Zobrazeno 1 - 10
of 77
pro vyhledávání: '"Henrik Ewald"'
Autor:
Henriette N. Buttenschøn, Torben A Kruse, Walter J. Muir, Anthony J. Pelosi, Douglas Blackwood, V. Murray, Leslie Foldager, Ole Mors, Henrik Ewald, M.D. Lundorf
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. :94-101
Recent evidence from postmortem studies suggests that GAD1 encoding the gamma-aminobutyric acid (GABA) synthetic enzyme GAD67 is a functional candidate susceptibility gene for both bipolar affective disorder (BPAD) and schizophrenia. Previous studies
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb4d5189f1f1136f64af6309cb2f9973
https://doi.org/10.1002/ajmg.b.30137
https://doi.org/10.1002/ajmg.b.30137
Autor:
L. Blanco, A. El Daoud, Torben A Kruse, Torben F. Ørntoft, F. Wikman, Ole Mors, Tove H. Jorgensen, Henriette N. Buttenschøn, Henrik Ewald, Thomas Damm Als, M. Torralba, B.M. Teruel, T.J. Flint
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. :25-30
Homozygosity mapping is a very powerful method for finding rare recessive disease genes in monogenic disorders and may also be useful for locating risk genes in complex disorders, late onset disorders where parents often are not available, and for ra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f658e14fb26c65bc0dcda289e7094568
https://doi.org/10.1002/ajmg.b.30106
https://doi.org/10.1002/ajmg.b.30106
Autor:
Henriette N. Buttenschøn, Tove H. Jorgensen, Thomas Damm Als, Henrik Ewald, Anders D. Børglum, August G. Wang
Publikováno v:
Human Genetics. 115:19-28
Historical, archaeological and linguistic sources suggest that the ancestors of the present day population in the Faroe Islands may have their origin in several different regions surrounding the North Atlantic Ocean. In this study we use binary and m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b6ef6858ee08e3dbfe10deb7f1175ec
https://doi.org/10.1007/s00439-004-1117-7
https://doi.org/10.1007/s00439-004-1117-7
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
Publikováno v:
Schizophrenia Research. 55:93-98
The few studies that have examined whether head injury is a risk factor for later schizophrenia have had important methodological problems.We examined the rates of head injury among 8288 persons in the 15 years up to their first admission with schizo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c16d8a59c2565a2bccbcad585289205
https://doi.org/10.1016/s0920-9964(01)00205-5
https://doi.org/10.1016/s0920-9964(01)00205-5
Autor:
Marlene Briciet Lauritsen, Torben A Kruse, Anders D. Børglum, Anne Philippe, Catalina Betancur, Henrik Ewald, Marion Leboyer
Publikováno v:
American Journal of Medical Genetics. 114:466-470
Though genetic risk factors are important for the development of autism, no specific risk alleles have yet been identified. DOPA decarboxylase (DDC) is involved in both the catecholaminergic and serotonergic pathways and may be considered a functiona
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef54cf69d3afb3b30914fc08c5bdf2f8
https://doi.org/10.1002/ajmg.10379
https://doi.org/10.1002/ajmg.10379
Autor:
Tove H. Jorgensen, M. Pinaud, Henrik Ewald, Maria Vang, A.G. Wang, Torben A Kruse, Anders D. Børglum, Ole Mors, Hans Atli Dahl, T.J. Flint
Publikováno v:
American Journal of Medical Genetics. 114:245-252
Chromosome 22q may harbor risk genes for schizophrenia and bipolar affective disorder. This is evidenced through genetic mapping studies, investigations of cytogenetic abnormalities, and direct examination of candidate genes. Patients with schizophre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f42a939b9feac8b44ede26f8f6f60b5
https://doi.org/10.1002/ajmg.10191
https://doi.org/10.1002/ajmg.10191
Publikováno v:
Journal of Autism and Developmental Disorders. 32:115-119
Possible associations between autism and specific medical disorders have been suggested, and this could be of relevance in the clinical examination and treatment of patients and may help to identify factors involved in the etiology or pathophysiology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36e5b510ebff20d68b9aeb0ff8f023eb
https://doi.org/10.1023/a:1014840622023
https://doi.org/10.1023/a:1014840622023
Autor:
Walter J. Muir, Irene McKee, David A. Collier, Torben A Kruse, V. Murray, George Kirov, Anders D. Børglum, Michael John Owen, Douglas Blackwood, Ole Mors, Henrik Ewald, Nicholas John Craddock
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. :18-22
Dopa decarboxylase (DDC) catalyses the synthesis of both dopamine and serotonin as well as trace amines suggested to possess neuromodulating capabilities. We have previously reported evidence suggesting an association between DDC and bipolar affectiv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::70dee3041faf5c360b4675d0e7aef8fa
https://doi.org/10.1002/ajmg.b.10030
https://doi.org/10.1002/ajmg.b.10030
Publikováno v:
Acta Psychiatrica Scandinavica. 103:411-427
Objective: To review systematically the empirical evidence for the involvement of genetic risk factors in infantile autism. Method: We aimed at including all relevant papers written in English. We conducted a Medline search in September 2000. In addi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8a2fc8ac4460ddd8d381136c87871f9e
https://doi.org/10.1034/j.1600-0447.2001.00086.x
https://doi.org/10.1034/j.1600-0447.2001.00086.x