For researchers

Is your paper here?

2,675 papers hold this site up. Every variant and condition page names the research it was written from, and this is that list, gathered from the pages themselves. Search your name, your journal, or a PMID.

25 matches for Bønnelykke K, showing the first 20.

Genome-wide association study identifies 74 loci associated with educational attainment
LifeLines Cohort Study
Nature · 2016 · PMID 27225129 · open access
12 pages+
rs56044892 rs12410444 rs12754946 rs1008078 rs17372140 rs78365243
Genome-wide associations for birth weight and correlations with adult disease
CHARGE Consortium Hematology Working Group · Early Growth Genetics (EGG) Consortium
Nature · 2016 · PMID 27680694
12 pages+
rs35261542 rs28510415 rs700059 rs3753639 rs62466330 rs6016377
Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks
Australian Asthma Genetics Consortium (AAGC) collaborators
Nature genetics · 2018 · PMID 29273806 · open access
12 pages+
rs2952156 rs17806299 rs4988958 rs2596464 rs6893213 rs1663687
Life-Course Genome-wide Association Study Meta-analysis of Total Body BMD and Assessment of Age-Specific Effects
American journal of human genetics · 2018 · PMID 29304378
12 pages+
rs71569047 rs10450586 rs34406563 rs7112229 rs11606709 rs4647728
Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis
23andMe Research Team · AAGC collaborators
Nature genetics · 2018 · PMID 30013184
12 pages+
rs9282864 rs12657787 rs2164068 rs3787184 rs7717955 rs28361986
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
EGG Consortium
Nature genetics · 2019 · PMID 31043758
12 pages+
rs6575803 rs75844534 rs10181515 rs7886910 rs732563 rs13271368
The trans-ancestral genomic architecture of glycemic traits
Lifelines Cohort Study · Meta-Analysis of Glucose and Insulin-related Traits Consortium (MAGIC)
Nature genetics · 2021 · PMID 34059833 · open access
12 pages+
rs118164457 rs182859029 rs7063597 rs3752435 rs4317621 rs4731113
A saturated map of common genetic variants associated with human height
23andMe Research Team · VA Million Veteran Program and 5 more consortia
Nature · 2022 · PMID 36224396 · open access
12 pages+
rs13010821 rs13164873 rs16826031 rs16995249 rs17128737 rs17202814
European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation
23andMe Research Team · Estonian Biobank Research Team
Nature communications · 2023 · PMID 37794016 · open access
12 pages+
rs4312054 rs6023002 rs705699 rs117137535 rs11236813 rs56308324
131 genetic loci highlight immunological pathways and tissues in nasal polyposis and asthma
FinnGen
Nature communications · 2025 · PMID 41213931 · open access
12 pages+
rs2891058 rs116877855 rs62408224 rs9828592 rs113372064 rs11894248
Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis
Australian Asthma Genetics Consortium (AAGC)
Nature genetics · 2015 · PMID 26482879 · open access
11 pages
rs112111458 rs10214237 rs6473227 rs6602364 rs7127307 rs2143950
Bivariate genome-wide association meta-analysis of pediatric musculoskeletal traits reveals pleiotropic effects at the SREBF1/TOM1L2 locus
Nature communications · 2017 · PMID 28743860 · open access
11 pages
rs3765350 rs6726821 rs2110281 rs12283755 rs6684375 rs13245690
Bone mineral density loci specific to the skull portray potential pleiotropic effects on craniosynostosis
Communications biology · 2023 · PMID 37402774 · open access
11 pages
rs11029963 rs11993347 rs12107945 rs113622822 rs34814687 rs13204469
Genome-wide association meta-analysis of childhood ADHD symptoms and diagnosis identifies new loci and potential effector genes
Nature genetics · 2025 · PMID 40962958
9 pages
rs7708883 rs4462678 rs9959583 rs4131786 rs1435746 rs7100410
Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index
Bone Mineral Density in Childhood Study (BMDCS) · Early Genetics and Lifecourse Epidemiology (EAGLE) consortium and 2 more consortia
Human molecular genetics · 2016 · PMID 26604143
8 pages
rs12041852 rs13253111 rs13387838 rs17024393 rs3829849 rs7550711
Meta-analysis of genome-wide association studies identifies ten loci influencing allergic sensitization
AAGC
Nature genetics · 2013 · PMID 23817571
7 pages
rs6906021 rs3771175 rs17616434 rs17454584 rs1059513 rs6932730
Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4
Australian Asthma Genetics Consortium (AAGC)
Nature communications · 2021 · PMID 34785669 · open access
6 pages
rs2844594 rs3848669 rs13208697 rs4372325 rs12334935 rs2918299
Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization
EPIC-Interact Consortium · Understanding Society Scientific Group
Wellcome open research · 2023 · PMID 39280063 · open access
6 pages
rs56381411 rs3784634 rs5400 rs17853166 rs75619922 rs7225887
Genome-wide analysis identifies 12 loci influencing human reproductive behavior
BIOS Consortium · LifeLines Cohort Study
Nature genetics · 2016 · PMID 27798627
4 pages
rs10908557 rs6885307 rs2347867 rs2721195
Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variants
EArly Genetics & Lifecourse Epidemiology (EAGLE) Consortium
The Journal of allergy and clinical immunology · 2014 · PMID 24315451
3 pages
rs3751972 rs2016444 rs12500579

Showing 20 of 25 · page 1 of 2

Questions about this list

Why is my paper here? I never gave you permission.

Nothing of your paper is reproduced here. This page records that a MyGeneLog™ page cites your work, and links to the paper on PubMed — which is what a citation is. Your title and author list come from Europe PMC, the same public record a library catalogue uses.

Why are all the authors listed instead of "et al."?

Because a study that needed 622 people is a different kind of study from one that needed four, and "et al." erases that. Twelve names show and the rest are one click away. Everyone is searchable, including the 187th name on a consortium paper — that person exists and may be looking for it.

My name is misspelt, or the paper is wrong.

Tell us and it is fixed. Names come from the public record and initials are inconsistent across databases; where two people share a form of a name we cannot separate them, and we would rather be corrected than guess.

My paper is not here. Does that mean you rejected it?

No. This catalogue is assembled from what a small team could read, and it is thinnest outside European-ancestry cohorts. A paper is absent because nobody has got to it, not because it was assessed and turned down.

Which pages rest on a paper?

Each row lists them, up to six, and links to each one. The count beside a row is how many pages cite it in total.

How often does this change?

It is rebuilt from the pages every hour. A paper appears the moment a page starts resting on it and disappears if that page stops — there is no separate list to keep in step, because the citation lives on the page that makes the claim.