Quem Somos

Publicações dos pesquisadores do Genoma USP - 2025

1. Adami FL, de Castro MV, Almeida BDS, Daher IP, Yamamoto MM, Souza Santos K, Zatz M, Naslavsky MS, Rosa DS, Cunha-Neto E, de Oliveira VL, Kalil J, Boscardin SB. Corrigendum: Anti-RBD IgG antibodies from endemic coronaviruses do not protect against the acquisition of SARS-CoV-2 infection among exposed uninfected individuals. Front Immunol. 2025 Apr 1;16:1598312. doi: 10.3389/fimmu.2025.1598312. eCollection 2025.

2. Asadollahi R, Ahmad A, Boonsawat P, Shahanoor Hinzen J, Lohse M, Bouazza-Arostegui B, Sun S, Utesch T, Sommer JD, Ilic D, Padmanarayana M, Fischermanns K, Ranjan M, Boll M, Ka C, Piton A, Mattioli F, Isidor B, Õunap K, Reinson K, Wojcik MH, Marshall CR, Mercimek-Andrews S, Matsumoto N, Miyake N, Stephan BO, Honjo RS, Bertola DR, et.al. Pathogenic UNC13A variants cause a neurodevelopmental syndrome by impairing synaptic function. Nat Genet. 2025 Nov;57(11):2691-2704. doi: 10.1038/s41588-025-02361-5. Epub 2025 Oct 22. PMID: 41125872; PMCID: PMC12597829.

3. Alves Paiva RD, Coa LL, Sielski M, Godoy JA, Azevedo J, Oliveira D, Alvarez KC, Okamoto OK, Kutner JM, Hamerschlak N, Kerbauy LN. Stability plan for advanced cell therapy NK cells: an off the shelf strategy for adoptive immunotherapy against acute myeloid leukemia. Cytotherapy, v.27(5), 2025, S181-S182, ISSN 1465-3249, https://doi.org/10.1016/j.jcyt.2025.03.366.

4. Avila Martins CC, Maschietto M, Kimura L, Alvizi L, Nunes K, Magalhães Borges V, Victorino Krepischi AC, Mingroni-Netto RC. Differential methylation in blood pressure control genes is associated to essential hypertension in African Brazilian populations. Epigenetics. 2025 Dec;20(1):2477850. doi: 10.1080/15592294.2025.2477850. Epub 2025 Mar 27.

5. Bortolin RH, de Souza Leite F, Luchessi AD, Esposito J, Barbosa IN, Freitas RCC, Sonawane AR, Singh SA, Aikawa E, Telles-Silva KA, Hirata TDC, Rosa Neta AP, Goulart E, Caires-Júnior LC, Mata Martins TMD, Semedo P, Moreira DP, Naslavsky M, Faludi AA, Gonçalves RM, Araujo DB, Malaquias VB, Ferreira GM, DeOcesano-Pereira C, Chudzinski-Tavassi AM, Pu WT, Zatz M, Hirata RDC, Hirata MH. Translational insights into statin-induced myotoxicity: Differential impact of lipophilic and hydrophilic statins on iPSC-derived skeletal muscle cells from patients with familial hypercholesterolemia. 2. Toxicology. 2025 Aug;515:154159. doi: 10.1016/j.tox.2025.154159. Epub 2025 Apr 18.

