| Home > Publications Database > Investigation of the role of TCF4 rare sequence variants in schizophrenia. > print |
| 001 | 137970 | ||
| 005 | 20240321220340.0 | ||
| 024 | 7 | _ | |a 10.1002/ajmg.b.32318 |2 doi |
| 024 | 7 | _ | |a pmid:26010163 |2 pmid |
| 024 | 7 | _ | |a 0148-7299 |2 ISSN |
| 024 | 7 | _ | |a 1096-8628 |2 ISSN |
| 024 | 7 | _ | |a 1552-4841 |2 ISSN |
| 024 | 7 | _ | |a 1552-485X |2 ISSN |
| 024 | 7 | _ | |a altmetric:4062203 |2 altmetric |
| 037 | _ | _ | |a DZNE-2020-04292 |
| 041 | _ | _ | |a English |
| 082 | _ | _ | |a 610 |
| 100 | 1 | _ | |a Basmanav, F Buket |0 P:(DE-HGF)0 |b 0 |
| 245 | _ | _ | |a Investigation of the role of TCF4 rare sequence variants in schizophrenia. |
| 260 | _ | _ | |a Hoboken, NJ |c 2015 |b Wiley-Liss |
| 264 | _ | 1 | |3 online |2 Crossref |b Wiley |c 2015-05-22 |
| 264 | _ | 1 | |3 print |2 Crossref |b Wiley |c 2015-07-01 |
| 336 | 7 | _ | |a article |2 DRIVER |
| 336 | 7 | _ | |a Output Types/Journal article |2 DataCite |
| 336 | 7 | _ | |a Journal Article |b journal |m journal |0 PUB:(DE-HGF)16 |s 1587731064_21493 |2 PUB:(DE-HGF) |
| 336 | 7 | _ | |a ARTICLE |2 BibTeX |
| 336 | 7 | _ | |a JOURNAL_ARTICLE |2 ORCID |
| 336 | 7 | _ | |a Journal Article |0 0 |2 EndNote |
| 520 | _ | _ | |a Investigation of the role of TCF4 rare sequence variants in schizophrenia. |
| 536 | _ | _ | |a 345 - Population Studies and Genetics (POF3-345) |0 G:(DE-HGF)POF3-345 |c POF3-345 |f POF III |x 0 |
| 542 | _ | _ | |i 2015-09-01 |2 Crossref |u http://doi.wiley.com/10.1002/tdm_license_1.1 |
| 588 | _ | _ | |a Dataset connected to CrossRef, PubMed, |
| 650 | _ | 7 | |a Basic Helix-Loop-Helix Leucine Zipper Transcription Factors |2 NLM Chemicals |
| 650 | _ | 7 | |a TCF4 protein, human |2 NLM Chemicals |
| 650 | _ | 7 | |a Transcription Factor 4 |2 NLM Chemicals |
| 650 | _ | 7 | |a Transcription Factors |2 NLM Chemicals |
| 650 | _ | 2 | |a White People: genetics |2 MeSH |
| 650 | _ | 2 | |a Basic Helix-Loop-Helix Leucine Zipper Transcription Factors: genetics |2 MeSH |
| 650 | _ | 2 | |a European Continental Ancestry Group: genetics |2 MeSH |
| 650 | _ | 2 | |a Female |2 MeSH |
| 650 | _ | 2 | |a Genetic Predisposition to Disease |2 MeSH |
| 650 | _ | 2 | |a Genetic Variation |2 MeSH |
| 650 | _ | 2 | |a Genotype |2 MeSH |
| 650 | _ | 2 | |a Humans |2 MeSH |
| 650 | _ | 2 | |a Male |2 MeSH |
| 650 | _ | 2 | |a Schizophrenia: genetics |2 MeSH |
| 650 | _ | 2 | |a Transcription Factor 4 |2 MeSH |
| 650 | _ | 2 | |a Transcription Factors: genetics |2 MeSH |
| 700 | 1 | _ | |a Forstner, Andreas J |0 P:(DE-HGF)0 |b 1 |
| 700 | 1 | _ | |a Fier, Heide |0 P:(DE-HGF)0 |b 2 |
| 700 | 1 | _ | |a Herms, Stefan |0 P:(DE-HGF)0 |b 3 |
| 700 | 1 | _ | |a Meier, Sandra |0 P:(DE-HGF)0 |b 4 |
