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18. da Silva Montenegro EM, Costa CS, Campos G, Scliar M, de Almeida TF, Zachi EC, Silva IMW, Chan AJS, Zarrei M, Lourenço NCV, Yamamoto GL, Scherer S, Passos-Bueno MR. Meta-Analyses Support Previous and Novel Autism Candidate Genes: Outcomes of an Unexplored Brazilian Cohort. Autism Res. 2020 Feb;13(2):199-206. doi: 10.1002/aur.2238. Epub 2019 Nov 6.PMID: 31696658
19. da Silva Filho LVRF, Maróstica PJC, Athanazio RA, Reis FJC, Damaceno N, Paes AT, Hira AY, Schlesinger D, Kok F, Amaral MD; Brazilian Cystic Fibrosis Patient Registry Contributors Team. Extensive CFTR sequencing through NGS in Brazilian individuals with cystic fibrosis: unravelling regional discrepancies in the country . J Cyst Fibros. 2020 Aug 17:S1569-1993(20)30822-5. doi: 10.1016/j.jcf.2020.08.007. Online ahead of print.PMID: 32819855;
20. de Assis LVM, Mendes D, Silva MM, Kinker GS, Pereira-Lima I, Moraes MN, Menck CFM, Castrucci AML. Melanopsin mediates UVA-dependent modulation of proliferation, pigmentation, apoptosis, and molecular clock in normal and malignant melanocytes. Biochim Biophys Acta Mol Cell Res. 2020 Oct;1867(10):118789. doi: 10.1016/j.bbamcr.2020.118789. Epub 2020 Jul 6.PMID: 32645331.
21. de Lima-Pardini AC, Coelho DB, Nucci MP, Boffino CC, Batista AX, de Azevedo Neto RM, Silva-Batista C, Barbosa ER, Cohen RG, Horak FB, Teixeira LA, Amaro E Jr. Brain networks associated with anticipatory postural adjustments in Parkinson's disease patients with freezing of gait. Neuroimage Clin. 2020;28:102461. doi: 10.1016/j.nicl.2020.102461. Epub 2020 Oct 8.PMID: 33395957 Free PMC article.
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26. Fuentes-León F, Peres de Oliveira A, Quintero-Ruiz N, Munford V, Satoru Kajitani G, Coimbra Brum A, Schuch AP, Colepicolo P, Sánchez-Lamar A, Menck CFM. DNA Damage Induced by Late Spring Sunlight in Antarctica. Photochem Photobiol. 2020 Nov;96(6):1215-1220. doi: 10.1111/php.13307. Epub 2020 Jul 24.PMID: 32614978
27. Galleni Leão L, Santos Souza L, Nogueira L, Pavanello RCM, Gurgel-Giannetti J, Reed UC, Oliveira ASB, Cuperman T, Cotta A, FPaim J, Zatz M, Vainzof M. Dominant or recessive mutations in the RYR1 gene causing central core myopathy in Brazilian patients. Acta Myol. 2020 Dec 1;39(4):274-282. doi: 10.36185/2532-1900-030. eCollection 2020 Dec.PMID: 33458582.
28. Gracitelli CPB, Gerente VM, Furlanetto RL, Amaro E Jr, Paranhos A Jr. Magnetic Resonance Imaging for Glaucoma Evaluation. J Glaucoma. 2020 Aug;29(8):622-626. doi: 10.1097/IJG.0000000000001558.PMID: 32459691 Review.
29. Gracitelli CPB, Duque-Chica GL, Sanches LG, Moura AL, Nagy BV, Teixeira SH, Amaro E Jr, Ventura DF, Paranhos A Jr. Structural Analysis of Glaucoma Brain and its Association With Ocular Parameters. J Glaucoma. 2020 May;29(5):393-400. doi: 10.1097/IJG.0000000000001470.PMID: 32079996
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31. Griesi-Oliveira K, Fogo MS, Pinto BGG, Alves AY, Suzuki AM, Morales AG, Ezquina S, Sosa OJ, Sutton GJ, Sunaga-Franze DY, Bueno AP, Seabra G, Sardinha L, Costa SS, Rosenberg C, Zachi EC,Sertie AL, Martins-de-Souza D, Reis EM, Voineagu I, Passos-Bueno MR. Transcriptome of iPSC-derived neuronal cells reveals a module of co-expressed genes consistently associated with autism spectrum disorder. Mol Psychiatry. 2020 Feb 14. doi: 10.1038/s41380-020-0669-9. Online ahead of print.PMID: 32060413
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36. Jacobacci F, Jovicich J, Lerner G, Amaro E Jr, Armony JL, Doyon J, Della-Maggiore V. Improving Spatial Normalization of Brain Diffusion MRI to Measure Longitudinal Changes of Tissue Microstructure in the Cortex and White Matter. J Magn Reson Imaging. 2020 Feb 14. doi: 10.1002/jmri.27092. Online ahead of print.
