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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- Metabolism and Genetic Disorders
Papers in
- Genetics 15
- Genomics and Rare Diseases 9
- BRCA gene mutations in cancer 3
- Genetics and Neurodevelopmental Disorders 2
- Cleft Lip and Palate Research 2
- Genomic variations and chromosomal abnormalities 2
- Craniofacial Disorders and Treatments 2
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- Mitochondrial Function and Pathology 3
- Congenital heart defects research 2
- Co-authors
- Banu Arun (1 shared paper)Jessica Profato (1 shared paper)Yuanqing Ye (1 shared paper)Denise Nebgen (1 shared paper)Jennifer K. Litton (1 shared paper)Seema R. Lalani (4 shared papers)Susan K. Peterson (1 shared paper)Claire N. Singletary (1 shared paper)
- Journals
- Genetics in Medicine (6 papers)Human Molecular Genetics (1 paper)Biochemical and Biophysical Research Communications (1 paper)The Oncologist (1 paper)Frontiers in Cell and Developmental Biology (1 paper)
- Partner nations
- United StatesHong KongChina
In The Last Decade
Haley Streff
20 papers receiving 193 citations
Peers
Comparison fields: 5 of 47
- Genetics 84
- Clinical Biochemistry 12
- Molecular Biology 93
- Cancer Research 17
- 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 25 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2016 | 38 | |
| 2 | 2021 | 20 | |
| 3 | 2019 | 18 | |
| 4 | 2018 | 16 | |
| 5 | 2018 | 16 | |
| 6 | 2021 | 12 | |
| 7 | 2016 | 12 | |
| 8 | 2019 | 11 | |
| 9 | 2020 | 9 | |
| 10 | 2021 | 8 | |
| 11 | 2021 | 8 | |
| 12 | 2021 | 6 | |
| 13 | 2023 | 5 | |
| 14 | 2022 | 4 | |
| 15 | 2023 | 4 | |
| 16 | 2018 | 3 | |
| 17 | 2023 | 2 | |
| 18 | 2019 | 2 | |
| 19 | 2023 | 2 | |
| 20 | 2020 | 1 |
About Haley Streff
Haley Streff is a scholar working on Genetics, Molecular Biology, Physiology, Cardiology and Cardiovascular Medicine and Oncology, having authored 25 papers that have together received 197 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (9 papers), BRCA gene mutations in cancer (3 papers), Mitochondrial Function and Pathology (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Congenital heart defects research (2 papers), Cleft Lip and Palate Research (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Craniofacial Disorders and Treatments (2 papers). The work is most often cited by research in Genetics (84 citations), Clinical Biochemistry (12 citations), Molecular Biology (93 citations), Cancer Research (17 citations) and Aging (2 citations). Haley Streff has collaborated with scholars based in United States, Hong Kong and China. Frequent co-authors include Banu Arun, Jessica Profato, Yuanqing Ye, Denise Nebgen, Jennifer K. Litton, Seema R. Lalani, Susan K. Peterson, Claire N. Singletary, Weimin Bi and Bret L. Bostwick. Their work appears in journals such as Genetics in Medicine, Human Molecular Genetics, Biochemical and Biophysical Research Communications, The Oncologist 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.