For researchers

Is your paper here?

2,663 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.

40 matches for Grant SF, showing the first 20.

GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children
Human molecular genetics · 2013 · PMID 23263863
4 pages
rs2340727 rs4657616 rs7203560 rs5987027
Genetic effects on the timing of parturition and links to fetal birth weight
Early Growth Genetics Consortium · Estonian Biobank Research Team and 1 more consortia
Nature genetics · 2023 · PMID 37012456 · open access
4 pages
rs113828443 rs34555419 rs6472846 rs28654158
A genome-wide association meta-analysis of diarrhoeal disease in young children identifies FUT2 locus and provides plausible biological pathways
Human molecular genetics · 2016 · PMID 27559109
3 pages
rs8111874 rs35106244 Diarrhoeal Disease in Infancy
Multidimensional Bone Density Phenotyping Reveals New Insights Into Genetic Regulation of the Pediatric Skeleton
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2018 · PMID 29240982
3 pages
rs58649746 rs75321045 rs34249834
Large trans-ethnic meta-analysis identifies AKR1C4 as a novel gene associated with age at menarche
Human reproduction (Oxford, England) · 2021 · PMID 34021356
3 pages
rs2095812 rs9401883 rs182498797
Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits-The Hispanic/Latino Anthropometry Consortium
HGG advances · 2022 · PMID 35399580 · open access
3 pages
rs3751813 rs6817771 rs9922708
A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene
Nature · 2007 · PMID 17632545
2 pages
rs2903692 rs2647044
Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease
Nature genetics · 2008 · PMID 18758464
2 pages
rs2315008 Ulcerative Colitis
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry
NABEC Consortium · UKBEC Consortium and 2 more consortia
Nature genetics · 2013 · PMID 23583978 · open access
2 pages
rs348495 rs10261878
Genome-wide association of body fat distribution in African ancestry populations suggests new loci
PLoS genetics · 2013 · PMID 23966867 · open access
2 pages
rs6931262 rs2075064
A novel common variant in DCST2 is associated with length in early life and height in adulthood
Early Genetics and Lifecourse Epidemiology (EAGLE) Consortium · Genetic Investigation of ANthropometric Traits (GIANT) Consortium and 1 more consortia
Human molecular genetics · 2015 · PMID 25281659 · open access
2 pages
rs1380294 rs905938
A Genomewide Association Study Identifies Two Sex-Specific Loci, at SPTB and IZUMO3, Influencing Pediatric Bone Mineral Density at Multiple Skeletal Sites
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2017 · PMID 28181694
2 pages
rs6963115 rs34770628
First Genome-Wide Association Study of Latent Autoimmune Diabetes in Adults Reveals Novel Insights Linking Immune and Metabolic Diabetes
Bone Mineral Density in Childhood Study
Diabetes care · 2018 · PMID 30254083 · open access
2 pages
rs1983890 Latent Autoimmune Diabetes in Adults (LADA)
Rare Genetic Variants of Large Effect Influence Risk of Type 1 Diabetes
DCCT/EDIC Research Group
Diabetes · 2020 · PMID 32005708 · open access
2 pages
rs2128344 rs60587303
Genome-wide association studies and fine-mapping identify genomic loci for n-3 and n-6 polyunsaturated fatty acids in Hispanic American and African American cohorts
Communications biology · 2023 · PMID 37587153 · open access
2 pages
rs717894 rs57112407
Genome-wide analyses of neonatal jaundice reveal a marked departure from adult bilirubin metabolism
Nature communications · 2024 · PMID 39214992 · open access
2 pages
rs149247216 rs5942980
Common variants at 6q22 and 17q21 are associated with intracranial volume
Early Growth Genetics Consortium · Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium
Nature genetics · 2012 · PMID 22504418
1 page
rs4273712
Common variants at 12q15 and 12q24 are associated with infant head circumference
Cohorts for Heart and Aging Research in Genetic Epidemiology (CHARGE) Consortium · Early Genetics & Lifecourse Epidemiology (EAGLE) consortium and 1 more consortia
Nature genetics · 2012 · PMID 22504419
1 page
rs1042725
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
Early Growth Genetics (EGG) Consortium
Human molecular genetics · 2018 · PMID 29309628 · open access
1 page
rs2971669
Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity
Diabetes · 2020 · PMID 32917775
1 page
rs791600

Showing 20 of 40 · page 2 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.