Jodi D. Hoffman
Impact in
- Genetics top 5%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
- Craniofacial Disorders and Treatments
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 18
- Genomics and Rare Diseases 7
- BRCA gene mutations in cancer 5
- Genomic variations and chromosomal abnormalities 3
- Connective tissue disorders research 3
- Craniofacial Disorders and Treatments 3
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- CRISPR and Genetic Engineering 2
- Co-authors
- Paige Kaplan (3 shared papers)Kenneth Ward (2 shared papers)Karen W. Gripp (1 shared paper)Deborah L. Stabley (1 shared paper)Linda K. Nicholson (1 shared paper)Katia Sol‐Church (1 shared paper)Elaine H. Zackai (3 shared papers)Karen L. Ciprero (1 shared paper)
- Journals
- Prenatal Diagnosis (4 papers)American Journal of Obstetrics and Gynecology (2 papers)European Journal of Medical Genetics (1 paper)PLoS ONE (1 paper)Human Mutation (1 paper)
- Partner nations
- United StatesCanadaGermany
In The Last Decade
Jodi D. Hoffman
31 papers receiving 642 citations
Peers
Comparison fields: 5 of 69
- Genetics 330
- Pediatrics, Perinatology and Child Health 101
- Medical Terminology 1
- Clinical Biochemistry 28
- Genetics 36
Countries citing papers authored by Jodi D. Hoffman
This map shows the geographic impact of Jodi D. Hoffman'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 Jodi D. Hoffman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jodi D. Hoffman more than expected).
Fields of papers citing papers by Jodi D. Hoffman
This network shows the impact of papers produced by Jodi D. Hoffman. 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 Jodi D. Hoffman. The network helps show where Jodi D. Hoffman may publish in the future.
Co-authors
The 25 scholars most cited alongside Jodi D. Hoffman, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 33 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2018 | 88 | |
| 2 | 2005 | 62 | |
| 3 | 2006 | 60 | |
| 4 | 2008 | 47 | |
| 5 | 2014 | 36 | |
| 6 | 2006 | 32 | |
| 7 | 2020 | 29 | |
| 8 | 2005 | 28 | |
| 9 | 2019 | 26 | |
| 10 | 2013 | 26 | |
| 11 | 1998 | 25 | |
| 12 | 1999 | 22 | |
| 13 | 1994 | 21 | |
| 14 | 2005 | 20 | |
| 15 | 2006 | 20 | |
| 16 | 2013 | 20 | |
| 17 | 2009 | 18 | |
| 18 | 2015 | 17 | |
| 19 | 2014 | 15 | |
| 20 | 2012 | 11 |
About Jodi D. Hoffman
Jodi D. Hoffman is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Physiology and Epidemiology, having authored 33 papers that have together received 667 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (7 papers), Prenatal Screening and Diagnostics (6 papers), BRCA gene mutations in cancer (5 papers), Lysosomal Storage Disorders Research (4 papers), Genomic variations and chromosomal abnormalities (3 papers), Connective tissue disorders research (3 papers), Craniofacial Disorders and Treatments (3 papers) and CRISPR and Genetic Engineering (2 papers). The work is most often cited by research in Genetics (330 citations), Pediatrics, Perinatology and Child Health (101 citations), Medical Terminology (1 citation), Clinical Biochemistry (28 citations) and Genetics (36 citations). Jodi D. Hoffman has collaborated with scholars based in United States, Canada and Germany. Frequent co-authors include Paige Kaplan, Kenneth Ward, Karen W. Gripp, Deborah L. Stabley, Linda K. Nicholson, Katia Sol‐Church, Elaine H. Zackai, Karen L. Ciprero, Kathleen E. Sullivan and Elizabeth A. Gilliam. Their work appears in journals such as Prenatal Diagnosis, American Journal of Obstetrics and Gynecology, European Journal of Medical Genetics, PLoS ONE and Human Mutation.
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.