Insights into human genetic variation and population history from 929 diverse genomes

Fast and accurate short read alignment with Burrows-Wheeler transform

Li, H., & Durbin, R. (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp324 · Cited by 58,607

RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies

Stamatakis, A. (2014) · Bioinformatics · doi:10.1093/bioinformatics/btu033 · Cited by 32,291

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

McKenna, A., Hanna, M., Banks, E., Sivachenko, A., Cibulskis, K., Kernytsky, A., Garimella, K., Altshuler, D., Gabriel, S., Daly, M., et al. (2010) · Genome Research · doi:10.1101/gr.107524.110 · Cited by 27,895

BEDTools: a flexible suite of utilities for comparing genomic features

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A global reference for human genetic variation

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BEAST: Bayesian evolutionary analysis by sampling trees

Drummond, A. J., & Rambaut, A. (2007) · BMC Evolutionary Biology · doi:10.1186/1471-2148-7-214 · Cited by 13,104

Mathematical model for studying genetic variation in terms of restriction endonucleases.

Nei, M., & Li, W. (1979) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.76.10.5269 · Cited by 10,501

Fast model-based estimation of ancestry in unrelated individuals

Alexander, D. H., Novembre, J., & Lange, K. (2009) · Genome Research · doi:10.1101/gr.094052.109 · Cited by 9,898

dbSNP: the NCBI database of genetic variation

Sherry, S. T. (2001) · Nucleic Acids Research · doi:10.1093/nar/29.1.308 · Cited by 7,502

A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data

Li, H. (2011) · Bioinformatics · doi:10.1093/bioinformatics/btr509 · Cited by 6,454

Tracing Scots Pine Expansion in Europe Using Patterns of Rare Alleles

Kastally, C., Tyrmi, J. S., Bastien, C., Cervera, M., VENDRAMIN, G. G., Savolainen, O., & Pyhäjärvi, T. (2025) · Ecology and Evolution · doi:10.1002/ece3.72433 · Cited by 2

Ancient Yellow River ancestry and divergent admixture histories in the Qiang people

Zeng, W., Yang, Z., Lü, Y., Lei, C., Gao, Y., Yang, Y., Wang, X., Jiayou, C., & Sf, X. (2026) · Science Advances · doi:10.1126/sciadv.ady6667 · Cited by 2

Multi-trait and multi-ancestry genetic analysis of comorbid lung diseases and traits improves genetic discovery and polygenic risk prediction

He, Y., Lu, W., Jee, Y. H., Shih, M.-Y., Wang, Y., Tsuo, K., Qian, D. C., Diao, J. A., Huang, H., Patel, C. J., et al. (2026) · Nature Genetics · doi:10.1038/s41588-025-02470-1 · Cited by 6

From unsupervised selection of AIMs to likelihood-based BGA inference: Challenges revealed by OpenADMIXTURE and GENOGEOGRAPHER

Resutik, P., Gysi, M., Lemmin, T., Kratzer, A., Haas, C., & Arora, N. (2026) · Forensic Science International Genetics · doi:10.1016/j.fsigen.2026.103433 · Cited by 3

Importance of genetic ancestry in pharmacogenomics for precision medicine

Venkatesh, R., Keat, K., Salvatore, M., Cindi, Z., Hall, M. A., & Ritchie, M. D. (2025) · Pharmacogenomics · doi:10.1080/14622416.2026.2620360 · Cited by 3

A catalogue of early diverged contemporary human genome variation reveals distinct Khoe-San populations

Jaratlerdsiri, W., Soh, P. X. Y., Gong, T., Jiang, J., Simayi, Z., Petersen, D. C., Holland, E., Chan, E. K. F., Theron, K. E., Haacke, W., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-69269-4 · Cited by 2

Analysis of medieval burials from Ibiza reveals genetic and pathogenic diversity during the Islamic period

Varela, R., Pochon, Z., Mas-Sandoval, À., Yaka, R., Fortes‐Lima, C., Ruiz, A. G.-R., Márquez‐Grant, N., Marí, J., Echávarri, G. G., Abárzuza, A. F., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-70615-9 · Cited by 2

