Anthony P. Monaco

Wellcome Trust Centre for Human Genetics, University of Oxford

Research Area

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 2	2010

Other Publications

Article	Year
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia. Nature genetics\| PubMed ID: 11743577	2002
A genomewide linkage screen for relative hand skill in sibling pairs. American journal of human genetics\| PubMed ID: 11774074	2002
Hailey-Hailey disease: molecular and clinical characterization of novel mutations in the ATP2C1 gene. The Journal of investigative dermatology\| PubMed ID: 11841554	2002
Molecular characterization and expression analysis of Mtmr2, mouse homologue of MTMR2, the Myotubularin-related 2 gene, mutated in CMT4B. Gene\| PubMed ID: 11867209	2002
Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1. Psychiatric genetics\| PubMed ID: 11901358	2002
A genomewide scan for loci involved in attention-deficit/hyperactivity disorder. American journal of human genetics\| PubMed ID: 11923911	2002
Clinical features and molecular bases of neuroacanthocytosis. Journal of molecular medicine (Berlin, Germany)\| PubMed ID: 12185448	2002
Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism. American journal of human genetics\| PubMed ID: 12187510	2002
Molecular evolution of FOXP2, a gene involved in speech and language. Nature\| PubMed ID: 12192408	2002
Enteric drainage of a pancreas allograft is safe for patients with celiac sprue. Clinical transplantation\| PubMed ID: 12225438	2002
Autism: in search of susceptibility genes. Neuromolecular medicine\| PubMed ID: 12230302	2002
Immunologic mechanisms in tolerance produced in mice with nonradiation-based lymphoablation and donor-specific bone marrow. Transplantation\| PubMed ID: 12352905	2002
Management of thrombophilia in renal transplant patients. American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons\| PubMed ID: 12392294	2002
Novel membrane traffic steps regulate the exocytosis of the Menkes disease ATPase. Human molecular genetics\| PubMed ID: 12393797	2002
Molecular genetics of speech and language disorders. Current opinion in pediatrics\| PubMed ID: 12436038	2002
Talking genes - the molecular basis of language impairment. Biologist (London, England)\| PubMed ID: 12486301	2002
Prevention of autoimmune diabetes by FTY720 in nonobese diabetic mice. Transplantation\| PubMed ID: 12499880	2002
Deciphering the genetic basis of speech and language disorders. Annual review of neuroscience\| PubMed ID: 12524432	2003
Use of multivariate linkage analysis for dissection of a complex cognitive trait. American journal of human genetics\| PubMed ID: 12587094	2003
Confirmatory evidence for linkage of relative hand skill to 2p12-q11. American journal of human genetics\| PubMed ID: 12596796	2003
Chorea-acanthocytosis: clinical and genetic findings in three families from the Arabian peninsula. Movement disorders : official journal of the Movement Disorder Society\| PubMed ID: 12671946	2003
A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11. American journal of human genetics\| PubMed ID: 12687500	2003
Genomic studies of gene expression: regulation of the Wilson disease gene. Genomics\| PubMed ID: 12782122	2003
The Menkes disease ATPase (ATP7A) is internalized via a Rac1-regulated, clathrin- and caveolae-independent pathway. Human molecular genetics\| PubMed ID: 12812980	2003
Chimerism in organ transplantation: conflicting experiments and clinical observations. Transplantation\| PubMed ID: 12819484	2003
Myotubularin-related 2 protein phosphatase and neurofilament light chain protein, both mutated in CMT neuropathies, interact in peripheral nerve. Human molecular genetics\| PubMed ID: 12837694	2003
The genetic basis of dyslexia. Lancet neurology\| PubMed ID: 12849333	2002
FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder. Brain : a journal of neurology\| PubMed ID: 12876151	2003
Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11. Human molecular genetics\| PubMed ID: 14583442	2003
Familial and genetic effects on motor coordination, laterality, and reading-related cognition. The American journal of psychiatry\| PubMed ID: 14594743	2003