6. Borda V, Loesch DP, Guo B, Laboulaye R, Veliz-Otani D, French JN, Leal TP, Gogarten SM, Ikpe S, Gouveia MH, Mendes M, Abecasis GR, Alvim I, Arboleda-Bustos CE, Arboleda G, Arboleda H, Barreto ML, Barwick L, Bezzera MA, Blangero J, Borges V, Caceres O, Cai J, Chana-Cuevas P, Chen Z, Custer B, Dean M, Dinardo C, Domingos I, Duggirala R, Dieguez E, Fernandez W, Ferraz HB, Gilliland F, Guio H, Horta B, Curran JE, Johnsen JM, Kaplan RC, Kelly S, Kenny EE, Konkle BA, Kooperberg C, Lescano A, Lima-Costa MF, Loos RJF, Manichaikul A, Meyers DA, Naslavsky MS, Nickerson DA, North KE, Padilla C, Preuss M, Raggio V, Reiner AP, Rich SS, Rieder CR, Rienstra M, Rotter JI, Rundek T, Sacco RL, Sanchez C, Sankaran VG, Santos-Lobato BL, Schumacher-Schuh AF, Scliar MO, Silverman EK, Sofer T, Lasky-Su J, Tumas V, Weiss ST; Latin American Research Borges VM, Horimoto ARVR, Wijsman EM, Kimura L, Nunes K, Nato AQ Jr, Mingroni-Netto RC. Genomic Exploration of Essential Hypertension in African-Brazilian Quilombo Populations: A Comprehensive Approach With Pedigree Analysis and Family-Based Association Studies. J Am Heart Assoc. 2025 Apr;14(7):e036193. doi: 10.1161/JAHA.124.036193. Epub 2025 Mar 21.

7. Bortolin RH, de Souza Leite F, Luchessi AD, Esposito J, Barbosa IN, Freitas RCC, Sonawane AR, Singh SA, Aikawa E, Telles-Silva KA, Hirata TDC, Rosa Neta AP, Goulart E, Caires-Júnior LC, Mata Martins TMD, Semedo P, Moreira DP, Naslavsky M, Faludi AA, Gonçalves RM, Araujo DB, Malaquias VB, Ferreira GM, DeOcesano-Pereira C, Chudzinski-Tavassi AM, Pu WT, Zatz M, Hirata RDC, Hirata MH. Translational insights into statin-induced myotoxicity: Differential impact of lipophilic and hydrophilic statins on iPSC-derived skeletal muscle cells from patients with familial hypercholesterolemia.Toxicology. 2025 Aug;515:154159. doi: 10.1016/j.tox.2025.154159. Epub 2025 Apr 18.

8. Bossolani-Martins AL, Meira JGC, Kobayashi GS, Barbosa-Gonçalves A, Passos-Bueno MR, Fett-Conte AC. Van der Woude syndrome and amniotic band sequence: A clue to a common genetic etiology? A case report. Genet Mol Biol. 2025 Feb 17;48(1):e20240123. doi: 10.1590/1678-4685-GMB-2024-0123. eCollection 2025.

9. Bruxel EM, Rovaris DL, Belangero SI, Chavarría-Soley G, Cuellar-Barboza AB, Martínez-Magaña JJ, Nagamatsu ST, Nievergelt CM, Núñez-Ríos DL, Ota VK, Peterson RE, Sloofman LG, Adams AM, Albino E, Alvarado AT, Andrade-Brito D, Arguello-Pascualli PY, Bandeira CE, Bau CHD, Bulik CM, Buxbaum JD, Cappi C, Corral-Frias NS, Corrales A, Corsi-Zuelli F, Crowley JJ, Cupertino RB, da Silva BS, De Almeida SS, De la Hoz JF, Forero DA, Fries GR, Gelernter J, González-Giraldo Y, Grevet EH, Grice DE, Hernández-Garayua A, Hettema JM, Ibáñez A, Ionita-Laza I, Lattig MC, Lima YC, Lin YS, López-León S, Loureiro CM, Martínez-Cerdeño V, Martínez-Levy GA, Melin K, Moreno-De-Luca D, Muniz Carvalho C, Olivares AM, Oliveira VF, Ormond R, Palmer AA, Panzenhagen AC, Passos-Bueno MR, Peng Q, Pérez-Palma E, Prieto ML, Roussos P, Sanchez-Roige S, Santamaría-García H, Shansis FM, Sharp RR, Storch EA, Tavares MEA, Tietz GE, Torres-Hernández BA, Tovo-Rodrigues L, Trelles P, Trujillo-ChiVacuan EM, Velásquez MM, Vera-Urbina F, Voloudakis G, Wegman-Ostrosky T, Zhen-Duan J, Zhou H; Latin American Genomics Consortium; Santoro ML, Nicolini H, Atkinson EG, Giusti-Rodríguez P, Montalvo-Ortiz JL. Psychiatric genetics in the diverse landscape of Latin American populations. Nat Genet. 2025 May;57(5):1074-1088. doi: 10.1038/s41588-025-02127-z. Epub 2025 Apr 2.PMID: 40175716

