Haley Streff
Impact in
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- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
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- Cancer Genomics and Diagnostics
Papers in
- Genetics 19
- Genomics and Rare Diseases 11
- BRCA gene mutations in cancer 5
- Ocular Disorders and Treatments 3
- Genetics and Neurodevelopmental Disorders 3
- Genomic variations and chromosomal abnormalities 3
- Cleft Lip and Palate Research 2
- Craniofacial Disorders and Treatments 2
- Co-authors
- Seema R. Lalani (4 shared papers)Susan K. Peterson (1 shared paper)Banu Arun (1 shared paper)Claire N. Singletary (1 shared paper)Jessica Profato (1 shared paper)Denise Nebgen (1 shared paper)Jennifer K. Litton (1 shared paper)Yuanqing Ye (1 shared paper)
- Journals
- Genetics in Medicine (6 papers)Scientific Reports (1 paper)Human Molecular Genetics (1 paper)European Journal of Human Genetics (1 paper)Frontiers in Cell and Developmental Biology (1 paper)
- Partner nations
- United StatesChinaHong Kong
In The Last Decade
Haley Streff
20 papers receiving 184 citations
Peers
Comparison fields: 5 of 49
- Genetics 93
- Cancer Research 23
- Clinical Biochemistry 10
- Molecular Biology 100
- Aging 2
Countries citing papers authored by Haley Streff
This map shows the geographic impact of Haley Streff'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 Haley Streff with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Haley Streff more than expected).
Fields of papers citing papers by Haley Streff
This network shows the impact of papers produced by Haley Streff. 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 Haley Streff. The network helps show where Haley Streff may publish in the future.
Co-authors
The 25 scholars most cited alongside Haley Streff, 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 24 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2016 | 37 | |
| 2 | 2021 | 19 | |
| 3 | 2019 | 16 | |
| 4 | 2018 | 16 | |
| 5 | 2018 | 15 | |
| 6 | 2021 | 11 | |
| 7 | 2019 | 11 | |
| 8 | 2016 | 11 | |
| 9 | 2020 | 9 | |
| 10 | 2021 | 8 | |
| 11 | 2021 | 8 | |
| 12 | 2021 | 6 | |
| 13 | 2022 | 4 | |
| 14 | 2023 | 4 | |
| 15 | 2023 | 4 | |
| 16 | 2018 | 3 | |
| 17 | 2019 | 2 | |
| 18 | 2023 | 2 | |
| 19 | 2020 | 1 | |
| 20 | 2023 | 1 |
About Haley Streff
Haley Streff is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Physiology and Cancer Research, having authored 24 papers that have together received 188 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (11 papers), BRCA gene mutations in cancer (5 papers), Ocular Disorders and Treatments (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Biomedical Ethics and Regulation (2 papers), Cleft Lip and Palate Research (2 papers) and Craniofacial Disorders and Treatments (2 papers). The work is most often cited by research in Genetics (93 citations), Cancer Research (23 citations), Clinical Biochemistry (10 citations), Molecular Biology (100 citations) and Aging (2 citations). Haley Streff has collaborated with scholars based in United States, China and Hong Kong. Frequent co-authors include Seema R. Lalani, Susan K. Peterson, Banu Arun, Claire N. Singletary, Jessica Profato, Denise Nebgen, Jennifer K. Litton, Yuanqing Ye, Mari Tokita and Bret L. Bostwick. Their work appears in journals such as Genetics in Medicine, Scientific Reports, Human Molecular Genetics, European Journal of Human Genetics and Frontiers in Cell and Developmental Biology.
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.