Unraveling the genetic landscape and admixture dynamics of urban populations across Peru

Borda, V., Cáceres, O., Sánchez, C., Padilla, C., Véliz-Otani, D., de Aquino, M. M., Silva-Carvalho, C., Alvim, I., Maron, B. A., Gouveia, M. H., et al. (2026) · Communications Biology · doi:10.1038/s42003-026-09671-2 · Cited by 3

Metabolomic ageing (MileAge) in mid‐life predicts incident vascular, unspecified and all‐cause dementia

Mutz, J., Gilchrist, L., Pain, O., Proitsi, P., & Lewis, C. M. (2026) · Alzheimer s & Dementia · doi:10.1002/alz.71280 · Cited by 3

Revisiting retinal and macular degeneration in the genomics era

Swaroop, A., & Roska, B. (2026) · Nature Reviews Genetics · doi:10.1038/s41576-026-00960-4 · Cited by 2

Carrier Frequencies of Medically Actionable Pathogenic Variants in the Russian Population

Suvorova, Y. M., Monakhova, A., Chekanov, N., Musharova, O., Moskovkina, E., Zaigrin, I. V., Antonov, I., Klimchuk, O., Pustoshilov, D., Zorina, D., et al. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27125344 · Cited by 2

Genome-wide analysis implicates inner ear development in Ménière disease

Shi, Z., Mandla, R., Li, J., Li, X., Zhang, Z., Chen, S., Lapinska, S., Flynn-Carroll, A. O., Paşaniuc, B., Epstein, D. J., et al. (2026) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2026.05.011 · Cited by 2

PGS Browser: a public platform for personalized polygenic score analysis and interpretation

Kolosov, N., Reeve, M. P., Parolo, P. D. B., Kurki, M., FinnGen, Parolo, P. D. B., Llorens, V., Sipila, T. P., Heřman, A., Молотков, И. И., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-74461-7 · Cited by 2

Evolution of CTCF binding sites in the human genome

Zhu, K., Zhuo, J., & Zhen, Y. (2026) · Molecular Biology and Evolution · doi:10.1093/molbev/msag167 · Cited by 3

Optimizing hard cutoff quality control metrics for IBD segment inference and genotyping accuracy in low-coverage sequencing data

Huang, M., Hughes-Stamm, S. R., Muenzler, M., & Woerner, A. E. (2026) · Forensic Science International Genetics · doi:10.1016/j.fsigen.2026.103585 · Cited by 2

VN1K is a pangenome-informed multi-omics and phenomics resource for the Vietnamese population

Tran, T. T. H., Hoang, T. H., Tran, M. H., Pham, T. M., Nguyen, N. N., Vu, G. M., Duong, V. C., Vu, Q. T., Nguyen, N. T., Hien, V. Q., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-75375-0 · Cited by 4

The rise and fall of language diversity through the Holocene

Blasí, D. E., Hamilton, M. J., Gray, R. D., & Bowern, C. (2026) · Science · doi:10.1126/science.adx4343 · Cited by 2

Characterizing features of the genetic architecture underlying autism from a multi-ancestry perspective

de Aquino, M. M., Xu, C. Y., Engchuan, W., Trost, B., Zhou, X., Miwa, B., Salazar, N. B., Iglar, J., Thiruvahindrapuram, B., Wallich, L., et al. (2026) · Molecular Psychiatry · doi:10.1038/s41380-026-03886-9 · Cited by 2

Eurasiaplex-2: Shifting the focus to SNPs with high population specificity increases the power of forensic ancestry marker sets

Phillips, C., de la Puente, M., Ruiz-Ramírez, J., Staniewska, A., Ambroa-Conde, A., Freire-Aradas, A., Mosquera‐Miguel, A., Rodríguez, A., & Lareu, M. V. (2022) · Forensic Science International Genetics · doi:10.1016/j.fsigen.2022.102780 · Cited by 2

