ArticleGenome research2024
Independent expansion, selection, and hypervariability of the
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Article in Genome research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.
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16citing papers in PubMed
–field-weighted citation impact
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
16 citing papers in PubMed.
- Whole genome sequencing of 1427 Mexican individuals from the oriGen cohort.Nature communications · 2026Article
- HPRC2: A human pangenome reference with near-complete coverage of common genetic variation.bioRxiv : the preprint server for biology · 2026Article
- Genetic diversity and regulatory features of human-specific NOTCH2NL duplications.Cell genomics · 2026Article
- Article
- Structural variations in evolutionary novel genomic regions: new insights into neurodevelopmental disorders by long-read DNA Sequencing.Molecular medicine (Cambridge, Mass.) · 2026Article
- Machine learning-based prediction of human structural variation and characterization of associated sequence determinants.bioRxiv : the preprint server for biology · 2026Article
- The effect of human-specific genetic variants on neuronal spinogenesis.Frontiers in genetics · 2026Review
- Structural variation, selection, and diversification of the NPIP gene family from the human pangenome.Cell genomics · 2025Article
- Article
- Human-specific gene expansions contribute to brain evolution.bioRxiv : the preprint server for biology · 2025Article
- Complete sequencing of ape genomes.Nature · 2025Article
- Structural polymorphism and diversity of human segmental duplications.Nature genetics · 2025Article
- Human-specific genetic hallmarks in neocortical development: focus on neural progenitors.Current opinion in genetics & development · 2024Review
- Complete sequencing of ape genomes.bioRxiv : the preprint server for biology · 2024Article
- Deciphering the role of structural variation in human evolution: a functional perspective.Current opinion in genetics & development · 2024Review
- Structural polymorphism and diversity of human segmental duplications.bioRxiv : the preprint server for biology · 2024Article
Corrections and comments
- Update of
Authors and funding
12 authors.
Xavi GuitartDepartment of Genome Sciences, University of Washington School of Medicine, Seattle, Washington 98195, USA.ORCID 0000-0002-4128-4375
David PorubskyDepartment of Genome Sciences, University of Washington School of Medicine, Seattle, Washington 98195, USA.ORCID 0000-0001-8414-8966
DongAhn YooDepartment of Genome Sciences, University of Washington School of Medicine, Seattle, Washington 98195, USA.ORCID 0000-0003-0033-3721
Max L DoughertyTisch Cancer Institute, Division of Hematology and Medical Oncology, The Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA.
Philip C DishuckDepartment of Genome Sciences, University of Washington School of Medicine, Seattle, Washington 98195, USA.ORCID 0000-0003-2223-9787
Katherine M MunsonDepartment of Genome Sciences, University of Washington School of Medicine, Seattle, Washington 98195, USA.ORCID 0000-0001-8413-6498
Alexandra P LewisDepartment of Genome Sciences, University of Washington School of Medicine, Seattle, Washington 98195, USA.
Kendra HoekzemaDepartment of Genome Sciences, University of Washington School of Medicine, Seattle, Washington 98195, USA.ORCID 0000-0002-8058-0177
Jordan KnuthDepartment of Genome Sciences, University of Washington School of Medicine, Seattle, Washington 98195, USA.
Stephen ChangDepartment of Biochemistry.
Tomi PastinenDepartment of Pediatrics, Genomic Medicine Center, Children's Mercy Kansas City, Kansas City, Missouri 64108, USA.ORCID 0000-0003-4016-5021
Evan E EichlerDepartment of Genome Sciences, University of Washington School of Medicine, Seattle, Washington 98195, USA; ee3@uw.edu.ORCID 0000-0002-8246-4014
Funding
Identifying and Characterizing the Full Spectrum of Haplotype-resolved Structural Variation in Human GenomesU24HG007497 · NHGRI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI Evan Eichler, Jan Oliver Korbel · 2019 to 2026
$17.2MSequence and Assembly of Segmental DuplicationsR01HG002385 · NHGRI · UNIVERSITY OF WASHINGTON · PI Evan Eichler · 2001 to 2026
$13.3MAn Integrative Analysis of Structural Variation for the 1000 Genomes ProjectU41HG007497 · NHGRI · JACKSON LABORATORY · PI LEE, CHARLES · 2013 to 2017
$13.0MSequence-resolved structural variation of human genomesR01HG010169 · NHGRI · UNIVERSITY OF WASHINGTON · PI Evan Eichler · 2018 to 2026
$4.5MNHGRI NIH HHS R01 HG002385NHGRI NIH HHS R01 HG010169NHGRI NIH HHS U24 HG007497NHGRI NIH HHS U41 HG007497
Abstract
PubMed holds no abstract for this paper.
Indexed as
GTPase-Activating ProteinsMultigene FamilySelection, GeneticAnimalsChromosomes, Human, Pair 17DNA Copy Number VariationsEvolution, MolecularGene DuplicationHumansNerve Tissue ProteinsPrimatesProto-Oncogene ProteinsGTPase-Activating ProteinsNerve Tissue ProteinsProto-Oncogene ProteinsTBC1D3 protein, human
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.