| Discipline name | Position | Best Scientists | Publications | D-Index |
|---|---|---|---|---|
| Medicine | 1236 | 185 | 166 | 19 |
Familial Cancer tackles a plethora of topics, such as Internal medicine, Epidemiology, Cancer, Oncology and Human genetics. In Familial Cancer, Gastroenterology, Germline mutation and Pathology are investigated in conjunction with one another to address concerns in Internal medicine research. The journal explores topics in Germline mutation which can be helpful for research in disciplines like Cancer research, Gene mutation and Germline.
The journal focuses on Epidemiology but the discussions also offer insight into other areas such as Cohort, Family medicine, Gynecology, Family history and Genetic testing. The tackled Genetic testing research is interrelated with Genetic counseling which concerns subjects like Psychiatry. While work presented in Familial Cancer provided substantial information on Cancer, it also covered topics in Pediatrics and Age of onset.
Some problems in Oncology that were presented in the journal overlapped with concepts under Penetrance, Disease and Genotype. It focuses on Human genetics research as part of the broader topic of Genetics. The featured Lynch syndrome studies mainly concentrate on MSH2 but also cover areas of interest in MLH1 and MSH6.
The published articles tackle a plethora of topics, such as Internal medicine, Cancer, Epidemiology, Oncology and Lynch syndrome. In addition to Internal medicine research, the most cited articles aim to explore topics under Gastroenterology, Gene mutation and Pathology. The most cited papers explore issues in Lynch syndrome which can be linked to other research areas like Germline mutation, MSH2, Microsatellite instability and Human genetics.
The topics of Internal medicine, Epidemiology, Human genetics, Cancer and Oncology are the focal point of discussions in the journal. Colorectal cancer, Breast cancer, Family history and Disease are among the concentrations of Internal medicine that garnered much attention in it. While Familial Cancer focused on Epidemiology, it was also able to explore topics like Family medicine, Lynch syndrome, Genetic testing and Cohort.
It explores issues in Human genetics which can be linked to other research areas like Bioinformatics, MEDLINE, Germline and Library science. Topics in Cancer were tackled in line with various other fields like Observational study, Medical diagnosis and Hereditary diffuse gastric cancer. The presented Oncology research focuses mostly on Germline mutation and, on occasion, topics in Gene mutation.
A key indicator for each journal is its effectiveness in reaching other researchers with the papers published at that venue.
The chart below presents the interquartile range (first quartile 25%, median 50% and third quartile 75%) of the number of citations of articles over time.
The top authors publishing in Familial Cancer (based on the number of publications) are:
The overall trend for top authors publishing in this journal is outlined below. The chart shows the number of publications at each edition of the journal for top authors.
Only papers with recognized affiliations are considered
The top affiliations publishing in Familial Cancer (based on the number of publications) are:
The overall trend for top affiliations publishing in this journal is outlined below. The chart shows the number of publications at each edition of the journal for top affiliations.
The publication chance index shows the ratio of articles published by the best research institutions in the journal edition to all articles published within that journal. The best research institutions were selected based on the largest number of articles published during all editions of the journal.
The chart below presents the percentage ratio of articles from top institutions (based on their ranking of total papers).Top affiliations were grouped by their rank into the following tiers: top 1-10, top 11-20, top 21-50, and top 51+. Only articles with a recognized affiliation are considered.
During the most recent 2021 edition, 4.49% of publications had an unrecognized affiliation. Out of the publications with recognized affiliations, 20.00% were posted by at least one author from the top 10 institutions publishing in the journal. Another 24.71% included authors affiliated with research institutions from the top 11-20 affiliations. Institutions from the 21-50 range included 22.35% of all publications and 32.94% were from other institutions.
A very common phenomenon observed among researchers publishing scientific articles is the intentional selection of journals they have already attended in the past. In particular, it is worth analyzing the case when the authors participate in the same journal from year to year.
The Returning Authors Index presented below illustrates the ratio of authors who participated in both a given as well as the previous edition of the journal in relation to all participants in a given year.
The graph below shows the Returning Institution Index, illustrating the ratio of institutions that participated in both a given and the previous edition of the conference in relation to all affiliations present in a given year.
Our experience to innovation index was created to show a cross-section of the experience level of authors publishing in a journal. The index includes the authors publishing at the last edition of a journal, grouped by total number of publications throughout their academic career (P) and the total number of citations of these publications ever received (C).
The group intervals were selected empirically to best show the diversity of the authors' experiences, their labels were selected as a convenience, not as judgment. The authors were divided into the following groups:
The chart below illustrates experience levels of first authors in cases of publications with multiple authors.
It would be beneficial to provide an understanding of the nature and extent of collaborations between different research institutions in the field of Familial Cancer research. This could shed light on the key players and the nature of their collaborations, fostering improved communication and synergy in future research endeavors. Several research collaborations exist amongst institutions in the field of Familial Cancer. To illustrate this, authors from diverse geographical and institutional backgrounds often co-author research papers. This cooperative effort epitomizes the integrated approach necessary for advancements in Familial Cancer research. For instance, in a recent publication, our Access to Genomic Information: Legal Implications, authors from the Institute of Human Genetics, Maastricht University, and Mayo Clinic worked together, showcasing a transatlantic collaborative effort. Collaborations like this are increasingly common within the research community, especially in areas like Familial Cancer that require a diverse range of expertise. Collaborations not only facilitate knowledge sharing but also provide opportunities for unique research perspectives that might not have been possible within one institution. For a deeper exploration of research collaborations and educational opportunities towards Familial Cancer, consider examining the lpn programs in wisconsin. These programs offer a wealth of information on Familial Cancer, as well as significant opportunities for partnerships and collaborations.
Virginie Marcel;Janice Kielbassa;Virginie Marchand;Kundhavai S Natchiar
(2020)Heald B;Hampel H;Church J;Dudley B
(2020)Claire Palles;Lynn Martin;Enric Domingo;Laura Chegwidden
(2021)J. A. Hol;M. C. J. Jongmans;A. S. Littooij;R. R. de Krijger
(2020)M. C. Frühwald;K. Nemes;H. Boztug;M. C. A. Cornips
(2021)Jette J Bakhuizen;Helen Hanson;Karin van der Tuin;Fiona Lalloo
(2021)L Guerrini-Rousseau;M J Smith;C P Kratz;B Doergeloh
(2021)Holly Ni Raghallaigh;Rosalind Eeles
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