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White-matter microstructure and gray-matter volumes in adolescents with subthreshold bipolar symptomsMARTINOT, M-L. Paillère; LEMAITRE, H; CONROD, P et al.Molecular psychiatry. 2014, Vol 19, Num 4, pp 462-470, issn 1359-4184, 9 p.Article

Genetic Risk For Nicotine Dependence in the Cholinergic System and Activation of the Brain Reward System in Healthy AdolescentsNEES, F; WITT, S. H; FRANK, J et al.Neuropsychopharmacology (New York, NY). 2013, Vol 38, Num 11, pp 2081-2089, issn 0893-133X, 9 p.Article

Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from EuropeRIETSCHEL, M; MATTHEISEN, M; STROHMAIER, J et al.Molecular psychiatry. 2012, Vol 17, Num 9, pp 906-917, issn 1359-4184, 12 p.Article

Independent evidence for the selective influence of GABAA receptors on one component of the bipolar disorder phenotypeBREUER, R; HAMSHERE, M. L; NÖTHEN, M. M et al.Molecular psychiatry. 2011, Vol 16, Num 6, pp 587-589, issn 1359-4184, 3 p.Article

Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2O'DONOVAN, M. C; NORTON, N; HOLMANS, P et al.Molecular psychiatry. 2009, Vol 14, Num 1, pp 30-36, issn 1359-4184, 7 p.Article

No evidence for linkage by transmission disequilibrium test analysis of microsatellite marker D22S278 and schizophrenia in a Palestinian Arab and in a German populationDOBRUSIN, M; CORBEX, Marilys; GATHAS, S et al.American journal of medical genetics. 2001, Vol 105, Num 4, pp 328-331, issn 0148-7299Article

Pemphigus chronicus benignus familiaris (Morbus Hailey-Hailey) und bipolare affektive Erkrankung bei drei Mitgliedern einer Familie = Hailey-Hailey disease and bipolar affective disorder in three members of the same familyWILK, M; RIETSCHEL, M; KÖRNER, J et al.Hautarzt. 1994, Vol 45, Num 5, pp 313-317, issn 0017-8470Conference Paper

Linakge analysis of spinal muscular atrophyDANIELS, R. J; THOMAS, N. H; RIETSCHEL, M et al.Genomics (San Diego, Calif.). 1992, Vol 12, Num 2, pp 335-339, issn 0888-7543Article

Postnatal shor stature, microcephaly, severe syndactyly of hands and feet, dysmorphic face, and mental retardation : a new syndrome ?ZERRES, K; RIETSCHEL, M; RIETSCHEL, E et al.Journal of medical genetics. 1992, Vol 29, Num 4, pp 269-271, issn 0022-2593Conference Paper

MASA syndrome : clinical variability and linkage analysisRIETSCHEL, M; FRIEDL, W; UHLHAAS, S et al.American journal of medical genetics. 1991, Vol 41, Num 1, pp 10-14, issn 0148-7299Article

Common variation in NCAN, a risk factor for bipolar disorder and schizophrenia, influences local cortical folding in schizophreniaSCHULTZ, C. C; MÜHLEISEN, T. W; KIEHNTOPF, M et al.Psychological medicine (Print). 2014, Vol 44, Num 4, pp 811-820, issn 0033-2917, 10 p.Article

Estimating the heritability of reporting stressful life events captured by common genetic variantsPOWER, R. A; WINGENBACH, T; JONES, L et al.Psychological medicine (Print). 2013, Vol 43, Num 9, pp 1965-1971, issn 0033-2917, 7 p.Article

Genome-wide association analysis of copy number variation in recurrent depressive disorderRUCKER, Jjh; BREEN, G; CRADDOCK, N et al.Molecular psychiatry. 2013, Vol 18, Num 2, pp 183-189, issn 1359-4184, 7 p.Article

Non-steroidal anti-inflammatory drugs and efficacy of antidepressants in major depressive disorderUHER, R; CARVER, S; PLACENTINO, A et al.Psychological medicine (Print). 2012, Vol 42, Num 10, pp 2027-2035, issn 0033-2917, 9 p.Article

TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studiesERHARDT, A; CZIBERE, L; HECK, A et al.Molecular psychiatry. 2011, Vol 16, Num 6, pp 647-663, issn 1359-4184, 17 p.Article

Genetic variation of the FAT gene at 4q35 is associated with bipolar affective disorderABOU JAMRA, R; BECKER, T; NÖTHEN, M. M et al.Molecular psychiatry. 2008, Vol 13, Num 3, pp 277-284, issn 1359-4184, 8 p.Article

Family-based and case-control study of catechol-O-methyltransferase in schizophrenia among Palestinian ArabsKREMER, I; PINTO, M; GOICHMAN, R et al.American journal of medical genetics. 2003, Vol 119B, Num 1, pp 35-39, issn 0148-7299, 5 p.Article

Efficacy and side-effects of clozapine not associated with variation in the 5-HT2C receptorRIETSCHEL, M; NABER, D; FIMMERS, R et al.Neuroreport (Oxford). 1997, Vol 8, Num 8, pp 1999-2003, issn 0959-4965Article

Efficacy and side-effects of clozapine : Testing for association with allelic variation in the dopamine D4 receptor geneRIETSCHEL, M; NABER, D; OBERLÄNDER, H et al.Neuropsychopharmacology (New York, NY). 1996, Vol 15, Num 5, pp 491-496, issn 0893-133XArticle

Human dopamine D4 receptor gene : frequent occurrence of a null allele and observation of homozygosityNÖTHEN, M. M; CICHON, S; KÖRNER, J et al.Human molecular genetics (Print). 1994, Vol 3, Num 12, pp 2207-2212, issn 0964-6906Article

Familial cosegregation of affective disorder and Hailey-Hailey diseaseKÖRNER, J; RIETSCHEL, M; NÖTHEN, M. M et al.British journal of psychiatry (Print). 1993, Vol 163, Num JUL, pp 109-110, issn 0007-1250Article

Pregnancy and spinal muscular atrophyRUDNIK-SCHONEBORN, S; ZERRES, K; IGNATIUS, J et al.Journal of neurology. 1992, Vol 239, Num 1, pp 26-30, issn 0340-5354Article

Depressive disorder moderates the effect of the FTO gene on body mass indexRIVERA, M; COHEN-WOODS, S; MORS, O et al.Molecular psychiatry. 2012, Vol 17, Num 6, pp 604-611, issn 1359-4184, 8 p.Article

GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophreniaCHEN, X; LEE, G; LEVINSON, D. F et al.Molecular psychiatry. 2011, Vol 16, Num 11, pp 1117-1129, issn 1359-4184, 13 p.Article

Genome-wide association for major depressive disorder : a possible role for the presynaptic protein piccoloSULLIVAN, P. F; DE GEUS, E. J. C; COVENTRY, W. L et al.Molecular psychiatry. 2009, Vol 14, Num 4, pp 359-375, issn 1359-4184, 17 p.Article

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