Open Access

Molecular Cytogenetics: the first impact factor (2.36)

Molecular Cytogenetics20136:28

DOI: 10.1186/1755-8166-6-28

Received: 18 July 2013

Accepted: 18 July 2013

Published: 24 July 2013

We are pleased to announce that Molecular Cytogenetics has received its first official Impact Factor of 2.36 in June 2013.

We sincerely thank our distinguished international editorial board for their efforts on behalf of the journal, and our publisher, BioMed Central, for their in-house contribution to the speed and efficiency with which manuscripts are processed. Most important of all, of course, are our authors and reviewers [1], and to them we extend our particular thanks.

Since it was launched in 2008, Molecular Cytogenetics has considered 204 and published 179 articles, giving an acceptance rate of 86%. This exemplifies the journal’s inclusive editorial policy to publish manuscripts that are scientifically sound, and not just based on perceived impact. These articles cover a wide range of topics in molecular cytogenetics, including clinical and tumor cytogenetics, interphase architecture and karyotype evolution studies not only in human but also in other vertebrates. The journal is also open for molecular cytogenetic-based studies in any species, including invertebrates as well as plants. A rapid review process ensures that papers are published in a timely manner [1]. Our average time from submission to the first decision is 20 days, even under our stringent peer review process. As an open access journal, all papers are made immediately and freely available and articles are being accessed more than ever, with around 27,000 accesses per month. Table 1 shows the 10 most highly accessed articles published in Molecular Cytogenetics during the journal’s 5 years of publishing and Table 2 shows some additional highly cited articles. Authors can also access statistics about their article, such as how many times it has been accessed and discussed on social media websites. These statistics can be viewed by selecting ‘Article metrics’ in the right hand column of each article. In addition, all Molecular Cytogenetics articles are mobile-device optimized to facilitate easy reading on phones and tablets.
Table 1

Highly assessed/cited papers published in Molecular Cytogenetics (information valid for the end of June 2013)

Reference

Title

Authors

Year/volume/number

Accesses

Citations

[2]

On the origin of trisomy 21 Down syndrome

Maj A Hultén, Suketu D Patel, Maira Tankimanova, Magnus Westgren, Nikos Papadogiannakis, Anna Jonsson, Erik Iwarsson

Molecular Cytogenetics 2008, 1:21

15036

56

[3]

Human interphase chromosomes: a review of available molecular cytogenetic technologies

Svetlana G Vorsanova, Yuri B Yurov, Ivan Y Iourov

Molecular Cytogenetics 2010, 3:1

14502

35

[4]

FISH mapping of Philadelphia negative BCR/ABL1 positive CML

Anna Virgili, Diana Brazma, Alistair G Reid, Julie Howard-Reeves, Mikel Valgañón, Anastasios Chanalaris, Valeria AS De Melo, David Marin, Jane F Apperley, Colin Grace, Ellie P Nacheva

Molecular Cytogenetics 2008, 1:14

10908

19

[5]

Selection of single blastocysts for fresh transfer via standard morphology assessment alone and with array CGH for good prognosis IVF patients: results from a randomized pilot study

Zhihong Yang, Jiaen Liu, Gary S Collins, Shala A Salem, Xiaohong Liu, Sarah S Lyle, Alison C Peck, E Sills, Rifaat D Salem

Molecular Cytogenetics 2012, 5:24

9981

33

[6]

Mosaic 22q11.2 microdeletion syndrome: diagnosis and clinical manifestations of two cases

Ashutosh Halder, Manish Jain, Madhulika Kabra, Neerja Gupta

Molecular Cytogenetics 2008, 1:18

9728

17

[7]

Fluorescence in situ hybridization in combination with the comet assay and micronucleus test in genetic toxicology

Galina G Hovhannisyan

Molecular Cytogenetics 2010, 3:17

8963

16

[8]

The genome diversity and karyotype evolution of mammals

Alexander S Graphodatsky, Vladimir A Trifonov, Roscoe Stanyon

Molecular Cytogenetics 2011, 4:22

8794

11

[9]

Cytogenetic contribution to uniparental disomy (UPD)

Thomas Liehr

Molecular Cytogenetics 2010, 3:8

8348

28

[10]

The hierarchically organized splitting of chromosomal bands for all human chromosomes

Nadezda Kosyakova, Anja Weise, Kristin Mrasek, Uwe Claussen, Thomas Liehr, Heike Nelle

Molecular Cytogenetics 2009, 2:4

7881

5

[11]

Autistic disorder associated with a paternally derived unbalanced translocation leading to duplication of chromosome 15pter-q13.2: a case report

David J Wu, Nicholas J Wang, Jennette Driscoll, Naghmeh Dorrani, Dahai Liu, Marian Sigman, N Carolyn Schanen

Molecular Cytogenetics 2009, 2:27

7801

6

Table 2

Highly cited papers additional to those highly accessed

Reference

Title

Authors

Year/volume/number

Citations

[12]

Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication

Blake C Ballif, Aaron Theisen, Justine Coppinger, Gordon C Gowans, Joseph H Hersh, Suneeta Madan-Khetarpal, Karen R Schmidt, Raymond Tervo, Luis F Escobar, Christopher A Friedrich, Marie McDonald, Lindsey Campbell, Jeffrey E Ming, Elaine H Zackai, Bassem A Bejjani, Lisa G Shaffer

Molecular Cytogenetics 2008, 1:8

117

[13]

Chromosomal mosaicism goes global

Ivan Y Iourov, Svetlana G Vorsanova, Yuri B Yurov

Molecular Cytogenetics 2008, 1:26

74

[14]

Microdeletion of 6q16. 1 encompassing EPHA7 in a child with mild neurological abnormalities and dysmorphic features: case report

Traylor RN, Fan Z, Hudson B, Rosenfeld JA, Shaffer LG, Torchia BS, Ballif BC

Molecular Cytogenetics 2009, 2:17

41

[15]

Comparative analysis of copy number detection by whole-genome BAC and oligonucleotide array CGH

Neill NJ, Torchia BS, Bejjani BA, Shaffer LG, Ballif BC

Molecular Cytogenetics 2010, 3:11

40

[16]

Cryptic genomic imbalances in patients with de novo or familial apparently balanced translocations and abnormal phenotype

Sismani C, Kitsiou-Tzeli S, Ioannides M, Christodoulou C, Anastasiadou V, Stylianidou G, Papadopoulou E, Kanavakis E, Kosmaidou-Aravidou Z, Patsalis PC

Molecular Cytogenetics 2008, 1:15

39

[17]

Chromosome distribution in human sperm - a 3D multicolor banding-study

Manvelyan M, Hunstig F, Bhatt S, Mrasek K, Pellestor F, Weise A, Simonyan I, Aroutiounian R, Liehr T

Molecular Cytogenetics 2008, 1:25

34

[18]

GIN'n'CIN hypothesis of brain aging: deciphering the role of somatic genetic instabilities and neural aneuploidy during ontogeny

Yurov YB, Vorsanova SG, Iourov IY

Molecular Cytogenetics 2009, 2:23

29

Recently an obituary of a key person in our field, Prof. Dr. Lore Zech, inventor of banding cytogenetics was published and highly recognized in the community [19]. To reflect the needs of our community, in addition to publishing articles recognizing key contributions from the field of molecular cytogenetics, we are very pleased to launch our new journal blog to promote interaction among researchers. In this blog, we will engage in specific discussions with regards to new directions in the field and newly emerging technologies, as well as feedback from recent meetings/articles and more. The blog can be accessed at [20], and also through the journal homepage.

The field of molecular cytogenetics is now entering an exciting time. Following various large-scale sequencing projects that have revealed a high level of genetic heterogeneity, it is clear that single-cell resolution and cell population dynamics are essential to understanding the mechanisms of many common and complex diseases. Thus molecular cytogenetics has become increasingly important as it provides information on both individual cells and cell populations. We hope our journal Molecular Cytogenetics will promote the popularity of the molecular cytogenetic approach during the post-genomic era.

With the help of its readers and authors we look forward to the continuing growth of Molecular Cytogenetics.

Declarations

Acknowledgements

We would like to express our appreciation to Mr. Sam Rose, our Journal Development Editor at BioMed Central, for his enthusiasm and efficiency in promoting the success of Molecular Cytogenetics.

Authors’ Affiliations

(1)
Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University
(2)
Wayne State University School of Medicine
(3)
National Research Center of Mental Health, Russian Academy of Medical Sciences
(4)
Ameripath Florida

