Evidence map›Paper›PMID 41867727›Full record

ArticlebioRxiv : the preprint server for biology2026

Somatic mutation in human cerebellum illustrates neuron type-specific patterns of age-related mutation.

Kow Essuman, Yingxi Yang, Eitan Goodman, Christie N Cambridge, Chunhui Cai, Zheming An, Shulin Mao, Monica Devi Manam, Benjamin Finander, Sattar Khoshkhoo and 3 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Kow EssumanDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA, USA.ORCID 0000-0002-6781-7248
Yingxi YangDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA, USA.
Eitan GoodmanDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA, USA.
Christie N CambridgeDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA, USA.
Chunhui CaiResearch Informatics, Department of Information Technology, Boston Children's Hospital, Boston, MA, USA.
Zheming AnDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA, USA.
Shulin MaoDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA, USA.
Monica Devi ManamDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA, USA.
Benjamin FinanderDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA, USA.
Sattar KhoshkhooDepartment of Neurology, Mass General Brigham, Boston, MA, USA.
Liang SunResearch Informatics, Department of Information Technology, Boston Children's Hospital, Boston, MA, USA.
August Yue HuangDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA, USA.ORCID 0000-0002-0416-2854
Christopher A WalshDivision of Genetics and Genomics, Manton Center for Orphan Disease Research, Boston Children's Hospital, Boston, MA, USA.

Funding

Cell Identity Determination In Human Brain: Somatic Mutation and Cell LineageR01NS032457 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI Alice Eunjung Lee, Christopher A. Walsh · 1995 to 2026
$12.7M
Role of clonal somatic mutations in microglia and Alzheimer’s diseaseR01AG088082 · NIA · BOSTON CHILDREN'S HOSPITAL · PI Yue Huang · 2024 to 2026
$4.4M
Rates and mechanisms of age-related somatic mutation in normal and Alzheimer brainR01AG070921 · NIA · BOSTON CHILDREN'S HOSPITAL · PI LEE, ALICE EUNJUNG, WALSH, CHRISTOPHER A. · 2021 to 2025
$4.3M
Detection and Characterization of Somatic Mutations in Human Tissue Utilizing Duplex-Consensus SequencingUH3NS132144 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI Sangita Choudhury, Alice Eunjung Lee · 2025 to 2026
$1.5M
Development of an Efficient High Throughput Technique for the Identification of High-Impact Non-Coding Somatic Variants Across Multiple Tissue TypesUH3NS132138 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI Peter J Park, Christopher A. Walsh · 2025 to 2026
$1.4M
Genetic and Cellular Mechanisms of Temporal Lobe EpilepsyK08NS128272 · NINDS · BRIGHAM AND WOMEN'S HOSPITAL · PI Sattar Khoshkhoo · 2022 to 2026
$1.2M
Role of clonal somatic mutations in microglia activation and Alzheimer’s diseaseR56AG079857 · NIA · BOSTON CHILDREN'S HOSPITAL · PI HUANG, YUE, LEE, EUNJUNG ALICE · 2023 to 2023
$883k
Detection and Characterization of Somatic Mutations in Human Tissue Utilizing Duplex-Consensus SequencingUG3NS132144 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI CHOUDHURY, SANGITA, LEE, EUNJUNG ALICE · 2023 to 2024
$877k
Development of an Efficient High Throughput Technique for the Identification of High-Impact Non-Coding Somatic Variants Across Multiple Tissue TypesUG3NS132138 · NINDS · BOSTON CHILDREN'S HOSPITAL · PI PARK, PETER J, WALSH, CHRISTOPHER A. · 2023 to 2024
$870k
NIA NIH HHS R01 AG070921NIA NIH HHS R01 AG088082NIA NIH HHS R56 AG079857NINDS NIH HHS K08 NS128272NINDS NIH HHS L30 NS118655NINDS NIH HHS R01 NS032457NINDS NIH HHS UG3 NS132138NINDS NIH HHS UG3 NS132144NINDS NIH HHS UH3 NS132138NINDS NIH HHS UH3 NS132144
6 · The paper itself

Abstract

Human neurodegenerative disorders are characterized by exquisite specificity for neuronal types, but the basis of this is unknown. Here, we show that cerebellar granule neurons (GN)-the most abundant neuronal type in the human brain-accumulate somatic mutations in patterns highly distinct from cerebral cortical neurons, and more closely resembling oligodendroglia and other dividing cells. We find shared mutational signatures between normal aging GNs and medulloblastoma subtypes, suggesting the GN lineage as a tumor cell of origin. Whole-genome sequence of multiple single GNs from the same donor allowed analysis of specific times of neurogenesis, revealing a rich lineage tree that includes GNs that become postmitotic 2 years or more after birth, yet migrating postnatally to populate both the cerebellar vermis and the distant cerebellar hemisphere. Our results show that neuronal type-specific somatic mutation patterns enlighten normal development, cancer origins and potentially the cell type-specificity of neurodegeneration.

Identifiers

PMID41867727
PMCPMC13001421

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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.