Elly Brokamp
Impact in
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- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 7
- Genomics and Rare Diseases 4
- BRCA gene mutations in cancer 3
- Genetics and Neurodevelopmental Disorders 2
- Forensic and Genetic Research 1
- Nutrition, Genetics, and Disease 1
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- Autism Spectrum Disorder Research 2
- Co-authors
- Jessica Duis (3 shared papers)Nathan C. Bingham (1 shared paper)Pieter Joost van Wattum (1 shared paper)Parisa Salehi (1 shared paper)Rizwan Hamid (3 shared papers)Anna K. Childers (1 shared paper)Ann Scheimann (1 shared paper)Ashley H. Shoemaker (1 shared paper)
- Journals
- Genetics in Medicine (2 papers)Arthritis Research & Therapy (1 paper)Molecular Case Studies (1 paper)Journal of Genetic Counseling (2 papers)American Journal of Medical Genetics Part A (1 paper)
- Partner nations
- United StatesAustraliaItaly
In The Last Decade
Elly Brokamp
8 papers receiving 172 citations
Peers
Comparison fields: 5 of 46
- Genetics 132
- Anatomy 3
- Pediatrics, Perinatology and Child Health 25
- Cancer Research 19
- Pathology and Forensic Medicine 18
Countries citing papers authored by Elly Brokamp
This map shows the geographic impact of Elly Brokamp'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 Elly Brokamp with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Elly Brokamp more than expected).
Fields of papers citing papers by Elly Brokamp
This network shows the impact of papers produced by Elly Brokamp. 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 Elly Brokamp. The network helps show where Elly Brokamp may publish in the future.
Co-authors
The 25 scholars most cited alongside Elly Brokamp, 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 | 2019 | 55 | |
| 2 | 2020 | 53 | |
| 3 | 2022 | 19 | |
| 4 | 2019 | 19 | |
| 5 | 2021 | 15 | |
| 6 | 2018 | 11 | |
| 7 | 2019 | 4 | |
| 8 | The Utility of Genomic Variant Databases in Genetic Counseling | 2016 | 1 |
| 9 | 2025 | 0 |
About Elly Brokamp
Elly Brokamp is a scholar working on Genetics, Cognitive Neuroscience, Surgery, Molecular Biology and Genetics, having authored 9 papers that have together received 177 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (4 papers), BRCA gene mutations in cancer (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Autism Spectrum Disorder Research (2 papers), Forensic and Genetic Research (1 paper), Nutrition, Genetics, and Disease (1 paper), Medical Coding and Health Information (1 paper) and Genetic factors in colorectal cancer (1 paper). The work is most often cited by research in Genetics (132 citations), Anatomy (3 citations), Pediatrics, Perinatology and Child Health (25 citations), Cancer Research (19 citations) and Pathology and Forensic Medicine (18 citations). Elly Brokamp has collaborated with scholars based in United States, Australia and Italy. Frequent co-authors include Jessica Duis, Nathan C. Bingham, Pieter Joost van Wattum, Parisa Salehi, Rizwan Hamid, Anna K. Childers, Ann Scheimann, Ashley H. Shoemaker, Jennifer L. Miller and Althea Robinson Shelton. Their work appears in journals such as Genetics in Medicine, Arthritis Research & Therapy, Molecular Case Studies, Journal of Genetic Counseling 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.