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Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease

PloS one, 2009-08, Vol.4 (8), p.e6501-e6501

2009

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Autophagy Markers Are Altered in Alzheimer's Disease, Dementia with Lewy Bodies and Frontotemporal Dementia

International journal of molecular sciences, 2024-01, Vol.25 (2), p.1125

2024

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Pseudoexfoliation syndrome-associated genetic variants affect transcription factor binding and alternative splicing of LOXL1

Nature communications, 2017-05, Vol.8 (1), p.15466-15466, Article 15466

2017

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The PINK1 p.Asn521Thr Variant Is Associated with Earlier Disease Onset in GRN/C9orf72 Frontotemporal Lobar Degeneration

International journal of molecular sciences, 2022-11, Vol.23 (21), p.12847

2022

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Identification of a cytokine profile in serum and cerebrospinal fluid of pediatric and adult spinal muscular atrophy patients and its modulation upon nusinersen treatment

Frontiers in cellular neuroscience, 2022-08, Vol.16, p.982760-982760

2022

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Broadening the Genetic Spectrum of Painful Small-Fiber Neuropathy through Whole-Exome Study in Early-Onset Cases

International journal of molecular sciences, 2024-07, Vol.25 (13), p.7248

2024

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Peripheral Ion Channel Genes Screening in Painful Small Fiber Neuropathy

International journal of molecular sciences, 2022-11, Vol.23 (22), p.14095

2022

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A novel network analysis approach reveals DNA damage, oxidative stress and calcium/cAMP homeostasis-associated biomarkers in frontotemporal dementia

PloS one, 2017-10, Vol.12 (10), p.e0185797-e0185797

2017

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Peripheral Ion Channel Gene Screening in Painful- and Painless-Diabetic Neuropathy

International journal of molecular sciences, 2022-06, Vol.23 (13), p.7190

2022

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Association of colorectal cancer with genetic and epigenetic variation in PEAR1-A population-based cohort study

PloS one, 2022-04, Vol.17 (4), p.e0266481

2022

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Archival skin biopsy specimens as a tool for miRNA-based diagnosis: Technical and post-analytical considerations

Molecular therapy. Methods & clinical development, 2023-12, Vol.31, p.101116-101116, Article 101116

2023

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Genetics can contribute to the prognosis of Brugada syndrome: a pilot model for risk stratification

European journal of human genetics : EJHG, 2013-09, Vol.21 (9), p.911-917

2013

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Semantic and right temporal variant of FTD: Next generation sequencing genetic analysis on a single-center cohort

Frontiers in aging neuroscience, 2022-12, Vol.14, p.1085406-1085406

2022

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Association Analysis of Noncoding Variants in Neuroligins 3 and 4X Genes with Autism Spectrum Disorder in an Italian Cohort

International journal of molecular sciences, 2016-10, Vol.17 (10), p.1765-1765

2016

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Genes involved in vasoconstriction and vasodilation system affect salt-sensitive hypertension

PloS one, 2011-05, Vol.6 (5), p.e19620

2011

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Muscle and Muscle-like Autoantigen Expression in Myasthenia Gravis Thymus: Possible Molecular Hint for Autosensitization

Biomedicines, 2023-02, Vol.11 (3), p.732

2023

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Genome-Wide Meta-Analysis of Blood Pressure Response to β1-Blockers: Results From ICAPS (International Consortium of Antihypertensive Pharmacogenomics Studies)

Journal of the American Heart Association, 2019-08, Vol.8 (16), p.e013115-e013115

2019

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Dissecting the Polygenic Basis of Primary Hypertension: Identification of Key Pathway-Specific Components

Frontiers in cardiovascular medicine, 2022-02, Vol.9, p.814502-814502

2022

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Adducin- and ouabain-related gene variants predict the antihypertensive activity of rostafuroxin, part 2: clinical studies

Science translational medicine, 2010-11, Vol.2 (59), p.59ra87

2010

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Diagnostic criteria for small fibre neuropathy in clinical practice and research

Brain (London, England : 1878), 2019-12, Vol.142 (12), p.3728-3736

2019

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PEAR1 is not a major susceptibility gene for cardiovascular disease in a Flemish population

BMC medical genetics, 2017-04, Vol.18 (1), p.45-45, Article 45

2017

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SNPLims: a data management system for genome wide association studies

BMC bioinformatics, 2008-03, Vol.9 Suppl 2 (S2), p.S13-S13, Article S13

2008

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Congenital insensitivity to pain: a novel mutation affecting a U12-type intron causes multiple aberrant splicing of SCN9A

Pain (Amsterdam), 2022-07, Vol.163 (7), p.e882-e887

2022

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Modelling the interaction of steroid receptors with endocrine disrupting chemicals

BMC bioinformatics, 2005-12, Vol.6 Suppl 4 (Suppl 4), p.S10-S10, Article S10

2005

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Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease

Autophagy Markers Are Altered in Alzheimer's Disease, Dementia with Lewy Bodies and Frontotemporal Dementia

Pseudoexfoliation syndrome-associated genetic variants affect transcription factor binding and alternative splicing of LOXL1

The PINK1 p.Asn521Thr Variant Is Associated with Earlier Disease Onset in GRN/C9orf72 Frontotemporal Lobar Degeneration

Identification of a cytokine profile in serum and cerebrospinal fluid of pediatric and adult spinal muscular atrophy patients and its modulation upon nusinersen treatment

Broadening the Genetic Spectrum of Painful Small-Fiber Neuropathy through Whole-Exome Study in Early-Onset Cases

Peripheral Ion Channel Genes Screening in Painful Small Fiber Neuropathy

A novel network analysis approach reveals DNA damage, oxidative stress and calcium/cAMP homeostasis-associated biomarkers in frontotemporal dementia

Peripheral Ion Channel Gene Screening in Painful- and Painless-Diabetic Neuropathy

Association of colorectal cancer with genetic and epigenetic variation in PEAR1-A population-based cohort study

Archival skin biopsy specimens as a tool for miRNA-based diagnosis: Technical and post-analytical considerations

Genetics can contribute to the prognosis of Brugada syndrome: a pilot model for risk stratification

Semantic and right temporal variant of FTD: Next generation sequencing genetic analysis on a single-center cohort

Association Analysis of Noncoding Variants in Neuroligins 3 and 4X Genes with Autism Spectrum Disorder in an Italian Cohort

Target Sequencing, Cell Experiments, and a Population Study Establish Endothelial Nitric Oxide Synthase (eNOS) Gene as Hypertension Susceptibility Gene

Genes involved in vasoconstriction and vasodilation system affect salt-sensitive hypertension

Muscle and Muscle-like Autoantigen Expression in Myasthenia Gravis Thymus: Possible Molecular Hint for Autosensitization

Genome-Wide Meta-Analysis of Blood Pressure Response to β1-Blockers: Results From ICAPS (International Consortium of Antihypertensive Pharmacogenomics Studies)

Dissecting the Polygenic Basis of Primary Hypertension: Identification of Key Pathway-Specific Components

Adducin- and ouabain-related gene variants predict the antihypertensive activity of rostafuroxin, part 2: clinical studies

Diagnostic criteria for small fibre neuropathy in clinical practice and research

PEAR1 is not a major susceptibility gene for cardiovascular disease in a Flemish population

SNPLims: a data management system for genome wide association studies

Congenital insensitivity to pain: a novel mutation affecting a U12-type intron causes multiple aberrant splicing of SCN9A

Modelling the interaction of steroid receptors with endocrine disrupting chemicals

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