Zobrazeno 1 - 10 of 28 pro vyhledávání: '"I. Bannoura"'
1
Transmission disequilibrium and haplotype analyses of the G72/G30 locus: Suggestive linkage to schizophrenia in Palestinian Arabs living in the North of Israel
Autor: I. Murad, M. Dobrusin, Alina Cholostoy, U. Bening‐Abu‐Shach, Michael Korostishevsky, I. Bannoura, Wolfgang Maier, Ruth Navon, Robert H. Belmaker, M. Kaganovich, Richard P. Ebstein, Ilana Kremer, Marcella Rietschel, M. Muhaheed
Publikováno v: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. :91-95
Association of the G72/G30 locus with schizophrenia was recently reported in French Canadian, Russian, and Ashkenazi populations using case-control studies. In the present study we hypothesize the existence of a G72/G30 risk allele over-transmitted t
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4514e1dce1bfe101e923c5c132bc314f
https://doi.org/10.1002/ajmg.b.30212
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2
A family-based study of the Cys23Ser 5HT2C serotonin receptor polymorphism in schizophrenia
Autor: Marcella Rietschel, Thomas G. Schulze, Wolfgang Maier, M. Muhaheed, I. Murad, Alon Reshef, V. Tsenter, M. Dobrusin, S. Gathas, Richard P. Ebstein, I. Bannoura, Ilana Kremer, Monica Blanaru, Daniel J. Müller, Robert H. Belmaker
Publikováno v: American Journal of Medical Genetics. 105:236-238
The 5HT2C receptor has a high affinity for clozapine, a nontypical neuroleptic, and has therefore been postulated to play a role in mediating negative symptoms and neuroleptic response in schizophrenia. In the current study, the Cys23Ser 5HT2C seroto
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8df21e332f6ff84db2ae709e31980a93
https://doi.org/10.1002/ajmg.1260
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3
No association between the dopamine D3 receptorBal I polymorphism and schizophrenia in a family-based study of a Palestinian Arab population
Autor: I. Murad, Daniel J. Müller, Dieter B. Wildenauer, M. Blanaru, S. Gathas, Marcella Rietschel, Alon Reshef, Richard P. Ebstein, Ilana Kremer, I. Bannoura, M. Dobrusin, W. Maier, Thomas G. Schulze, S. G. Schwab, Robert H. Belmaker, Mustafa Mujaheed, Rachel Bachner-Melman
Publikováno v: American Journal of Medical Genetics. 96:778-780
Several recent meta-analyses appear to show a weak but significant effect of both forms of the gly/ser DRD3 polymorphism in conferring risk for schizophrenia. Since most studies have employed the artifact-prone case-control design, we thought it wort
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8f2dd25bc4d88a5743f39f38ced07836
https://doi.org/10.1002/1096-8628(20001204)96:6<778::aid-ajmg16>3.0.co
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4
Examination of IMPA1 and IMPA2 genes in manic-depressive patients: association between IMPA2 promoter polymorphisms and bipolar disorder
Autor: Jan Øystein Berle, M Mujahed, Douglas F. Levinson, Claudine Laurent, Jacques Mallet, Anders Molven, Vidar M. Steen, Rolv T. Lie, J.F. Deleuze, I Bannoura, I Murad, Gry Sjøholt, Richard P. Ebstein
Publikováno v: Molecular psychiatry. 9(6)
Manic-depressive (bipolar) illness is a serious psychiatric disorder with a strong genetic predisposition. The disorder is likely to be multifactorial and etiologically complex, and the causes of genetic susceptibility have been difficult to unveil.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b47b63e8cdea31769b5788c015b0ab6
https://pubmed.ncbi.nlm.nih.gov/14699425
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5
No evidence for linkage by transmission disequilibrium test analysis of microsatellite marker D22S278 and schizophrenia in a Palestinian Arab and in a German population
Autor: M, Dobrusin, M, Corbex, I, Kremer, I, Murad, M, Muhaheed, I, Bannoura, D J, Müller, T G, Schulze, A, Reshef, M, Blanaru, S, Gathas, M, Rietschel, R H, Belmaker, W, Maier, R P, Ebstein
Publikováno v: American journal of medical genetics. 105(4)
Linkage for a schizophrenia susceptibility locus on chromosome region 22q12-q13 was initially suggested by independent studies from two groups and confirmed in a combined analysis of data for the microsatellite marker D22S278 in multiply affected sch
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a169faa110d6fc53af687c8127086a6f
https://pubmed.ncbi.nlm.nih.gov/11378845
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6
A family-based study of the Cys23Ser 5HT2C serotonin receptor polymorphism in schizophrenia
Autor: I, Murad, I, Kremer, M, Dobrusin, M, Muhaheed, I, Bannoura, D J, Müller, T G, Schulze, A, Reshef, M, Blanaru, S, Gathas, V, Tsenter, M, Rietschel, R H, Belmaker, W, Maier, R P, Ebstein
Publikováno v: American journal of medical genetics. 105(3)
The 5HT2C receptor has a high affinity for clozapine, a nontypical neuroleptic, and has therefore been postulated to play a role in mediating negative symptoms and neuroleptic response in schizophrenia. In the current study, the Cys23Ser 5HT2C seroto
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::41abf8048aa60115061159cbfbddc6fc
https://pubmed.ncbi.nlm.nih.gov/11353441
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7
No association between the dopamine D3 receptor Bal I polymorphism and schizophrenia in a family-based study of a Palestinian Arab population
Autor: I, Kremer, M, Rietschel, M, Dobrusin, M, Mujaheed, I, Murad, M, Blanaru, I, Bannoura, D J, Müller, T G, Schulze, A, Reshef, S, Gathas, S, Schwab, D, Wildenauer, R, Bachner-Melman, R H, Belmaker, W, Maier, R P, Ebstein
Publikováno v: American journal of medical genetics. 96(6)
Several recent meta-analyses appear to show a weak but significant effect of both forms of the gly/ser DRD3 polymorphism in conferring risk for schizophrenia. Since most studies have employed the artifact-prone case-control design, we thought it wort
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::6b6b0a8d7213c133e5f5ea6a4b3b69e5
https://pubmed.ncbi.nlm.nih.gov/11121180
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9
Akademický článek
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10
Akademický článek
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