References

  1. Liehr T, Heng H, Yurov YB: Reviewer acknowledgement 2013. Mol Cytogenet 2013, 6: 9. 10.1186/1755-8166-6-9PubMed CentralView ArticlePubMedGoogle Scholar
  2. Hultén MA, Patel SD, Tankimanova M, Westgren M, Papadogiannakis N, Jonsson AM, Iwarsson E: On the origin of trisomy 21 down syndrome. Mol Cytogenet 2008, 1: 21. 10.1186/1755-8166-1-21PubMed CentralView ArticlePubMedGoogle Scholar
  3. Vorsanova SG, Yurov YB, Iourov IY: Human interphase chromosomes: a review of available molecular cytogenetic technologies. Mol Cytogenet 2010, 3: 1. 10.1186/1755-8166-3-1PubMed CentralView ArticlePubMedGoogle Scholar
  4. Virgili A, Brazma D, Reid AG, Howard-Reeves J, Valgañón M, Chanalaris A, De Melo VA, Marin D, Apperley JF, Grace C, Nacheva EP: FISH mapping of Philadelphia negative BCR/ABL1 positive CML. Mol Cytogenet 2008, 1: 14. 10.1186/1755-8166-1-14PubMed CentralView ArticlePubMedGoogle Scholar
  5. Yang Z, Liu J, Collins GS, Salem SA, Liu X, Lyle SS, Peck AC, Sills ES, Salem RD: Selection of single blastocysts for fresh transfer via standard morphology assessment alone and with array CGH for good prognosis IVF patients: results from a randomized pilot study. Mol Cytogenet 2012, 5: 24. 10.1186/1755-8166-5-24PubMed CentralView ArticlePubMedGoogle Scholar
  6. Halder A, Jain M, Kabra M, Gupta N: Mosaic 22q11.2 Microdeletion syndrome: diagnosis and clinical manifestations of two cases. Mol Cytogenet 2008, 1: 18. 10.1186/1755-8166-1-18PubMed CentralView ArticlePubMedGoogle Scholar
  7. Hovhannisyan GG: Fluorescence in situ hybridization in combination with the comet assay and micronucleus test in genetic toxicology. Mol Cytogenet 2010, 3: 17. 10.1186/1755-8166-3-17PubMed CentralView ArticlePubMedGoogle Scholar
  8. Graphodatsky AS, Trifonov VA, Stanyon R: The genome diversity and karyotype evolution of mammals. Mol Cytogenet 2011, 4: 22. 10.1186/1755-8166-4-22PubMed CentralView ArticlePubMedGoogle Scholar
  9. Liehr T: Cytogenetic contribution to uniparental disomy (UPD). Mol Cytogenet 2010, 3: 8. 10.1186/1755-8166-3-8PubMed CentralView ArticlePubMedGoogle Scholar
  10. Kosyakova N, Weise A, Mrasek K, Claussen U, Liehr T, Nelle H: The hierarchically organized splitting of chromosomal bands for all human chromosomes. Mol Cytogenet 2009, 2: 4. 10.1186/1755-8166-2-4PubMed CentralView ArticlePubMedGoogle Scholar
  11. Wu DJ, Wang NJ, Driscoll J, Dorrani N, Liu D, Sigman M, Schanen NC: Autistic disorder associated with a paternally derived unbalanced translocation leading to duplication of chromosome 15pter-q13.2: a case report. Mol Cytogenet 2009, 2: 27. 10.1186/1755-8166-2-27PubMed CentralView ArticlePubMedGoogle Scholar
  12. Ballif BC, Theisen A, Coppinger J, Gowans GC, Hersh JH, Madan-Khetarpal S, Schmidt KR, Tervo R, Escobar LF, Friedrich CA, McDonald M, Campbell L, Ming JE, Zackai EH, Bejjani BA, Shaffer LG: Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization of the reciprocal microduplication. Mol Cytogenet 2008, 1: 8. 10.1186/1755-8166-1-8PubMed CentralView ArticlePubMedGoogle Scholar
  13. Iourov IY, Vorsanova SG, Yurov YB: Chromosomal mosaicism goes global. Mol Cytogenet 2008, 1: 26. 10.1186/1755-8166-1-26PubMed CentralView ArticlePubMedGoogle Scholar
  14. Traylor RN, Fan Z, Hudson B, Rosenfeld JA, Shaffer LG, Torchia BS, Ballif BC: Microdeletion of 6q16.1 encompassing EPHA7 in a child with mild neurological abnormalities and dysmorphic features: case report. Mol Cytogenet 2009, 2: 17. 10.1186/1755-8166-2-17PubMed CentralView ArticlePubMedGoogle Scholar
  15. Neill NJ, Torchia BS, Bejjani BA, Shaffer LG, Ballif BC: Comparative analysis of copy number detection by whole-genome BAC and oligonucleotide array CGH. Mol Cytogenet 2010, 3: 11. 10.1186/1755-8166-3-11PubMed CentralView ArticlePubMedGoogle Scholar
  16. Sismani C, Kitsiou-Tzeli S, Ioannides M, Christodoulou C, Anastasiadou V, Stylianidou G, Papadopoulou E, Kanavakis E, Kosmaidou-Aravidou Z, Patsalis PC: Cryptic genomic imbalances in patients with de novo or familial apparently balanced translocations and abnormal phenotype. Mol Cytogenet 2008, 1: 15. 10.1186/1755-8166-1-15PubMed CentralView ArticlePubMedGoogle Scholar
  17. Manvelyan M, Hunstig F, Bhatt S, Mrasek K, Pellestor F, Weise A, Simonyan I, Aroutiounian R, Liehr T: Chromosome distribution in human sperm - a 3D multicolor banding-study. Mol Cytogenet 2008, 1: 25. 10.1186/1755-8166-1-25PubMed CentralView ArticlePubMedGoogle Scholar
  18. Yurov YB, Vorsanova SG, Iourov IY: GIN'n'CIN hypothesis of brain aging: deciphering the role of somatic genetic instabilities and neural aneuploidy during ontogeny. Mol Cytogenet 2009, 2: 23. 10.1186/1755-8166-2-23PubMed CentralView ArticlePubMedGoogle Scholar
  19. Schlegelberger B: In memoriam: Prof. Dr. rer. nat. Dr. med. h.c. Lore Zech; 24.9.1923 - 13.3.2013: honorary member of the European society of human genetics, honorary member of the German society of human genetics, doctor laureate, the University of Kiel, Germany. Mol Cytogenet 2013, 6: 20. 10.1186/1755-8166-6-20PubMed CentralView ArticlePubMedGoogle Scholar
  20. Molecular cytogenetics blog. http://blogs.biomedcentral.com/molcyt

Copyright

© Liehr et al.; licensee BioMed Central Ltd. 2013

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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