Maria Luiza Petzl‐erler - Genetic Mutations

Author Information

Maria Luiza Petzl-Erler is affiliated with the Laboratory of Human Molecular Genetics at the Department of Genetics, Universidade Federal do Paraná in Curitiba, Brazil. Her work focuses on areas within the field of genetics, particularly involving molecular genetics and its application to various human populations and diseases.

Research Contributions

Maria Luiza Petzl-Erler has made significant contributions to the field of genetics, with a particular focus on population genetics and the genetic basis of diseases. Her recent research includes studies on uniparental markers to understand ancestry and admixture in Brazil, the genetic structure of Amerindian populations, genetic associations related to diseases like pemphigus foliaceus, and the genetic diversity among Native American populations. Additionally, she has explored the genetic factors associated with diseases such as COVID-19 and Alzheimer's disease. Her work often involves examining genetic diversity and its implications for health and disease susceptibility.

Aliases

Maria Luiza Petzl-Erler has published under several aliases, including M Luiza Petzl-erler, M. Luiza Petzl-erler, María Luiza Petzl-erler, and others. These variations reflect common practices in academic publishing where authors might use different versions of their names across different publications.

Publication and Citation Metrics

Metric	Value
Citation Count	6543
h-index	36
Paper Count	176

Publications:

Uniparental markers reveal new insights on subcontinental ancestry and sex-biased admixture in Brazil.

DOI: 10.1007/s00438-022-01857-7

Year: 2022

Population structure and forensic genetic analyses in Guarani and Kaingang Amerindian populations from Brazil.

DOI: 10.1016/j.fsigen.2022.102678

Year: 2022

Genetic Associations and Differential mRNA Expression Levels of Host Genes Suggest a Viral Trigger for Endemic Pemphigus Foliaceus

DOI: 10.3390/v14050879

Year: 2022

Single Nucleotide Variants as Proxies for HLA-A*31:01 in Native American Populations

DOI: 10.3389/fphar.2022.849136

Year: 2022

Tracing the Distribution of European Lactase Persistence Genotypes Along the Americas

DOI: 10.3389/fgene.2021.671079

Year: 2021

Genetic association and differential expression of HLAComplexGroup lncRNAs in pemphigus.

DOI: 10.1016/j.jaut.2021.102705

Year: 2021

An immunogenetic view of COVID-19

DOI: 10.1590/1678-4685-GMB-2021-0036

Year: 2021

COVID-19: The question of genetic diversity and therapeutic intervention approaches.

DOI: 10.1590/1678-4685-gmb-2020-0452

Year: 2021

GWAS-Top Polymorphisms Associated With Late-Onset Alzheimer Disease in Brazil: Pointing Out Possible New Culprits Among Non-Coding RNAs

DOI: 10.3389/fmolb.2021.632314

Year: 2021

Remarkably low KIR and HLA diversity in Amerindians reveals signatures of strong purifying selection shaping the centromeric KIR region.

DOI: 10.1093/molbev/msab298

Year: 2021

Can Nucleotide Mutations Be Repaired?

How Does Genetic Drift Play a Role?

What is Genetic Sequencing?

What Measures Can Be Taken to Mitigate the Risks?

What is Meiosis?

What Types of Prenatal Tests Are Available?

How are Autosomal Recessive Disorders Diagnosed?

What is Gene Cloning?

What Are the Consequences of Gene Amplification?

What is Cellular Heterogeneity?

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