Aberrant trafficking of transmembrane proteins in human disease. Trends in cell biology\| PubMed ID: 14624842	2003
Geographic disparities in access to organ transplantation. Transplantation\| PubMed ID: 14627920	2003
Tolerance comes of age. Editorial comment. Transplantation\| PubMed ID: 14657673	2003
Actin and microtubule regulation of trans-Golgi network architecture, and copper-dependent protein transport to the cell surface. Molecular membrane biology\| PubMed ID: 14668139	2004
Regulatory T cells finally get the attention they deserve. Transplantation\| PubMed ID: 14726757	2004
A meta-analysis from the Cochrane Library reviewing interleukin 2 receptor antagonists in renal transplantation. Transplantation\| PubMed ID: 14742975	2004
Clinical Tolerance: the end of the beginning. Transplantation\| PubMed ID: 15077038	2004
Renal transplant survival from older donors: a single center experience. Archives of surgery (Chicago, Ill. : 1960)\| PubMed ID: 15078705	2004
HLA in the allocation of cadaver kidneys: a global perspective. Transplantation\| PubMed ID: 15084945	2004
Chorein detection for the diagnosis of chorea-acanthocytosis. Annals of neurology\| PubMed ID: 15293285	2004
Active role of chimerism in transplantation tolerance induced by antilymphocyte serum, sirolimus, and bone-marrow-cell infusion. Transplantation\| PubMed ID: 15385800	2004
Ethical issues and xenotransplantation. Transplantation\| PubMed ID: 15502701	2004
A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States. American journal of human genetics\| PubMed ID: 15514892	2004
Mutation screening and association analysis of six candidate genes for autism on chromosome 7q. European journal of human genetics : EJHG\| PubMed ID: 15523497	2005
Care of the live kidney donor: consensus on the ultimate gift. Transplantation\| PubMed ID: 15785360	2005
Early clinical heterogeneity in choreoacanthocytosis. Archives of neurology\| PubMed ID: 15824261	2005
Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT. American journal of human genetics\| PubMed ID: 15830322	2005
The beginning of clinical tolerance in solid organ allografts. Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation\| PubMed ID: 15859922	2004
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits. American journal of human genetics\| PubMed ID: 15877281	2005
Reduction in calcineurin inhibitor exposure and maintenance of effective immunosuppression: clinical experience with everolimus (Certican). Transplantation\| PubMed ID: 15880017	2005
Prevention and cure of autoimmune diabetes in nonobese diabetic mice by continuous administration of FTY720. Transplantation\| PubMed ID: 15880042	2005
On the intraoperative molecular status of renal allografts after vascular reperfusion and clinical outcomes. Journal of the American Society of Nephrology : JASN\| PubMed ID: 15888558	2005
Pancreatic islet transplantation: is the glass half-empty or half-full? Transplantation\| PubMed ID: 15912089	2005
Identification of a VPS13A founder mutation in French Canadian families with chorea-acanthocytosis. Neurogenetics\| PubMed ID: 15918062	2005
Familial temporal lobe epilepsy as a presenting feature of choreoacanthocytosis. Epilepsia\| PubMed ID: 16060937	2005
Older living donors provide excellent quality kidneys: a single center experience (older living donors). Clinical transplantation\| PubMed ID: 16146550	2005
Genetic influences on language impairment and phonological short-term memory. Trends in cognitive sciences\| PubMed ID: 16188486	2005
SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample. European journal of human genetics : EJHG\| PubMed ID: 16205742	2006
Intensive care unit extubation does not preclude extrarenal organ recovery from donors after cardiac death. Transplantation\| PubMed ID: 16314792	2005
Good samaritan kidney donation. Transplantation\| PubMed ID: 16340776	2005
Utility of a mathematical nomogram to predict delayed graft function: a single-center experience. Transplantation\| PubMed ID: 16436956	2006
