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NOTHEN MM
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DELMO C
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BECKMANN H
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Citation: J. Deckert et al., SYSTEMATIC MUTATION SCREENING AND ASSOCIATION STUDY OF THE A(1) AND A(2A) ADENOSINE RECEPTOR GENES IN PANIC DISORDER SUGGEST A CONTRIBUTIONOF THE A(2A) GENE TO THE DEVELOPMENT OF DISEASE, Molecular psychiatry, 3(1), 1998, pp. 81-85
Citation: W. Maier et R. Laszig, COMPLICATIONS OF ENDONASAL SINUS SURGERY - DIAGNOSTIC AND THERAPEUTICCONSEQUENCES, Laryngo-, Rhino-, Otologie, 77(7), 1998, pp. 402-409
Citation: R. Heun et al., RELIABILITY OF INTERVIEW INFORMATION IN A FAMILY STUDY IN THE ELDERLY, Social psychiatry and psychiatric epidemiology, 33(3), 1998, pp. 140-144
Authors:
VALLADA H
CURTIS D
SHAM P
KUNUGI H
ZHAO JH
MURRAY R
MCGUFFIN P
NANKO S
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GILL M
COLLIER DA
ANTONARAKIS S
HOUSMAN D
KAZAZIAN H
NESTADT G
PULVER AE
STRAUB RE
MACLEAN CJ
WALSH D
KENDLER KS
DELISI L
POLYMEROPOULOS M
COON H
BYERLEY W
LOFTHOUSE R
GERSHON E
GOLDIN L
FREEDMAN R
LAURENT C
BODEAUPEAN S
DAMATO T
JAY M
CAMPION D
MALLET J
WILDENAUER DB
LERER B
ALBUS M
ACKENHEIL M
EBSTEIN RP
HALLMAYER J
MAIER W
GURLING H
CURTIS D
KALSI G
BRYNJOLFSSON J
SIGMUNDSON T
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MURI W
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HWU HG
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WIESE C
KRISTBJARNARSON H
LEVINSON DF
MOWRY BJ
DONISKELLER H
HAYWARD NK
CROWE RR
SILVERMAN JM
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READ CM
Citation: H. Vallada et al., A TRANSMISSION DISEQUILIBRIUM AND LINKAGE ANALYSIS OF D22S278 MARKER ALLELES IN 574 FAMILIES - FURTHER SUPPORT FOR A SUSCEPTIBILITY LOCUS FOR SCHIZOPHRENIA AT 22Q12, Schizophrenia research, 32(2), 1998, pp. 115-121
Authors:
SCHWAB SG
KNAPP M
FREYMANN J
ALBUS M
LERER B
HALLMAYER J
MAIER W
WILDENAUER DB
Citation: Sg. Schwab et al., THE HLA DRB1 GENE LOCUS IN SCHIZOPHRENIA - AN ASSOCIATION STUDY IN 55FAMILIES WITH LINKAGE TO CHROMOSOME 6P, Schizophrenia research, 29(1-2), 1998, pp. 133-133
Citation: W. Maier et al., SPECIAL FEATURE - FAMILY-GENETIC RESEARCH STRATEGIES FOR PERSONALITY-DISORDERS, Journal of personality disorders, 12(3), 1998, pp. 262-276
Authors:
MAIER W
COSENTINO F
LUTOLF R
FLEISCH M
SEILER C
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Citation: W. Maier et al., TETRAHYDROBIOPTERIN IMPROVES ENDOTHELIAL FUNCTION IN PATIENTS WITH CORONARY-ARTERY DISEASE, Journal of the American College of Cardiology, 31(2), 1998, pp. 178-179
Citation: W. Maier et B. Meier, INTERVENTIONAL CARDIOLOGY IN PERSPECTIVE - IMPACT ON CARDIAC REHABILITATION, European heart journal, 19, 1998, pp. 24-28
Authors:
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LEBOYER M
GANSICKE M
WEIFFENBACH O
BIANCALANA V
CORNILLETLEFEBRE P
CROQUETTE MF
FROSTER U
SCHWAB SG
POUSTKA F
HAUTZINGER M
MAIER W
Citation: P. Franke et al., GENOTYPE-PHENOTYPE RELATIONSHIP IN FEMALE CARRIERS OF THE PREMUTATIONAND FULL MUTATION OF FMR-1, Psychiatry research, 80(2), 1998, pp. 113-127
Authors:
WILDENAUER DB
SCHWAB SG
HALLMAYER J
LERER B
ALBUS M
BORRMAN M
LICHTERMANN D
DREIKORN B
HANSES C
ECKSTEIN GN
ZILL P
HONIG S
KANYA K
SEGMAN R
EBSTEIN RE
TRIXLER M
RIETSCHEL M
MAIER W
