Preprint / Version 1

The ‘Obesity Knowledge Portal’: an AI-powered integrative platform for exploration of obesity genetics

This article is a preprint and has not been certified by peer review.

Authors

    Yifan Liang,  
    Yifan Liang
    • Fudan University image/svg+xml
    • Shanghai Key Laboratory of Metabolic Remodelling and Health, Institute of Metabolism and Integrative Biology, School of Basic Medical Sciences, Centre for Evolutionary Biology, Fudan University, Shanghai, 200438, China
    Shiqi Ao,  
    Shiqi Ao
    • Shanghai Key Laboratory of Metabolic Remodelling and Health, Institute of Metabolism and Integrative Biology, School of Basic Medical Sciences, Centre for Evolutionary Biology, Fudan University, Shanghai, 200438, China
    Wei Xu,   Baoguo Li,   Jun-feng Bi,   Tong-jin Zhao,   Peng Li,  
    Peng Li
    • State Key Laboratory of Metabolic Dysregulation & Prevention and Treatment of Esophageal Cancer, Tianjian Laboratory of Advanced Biomedical Sciences, Academy of Medical Sciences, Zhengzhou University, Zhengzhou, 450001, China
    John R. Speakman,  
    John R. Speakman
    • Shenzhen Key Laboratory of Metabolic Health, Center for Energy Metabolism and Reproduction, Shenzhen Institute of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, China
    • State Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, 100101, China
    • Institute of Health Sciences, China Medical University, Shenyang, Liaoning, 110122, China
    • Faculty of Pharmacy, Shenzhen University of Advanced Technology, Shenzhen, 518107, Guangdong, China
    • School of Biological Sciences, University of Aberdeen, AB24 2TZ, Aberdeen, UK
    Guanlin Wang
    Guanlin Wang
Categories
Keywords
obesity; knowledge portal; AI; large language model; GWAS; precision medicine

Abstract

Obesity is a chronic, multifactorial disease in which genetics plays a major role. Genome-wide association studies (GWAS) have identified thousands of loci associated with obesity and related traits, however, translating these findings into mechanistic understanding and clinical application remains challenging. Here we present an open-access and AI-powered web platform, Obesity Knowledge Portal (OKP, https://obesityknowledge.org), which covers 166,582 curated variant-trait associations mapped to 11,298 unique genes from published GWAS and UK Biobank summary statistics, a manually curated database of 49 clinical-stage obesity therapeutics with gene-level GWAS evidence annotation, and a domain-specific AI assistant built on Retrieval-Augmented Generation (RAG) of 10,198 peer-reviewed publications. The portal provides three core analytical capabilities: interactive exploration of gene- and variant-level associations across multiple datasets with cross-linking to clinical-stage drug targets; a genomic target prioritisation algorithm that combines statistical significance and variant density to prioritise novel candidates from genes not targeted by existing therapeutics, and literature-grounded interpretation of genetic and pharmacological queries through a scope-restricted LLM-driven contextualisation system. We demonstrate the portal’s utility through case studies at the FTO locus and an integrated pharmacogenomic analysis of the GLP-1/incretin axis. The OKP is freely available and aims to support the translation of genetic discoveries into therapeutic hypotheses for obesity.

References

1. Afshin, A., Forouzanfar, M.H., Reitsma, M.B., Sur, P., Estep, K., Lee, A., Marczak, L., Mokdad, A.H., Moradi-Lakeh, M., Naghavi, M., et al. (2017). Health Effects of Overweight and Obesity in 195 Countries over 25 Years. N Engl J Med 377, 13-27. 10.1056/NEJMoa1614362.

2. Phelps, N.H., Singleton, R.K., Zhou, B., Heap, R.A., Mishra, A., Bennett, J.E., Paciorek, C.J., Lhoste, V.P.F., Carrillo-Larco, R.M., Stevens, G.A., et al. (2024). Worldwide trends in underweight and obesity from 1990 to 2022: a pooled analysis of 3663 population-representative studies with 222 million children, adolescents, and adults. The Lancet 403, 1027-1050. 10.1016/S0140-6736(23)02750-2.

3. Maes, H.H., Neale, M.C., and Eaves, L.J. (1997). Genetic and environmental factors in relative body weight and human adiposity. Behav Genet 27, 325-351. 10.1023/a:1025635913927.

