Whitney Neufeld‐Kaiser
- Genetics top 10%
- Genomic variations and chromosomal abnormalities 4
- BRCA gene mutations in cancer 3
- Genomics and Rare Diseases 2
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- Prenatal Screening and Diagnostics 3
- Childhood Cancer Survivors' Quality of Life 2
- Fetal and Pediatric Neurological Disorders 2
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- Congenital heart defects research 3
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- Parvovirus B19 Infection Studies 2
- Co-authors
- Yajuan J. LiuKathryn F. PetersRobin L. BennettBonnie Jeanne BatyWendy McKinnonKwang‐Ting ChengRick A. MartinPamela Flodman
- Partner nations
- United StatesSouth AfricaCanada
In The Last Decade
Whitney Neufeld‐Kaiser
12 papers receiving 295 citations
Peers
Comparison fields: 5 of 58
- Genetics 219
- Pediatrics, Perinatology and Child Health 84
- Urology 11
- Cancer Research 25
- Molecular Biology 101
Countries citing papers authored by Whitney Neufeld‐Kaiser
This map shows the geographic impact of Whitney Neufeld‐Kaiser'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 Whitney Neufeld‐Kaiser with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Whitney Neufeld‐Kaiser more than expected).
Fields of papers citing papers by Whitney Neufeld‐Kaiser
This network shows the impact of papers produced by Whitney Neufeld‐Kaiser. 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 Whitney Neufeld‐Kaiser. The network helps show where Whitney Neufeld‐Kaiser may publish in the future.
Co-authorship network
The 25 scholars most cited alongside Whitney Neufeld‐Kaiser, 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 | 2025 | 1 | |
| 2 | 2023 | 1 | |
| 3 | 2020 | 6 | |
| 4 | 2020 | 10 | |
| 5 | 2019 | 12 | |
| 6 | 2018 | 18 | |
| 7 | 2017 | 30 | |
| 8 | 2017 | 0 | |
| 9 | 2015 | 30 | |
| 10 | 2009 | 21 | |
| 11 | 2002 | 57 | |
| 12 | 2000 | 43 | |
| 13 | Predisposition genetic testing for late-onset disorders in adults. A position paper of the National Society of Genetic Counselors. | 1997 | 86 |
About Whitney Neufeld‐Kaiser
Whitney Neufeld‐Kaiser is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Periodontics, having authored 13 papers that have together received 315 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), BRCA gene mutations in cancer (3 papers), Prenatal Screening and Diagnostics (3 papers), Congenital heart defects research (3 papers), Genomics and Rare Diseases (2 papers), Childhood Cancer Survivors' Quality of Life (2 papers), Fetal and Pediatric Neurological Disorders (2 papers) and Parvovirus B19 Infection Studies (2 papers). The work is most often cited by research in Genetics (219 citations), Pediatrics, Perinatology and Child Health (84 citations) and Urology (11 citations). Whitney Neufeld‐Kaiser has collaborated with scholars based in United States, South Africa and Canada. Frequent co-authors include Yajuan J. Liu, Kathryn F. Peters, Robin L. Bennett, Bonnie Jeanne Baty, Wendy McKinnon, Kwang‐Ting Cheng, Rick A. Martin, Pamela Flodman, Andrew Cheng and David W. Furnas. Their work appears in journals such as Human Mutation, Frontiers in Genetics, BMC Medicine, Journal of Perinatology and BMC Cardiovascular Disorders.
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.