Comprehensive Genetic Analysis of Druze Provides Insights into Carrier Screening

Avnat, E., Shapira, G., Shoval, S., Israel‐Elgali, I., Alkelai, A., Shuldiner, A. R., Gonzaga-Jauregui, C. G., Zidan, J., Maray, T., Shomron, N., et al. (2023) · Genes · doi:10.3390/genes14040937 · Cited by 2

Exploring the Neandertal legacy of pancreatic ductal adenocarcinoma risk in Eurasians

Piccardi, M., Gentiluomo, M., Bertoncini, S., Pezzilli, R., Erőss, B. M., Bunduc, Ș., Uzunoglu, F. G., Talar‐Wojnarowska, R., Vanagas, T., Sperti, C., et al. (2023) · Biological Research · doi:10.1186/s40659-023-00457-y · Cited by 2

Y-chromosomal STRs Mutation Rates in the Yakut Population

Adamov, D. S., & Федорова, С. А. (2024) · Russian Journal of Genetics · doi:10.1134/s1022795424040021 · Cited by 2

Human genetic ancestry, Mycobacterium tuberculosis diversity, and tuberculosis disease severity in Dar es Salaam, Tanzania

Zwyer, M., Xu, Z. M., Ross, A. J., Hella, J., Sasamalo, M., Rotival, M., Hiza, H. C., Rutaihwa, L. K., Borrell, S., Reither, K., et al. (2026) · eLife · doi:10.7554/elife.103533.3 · Cited by 2

AI for precision medicine must keep non-random complexity in mind to support equity in outcomes

Smarr, B. L. (2024) · IEEE International Conference on e-Science · doi:10.1109/e-science62913.2024.10678664 · Cited by 2

Inference of genetic ancestry from a multi-gene cancer panel in Colombian women with cancer

Zambrano, Y., Mejía‐García, A., Morales-Suárez, P. D., Tsao, H. M., Rey-Vargas, L., Ovalle, W. J. M., Huertas-Caro, C. A., Sanabria‐Salas, M. C., Riaño-Moreno, J. C., Rodriguez, J. L., et al. (2024) · Breast Cancer Research and Treatment · doi:10.1007/s10549-024-07557-7 · Cited by 2

A genomic tale of inbreeding in western Mediterranean human populations

Hernández, C. L., Sánchez-Martínez, L. J., Ceballos, F. C., Dugoujon, J. M., Pereira, L., & Calderón, R. (2025) · Human Genetics · doi:10.1007/s00439-025-02747-9 · Cited by 2

Phylogenetics and genomic variation of Hepatocystis isolated from shotgun sequencing of wild primate hosts

Haffener, P. E., Hopson, H. D., Herbert-Mainero, A., Ramirez, A., & Leffler, E. M. (2025) · PLoS Pathogens · doi:10.1371/journal.ppat.1013240 · Cited by 2

Historical comparative linguistics and language classification

Barlow, R., & Campbell, L. R. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.3 · Cited by 2

Bayesian phylogenetics for language prehistory— and archaeology

Heggarty, P., & Powell, A. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.11 · Cited by 2

Linguistic phylogeography

Wichmann, S. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.6 · Cited by 2

Archaeolinguistics of Papuan languages

Schapper, A., Gaffney, D., & Brucato, N. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.26 · Cited by 2

Investigating the demographic history of Sindhi population inhabited in West Coast India

Kumar, L., Nongmaithem, S. S., Kumar, S., & Kumarasamy Thangaraj, K. (2025) · Human Genomics · doi:10.1186/s40246-025-00822-w · Cited by 2

CLUES2 Companion: computational pipelines to estimate, visualize, and date selection on multi-locus sites

Lisi, A., & Campbell, M. C. (2024) · Bioinformatics Advances · doi:10.1093/bioadv/vbaf277 · Cited by 2

Genetic ancestry proportion influences risk of adverse events from tuberculosis treatment in Brazil

Piekos, J. A., Amorim, G., Ridolfi, F. M., Cordeiro‐Santos, M., Kritski, A. L., Figueiredo, M. C., Andrade, B. C. O. P., Santos, A. R., Haas, D. W., Sterling, T. R., et al. (2026) · Human Genetics · doi:10.1007/s00439-025-02809-y · Cited by 2