| 700 | 1 | _ | |a Degenhardt, Franziska |0 P:(DE-HGF)0 |b 5 |
| 700 | 1 | _ | |a Hoffmann, Per |0 P:(DE-HGF)0 |b 6 |
| 700 | 1 | _ | |a Barth, Sandra |0 P:(DE-HGF)0 |b 7 |
| 700 | 1 | _ | |a Fricker, Nadine |0 P:(DE-HGF)0 |b 8 |
| 700 | 1 | _ | |a Strohmaier, Jana |0 P:(DE-HGF)0 |b 9 |
| 700 | 1 | _ | |a Witt, Stephanie H |0 P:(DE-HGF)0 |b 10 |
| 700 | 1 | _ | |a Ludwig, Michael |0 P:(DE-HGF)0 |b 11 |
| 700 | 1 | _ | |a Schmael, Christine |0 P:(DE-HGF)0 |b 12 |
| 700 | 1 | _ | |a Moebus, Susanne |0 P:(DE-HGF)0 |b 13 |
| 700 | 1 | _ | |a Maier, Wolfgang |0 P:(DE-HGF)0 |b 14 |
| 700 | 1 | _ | |a Mössner, Rainald |0 P:(DE-HGF)0 |b 15 |
| 700 | 1 | _ | |a Rujescu, Dan |0 P:(DE-HGF)0 |b 16 |
| 700 | 1 | _ | |a Rietschel, Marcella |0 P:(DE-HGF)0 |b 17 |
| 700 | 1 | _ | |a Lange, Christoph |0 P:(DE-2719)9000181 |b 18 |u dzne |
| 700 | 1 | _ | |a Nöthen, Markus M |0 P:(DE-HGF)0 |b 19 |
| 700 | 1 | _ | |a Cichon, Sven |0 P:(DE-HGF)0 |b 20 |e Corresponding author |
| 773 | 1 | 8 | |a 10.1002/ajmg.b.32318 |b : Wiley, 2015-05-22 |n 5 |p 354-362 |3 journal-article |2 Crossref |t American Journal of Medical Genetics Part B: Neuropsychiatric Genetics |v 168 |y 2015 |x 1552-4841 |
| 773 | _ | _ | |a 10.1002/ajmg.b.32318 |g Vol. 168B, no. 5, p. 354 - 362 |0 PERI:(DE-600)2143866-3 |n 5 |q 168B:5<354 - 362 |p 354-362 |t American journal of medical genetics / B |v 168 |y 2015 |x 1552-4841 |
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| 913 | 1 | _ | |a DE-HGF |b Forschungsbereich Gesundheit |l Erkrankungen des Nervensystems |1 G:(DE-HGF)POF3-340 |0 G:(DE-HGF)POF3-345 |2 G:(DE-HGF)POF3-300 |v Population Studies and Genetics |x 0 |
| 914 | 1 | _ | |y 2015 |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0300 |2 StatID |b Medline |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0310 |2 StatID |b NCBI Molecular Biology Database |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0200 |2 StatID |b SCOPUS |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0199 |2 StatID |b Clarivate Analytics Master Journal List |
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| 915 | _ | _ | |a WoS |0 StatID:(DE-HGF)0111 |2 StatID |b Science Citation Index Expanded |
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| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)1050 |2 StatID |b BIOSIS Previews |
| 915 | _ | _ | |a JCR |0 StatID:(DE-HGF)0100 |2 StatID |b AM J MED GENET C : 2017 |
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| 920 | 1 | _ | |0 I:(DE-2719)7000008 |k U T4 Researchers - Bonn |l U T4 Researchers - Bonn |x 0 |
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| 980 | _ | _ | |a VDB |
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