Jorge I. Vélez
Jorge I. Vélez
Assistant Professor, Universidad del Norte
Verified email at - Homepage
TitleCited byYear
A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication
M Arcos-Burgos, M Jain, MT Acosta, S Shively, H Stanescu, D Wallis, ...
Molecular psychiatry 15 (11), 1053, 2010
Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly
E Roessler, MV Ouspenskaia, JD Karkera, JI Vélez, A Kantipong, ...
The American Journal of Human Genetics 83 (1), 18-29, 2008
Linear clinical progression, independent of age of onset, in Niemann–Pick disease, type C
NM Yanjanin, JI Vélez, A Gropman, K King, SE Bianconi, SK Conley, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153 …, 2010
Robotic approach for cervical cancer: comparison with laparotomy: a case control study
A Maggioni, L Minig, V Zanagnolo, M Peiretti, F Sanguineti, L Bocciolone, ...
Gynecologic oncology 115 (1), 60-64, 2009
Analysis of genotype–phenotype correlations in human holoprosencephaly
BD Solomon, S Mercier, JI Vélez, DE Pineda‐Alvarez, A Wyllie, N Zhou, ...
American Journal of Medical Genetics Part C: Seminars in Medical Genetics …, 2010
Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function
F Lacbawan, BD Solomon, E Roessler, K El-Jaick, S Domené, JI Velez, ...
Journal of medical genetics 46 (6), 389, 2009
Analysis of component findings in 79 patients diagnosed with VACTERL association
BD Solomon, DE Pineda‐Alvarez, MS Raam, SM Bous, AA Keaton, ...
American Journal of Medical Genetics Part A 152 (9), 2236-2244, 2010
The mutational spectrum of holoprosencephaly‐associated changes within the SHH gene in humans predicts loss‐of‐function through either key structural …
E Roessler, KB El‐Jaick, C Dubourg, JI Vélez, BD Solomon, ...
Human mutation 30 (10), E921-E935, 2009
Symptomatology of autism spectrum disorder in a population with neurofibromatosis type 1
KS Walsh, JI Vélez, PG Kardel, DM Imas, M Muenke, RJ Packer, ...
Developmental Medicine & Child Neurology 55 (2), 131-138, 2013
Cumulative ligand activity of NODAL mutations and modifiers are linked to human heart defects and holoprosencephaly
E Roessler, W Pei, MV Ouspenskaia, JD Karkera, JI Veléz, ...
Molecular genetics and metabolism 98 (1-2), 225-234, 2009
Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals
BD Solomon, F Lacbawan, S Mercier, NJ Clegg, MR Delgado, ...
Journal of medical genetics 47 (8), 513-524, 2010
A common genetic network underlies substance use disorders and disruptive or externalizing disorders
M Arcos-Burgos, JI Vélez, BD Solomon, M Muenke
Human Genetics, 1-13, 2012
A cooperative interaction between LPHN3 and 11q doubles the risk for ADHD
M Jain, JI Vélez, MT Acosta, LG Palacio, J Balog, E Roessler, D Pineda, ...
Molecular Psychiatry, 2011
Mutations in the human SIX3 gene in holoprosencephaly are loss of function
S Domene, E Roessler, KB El-Jaick, M Snir, JL Brown, JI Vélez, S Bale, ...
Human molecular genetics 17 (24), 3919-3928, 2008
Comparison between SVM and logistic regression: Which one is better to discriminate?
DA Salazar, JI Vélez, JC Salazar
Revista Colombiana de Estadística 35 (SPE2), 223-237, 2012
Utilizing prospective sequence analysis of SHH, ZIC2, SIX3 and TGIF in holoprosencephaly probands to describe the parameters limiting the observed frequency of mutant gene …
E Roessler, JI Vélez, N Zhou, M Muenke
Molecular genetics and metabolism 105 (4), 658-664, 2012
APOE* E2 allele delays age of onset in PSEN1 E280A Alzheimer’s disease
JI Vélez, F Lopera, D Sepulveda-Falla, HR Patel, AS Johar, A Chuah, ...
Molecular Psychiatry 21 (7), 916, 2016
A two-locus genetic interaction between LPHN3 and 11q predicts ADHD severity and long-term outcome
MT Acosta, JI Vélez, ML Bustamante, JZ Balog, M Arcos-Burgos, ...
Translational Psychiatry 1 (7), e17, 2011
Novel and rare functional genomic variants in multiple autoimmune syndrome and Sjögren’s syndrome
AS Johar, C Mastronardi, A Rojas-Villarraga, HR Patel, A Chuah, K Peng, ...
Journal of translational medicine 13 (1), 173, 2015
Pooling/bootstrap-based GWAS (pbGWAS) identifies new loci modifying the age of onset in PSEN1 p. Glu280Ala Alzheimer's disease
JI Vélez, SC Chandrasekharappa, E Henao, AF Martinez, U Harper, ...
Molecular Psychiatry, 2012
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