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A. Monaco · SciRah

Researcher profile · Semantic Scholar

A. Monaco

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A. Monaco — researcher profile on SciRah

h-index: 94
Works: 569
Citations: 44K

Most-cited papers

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
S. H. S. B. M. S. V. S. M. R. H. B. Lee Ripke Neale Faraone Purcell Perlis Mowry Thapa, Hong S. Lee, S. Ripke, B. Neale +367 more
2013Nature Genetics2,210 citations Open access
Semantic Scholar
Functional Impact of Global Rare Copy Number Variation in Autism Spectrum Disorder
D. Pinto, A. Pagnamenta, L. Klei, R. Anney +173 more
2010Nature2,062 citations Open access
Semantic Scholar
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
Colm Lizzy Phil H Laramie Neelroop N Stephen Stephan Be O'Dushlaine Rossin Lee Duncan Parikshak Newhouse R, C. O'Dushlaine, L. Rossin, P. Lee +372 more
2015Nature Neuroscience765 citations Open access
Semantic Scholar
A genome-wide scan for common alleles affecting risk for autism
R. Anney, L. Klei, D. Pinto, R. Regan +162 more
2010Human Molecular Genetics605 citations Open access
Semantic Scholar
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments
C. Leblond, C. Nava, A. Polge, J. Gauthier +56 more
2014PLoS Genetics579 citations Open access
Semantic Scholar
Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders
C. Leblond, J. Heinrich, R. Delorme, C. Proepper +56 more
2012PLoS Genetics401 citations Open access
Semantic Scholar
Individual common variants exert weak effects on the risk for autism spectrum disorders
R. Anney, L. Klei, D. Pinto, J. Almeida +133 more
2012Human Molecular Genetics374 citations Open access
Semantic Scholar
Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects
D. Newbury, S. Paracchini, T. Scerri, L. Winchester +6 more
2010Behavior Genetics235 citations Open access
Semantic Scholar
Donation After Circulatory Death: Current Practices, Ongoing Challenges, and Potential Improvements
P. Morrissey, A. Monaco
2014Transplantation231 citations Open access
Semantic Scholar
Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder
R. Maier, G. Moser, Guo-Bo Chen, S. Ripke +373 more
2015American Journal of Human Genetics226 citations Open access
Semantic Scholar
A whole-genome scan and fine-mapping linkage study of auditory-visual synesthesia reveals evidence of linkage to chromosomes 2q24, 5q33, 6p12, and 12p12.
Julian E. Asher, J. Lamb, D. Brocklebank, J. Cazier +5 more
2009American Journal of Human Genetics213 citations Open access
Semantic Scholar
Disruption at the PTCHD1 locus on Xp22.11 in autism spectrum disorder and intellectual disability
A. Noor, Annabel C. Whibley, C. Marshall, P. Gianakopoulos +52 more
2010Science Translational Medicine207 citations Open access
Semantic Scholar
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
J. Casey, T. Magalhães, J. Conroy, R. Regan +122 more
2011Human Genetics203 citations Open access
Semantic Scholar
DCDC2, KIAA0319 and CMIP Are Associated with Reading-Related Traits
T. Scerri, A. Morris, Lyn-Louise Buckingham, D. Newbury +4 more
2011Biological Psychiatry191 citations Open access
Semantic Scholar
Common Variants in Left/Right Asymmetry Genes and Pathways Are Associated with Relative Hand Skill
William M. Brandler, A. Morris, D. Evans, T. Scerri +11 more
2013PLoS Genetics154 citations Open access
Semantic Scholar
Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia
A. Pagnamenta, E. Bacchelli, M. D. de Jonge, G. Mirza +23 more
2010Biological Psychiatry152 citations Open access
Semantic Scholar
Identification of FOXP1 Deletions in Three Unrelated Patients with Mental Retardation and Significant Speech and Language Deficits
D. Horn, J. Kapeller, Núria Rivera-Brugués, U. Moog +19 more
2010Human Mutation149 citations Open access
Semantic Scholar
Human VPS13A is associated with multiple organelles and influences mitochondrial morphology and lipid droplet motility
Wondwossen M. Yeshaw, M. van der Zwaag, Francesco Pinto, L. Lahaye +9 more
2019eLife148 citations Open access
Semantic Scholar
A 15q13.3 microdeletion segregating with autism
A. Pagnamenta, Kirsty Wing, E. S. Akha, S. Knight +9 more
2009European Journal of Human Genetics146 citations Open access
Semantic Scholar
The Role of mTOR Inhibitors in the Management of Posttransplant Malignancy
A. Monaco
2009Transplantation139 citations Open access
Semantic Scholar
PCSK6 is associated with handedness in individuals with dyslexia
T. Scerri, William M. Brandler, S. Paracchini, A. Morris +5 more
2010Human Molecular Genetics134 citations Open access
Semantic Scholar
Discovery of 42 genome-wide significant loci associated with dyslexia
C. Doust, P. Fontanillas, E. Eising, S. Gordon +141 more
2021Nature Genetics121 citations Open access
Semantic Scholar
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people
E. Eising, Nazanin Mirza-Schreiber, E. D. de Zeeuw, Carol A. Wang +91 more
2022Proceedings of the National Academy of Sciences of the United States of America107 citations Open access
Semantic Scholar
Recent advances in the genetics of language impairment
D. Newbury, S. Fisher, A. Monaco
2010Genome Medicine106 citations Open access
Semantic Scholar
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability
A. Pagnamenta, Hameed Khan, S. Walker, D. Gerrelli +15 more
2010Journal of Medical Genetics101 citations Open access
Semantic Scholar
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia
A. Gialluisi, T. Andlauer, Nazanin Mirza-Schreiber, K. Moll +45 more
2020Molecular Psychiatry100 citations Open access
Semantic Scholar
Associations of HLA alleles with specific language impairment
R. Nudel, N. Simpson, G. Baird, A. O'Hare +9 more
2014Journal of Neurodevelopmental Disorders92 citations Open access
Semantic Scholar
Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia
A. Gialluisi, T. Andlauer, Nazanin Mirza-Schreiber, K. Moll +41 more
2018bioRxiv91 citations Open access
Semantic Scholar
Linkage and candidate gene studies of autism spectrum disorders in European populations
R. Holt, G. Barnby, E. Maestrini, E. Bacchelli +9 more
2010European Journal of Human Genetics91 citations Open access
Semantic Scholar
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment
R. Nudel, N. Simpson, G. Baird, A. O'Hare +10 more
2014Genes, Brain and Behavior79 citations Open access
Semantic Scholar
Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry
I. Sousa, T. Clark, R. Holt, A. Pagnamenta +7 more
2010Molecular Autism74 citations Open access
Semantic Scholar
Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort
J. Becker, D. Czamara, T. Scerri, F. Ramus +37 more
2013European Journal of Human Genetics66 citations Open access
Semantic Scholar
Trafficking of the Menkes copper transporter ATP7A is regulated by clathrin-, AP-2–, AP-1–, and Rab22-dependent steps
Zoe G. Holloway, A. Velayos-Baeza, G. Howell, C. Levecque +3 more
2013Molecular Biology of the Cell63 citations Open access
Semantic Scholar
The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism
D. Hadley, Zhi-Liang Wu, Charlly Kao, A. Kini +94 more
2014Nature Communications59 citations Open access
Semantic Scholar
Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population
Pía Villanueva, D. Newbury, L. Jara, Zulema De Barbieri +6 more
2011European Journal of Human Genetics55 citations Open access
Semantic Scholar
The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on
Luiz G. Guidi, A. Velayos-Baeza, I. Martinez-Garay, A. Monaco +3 more
2018European Journal of Neuroscience53 citations Open access
Semantic Scholar
The Dyslexia-susceptibility Protein KIAA0319 Inhibits Axon Growth Through Smad2 Signaling
F. Franquinho, Joana Nogueira-Rodrigues, J. Duarte, Sofia Esteves +6 more
2017Cerebral Cortex53 citations Open access
Semantic Scholar
Rabbit Antithymocyte Globulin (Thymoglobulin®)
A. Gaber, A. Monaco, James A. Russell, Y. Lebranchu +1 more
2010Drugs53 citations
Semantic Scholar
The Dyslexia Candidate Locus on 2p12 Is Associated with General Cognitive Ability and White Matter Structure
T. Scerri, F. Darki, D. Newbury, A. Whitehouse +12 more
2012PLoS ONE50 citations Open access
Semantic Scholar
Identification of VPS13C as a Galectin-12-Binding Protein That Regulates Galectin-12 Protein Stability and Adipogenesis
Riyao Yang, Huiting Xue, Lan Yu, A. Velayos-Baeza +2 more
2016PLoS ONE46 citations Open access
Semantic Scholar
Links between genetics and pathophysiology in the autism spectrum disorders
R. Holt, A. Monaco
2011EMBO Molecular Medicine46 citations Open access
Semantic Scholar
Reading and Language Disorders: The Importance of Both Quantity and Quality
D. Newbury, A. Monaco, S. Paracchini
2014Genes45 citations Open access
Semantic Scholar
Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia
S. Vernes, K. Macdermot, A. Monaco, S. Fisher
2009European Journal of Human Genetics45 citations Open access
Semantic Scholar
Demographic history, current expansion and future management challenges of wild boar populations in the Balkans and Europe
N. Veličković, E. Ferreira, M. Djan, M. Ernst +3 more
2016Heredity44 citations Open access
Semantic Scholar
Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18
T. Scerri, S. Paracchini, A. Morris, I. L. MacPhie +7 more
2010PLoS ONE44 citations Open access
Semantic Scholar
A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3
A. Pagnamenta, R. Holt, Mohammed Yusuf, D. Pinto +5 more
2011Journal of Neurodevelopmental Disorders43 citations Open access
Semantic Scholar
Infection and Malignancy Outweigh Cardiovascular Mortality in Kidney Transplant Recipients: Post Hoc Analysis of the FAVORIT Trial.
L. Weinrauch, J. D'Elia, M. Weir, S. Bunnapradist +4 more
2017American Journal of Medicine42 citations
Semantic Scholar
The dyslexia-associated protein KIAA0319 interacts with adaptor protein 2 and follows the classical clathrin-mediated endocytosis pathway
C. Levecque, A. Velayos-Baeza, Zoe G. Holloway, A. Monaco
2009American Journal of Physiology - Cell Physiology40 citations Open access
Semantic Scholar
The Dyslexia-associated KIAA0319 Protein Undergoes Proteolytic Processing with γ-Secretase-independent Intramembrane Cleavage
A. Velayos-Baeza, C. Levecque, Kazuhiro Kobayashi, Zoe G. Holloway +1 more
2010Journal of Biological Chemistry39 citations Open access
Semantic Scholar
Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder
D. Newbury, F. Mari, Elham Sadighi Akha, K. Macdermot +6 more
2012European Journal of Human Genetics38 citations Open access
Semantic Scholar

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