10. BW Souza, GL Yamamoto, IA Zogbi, PV Andrade, JM Santos, LN Feitosa. Vainzof M. Rare Duplication in the RYR1 Gene Causing Malignant Hyperthermia and Clinical Variability. Genes 16(11), 1252, 2025.

11. Chatterjee S, Ishida M, Bertola DR, Agwu JC, Gaston-Massuet C, McGuffin LJ, Storr HL, Maharaj AV. Pathogenesis of Noonan syndrome is modulated by NOC2L, a novel interactor of LZTR1 leading to impaired p53 signalling. J Clin Endocrinol Metab. 2025 Nov 1:dgaf602. doi: 10.1210/clinem/dgaf602. Epub ahead of print. PMID: 41175093.

12. Costa CIS, Madanelo L, Wang JYT, da Silva Campos G, De Sanctis Girardi AC, Scliar M, Monfardini F, de Cássia Mingroni Pavanello R, Cória VR, Vibranovski MD, Krepischi AC, Lourenço NCV, Zatz M, Yamamoto GL, Zachi EC, Passos-Bueno MR. Understanding rare variant contributions to autism: lessons from dystrophin-deficient model. NPJ Genom Med. 2025 Mar 6;10(1):18. doi: 10.1038/s41525-025-00469-5.

13. Corradi C, Moreno NC, Quintero-Ruiz N, Silva Leandro GD, Teatin Latancia M, de Souza TA, Munford V, Menck CFM. Uncovering the Role of DNA Repair Impairment in UVA-Induced. Mutagenesis in Human Xeroderma Pigmentosum Variant Cells. Mol Carcinog. 64(11): 1823-1837, 2025.

14. Dos Santos Silva M, Micheletti L, Souza R, Souza B, Andrade P, Vainzof M, Silva H. Anabolic androgenic steroids and illicit drugs as potential modulating factors in malignant hyperthermia: a case series. Anaesthesiol Intensive Ther. 2025 Jul 23;57(1):170-173. doi: 10.5114/ait/207611. PMID: 40734645; PMCID: PMC12329499.

15. Fajardo TCG, Quadros Junior AC, Pinto CAL, Santos GRD, Silva ACBD, Catalan DT, Bertozzi APAP, Gazeta RE, Moron AF, Passos SD; Jundiai Zika Cohort Group; Mello AS, Soriano-Arandes A, Alarcon A, Garcia-Alix A, Silva ABD, Ventura DF, Oliveira DBL, Tambalo DS, Lima DDS, Fujiwara DT, Durigon EL, Bagne ER, Velasco FG, Baran LCP, Arita FN, Hernandez FDM, Almeida JPG, Camandulli KR, Castro LP, Machado MB, Zatz M, Rodrigues MMD, Rizzo MFV, Farrão MA, Leite MNB, Florence Filho N, Loiola PC, Prestes R, Dezena RCA, Bonon SHA, Vranjac S, Rosemberg S, Sarmento SGP, Witkinchi SS, Souza TG, Pandini VCM, Paiva VP. Serology survey of chikungunya virus in high-risk pregnant women and placental tissue findings. Rev Inst Med Trop Sao Paulo. 2025 Jul 7;67:e43. doi: 10.1590/S1678-9946202567043. PMID: 40638511; PMCID: PMC12233753.

