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Fragile X syndrome in the largest world clustering. I. Genetic epidemiology and founder effect outline

American journal of medical genetics. Part A, 2024-05, Vol.194 (5), p.e63523-n/a

2024

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Diagnostic yield of chromosomal microarray in the largest Latino clinical cohort

American journal of medical genetics. Part A, 2024-02, Vol.194 (2), p.218-225

2024

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Linear clinical progression, independent of age of onset, in Niemann-Pick disease, type C

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2010-01, Vol.153B (1), p.132-140

2010

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Origin of the PSEN1 E280A mutation causing early-onset Alzheimer's disease

Alzheimer's & dementia, 2014-10, Vol.10 (5), p.S277-S283.e10

2014

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Support for association between ADHD and two candidate genes: NET1 and DRD1

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2005-04, Vol.134B (1), p.67-72

2005

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Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: A Comprehensive Review

Diagnostics (Basel), 2019-08, Vol.9 (3), p.91

2019

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A multifactorial model of pathology for age of onset heterogeneity in familial Alzheimer’s disease

Acta neuropathologica, 2021-02, Vol.141 (2), p.217-233

2021

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ADGRL3 genomic variation implicated in neurogenesis and ADHD links functional effects to the incretin polypeptide GIP

Scientific reports, 2022-09, Vol.12 (1), p.15922-15922, Article 15922

2022

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Genetic modifiers of cognitive decline in PSEN1 E280A Alzheimer's disease

Alzheimer's & dementia, 2024-04, Vol.20 (4), p.2873-2885

2024

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Role of the IL-1 Pathway in Dopaminergic Neurodegeneration and Decreased Voluntary Movement

Molecular neurobiology, 2017-08, Vol.54 (6), p.4486-4495

2017

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Neural Plasticity during Aging

Neural plasticity, 2019-01, Vol.2019, p.6042132-3

2019

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Polyautoimmunity in Sjögren Syndrome

Rheumatic diseases clinics of North America, 2016-08, Vol.42 (3), p.457-472

2016

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The Mendelian Legacy to Mental and Behavioral Disorders

International journal of psychological research, 2020-01, Vol.13 (1), p.6-8

2020

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Long Non-Coding RNAs and Alzheimer’s Disease: Towards Personalized Diagnosis

International journal of molecular sciences, 2024-07, Vol.25 (14), p.7641

2024

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Distinctive adaptive response to repeated exposure to hydrogen peroxide associated with upregulation of DNA repair genes and cell cycle arrest

Redox biology, 2016-10, Vol.9 (C), p.124-133

2016

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Chikungunya outbreak (2015) in the Colombian Caribbean: Latent classes and gender differences in virus infection

PLoS neglected tropical diseases, 2020-06, Vol.14 (6), p.e0008281

2020

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Reproductive success is predicted by social dynamics and kinship in managed animal populations

F1000 research, 2016, Vol.5, p.870-870

2016

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Familial Alzheimer’s Disease and Recessive Modifiers

Molecular neurobiology, 2020-02, Vol.57 (2), p.1035-1043

2020

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Uncovering the Genetic and Molecular Features of Huntington’s Disease in Northern Colombia

International journal of molecular sciences, 2023-11, Vol.24 (22), p.16154

2023

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A common genetic network underlies substance use disorders and disruptive or externalizing disorders

Human genetics, 2012-06, Vol.131 (6), p.917-929

2012

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Screening of human LPHN3 for variants with a potential impact on ADHD susceptibility

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2011-01, Vol.156B (1), p.11-18

2011

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From the black widow spider to human behavior: Latrophilins, a relatively unknown class of G protein-coupled receptors, are implicated in psychiatric disorders

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2011-01, Vol.156B (1), p.1-10

2011

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Mutations modifying sporadic Alzheimer's disease age of onset

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2016-12, Vol.171B (8), p.1116-1130

2016

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Early Interstitial Lung Disease in Familial Pulmonary Fibrosis

American journal of respiratory and critical care medicine, 2007-10, Vol.176 (7), p.698-705

2007

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Common interacting genetic variation shapes susceptibility to type 1 diabetes in a Colombian Caribbean community: In search of shared genetic markers

Genes & diseases, 2024-07, Vol.11 (4), p.101058-101058, Article 101058

2024

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Fragile X syndrome in the largest world clustering. I. Genetic epidemiology and founder effect outline

Diagnostic yield of chromosomal microarray in the largest Latino clinical cohort

Linear clinical progression, independent of age of onset, in Niemann-Pick disease, type C

Origin of the PSEN1 E280A mutation causing early-onset Alzheimer's disease

Support for association between ADHD and two candidate genes: NET1 and DRD1

Myalgic Encephalomyelitis/Chronic Fatigue Syndrome: A Comprehensive Review

A multifactorial model of pathology for age of onset heterogeneity in familial Alzheimer’s disease

ADGRL3 genomic variation implicated in neurogenesis and ADHD links functional effects to the incretin polypeptide GIP

Genetic modifiers of cognitive decline in PSEN1 E280A Alzheimer's disease

Role of the IL-1 Pathway in Dopaminergic Neurodegeneration and Decreased Voluntary Movement

Neural Plasticity during Aging

Polyautoimmunity in Sjögren Syndrome

The Mendelian Legacy to Mental and Behavioral Disorders

Long Non-Coding RNAs and Alzheimer’s Disease: Towards Personalized Diagnosis

Distinctive adaptive response to repeated exposure to hydrogen peroxide associated with upregulation of DNA repair genes and cell cycle arrest

Chikungunya outbreak (2015) in the Colombian Caribbean: Latent classes and gender differences in virus infection

Reproductive success is predicted by social dynamics and kinship in managed animal populations

Familial Alzheimer’s Disease and Recessive Modifiers

Uncovering the Genetic and Molecular Features of Huntington’s Disease in Northern Colombia

A common genetic network underlies substance use disorders and disruptive or externalizing disorders

Screening of human LPHN3 for variants with a potential impact on ADHD susceptibility

From the black widow spider to human behavior: Latrophilins, a relatively unknown class of G protein-coupled receptors, are implicated in psychiatric disorders

Mutations modifying sporadic Alzheimer's disease age of onset

Early Interstitial Lung Disease in Familial Pulmonary Fibrosis

Common interacting genetic variation shapes susceptibility to type 1 diabetes in a Colombian Caribbean community: In search of shared genetic markers

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