Mauricio Arcos‐Burgos

Author

Also Known As

Arcos-Burgos M., Arcos-Burgos, M, Arcos-Burgos, M., Arcos-Burgos, Mauricio, Ariel F. Martinez, Ferreira de Lima, Renata L.L., Karen Stern, M Arcos, M Arcos-Burgos, M Arcos‐Burgos

229

Publications

11.4K

Citations

H-Index

122

Concepts

All Affiliations

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

About

Mauricio Arcos‐Burgos is an author at Universidad de Antioquia specializing in medicine, genetics, and psychiatry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	26	40	3.7K
2	Public Health	11	11	454
3	Natural Sciences	4	4	188
4	Health Sciences	3	3	41
5	Engineering	1	1	26

Mauricio Arcos‐Burgos

Publications

8.7K

Citations

H-Index

Page 1

	Year	Citations
Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes Shinji Kondo, Brian C. Schutte, Rebecca J. Richardson, Nature Genetics Developmental AnomalyPopliteal Pterygium SyndromesMendelian DisorderGenetic DisorderGenetics	2002	891
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4 Terri H. Beaty, Jeffrey C. Murray, Mary L. Marazita, Nature Genetics Genome-wide Association StudyAllelic VariantDevelopmental BiologyGeneticsCleft Palate Identifies	2010	583
Interferon Regulatory Factor 6 ( <i>IRF6</i> ) Gene Variants and the Risk of Isolated Cleft Lip or Palate Theresa M. Zucchero, Margaret E. Cooper, Brion S. Maher, New England Journal of Medicine	2004	581
Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, and <i>KCNJ10</i> Mutations Detlef Böckenhauer, Sally Feather, Horia Stanescu, New England Journal of Medicine	2009	568
Risk HLA-DQA1 and PLA <sub>2</sub> R1 Alleles in Idiopathic Membranous Nephropathy H.C. Stanescu, Mauricio Arcos‐Burgos, Alan Medlar, New England Journal of Medicine	2011	508
Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder Robert Kleta, Elisa Romeo, Zorica Ristic, Nature Genetics Mendelian DisorderGenetic DisorderCause Hartnup DisorderGeneticsInherited Metabolic Disease	2004	308
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
Young adult outcomes in the follow‐up of the multimodal treatment study of attention‐deficit/hyperactivity disorder: symptom persistence, source discrepancy, and height suppression James M. Swanson, L. Eugene Arnold, Brooke S. G. Molina, Journal of Child Psychology and Psychiatry	2017	276
A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13 Elizabeth J. Leslie, Jenna C. Carlson, John R. Shaffer, Human Molecular Genetics	2016	224
Support for association between ADHD and two candidate genes: <i>NET1</i> and <i>DRD1</i> Aaron J. Bobb, Anjené Addington, Ellen Sidransky, American Journal of Medical Genetics Part B Neuropsychiatric Genetics	2005	221

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