16. Fatori D, Shephard E, Benette D, Naspolini NF, Guzman GC, Wang JYT, Tótolo P, Mafra AL, Isaias C, Dos Santos DP, Russo FB, Kobayashi G, Argeu A, Teixeira M, Mattiello-Sverzut AC, Fernandes MTB, Petian-Alonso DC, Brentani H, Scliar M, Schüroff PA, Zuccolo P, Lerner R, Geraldini S, Euclydes VLV, Matijasevich A, de Campos AC, de Carvalho ACP, Fujita A, Taddei CR, Passos-Bueno MR, Beltrão-Braga P, Polanczyk GV. Identifying biomarkers and trajectories of executive functions and language development in the first 3 years of life: Design, methods, and findings of the Germina cohort study. Dev Psychopathol. 2025 Mar 5:1-11. doi: 10.1017/S0954579425000069. Online ahead of print.

17. Ferreira Jr RS, Mantovani CK, Ferreira ASBS, Nascimento LO, Ferrari MFR, Kawano DF, Massirer KB, Anhê GF, Anholon R, Caricati CP, Ortega LM, Guilbert S, Lambe T, Oliveira-Filho JP, Clemens SAC, Barraviera B. Translational science at the undergraduate level: awakening talents to overcome the valley of death - case report. J Venom Anim Toxins Incl Trop Dis. 2025 May:e20250005. doi: 10.1590/1678-9199-JVATITD-2025-0005. eCollection 2025. Affiliations Expand

18. Fridman C, Batista JPG, Bianchini PV, Batistutti VP, de Sá Osório P, de Mello Andrade L, Levi JE, Krepischi ACV, Villela D, Rosenberg C. Uniparental disomy (UPD) as the cause of inconsistencies in parentage tests: report of maternal UPD of chromosome 2 and review of the literature. Int J Legal Med. 2025 Mar 1. doi: 10.1007/s00414-025-03428-y. Online ahead of print.

19. Garcia FM, de Sousa VP, Silva-Dos-Santos PPE, Fernandes IS, Serpa FS, de Paula F, Mill JG, Bueno MRP, Errera FIV. Copy Number Variation in Asthma: An Integrative Review. Clin Rev Allergy Immunol. 2025 Jan 4;68(1):4. doi: 10.1007/s12016-024-09015-0.PMID: 39755867 Review.

20. Gear R, Kalitsis P, Glass M, Isidor B, Vincent-Delorme C, Petit F, Verhagen JMA, Jorge A, Krepischi ACV, Osei-Owusu I, Martinez E, O'Donnell-Luria A, de Leeuw N, Ruggiero S, Helbig I, David F 1st, Brown NJ. AP2M1 Is a Candidate Gene for Microcephaly and Intellectual Disability in 3q27.1 Deletions. Am J Med Genet A. 2025 Nov;197(11):e64153. doi: 10.1002/ajmg.a.64153. Epub 2025 Jul 9. PMID: 40631915; PMCID: PMC12286883.

21. Gomes AO, Andrade PV, Santos JM, Souza LS, Oliveira ASB, Vainzof M, Silva HCA. Association between joint dislocation and malignant hyperthermia. Anaesth Rep. 2025 Jul 9;13(2):e70021. doi: 10.1002/anr3.70021.

22. Hui Ling Ma, Raiane de Oliveira Ferreira, Danyllo Felipe de Oliveira, Alice Kei Endo, Okamoto OK, Zatz M. 3D bioprinted neural progenitor cell constructs for enhancing ex vivo brain integration and neuron-astrocyte differentiation. Bioprinting. E00424, 2025.

