Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Sarah H. Shaw"'
Autor:
Sarah H. Shaw, Simon E. Fisher, Alex J. Richardson, Clyde Francks, John F. Stein, Anthony P. Monaco, Lynn E. DeLisi
Publikováno v:
Human Molecular Genetics
Schizophrenia and non-right-handedness are moderately associated, and both traits are often accompaniedby abnormalities of asymmetrical brain morphology or function. We have found linkage previously ofchromosome 2p12–q11 to a quantitative measure o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4085c9e7a16be519f7d13c1253c4130b
https://doi.org/10.1093/hmg/ddg362
https://doi.org/10.1093/hmg/ddg362
Autor:
Nicholas J. Schork, Don Hutchison, Ken Abel, Lynn E. DeLisi, Robin Sherrington, Robert Saiz, Sarah H. Shaw
Publikováno v:
American Journal of Medical Genetics. 114:205-213
To assess the utility of linkage disequilibrium (LD) as a tool for fine-mapping disease genes in non-isolated populations, we have assessed the linkage disequilibrium strength among a series of single nucleotide polymorphisms (SNPs) in an approximate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca0651dcfe822bf0de83f962c4f94518
https://doi.org/10.1002/ajmg.10151
https://doi.org/10.1002/ajmg.10151
Autor:
Alan Buckler, Sarah H. Shaw, Luis García-Villarreal, Paula Bauer, Antonio Tugores, Jeanne Geskes, Susan Daniels, Margaret Galvin, David Cotton, Angel Sierra-Hernández
Publikováno v:
Hepatology. 32:1329-1336
The molecular basis of Wilson disease (WD), an autosomal recessive disorder, is the presence of mutations in the ATP7B gene, a copper transporting ATPase. Hospital records indicated a higher prevalence of WD (1 in 2,600) in some counties in the north
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b85da7896f583a6760df99f16142681f
https://doi.org/10.1053/jhep.2000.20152
https://doi.org/10.1053/jhep.2000.20152
Autor:
Antonio Vita, Gail Shields, Lynn E. DeLisi, Margherita Comazzi, John Stewart, B. Nanthakumar, M. De Hert, Sarah H. Shaw, Kamran Razi, Angela B. Smith, Timothy J. Crow, Robin Sherrington, J. Loftus, Veronica W. Larach, N.A. Wellman
Publikováno v:
American Journal of Medical Genetics. 96:335-341
The hypothesis that a gene for susceptibility to psychosis (specifically in the X-Y homologous class) is located on the sex chromosomes has been proposed. Such a gene would account for the excess of sex chromosome anomalous males and females in popul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb89a30ef8efbdc2b147384d0ec74490
https://doi.org/10.1002/1096-8628(20000612)96:3<335::aid-ajmg20>3.0.co
https://doi.org/10.1002/1096-8628(20000612)96:3<335::aid-ajmg20>3.0.co
Autor:
Robert Saiz, Stefan Schreiber, Silvia Mascheretti, Pieter C. F. Stokkers, Sarah H. Shaw, Nancy J. Leysens, Nicholas J. Lynch, Annette Lantermann, Mark E. Curran, John E. Lennard-Jones, Christopher G. Mathew, Phil Morin, Alastair Forbes, Stephen Bridger, Mudassar M. Mirza, Sander J. H. van Deventer, A Macpherson, Jochen Hampe
Publikováno v:
American journal of human genetics, 65(6), 1647-1655. Cell Press
Inflammatory bowel disease (IBD) is characterized by a chronic relapsing intestinal inflammation. IBD is subdivided into Crohn disease and ulcerative colitis phenotypes. Given the immunologic dysregulation in IBD, the human-leukocyte-antigen region o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::081363678ea6762071110b621b2058fc
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
https://doi.org/10.1002/(sici)1096-8628(19980907)81:5<420::aid-ajmg11>3.0.co
Autor:
Tara C. Matise, Sarah H. Shaw, Jean Weissenbach, Bonnie Thiel, Charles W. Richard, Joan E. Farr, Aravinda Chakaravarti
Publikováno v:
Genomics. 27:502-510
We have constructed a high-resolution physical map of the long arm of human chromosome 13 using a panel of 94 radiation hybrids. A comprehensive map of 95 chromosome 13-specific sequence tagged sites (STSs) spanning 13q from the presumed centromere a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba34d13e2cc4f2fe65260f00c38bcd07
https://doi.org/10.1006/geno.1995.1083
https://doi.org/10.1006/geno.1995.1083
Autor:
Christoph Gasche, Alexander Zdanov, Alfred Gangl, Walter Reinisch, Sarah H. Shaw, Petra Zwirn, Brian M. J. Foxwell, Paul Grundtner, Usha Sarma, Lynn M. Williams
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 170(11)
IL-10-deficient mice exhibit spontaneous enterocolitis and other symptoms akin to Crohn’s disease, indicating that IL-10 might regulate normal physiology in the gut. However, clinical trials with IL-10 in Crohn’s disease were disappointing, altho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a8ea71f84e911767d90d11ccb8bd130
https://pubmed.ncbi.nlm.nih.gov/12759436
https://pubmed.ncbi.nlm.nih.gov/12759436
Autor:
Jochen Hampe, Mark E. Curran, Sarah H. Shaw, Christopher G. Mathew, Ray White, Stefan Schreiber
Publikováno v:
Human genetics. 113(6)
Previously we have conducted a genome-wide search for inflammatory bowel disease susceptibility loci in a large European cohort. Results from this study demonstrated suggestive evidence of linkage to loci at chromosomes 1q, 6p, and 10p and replicated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8677c423dc14ecd36a5b1ad3adb4ede5
https://pubmed.ncbi.nlm.nih.gov/13680363
https://pubmed.ncbi.nlm.nih.gov/13680363
Autor:
Timothy J. Crow, Margherita Comazzi, Kamran Razi, N.A. Wellman, Angela B. Smith, Antonio Vita, John Stewart, Betsy Nanthakumar, Gail Shields, Lynn E. DeLisi, Robin Sherrington, J. Loftus, Veronica W. Larach, Sarah H. Shaw, Thomas G. Heffner
Publikováno v:
Università degli Studi di Brescia-IRIS
Some genome-wide scans and association studies for schizophrenia susceptibility genes have yielded significant positive findings, but there is disagreement between studies on their locations, and no mutation has yet been found in any gene. Since schi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49f8764625602f0458e603437fd0e0ae
https://pubmed.ncbi.nlm.nih.gov/12611866
https://pubmed.ncbi.nlm.nih.gov/12611866