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Evidence for linkage to psychosis and cerebral asymmetry (relative hand skill) on the X chromosome

Autor: Lynn E. DeLisi, J. Loftus, J. Rue, Gail Shields, John Stewart, Paula Peterson, J.C. Dann, Shinichiro Nanko, Timothy J. Crow, Angela B. Smith, Antonio Vita, S. H. Laval, R.J. Butler, Sarah H. Shaw, Margherita Comazzi, S.J. Leask, N. Bass

Publikováno v: Università degli Studi di Brescia-IRIS

The hypothesis that psychosis arises as a part of the genetic diversity associated with the evolution of language generates the prediction that illness will be linked to a gene determining cerebral asymmetry, which, from the evidence of sex chromosom

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a108cff078f242669e6b439bd27a8106
https://doi.org/10.1002/(sici)1096-8628(19980907)81:5<420::aid-ajmg11>3.0.co

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Limb-girdle muscular dystrophies--from genetics to molecular pathology

Autor: S H, Laval, K M D, Bushby

Publikováno v: Neuropathology and applied neurobiology. 30(2)

The limb-girdle muscular dystrophies are a diverse group of muscle-wasting disorders characteristically affecting the large muscles of the pelvic and shoulder girdles. Molecular genetic analyses have demonstrated causative mutations in the genes enco

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::7e02fad44793743969d96dd834c08b70
https://pubmed.ncbi.nlm.nih.gov/15043707

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Partial sequence data from three evolutionarily conserved loci from the proximal short arm of the human X chromosome; assignment of DXF34S1 to Xp11.21-cen

Autor: G Maslen, Yvonne Boyd, S. H. Laval, V Reed

Publikováno v: Europe PubMed Central

DNA sequence data have been obtained from three clones derived from the human X chromosome which contain evolutionarily conserved sequences. Primers have been designed which enable these loci to be defined as sequence-tagged-sites (STS’s). The assi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce3cd154154d6543863a37e22015cf1b
https://doi.org/10.1159/000133460

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The X-chromosome and susceptibility to ankylosing spondylitis

Autor: E, Hoyle, S H, Laval, A, Calin, B P, Wordsworth, M A, Brown

Publikováno v: Arthritis and rheumatism. 43(6)

Ankylosing spondylitis (AS) affects 0.25-1.0% of the population, and its etiology is incompletely understood. Susceptibility to this highly familial disease (lambda(s) = 58) is primarily genetically determined. There is a significant sex bias in AS,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b16ec48c65df6ebcbad3781ab46df645
https://pubmed.ncbi.nlm.nih.gov/10857794

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A genome-wide search for schizophrenia susceptibility genes

Autor: S H, Shaw, M, Kelly, A B, Smith, G, Shields, P J, Hopkins, J, Loftus, S H, Laval, A, Vita, M, De Hert, L R, Cardon, T J, Crow, R, Sherrington, L E, DeLisi

Publikováno v: American journal of medical genetics. 81(5)

We completed a systematic genome-wide search for evidence of loci linked to schizophrenia using a collection of 70 pedigrees containing multiple affected individuals according to three phenotype classifications: schizophrenia only (48 pedigrees; 70 s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f4c3142be818b442de9e141707da5726
https://pubmed.ncbi.nlm.nih.gov/9754621

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