23. Inoue Y, Tsuchida N, Kim CA, de Oliveira Stephan B, Castro MAA, Honjo RS, Bertola DR, Uchiyama Y, Hamanaka K, Fujita A, Koshimizu E, Misawa K, Miyatake S, Mizuguchi T, Matsumoto N. Correction: Novel compound heterozygous ABCA2 variants cause IDPOGSA, a variable phenotypic syndrome with intellectual disability. J Hum Genet. 2025 Nov 10. doi: 10.1038/s10038-025-01422-1. Epub ahead of print. Erratum for: J Hum Genet. 2024 Apr;69(3-4):163-167. doi: 10.1038/s10038-024-01219-8. PMID: 41207891.

24. Kajitani GS, Tomaz MA, Leandro GDS, Quayle C, Rocha LCM, de Souza TA, Moreira LM, Rosse I, Menck CFM, Garcia CCM . Altered pathways in Cockayne syndrome: Involvement of MAPK, PI3K-Akt, extracellular matrix, inflammation, and neuronal signaling. DNA Repair (Amst).152:103861, 2-25, 2025.

25. Kim GJ, Malaquias AC, Bertola DR, Rezende RC, Cellin LP, Pires LVL, Santillan-Vasconez AM, Lerario AM, Scalco RDC, Jorge AAL. Non-RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome. Am J Med Genet A. 2025 Oct 25:e64291. doi: 10.1002/ajmg.a.64291. Epub ahead of print. PMID: 41137536.

26. Koko M, Satterstrom FK; Autism Sequencing Consortium; APEX consortium; Warrier V, Martin H.(Collaborators: Passos-Bueno MR et al) . Contribution of autosomal rare and de novo variants to sex differences in autism. Am J Hum Genet. 2025 Mar 6;112(3):599-614. doi: 10.1016/j.ajhg.2025.01.016. Epub 2025 Feb 14.PMID: 39954678 Free PMC article.

27. Landry C, Costanzo JP, Mitne-Neto M, Zatz M, Schaffer AE, Hatzoglou M, Muotri AR, Miranda HC. Convergent activation of the integrated stress response and ER-mitochondria uncoupling in VAPB-associated ALS. EMBO Mol Med. 2025 Sep;17(9):2299-2331. doi: 10.1038/s44321-025-00279-3. Epub 2025 Aug 5. PMID: 40764463; PMCID: PMC12423299.

28. Leoncio JC, Batissoco AC, Alegria TGP, Gomes F, Netto LES, Mingroni-Netto RC, Haddad LA. Direct connexin-26 interactions with membrane proteins functionally relevant to the cochlea. Hum Genet. 2025 Oct;144(9-10):983-1000. doi: 10.1007/s00439-025-02769-3. Epub 2025 Aug 13. PMID: 40801940.

29. Leite JMRS, Pereira JL, Alves de Souza C, Pavan Soler JM, Mingroni-Netto RC, Fisberg RM, Rogero MM, Sarti FM. Novel loci linked to serum lipid traits are identified in a genome-wide association study of a highly admixed Brazilian population - the 2015 ISA Nutrition. Lipids Health Dis. 2024 Jul 26;23(1):229. doi: 10.1186/s12944-024-02085-1.PMID: 39060932.

30. Ma HL, Garcia LSA, Ishiba R, Dametto LC, da Silva Moraes KA, Oliveira Ferreira R, Okamoto OK, Zatz M. Modeling glioblastoma in 3D hydrogels enables investigation of Zika virus targeting and immune modulation in oncolytic virotherapy. Biomater Adv. 2026 Feb;179:214492. doi: 10.1016/j.bioadv.2025.214492. Epub 2025 Sep 11. PMID: 40957303.

31. Moreira R, Nascimento H, Martins TMDM, Barbieri G, Pires P, Carvalho LN, Rosa LR, Almeida A, Pessuti CL, Ferrer H, Gomes JÁP, Goulart E, Raia S, Belfort R Jr. Porcine Corneal Tissue and Xenozoonotic Risks: A Review of the Current Evidence. Xenotransplantation. 2025 Nov-Dec;32(6):e70068. doi: 10.1111/xen.70068. PMID: 41200999; PMCID: PMC12593271.

