Article in Science advances, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
0numbers the graph read from it
0cells of the map it votes in
3citing 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.
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
19 authors.
Mengge WangDepartment of Laboratory Medicine/Clinical Laboratory Medicine Research Center & Institute of Rare Diseases, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, Sichuan 610000, China.ORCID 0000-0002-3673-1855
Yunhui LiuDepartment of Laboratory Medicine/Clinical Laboratory Medicine Research Center & Institute of Rare Diseases, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, Sichuan 610000, China.ORCID 0009-0005-7252-5169
Lintao LuoDepartment of Laboratory Medicine/Clinical Laboratory Medicine Research Center & Institute of Rare Diseases, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, Sichuan 610000, China.ORCID 0009-0001-5790-4866
Zhiyong WangDepartment of Laboratory Medicine/Clinical Laboratory Medicine Research Center & Institute of Rare Diseases, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, Sichuan 610000, China.ORCID 0009-0001-9573-7106
Yuhang FengDepartment of Laboratory Medicine/Clinical Laboratory Medicine Research Center & Institute of Rare Diseases, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, Sichuan 610000, China.ORCID 0000-0002-3321-0827
Ting YangDepartment of Laboratory Medicine/Clinical Laboratory Medicine Research Center & Institute of Rare Diseases, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, Sichuan 610000, China.ORCID 0009-0005-0252-3934
Jing ChenDepartment of Laboratory Medicine/Clinical Laboratory Medicine Research Center & Institute of Rare Diseases, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, Sichuan 610000, China.
Yufeng LiuDepartment of Laboratory Medicine/Clinical Laboratory Medicine Research Center & Institute of Rare Diseases, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, Sichuan 610000, China.
Yuguo HuangDepartment of Laboratory Medicine/Clinical Laboratory Medicine Research Center & Institute of Rare Diseases, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, Sichuan 610000, China.ORCID 0000-0003-4523-2289
Qiuxia SunDepartment of Laboratory Medicine/Clinical Laboratory Medicine Research Center & Institute of Rare Diseases, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, Sichuan 610000, China.ORCID 0009-0007-4335-6364
Shuhan DuanDepartment of Laboratory Medicine/Clinical Laboratory Medicine Research Center & Institute of Rare Diseases, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, Sichuan 610000, China.
Xinyu LinDepartment of Laboratory Medicine/Clinical Laboratory Medicine Research Center & Institute of Rare Diseases, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, Sichuan 610000, China.
Jie ZhongDepartment of Laboratory Medicine/Clinical Laboratory Medicine Research Center & Institute of Rare Diseases, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, Sichuan 610000, China.ORCID 0000-0003-0354-9448
Bowen LiDepartment of Laboratory Medicine/Clinical Laboratory Medicine Research Center & Institute of Rare Diseases, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, Sichuan 610000, China.ORCID 0000-0001-5684-9925
Kaijun LiuInstitute of 23Mofang, Tianfu Software Park, Chengdu 610042, China.ORCID 0009-0006-6600-871X
Chao LiuAnti-Drug Technology Center of Guangdong Province, Guangzhou 510230, China.ORCID 0000-0001-5633-3929
Renkuan TangDepartment of Forensic Medicine, College of Basic Medicine, Chongqing Medical University, Chongqing 400331, China.ORCID 0000-0003-0008-1288
Guanglin HeDepartment of Laboratory Medicine/Clinical Laboratory Medicine Research Center & Institute of Rare Diseases, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, Sichuan 610000, China.ORCID 0000-0002-6614-5267
Funding
No grant is acknowledged in the PubMed record.
6 · The paper itself
Abstract
The scale and timing of genetic contributions from ancient millet- and rice-farming populations in China to Southeast Asian populations remain incompletely understood, particularly concerning Y-chromosome diversity. Here, a comprehensive dataset of Chinese Y-chromosome variations, including 1507 high-coverage sequences from ethnolinguistically diverse groups, was analyzed alongside 780 ancient genomes from eastern Eurasia and 1748 low-coverage sequences from Southeast Asia. We reconstructed a high-resolution, time-calibrated Y-chromosome phylogeny, revealing multiple male-biased expansions associated with Neolithic cultural innovations in South China. These expansions markedly shaped the paternal ancestry of both South China and mainland Southeast Asia. Founding lineages linked to Hmong-Mien and Tai-Kadai speakers were traced, revealing notable growth during the Middle Neolithic. Phylogeographic structure, network analyses, and haplogroup distributions indicate complex demographic interactions that established the genetic legacy of Neolithic farmers in Southeast Asia. These findings highlight recurrent southward migrations of Chinese farmer-related groups and their enduring influence on the paternal genetic landscape of ancient and present-day Southeast Asians.
Indexed as
Asian PeopleChromosomes, Human, YFarmersHuman MigrationAsia, SoutheasternChinaGenetics, PopulationGenetic VariationHaplotypesHistory, AncientHumansMalePhylogenyPhylogeography
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 Socratic graph.
Multiple southward migrations of Neolithic Chinese farmers into Southeast Asia revealed from large-scale Y-chromosome sequences. · full record | Socratic