2018 - Fellow of the American Academy of Arts and Sciences
His primary areas of investigation include Genetics, Autism, Locus, Gene and Genetic linkage. His research on Genetics often connects related topics like Molecular biology. His study in Molecular biology is interdisciplinary in nature, drawing from both Complementary DNA, Duchenne muscular dystrophy and Exon.
His Autism research integrates issues from Single-nucleotide polymorphism and Intellectual disability. His Genetic linkage research also works with subjects such as
Genetics, Transplantation, Immunology, Surgery and Gene are his primary areas of study. Anthony P. Monaco regularly links together related areas like Autism in his Genetics studies. His biological study spans a wide range of topics, including Single-nucleotide polymorphism and Candidate gene.
His studies deal with areas such as Immunosuppression, Kidney and Pathology as well as Transplantation. His Gene study frequently draws connections to other fields, such as Molecular biology. Anthony P. Monaco has included themes like Gastroenterology and Diabetes mellitus, Endocrinology in his Internal medicine study.
His scientific interests lie mostly in Genetics, Autism, Genome-wide association study, Dyslexia and Transplantation. His research related to Single-nucleotide polymorphism, Copy-number variation, Candidate gene, Locus and Gene might be considered part of Genetics. His work is dedicated to discovering how Candidate gene, Genetic association are connected with Genetic linkage and other disciplines.
Many of his studies involve connections with topics such as Intellectual disability and Autism. His Genome-wide association study research includes themes of Schizophrenia, Bipolar disorder, Specific language impairment, Genomics and Allele. The Reading disability research he does as part of his general Dyslexia study is frequently linked to other disciplines of science, such as Clinical psychology and Cognition, therefore creating a link between diverse domains of science.
Anthony P. Monaco mostly deals with Genetics, Autism, Genome-wide association study, Single-nucleotide polymorphism and Copy-number variation. His Genetics study frequently draws connections to adjacent fields such as Specific language impairment. His Specific language impairment study incorporates themes from CNTNAP2 and Communication disorder.
His Copy-number variation research includes elements of Genetic variation, Bioinformatics and Genetic architecture. The concepts of his Locus study are interwoven with issues in Heterologous, Immunology, Lymphocyte and Immunologic Tolerance. His Genetic association research is multidisciplinary, incorporating perspectives in Psychiatric genetics and Genomics.
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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;E.P. Hoffman;C.J. Bertelson;A.P. Monaco.
Cell (1987)
A forkhead-domain gene is mutated in a severe speech and language disorder
Cecilia S. L. Lai;Simon E. Fisher;Jane A. Hurst;Faraneh Vargha-Khadem.
Nature (2001)
Molecular evolution of FOXP2, a gene involved in speech and language
Wolfgang Enard;Molly Przeworski;Simon E. Fisher;Cecilia S. L. Lai.
Nature (2002)
Functional impact of global rare copy number variation in autism spectrum disorders
Dalila Pinto;Alistair T. Pagnamenta;Lambertus Klei;Richard Anney.
Nature (2010)
The Complete Sequence of Dystrophin Predicts a Rod-Shaped Cytoskeletal Protein
M. Koenig;M. Koenig;A.P. Monaco;A.P. Monaco;L.M. Kunkel;L.M. Kunkel;L.M. Kunkel.
Cell (1988)
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
S. Hong Lee;Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Stephen V. Faraone.
Nature Genetics (2013)
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Peter Szatmari;Andrew D. Paterson;Lonnie Zwaigenbaum;Wendy Roberts.
Nature Genetics (2007)
An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus.
Anthony P. Monaco;Corlee J. Bertelson;Corlee J. Bertelson;Sabina Liechti-Gallati;Hans Moser.
Genomics (1988)
Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene.
Anthony P. Monaco;Anthony P. Monaco;Rachael L. Neve;Rachael L. Neve;Chris Colletti-Feener;Corlee J. Bertelson.
Nature (1986)
Cloning the gene for an inherited human disorder—chronic granulomatous disease—on the basis of its chromosomal location
B. Royerpokora;L. M. Kunkel;A. P. Monaco;S. C. Goff.
Nature (1986)
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