| Home > Publications Database > Inherited genetic susceptibility to monoclonal gammopathy of unknown significance. > print |
| 001 | 137392 | ||
| 005 | 20240321220236.0 | ||
| 024 | 7 | _ | |a 10.1182/blood-2013-10-532283 |2 doi |
| 024 | 7 | _ | |a pmid:24449210 |2 pmid |
| 024 | 7 | _ | |a 0006-4971 |2 ISSN |
| 024 | 7 | _ | |a 1528-0020 |2 ISSN |
| 024 | 7 | _ | |a altmetric:2069161 |2 altmetric |
| 037 | _ | _ | |a DZNE-2020-03714 |
| 041 | _ | _ | |a English |
| 082 | _ | _ | |a 610 |
| 100 | 1 | _ | |a Weinhold, Niels |b 0 |
| 245 | _ | _ | |a Inherited genetic susceptibility to monoclonal gammopathy of unknown significance. |
| 260 | _ | _ | |a Stanford, Calif. |c 2014 |b HighWire Press |
| 264 | _ | 1 | |3 print |2 Crossref |b American Society of Hematology |c 2014-04-17 |
| 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 1590421034_3986 |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 Inherited genetic susceptibility to monoclonal gammopathy of unknown significance. |
| 536 | _ | _ | |a 345 - Population Studies and Genetics (POF3-345) |0 G:(DE-HGF)POF3-345 |c POF3-345 |f POF III |x 0 |
| 588 | _ | _ | |a Dataset connected to CrossRef, PubMed, |
| 650 | _ | 2 | |a Aged |2 MeSH |
| 650 | _ | 2 | |a Aged, 80 and over |2 MeSH |
| 650 | _ | 2 | |a Disease Progression |2 MeSH |
| 650 | _ | 2 | |a Female |2 MeSH |
| 650 | _ | 2 | |a Genetic Association Studies |2 MeSH |
| 650 | _ | 2 | |a Genetic Predisposition to Disease |2 MeSH |
| 650 | _ | 2 | |a Genotype |2 MeSH |
| 650 | _ | 2 | |a Germany: epidemiology |2 MeSH |
| 650 | _ | 2 | |a Humans |2 MeSH |
| 650 | _ | 2 | |a Male |2 MeSH |
| 650 | _ | 2 | |a Middle Aged |2 MeSH |
| 650 | _ | 2 | |a Monoclonal Gammopathy of Undetermined Significance: epidemiology |2 MeSH |
| 650 | _ | 2 | |a Monoclonal Gammopathy of Undetermined Significance: genetics |2 MeSH |
| 650 | _ | 2 | |a Monoclonal Gammopathy of Undetermined Significance: pathology |2 MeSH |
| 650 | _ | 2 | |a Multiple Myeloma: epidemiology |2 MeSH |
| 650 | _ | 2 | |a Multiple Myeloma: genetics |2 MeSH |
| 650 | _ | 2 | |a Polymorphism, Single Nucleotide |2 MeSH |
| 700 | 1 | _ | |a Johnson, David C |b 1 |
| 700 | 1 | _ | |a Rawstron, Andrew C |b 2 |
| 700 | 1 | _ | |a Försti, Asta |b 3 |
| 700 | 1 | _ | |a Doughty, Chi |b 4 |
| 700 | 1 | _ | |a Vijayakrishnan, Jayaram |b 5 |
| 700 | 1 | _ | |a Broderick, Peter |b 6 |
| 700 | 1 | _ | |a Dahir, Nasrin B |b 7 |
| 700 | 1 | _ | |a Begum, Dil B |b 8 |
| 700 | 1 | _ | |a Hosking, Fay J |b 9 |
| 700 | 1 | _ | |a Yong, Kwee |b 10 |
| 700 | 1 | _ | |a Walker, Brian A |b 11 |
| 700 | 1 | _ | |a Hoffmann, Per |b 12 |
| 700 | 1 | _ | |a Mühleisen, Thomas W |b 13 |
| 700 | 1 | _ | |a Langer, Christian |b 14 |
| 700 | 1 | _ | |a Dörner, Elisabeth |b 15 |
| 700 | 1 | _ | |a Jöckel, Karl-Heinz |b 16 |
| 700 | 1 | _ | |a Eisele, Lewin |b 17 |
| 700 | 1 | _ | |a Nöthen, Markus M |0 P:(DE-2719)9000400 |b 18 |u dzne |
| 700 | 1 | _ | |a Hose, Dirk |b 19 |
| 700 | 1 | _ | |a Davies, Faith E |b 20 |
| 700 | 1 | _ | |a Goldschmidt, Hartmut |b 21 |
| 700 | 1 | _ | |a Morgan, Gareth J |b 22 |
| 700 | 1 | _ | |a Hemminki, Kari |b 23 |
| 700 | 1 | _ | |a Houlston, Richard S |0 P:(DE-HGF)0 |b 24 |e Corresponding author |
| 773 | 1 | 8 | |a 10.1182/blood-2013-10-532283 |b : American Society of Hematology, 2014-04-17 |n 16 |p 2513-2517 |3 journal-article |2 Crossref |t Blood |v 123 |y 2014 |x 0006-4971 |