4. Loos, R.J.F., and Yeo, G.S.H. (2022). The genetics of obesity: from discovery to biology. Nat Rev Genet 23, 120-133. 10.1038/s41576-021-00414-z.

5. Silventoinen, K., Rokholm, B., Kaprio, J., and Sørensen, T.I. (2010). The genetic and environmental influences on childhood obesity: a systematic review of twin and adoption studies. Int J Obes (Lond) 34, 29-40. 10.1038/ijo.2009.177.

6. Frayling, T.M., Timpson, N.J., Weedon, M.N., Zeggini, E., Freathy, R.M., Lindgren, C.M., Perry, J.R., Elliott, K.S., Lango, H., Rayner, N.W., et al. (2007). A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity. Science 316, 889-894. 10.1126/science.1141634.

7. Locke, A.E., Kahali, B., Berndt, S.I., Justice, A.E., Pers, T.H., Day, F.R., Powell, C., Vedantam, S., Buchkovich, M.L., Yang, J., et al. (2015). Genetic studies of body mass index yield new insights for obesity biology. Nature 518, 197-206. 10.1038/nature14177.

8. Yengo, L., Sidorenko, J., Kemper, K.E., Zheng, Z., Wood, A.R., Weedon, M.N., Frayling, T.M., Hirschhorn, J., Yang, J., and Visscher, P.M. (2018). Meta-analysis of genome-wide association studies for height and body mass index in ∼700000 individuals of European ancestry. Hum Mol Genet 27, 3641-3649. 10.1093/hmg/ddy271.

9. Pulit, S.L., Stoneman, C., Morris, A.P., Wood, A.R., Glastonbury, C.A., Tyrrell, J., Yengo, L., Ferreira, T., Marouli, E., Ji, Y., et al. (2019). Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. Hum Mol Genet 28, 166-174. 10.1093/hmg/ddy327.

10. Huang, J., Huffman, J.E., Huang, Y., Do Valle, Í., Assimes, T.L., Raghavan, S., Voight, B.F., Liu, C., Barabási, A.L., Huang, R.D.L., et al. (2022). Genomics and phenomics of body mass index reveals a complex disease network. Nat Commun 13, 7973. 10.1038/s41467-022-35553-2.

11. Karczewski, K.J., Gupta, R., Kanai, M., Lu, W., Tsuo, K., Wang, Y., Walters, R.K., Turley, P., Callier, S., Shah, N.N., et al. (2025). Pan-UK Biobank genome-wide association analyses enhance discovery and resolution of ancestry-enriched effects. Nat Genet 57, 2408-2417. 10.1038/s41588-025-02335-7.

12. Speliotes, E.K., Willer, C.J., Berndt, S.I., Monda, K.L., Thorleifsson, G., Jackson, A.U., Lango Allen, H., Lindgren, C.M., Luan, J., Mägi, R., et al. (2010). Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat Genet 42, 937-948. 10.1038/ng.686.

13. Willer, C.J., Speliotes, E.K., Loos, R.J., Li, S., Lindgren, C.M., Heid, I.M., Berndt, S.I., Elliott, A.L., Jackson, A.U., Lamina, C., et al. (2009). Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. Nat Genet 41, 25-34. 10.1038/ng.287.

14. Timshel, P.N., Thompson, J.J., and Pers, T.H. (2020). Genetic mapping of etiologic brain cell types for obesity. Elife 9. 10.7554/eLife.55851.

15. Aguet, F., Brown, A.A., Castel, S.E., Davis, J.R., He, Y., Jo, B., Mohammadi, P., Park, Y., Parsana, P., Segrè, A.V., et al. (2017). Genetic effects on gene expression across human tissues. Nature 550, 204-213. 10.1038/nature24277.

16. Consortium, T.G., Aguet, F., Anand, S., Ardlie, K.G., Gabriel, S., Getz, G.A., Graubert, A., Hadley, K., Handsaker, R.E., Huang, K.H., et al. (2020). The GTEx Consortium atlas of genetic regulatory effects across human tissues. Science 369, 1318-1330. doi:10.1126/science.aaz1776.

17. Wu, Y., Rudolf, A.M., Wang, L., Zhang, Z., Niu, C., Xia, F., Li, M., Wang, A., Derous, D., Mitchell, S.E., et al. (2026). The susceptibility to weight gain in male C57BL/6N mice fed high fat diet is due to a small set of genes predominantly not expressed in the brain: I target identification. Proceedings of the National Academy of Sciences, accepted.

