Publications by authors named "Nadia Pinto"

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Statistical interpretation of cases involving mixtures: A Spanish and Portuguese-Speaking Working Group (GHEP-ISFG) collaborative exercise.
Camila Costa, Juan Carlos Álvarez, Sofia Angeletti, Sebastian Biagini, Mariela Caputo, Nádia Pinto

Forensic Sci Int Genet· February 2026

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MHappaMundi: A custom AmpliSeq microhaplotype panel for ancestry inference.
Pedro Rodrigues, Nádia Pinto, Maria João Prata, Rodrigo Flores-Espinoza, Germán Burgos

Forensic Sci Int Genet· February 2026

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Hereditary diffuse gastric cancer spectrum associated with germline loss of function revealed by clinical and molecular data from 351 carrier families and over 37 000 non-carrier controls.
Silvana Lobo, Alexandre Dias, Ana Maria Pedro, Marta Ferreira, André Pinto-Oliveira, Nádia Pinto

Gut· November 2025

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The impact of considering different numbers of contributors in identification problems involving real casework mixture samples.
Camila Costa, Carolina Figueiredo, Sandra Costa, Paulo Miguel Ferreira, António Amorim, Nádia Pinto

Int J Legal Med· September 2025

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Stutter Modeling in Probabilistic Genotyping for Forensic DNA Analysis: A Casework-Driven Assessment.
Camila Costa, Érica Pereira, Sandra Costa, Paulo Miguel Ferreira, António Amorim, Nádia Pinto

Genes (Basel)· September 2025

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Navigating the blurred boundary: Neuropathologic changes versus clinical symptoms in Alzheimer's disease, and its consequences for research in genetics.
Catarina Xavier, Nádia Pinto

J Alzheimers Dis· April 2025

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Enhancing the Potential of Microhaplotypes for Forensic Applications: Insights from Afghan and Somali Populations.
Pedro Rodrigues, Nádia Pinto, Tess Otterlund, Carina G Jønck, Maria João Prata

Genes (Basel)· April 2025

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[Role of ultrasound in critically ill patients with heart failure].
Julieta Lozita, Juan Pablo Leopoldo Ricarte Bratti, Judith Mailen Vicentin, Nadia Elizabeth Pinto

Rev Fac Cien Med Univ Nac Cordoba· March 2025

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A mathematical framework for genetic relatedness analysis involving X chromosome aneuploidies.
Marisa Faustino, Leonor Gusmão, António Amorim, Daniel Kling, Nádia Pinto

Forensic Sci Int Genet· January 2025

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The impact of parameter variation in the quantification of forensic genetic evidence.
Camila Costa, Carolina Figueiredo, Sandra Costa, Paulo Miguel Ferreira, António Amorim, Nádia Pinto

Sci Rep· January 2025

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Integrating functional scoring and regulatory data to predict the effect of non-coding SNPs in a complex neurological disease.
Daniela Felício, Miguel Alves-Ferreira, Mariana Santos, Marlene Quintas, Alexandra M Lopes, Nádia Pinto

Brief Funct Genomics· March 2024

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Microsatellites' mutation modeling through the analysis of the Y-chromosomal transmission: Results of a GHEP-ISFG collaborative study.
Sofia Antão-Sousa, Leonor Gusmão, Nidia M Modesti, Sofía Feliziani, Marisa Faustino, Nadia Pinto

Forensic Sci Int Genet· March 2024

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The sequence of the repetitive motif influences the frequency of multistep mutations in Short Tandem Repeats.
Sofia Antão-Sousa, Nádia Pinto, Pablo Rende, António Amorim, Leonor Gusmão

Sci Rep· June 2023

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Non-coding variants in VAMP2 and SNAP25 affect gene expression: potential implications in migraine susceptibility.
Daniela Felício, Andreia Dias, Sandra Martins, Estefânia Carvalho, Alexandra M Lopes, Nádia Pinto

J Headache Pain· June 2023

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Genotype-first approach to identify associations between CDH1 germline variants and cancer phenotypes: a multicentre study by the European Reference Network on Genetic Tumour Risk Syndromes.
José Garcia-Pelaez, Rita Barbosa-Matos, Silvana Lobo, Alexandre Dias, Luzia Garrido, Nádia Pinto, Carla Pinto

Lancet Oncol· January 2023

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Quantification of forensic genetic evidence: Comparison of results obtained by qualitative and quantitative software for real casework samples.
Camila Costa, Carolina Figueiredo, António Amorim, Sandra Costa, Paulo Miguel Ferreira, Nádia Pinto

Forensic Sci Int Genet· July 2022

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Estimations of Mutation Rates Depend on Population Allele Frequency Distribution: The Case of Autosomal Microsatellites.
Sofia Antão-Sousa, Eduardo Conde-Sousa, Leonor Gusmão, António Amorim, Nádia Pinto

Genes (Basel)· July 2022

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A High Methylation Level of a Novel -284 bp CpG Island in the Gene Promoter Is Potentially Associated with Migraine in Women.
Estefânia Carvalho, Andreia Dias, Alda Sousa, Alexandra M Lopes, Sandra Martins, Nádia Pinto

Brain Sci· April 2022

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Influence of PICALM and CLU risk variants on beta EEG activity in Alzheimer's disease patients.
Aarón Maturana-Candelas, Carlos Gómez, Jesús Poza, Víctor Rodríguez-González, Vìctor Gutiérrez-de Pablo, Nadia Pinto

Sci Rep· October 2021

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Risk Variants in Three Alzheimer's Disease Genes Show Association with EEG Endophenotypes.
Ana Macedo, Carlos Gómez, Miguel Ângelo Rebelo, Jesús Poza, Iva Gomes, Nádia Pinto

J Alzheimers Dis· September 2021

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4SpecID: Reference DNA Libraries Auditing and Annotation System for Forensic Applications.
Luís Neto, Nádia Pinto, Alberto Proença, António Amorim, Eduardo Conde-Sousa

Genes (Basel)· January 2021

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Variants in an Iberian Alzheimer Cohort Detected through an Optimized Sanger Sequencing Protocol.
Ricardo D González, Iva Gomes, Catarina Gomes, Rita Rocha, Luís Durães, Nádia Pinto

Genes (Basel)· December 2020

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Genome-Wide Scan for Five Brain Oscillatory Phenotypes Identifies a New QTL Associated with Theta EEG Band.
Miguel Ângelo Rebelo, Carlos Gómez, Iva Gomes, Jesús Poza, Sandra Martins, Nádia Pinto

Brain Sci· November 2020

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Twenty Years Later: A Comprehensive Review of the X Chromosome Use in Forensic Genetics.
Iva Gomes, Nádia Pinto, Sofia Antão-Sousa, Verónica Gomes, Leonor Gusmão

Front Genet· September 2020

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Relationship between the Presence of the 4 Allele and EEG Complexity along the Alzheimer's Disease Continuum.
Víctor Gutiérrez-de Pablo, Carlos Gómez, Jesús Poza, Aarón Maturana-Candelas, Sandra Martins, Nádia Pinto

Sensors (Basel)· July 2020

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