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One or more keywords matched the following items that are connected to Monaco, Anthony
Item TypeName
Academic Article Isolation of a candidate gene for Norrie disease by positional cloning.
Academic Article Familial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16.
Academic Article Chorea-acanthocytosis: genetic linkage to chromosome 9q21.
Academic Article Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia.
Academic Article Refined linkage disequilibrium and physical mapping of the gene locus for X-linked dystonia-parkinsonism (DYT3).
Academic Article Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects.
Academic Article Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1.
Academic Article Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects.
Academic Article Report of the committee on the genetic constitution of the X chromosome.
Academic Article Construction of a human X-chromosome-enriched phage library which facilitates analysis of specific loci.
Academic Article Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6.
Academic Article Linkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndrome.
Academic Article Autism: in search of susceptibility genes.
Academic Article Strategies for autism candidate gene analysis.
Academic Article McLeod syndrome and neuroacanthocytosis with a novel mutation in the XK gene.
Academic Article The genetic basis of dyslexia.
Academic Article Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairment.
Academic Article Autism: recent molecular genetic advances.
Academic Article The chorea of McLeod syndrome.
Academic Article Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism.
Academic Article DNA linkage analysis of X chromosome-linked chronic granulomatous disease.
Academic Article Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci.
Academic Article Linkage and candidate gene studies of autism spectrum disorders in European populations.
Academic Article Recombination with pERT87 (DXS164) in families with X-linked muscular dystrophy.
Academic Article Pooled genome-wide linkage data on 424 ADHD ASPs suggests genetic heterogeneity and a common risk locus at 5p13.
Academic Article Genome maps III. 1992. Wall Chart.
Academic Article A physical map of 4 million bp around the Duchenne muscular dystrophy gene on the human X-chromosome.
Academic Article The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder.
Academic Article Identifying autism susceptibility genes.
Academic Article Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families.
Academic Article Association between X-linked mixed deafness and mutations in the POU domain gene POU3F4.
Academic Article A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene.
Academic Article Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairment.
Academic Article CMIP and ATP2C2 modulate phonological short-term memory in language impairment.
Academic Article Localization of tub and uncoupling proteins (Ucp) 2 and 3 to a region of rat chromosome 1 linked to glucose intolerance and adiposity in the Goto-Kakizaki (GK) type 2 diabetic rat.
Academic Article Association of infantile convulsions with paroxysmal dyskinesias (ICCA syndrome): confirmation of linkage to human chromosome 16p12-q12 in a Chinese family.
Academic Article A sibling-pair based approach for mapping genetic loci that influence quantitative measures of reading disability.
Academic Article Fine mapping of the McLeod locus (XK) to a 150-380-kb region in Xp21.
Academic Article Localisation of a gene implicated in a severe speech and language disorder.
Academic Article Menkes and Wilson diseases.
Academic Article Identification of YAC and cosmid clones encompassing the ZFX-POLA region using irradiation hybrid cell lines.
Academic Article A gene-based genetic linkage and comparative map of the rat X chromosome.
Academic Article A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia.
Academic Article Dystrophin expression and genotypic analysis of two cases of benign X linked myopathy (McLeod's syndrome).
Academic Article A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11.
Academic Article A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31-q14.3.
Academic Article Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
Academic Article Multivariate linkage analysis of specific language impairment (SLI).
Academic Article Confirmatory evidence for linkage of relative hand skill to 2p12-q11.
Academic Article Familial and genetic effects on motor coordination, laterality, and reading-related cognition.
Academic Article Isolation and characterization of a MAGE gene family in the Xp21.3 region.
Academic Article 2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the RPS4X, PHKA1, XIST and DXS128E genes.
Academic Article Regional localization of the murine Duchenne muscular dystrophy gene on the mouse X chromosome.
Academic Article Analysis of Mnk, the murine homologue of the locus for Menkes disease, in normal and mottled (Mo) mice.
Academic Article Identification of candidate genes for dyslexia susceptibility on chromosome 18.
Academic Article A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome.
Academic Article Cloning the Wilson disease gene.
Academic Article Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population.
Academic Article X linked Charcot-Marie-Tooth disease (CMTX1): a study of 15 families with 12 highly informative polymorphisms.
Academic Article Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy.
Academic Article Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability.
Academic Article Physical mapping of Xq24-25 around loci closely linked to the X-linked lymphoproliferative syndrome locus: an overlapping YAC map and linkage between DXS12, DXS42, and DXS37.
Academic Article Construction of two YAC contigs in human Xp11.23-p11.22, one encompassing the loci OATL1, GATA, TFE3, and SYP, the other linking DXS255 to DXS146.
Concept Genetic Linkage
Search Criteria
  • Genetic Linkage
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.