18. Markham, A. (2021). Setmelanotide: First Approval. Drugs 81, 397-403. 10.1007/s40265-021-01470-9.

19. Wilding, J.P.H., Batterham, R.L., Calanna, S., Davies, M., Gaal, L.F.V., Lingvay, I., McGowan, B.M., Rosenstock, J., Tran, M.T.D., Wadden, T.A., et al. (2021). Once-Weekly Semaglutide in Adults with Overweight or Obesity. New England Journal of Medicine 384, 989-1002. doi:10.1056/NEJMoa2032183.

20. Garvey, W.T., Batterham, R.L., Bhatta, M., Buscemi, S., Christensen, L.N., Frias, J.P., Jódar, E., Kandler, K., Rigas, G., Wadden, T.A., and Wharton, S. (2022). Two-year effects of semaglutide in adults with overweight or obesity: the STEP 5 trial. Nat Med 28, 2083-2091. 10.1038/s41591-022-02026-4.

21. Jastreboff, A.M., Aronne, L.J., Ahmad, N.N., Wharton, S., Connery, L., Alves, B., Kiyosue, A., Zhang, S., Liu, B., Bunck, M.C., and Stefanski, A. (2022). Tirzepatide Once Weekly for the Treatment of Obesity. New England Journal of Medicine 387, 205-216. doi:10.1056/NEJMoa2206038.

22. Jastreboff, A.M., Kaplan, L.M., Frías, J.P., Wu, Q., Du, Y., Gurbuz, S., Coskun, T., Haupt, A., Milicevic, Z., and Hartman, M.L. (2023). Triple–Hormone-Receptor Agonist Retatrutide for Obesity — A Phase 2 Trial. New England Journal of Medicine 389, 514-526. doi:10.1056/NEJMoa2301972.

23. Giblin, K., Kaplan, L.M., Somers, V.K., Le Roux, C.W., Hunter, D.J., Wu, Q., Lalonde, A., Ahmad, N., and Bethel, M.A. (2026). Retatrutide for the treatment of obesity, obstructive sleep apnea and knee osteoarthritis: Rationale and design of the TRIUMPH registrational clinical trials. Diabetes Obes Metab 28, 83-93. 10.1111/dom.70209.

24. Gao, W., Liu, L., Huh, E., Gbahou, F., Cecon, E., Oshima, M., Houzé, L., Katsonis, P., Hegron, A., Fan, Z., et al. (2023). Human GLP1R variants affecting GLP1R cell surface expression are associated with impaired glucose control and increased adiposity. Nat Metab 5, 1673-1684. 10.1038/s42255-023-00889-6.

25. Lagou, V., Jiang, L., Ulrich, A., Zudina, L., González, K.S.G., Balkhiyarova, Z., Faggian, A., Maina, J.G., Chen, S., Todorov, P.V., et al. (2023). GWAS of random glucose in 476,326 individuals provide insights into diabetes pathophysiology, complications and treatment stratification. Nat Genet 55, 1448-1461. 10.1038/s41588-023-01462-3.

26. Dawed, A.Y., Mari, A., Brown, A., McDonald, T.J., Li, L., Wang, S., Hong, M.G., Sharma, S., Robertson, N.R., Mahajan, A., et al. (2023). Pharmacogenomics of GLP-1 receptor agonists: a genome-wide analysis of observational data and large randomised controlled trials. Lancet Diabetes Endocrinol 11, 33-41. 10.1016/s2213-8587(22)00340-0.

27. Kizilkaya, H.S., Sørensen, K.V., Madsen, J.S., Lindquist, P., Douros, J.D., Bork-Jensen, J., Berghella, A., Gerlach, P.A., Gasbjerg, L.S., Mokrosiński, J., et al. (2024). Characterization of genetic variants of GIPR reveals a contribution of β-arrestin to metabolic phenotypes. Nat Metab 6, 1268-1281. 10.1038/s42255-024-01061-4.

28. Sollis, E., Mosaku, A., Abid, A., Buniello, A., Cerezo, M., Gil, L., Groza, T., Güneş, O., Hall, P., Hayhurst, J., et al. (2023). The NHGRI-EBI GWAS Catalog: knowledgebase and deposition resource. Nucleic Acids Res 51, D977-d985. 10.1093/nar/gkac1010.

