Anthony P Monaco

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Simon E. FisherDirector, Max Planck Institute for PsycholinguisticsCorreu electrònic verificat a mpi.nl
Silvia ParacchiniProfessor, University of St AndrewsCorreu electrònic verificat a st-andrews.ac.uk
Prof. dr. Clyde FrancksMax Planck Institute & Radboud University Medical Center, Nijmegen, the NetherlandsCorreu electrònic verificat a mpi.nl
Alex J. RichardsonSenior Research Associate, University of OxfordCorreu electrònic verificat a dpag.ox.ac.uk
Janine LambReader in Complex Human Genetics/Genomics, University of ManchesterCorreu electrònic verificat a manchester.ac.uk
Thomas ScerriPostdoctoral Fellow, Bioinformatics Division, Walter and Eliza Hall Instutite of Medical ResearchCorreu electrònic verificat a wehi.edu.au
Joel B. TalcottProfessor of Developmental Cognitive Neuroscience, Aston Brain Centre, Aston UniversityCorreu electrònic verificat a aston.ac.uk
Eric P HoffmanProfessor, Department of Pharmaceutical Sciences, Binghamton UniversityCorreu electrònic verificat a binghamton.edu
Kay DaviesProfessor of Genetics University of OxfordCorreu electrònic verificat a dpag.ox.ac.uk
John DeFriesFaculty Fellow, Institute for Behavioral GeneticsCorreu electrònic verificat a colorado.edu
Richard OlsonUniversity of ColoradoCorreu electrònic verificat a colorado.edu
Bruce F. PenningtonProfessor of PsychologyCorreu electrònic verificat a du.edu
Andrew MorrisProfessor of Statistical GeneticsCorreu electrònic verificat a liverpool.ac.uk
jean louis mandelprof. Collège de france (chaire génétique humaine), responsable labo. diagnostic génét. CHUCorreu electrònic verificat a igbmc.fr
Sreenivasan PonnambalamReader in Human Disease Biology, University of Leeds, UKCorreu electrònic verificat a leeds.ac.uk
Daniel E. WeeksProfessor of Human Genetics and Biostatistics, University of PittsburghCorreu electrònic verificat a pitt.edu
Sue Pavitt nee RiderProfessor in Translation & Applied Health Research, Director of Dental Translation and ClinicalCorreu electrònic verificat a leeds.ac.uk
Justin Paul RubioAssociate Prof of Human Genetics, The Florey Institute of Neuroscience andCorreu electrònic verificat a unimelb.edu.au
Lon CardonChief Scientific Officer, BioMarin PharmaceuticalCorreu electrònic verificat a bmrn.com
Laura WinchesterOxford UniversityCorreu electrònic verificat a psych.ox.ac.uk

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Anthony P Monaco

President, Tufts University

Correu electrònic verificat a tufts.edu - Pàgina d'inici

neurodevelopmental disorders human genetics neuroscience autism dyslexia


Títol Ordena per cites Ordena per any Ordena per títol	Citada per Citada per	Any
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	3115	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	2992	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	2388	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	2352	2002
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein M Koenig, AP Monaco, LM Kunkel Cell 53 (2), 219-228, 1988	2015	1988
Mapping autism risk loci using genetic linkage and chromosomal rearrangements Nature genetics 39 (3), 319-328, 2007	1675	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	1622	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	1435	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	1138	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	1079	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	1018	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	976	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	895	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	889	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	873	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	850	1998
A genome-wide linkage and association scan reveals novel loci for autism LA Weiss, DE Arking, ... Nature 461 (7265), 802-808, 2009	814	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	741	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	672	2014

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