32. Mason CE, Hajirasouliha I. CAMP: A modular metagenomics analysis system for integrated multi-step data exploration. bioRxiv [Preprint]. 2024 Sep 14:2023.04.09.536171. doi: 10.1101/2023.04.09.536171.PMID: 37066359 Free PMC article. Preprint.

33. Mitsugi TG, Sherwood M, Jandrey EHF, Assoni AF, Bell J, Coke B, Skipp P, Ewing R, Okamoto OK. Integrated interactome, proteomic and functional analyses reveal molecular pathways driving L1TD1-induced aggressiveness in CNS embryonal tumor cells. FEBS Lett. 2025 Apr;599(7):1029-1045. doi: 10.1002/1873-3468.70002. Epub 2025 Feb 6.PMID: 39912397

34. Nascimento JA, Bazán PR, Azevedo Neto RM, Silva ES, Soares DA, Balardin JB, Amaro Junior E. Assessing webcam-based eye-tracking during comic reading in the classroom: a feasibility study. Einstein (Sao Paulo). 2025 Apr 7;23:eAO0911. doi: 10.31744/einstein_journal/2025AO0911. eCollection 2025.PMID: 40197878 Free PMC article.

35. Naspolini NF, Schüroff PA, Vanzele PAR, Pereira-Santos D, Valim TA, Bonham KS, Fujita A, Passos-Bueno MR, Beltrão-Braga PCB, Carvalho ACPLF, Klepac-Ceraj V, Polanczyk GV, Campos AC, Taddei CR. Exclusive breastfeeding is associated with the gut microbiome maturation in infants according to delivery mode. Gut Microbes. 2025 Dec;17(1):2493900. doi: 10.1080/19490976.2025.2493900. Epub 2025 Apr 16.PMID: 40237336 Free PMC article.

36. Paes VR, Justo AFO, Rodriguez RD, Naslavsky MS, Renata Leite REP, Pasqualucci CA, Zatz M, Jacob-Filho W, Suemoto CK, Grinberg LT. Lewy body disease stages through aging and correlations with clinical and neuropathological profile on a population-based brain bank. Alzheime'r & Dementia. First published: 03 January 2025 https://doi.org/10.1002/alz.092753

37. Pires LVL, Da Cás E, de Melo LC, Nakaie CMA, Aiello VD, Yamamoto GL, Honjo RS, Kim CA, Bertola DR. Plastic Bronchitis in Noonan Syndrome: Further Evidence Suggesting a Higher Risk of Lymphatic Abnormalities in Individuals Harboring Variants in PTPN11 Residue p.Phe285. Mol Syndromol. 2025 Apr;16(2):165-170. doi: 10.1159/000540570. Epub 2024 Aug 22. PMID: 4017683

38. Pasa ID, Frey AC, Ferraciolli SF, Lucato LT, Azevedo Carvalho M, Pagotto MVC, Burlacchini De Carvalho MH, Pulcineli Vieira Francisco R, Honjo RS, Bertola DR, Kim CA. A Novel NOTCH3 Variant Leading to Lateral Meningocele Syndrome: Prenatal Diagnosis and Possible Expansion of the Phenotype. Mol Syndromol. 2025 Aug;16(4):384-389. doi: 10.1159/000542432. Epub 2024 Nov 7. PMID: 40771185; PMCID: PMC12324726.

39. Piai CB, Salti GYG, Allegro MC, Betty PB, de Souza Valente F, Pasa ID, de Oliveira Stephan B, Linnenkamp BDW, Honjo RS, Bertola DR, Sakamoto M, Inoue Y, Saida K, Tsuchida N, Miyake N, Matsumoto N, Kim CA. Blended Phenotypes in Individuals With Rare Diseases: A Brazilian Case Series. Am J Med Genet A. 2025 Dec;197(12):e64209. doi: 10.1002/ajmg.a.64209. Epub 2025 Aug 5. PMID: 40762225.

