Anthony P Monaco

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Simon E. FisherDirector, Max Planck Institute for PsycholinguisticsVerified email at mpi.nl
Silvia ParacchiniProfessor, University of St AndrewsVerified email at st-andrews.ac.uk
Prof. dr. Clyde FrancksMax Planck Institute & Radboud University Medical Center, Nijmegen, the NetherlandsVerified email at mpi.nl
Alex J. RichardsonSenior Research Associate, University of OxfordVerified email at dpag.ox.ac.uk
Janine LambReader in Complex Human Genetics/Genomics, University of ManchesterVerified email at manchester.ac.uk
Thomas ScerriPostdoctoral Fellow, Bioinformatics Division, Walter and Eliza Hall Instutite of Medical ResearchVerified email at wehi.edu.au
Joel B. TalcottProfessor of Developmental Cognitive Neuroscience, Aston Brain Centre, Aston UniversityVerified email at aston.ac.uk
Huntington F WillardGenome Medical, IncVerified email at genomemedical.com
Kay DaviesProfessor of Genetics University of OxfordVerified email at dpag.ox.ac.uk
Eric P HoffmanProfessor, Department of Pharmaceutical Sciences, Binghamton UniversityVerified email at binghamton.edu
John DeFriesFaculty Fellow, Institute for Behavioral GeneticsVerified email at colorado.edu
Richard OlsonUniversity of ColoradoVerified email at colorado.edu
Bruce F. PenningtonProfessor of PsychologyVerified email at du.edu
Andrew MorrisProfessor of Statistical GeneticsVerified email at liverpool.ac.uk
jean louis mandelprof. Collège de france (chaire génétique humaine), responsable labo. diagnostic génét. CHUVerified email at igbmc.fr
Sreenivasan PonnambalamReader in Human Disease Biology, University of Leeds, UKVerified email at leeds.ac.uk
Daniel E. WeeksProfessor of Human Genetics and Biostatistics, University of PittsburghVerified email at pitt.edu
Sue Pavitt nee RiderProfessor in Translation & Applied Health Research, Director of Dental Translation and ClinicalVerified email at leeds.ac.uk
Justin Paul RubioAssociate Prof of Human Genetics, The Florey Institute of Neuroscience andVerified email at unimelb.edu.au
Lon CardonChief Scientific Officer, BioMarin PharmaceuticalVerified email at bmrn.com

Anthony P Monaco

President, Tufts University

Verified email at tufts.edu - Homepage

neurodevelopmental disorders human genetics neuroscience autism dyslexia


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Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals M Koenig, EP Hoffman, CJ Bertelson, AP Monaco, C Feener, LM Kunkel Cell 50 (3), 509-517, 1987	2988	1987
A forkhead-domain gene is mutated in a severe speech and language disorder CSL Lai, SE Fisher, JA Hurst, F Vargha-Khadem, AP Monaco Nature 413 (6855), 519-523, 2001	2866	2001
Molecular evolution of FOXP2, a gene involved in speech and language W Enard, M Przeworski, SE Fisher, CSL Lai, V Wiebe, T Kitano, ... Nature 418 (6900), 869-872, 2002	2234	2002
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ... Nature genetics 45 (9), 984-994, 2013	2231	2013
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	2231	2010
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein M Koenig, AP Monaco, LM Kunkel Cell 53 (2), 219-228, 1988	1972	1988
Mapping autism risk loci using genetic linkage and chromosomal rearrangements Nature genetics 39 (3), 319-328, 2007	1606	2007
An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus AP Monaco, CJ Bertelson, S Liechti-Gallati, H Moser, LM Kunkel Genomics 2 (1), 90-95, 1988	1533	1988
Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene AP Monaco, RL Neve, C Colletti-Feener, CJ Bertelson, DM Kurnit, ... Nature 323 (6089), 646-650, 1986	1391	1986
Cloning the gene for an inherited human disorder—chronic granulomatous disease—on the basis of its chromosomal location B Royer-Pokora, LM Kunkel, AP Monaco, SC Goff, PE Newburger, ... Nature 322 (6074), 32-38, 1986	1062	1986
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders D Pinto, E Delaby, D Merico, M Barbosa, A Merikangas, L Klei, ... The American Journal of Human Genetics 94 (5), 677-694, 2014	1013	2014
An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita E Zanaria, F Muscatelli, B Bardoni, TM Strom, S Guioli, W Guo, E Lalli, ... Nature 372 (6507), 635-641, 1994	970	1994
Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease A Sakuntabhai, V Ruiz-Perez, S Carter, N Jacobsen, S Burge, S Monk, ... Nature genetics 21 (3), 271-277, 1999	931	1999
Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism F Muscatelli, TM Strom, AP Walker, E Zanaria, D Récan, A Meindl, ... Nature 372 (6507), 672-676, 1994	834	1994
Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein J Chelly, Z Tümer, T Tønnesen, A Petterson, Y Ishikawa-Brush, ... Nature genetics 3 (1), 14-19, 1993	833	1993
A functional genetic link between distinct developmental language disorders SC Vernes, DF Newbury, BS Abrahams, L Winchester, J Nicod, M Groszer, ... New England Journal of Medicine 359 (22), 2337-2345, 2008	830	2008
Localisation of a gene implicated in a severe speech and language disorder SE Fisher, F Vargha-Khadem, KE Watkins, AP Monaco, ME Pembrey Nature genetics 18 (2), 168-170, 1998	814	1998
A genome-wide linkage and association scan reveals novel loci for autism LA Weiss, DE Arking, ... Nature 461 (7265), 802-808, 2009	748	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	690	2010
Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion. LM Kunkel, AP Monaco, W Middlesworth, HD Ochs, SA Latt Proceedings of the National Academy of Sciences 82 (14), 4778-4782, 1985	620	1985

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