Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Renee F. Badenhop"'
Autor:
Ian P. Blair, Jennifer A. Donald, Zhixin Liu, Anna Scimone, Janice M. Fullerton, Peter R. Schofield, Mary Van Herten, Philip B. Mitchell, Renee F. Badenhop
Publikováno v:
Psychiatric Genetics. 18:156-161
Despite many studies into the genetics of bipolar disorder (BP), the molecular causes underlying susceptibility to BP remain unclear. The aim of this study was to identify chromosomal regions linked to BP in a new Australian extended pedigree cohort.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20d971d1e71062769583aa1bb3f0122b
https://doi.org/10.1097/ypg.0b013e3282fa1861
https://doi.org/10.1097/ypg.0b013e3282fa1861
Autor:
M J Moses, Renee F. Badenhop, Jennifer A. Donald, Ian P. Blair, Anna Scimone, Nicholas P. Kerr, Peter R. Schofield, Philip B. Mitchell
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. :56-59
Bipolar affective disorder is a major psychiatric illness with a population prevalence of up to 1.6%. The disorder is genetically complex. To date, no specific gene or DNA sequence variation that predisposes to the disorder has been described, howeve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c61b247a28e7949cc73404b51b221ec0
https://doi.org/10.1002/ajmg.b.30131
https://doi.org/10.1002/ajmg.b.30131
Autor:
J. Raymond DePaulo, Martin Alda, S H Juo, Philip B. Mitchell, Peter P. Zandi, Peter M. Visscher, Melvin G. McInnis, Johannes Schumacher, Michael Gill, Jenny Ekholm, Howard J. Edenberg, Stylianos E. Antonarakis, Nelson B. Freimer, Cathryn M. Lewis, Peter R. Schofield, Tatiana Foroud, Victor I. Reus, Jennifer A. Donald, Henrik Ewald, Takeo Yoshikawa, Conrad T. Gilliam, Rolf Adolfsson, Alison Goate, Theodore Reich, William Byerley, Elliot S. Gershon, Andrew McQuillin, Jouko Lönnqvist, Phil Bennett, Hugh Gurling, Paul Grof, Francis J. McMahon, Christine Windemuth, Judith A. Badner, L. J. Adams, John P. Rice, Wolfgang Maier, Michael Escamilla, Gursharan Kalsi, John I. Nurnberger, Douglas F. Levinson, Douglas Blackwood, Gustavo Turecki, Virginia L. Willour, Uppala Radhakrishna, Miron Baron, Hermann Luebbert, Jianjun Liu, Stuart MacGregor, Lynn R. Goldin, Eric Shink, Walter J. Muir, Pedro León, Torben A Kruse, Wade H. Berrettini, Nicholas John Craddock, Jurgen Del-Favero, John R. Kelsoe, Hilary Coon, Julien Mendlewicz, Sevilla D. Detera-Wadleigh, Jean-Louis Blouin, Leena Peltonen, Nurten A. Akarsu, Marcella Rietschel, Jean Morissette, Markus M. Nöthen, Christine Van Broeckhoven, M. Anne Spence, Peter Propping, Sven Cichon, Ole Mors, Nicholas Barden, Renee F. Badenhop, Stephan Claes, L. Alison McInnes, Ricardo Segurado, Guy A. Rouleau
Publikováno v:
ResearcherID
American Journal of Human Genetics, Vol. 73, No 1 (2003) pp. 49-62
American Journal of Human Genetics, Vol. 73, No 1 (2003) pp. 49-62
PUBLISHED
PMID: 12802785
Genome scans of bipolar disorder (BPD) have not produced consistent evidence for linkage. The rank-based genome scan meta-analysis (GSMA) method was applied to 18 BPD genome scan data sets in an effort to identify r
PMID: 12802785
Genome scans of bipolar disorder (BPD) have not produced consistent evidence for linkage. The rank-based genome scan meta-analysis (GSMA) method was applied to 18 BPD genome scan data sets in an effort to identify r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90680cf9fa645871cd26143366cb38a3
Autor:
L. J. Adams, A Rosso, Renee F. Badenhop, Jennifer A. Donald, M J Moses, Philip B. Mitchell, Peter R. Schofield, K R Ewen-White, Anna Scimone
Publikováno v:
Molecular Psychiatry. 7:851-859
