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Molecular Cytogenetics is a peer-reviewed journal published by BMC (BioMed Central), covering Genomic variations and chromosomal abnormalities, Prenatal Screening and Diagnostics, Chromosomal and Genetic Variations. Over its lifetime it has published 1,227 papers, which have received 17,328 citations.
| Publisher | BMC (BioMed Central) |
|---|---|
| Reference style | Numbered (Vancouver) Numbered — [1], [2] in the text 1. Smith A, Jones B, Lee C. A representative article title. Molecular Cytogenetics. 2023;12(3):45–58.
Formats any DOI in Molecular Cytogenetics style. No sign-up. |
| Publishes research in | Genomic variations and chromosomal abnormalities Prenatal Screening and Diagnostics Chromosomal and Genetic Variations Genetic Syndromes and Imprinting Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities |
| ISSN | 1755-8166 |
| Citation impact (2-yr) | 1.32 |
| h-index | 54 |
| i10-index | 495 |
| Article processing charge | $2,318 |
| Open access | Yes — indexed in DOAJ |
| Top institutions publishing here | Jena University Hospital |
| Journal website | molecularcytogenetics.biomedcentral.com |
| You get | A submission-ready PDF and the editable LaTeX source — ready to submit. |
Citations each year’s papers have accumulated so far — the most recent years are still building up.
BACKGROUND: Single embryo transfer (SET) remains underutilized as a strategy to reduce multiple gestation risk in IVF, and its overall lower pregnancy rate underscores the need for improved techniques to select one embryo for fresh transfer. This study explored use of comprehensive chromosomal screening by array CGH (aCGH) to provide this advantage and improve pregnancy…
BACKGROUND: Interstitial deletions of 3q29 have been recently described as a microdeletion syndrome mediated by nonallelic homologous recombination between low-copy repeats resulting in an ~1.6 Mb common-sized deletion. Given the molecular mechanism causing the deletion, the reciprocal duplication is anticipated to occur with equal frequency, although only one family with this duplication has been reported.…
Uniparental disomy (UPD) is often considered as an event to be characterized exclusively by molecular genetic or epigenetic approaches. This review shows that at least one third of UPD cases emerge in connection with or due to a chromosomal rearrangement. Thus, additional (molecular) cytogenetic characterization of UPD cases is essential. Up to now > 1,100…
: Intercellular differences of chromosomal content in the same individual are defined as chromosomal mosaicism (alias intercellular or somatic genomic variations or, in a number of publications, mosaic aneuploidy). It has long been suggested that this phenomenon poorly contributes both to intercellular (interindividual) diversity and to human disease. However, our views have recently become to…
The past decade has witnessed an explosion of genome sequencing and mapping in evolutionary diverse species. While full genome sequencing of mammals is rapidly progressing, the ability to assemble and align orthologous whole chromosome regions from more than a few species is still not possible. The intense focus on building of comparative maps for companion…