Inversion of k-Nearest Neighbours Algorithm for Extracting SNPs Discriminating Human Populations

Gu, H., & Ding, X. (2021) · Lecture notes in computer science · doi:10.1007/978-3-030-84532-2_10 · Cited by 2

A Reference Genome Assembly and Initial Polymorphism Data for Aotus nancymaae

Rogers, J., Harris, R. A., Raveendran, M., Williams, L. E., & Worley, K. C. (2023) · Developments in primatology · doi:10.1007/978-3-031-13555-2_8 · Cited by 2

When Past and Present Collide

Zakai, S. (2018) · Routledge eBooks · doi:10.4324/9781315110646-7 · Cited by 2

Inter-ethnic genetic variations and novel variant identification in the partial sequences of CYP2B6 gene in Pakistani population

Ahmed, S., Khan, H., Khan, A., Bangash, M. H., Hussain, A., Qayum, M., & Hamdard, M. H. (2021) · PeerJ · doi:10.7717/peerj.11149 · Cited by 2

Cross-continental admixture in the Kho population from northwest Pakistan

Khan, A., Vallini, L., Aziz, S., Khan, H., Zaib, K., Nigar, K., Ayub, Q., Wang, L.-X., Pagani, L., & Wen, S. (2022) · European Journal of Human Genetics · doi:10.1038/s41431-022-01057-2 · Cited by 2

Sequence diversity of the uniparentally transmitted portions of the genome in the resident population of Catalonia

Font‐Porterias, N., García-Fernández, C., Aizpurua-Iraola, J., Comas, D., Torrents, D., de Cid, R., & Calafell, F. (2022) · Forensic Science International Genetics · doi:10.1016/j.fsigen.2022.102783 · Cited by 2

Paleogenomic insights into cooperation in the ancient Andes from positive selection on oxytocin pathway genes

Joseph, S. K., Wagman, E. K., Diab, N., Ryu, N., Lee, M., Haas, R., Rilling, J. K., Aldenderfer, M. S., & Lindo, J. (2024) · Genes Brain & Behavior · doi:10.1111/gbb.12877 · Cited by 2

Global Picture of Genetic Relatedness and the Evolution of Humankind

Khvorykh, G. V., Mulyar, O. A., Fedorova, L. V., Владимирович, Х. А., Limborska, S. A., & Fedorov, A. (2020) · Biology · doi:10.3390/biology9110392 · Cited by 2

An integrated personal and population-based Egyptian genome referencePreprint

Wohlers, I., Künstner, A., Munz, M., Olbrich, M. R., Fähnrich, A., Calonga-Solís, V., Ma, C., Hirose, M., El-Mosallamy, S., Salama, M., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/681254 · Cited by 2

Human Origins in Southern African Palaeo-wetlands? Strong Claims from Weak EvidencePreprint

Schlebusch, C. M., Loog, L., Groucutt, H. S., King, T. E., Rutherford, A. D., Barbieri, C., Barbujani, G., Chikhi, L., Jakobsson, M., Eriksson, A., et al. (2019) · Preprints.org · doi:10.20944/preprints201911.0193.v1 · Cited by 2

Reply to: On powerful GWAS in admixed populations

Atkinson, E. G., Bloemendal, A., Maihofer, A. X., Nievergelt, C. M., Daly, M. J., & Neale, B. M. (2021) · Nature Genetics · doi:10.1038/s41588-021-00975-z · Cited by 2

Differentiated genomic footprints and connections inferred from 440 Hmong-Mien genomes suggest their isolation and long-distance migrationPreprint

He, G., Chen, J., Liu, Y., Hu, R., Wang, P., Duan, S., Sun, Q., Tang, R., Yang, J., Wang, Z., et al. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.01.14.523079 · Cited by 2

Modeling of African population history using f -statistics can be highly biased and is not addressed by previously suggested SNP ascertainment schemesPreprint

Flegontov, P., Işıldak, U., Maier, R., Yüncü, E., Changmai, P., & Reich, D. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.01.22.525077 · Cited by 2

