Jorge I. Vélez - Concepedia

Author

Jorge I. Vélez

Also Known As

J I Velez, J I Vélez, J. I. Vélez, J.I. Vélez, JORGE I VÉLEZ, Jorge I Velez, Jorge I Vélez, Jorge I. Velez, Jorge I. Vélez, Jorge Ivan Velez

119

Publications

3.5K

Citations

H-Index

156

Concepts

All Affiliations

Universidad del Norte Universidad de Antioquia National Human Genome Research Institute National Institutes of Health Australian National University

About

Jorge I. Vélez is an author at Universidad del Norte specializing in medicine, genetics, and social sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	22	1.3K
2	Engineering	6	6	143
3	Public Health	6	6	237
4	Education	2	2	79
5	Health Sciences	1	1	17

Jorge I. Vélez

Publications

2.8K

Citations

H-Index

Page 1

	Year	Citations
A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication Mauricio Arcos‐Burgos, Mahim Jain, Maria T. Acosta, Molecular Psychiatry AdhdPsychiatryPsychotropic MedicationPsychopharmacologyStimulant Medication	2010	291
Linear clinical progression, independent of age of onset, in Niemann–Pick disease, type C Nicole M. Yanjanin, Jorge I. Vélez, Andrea Gropman, American Journal of Medical Genetics Part B Neuropsychiatric Genetics	2009	197
Reduced NODAL Signaling Strength via Mutation of Several Pathway Members Including FOXH1 Is Linked to Human Heart Defects and Holoprosencephaly Erich Roessler, Maia V. Ouspenskaia, Jayaprakash D. Karkera, The American Journal of Human Genetics Transcriptional RegulationDevelopmental BiologyNodal Signaling StrengthSignaling PathwayGenetic Disorder	2008	174
Symptomatology of autism spectrum disorder in a population with neurofibromatosis type 1 Karin S. Walsh, Jorge I. Vélez, P. Kardel, Developmental Medicine & Child Neurology	2012	131
Robotic approach for cervical cancer: Comparison with laparotomy A case control study Angelo Maggioni, Lucas Minig, Vanna Zanagnolo, Gynecologic Oncology Robotic ApproachSurgical OncologyCervical CancerComputer-assisted SurgeryMedicine	2009	129
APOE*E2 allele delays age of onset in PSEN1 E280A Alzheimer’s disease Jorge I. Vélez, Francisco Lopera, Diego Sepúlveda‐Falla, Molecular Psychiatry	2015	106
Clinical spectrum of <i>SIX3</i>-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function Felicitas Lacbawan, Benjamin D. Solomon, Erich Roessler, Journal of Medical Genetics	2009	98
Analysis of component findings in 79 patients diagnosed with VACTERL association Benjamin D. Solomon, Daniel Pineda‐Alvarez, Manu S. Raam, American Journal of Medical Genetics Part A Component FeaturesDisease DiagnosisComponent FindingsMedicinePathogenesis	2010	95
The mutational spectrum of holoprosencephaly-associated changes within the<i>SHH</i>gene in humans predicts loss-of-function through either key structural alterations of the ligand or its altered synthesis Erich Roessler, Kênia Balbi El-Jaick, Christèle Dubourg, Human Mutation GeneticsDisease Gene IdentificationSignaling PathwayHoloprosencephaly-associated ChangesMutational Spectrum	2009	86
Mutations in <i>ZIC2</i> in human holoprosencephaly: description of a Novel <i>ZIC2</i> specific phenotype and comprehensive analysis of 157 individuals B. D. Solomon, Felicitas Lacbawan, Sandra Mercier, Journal of Medical Genetics	2009	83

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