Leveraging base-pair mammalian constraint to understand genetic variation and human disease is a research paper published in Science (2023). On theSindex it has a DataRank of 0. It has been cited 121 times.
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NHGRI NIH HHS
Grant: R01 HG008742
NIMH NIH HHS
Grant: R01 MH118278
NHGRI NIH HHS
Grant: U01 HG011720
NHGRI NIH HHS
Grant: R00 HG010160
NCI NIH HHS
Grant: R37 CA218570
NIMH NIH HHS
Grant: U01 MH116438
NHGRI NIH HHS
Grant: U24 HG007234
NIDA NIH HHS
Grant: F30 DA053020
NIGMS NIH HHS
Grant: R35 GM147789
NHGRI NIH HHS
Grant: U41 HG002371
NIEHS NIH HHS
Grant: R01 ES033630
NIMH NIH HHS
Grant: R01 MH124839
NHGRI NIH HHS
Grant: R01 HG010485
NIDA NIH HHS
Grant: DP1 DA046585
National Institutes of Health
Grant: 5R00HG010160-04
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National Health and Medical Research Council (NHMRC)
Grant: 1113400
Complex trait genomics
National Institutes of Health
Grant: 5R01ES033630-04
Modeling the interaction of physiological and environmental stressors on common variants to psychiatric traits
Wellcome Trust
Grant: unidentified
unidentified
National Institutes of Health
Grant: 5U41HG002371-21
The UCSC Genome Browser
National Institutes of Health
Grant: 5F30DA053020-03
Integrating primate-rodent cell types and epigenomics to identify conservation in substance addiction
National Institutes of Health
Grant: 5R01MH124839-02
3/7 Psychiatric Genomics Consortium: Advancing Discovery and Impact
National Institutes of Health
Grant: 1U01HG011720-01
Polygenic risk scores and health disparities: the role of blood cells immune response and evolutionary adaptation
National Institutes of Health
Grant: 5U01MH116438-04
Massively parallel characterization of psychiatric disease associated regulatory elements in defined cell types
National Institutes of Health
Grant: 5R01MH118278-03
Predicting the multi-omic impact of psychiatric GWAS associations
National Institutes of Health
Grant: 5R35GM147789-02
Characterizing genetic signatures of natural selection to understand human diseases
National Institutes of Health
Grant: 5R01HG008742-02
The 200 mammals project: sequencing genomes by a novel cost-effective method, yielding a high resolution annotation of the human genome.
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Sustainable Development Goals