A collection of read depth profiles at structural variant breakpoints

Bezdvornykh, I., Cherkasov, N., Kanapin, A. A., & Samsonova, A. A. (2023) · Scientific Data · doi:10.1038/s41597-023-02076-4 · Cited by 2

FOG2 coding variant Ser657Gly is associated with Coronary Microvascular Disease through altered hypoxia-mediated gene transcriptionPreprint

Guerraty, M. A., Verma, S. S., Ko, Y. A., McQuillan, M. A., Conlon, D., Tobias, J. W., Levin, M. G., Haury, W. R., Zhang, C., Judy, R., et al. (2023) · medRxiv · doi:10.1101/2023.05.22.23290352 · Cited by 2

Federated analysis of the contribution of recessive coding variants to 29,745 developmental disorder patients from diverse populationsPreprint

Chundru, V. K., Zhang, Z., Walter, K., Lindsay, S., Danecek, P., Eberhardt, R. Y., Gardner, E. J., Malawsky, D. S., Wigdor, E. M., Torene, R. I., et al. (2023) · medRxiv · doi:10.1101/2023.07.24.23293070 · Cited by 2

Imputation of race and ethnicity categories using continental genetic ancestry from real-world genomic testing dataPreprint

Rhead, B. L., Haffener, P. E., Pouliot, Y., & Vega, F. M. D. L. (2023) · medRxiv · doi:10.1101/2023.08.04.23293679 · Cited by 2

Unified Multi-caller Ensemble (UME) generates an unbiased maize haplotype map for variable coverage whole genome dataPreprint

Vallebueno‐Estrada, M., & Swarts, K. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.12.07.570552 · Cited by 2

Segmental Duplications and CNVs

Balaresque, P. L., & Delehelle, F. (2023) · Wiley eBooks · doi:10.1002/9781394264902.ch2 · Cited by 2

Genetic Ancestry and Somatic Mutations in Lung Adenocarcinoma: Insights from Real-World Clinico-Genomic DataPreprint

Rhead, B. L., Pouliot, Y., Guinney, J., & Vega, F. M. D. L. (2024) · medRxiv · doi:10.1101/2024.04.24.24306316 · Cited by 2

Systematic comparison of phenome-wide admixture mapping and genome-wide association in a diverse biobankPreprint

Cullina, S., Shemirani, R., Asgari, S., & Kenny, E. E. (2024) · medRxiv · doi:10.1101/2024.11.18.24317494 · Cited by 2

Within-Family GWAS does not Ameliorate the Decline in Prediction Accuracy across PopulationsPreprint

Zhang, L., & Conley, D. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.12.12.628188 · Cited by 2

Population-scale inheritance analysis of 858,635 individuals reveals North Sea migration from the Middle Ages to the Industrial RevolutionPreprint

Zhang, X., Holm, P., Scally, A., Banasik, K., Mortensen, L. H., Fitzgerald, T. W., Westergaard, D., Chmura, P. J., Ostrowski, S. R., Sørensen, E., et al. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.03.19.643007 · Cited by 2

Revisiting the Evolution of Lactase Persistence: Insights from South Asian GenomesPreprint

Kerdoncuff, É., Marohn, M., Cramer, N., Dey, S., Kardia, S. L. R., Kumarasamy Thangaraj, K., Ségurel, L., Lee, J., Dey, A. B., & Moorjani, P. (2025) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2025.11.05.686799 · Cited by 2

Admixture mapping identifies complex trait associations with local ancestry in the All of Us Research ProgramPreprint

Rivera, W. G. G., Liu, Y., Mirmira, T., Ma, N., Kim, J., Antonio, M. D., Dube, U., Frazer, K. A., & Gymrek, M. (2025) · medRxiv · doi:10.64898/2025.12.29.25343152 · Cited by 2

High-resolution population structure inference using genome-wide short tandem repeat variationsPreprint

Xia, F., Baudis, M., & Anisimova, M. O. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.02.20.707006 · Cited by 2

Point cloud local ancestry inference (PCLAI): continuous coordinate-based ancestry along the genomePreprint

Geleta, M., Montserrat, D. M., Ioannidis, N. M., & Ioannidis, A. G. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.03.23.713813 · Cited by 4