Bipolar affective disorder is a severe mood disorder that afflicts approximately 1% of the population worldwide. Twin and adoption studies have indicated that genetic factors contribute to the disorder and while many chromosomal regions have been imp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7477da8de10bea98e8e813bb109df7cb
https://doi.org/10.1038/sj.mp.4001114
https://doi.org/10.1038/sj.mp.4001114
Autor:
Rod Mckenzie, John B.J. Kwok, Renee F. Badenhop, Philip B. Mitchell, Georgina Luscombe, Henry Brodaty, Peter R. Schofield
Publikováno v:
Human Genetics. 110:8-14
Idiopathic basal ganglia calcification (IBGC) is characterised by radiological, neurological, cognitive and psychiatric abnormalities. The associations between these abnormal phenotypes and abnormal genes remain unclear despite the recent mapping to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88620cb4e0b791d3cc0da32f10efe800
https://doi.org/10.1007/s00439-001-0650-x
https://doi.org/10.1007/s00439-001-0650-x
Autor:
Bora E. Baysal, Renee F. Badenhop, Peter E.M. Taschner, Reginald S. A. Lord, Peter R. Schofield, Sanjay M. Cherian
Publikováno v:
Genes, Chromosomes and Cancer. 31:255-263
Paraganglioma (PGL) is a rare disorder characterized by tumors of the head and neck region. Between 10% and 50% of cases of PGL are familial, and the disease is autosomal dominant and subject to age-dependent penetrance and imprinting. The paragangli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9dc29ee9f2423245b7a33d2200d1d44
https://doi.org/10.1002/gcc.1142
https://doi.org/10.1002/gcc.1142
Publikováno v:
Circulation. 93:2092-2096
Background Recently we found that the deletion (D) allele of the insertion/deletion (I/D) polymorphism of the ACE gene in 404 children was associated with a history of coronary artery disease (CAD) in their grandparents. This led us to explore polymo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c645a5f1b3933627c88ff60f7fe09fc7
https://doi.org/10.1161/01.cir.93.12.2092
https://doi.org/10.1161/01.cir.93.12.2092
Publikováno v:
Circulation. 91:1655-1658
Background It has been suggested that the insertion/deletion (I/D) polymorphism of the angiotensin-converting enzyme (ACE) gene is an independent risk factor for coronary artery disease. The D/D genotype, which is associated with higher levels of cir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b60a8de7a696ec295f617989fbc2c44
https://doi.org/10.1161/01.cir.91.6.1655
https://doi.org/10.1161/01.cir.91.6.1655
Autor:
Jennifer A. Donald, John B.J. Kwok, Philip B. Mitchell, Renee F. Badenhop, Peter R. Schofield, Ian P. Blair, L. J. Adams, M J Moses, Anna Scimone, George Kirov, Albert Chetcuti, Michael John Owen, Elaine K. Green, Nicholas John Craddock
Publikováno v:
Molecular psychiatry. 11(4)
A susceptibility locus for bipolar disorder was previously localized to chromosome 4q35 by genetic linkage analysis. We have applied a positional cloning strategy, combined with association analysis and provide evidence that a cadherin gene, FAT, con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39f1c97d04224e93d07adbc35d33d361
https://pubmed.ncbi.nlm.nih.gov/17895925
https://pubmed.ncbi.nlm.nih.gov/17895925
Autor:
Philip B. Mitchell, Peter R. Schofield, Jennifer A. Donald, M J Moses, Ian P. Blair, Anna Scimone, Renee F. Badenhop
Publikováno v:
Psychiatric genetics. 15(3)
The cause of bipolar disorder remains unknown, with little knowledge of the underlying biological, anatomical, biochemical, or genetic defect. The disorder is genetically complex, with an increasing number of loci being implicated through genetic lin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df23a0efb40685478512b1600f4a8576
https://pubmed.ncbi.nlm.nih.gov/16094255
https://pubmed.ncbi.nlm.nih.gov/16094255