40. Porras LM, Rodríguez-Lausell I, Iglesias-Maldonado G, Tuliao EVF, Martínez G, Leveque C, Tobon J, Eloy R, Belangero S, Bulik CM, Loureiro CM, Carvalho CM, Ota V, Rovaris DL, Storch EA, Vacuan EMT, Velasquez MM; Latin American Genomics Consortium; Santoro ML, Nicolini H, Atkinson EG, Montalvo-Ortiz JL, Giusti-Rodríguez P. Functional Genomics Studies of Psychiatric Disorders in Individuals of Latin American Populations: A Scoping Review. Am J Med Genet B Neuropsychiatr Genet. 2025 Sep 27. doi: 10.1002/ajmg.b.33063. Epub ahead of print. PMID: 41014243.

41. Portela FSO, Louzada ACS, da Silva MFA, Portugal MFC, Galvão FA, Teivelis MP, Junior EA, Wolosker N. Analysis of 19 439 lower limb amputations in children in Brazilian health system over 14 years. Inj Prev. 2025 Jan 7:ip-2024-045472. doi: 10.1136/ip-2024-045472. Online ahead of print.PMID: 39773851

42. Quintero-Ruiz N, Corradi C, Moreno NC, de Souza TA, Menck CFM. UVA-light-induced mutagenesis in the exome of human nucleotide excision repair-deficient cells. Photochem Photobiol Sci. 2025 Mar;24(3):429-449. doi: 10.1007/s43630-025-00697-9. Epub 2025 Mar 10.PMID: 40063310

43. Quiñones-Vega M, Sosa-Acosta P, Guedes JS, Pinto de Almeida N, V de Castro M, Silva MVR, Dell'Aquila LP, Razuk-Filho Á, Batista-Júnior PB, Zatz M, Nogueira FCS, Domont GB. Proteomics and Metabolomics Profiles of Unvaccinated Nonagenarian Patients with Severe SARS-CoV-2 Infection. J Proteome Res. 2025 Nov 7;24(11):5453-5466. doi: 10.1021/acs.jproteome.5c00251. Epub 2025 Sep 25. PMID: 40997940; PMCID: PMC12604035.

44. Ramos LC, Kobachuk LDG, Nadur DM, Sabbag LR, Rosário MMTD, Naslavsky MS, Mendes-Junior CT, Castelli EC. Assessing the performance of multi-InDel panels for human identification among admixed Brazilians. Forensic Sci Int Genet. 2025

45. Rodrigues MAS, Rodrigues TP, Bach ABM, Paulo AJM, Nasvlasky MS, Duarte YAO, Zatz M, Amaro Junior E. Exploring the relationship between cognitive performance and magnetic resonance imaging diffusion parameters in elderly individuals. Einstein (Sao Paulo). 2025 Oct 17;23:eAO1467. doi: 10.31744/einstein_journal/2024AO1467. PMID: 41124430.

46. Rosa-Ribeiro R, Falco ML, Sena de Souza J, Okamoto OK, Weinlich R. Unraveling Zika virus-induced cell death pathways in eradicating embryonal central nervous system tumors. Neuroscience. 2025 Aug 30;582:126-133. doi: 10.1016/j.neuroscience.2025.07.039. Epub 2025 Jul 23. PMID: 40712830.

47. Santos RC, Lima LFCDMS, Andrade PV, Santos JM, Galleni L, Ribeiro-Jr AF, Souza LS, Schmidt B, Oliveira ASB, Amaral JLG, Vainzof M, Silva HCA. Report of Joint hypermobility in malignant hyperthermia susceptible patients: Observational study with a case-control descriptive design. Heliyon, 11, e41776, 2025

48. Semzezem C, Gomes KFB, Santos AS, Brochet P, Crisostomo LG, Correia MRS, Frade-Barros AF, Brito LA, Passos-Bueno MR, Chevillard C, Cunha-Neto E, da Silva MER. IL17RA and IL21R polymorphisms influence type 1 diabetes predisposition and autoimmune phenotypes.Front Endocrinol (Lausanne). 2025 Sep 4;16:1620509. doi: 10.3389/fendo.2025.1620509.

