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Nadia Pinto

Has grant

Associate Researcher

i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto

Portugal

Research Interests

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Recent Grants

Grant: Close

AgeAD - Genomic Signatures of Age-of-Onset Variation in Sporadic Alzheimer's Disease

Open Date: 2026-03-01

Close Date:

Grant: Close

CapCell - “Innovative forensic trace investigation via microfluidics and single-cell genomics”

Open Date: 2025-09-01

Close Date:

Grant: Close

ForMat - “Forensic methylation analysis toolsets”

Open Date: 2025-09-01

Close Date:

Grant: Open

Natural Traces in forensic investigations - how the analysis of non-human evidence can solve crime

Open Date: 2024-03-01

Close Date: 2027-10-01

Grant: Close

The chronnectomic brain: uncovering the neuropathological fingerprints in dementia

Open Date: 2023-09-01

Close Date:

Articles (19)

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2022

Collaborators (17)

Antonio Amorim

Prof

University of Porto

PORTUGAL

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Claus Børsting

Senior researcher

University of Copenhagen

DENMARK

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Chrystelle Colas

Institut Curie

FRANCE

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Carla Oliveira

Principal Investigator

University of Porto

PORTUGAL

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Carlos Gómez

Associate Professor

Universidad de Valladolid

SPAIN

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Jesus Poza

Associate Professor

Universidad de Valladolid

SPAIN

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Srdjan Novaković

University of Ljubljana

SLOVENIA

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Laura Cainé

Professora Auxiliar Convidada

Instituto de Ciências Biomédicas Abel Salazar

PORTUGAL

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Paulo Basta

Senior Researcher

Oswaldo Cruz Foundation

BRAZIL

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Iva Gomes

Associate Researcher

i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto

PORTUGAL

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Catarina Xavier

Junior researcher

i3S - Instituto de Investigação e Inovação em Saúde, Universidade do Porto

PORTUGAL

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Jose Luis Soto

Associate Professor

Universidad de Alicante

SPAIN

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Carmen Tomas Mas

Københavns Universitet

DENMARK

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Manuel António Rodrigues Teixeira

Director

Universidade do Porto Instituto de Ciências Biomédicas Abel Salazar

PORTUGAL

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Roberto Hornero

Full Professor

Universidad de Valladolid

SPAIN

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Carolina Lemos

Instituto de Ciências Biomédicas Abel Salazar

PORTUGAL

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Maria J. Prata

University of Porto

PORTUGAL

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Nadia Pinto

Research Interests

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Recent Grants

Articles (19)

MHappaMundi: A custom AmpliSeq microhaplotype panel for ancestry inference

Statistical interpretation of cases involving mixtures: A Spanish and Portuguese-Speaking Working Group (GHEP-ISFG) collaborative exercise

Navigating population-level coancestry in forensic mixture analysis

Effect of MAPT gene variations on the brain electrical activity: A multiplex network study

Hereditary diffuse gastric cancer spectrum associated with germline CTNNA1 loss of function revealed by clinical and molecular data from 351 carrier families and over 37 000 non-carrier controls

António Amorim (in memoriam)

X-chromosomal STRs: Metapopulations and mutation rates

Applications of Haplodiploid Markers in Forensic Genetics

Stutter Modeling in Probabilistic Genotyping for Forensic DNA Analysis: A Casework-Driven Assessment

The impact of considering different numbers of contributors in identification problems involving real casework mixture samples

Enhancing the Potential of Microhaplotypes for Forensic Applications: Insights from Afghan and Somali Populations

Navigating the blurred boundary: Neuropathologic changes versus clinical symptoms in Alzheimer’s disease, and its consequences for research in genetics

The impact of parameter variation in the quantification of forensic genetic evidence

A mathematical framework for genetic relatedness analysis involving X chromosome aneuploidies

Microsatellites' mutation modeling through the analysis of the Y-chromosomal transmission

The sequence of the repetitive motif influences the frequency of multistep mutations in Short Tandem Repeats

Non-coding variants in VAMP2 and SNAP25 affect gene expression: potential implications in migraine susceptibility

Integrating functional scoring and regulatory data to predict the effect of non-coding SNPs in a complex neurological disease

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.

Collaborators (17)

Antonio Amorim

Claus Børsting

Chrystelle Colas

Carla Oliveira

Carlos Gómez

Jesus Poza

Srdjan Novaković

Laura Cainé

Paulo Basta

Iva Gomes

Catarina Xavier

Jose Luis Soto

Carmen Tomas Mas

Manuel António Rodrigues Teixeira

Roberto Hornero

Carolina Lemos

Maria J. Prata

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