A Tale of Native American Whole-Genome Sequencing and Other Technologies

Aguilar-Ordóñez, I., Guzmán-Linares, J., Ballesteros-Villascán, J., Mirón-Toruño, F., Pérez-González, A. P., García-López, J., Cruz-López, F., & Morett, E. (2022) · Diversity · doi:10.3390/d14080647 · Cited by 1

On whole-genome demography of world’s ethnic groups and individual genomic identity

Kim, B.-J., Choi, J., & Kim, S. (2023) · Scientific Reports · doi:10.1038/s41598-023-32325-w · Cited by 1

Genetic factors for differentiated thyroid cancer in French Polynesia: new candidate loci

Zidane, M., Haber, M., Truong, T., Rachédi, F., Ory, C., Chevillard, S., Blanché, H., Olaso, R., Boland, A., Conte, É., et al. (2023) · Precision Clinical Medicine · doi:10.1093/pcmedi/pbad015 · Cited by 1

The complex genetic landscape of southwestern Chinese populations contributed to their extensive ethnolinguistic diversity

Wang, M., Duan, S., Sun, Q., Liu, Y., Tang, R., Yang, J., Chen, P., Liu, C., Sun, H., & He, G. (2023) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2023.1235655 · Cited by 1

Reconstruct recent multi-population migration history by using identical-by-descent sharing

Zhang, W., Yuan, K., Wen, R., Li, H., & Ni, X. (2024) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/j.jgg.2024.02.006 · Cited by 1

Urofacial (Ochoa) syndrome with a founder pathogenic variant in the HPSE2 gene: a case report and mutation origin

Valle-Peréz, M. D., Mejía‐García, A., Echeverri-López, D., Gallo-Bonilla, K., Moreno, J., Villegas‐Lanau, A., Chvatal‐Medina, M., Restrepo, J. E., Montoya, G. P. C., & Zapata, W. (2024) · Journal of Applied Genetics · doi:10.1007/s13353-024-00896-7 · Cited by 1

Forensic Biogeographical Ancestry Inference in the Philippines: Considerations for Future Implementation

Soliven, N. F. J. A., Daniel, R., Delfin, F. C., Fontanilla, I. K. C., & Ungria, M. C. A. D. (2024) · Current Molecular Biology Reports · doi:10.1007/s40610-024-00163-y · Cited by 1

Genetic Changes, Epigenetic Modifications and Antibiotic Resistance Caused by Bacterial Infection

Hashemzadeh, M., & Dezfuli, A. A. Z. (2024) · Genetics. · doi:10.5772/intechopen.1006623 · Cited by 1

A multi-ancestry genome-wide association study identifies novel candidate loci in the RARB gene associated with hypertensive disorders of pregnancy

Mack, J. A., Akhtari, F. S., Burkholder, A., House, J. S., Sovio, U., Smith, G. C. S., Schmitt, C., Fargo, D. C., Hall, J. E., & Motsinger‐Reif, A. A. (2024) · Human Genetics and Genomics Advances · doi:10.1016/j.xhgg.2024.100385 · Cited by 2

A simple demonstration of a privacy-preserving de-centralised genotype imputation workflow

Letaillandier, A., Druet, D. P., Ludwig, T. E., Marenne, G., & Herzig, A. F. (2026) · PLoS ONE · doi:10.1371/journal.pone.0353078 · Cited by 1

Rethinking GWAS: how lessons from genetic screens and artificial intelligence could reveal biological mechanisms

Hazelett, D. J. (2025) · Bioinformatics · doi:10.1093/bioinformatics/btaf153 · Cited by 1

Decoding maternal genetic background of Chinese Tujia people through extensive mitochondrial genome analyses

Chen, C., Chen, M., Luo, L., Zhu, Y., Chen, H., Zhao, M., Cao, Y., Li, Y., Li, L., Shen, C., et al. (2025) · Frontiers in Ecology and Evolution · doi:10.3389/fevo.2025.1636099 · Cited by 1

Archaeolinguistics of the languages of the Andes

Urban, M., Barbieri, C., & Rademaker, K. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.33 · Cited by 1

