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Paper · 26432243

Human genomics: The end of the start for population sequencing.

Birney E and 1 other. Nature, 2015. Cited by 61 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Human genomics: The end of the start for population sequencing. Papers, record 26432243. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/26432243

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Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title
Human genomics: The end of the start for population sequencing.
PubMed
Journal
Nature
PubMed
Year
2015
PubMed
Publication types
Journal Article, Comment
PubMed
Citations, by iCite
61
iCite
Relative citation ratio, by iCite
1.71
iCite
Revised in PubMed
2018-12-02
PubMed

Authors2

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

OrderAuthorForenameKindORCID iD
1Birney EEwan
2Soranzo NNicole

Source PubMed

Topics7

NLM's MeSH indexing of the paper, its major topics first.

MeSH termMajor
Genetic VariationMajor topic
Genetics, PopulationMajor topic
Genome, HumanMajor topic
GenomicsMajor topic
InternationalityMajor topic
Physical Chromosome MappingMajor topic
Humans

Source PubMed

Grants0

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

None in this release.

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections2

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

KindPMIDTitleIn PapersSource
Comment on26,432,245A global reference for human genetic variation.https://conductscience.org/library/papers/26432245PubMed
Comment on26,432,246An integrated map of structural variation in 2,504 human genomes.https://conductscience.org/library/papers/26432246PubMed

References4

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

OrderPMIDTitleJournalYearIn PapersSource
121,358,748Genome structural variation discovery and genotyping.Nat Rev Genet2011https://conductscience.org/library/papers/21358748PubMed
223,128,226An integrated map of genetic variation from 1,092 human genomes.Nature2012https://conductscience.org/library/papers/23128226PubMed
326,432,245A global reference for human genetic variation.Nature2015https://conductscience.org/library/papers/26432245PubMed
426,432,246An integrated map of structural variation in 2,504 human genomes.Nature2015https://conductscience.org/library/papers/26432246PubMed

Cited by45

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 61 citations.

PMIDTitleJournalYearIn PapersSource
42,284,538Genomic Features Do Not Account for Differences in Multiple Myeloma Risk by Ancestry.Blood Cancer Discov2026https://conductscience.org/library/papers/42284538PubMed
41,793,414Sequencing and health data resource of children of African ancestry.Genet Med2026https://conductscience.org/library/papers/41793414PubMed
41,571,639Cross-ancestry comparison of aptamer and antibody protein measures.Nat Commun2026https://conductscience.org/library/papers/41571639PubMed
40,849,414Large-scale GWAS of strabismus identifies risk loci and provides support for a link with maternal smoking.Nat Commun2025https://conductscience.org/library/papers/40849414PubMed
40,801,674Whole Exome Sequencing Study Uncovers Novel Candidate Genes and Protein-Coding Variants for Cataract.Invest Ophthalmol Vis Sci2025https://conductscience.org/library/papers/40801674PubMed
40,723,922Genetic Diversity in the Suppressyn Gene Sequence: From Polymorphisms to Loss-of-Function Mutations.Biomolecules2025https://conductscience.org/library/papers/40723922PubMed
40,098,727Subclinical parents assist in the detection of genetic variants in keratoconus by trio-based whole-exome sequencing.Mol Vis2025https://conductscience.org/library/papers/40098727PubMed
38,982,300Short Tandem Repeats in the era of next-generation sequencing: from historical loci to population databases.Eur J Hum Genet2024https://conductscience.org/library/papers/38982300PubMed
38,832,639Extended haplotype with rs41524547-G defines the ancestral origin of SCA10.Hum Mol Genet2024https://conductscience.org/library/papers/38832639PubMed
37,351,342A multiethnic genome-wide analysis of 19,420 individuals identifies novel loci associated with axial length and shared genetic influences with refractive error and myopia.Front Genet2023https://conductscience.org/library/papers/37351342PubMed

1 to 10 of 45

See all 45 cited by

Genes0

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

None in this release.

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed
2026-11-06
PubMed
iCite
2026-11-05
iCite
PMC's ID file
2026-11-05
PMC's ID file
NIH RePORTER's grant and paper links
2026-11-01
NIH RePORTER's grant and paper links
Trials
2026-11-12
Gene search
2026-11-11
Pipelines
2026-09-18

Sources 11

  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • HGNCCC0
  • iCiteCC BY 4.0
  • NCBI GenePublic domain (US government)
  • NIH RePORTER's grant and paper linksPublic domain
  • Open TargetsCC0 1.0
  • PMC's ID filePublic domain (US government)
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • HGNCCC0: https://www.genenames.org/about/license/
  • iCiteCC BY 4.0
  • NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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