Anthony P Monaco
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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
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
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
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
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
The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein
M Koenig, AP Monaco, LM Kunkel
Cell 53 (2), 219-228, 1988
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Nature genetics 39 (3), 319-328, 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
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
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
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
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
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
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
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
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
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
A genome-wide linkage and association scan reveals novel loci for autism
LA Weiss, DE Arking, ...
Nature 461 (7265), 802-808, 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
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
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