Mirian Yumie Nishi (Mirian Yumi Nishi, Mirian Y Nishi, Miriam Y Nishi)

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 8

Top Topics

Transcranial Magnetic Stimulation

Polycystic Ovary Syndrome

Top Venues

Molecular genetics & genomic medicine

Clinics (Sao Paulo, Brazil)

Endocrine pathology

This page only lists publications with an associated author ORCID identifier.

Publications

Maria Luiza Anhaia de Arruda Botelho, Mirian Yumie Nishi, Karina Braga Ribeiro, Maria Claudia Nogueira Zerbini
Morphological Harbingers of ARMC5-Pathogenic Variant-Related Bilateral Macronodular Adrenocortical Disease. Endocrine pathology (2023)
José Antonio Diniz Faria, Daniela R Moraes, Leslie Domenici Kulikowski, Rafael Loch Bastista, Nathalia Lisboa Gomes, Mirian Yumie Nishi, Evelin Zanardo, Carolina Kymie Vasques Nonaka, Bruno Solano de Freitas Souza, Berenice Bilharinho Mendonca, Sorahia Domenice
Cytogenomic Investigation of Syndromic Brazilian Patients with Differences of Sexual Development. Diagnostics (Basel, Switzerland) 13 (13) (2023)
Felipe Martins Elias, Mirian Yumie Nishi, Maria Helena Palma Sircili, Rafael Loch Bastista, Nathalia Lisboa Gomes, Maria Tereza Martins Ferrari, Elaine Maria Frade Costa, Francisco Tibor Denes, Berenice Bilharinho Mendonca, Sorahia Domenice
Elevated plasma miR-210 expression is associated with atypical genitalia in patients with 46,XY differences in sex development. Molecular genetics & genomic medicine (2022)
Raiane P Crespo, Thais P Rocha, Luciana R Montenegro, Mirian Yumie Nishi, Alexander Augusto de Lima Jorge, Gustavo Arantes Rosa Maciel, Edmund Chada Baracat, Ana Claudia L Xavier, Berenice Bilharinho de Mendonca, Larissa Garcia Gomes
High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort. Journal of the Endocrine Society 6 (9) (2022)
Luciana Ribeiro Montenegro, Antonio Marcondes Lerario, Mirian Yumie Nishi, Alexander Augusto de Lima Jorge, Berenice Bilharinho de Mendonca
Performance of mutation pathogenicity prediction tools on missense variants associated with 46,XY differences of sex development. Clinics (Sao Paulo, Brazil) 76 (2021)
Vania Balderrama Brondani, Luciana Montenegro, Amanda Meneses Ferreira Lacombe, Breno Marchiori Magalhães, Mirian Yumie Nishi, Mariana Ferreira de Assis Funari, Amanda de Moraes Narcizo, Lais Cavalca Cardoso, Sheila Aparecida Coelho Siqueira, Maria Claudia Nogueira Zerbini, Francisco Tibor Denes, Ana Claudia Latronico, Berenice Bilharinho Mendonca, Madson Queiroz Almeida, Antonio Marcondes Lerario, Ibere Cauduro Soares, Maria Candida Barisson Villares Fragoso
High Prevalence of Alterations in DNA Mismatch Repair Genes of Lynch Syndrome in Pediatric Patients with Adrenocortical Tumors Carrying a Germline Mutation on TP53. Cancers 12 (3) (2020)
Monica Malheiros França, Mariana F A Funari, Antonio M Lerario, Mariza G Santos, Mirian Yumie Nishi, Sorahia Domenice, Daniela R Moraes, Everlayny F Costalonga, Gustavo A R Maciel, Andréa Trevas Maciel-Guerra, Gil Guerra-Junior, Berenice B Mendonca
Screening of targeted panel genes in Brazilian patients with primary ovarian insufficiency. PloS one 15 (10) (2020)
Nathalia Lisboa Gomes, Antônio Marcondes Lerário, Aline Zamboni Machado, Daniela Rodrigues de Moraes, Thatiana Evilen da Silva, Ivo J P Arnhold, Rafael Loch Batista, José Antônio Diniz Faria Júnior, Elaine Maria Costa, Mirian Yumie Nishi, Marlene Inacio, Sorahia Domenice, Berenice Bilharinho de Mendonca
Long-term outcomes and molecular analysis of a large cohort of patients with 46,XY disorder of sex development due to partial gonadal dysgenesis. Clinical endocrinology 89 (2) (2018)