Michael Cuccaro
Michael Cuccaro
Associate Professor, Human Genetics, University of Miami Miller School of Medicine
Adresă de e-mail confirmată pe med.miami.edu
Citat de
Citat de
Functional impact of global rare copy number variation in autism spectrum disorders
D Pinto, AT Pagnamenta, L Klei, R Anney, D Merico, R Regan, J Conroy, ...
Nature 466 (7304), 368-372, 2010
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Nature genetics 39 (3), 319-328, 2007
Common genetic variants on 5p14. 1 associate with autism spectrum disorders
K Wang, H Zhang, D Ma, M Bucan, JT Glessner, BS Abrahams, ...
Nature 459 (7246), 528-533, 2009
A genome-wide linkage and association scan reveals novel loci for autism
LA Weiss, DE Arking, ...
Nature 461 (7265), 802-808, 2009
A genome-wide scan for common alleles affecting risk for autism
R Anney, L Klei, D Pinto, R Regan, J Conroy, TR Magalhaes, C Correia, ...
Human molecular genetics 19 (20), 4072-4082, 2010
Genomic and epigenetic evidence for oxytocin receptor deficiency in autism
SG Gregory, JJ Connelly, AJ Towers, J Johnson, D Biscocho, ...
BMC medicine 7, 1-13, 2009
Autism and maternally derived aberrations of chromosome 15q
RJ Schroer, MC Phelan, RC Michaelis, EC Crawford, SA Skinner, ...
American journal of medical genetics 76 (4), 327-336, 1998
Repetitive behaviors in autism: Relationships with associated clinical features
RL Gabriels, ML Cuccaro, DE Hill, BJ Ivers, E Goldson
Research in developmental disabilities 26 (2), 169-181, 2005
Fine mapping of autistic disorder to chromosome 15q11-q13 by use of phenotypic subtypes
Y Shao, ML Cuccaro, ER Hauser, KL Raiford, MM Menold, CM Wolpert, ...
The American Journal of Human Genetics 72 (3), 539-548, 2003
Individual common variants exert weak effects on the risk for autism spectrum disorders
R Anney, L Klei, D Pinto, J Almeida, E Bacchelli, G Baird, N Bolshakova, ...
Human molecular genetics 21 (21), 4781-4792, 2012
Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism
DQ Ma, PL Whitehead, MM Menold, ER Martin, AE Ashley-Koch, H Mei, ...
The American Journal of Human Genetics 77 (3), 377-388, 2005
Factor analysis of restricted and repetitive behaviors in autism using the Autism Diagnostic Interview-R
ML Cuccaro, Y Shao, J Grubber, M Slifer, CM Wolpert, SL Donnelly, ...
Child psychiatry and human development 34, 3-17, 2003
Identification of MeCP2 mutations in a series of females with autistic disorder
RM Carney, CM Wolpert, SA Ravan, M Shahbazian, A Ashley-Koch, ...
Pediatric neurology 28 (3), 205-211, 2003
Genomic screen and follow‐up analysis for autistic disorder
Y Shao, CM Wolpert, KL Raiford, MM Menold, SL Donnelly, SA Ravan, ...
American journal of medical genetics 114 (1), 99-105, 2002
Race and gender differences in the treatment of psychiatric disorders in young adolescents
SP Cuffe, JL Waller, ML Cuccaro, AJ Pumariega, CZ Garrison
Journal of the American Academy of Child & Adolescent Psychiatry 34 (11 …, 1995
A genome‐wide association study of autism reveals a common novel risk locus at 5p14. 1
D Ma, D Salyakina, JM Jaworski, I Konidari, PL Whitehead, AN Andersen, ...
Annals of human genetics 73 (3), 263-273, 2009
Genetic studies of autistic disorder and chromosome 7
A Ashley-Koch, CM Wolpert, MM Menold, L Zaeem, S Basu, SL Donnelly, ...
Genomics 61 (3), 227-236, 1999
Analysis of the RELN gene as a genetic risk factor for autism
DA Skaar, Y Shao, JL Haines, JE Stenger, J Jaworski, ER Martin, ...
Molecular psychiatry 10 (6), 563-571, 2005
Accelerated head growth in early development of individuals with autism
YA Dementieva, DD Vance, SL Donnelly, LA Elston, CM Wolpert, ...
Pediatric neurology 32 (2), 102-108, 2005
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
JP Casey, T Magalhaes, JM Conroy, R Regan, N Shah, R Anney, ...
Human genetics 131, 565-579, 2012
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