Anthony P Monaco

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Simon E. FisherDirector, Max Planck Institute for PsycholinguisticsEmail verificata su mpi.nl
Silvia ParacchiniProfessor, University of St AndrewsEmail verificata su st-andrews.ac.uk
Prof. dr. Clyde FrancksMax Planck Institute & Radboud University Medical Center, Nijmegen, the NetherlandsEmail verificata su mpi.nl
Alex J. RichardsonSenior Research Associate, University of OxfordEmail verificata su dpag.ox.ac.uk
Janine LambReader in Complex Human Genetics/Genomics, University of ManchesterEmail verificata su manchester.ac.uk
Thomas ScerriPostdoctoral Fellow, Bioinformatics Division, Walter and Eliza Hall Instutite of Medical ResearchEmail verificata su wehi.edu.au
Joel B. TalcottProfessor of Developmental Cognitive Neuroscience, Aston Brain Centre, Aston UniversityEmail verificata su aston.ac.uk
Eric P HoffmanProfessor, Department of Pharmaceutical Sciences, Binghamton UniversityEmail verificata su binghamton.edu
Kay DaviesProfessor of Genetics University of OxfordEmail verificata su dpag.ox.ac.uk
John DeFriesFaculty Fellow, Institute for Behavioral GeneticsEmail verificata su colorado.edu
Richard OlsonUniversity of ColoradoEmail verificata su colorado.edu
Bruce F. PenningtonProfessor of PsychologyEmail verificata su du.edu
Andrew MorrisProfessor of Statistical GeneticsEmail verificata su liverpool.ac.uk
jean louis mandelprof. Collège de france (chaire génétique humaine), responsable labo. diagnostic génét. CHUEmail verificata su igbmc.fr
Sreenivasan PonnambalamReader in Human Disease Biology, University of Leeds, UKEmail verificata su leeds.ac.uk
Daniel E. WeeksProfessor of Human Genetics and Biostatistics, University of PittsburghEmail verificata su pitt.edu
Sue Pavitt nee RiderProfessor in Translation & Applied Health Research, Director of Dental Translation and ClinicalEmail verificata su leeds.ac.uk
Justin Paul RubioAssociate Prof of Human Genetics, The Florey Institute of Neuroscience andEmail verificata su unimelb.edu.au
Lon CardonChief Scientific Officer, BioMarin PharmaceuticalEmail verificata su bmrn.com
Laura WinchesterOxford UniversityEmail verificata su psych.ox.ac.uk

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Anthony P Monaco

University Professor and President emeritus, Tufts University

Email verificata su tufts.edu

neurodevelopmental disorders human genetics neuroscience autism dyslexia


Titolo Ordina per citazioni Ordina per anno Ordina per titolo	Citata da Citata da	Anno
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	3122	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	2962	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	2432	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	2416	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	2339	2002
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein M Koenig, AP Monaco, LM Kunkel Cell 53 (2), 219-228, 1988	2016	1988
Mapping autism risk loci using genetic linkage and chromosomal rearrangements Nature genetics 39 (3), 319-328, 2007	1646	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	1607	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	1428	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	1135	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	1099	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	1022	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	972	1999
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	884	2008
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	884	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	868	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	846	1998
A genome-wide linkage and association scan reveals novel loci for autism LA Weiss, DE Arking, ... Nature 461 (7265), 802-808, 2009	815	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	735	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	671	2014

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