29. Costanzo, M.C., von Grotthuss, M., Massung, J., Jang, D., Caulkins, L., Koesterer, R., Gilbert, C., Welch, R.P., Kudtarkar, P., Hoang, Q., et al. (2023). The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits. Cell Metab 35, 695-710.e696. 10.1016/j.cmet.2023.03.001.

30. Ochoa, D., Hercules, A., Carmona, M., Suveges, D., Baker, J., Malangone, C., Lopez, I., Miranda, A., Cruz-Castillo, C., Fumis, L., et al. (2023). The next-generation Open Targets Platform: reimagined, redesigned, rebuilt. Nucleic Acids Res 51, D1353-d1359. 10.1093/nar/gkac1046.

31. Thirunavukarasu, A.J., Ting, D.S.J., Elangovan, K., Gutierrez, L., Tan, T.F., and Ting, D.S.W. (2023). Large language models in medicine. Nature Medicine 29, 1930-1940. 10.1038/s41591-023-02448-8.

32. Lab, N. (2018). UK Biobank — Neale Lab. http://www.nealelab.is/uk-biobank/.

33. Knox, C., Wilson, M., Klinger, C.M., Franklin, M., Oler, E., Wilson, A., Pon, A., Cox, J., Chin, N.E.L., Strawbridge, S.A., et al. (2024). DrugBank 6.0: the DrugBank Knowledgebase for 2024. Nucleic Acids Res 52, D1265-d1275. 10.1093/nar/gkad976.

34. Zdrazil, B., Felix, E., Hunter, F., Manners, E.J., Blackshaw, J., Corbett, S., de Veij, M., Ioannidis, H., Lopez, D.M., Mosquera, Juan F., et al. (2023). The ChEMBL Database in 2023: a drug discovery platform spanning multiple bioactivity data types and time periods. Nucleic Acids Research 52, D1180-D1192. 10.1093/nar/gkad1004.

35. Reimers, N., and Gurevych, I. (2019). Sentence-bert: Sentence embeddings using siamese bert-networks. pp. 3982-3992.

36. Pruim, R.J., Welch, R.P., Sanna, S., Teslovich, T.M., Chines, P.S., Gliedt, T.P., Boehnke, M., Abecasis, G.R., and Willer, C.J. (2010). LocusZoom: regional visualization of genome-wide association scan results. Bioinformatics 26, 2336-2337. 10.1093/bioinformatics/btq419.

37. Szklarczyk, D., Kirsch, R., Koutrouli, M., Nastou, K., Mehryary, F., Hachilif, R., Gable, A.L., Fang, T., Doncheva, N.T., Pyysalo, S., et al. (2023). The STRING database in 2023: protein-protein association networks and functional enrichment analyses for any sequenced genome of interest. Nucleic Acids Res 51, D638-d646. 10.1093/nar/gkac1000.

38. Gillespie, M., Jassal, B., Stephan, R., Milacic, M., Rothfels, K., Senff-Ribeiro, A., Griss, J., Sevilla, C., Matthews, L., Gong, C., et al. (2022). The reactome pathway knowledgebase 2022. Nucleic Acids Res 50, D687-d692. 10.1093/nar/gkab1028.

39. Kanehisa, M., Furumichi, M., Sato, Y., Kawashima, M., and Ishiguro-Watanabe, M. (2023). KEGG for taxonomy-based analysis of pathways and genomes. Nucleic Acids Res 51, D587-d592. 10.1093/nar/gkac963.

40. Stelzer, G., Rosen, N., Plaschkes, I., Zimmerman, S., Twik, M., Fishilevich, S., Stein, T.I., Nudel, R., Lieder, I., Mazor, Y., et al. (2016). The GeneCards Suite: From Gene Data Mining to Disease Genome Sequence Analyses. Curr Protoc Bioinformatics 54, 1.30.31-31.30.33. 10.1002/cpbi.5.

41. Jia, G., Fu, Y., Zhao, X., Dai, Q., Zheng, G., Yang, Y., Yi, C., Lindahl, T., Pan, T., Yang, Y.G., and He, C. (2011). N6-methyladenosine in nuclear RNA is a major substrate of the obesity-associated FTO. Nat Chem Biol 7, 885-887. 10.1038/nchembio.687.

