|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
|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
|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 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
|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
|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
|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
|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
|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
|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
|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 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
|The PHF21B gene is associated with major depression and modulates the stress response|
ML Wong, M Arcos-Burgos, S Liu, JI Velez, C Yu, BT Baune, MC Jawahar, ...
Molecular Psychiatry, 2016
|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
|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