P. Marques

发表

Genes from the TAS1R and TAS2R Families of Taste Receptors: Looking for Signatures of Their Adaptive Role in Human Evolution

A. Amorim, C. Valente, L. Alvarez, 2018, Genome biology and evolution.

Intronic variation of the SOHLH2 gene confers risk to male reproductive impairment.

P. Marques, S. Seixas, L. Bassas, 2020, Fertility and sterility.

Known Mutations at the Cause of Alpha-1 Antitrypsin Deficiency an Updated Overview of SERPINA1 Variation Spectrum

P. Marques, S. Seixas, 2021, The application of clinical genetics.

Profiling of lung microbiota discloses differences in adenocarcinoma and squamous cell carcinoma

R. Matthiesen, P. Marques, S. Seixas, 2019, Scientific Reports.

Sequence variation at KLK and WFDC clusters and its association to semen hyperviscosity and other male infertility phenotypes.

V. Quesada, Diana A. Puente, R. Matthiesen, 2016, Human reproduction.

TACG_A_257511 173..194

P. Marques, S. Seixas, 2021 .

Common genetic variation in KATNAL1 non‐coding regions is involved in the susceptibility to severe phenotypes of male infertility

P. Marques, S. Seixas, L. Bassas, 2022, Andrology.

Semen quality is affected by HLA class I alleles together with sexually transmitted diseases

P. Marques, S. Seixas, B. Cavadas, 2019, Andrology.

DNA methylation imprinting errors in spermatogenic cells from maturation arrest azoospermic patients

M. Sousa, P. Marques, A. Barros, 2017, Andrology.

Immune and spermatogenesis-related loci are involved in the development of extreme patterns of male infertility

P. Marques, S. Seixas, L. Bassas, 2022, Communications Biology.

Adaptive Evolution Favoring KLK4 Downregulation in East Asians.

V. Quesada, P. Marques, S. Seixas, 2016, Molecular biology and evolution.

Evaluation of Male Fertility-Associated Loci in a European Population of Patients with Severe Spermatogenic Impairment

P. Marques, S. Seixas, L. Bassas, 2020, Journal of personalized medicine.

Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia

P. Marques, S. Seixas, L. Bassas, 2022, Frontiers in Cell and Developmental Biology.

Common Variation in the PIN1 Locus Increases the Genetic Risk to Suffer from Sertoli Cell-Only Syndrome

P. Marques, S. Seixas, L. Bassas, 2022, Journal of personalized medicine.

Characterization of microbiota in male infertility cases uncovers differences in seminal hyperviscosity and oligoasthenoteratozoospermia possibly correlated with increased prevalence of infectious bacteria

P. Marques, S. Seixas, B. Cavadas, 2018, American journal of reproductive immunology.

The mutational spectrum of WT1 in male infertility.

A. Amorim, M. Sousa, P. Marques, 2015, The Journal of urology.

Adaptive Evolution and Divergence of SERPINB3: A Young Duplicate in Great Apes

R. Matthiesen, P. Marques, S. Seixas, 2014, PloS one.

Rare double sex and mab‐3‐related transcription factor 1 regulatory variants in severe spermatogenic failure

D. Conrad, P. Marques, S. Seixas, 2015, Andrology.

Effect and in silico characterization of genetic variants associated with severe spermatogenic disorders in a large Iberian cohort

P. Marques, S. Seixas, L. Bassas, 2021, Andrology.

Severe α‐1 antitrypsin deficiency caused by Q0Ourém allele: clinical features, haplotype characterization and history

P. Marques, S. Seixas, J. Rocha, 2012, Clinical genetics.

Comparative analysis of the bronchoalveolar microbiome in Portuguese patients with different chronic lung disorders

M. Pérez‐Losada, R. Matthiesen, P. Marques, 2021, Scientific Reports.

SERPINA2 Is a Novel Gene with a Divergent Function from SERPINA1

P. Marques, S. Seixas, P. Castro, 2013, PloS one.