42. Zhao, X., Yang, Y., Sun, B.F., Shi, Y., Yang, X., Xiao, W., Hao, Y.J., Ping, X.L., Chen, Y.S., Wang, W.J., et al. (2014). FTO-dependent demethylation of N6-methyladenosine regulates mRNA splicing and is required for adipogenesis. Cell Res 24, 1403-1419. 10.1038/cr.2014.151.

43. Merkestein, M., Laber, S., McMurray, F., Andrew, D., Sachse, G., Sanderson, J., Li, M., Usher, S., Sellayah, D., Ashcroft, F.M., and Cox, R.D. (2015). FTO influences adipogenesis by regulating mitotic clonal expansion. Nat Commun 6, 6792. 10.1038/ncomms7792.

44. Drucker, D.J. (2022). GLP-1 physiology informs the pharmacotherapy of obesity. Mol Metab 57, 101351. 10.1016/j.molmet.2021.101351.

45. Müller, T.D., Blüher, M., Tschöp, M.H., and DiMarchi, R.D. (2022). Anti-obesity drug discovery: advances and challenges. Nat Rev Drug Discov 21, 201-223. 10.1038/s41573-021-00337-8.

46. Grant, S.F., Thorleifsson, G., Reynisdottir, I., Benediktsson, R., Manolescu, A., Sainz, J., Helgason, A., Stefansson, H., Emilsson, V., Helgadottir, A., et al. (2006). Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetes. Nat Genet 38, 320-323. 10.1038/ng1732.

47. Florez, J.C., Jablonski, K.A., Bayley, N., Pollin, T.I., de Bakker, P.I., Shuldiner, A.R., Knowler, W.C., Nathan, D.M., and Altshuler, D. (2006). TCF7L2 polymorphisms and progression to diabetes in the Diabetes Prevention Program. N Engl J Med 355, 241-250. 10.1056/NEJMoa062418.

48. Mahajan, A., Spracklen, C.N., Zhang, W., Ng, M.C.Y., Petty, L.E., Kitajima, H., Yu, G.Z., Rüeger, S., Speidel, L., Kim, Y.J., et al. (2022). Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation. Nat Genet 54, 560-572. 10.1038/s41588-022-01058-3.

49. Saeed, S., Bonnefond, A., Tamanini, F., Mirza, M.U., Manzoor, J., Janjua, Q.M., Din, S.M., Gaitan, J., Milochau, A., Durand, E., et al. (2018). Loss-of-function mutations in ADCY3 cause monogenic severe obesity. Nat Genet 50, 175-179. 10.1038/s41588-017-0023-6.

50. Grarup, N., Moltke, I., Andersen, M.K., Dalby, M., Vitting-Seerup, K., Kern, T., Mahendran, Y., Jørsboe, E., Larsen, C.V.L., Dahl-Petersen, I.K., et al. (2018). Loss-of-function variants in ADCY3 increase risk of obesity and type 2 diabetes. Nat Genet 50, 172-174. 10.1038/s41588-017-0022-7.

51. Shungin, D., Winkler, T.W., Croteau-Chonka, D.C., Ferreira, T., Locke, A.E., Mägi, R., Strawbridge, R.J., Pers, T.H., Fischer, K., Justice, A.E., et al. (2015). New genetic loci link adipose and insulin biology to body fat distribution. Nature 518, 187-196. 10.1038/nature14132.

52. Bradfield, J.P., Taal, H.R., Timpson, N.J., Scherag, A., Lecoeur, C., Warrington, N.M., Hypponen, E., Holst, C., Valcarcel, B., Thiering, E., et al. (2012). A genome-wide association meta-analysis identifies new childhood obesity loci. Nat Genet 44, 526-531. 10.1038/ng.2247.

53. Littleton, S.H., Trang, K.B., Volpe, C.M., Cook, K., DeBruyne, N., Maguire, J.A., Weidekamp, M.A., Hodge, K.M., Boehm, K., Lu, S., et al. (2024). Variant-to-function analysis of the childhood obesity chr12q13 locus implicates rs7132908 as a causal variant within the 3' UTR of FAIM2. Cell Genom 4, 100556. 10.1016/j.xgen.2024.100556.

54. Harding, S.D., Armstrong, J.F., Faccenda, E., Southan, C., Alexander, S.P.H., Davenport, A.P., Spedding, M., and Davies, J.A. (2024). The IUPHAR/BPS Guide to PHARMACOLOGY in 2024. Nucleic Acids Res 52, D1438-d1449. 10.1093/nar/gkad944.