Indo-European archaeolinguistics

Lubotsky, A., & Pronk, T. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.18 · Cited by 2

Austronesian archaeolinguistics

Spriggs, M., Geraghty, P., & Liu, Y.-C. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.25 · Cited by 2

Uralic archaeolinguistics

Vesakoski, O., Salmela, E., & Piezonka, H. (2025) · Oxford University Press eBooks · doi:10.1093/oxfordhb/9780192868350.013.19 · Cited by 3

A multi-ancestry polygenic risk score for body mass index predicts longitudinal weight change

Lu, T., Stalter, L. N., Lauer, K. V., Hanlon, B. M., Zhang, W., & Funk, L. M. (2026) · Genome Medicine · doi:10.1186/s13073-026-01741-8 · Cited by 1

The AADR Visualizer: an ArcGIS online visualizer for ancient human DNA from the Allen Ancient DNA Resource

Yi, W., Delroba, E., Zizzamia, B., Spera, S. A., & Yang, M. A. (2024) · Bioinformatics Advances · doi:10.1093/bioadv/vbaf199 · Cited by 1

Immunogenetic polymorphism of human platelet antigens in the Saudi population: Insights into genetic diversity and alloimmune risk

Alsuhaibani, O., Chatti, N., AlZahrani, S., AlHajuj, M., Malhani, D., AlDosseri, A., Albasri, J., Elyamany, G., & Skouri, H. (2025) · Vox Sanguinis · doi:10.1111/vox.70093 · Cited by 1

An efficient LASSO framework for admixture-aware polygenic scores

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GViNC: an innovative framework for genome graph comparison reveals hidden patterns in the genetic diversity of human populations

Kamaraj, V., Gupta, A., Raman, K., Narayanan, M., & Sinha, H. (2025) · NAR Genomics and Bioinformatics · doi:10.1093/nargab/lqaf121 · Cited by 3

Mutation ages and population origins inferred from genomes in structured populations

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CEP76 impairment at the centrosome-cilium interface contributes to a spectrum of ciliopathies

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A historical and technological perspective on the evolution of the human brain transcriptome

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African-ancestry-specific variant IKKβ p.Glu502Lys confers high lupus risk

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Uncovering the Genetic Structure of the Sekler Population in Transylvania Through Genome-Wide Autosomal Data

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Coancestry superposed on admixed populations yields measures of relatedness at individual-level resolution

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An ancient DNA perspective on the Russian conquest of Yakutia

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Cosmopolitanism in the depths of Barbaricum evidenced by archaeogenomic data from the Late Iron Age Goth community of the Masłomęcz group

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Strategies in Global Ancestry and Local Ancestry Inference

Akgün, B., & Rajabli, F. (2026) · Current Protocols · doi:10.1002/cpz1.70321 · Cited by 2

Phenome-Wide Mendelian Randomization Identifying Circulating Proteins for Cardiovascular Traits in Populations of African Ancestry

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Multiple-testing corrections in case-control studies using identity-by-descent segments

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Autosomal str allele frequencies, forensic parameters and population structure in four underrepresented indigenous groups from Paraguay

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A decade of discovery: Leveraging genomic data in the ABCD study to illuminate adolescent neurodevelopment

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High-resolution analysis of recent population structure using rare variants

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Cumulative genetic risk for asthma contributes to disease severity in children with asthma

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Intrahost mutational dynamics parallel long-term genome evolution in endosymbionts

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Population Genomics Insights into Pharmacogenomic Differentiation Between East Asians and Europeans

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Whole‐Genome Sequencing Pilot of the Central Asian Genomic Diversity Project Reveals Distinct Histories, Adaptation, and Introgression

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Diverse human genomes

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Am. J. Hum. Genet. 72:1171–1186, 2003 Features of Evolution and Expansion of Modern Humans, Inferred from Genomewide Microsatellite

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Features of Evolution and Expansion of Modern Humans, Inferred from Genomewide Microsatellite Markers

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Genetics and Genomics of Human Population Structure

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Human demographic history : Insights on the human past based on genomes from Southern through Central Africa

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