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List of works by Jorge I Velez

A Lachnospiraceae-dominated bacterial signature in the fecal microbiota of HIV-infected individuals from Colombia, South America.

scientific article published on 14 March 2018

A Mutation in DAOA Modifies the Age of Onset in PSEN1 E280A Alzheimer's Disease

scientific article published on 5 January 2016

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

scientific article

A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD.

scientific article

A two-locus genetic interaction between LPHN3 and 11q predicts ADHD severity and long-term outcome

scientific article published on 5 July 2011

ADGRL3 (LPHN3) variants predict substance use disorder

scientific article published on 29 January 2019

ADHD Endophenotypes in Caribbean Families.

scientific article published in March 2018

APOE*E2 allele delays age of onset in PSEN1 E280A Alzheimer's disease

scientific article

Analysis of brain metabolism by proton magnetic resonance spectroscopy (1H-MRS) in attention-deficit/hyperactivity disorder suggests a generalized differential ontogenic pattern from controls

scientific article

Analysis of component findings in 79 patients diagnosed with VACTERL association.

scientific article published in September 2010

Changes in short-term health-related quality of life in women undergoing gynecologic oncologic laparotomy: an associated factor analysis.

scientific article

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

scientific article published on 03 June 2020

Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly

scientific article

Definition of mutations in polyautoimmunity

scientific article

Evaluation of laparoscopic management of gynecologic emergencies by residents

scientific article published on 26 June 2010

Exosomes: Potential Disease Biomarkers and New Therapeutic Targets

scientific article published in 2021

Familial Alzheimer's Disease and Recessive Modifiers

scientific article published on 29 October 2019

GWAS reveals new recessive loci associated with non-syndromic facial clefting

scientific article

Genetic Variation Underpinning ADHD Risk in a Caribbean Community

scientific article published on 16 August 2019

How Is Temporal Processing Affected in Children with Attention-deficit/hyperactivity Disorder?

scientific article published on 15 May 2020

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

scientific article

Linkage and association analysis of ADHD endophenotypes in extended and multigenerational pedigrees from a genetic isolate.

scientific article published on 24 November 2015

Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals

scientific article published on 2 December 2009

Mutations in sphingolipid metabolism genes are associated with ADHD

scientific article published on 13 July 2020

Mutations in the human SIX3 gene in holoprosencephaly are loss of function

scientific article

Mutations modifying sporadic Alzheimer's disease age of onset

scientific article published on 30 August 2016

Neuropsychological performance in patients with asymptomatic HIV-1 infection.

scientific article published on 7 February 2018

Novel and rare functional genomic variants in multiple autoimmune syndrome and Sjögren's syndrome

scientific article published on 2 June 2015

Pooling/bootstrap-based GWAS (pbGWAS) identifies new loci modifying the age of onset in PSEN1 p.Glu280Ala Alzheimer's disease

scientific article published on 19 June 2012

Potential cognitive endophenotypes in multigenerational families: segregating ADHD from a genetic isolate

scientific article

Prepotent response inhibition and reaction times in children with attention deficit/hyperactivity disorder from a Caribbean community.

scientific article published on 25 February 2017

Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly

scientific article published on 5 June 2008

Retrospective assessment of childhood ADHD symptoms for diagnosis in adults: validity of a short 8-item version of the Wender-Utah Rating Scale

scientific article

Robotic approach for cervical cancer: comparison with laparotomy: a case control study.

scientific article

Symptomatology of autism spectrum disorder in a population with neurofibromatosis type 1.

scientific article

TGIF Mutations in Human Holoprosencephaly: Correlation between Genotype and Phenotype

scientific article published on January 2010

The PHF21B gene is associated with major depression and modulates the stress response.

scientific article

The allocation of valenced concepts onto 3D space.

scientific article published on 28 June 2017

Utilizing prospective sequence analysis of SHH, ZIC2, SIX3 and TGIF in holoprosencephaly probands to describe the parameters limiting the observed frequency of mutant gene×gene interactions

scientific article published on 12 January 2012

Validating the role of the Australian National University Alzheimer's Disease Risk Index (ANU-ADRI) and a genetic risk score in progression to cognitive impairment in a population-based cohort of older adults followed for 12 years

scientific article published on 04 March 2017

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