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Page 1
The Genomic Profile Associated with Risk of Severe Forms of COVID-19 in Amazonian Native American Populations.
Pastana LF, Silva TA, Gellen LPA, Vieira GM, de Assunção LA, Leitão LPC, da Silva NM, Coelho RCC, de Alcântara AL, Vinagre LWMS, Rodrigues JCG, Borges Leal DFDV, Fernandes MR, de Souza SJ, Kroll JE, Ribeiro-Dos-Santos AM, Burbano RMR, Guerreiro JF, de Assumpção PP, Ribeiro-Dos-Santos ÂC, Dos Santos SEB, Dos Santos NPC. Pastana LF, et al. Among authors: kroll je. J Pers Med. 2022 Apr 1;12(4):554. doi: 10.3390/jpm12040554. J Pers Med. 2022. PMID: 35455670 Free PMC article.
A Benchmark of In-House Homologous Recombination Repair Deficiency Testing Solutions for High-Grade Serous Ovarian Cancer Diagnosis.
Guarischi-Sousa R, Kroll JE, Bonaldi A, Pierry PM, Villela D, Souza CA, Silva JS, Bürger MC, Oliveira FA, de Paula MG, Meliso FM, de Almeida LG, Monfredini PM, de Oliveira AG, Milanezi F, Scapulatempo-Neto C, Yamamoto GL. Guarischi-Sousa R, et al. Among authors: kroll je. Diagnostics (Basel). 2023 Oct 24;13(21):3293. doi: 10.3390/diagnostics13213293. Diagnostics (Basel). 2023. PMID: 37958189 Free PMC article.
Identification of NUDT15 gene variants in Amazonian Amerindians and admixed individuals from northern Brazil.
Rodrigues JCG, Souza TP, Pastana LF, Ribeiro Dos Santos AM, Fernandes MR, Pinto P, Wanderley AV, Souza SJ, Kroll JE, Pereira AL, Magalhães L, Mercês LRD, Vidal AF, Vinasco-Sandoval T, Cavalcante GC, Guerreiro JF, Assumpção PP, Ribeiro-Dos-Santos Â, Santos S, Santos NPCD. Rodrigues JCG, et al. Among authors: kroll je. PLoS One. 2020 Apr 15;15(4):e0231651. doi: 10.1371/journal.pone.0231651. eCollection 2020. PLoS One. 2020. PMID: 32294118 Free PMC article.
Identification of Variants (rs11571707, rs144848, and rs11571769) in the BRCA2 Gene Associated with Hereditary Breast Cancer in Indigenous Populations of the Brazilian Amazon.
Dobbin EAF, Medeiros JAG, Costa MSCR, Rodrigues JCG, Guerreiro JF, Kroll JE, Souza SJ, de Assumpção PP, Ribeiro-Dos-Santos Â, Santos SEBD, Burbano RMR, Fernandes MR, Santos NPCD. Dobbin EAF, et al. Among authors: kroll je. Genes (Basel). 2021 Jan 22;12(2):142. doi: 10.3390/genes12020142. Genes (Basel). 2021. PMID: 33499154 Free PMC article.
Low-pass whole genome sequencing is a reliable and cost-effective approach for copy number variant analysis in the clinical setting.
Mazzonetto PC, Villela D, da Costa SS, Krepischi ACV, Milanezi F, Migliavacca MP, Pierry PM, Bonaldi A, Almeida LGD, De Souza CA, Kroll JE, Paula MG, Guarischi-Sousa R, Scapulatempo-Neto C, Rosenberg C. Mazzonetto PC, et al. Among authors: kroll je. Ann Hum Genet. 2024 Mar;88(2):113-125. doi: 10.1111/ahg.12532. Epub 2023 Oct 9. Ann Hum Genet. 2024. PMID: 37807935
Whole genome sequencing as a first-tier diagnostic test for infants in neonatal intensive care units: A pilot study in Brazil.
Migliavacca MP, Sobreira J, Bermeo D, Gomes M, Alencar D, Sussuchi L, Souza CA, Silva JS, Kroll JE, Burger M, Guarischi-Sousa R, Villela D, Yamamoto GL, Milanezi F, Horigoshi N, Cesar RG, de Carvalho WB, Honjo RS, Bertola DR, Kim CA, de Souza L, Procianoy RS, Silveria RC, Rosenberg C, Giugliani R, Campana GA, Scapulatempo-Neto C, Sobreira N. Migliavacca MP, et al. Among authors: kroll je. Am J Med Genet A. 2024 Jan 23. doi: 10.1002/ajmg.a.63544. Online ahead of print. Am J Med Genet A. 2024. PMID: 38258498
14 results