The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration. Human molecular genetics\| PubMed ID: 16600991	2006
Use of an immune function assay to monitor immunosuppression for treatment of post-transplant lymphoproliferative disorder. Pediatric transplantation\| PubMed ID: 16856999	2006
Editorial comment: the other consequences of CMV infection. Transplantation\| PubMed ID: 16858267	2006
Costs of ABO incompatible living donor transplantation are justified. Transplantation\| PubMed ID: 16858273	2006
Living kidney donation: evolution and technical aspects of donor nephrectomy. The Surgical clinics of North America\| PubMed ID: 16962411	2006
Cell biology of membrane trafficking in human disease. International review of cytology\| PubMed ID: 16984815	2006
Determination of the mutation spectrum of the EXT1/EXT2 genes in British Caucasian patients with multiple osteochondromas, and exclusion of six candidate genes in EXT negative cases. Human mutation\| PubMed ID: 17041877	2006
Introduction of Sir Peter John Morris. Transplantation\| PubMed ID: 17198240	2006
Reducing the financial disincentives to living kidney donation: will compensation help the way it is supposed to? Nature clinical practice. Nephrology\| PubMed ID: 17245328	2007
Mapping autism risk loci using genetic linkage and chromosomal rearrangements. Nature genetics\| PubMed ID: 17322880	2007
Multivariate linkage analysis of specific language impairment (SLI). Annals of human genetics\| PubMed ID: 17388790	2007
The genetic lexicon of dyslexia. Annual review of genomics and human genetics\| PubMed ID: 17444811	2007
Is there a rational solution to the kidney shortage? Medicine and health, Rhode Island\| PubMed ID: 17601289	2007
Editorial comment: a role for alloimmune response mediators in tolerance induction? Transplantation\| PubMed ID: 17632404	2007
Alternative splicing in the dyslexia-associated gene KIAA0319. Mammalian genome : official journal of the International Mammalian Genome Society\| PubMed ID: 17846832	2007
Activation of ADP-ribosylation factor regulates biogenesis of the ATP7A-containing trans-Golgi network compartment and its Cu-induced trafficking. American journal of physiology. Cell physiology\| PubMed ID: 17913844	2007
Instant electronic access to randomized controlled trials (RCT). Transplantation\| PubMed ID: 17989594	2007
Choreoacanthocytosis in a Mexican family. Archives of neurology\| PubMed ID: 17998451	2007
The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms. Human molecular genetics\| PubMed ID: 18063668	2008
SV40 infection associated with rituximab treatment after kidney transplantation in nonhuman primates. Transplantation\| PubMed ID: 18360273	2008
Oxidised LDL internalisation by the LOX-1 scavenger receptor is dependent on a novel cytoplasmic motif and is regulated by dynamin-2. Journal of cell science\| PubMed ID: 18544637	2008
Evidence in transplantation: randomized versus nonrandomized studies. Transplantation\| PubMed ID: 18622270	2008
Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population. The American journal of psychiatry\| PubMed ID: 18829873	2008
A functional genetic link between distinct developmental language disorders. The New England journal of medicine\| PubMed ID: 18987363	2008
MET and autism susceptibility: family and case-control studies. European journal of human genetics : EJHG\| PubMed ID: 19002214	2009
A 15q13.3 microdeletion segregating with autism. European journal of human genetics : EJHG\| PubMed ID: 19050728	2009
Transplantation: a report of progress. Transplantation\| PubMed ID: 19104394	2008
The role of mTOR inhibitors in the management of posttransplant malignancy. Transplantation\| PubMed ID: 19155967	2009
A whole-genome scan and fine-mapping linkage study of auditory-visual synesthesia reveals evidence of linkage to chromosomes 2q24, 5q33, 6p12, and 12p12. American journal of human genetics\| PubMed ID: 19200526	2009
Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairment. American journal of medical genetics. Part A\| PubMed ID: 19267418	2009
A common variant associated with dyslexia reduces expression of the KIAA0319 gene. PLoS genetics\| PubMed ID: 19325871	2009
Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia. European journal of human genetics : EJHG\| PubMed ID: 19352412	2009
Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection. European journal of human genetics : EJHG\| PubMed ID: 19384346	2009
The dyslexia-associated protein KIAA0319 interacts with adaptor protein 2 and follows the classical clathrin-mediated endocytosis pathway. American journal of physiology. Cell physiology\| PubMed ID: 19419997	2009
Editorial commentary: 2007 and 2008 Beaune seminars in transplantation research. Transplantation\| PubMed ID: 19424001	2009
CMIP and ATP2C2 modulate phonological short-term memory in language impairment. American journal of human genetics\| PubMed ID: 19646677	2009
Outcomes with conversion from calcineurin inhibitors to sirolimus after renal transplantation in the context of steroid withdrawal or steroid continuation. Transplantation\| PubMed ID: 19741466	2009
Gene expression profiling of the donor kidney at the time of transplantation predicts clinical outcomes 2 years after transplantation. Human immunology\| PubMed ID: 20156509	2010
Outcome and allocation of deceased heart-beating donor kidneys in the United kingdom. Transplantation\| PubMed ID: 20177336	2010
Recent advances in the genetics of language impairment. Genome medicine\| PubMed ID: 20193051	2010
Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia. Biological psychiatry\| PubMed ID: 20346443	2010
Rabbit antithymocyte globulin (thymoglobulin): 25 years and new frontiers in solid organ transplantation and haematology. Drugs\| PubMed ID: 20394456	2010
Linkage and candidate gene studies of autism spectrum disorders in European populations. European journal of human genetics : EJHG\| PubMed ID: 20442744	2010
Functional impact of global rare copy number variation in autism spectrum disorders. Nature\| PubMed ID: 20531469	2010
A genome-wide scan for common alleles affecting risk for autism. Human molecular genetics\| PubMed ID: 20663923	2010
Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry. Molecular autism\| PubMed ID: 20678249	2010
Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability. Science translational medicine\| PubMed ID: 20844286	2010
Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits. Human mutation\| PubMed ID: 20848658	2010
The dyslexia-associated KIAA0319 protein undergoes proteolytic processing with {gamma}-secretase-independent intramembrane cleavage. The Journal of biological chemistry\| PubMed ID: 20943657	2010
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability. Journal of medical genetics\| PubMed ID: 20972252	2011
PCSK6 is associated with handedness in individuals with dyslexia. Human molecular genetics\| PubMed ID: 21051773	2011
Identification of candidate genes for dyslexia susceptibility on chromosome 18. PloS one\| PubMed ID: 21060895	2010
Transplantation: a report of progress. Transplantation\| PubMed ID: 21160404	2010
Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population. European journal of human genetics : EJHG\| PubMed ID: 21248734	2011
DCDC2, KIAA0319 and CMIP are associated with reading-related traits. Biological psychiatry\| PubMed ID: 21457949	2011
A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3. Journal of neurodevelopmental disorders\| PubMed ID: 21484199	2011
Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism. Journal of neurodevelopmental disorders\| PubMed ID: 21484201	2011
Chronic renal allograft damage: not enough immunosuppression? Transplantation\| PubMed ID: 21519212	2011
Everolimus and long-term outcomes in renal transplantation: seeking an optimal strategy for immunosuppression. Transplantation\| PubMed ID: 21799391	2011
Links between genetics and pathophysiology in the autism spectrum disorders. EMBO molecular medicine\| PubMed ID: 21805639	2011
Chorea-acanthocytosis genotype in the original critchley kentucky neuroacanthocytosis kindred. Archives of neurology\| PubMed ID: 21987550	2011
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder. Human genetics\| PubMed ID: 21996756	2011