| 773 | _ | _ | |a 10.1182/blood-2013-10-532283 |g Vol. 123, no. 16, p. 2513 - 2517 |0 PERI:(DE-600)1468538-3 |n 16 |q 123:16<2513 - 2517 |p 2513-2517 |t Blood |v 123 |y 2014 |x 0006-4971 |
| 909 | C | O | |o oai:pub.dzne.de:137392 |p VDB |
| 910 | 1 | _ | |a Deutsches Zentrum für Neurodegenerative Erkrankungen |0 I:(DE-588)1065079516 |k DZNE |b 18 |6 P:(DE-2719)9000400 |
| 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 2014 |
| 915 | _ | _ | |a JCR |0 StatID:(DE-HGF)0100 |2 StatID |b BLOOD : 2017 |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0200 |2 StatID |b SCOPUS |
| 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)0320 |2 StatID |b PubMed Central |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0600 |2 StatID |b Ebsco Academic Search |
| 915 | _ | _ | |a Peer Review |0 StatID:(DE-HGF)0030 |2 StatID |b ASC |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0199 |2 StatID |b Clarivate Analytics Master Journal List |
| 915 | _ | _ | |a WoS |0 StatID:(DE-HGF)0110 |2 StatID |b Science Citation Index |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)0150 |2 StatID |b Web of Science Core Collection |
| 915 | _ | _ | |a WoS |0 StatID:(DE-HGF)0111 |2 StatID |b Science Citation Index Expanded |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)1110 |2 StatID |b Current Contents - Clinical Medicine |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)1030 |2 StatID |b Current Contents - Life Sciences |
| 915 | _ | _ | |a DBCoverage |0 StatID:(DE-HGF)1050 |2 StatID |b BIOSIS Previews |
| 915 | _ | _ | |a IF >= 15 |0 StatID:(DE-HGF)9915 |2 StatID |b BLOOD : 2017 |
| 920 | 1 | _ | |0 I:(DE-2719)6000011 |k Bonn Pre 2020 |l Bonn Pre 2020 |x 0 |
| 980 | _ | _ | |a journal |
| 980 | _ | _ | |a VDB |
| 980 | _ | _ | |a I:(DE-2719)6000011 |
| 980 | _ | _ | |a UNRESTRICTED |
| 999 | C | 5 | |a 10.1038/nrc3257 |9 -- missing cx lookup -- |2 Crossref |o 10.1038/nrc3257 |
| 999 | C | 5 | |a 10.1056/NEJMoa01133202 |9 -- missing cx lookup -- |2 Crossref |o 10.1056/NEJMoa01133202 |
| 999 | C | 5 | |a 10.1182/blood-2008-12-191676 |9 -- missing cx lookup -- |2 Crossref |o 10.1182/blood-2008-12-191676 |
| 999 | C | 5 | |a 10.1038/ng.993 |9 -- missing cx lookup -- |2 Crossref |o 10.1038/ng.993 |
| 999 | C | 5 | |a 10.1038/ng.2733 |9 -- missing cx lookup -- |2 Crossref |o 10.1038/ng.2733 |
| 999 | C | 5 | |a 10.1038/nature05911 |9 -- missing cx lookup -- |2 Crossref |o 10.1038/nature05911 |
| 999 | C | 5 | |a 10.1093/ije/dyi183 |9 -- missing cx lookup -- |2 Crossref |o 10.1093/ije/dyi183 |
| 999 | C | 5 | |a 10.1067/mhj.2002.123579 |9 -- missing cx lookup -- |2 Crossref |o 10.1067/mhj.2002.123579 |
| 999 | C | 5 | |y 1994 |2 Crossref |t Meta-analysis decision analysis and cost-effectivness analysis |o Pettiti Meta-analysis decision analysis and cost-effectivness analysis 1994 |
| 999 | C | 5 | |a 10.1002/sim.1186 |9 -- missing cx lookup -- |2 Crossref |o 10.1002/sim.1186 |
| 999 | C | 5 | |2 Crossref |o Greenberg |
| 999 | C | 5 | |a 10.1016/j.ajhg.2012.03.015 |9 -- missing cx lookup -- |2 Crossref |o 10.1016/j.ajhg.2012.03.015 |
| 999 | C | 5 | |a 10.1038/gene.2012.26 |9 -- missing cx lookup -- |2 Crossref |o 10.1038/gene.2012.26 |
| 999 | C | 5 | |a 10.1073/pnas.0608721104 |9 -- missing cx lookup -- |2 Crossref |o 10.1073/pnas.0608721104 |
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