49. Sennes MGS, Carvalho LML, Castro MAA, Toccoli GM, Farias SO, Fialho DMC, Bertollo EMG, Pavarino EC, de Athayde LS, Buck CB, Toralles MBP, Melaragno MI, Riegel-Giugliani M, Spolador GM, Otto PA, Piai CB, Kok F, Cechella CS, Rosenberg C, Llerena JC, Bertola DR, Raskin S, Kim CA, Krepischi ACV. Clinical and Molecular Characterization of Xia-Gibbs Syndrome: Expanding the Phenotypic Spectrum in a Brazilian Cohort. Clin Genet. 2025 Jun 11. doi: 10.1111/cge.14777.

50. Sherwood M, Mitsugi TG, Kaid C, Coke B, Zatz M, Maringer K, Okamoto OK, Ewing RM. Multi-omics analysis reveals key immunogenic signatures induced by oncolytic Zika virus infection of paediatric brain tumour cells. Sci Rep. 2025 Apr 16;15(1):13090. doi: 10.1038/s41598-025-97804-8.

51. Schwartz-Marin E, Jiwani T, Abel S, Egorova Y, M'charek A, Meyer D, Moreno Estrada A, Schramm K, Wade P, Naslavsky M. Genetic ancestry and the colonial legacies of race in genomics: a cross-disciplinary dialogue. Front Genet. 2025 Jan 23;15:1523406. doi: 10.3389/fgene.2024.1523406. eCollection 2024.

52. Suemoto CK,Leite REP, Paes VR, Rodriguez RD, Justo AFO, Naslavsky MS, Zatz M, Pasqualucci CA, Nitrini R, Ferriolli E, Jacob‐Filho W, Lea T Grinberg LT. Racial differences in neuropathology and cognitive abilities. Alzheimer's & Dementia. 2025 Jan 9;20(Suppl 7):e090333. doi: 10.1002/alz.090333

53. Silva HCA, Mendonça DC, Souza BW, Santos JM, Souza LS, Junior AFR, Vasconcelos FTGR, Andrade PV, Oliveira ASB, Vainzof M. Genetic Characteristics of Brazilian Patients with MH History. Genes (Basel). 2025 Sep 25;16(10):1127. doi: 10.3390/genes16101127. PMID: 41153347; PMCID: PMC12562892.

54. Sherwood M, Nicholas B, Bailey A, Mitsugi TG, Kaid C, Okamoto OK, et al. (2025) Identification of natural Zika virus peptides presented on the surface of paediatric brain tumour cells by HLA class I. PLoS One 20(10): e0335726. https://doi.org/10.1371/journal.pone.0335726.

55. Sherwood M, Mitsugi TG, Kaid C, Coke B, Zatz M, Maringer K, Okamoto OK, Ewing RM. Multi-omics analysis reveals key immunogenic signatures induced by oncolytic Zika virus infection of paediatric brain tumour cells. Sci Rep. 2025 Apr 16;15(1):13090. doi: 10.1038/s41598-025-97804-8. PMID: 40240536; PMCID: PMC12003866.

56. Suemoto CK, Paradela R, Leite REP, Paes VR, Pasqualucci CA, Ferriolli E, Zatz M, do Nascimento Santos G, de Alexandria MALS, Pereira AC, Fortea J, Naslavsky M, Grinberg LT. Apolipoprotein E and Alzheimer's disease pathology in a diverse autopsy study. Alzheimers Dement. 2025 Nov;21(11):e70927. doi: 10.1002/alz.70927.PMID: 41268805

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