Anthony P Monaco

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198619871988198919901991199219931994199519961997199819992000200120022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024179 492 707 864 658 686 849 896 883 1023 938 971 963 1026 1190 1248 1521 1564 1642 1776 1987 1941 2119 1976 2230 2698 2763 3009 3365 3111 2876 2852 2784 2613 2547 2660 2264 1918 1459

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

Ikuti

Anthony P Monaco

President, Tufts University

Email yang diverifikasi di tufts.edu - Beranda

neurodevelopmental disorders human genetics neuroscience autism dyslexia


Judul Urutkan menurut kutipan Urutkan menurut tahun Urutkan menurut judul	Dikutip oleh Dikutip oleh	Tahun
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	3097	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	2403	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	2361	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	2333	2002
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein M Koenig, AP Monaco, LM Kunkel Cell 53 (2), 219-228, 1988	2001	1988
Mapping autism risk loci using genetic linkage and chromosomal rearrangements Nature genetics 39 (3), 319-328, 2007	1669	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	1608	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	1421	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	1120	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	1071	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	970	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	887	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	884	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	869	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	808	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	737	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	658	2014

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