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38. Kaid C, Madi RADS, Astray R, Goulart E, Caires-Junior LC, Mitsugi TG, Moreno ACR, Castro-Amarante MF, Pereira LR, Porchia BFMM, de Andrade TO, Landini V, Sanches DS, Pires CG, Tanioka RKO, Pereira MCL, Barbosa IN, Massoco CO, Ferreira LCS, Okamoto OK, Zatz M. Safety, Tumor Reduction, and Clinical Impact of Zika Virus Injection in Dogs with Advanced-Stage Brain Tumors. Mol Ther. 2020 May 6;28(5):1276-1286. doi: 10.1016/j.ymthe.2020.03.004. Epub 2020 Mar 10.PMID: 32220305 Free article.
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42. Jacobacci F, Armony JL, Yeffal A, Lerner G, Amaro E Jr , Jovicich J, Doyon J, Della-Maggiore V. Rapid hippocampal plasticity supports motor sequence learning . Proc Natl Acad Sci U S A. 2020 Sep 22;117(38):23898-23903. doi: 10.1073/pnas.2009576117. Epub 2020 Sep 8.PMID: 32900965.
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44. Kumar A, Furtado VL, Gonçalves JM, Bannitz-Fernandes R, Netto LES, Araki K, Bertotti M. Amperometric microsensor based on nanoporous gold for ascorbic acid detection in highly acidic biological extracts . Anal Chim Acta. 2020 Jan 25;1095:61-70. doi: 10.1016/j.aca.2019.10.022. Epub 2019 Oct 16.PMID: 31864631.
45. Lerner LK, Nguyen TV, Castro LP, Vilar JB, Munford V, Le Guillou M, Mohammad MM, Vergé V, Rosselli F, Menck CFM, Sarasin A, Aoufouchi S. Large deletions in immunoglobulin genes are associated with a sustained absence of DNA Polymerase η. Sci Rep. 2020 Jan 28;10(1):1311. doi: 10.1038/s41598-020-58180-7.PMID: 31992747 Free PMC article.
46. Lima DDS, Baran LCP, Hamer RD, Costa MFD, Vidal KS, Damico FM, Barboni MTS, França VCRM, Martins CMG, Tabares HS, Dias SL, Silva LA, Decleva D, Zatz M, Bertozzi APAP, Gazeta RE, Passos SD, Ventura DF. Longitudinal visual acuity development in ZIKV-exposed children . J AAPOS. 2020 Feb;24(1):23.e1-23.e6. doi: 10.1016/j.jaapos.2019.11.005. Epub 2020 Jan 8.PMID: 31926367.
47. Louzada S, Algady W, Weyell E, Zuccherato LW, Brajer P, Almalki F, Scliar MO, Naslavsky MS, Yamamoto GL,Duarte YAO, Passos-Bueno MR, Zatz M, Yang F, Hollox EJ. Structural variation of the malaria-associated human glycophorin A-B-E region. BMC Genomics. 2020 Jun 29;21(1):446. doi: 10.1186/s12864-020-06849-8.PMID: 32600246 Free PMC article.
48. Machado DR, Kimura M, Duarte YAO, Lebrão ML. [Violence perpetrated against the elderly and health-related quality of life: a populational study in the city of São Paulo, Brazil]. Cien Saude Colet. 2020 Mar;25(3):1119-1128. doi: 10.1590/1413-81232020253.19232018. Epub 2018 Jul 30.PMID: 32159679.
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50. Mariano FV, Fidalgo F, Casarim ALM, Martins AS, Scarini JF, de Lima Souza RA, Egal ES, Kowalski LP, Krepischi ACV, Altemani A. Somatic copy number alterations in pleomorphic adenoma and recurrent pleomorphic adenoma. Oral Surg Oral Med Oral Pathol Oral Radiol. 2020 Jan;129(1):59-64. doi: 10.1016/j.oooo.2019.08.016. Epub 2019 Sep 2.PMID: 31607675.