55. Tsang, C.H., De Rosa, A., and Kozielewicz, P. (2025). Identification and molecular characterization of missense mutations in orphan G protein-coupled receptor GPR61 occurring in severe obesity. Mol Pharmacol 107, 100026. 10.1016/j.molpha.2025.100026.

56. Nogueira, P.A.S., Moura-Assis, A., Zanesco, A.M., Bombassaro, B., Gallo-Ferraz, A.L., Simões, M.R., Engel, D.F., Razolli, D.S., Gaspar, J.M., Junior, J.D., and Velloso, L.A. (2023). The orphan G protein-coupled receptor, GPR139, is expressed in the hypothalamus and is involved in the regulation of body mass, blood glucose, and insulin. Neurosci Lett 792, 136955. 10.1016/j.neulet.2022.136955.

57. Felix, J.F., Bradfield, J.P., Monnereau, C., van der Valk, R.J., Stergiakouli, E., Chesi, A., Gaillard, R., Feenstra, B., Thiering, E., Kreiner-Møller, E., et al. (2016). Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index. Hum Mol Genet 25, 389-403. 10.1093/hmg/ddv472.

58. Clément, K., van den Akker, E., Argente, J., Bahm, A., Chung, W.K., Connors, H., De Waele, K., Farooqi, I.S., Gonneau-Lejeune, J., Gordon, G., et al. (2020). Efficacy and safety of setmelanotide, an MC4R agonist, in individuals with severe obesity due to LEPR or POMC deficiency: single-arm, open-label, multicentre, phase 3 trials. Lancet Diabetes Endocrinol 8, 960-970. 10.1016/s2213-8587(20)30364-8.

59. Bonnefond, A., Bruner, W.S., Grant, S.F., Morandi, A., and Froguel, P. (2026). The genetics of obesity: aetiology, prevention and therapy. Nature Metabolism, 1-17.

60. Ghoussaini, M., Mountjoy, E., Carmona, M., Peat, G., Schmidt, E.M., Hercules, A., Fumis, L., Miranda, A., Carvalho-Silva, D., Buniello, A., et al. (2021). Open Targets Genetics: systematic identification of trait-associated genes using large-scale genetics and functional genomics. Nucleic Acids Res 49, D1311-d1320. 10.1093/nar/gkaa840.

61. Lorente, J.S., Sokolov, A.V., Ferguson, G., Schiöth, H.B., Hauser, A.S., and Gloriam, D.E. (2025). GPCR drug discovery: new agents, targets and indications. Nat Rev Drug Discov 24, 458-479. 10.1038/s41573-025-01139-y.

62. Hauser, A.S., Attwood, M.M., Rask-Andersen, M., Schiöth, H.B., and Gloriam, D.E. (2017). Trends in GPCR drug discovery: new agents, targets and indications. Nat Rev Drug Discov 16, 829-842. 10.1038/nrd.2017.178.

63. Liskiewicz, D., Novikoff, A., Khalil, A., Akindehin, S., Campbell, J.E., Candela, P., Castelino, R.L., Coupland, C., Culot, M., Dodson, W.S., et al. (2026). GLP-1R–GIPR–PPARα/γ/δ quintuple agonism corrects obesity and diabetes in mice. Nature 653, 776-785. 10.1038/s41586-026-10427-5.

64. Lewis, P., Perez, E., Piktus, A., Petroni, F., Karpukhin, V., Goyal, N., Küttler, H., Lewis, M., Yih, W.-t., and Rocktäschel, T. (2020). Retrieval-augmented generation for knowledge-intensive nlp tasks. Advances in neural information processing systems 33, 9459-9474.

65. Li, M., Kilicoglu, H., Xu, H., and Zhang, R. (2025). Biomedrag: A retrieval augmented large language model for biomedicine. Journal of Biomedical Informatics 162, 104769.

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2026-06-20

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Liang, Y., Ao, S., Xu, W., Li, B., Bi, J.- feng, Zhao, T.- jin, Li, P., Speakman, J. R., & Wang, G. (2026). The ‘Obesity Knowledge Portal’: an AI-powered integrative platform for exploration of obesity genetics. LangTaoSha Preprint Server. https://doi.org/10.65215/LTSpreprints.2026.06.20.000276

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The authors declare no competing interests to disclose.