Details

Aims and Scope

Advancing understanding of genetic syndromes through molecular insights

'Molecular Syndromology' aims to furnish the medical genetics community with clinically useful information regarding genetic and genomic disorders. The scope of Molecular Syndromology includes papers that elucidate the molecular and biochemical basis of the disease, genotype-phenotype correlations, and the prognosis and treatment options based on knowledge of the underlying mutation(s). To do so, Molecular Syndromology publishes research and review articles, case reports revealing novel genes, mutations and phenotypes, and summaries of symposia and workshops on themes with relevance to clinical genetics.

Bibliographic Details

Molecular Syndromology
Journal Abbreviation: Mol Syndromol
ISSN: 1661-8769 (Print)
e-ISSN: 1661-8777 (Online)
DOI: 10.1159/issn.1661-8769
karger.com/MSY

Indexing/Abstracting

Listed in bibliographic services, including:

PubMed | US National Library of Medicine
PubMed Central | US National Library of Medicine
Web of Science | Clarivate Analytics
Science Citation Index Expanded | Clarivate Analytics
Google Scholar | Google
Chemical Abstracts Service | American Chemical Society
Scopus | Elsevier
Embase | Elsevier
Pathway Studio | Elsevier
Health Research Premium Collection | ProQuest
Medical Database | ProQuest
Health & Medical Collection | ProQuest
ProQuest Central | ProQuest
WorldCat | OCLC

History

Founded 2010 by A. Rauch
Continued by M. Schmid (2011-2018)
Continued by Lisa. G. Shaffer (2012-2021)