Citation: Db. Wildenauer et al., GENOME SCAN FOR AUTOSOMAL GENES CONFERRING RISK TO SCHIZOPHRENIA IN AGERMAN ISRAELI SAMPLE/, American journal of medical genetics, 81(6), 1998, pp. 454-454
Authors:
HEUN R
PAPASSOTIROPOULOS A
JESSEN F
MAIER W
Citation: R. Heun et al., RISKS FOR PRIMARY PROGRESSIVE DEMENTIA AND FOR DEPRESSION IN FIRST-DEGREE RELATIVES OF PATIENTS WITH ALZHEIMERS-DISEASE AND GERIATRIC DEPRESSION, American journal of medical genetics, 81(6), 1998, pp. 457-457
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GRUNHAGE F
RIETSCHEL M
ALBUS M
MAIER W
PROPPING P
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Citation: F. Grunhage et al., SYSTEMATIC SEARCH FOR VARIATION IN THE HUMAN DOPAMINE TRANSPORTER GENE, American journal of medical genetics, 81(6), 1998, pp. 500-500
Authors:
RIETSCHEL M
SCHOOR A
ALBUS M
KREINER R
HELD T
KRAUSS H
KNAPP M
SCHULZE TG
MULLER DJ
PROPPING P
MAIER W
NOTHEN MM
Citation: M. Rietschel et al., ASSOCIATION STUDY OF THE TRYPTOPHAN-HYDROXYLASE GENE AND BIPOLAR AFFECTIVE-DISORDER USING FAMILY-BASED INTERNAL CONTROLS, American journal of medical genetics, 81(6), 1998, pp. 513-513
Authors:
DECKERT J
SYAGAILO Y
MODLICH O
NOTHEN MM
FRANKE P
MAIER W
BECKMANN H
PROPPING P
LESCH KP
Citation: J. Deckert et al., EVIDENCE FOR ASSOCIATION OF A MAO-A PROMOTER POLYMORPHISM WITH PANIC DISORDER IN FEMALE-PATIENTS, American journal of medical genetics, 81(6), 1998, pp. 514-515
Authors:
FREYMANN J
SCHWAB SG
KNAPP M
ALBUS M
LERER B
HALLMAYER J
MAIER W
WILDENAUER DB
Citation: J. Freymann et al., ASSOCIATION STUDIES OF HLA GENES IN FAMILIES WITH LINKAGE TO CHROMOSOME 6P, American journal of medical genetics, 81(6), 1998, pp. 517-517
Authors:
PAUS S
RIETSCHEL M
ALBUS M
MAIER W
PROPPING P
NOTHEN MM
Citation: S. Paus et al., SYSTEMATIC SCREENING FOR MUTATIONS IN THE HUMAN NMDAR1 GENE IN PATIENTS WITH SCHIZOPHRENIA, American journal of medical genetics, 81(6), 1998, pp. 519-519
Authors:
WILDENAUER DB
KNAPP M
ALBUS M
LERER B
BORRMANN M
SEGMAN R
LICHTERMANN D
HALLMAYER J
MAIER W
SCHWAB SG
Citation: Db. Wildenauer et al., ASSOCIATION LINKAGE DISEQUILIBRIUM OF G-OLF(ALPHA) IN 59 FAMILIES WITH SCHIZOPHRENIC INDEX PATIENTS IN THE PRESENCE OF LINKAGE/, American journal of medical genetics, 81(6), 1998, pp. 524-524
Authors:
SCHULZE TG
MAROLDT A
KRAUSS H
KNAPP M
MARWINSKI K
FERNANDEZ ANY
MULLER DJ
WEBER T
NOTHEN M
MAIER W
HELD T
RIETSCHEL M
Citation: Tg. Schulze et al., AFFECTIVE SYMPTOMS AND FAMILY HISTORY OF AFFECTIVE-DISORDER IN PATIENTS WITH TARDIVE-DYSKINESIA, American journal of medical genetics, 81(6), 1998, pp. 526-527
Authors:
SCHWAB SG
HALLMAYER J
ALBUS M
LERER B
HANSES C
KANYAS K
SEGMAN R
BORRMANN M
DREIKORN B
LICHTERMANN D
RIETSCHEL M
TRIXLER M
MAIER W
WILDENAUER DB
Citation: Sg. Schwab et al., A POTENTIAL SUSCEPTIBILITY LOCUS ON CHROMOSOME 10P14-P11 IN 72 FAMILIES WITH SCHIZOPHRENIA, American journal of medical genetics, 81(6), 1998, pp. 528-529
Authors:
HALLMAYER J
SCHWAB SG
ALBUS M
LERER B
ZILL P
HANSES C
LICHTERMANN D
KANYAS K
BORRMANN M
RIETSCHEL M
MAIER W
WILDENAUER DB
Citation: J. Hallmayer et al., A POTENTIAL SUSCEPTIBILITY LOCUS FOR SCHIZOPHRENIA ON 22Q12,13 - REEVALUATION IN 72 FAMILIES, American journal of medical genetics, 81(6), 1998, pp. 529-529
Authors:
ECKSTEIN GN
SCHWAB SG
MAIER W
WILDENAUER DB
Citation: Gn. Eckstein et al., SEARCHING FOR CANDIDATE GENES FOR SCHIZOPHRENIA IN CHROMOSOME 6P22,23- ISOLATION OF A BAC CONTIG SPANNING 3.5 MEGABASES, American journal of medical genetics, 81(6), 1998, pp. 530-530