Carol Bocchini
Impact in
- Genetics top 2%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Molecular Biology top 5%
- Bioinformatics and Genomic Networks
- Biomedical Text Mining and Ontologies
- Genomics and Phylogenetic Studies
- Gene expression and cancer classification
- RNA modifications and cancer
Papers in
- Genetics 8
- Genomics and Rare Diseases 7
- Nutrition, Genetics, and Disease 2
- BRCA gene mutations in cancer 2
- Genomic variations and chromosomal abnormalities 2
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- Biomedical Text Mining and Ontologies 3
- Genetics, Bioinformatics, and Biomedical Research 2
- Congenital heart defects research 2
- Co-authors
- Joanna Amberger (8 shared papers)Ada Hamosh (8 shared papers)Alan F. Scott (4 shared papers)François Schiettecatte (1 shared paper)Sonja A. Rasmussen (2 shared papers)V.A. McKusick (1 shared paper)Victor A. McKusick (1 shared paper)P. Pearson (1 shared paper)
- Journals
- Nucleic Acids Research (5 papers)Bioinformatics (1 paper)Human Mutation (1 paper)Genetics in Medicine (1 paper)American Journal of Medical Genetics Part A (1 paper)
- Partner nations
- United StatesGermanyPoland
In The Last Decade
Carol Bocchini
9 papers receiving 3.4k citations
Carol Bocchini's Hit Papers
Peers
Comparison fields: 5 of 122
- Genetics 888
- Molecular Biology 1.8k
- Pharmacology 213
- Cancer Research 265
- Computational Theory and Mathematics 305
Countries citing papers authored by Carol Bocchini
This map shows the geographic impact of Carol Bocchini's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Carol Bocchini with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Carol Bocchini more than expected).
Fields of papers citing papers by Carol Bocchini
This network shows the impact of papers produced by Carol Bocchini. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Carol Bocchini. The network helps show where Carol Bocchini may publish in the future.
Co-authors
The 14 scholars most cited alongside Carol Bocchini, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders Hit paper breakdown → | 2014 | 1713 |
| 2 | OMIM.org: leveraging knowledge across phenotype–gene relationships Hit paper breakdown → | 2018 | 617 |
| 3 | McKusick's Online Mendelian Inheritance in Man (OMIM(R)) Hit paper breakdown → | 2008 | 525 |
| 4 | 2011 | 256 | |
| 5 | 2021 | 99 | |
| 6 | ヒトのオンラインメンデル性遺伝(OMIM),ヒト遺伝子および遺伝子病の情報ベース | 2005 | 83 |
| 7 | 2014 | 59 | |
| 8 | 1994 | 54 | |
| 9 | 2020 | 14 |
About Carol Bocchini
Carol Bocchini is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Infectious Diseases and Organic Chemistry, having authored 9 papers that have together received 3.4k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (7 papers), Biomedical Text Mining and Ontologies (3 papers), Nutrition, Genetics, and Disease (2 papers), BRCA gene mutations in cancer (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Genetics, Bioinformatics, and Biomedical Research (2 papers), Congenital heart defects research (2 papers) and Genetic factors in colorectal cancer (1 paper). The work is most often cited by research in Genetics (888 citations), Molecular Biology (1.8k citations), Pharmacology (213 citations), Cancer Research (265 citations) and Computational Theory and Mathematics (305 citations). Carol Bocchini has collaborated with scholars based in United States, Germany and Poland. Frequent co-authors include Joanna Amberger, Ada Hamosh, Alan F. Scott, François Schiettecatte, Sonja A. Rasmussen, V.A. McKusick, Victor A. McKusick, P. Pearson, Clair A. Francomano and Damian Smedley. Their work appears in journals such as Nucleic Acids Research, Bioinformatics, Human Mutation, Genetics in Medicine and American Journal of Medical Genetics Part A.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.