Elly Brokamp
Impact in
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- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
Papers in
- Genetics 9
- Genomics and Rare Diseases 6
- BRCA gene mutations in cancer 4
- Genetics and Neurodevelopmental Disorders 1
- Genetic Syndromes and Imprinting 1
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- Autism Spectrum Disorder Research 2
- Co-authors
- Jessica Duis (3 shared papers)Anna K. Childers (1 shared paper)Pieter Joost van Wattum (1 shared paper)Ann Scheimann (1 shared paper)Althea Robinson Shelton (1 shared paper)Ashley H. Shoemaker (1 shared paper)Jennifer L. Miller (1 shared paper)Parisa Salehi (1 shared paper)
- Journals
- Genetics in Medicine (2 papers)Molecular Case Studies (1 paper)Arthritis Research & Therapy (1 paper)Journal of Genetic Counseling (3 papers)Molecular Genetics & Genomic Medicine (2 papers)
- Partner nations
- United StatesItalyJapan
In The Last Decade
Elly Brokamp
9 papers receiving 194 citations
Peers
Comparison fields: 5 of 45
- Genetics 140
- Anatomy 3
- Pediatrics, Perinatology and Child Health 23
- Developmental Biology 2
- Cancer Research 12
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 | 59 | |
| 2 | 2020 | 56 | |
| 3 | 2019 | 20 | |
| 4 | 2022 | 19 | |
| 5 | 2021 | 17 | |
| 6 | 2020 | 13 | |
| 7 | 2018 | 11 | |
| 8 | 2019 | 4 | |
| 9 | The Utility of Genomic Variant Databases in Genetic Counseling | 2016 | 1 |
| 10 | 2025 | 0 | |
| 11 | 2025 | 0 |
About Elly Brokamp
Elly Brokamp is a scholar working on Genetics, Cognitive Neuroscience, Molecular Biology, Pathology and Forensic Medicine and Pediatrics, Perinatology and Child Health, having authored 11 papers that have together received 200 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), BRCA gene mutations in cancer (4 papers), Autism Spectrum Disorder Research (2 papers), Genetics and Neurodevelopmental Disorders (1 paper), Ubiquitin and proteasome pathways (1 paper), Genetic Syndromes and Imprinting (1 paper), Family and Disability Support Research (1 paper) and Genetic factors in colorectal cancer (1 paper). The work is most often cited by research in Genetics (140 citations), Anatomy (3 citations), Pediatrics, Perinatology and Child Health (23 citations), Developmental Biology (2 citations) and Cancer Research (12 citations). Elly Brokamp has collaborated with scholars based in United States, Italy and Japan. Frequent co-authors include Jessica Duis, Anna K. Childers, Pieter Joost van Wattum, Ann Scheimann, Althea Robinson Shelton, Ashley H. Shoemaker, Jennifer L. Miller, Parisa Salehi, Rizwan Hamid and Nathan C. Bingham. Their work appears in journals such as Genetics in Medicine, Molecular Case Studies, Arthritis Research & Therapy, Journal of Genetic Counseling and Molecular Genetics & Genomic Medicine.
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.