Manuel Lemos

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Full Professor (Endocrinology)

Universidade da Beira Interior

Portugal

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About

Manuel Lemos is a Full Professor of Endocrinology at the University of Beira Interior, Portugal. His research areas include the genetic and functional analysis of endocrine disorders, with a focus on disorders such as Kallmann Syndrome and congenital hypogonadotropic hypogonadism. He has also explored the impact of maternal iodine concentration on child development and the regulation of drug resistance by sex steroids.

Recent Grants

Grant: Close

GenoPit - Genetic risk factors for pituitary adenomas: a national, multicenter, genetic and clinical analysis

Open Date: 2018-07-01

Close Date: 2021-06-01

Grant: Close

Molecular genetics and functional genomics of pituitary hormone deficiencies

Open Date: 2010-06-01

Close Date: 2013-11-30

Articles (13)

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2025

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2024

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2023

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2023

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2023

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2022

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2022

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2022

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2022

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2022

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2021

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2021

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2020

Collaborators (4)

Cecilia Santos

Universidade da Beira Interior

PORTUGAL

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Ivone Castro-Vale

Professora auxiliar

Universidade do Porto Faculdade de Medicina

PORTUGAL

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Telma Quintela

Universidade da Beira Interior

PORTUGAL

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Isabel Maria Theriaga Mendes Varanda Gonçalve

Assistant Professor

Universidade da Beira Interior

PORTUGAL

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Manuel Lemos

Research Interests

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About

Recent Grants

Articles (13)

Computational Resources and Infrastructures for a Novel Bioinformatics Laboratory: A Case Study

Kallmann Syndrome: Functional Analysis of a CHD7 Missense Variant Shows Aberrant RNA Splicing

Regulation of ABC transporters by sex steroids may explain differences in drug resistance between sexes

Low frequency of AIP mutations in patients with young-onset sporadic pituitary macroadenomas

Maternal Urinary Iodine Concentration during Pregnancy and Its Impact on Child Growth and Neurodevelopment: An 11-Year Follow-Up Study

A Common Variant in the <i>CDK8</i> Gene Is Associated with Sporadic Pituitary Adenomas in the Portuguese Population: A Case-Control Study

Disorder of Sex Development Due to 17-Beta-Hydroxysteroid Dehydrogenase Type 3 Deficiency: A Case Report and Review of 70 Different HSD17B3 Mutations Reported in 239 Patients

A Novel FGFR1 Missense Mutation in a Portuguese Family with Congenital Hypogonadotropic Hypogonadism

Iodine Supplementation in Pregnancy in an Iodine-Deficient Region: A Cross-Sectional Survey

Clinical, Genetic and Functional Characterization of a Novel AVPR2 Missense Mutation in a Woman with X-Linked Recessive Nephrogenic Diabetes Insipidus

The Glucocorticoid Receptor Gene (NR3C1) 9β SNP Is Associated with Posttraumatic Stress Disorder

Promoter Demethylation Upregulates STEAP1 Gene Expression in Human Prostate Cancer: In Vitro and In Silico Analysis

Age, Sex Hormones, and Circadian Rhythm Regulate the Expression of Amyloid-Beta Scavengers at the Choroid Plexus

Collaborators (4)

Cecilia Santos

Ivone Castro-Vale

Telma Quintela

Isabel Maria Theriaga Mendes Varanda Gonçalve

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