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Liya Regina Mikami

Observed names: L.R. Mikami, Liya Mikami, Liya R Mikami, Liya R. Mikami, Liya Regina MIKAMI, Liya Regina Mikami Wormsbecker, Mikami Liya Regina, Mikami, Liya, Mikami, Liya Regina
Observed institutions: Universidade Estadual de Maringá, Pontifícia Universidade Católica do Paraná, Universidade Presbiteriana Mackenzie, Faculdade Evangélica do Paraná, UniBrasil Centro Universitário, Universidade Federal do Paraná, University of Nebraska Medical Center
ORCID: 0000-0003-1234-7549
Observed ORCID: 0000-0003-1234-7549
OpenAlex ID: A5081043078
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies
2016 · Claire Redin, Harrison Brand, et al. · Nature Genetics · 341
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Four new mutations in the BCHE gene of human butyrylcholinesterase in a Brazilian blood donor sample
2005 · Ricardo L.R. Souza, Liya R. Mikami, et al. · Molecular Genetics and Metabolism · 55
Five new naturally occurring mutations of the BCHE gene and frequencies of 12 butyrylcholinesterase alleles in a Brazilian population
2008 · Liya R. Mikami, Stacy Wieseler, et al. · Pharmacogenetics and Genomics · 41
Association of variants of the −116 site of the butyrylcholinesterase BCHE gene to enzyme activity and body mass index
2008 · Lupe Furtado-Alle, Fabiana A. Andrade, et al. · Chemico-Biological Interactions · 36
Mutações Do Gene Do Receptor De Vitamina D E Níveis Séricos De Vitamina D Em Crianças Com Asma
2018 · Hevertton Luiz Bozzo Silva Santos, Silvia de Souza e Silva, et al. · Revista Paulista de Pediatria · 20
Two new mutations of the human BCHE gene (IVS3-14T>C and L574fsX576)
2008 · Fernando Parmo-Folloni, Kelly Nunes, et al. · Chemico-Biological Interactions · 9
Short-term Prophylaxis for Delivery in Pregnant Women with Hereditary Angioedema with Normal C1-Inhibitor
2020 · Caroline Guth de Freitas Batista de Moraes, Liya Regina Mikami, et al. · Revista Brasileira Ginecologia e Obstetrícia · 8
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Study of angiopoietin and plasminogen genes in hereditary angioedema
2020 · Tatielly Kruk, Herberto José Chong-Neto, et al. · Revista da Associação Médica Brasileira · 6
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Expression of three naturally occurring genetic variants (G75R, E90D, I99M) of the BCHE gene of human butyrylcholinesterase
2007 · Liya R. Mikami, Stacy Wieseler, et al. · Pharmacogenetics and Genomics · 5
Intolerância à lactose: diagnóstico clínico laboratorial e genético
2022 · Beatriz França Castellano, Carolina Maria Aumann Sardá, et al. · BioSCIENCE · 4
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Autism and duplication of 17q12q21.2 by array-CGH: a case report
2023 · Alana Weingartner, Naiara Bozza Pegoraro, et al. · Revista Paulista de Pediatria · 3
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Dopamine DRD4 gene polymorphism as a risk factor for epilepsy in autism spectrum disorder
2020 · Wehmuth Mariane, Antoniuk Sergio A, et al. · Journal of Biology and Medicine · 3
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Vitamin D Receptor Gene Mutations and Vitamin D Serum Levels in Asthmatic Children
2018 · Santos, Hevertton Luiz Bozzo Silva, Silva, Silvia de Souza e, et al. · Figshare · 3
Association between RAPH1 Gene Haplotypes and CHE2 Locus Phenotypes
2016 · Fabiana A. De Andrade, Meire S. Batistela, et al. · Annals of Human Genetics · 2
Nuclear halo from Bradysia hygida (Diptera:Sciaridae) salivary gland polytene cells
2005 · Celso Aparecido Polinarski, José Luis da Conceição Silva, et al. · Brazilian Archives of Biology and Technology · 2
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Variabilidade dos exons 2 e 4 do gene BCHE e sua relaçao com a atividade da butirilcolinesterase
2005 · Liya Regina Mikami · LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) · 2
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Drosophila Salivary Gland Polytene Nuclear Halo: A New Approach for Polytene Nuclear Matrix Analysis.
2001 · Liya Regina Mikami, Celso Aparecido Polinarski, et al. · CYTOLOGIA · 2
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P677: Whole-exome sequencing identifies new candidate genes for non-syndromic orofacial clefts
2026 · Vitor Henrique Bida, Felipe Ricardo Oliveira, et al. · Genetics in Medicine Open · 1
Aconselhamento genético e autismo: novas perspectivas para diagnóstico e intervenção
2025 · João Marcos Valentim Dos Santos, Isabela Garrett Portugal, et al. · BioSCIENCE · 1
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Como contornar o impacto das doenças genéticas na vida dos pacientes e seus familiares?
2025 · Fernanda Ritt De Souza, Cornelio Schwamabach, et al. · BioSCIENCE · 1
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Disbiose Da Microbiota Cervicovaginal No Desenvolvimento Do Câncer De Colo De Útero: Uma Revisão Narrativa
2022 · Gabriel Dziurkovski Machado, Felipe Mota Narciso de Morais, et al. · BioSCIENCE · 1
Relevância Do Diagnóstico Genético Na Identificação De Variantes Genéticas Raras Em Duas Famílias Brasileiras Com Síndrome De Alport: Relato De Caso
2022 · Isadora Kertscher, Fernada Arissa Takii, et al. · BioSCIENCE · 1
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Investigação genética relacionada a fisiopatologia e sintomas clínicos do Angioedema Hereditário
2020 · Tatielly Kruk, Lucas Marques Fortunato, et al. · Research Society and Development · 1
Síndromes cromossômicas: uma revisão
2014 · Jhulie Caroline Mirandola de Souza, Maria Marlene Solarewicz, et al. · Cadernos da Escola de Saúde · 1
Genetic Landscape and in Silico Predictions of Variants of Uncertain Significance (VUS) in a Southern Brazilian Hereditary Cancer Cohort
2026 · Fernanda Arissa Takii, Gabriel Dziurkovski Machado, et al. · Brazilian Journal of Oncology
Works count: 64
Citation count: 549
H-index: 7
I10-index: 5
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