Articles with public access mandates - Mauricio Arcos-Burgos MD, PhD.Learn more
Not available anywhere: 2
Alzheimer's disease: Age of Onset Modifier Genes in the World’s Largest Pedigree
JI Vélez Valbuena
The Australian National University, 2015
Mandates: US National Institutes of Health
Frontiers in genomic research: what the clinician needs to know.
ML Wong, M Arcos-Burgos, J Licinio
Psychiatric Times 25 (7), 44-44, 2008
Mandates: US National Institutes of Health
Available somewhere: 51
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
Mandates: US National Institutes of Health, Canadian Institutes of Health Research
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
Mandates: National Institute of Health and Medical Research, France
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
Mandates: US National Institutes of Health, German Research Foundation
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
Mandates: US National Institutes of Health, German Research Foundation
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
Mandates: US National Institutes of Health, US Department of Education, Autism Speaks …
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
Mandates: US National Institutes of Health, German Research Foundation
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
Mandates: US National Institutes of Health
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
Mandates: US National Institutes of Health, Danish National Research Foundation …
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
Mandates: US National Institutes of Health
FOXE1 association with both isolated cleft lip with or without cleft palate, and isolated cleft palate
LM Moreno, MA Mansilla, SA Bullard, ME Cooper, TD Busch, J Machida, ...
Human molecular genetics 18 (24), 4879-4896, 2009
Mandates: US National Institutes of Health
Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3p
M Gunay-Aygun, Y Zivony-Elboum, F Gumruk, D Geiger, M Cetin, ...
Blood, The Journal of the American Society of Hematology 116 (23), 4990-5001, 2010
Mandates: US National Institutes of Health
A genome-wide association study of nonsyndromic cleft palate identifies an etiologic missense variant in GRHL3
EJ Leslie, H Liu, JC Carlson, JR Shaffer, E Feingold, G Wehby, CA Laurie, ...
The American Journal of Human Genetics 98 (4), 744-754, 2016
Mandates: US National Institutes of Health
Mistargeting of peroxisomal EHHADH and inherited renal Fanconi's syndrome
ED Klootwijk, M Reichold, A Helip-Wooley, A Tolaymat, C Broeker, ...
New England Journal of Medicine 370 (2), 129-138, 2014
Mandates: US National Institutes of Health, German Research Foundation
Latent class subtyping of attention-deficit/hyperactivity disorder and comorbid conditions
MT Acosta, FX Castellanos, KL Bolton, JZ Balog, P Eagen, L Nee, J Jones, ...
Journal of the American Academy of Child & Adolescent Psychiatry 47 (7), 797-807, 2008
Mandates: US National Institutes of Health
A common genetic network underlies substance use disorders and disruptive or externalizing disorders
M Arcos-Burgos, JI Vélez, BD Solomon, M Muenke
Human Genetics 131, 917-929, 2012
Mandates: US National Institutes of Health
Prediction of susceptibility to major depression by a model of interactions of multiple functional genetic variants and environmental factors
ML Wong, C Dong, V Andreev, M Arcos-Burgos, J Licinio
Molecular psychiatry 17 (6), 624-633, 2012
Mandates: US National Institutes of Health
ADHD latent class clusters: DSM-IV subtypes and comorbidity
J Elia, M Arcos-Burgos, KL Bolton, PJ Ambrosini, W Berrettini, M Muenke
Psychiatry research 170 (2-3), 192-198, 2009
Mandates: US National Institutes of Health
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 17 (7), 741-747, 2012
Mandates: US National Institutes of Health, German Research Foundation
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