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Mauricio Arcos-Burgos MD, PhD.
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Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes
S Kondo, BC Schutte, RJ Richardson, BC Bjork, AS Knight, Y Watanabe, ...
Nature genetics 32 (2), 285-289, 2002
10732002
Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate
TM Zucchero, ME Cooper, BS Maher, S Daack-Hirsch, B Nepomuceno, ...
New England Journal of Medicine 351 (8), 769-780, 2004
7922004
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4
TH Beaty, JC Murray, ML Marazita, RG Munger, I Ruczinski, JB Hetmanski, ...
Nature genetics 42 (6), 525-529, 2010
6812010
Risk HLA-DQA1 and PLA2R1 Alleles in Idiopathic Membranous Nephropathy
HC Stanescu, M Arcos-Burgos, A Medlar, D Bockenhauer, A Kottgen, ...
New England Journal of Medicine 364 (7), 616-626, 2011
6322011
Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations
D Bockenhauer, S Feather, HC Stanescu, S Bandulik, AA Zdebik, ...
New England Journal of Medicine 360 (19), 1960-1970, 2009
6242009
Cognitive neuroscience of attention
MI Posner
Guilford Press, 2012
5422012
Clinical features of early-onset Alzheimer disease in a large kindred with an E280A presenilin-1 mutation
F Lopera, A Ardilla, A Martínez, L Madrigal, JC Arango-Viana, CA Lemere, ...
Jama 277 (10), 793-799, 1997
4561997
Genetics of population isolates
M Arcos‐Burgos, M Muenke
Clinical genetics 61 (4), 233-247, 2002
3542002
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), 1053-1066, 2010
3432010
Mutations in SLC6A19, encoding B0AT1, cause Hartnup disorder
R Kleta, E Romeo, Z Ristic, T Ohura, C Stuart, M Arcos-Burgos, MH Dave, ...
Nature genetics 36 (9), 999-1002, 2004
3292004
Young adult outcomes in the follow‐up of the multimodal treatment study of attention‐deficit/hyperactivity disorder: Symptom persistence, source discrepancy, and height suppression
JM Swanson, LE Arnold, BSG Molina, MH Sibley, LT Hechtman, ...
Journal of Child Psychology and Psychiatry 58 (6), 663-678, 2017
3222017
Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13. 2, 5q33. 3, 11q22, and 17p11
M Arcos-Burgos, FX Castellanos, D Pineda, F Lopera, JD Palacio, ...
The American Journal of Human Genetics 75 (6), 998-1014, 2004
3122004
Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35
ML Marazita, JC Murray, AC Lidral, M Arcos-Burgos, ME Cooper, ...
The American Journal of Human Genetics 75 (2), 161-173, 2004
3112004
Support for association between ADHD and two candidate genes: NET1 and DRD1
AJ Bobb, AM Addington, E Sidransky, MC Gornick, JP Lerch, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 134 …, 2005
2982005
Meta‐analysis of genome‐wide linkage scans of attention deficit hyperactivity disorder
K Zhou, A Dempfle, M Arcos‐Burgos, SC Bakker, T Banaschewski, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147 …, 2008
2742008
Myalgic encephalomyelitis/chronic fatigue syndrome: a comprehensive review
M Cortes Rivera, C Mastronardi, CT Silva-Aldana, M Arcos-Burgos, ...
Diagnostics 9 (3), 91, 2019
2472019
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
2232010
The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families
RF Clark, M Hutton, M Fuldner, S Froelich, E Karran, C Talbot, R Crook, ...
Nature genetics 11 (2), 219-222, 1995
2201995
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
EJ Leslie, JC Carlson, JR Shaffer, E Feingold, G Wehby, CA Laurie, ...
Human molecular genetics 25 (13), 2862-2872, 2016
2172016
Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association …
ML Marazita, AC Lidral, JC Murray, LL Field, BS Maher, ...
Human heredity 68 (3), 151-170, 2009
1842009
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