Anthony P Monaco

Cited by

	All	Since 2019
Citations	68325	13578
h-index	127	56
i10-index	313	165

3400

1700

850

2550

198619871988198919901991199219931994199519961997199819992000200120022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024179 492 707 864 658 686 849 897 887 1021 939 971 963 1026 1192 1248 1522 1564 1644 1776 1987 1940 2125 1976 2228 2698 2764 3012 3369 3109 2875 2852 2777 2612 2551 2672 2276 1917 1547

Public access

View all

59 articles

0 articles

available

not available

Based on funding mandates

Co-authors

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
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
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


Title Sort by citations Sort by year Sort by title	Cited by Cited by	Year
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	3100	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	2965	2001
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	2405	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	2367	2010
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	2336	2002
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein M Koenig, AP Monaco, LM Kunkel Cell 53 (2), 219-228, 1988	2004	1988
Mapping autism risk loci using genetic linkage and chromosomal rearrangements Nature genetics 39 (3), 319-328, 2007	1671	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	1615	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	1424	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	1127	2014
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	1074	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	1019	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	973	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	888	1994
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	885	2008
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	871	1993
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	847	1998
A genome-wide linkage and association scan reveals novel loci for autism LA Weiss, DE Arking, ... Nature 461 (7265), 802-808, 2009	810	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	738	2010
Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments CS Leblond, C Nava, A Polge, J Gauthier, G Huguet, S Lumbroso, ... PLoS genetics 10 (9), e1004580, 2014	662	2014

The system can't perform the operation now. Try again later.

Articles 1–20

Citations per year

Duplicate citations

Merged citations

Add co-authorsCo-authors

Follow

Cited by

Co-authors