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Sofia Dória

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Portugal

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Professors in Portugal Professors in Cell Biology Cell Biology professors in Portugal

About

Professor Sofia Dória is a faculty member at the Faculty of Medicine, specializing in reproductive health and genetic disorders. Her recent research includes topics such as immune dysregulation in pregnancy loss and genetic editing techniques for stem cells. She has published extensively on issues related to oocyte maturation, hereditary disorders, and chromosomal abnormalities in infertility. Based in Portugal, she contributes to understanding the genetic underpinnings of reproductive health and associated pathologies.

Recent Grants

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The role of (epi)genetic mechanisms in oocyte maturation and idiopathic pregnancy losses new insights into human reproduction

Open Date: 2021-11-01

Close Date: 2023-10-31

Articles (19)

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2025

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2020

Collaborators (13)

Carla Oliveira

Principal Investigator

University of Porto

PORTUGAL

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Dezso David

Instituto Nacional de Saúde Doutor Ricardo Jorge

PORTUGAL

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Ana Grangeia

Professora Auxiliar Convidada a tempo parcial

Universidade do Porto Faculdade de Medicina

PORTUGAL

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Carla Ramalho

Professora catedrática convidada

University of Porto

PORTUGAL

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Mário Sousa

Full Professor

Instituto de Ciências Biomédicas Abel Salazar

PORTUGAL

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Miguel Branco

Reader

Queen Mary University of London

UNITED KINGDOM

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Joel Pinto

Assistant Professor

Polytechnic Institute of Porto

PORTUGAL

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Daniel Sobral

Invited Researcher

Instituto Nacional de Saúde Doutor Ricardo Jorge

PORTUGAL

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Davide Carvalho

Head

PORTUGAL

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Cynthia Morton

The University of Manchester

UNITED KINGDOM

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Carla Pinto Moura

MD, PhD

Universidade do Porto Faculdade de Medicina

PORTUGAL

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Carolina Almeida

Faculty of Medicine of the University of Porto

PORTUGAL

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Joana Marques

Researcher

Universidade do Porto Faculdade de Medicina

PORTUGAL

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Sofia Dória

Research Interests

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About

Recent Grants

Articles (19)

Immune Dysregulation and Trophoblastic Dysfunction as a Potential Cause of Idiopathic Recurrent Pregnancy Loss

Transcriptomic analysis and epigenetic regulators in human oocytes at different stages of oocyte meiotic maturation

A protocol for karyotyping and genetic editing of induced pluripotent stem cells with homology-directed repair mediated CRISPR/Cas9

X-chromosome inactivation pattern and telomere length in recurrent pregnancy loss

Impact of copy number variants in epilepsy plus neurodevelopment disorders

Syncytiotrophoblast Markers Are Downregulated in Placentas from Idiopathic Stillbirths

Genetic study on candidates for oocyte donation

Kidney Failure Secondary to Hereditary Xanthinuria due to a Homozygous Deletion of the XDH Gene in the Absence of Overt Kidney Stone Disease

Balanced chromosomal rearrangements implicate YIPF5 and SPATC1L in non-obstructive oligoasthenozoospermia and oligozoospermia and of a derivative chromosome 22 in recurrent miscarriage

Copy number variations on chromosome 2: impact on human phenotype, a cross-sectional study

Klinefelter syndrome: The characterization of the clinical and sociological features of 51 patients.

Severe KIDAR syndrome caused by deletion in the AP1B1 gene: Report of a teenage patient and systematic review of the literature

The role of DNA hydroxymethylation and TET enzymes in placental development and pregnancy outcome

Clinical Findings on Chromosome 1 Copy Number Variations.

Clinical outcomes of 77 TESE treatment cycles in non-mosaic Klinefelter syndrome patients.

X-chromosome inactivation: implications in human disease

Deregulation of imprinted genes expression and epigenetic regulators in placental tissue from intrauterine growth restriction

12q14 microduplication: a new clinical entity reciprocal to the microdeletion syndrome?

46,XX male disorder of sexual development

Collaborators (13)

Carla Oliveira

Dezso David

Ana Grangeia

Carla Ramalho

Mário Sousa

Miguel Branco

Joel Pinto

Daniel Sobral

Davide Carvalho

Cynthia Morton

Carla Pinto Moura

Carolina Almeida

Joana Marques

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