Anthony P Monaco

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Citations	56655	12863
h-index	116	52
i10-index	305	157

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198619871988198919901991199219931994199519961997199819992000200120022003200420052006200720082009201020112012201320142015201620172018201920202021192 470 691 828 607 669 784 829 790 949 865 892 888 967 1144 1161 1422 1498 1593 1690 1844 1801 2052 1935 2181 2572 2654 2856 3141 2919 2649 2623 2553 2343 2316 374

Co-authors

Simon E. FisherDirector, Max Planck Institute for PsycholinguisticsVerified email at mpi.nl
Silvia ParacchiniUniversity of St AndrewsVerified email at st-andrews.ac.uk
Clyde FrancksMax Planck Institute for Psycholinguistics, Nijmegen, The NetherlandsVerified email at mpi.nl
Alex J. RichardsonSenior Research Associate, University of OxfordVerified email at dpag.ox.ac.uk
Thomas ScerriPostdoctoral Fellow, Bioinformatics Division, Walter and Eliza Hall Instutite of Medical ResearchVerified email at wehi.edu.au
Janine LambReader in Complex Human Genetics/Genomics, University of ManchesterVerified email at manchester.ac.uk
Huntington F WillardGenome Medical, IncVerified email at genomemedical.com
Kay DaviesProfessor of Genetics University of OxfordVerified email at dpag.ox.ac.uk
Joel B. TalcottProfessor of Developmental Cognitive Neuroscience, Aston Brain Centre, Aston UniversityVerified email at aston.ac.uk
Eric P HoffmanProfessor, Department of Pharmaceutical Sciences, Binghamton UniversityVerified email at binghamton.edu
Andrew MorrisProfessor of Statistical GeneticsVerified email at liverpool.ac.uk
Richard OlsonUniversity of ColoradoVerified email at colorado.edu
jean louis mandelprof. Collège de france (chaire génétique humaine), responsable labo. diagnostic génét. CHUVerified email at igbmc.fr
John DeFriesFaculty Fellow, Institute for Behavioral GeneticsVerified email at colorado.edu
Bruce F. PenningtonProfessor of PsychologyVerified email at du.edu
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
Stan NelsonProfessor of Human Genetics, UCLAVerified email at ucla.edu
Laura WinchesterOxford UniversityVerified email at psych.ox.ac.uk

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	2660	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	2486	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	2009	2002
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	1935	2010
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein M Koenig, AP Monaco, LM Kunkel Cell 53 (2), 219-228, 1988	1801	1988
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs SH Lee, S Ripke, BM Neale, SV Faraone, SM Purcell, RH Perlis, ... Nature genetics 45 (9), 984, 2013	1756	2013
Mapping autism risk loci using genetic linkage and chromosomal rearrangements P Szatmari, AD Paterson, L Zwaigenbaum, W Roberts, J Brian, XQ Liu, ... Nature genetics 39 (3), 319, 2007	1447	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	1324	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	1196	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	939	1986
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	905	1994
Mutations in ATP2A2, encoding a Ca 2+ pump, cause Darier disease A Sakuntabhai, V Ruiz-Perez, S Carter, N Jacobsen, S Burge, S Monk, ... Nature genetics 21 (3), 271-277, 1999	833	1999
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	774	1993
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	764	1994
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	750	2014
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	745	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	713	1998
A genome-wide linkage and association scan reveals novel loci for autism LA Weiss, DE Arking Nature 461 (7265), 802-808, 2009	653	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	595	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	558	1985

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