Publications by authors named "Monize Lazar"

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Childhood Hypophosphatasia Associated with a Novel Biallelic Variant at the TNSALP Dimer Interface.
Luciane Martins, Luis Gustavo F Lessa, Taccyanna M Ali, Monize Lazar, Chong A Kim

Int J Mol Sci· December 2022

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Nemaline Myopathy in Brazilian Patients: Molecular and Clinical Characterization.
Juliana Gurgel-Giannetti, Lucas Santos Souza, Guilherme L Yamamoto, Marina Belisario, Monize Lazar

Int J Mol Sci· October 2022

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Germline variants of Brazilian women with breast cancer and detection of a novel pathogenic ATM deletion in early-onset breast cancer.
Gabriel Bandeira, Katia Rocha, Monize Lazar, Suzana Ezquina, Guilherme Yamamoto

Breast Cancer· March 2021

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Altered muscle differentiation in X-linked myopathy with excessive autophagy.
Stephanie A Fernandes, Camila F Almeida, Lucas S Souza, Monize Lazar, Paula Onofre-Oliveira

Dis Model Mech· January 2020

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Exomic variants of an elderly cohort of Brazilians in the ABraOM database.
Michel Satya Naslavsky, Guilherme Lopes Yamamoto, Tatiana Ferreira de Almeida, Suzana A M Ezquina, Daniele Yumi Sunaga, Monize Lazar

Hum Mutat· July 2017

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What is the best way to determine the cause of adolescent idiopathic scoliosis?
Marcelo Wajchenberg, Delio Eulalio Martins, Monize Lazar

Ann Transl Med· March 2015

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Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility.
Rodrigo A Toledo, Roxanne Hatakana, Delmar M Lourenço, Susan C Lindsey, Cleber P Camacho, Monize Lazar

Endocr Relat Cancer· February 2015

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Mutations in PCYT1A cause spondylometaphyseal dysplasia with cone-rod dystrophy.
Guilherme L Yamamoto, Wagner A R Baratela, Tatiana F Almeida, Monize Lazar, Clara L Afonso

Am J Hum Genet· January 2014

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Assessing pathogenicity for novel mutation/sequence variants: the value of healthy older individuals.
Mayana Zatz, Rita de Cassia M Pavanello, Naila Cristina V Lourenço, Antonia Cerqueira, Monize Lazar

Neuromolecular Med· December 2012

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Downregulation of VAPB expression in motor neurons derived from induced pluripotent stem cells of ALS8 patients.
Miguel Mitne-Neto, Marcela Machado-Costa, Maria C N Marchetto, Mario H Bengtson, Claudio A Joazeiro, Monize Lazar

Hum Mol Genet· September 2011

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Genetic aspects of adolescent idiopathic scoliosis in a family with multiple affected members: a research article.
Marcelo Wajchenberg, Monize Lazar, Natale Cavaçana, Delio Eulalio Martins, Luciana Licinio

Scoliosis· April 2010

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