Publicacións en colaboración con investigadores/as de Universidade Do Porto (104)

2024

  1. Is There a Bias Towards Males in the Diagnosis of Autism? A Systematic Review and Meta-Analysis

    Neuropsychology Review

2022

  1. Genetic ancestry in Afro-descendants from the Andes and Pacific Coast regions of Ecuador

    Forensic Science International: Genetics Supplement Series, Vol. 8, pp. 254-256

  2. How Executive Functions Correlate with Intelligence in Children and Adolescents in Autism Spectrum Disorders

    Journal of Cognition and Development, Vol. 23, Núm. 5, pp. 776-790

2021

  1. Executive Functioning: A Mediator Between Sensory Processing and Behaviour in Autism Spectrum Disorder

    Journal of Autism and Developmental Disorders, Vol. 51, Núm. 6, pp. 2091-2103

2019

  1. Erratum to: Germline variation at 8q24 and prostate cancer risk in men of European ancestry (Nature Communications, (2018), 9, 1, (4616), 10.1038/s41467-018-06863-1)

    Nature Communications

  2. Genome-wide association study of germline variants and breast cancer-specific mortality

    British Journal of Cancer, Vol. 120, Núm. 6, pp. 647-657

  3. Spatially explicit analysis reveals complex human genetic gradients in the Iberian Peninsula

    Scientific Reports, Vol. 9, Núm. 1

2018

  1. Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants

    Nature Communications, Vol. 9, Núm. 1

  2. Germline variation at 8q24 and prostate cancer risk in men of European ancestry

    Nature Communications, Vol. 9, Núm. 1

2017

  1. A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar Ataxia

    American Journal of Human Genetics, Vol. 101, Núm. 1, pp. 87-103

  2. Forensic genetics and genomics: Much more than just a human affair

    PLoS Genetics, Vol. 13, Núm. 9

  3. Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

    Nature Genetics, Vol. 49, Núm. 12, pp. 1767-1778

2016

  1. Sequence variation between 462 human individuals fine-tunes functional sites of RNA processing

    Scientific Reports, Vol. 6

2015

  1. Completion of a worldwide reference panel of samples for an ancestry informative Indel assay

    Forensic Science International: Genetics, Vol. 17, pp. 75-80

  2. Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk

    Human Molecular Genetics, Vol. 24, Núm. 5, pp. 1478-1492

  3. Mosaic maternal ancestry in the Great Lakes region of East Africa

    Human Genetics, Vol. 134, Núm. 9, pp. 1013-1027

  4. Predicting proliferative vitreoretinopathy: Temporal and external validation of models based on genetic and clinical variables

    British Journal of Ophthalmology, Vol. 99, Núm. 1, pp. 41-48

  5. Recurrent Coding Sequence Variation Explains only A Small Fraction of the Genetic Architecture of Colorectal Cancer

    Scientific Reports, Vol. 5

2014

  1. Comparison of the genetic background of different Colombian populations using the SNPforID 52plex identification panel

    International Journal of Legal Medicine, Vol. 128, Núm. 1, pp. 19-25

  2. Update of the guidelines for the publication of genetic population data

    Forensic Science International: Genetics