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A decade of structural variants: description, history and methods to detect structural variation

Briefings in functional genomics, 2015-09, Vol.14 (5), p.305-314

2015

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Efficient and flexible Integration of variant characteristics in rare variant association studies using integrated nested Laplace approximation

PLoS computational biology, 2021-02, Vol.17 (2), p.e1007784

2021

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Genetic variants and abnormal processing of pre-miR-182, a circadian clock modulator, in major depression patients with late insomnia

Human molecular genetics, 2010-10, Vol.19 (20), p.4017-4025

2010

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Cluster analysis of clinical data identifies fibromyalgia subgroups

PloS one, 2013-09, Vol.8 (9), p.e74873-e74873

2013

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The early-life exposome modulates the effect of polymorphic inversions on DNA methylation

Communications biology, 2022-05, Vol.5 (1), p.455-455, Article 455

2022

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Allele balance bias identifies systematic genotyping errors and false disease associations

Human mutation, 2019-01, Vol.40 (1), p.115-126

2019

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Study of the Combined Effect of Maternal Tobacco Smoking and Polygenic Risk Scores on Birth Weight and Body Mass Index in Childhood

Frontiers in genetics, 2022-05, Vol.13, p.867611-867611

2022

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The total deviation index estimated by tolerance intervals to evaluate the concordance of measurement devices

BMC medical research methodology, 2010-04, Vol.10 (1), p.31-31, Article 31

2010

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A Brain-Derived Neurotrophic Factor Haplotype Is Associated with Therapeutic Response in Obsessive-Compulsive Disorder

Biological psychiatry (1969), 2009-10, Vol.66 (7), p.674-680

2009

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Detection of Significant Disease Risks Using a Spatial Conditional Autoregressive Model

Biometrics, 2008-12, Vol.64 (4), p.1043-1053

2008

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Huntington’s disease brain-derived small RNAs recapitulate associated neuropathology in mice

Acta neuropathologica, 2021-04, Vol.141 (4), p.565-584

2021

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Accounting for uncertainty when assessing association between copy number and disease: a latent class model

BMC bioinformatics, 2009-06, Vol.10 (172), p.172-172, Article 172

2009

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ALDH5A1 variability in opioid dependent patients could influence response to methadone treatment

European neuropsychopharmacology, 2014-03, Vol.24 (3), p.420-424

2014

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Specific small-RNA signatures in the amygdala at premotor and motor stages of Parkinson's disease revealed by deep sequencing analysis

Bioinformatics, 2016-03, Vol.32 (5), p.673-681

2016

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A High-Throughput Screening Identifies MicroRNA Inhibitors That Influence Neuronal Maintenance and/or Response to Oxidative Stress

Molecular therapy. Nucleic acids, 2019-09, Vol.17, p.374-387

2019

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Blood miRNA levels associated with ADHD traits in children across six European birth cohorts

BMC psychiatry, 2023-09, Vol.23 (1), p.1-696, Article 696

2023

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Changes in the stool and oropharyngeal microbiome in obsessive-compulsive disorder

Scientific reports, 2022-01, Vol.12 (1), p.1448-1448, Article 1448

2022

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A new tetra-plex fluorimetric assay for the quantification of cerebrospinal fluid β-amyloid42, total-tau, phospho-tau and α-synuclein in the differential diagnosis of neurodegenerative dementia

Journal of neurology, 2020-09, Vol.267 (9), p.2567-2581

2020

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MicroRNA profiling of Parkinson's disease brains identifies early downregulation of miR-34b/c which modulate mitochondrial function

Human molecular genetics, 2011-08, Vol.20 (15), p.3067-3078

2011

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Spatio-temporal analysis of mortality among children under the age of five in Manhiça (Mozambique) during the period 1997-2005

International journal of health geographics, 2011-02, Vol.10 (1), p.14-14, Article 14

2011

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Upregulation of a small vault RNA (svtRNA2-1a) is an early event in Parkinson disease and induces neuronal dysfunction

RNA biology, 2013-07, Vol.10 (7), p.1093-1106

2013

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IDENTIFYING VPS13A INTERACTING PARTNERS AND THEIR ROLE IN THE NEURONAL MITOCHONDRIAL FUNCTIONING IN A MODEL OF CHOREA-ACANTHOCYTOSIS

IBRO neuroscience reports, 2023-10, Vol.15, p.S482-S482

2023

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Common genetic variants associated with urinary phthalate levels in children: A genome-wide study

Environment international, 2024-08, Vol.190, p.108845, Article 108845

2024

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A decade of structural variants: description, history and methods to detect structural variation

Identification of autosomal cis expression quantitative trait methylation (cis eQTMs) in children's blood

Efficient and flexible Integration of variant characteristics in rare variant association studies using integrated nested Laplace approximation

Genetic variants and abnormal processing of pre-miR-182, a circadian clock modulator, in major depression patients with late insomnia

Cluster analysis of clinical data identifies fibromyalgia subgroups

The early-life exposome modulates the effect of polymorphic inversions on DNA methylation

Allele balance bias identifies systematic genotyping errors and false disease associations

Study of the Combined Effect of Maternal Tobacco Smoking and Polygenic Risk Scores on Birth Weight and Body Mass Index in Childhood

The total deviation index estimated by tolerance intervals to evaluate the concordance of measurement devices

A Brain-Derived Neurotrophic Factor Haplotype Is Associated with Therapeutic Response in Obsessive-Compulsive Disorder

Detection of Significant Disease Risks Using a Spatial Conditional Autoregressive Model

Huntington’s disease brain-derived small RNAs recapitulate associated neuropathology in mice

Accounting for uncertainty when assessing association between copy number and disease: a latent class model

ALDH5A1 variability in opioid dependent patients could influence response to methadone treatment

Specific small-RNA signatures in the amygdala at premotor and motor stages of Parkinson's disease revealed by deep sequencing analysis

A High-Throughput Screening Identifies MicroRNA Inhibitors That Influence Neuronal Maintenance and/or Response to Oxidative Stress

Blood miRNA levels associated with ADHD traits in children across six European birth cohorts

Changes in the stool and oropharyngeal microbiome in obsessive-compulsive disorder

A new tetra-plex fluorimetric assay for the quantification of cerebrospinal fluid β-amyloid42, total-tau, phospho-tau and α-synuclein in the differential diagnosis of neurodegenerative dementia

MicroRNA profiling of Parkinson's disease brains identifies early downregulation of miR-34b/c which modulate mitochondrial function

Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis

Spatio-temporal analysis of mortality among children under the age of five in Manhiça (Mozambique) during the period 1997-2005

Upregulation of a small vault RNA (svtRNA2-1a) is an early event in Parkinson disease and induces neuronal dysfunction

IDENTIFYING VPS13A INTERACTING PARTNERS AND THEIR ROLE IN THE NEURONAL MITOCHONDRIAL FUNCTIONING IN A MODEL OF CHOREA-ACANTHOCYTOSIS

Common genetic variants associated with urinary phthalate levels in children: A genome-wide study

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