 10, p. 1586, doi. 10.1093/cid/civ080
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- Article
Integrating genetics with newborn metabolomics in infantile hypertrophic pyloric stenosis.
- Published in:
- Metabolomics, 2021, v. 17, n. 1, p. 1, doi. 10.1007/s11306-020-01763-2
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- Article
No association between age at menarche and sex of offspring.
- Published in:
- Human Reproduction, 2011, v. 26, n. 11, p. 3202, doi. 10.1093/humrep/der306
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- Publication type:
- Article
X-Chromosomal Maternal and Fetal SNPs and the Risk of Spontaneous Preterm Delivery in a Danish/Norwegian Genome-Wide Association Study.
- Published in:
- PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0061781
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- Publication type:
- Article
Genetic Variability in Beta-Defensins Is Not Associated with Susceptibility to Staphylococcus aureus Bacteremia.
- Published in:
- PLoS ONE, 2012, v. 7, n. 2, p. 1, doi. 10.1371/journal.pone.0032315
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- Publication type:
- Article
246-OR: A Loss-of-Function Mutation in the Sucrase-Isomaltase Gene Is Linked to a Markedly Healthier Metabolic Profile in Greenlanders.
- Published in:
- Diabetes, 2020, v. 69, p. N.PAG, doi. 10.2337/db20-246-OR
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- Article
Sequence variants in oxytocin pathway genes and preterm birth: a candidate gene association study.
- Published in:
- BMC Medical Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2350-14-77
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- Article