User profiles for Aaron Kleinman
Aaron KleinmanComputational Biologist, 23andMe Verified email at 23andme.com Cited by 6531 |
Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals
Here we conducted a large-scale genetic association analysis of educational attainment in
a sample of approximately 1.1 million individuals and identify 1,271 independent genome-…
a sample of approximately 1.1 million individuals and identify 1,271 independent genome-…
An atlas of genetic influences on osteoporosis in humans and mice
Osteoporosis is a common aging-related disease diagnosed primarily using bone mineral
density (BMD). We assessed genetic determinants of BMD as estimated by heel quantitative …
density (BMD). We assessed genetic determinants of BMD as estimated by heel quantitative …
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences
Humans vary substantially in their willingness to take risks. In a combined sample of over 1
million individuals, we conducted genome-wide association studies (GWAS) of general risk …
million individuals, we conducted genome-wide association studies (GWAS) of general risk …
Whole‐genome sequencing identifies EN1 as a determinant of bone density and fracture
The extent to which low‐frequency (minor allele frequency (MAF) between 1–5%) and rare (MAF
≤ 1%) variants contribute to complex traits and disease in the general population is …
≤ 1%) variants contribute to complex traits and disease in the general population is …
Genetic evidence of assortative mating in humans
MR Robinson, A Kleinman, M Graff… - Nature Human …, 2017 - nature.com
In human populations, assortative mating is almost universally positive, with similarities
between partners for quantitative phenotypes 1 – 6 , common disease risk 1 , 3 , 7 – 10 , …
between partners for quantitative phenotypes 1 – 6 , common disease risk 1 , 3 , 7 – 10 , …
Resource profile and user guide of the Polygenic Index Repository
…, R Karlsson Linnér, R Ahlskog, A Kleinman… - Nature human …, 2021 - nature.com
Polygenic indexes (PGIs) are DNA-based predictors. Their value for research in many
scientific disciplines is growing rapidly. As a resource for researchers, we used a consistent …
scientific disciplines is growing rapidly. As a resource for researchers, we used a consistent …
[HTML][HTML] Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis
…, BS Hromatka, KE Huber, A Kleinman… - The Lancet …, 2017 - thelancet.com
Background Restless legs syndrome is a prevalent chronic neurological disorder with
potentially severe mental and physical health consequences. Clearer understanding of the …
potentially severe mental and physical health consequences. Clearer understanding of the …
[HTML][HTML] A genetic investigation of sex bias in the prevalence of attention-deficit/hyperactivity disorder
…, DA Hinds, BS Hromatka, KE Huber, A Kleinman… - Biological …, 2018 - Elsevier
Background Attention-deficit/hyperactivity disorder (ADHD) shows substantial heritability
and is two to seven times more common in male individuals than in female individuals. We …
and is two to seven times more common in male individuals than in female individuals. We …
Inherited myeloproliferative neoplasm risk affects haematopoietic stem cells
…, NA Furlotte, DA Hinds, KE Huber, A Kleinman… - Nature, 2020 - nature.com
Myeloproliferative neoplasms (MPNs) are blood cancers that are characterized by the
excessive production of mature myeloid cells and arise from the acquisition of somatic driver …
excessive production of mature myeloid cells and arise from the acquisition of somatic driver …
[HTML][HTML] Gene discovery and polygenic prediction from a 1.1-million-person GWAS of educational attainment
We conduct a large-scale genetic association analysis of educational attainment in a sample
of~ 1.1 million individuals and identify 1,271 independent genome-wide-significant SNPs. …
of~ 1.1 million individuals and identify 1,271 independent genome-wide-significant SNPs. …