51. Martins Trevisan C, Naslavsky MS, Monfardini F, Wang J, Zatz M, Peluso C, Pellegrino R, Mafra F, Hakonarson H, Ferreira FM, Nakaya H, Christofolini DM, Montagna E, Crandall KA, Barbosa CP, Bianco B. Variants in the Kisspeptin-GnRH Pathway Modulate the Hormonal Profile and Reproductive Outcomes. DNA Cell Biol. 2020 Jun;39(6):1012-1022. doi: 10.1089/dna.2019.5165. Epub 2020 Apr 29.PMID: 32352843.
52. Masuda HP, Nakabashi M, Morgante PG, Kajihara D, de Setta N, Menck CFM, Van Sluys MA. Evidence for sub-functionalization of tandemly duplicated XPB nucleotide excision repair genes in Arabidopsis thaliana. Gene. 2020 Sep 5;754:144818. doi: 10.1016/j.gene.2020.144818. Epub 2020 May 30.PMID: 32485308
53. Mendonça RH, Matsui C Jr, Polido GJ, Silva AMS, Kulikowski L, Torchio Dias A, Zanardo EA, Solla DJF, Gurgel-Giannetti J, de Moura ACML, Sampaio GPC, Oliveira ASB, de Souza PVS, Pinto WBVR, Gonçalves EA, Farias IB, Nardes F, Araújo APQC, Marques W Jr, Tomaselli PJ, Ribeiro MDO, Kitajima JP, Paoli Monteiro F, Saute JAM, Becker MM, Saraiva-Pereira ML, Brusius-Facchin AC, van der Linden V, Florêncio RN, Barbosa AVS, Machado-Costa MC, Pessoa ALS, Souza LS, Franca MC Jr, Kok F, Reed UC, Zanoteli E. Intragenic variants in the SMN1 gene determine the clinical phenotype in 5q spinal muscular atrophy. Neurol Genet. 2020 Sep 1;6(5):e505. doi: 10.1212/NXG.0000000000000505. eCollection 2020 Oct.PMID: 33062891 Free PMC article.
54. Miotto EC, Bazán PR, Batista AX, Conforto AB, Figueiredo EG, Martin MDGM, Avolio IB, Amaro E Jr, Teixeira MJ. Behavioral and Neural Correlates of Cognitive Training and Transfer Effects in Stroke Patients. Front Neurol. 2020 Sep 15;11:1048. doi: 10.3389/fneur.2020.01048. eCollection 2020.PMID: 33041987 Free PMC article.
55. Monteiro FP, Curry CJ, Hevner R, Elliott S, Fisher JH, Turocy J, Dobyns WB, Costa LA, Freitas E, Kitajima JP, Kok F. Biallelic loss of function variants in ATP1A2 cause hydrops fetalis, microcephaly, arthrogryposis and extensive cortical malformations. Eur J Med Genet. 2020 Jan;63(1):103624. doi: 10.1016/j.ejmg.2019.01.014. Epub 2019 Jan 25.PMID: 30690204
56. Moreno NC, de Souza TA, Garcia CCM, Ruiz NQ, Corradi C, Castro LP, Munford V, Ienne S, Alexandrov LB, Menck CFM. Whole-exome sequencing reveals the impact of UVA light mutagenesis in xeroderma pigmentosum variant human cells. Nucleic Acids Res. 2020 Feb 28;48(4):1941-1953. doi: 10.1093/nar/gkz1182.PMID: 31853541 Free PMC article.
57. Oliveira D, Morales-Vicente DA, Amaral MS, Luz L, Sertié AL, Leite FS, Navarro C, Kaid C, Esposito J, Goulart E, Caires L, Alves LM, Melo US, Figueiredo T, Mitne-Neto M,Okamoto OK, Verjovski-Almeida S, Zatz M. Different gene expression profiles in iPSC-derived motor neurons from ALS8 patients with variable clinical courses suggest mitigating pathways for neurodegeneration. Hum Mol Genet. 2020 Jun 3;29(9):1465-1475. doi: 10.1093/hmg/ddaa069.PMID: 32280986
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60. Onofre-Oliveira PCG, Vainzof M. Isolation and Characterization of Muscle-Derived Stem Cells from Dystrophic Mouse Models. Methods Mol Biol. 2020;2063:171-180. doi: 10.1007/978-1-0716-0138-9_13.PMID: 31667770
61. Peres de Oliveira A, Basei FL, Slepicka PF, de Castro Ferezin C, Melo-Hanchuk TD, de Souza EE, Lima TI, Dos Santos VT, Mendes D, Silveira LR, Menck CFM, Kobarg J. NEK10 interactome and depletion reveal new roles in mitochondria. Proteome Sci. 2020 Apr 28;18:4. doi: 10.1186/s12953-020-00160-w. eCollection 2020.PMID: 32368190 Free PMC article.
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