Whitney Neufeld‐Kaiser

655 citations
13 papers · 315 indexed · h-index 9
Topics
Genomic variations and chromosomal abnormalities (4 papers)BRCA gene mutations in cancer (3 papers)Prenatal Screening and Diagnostics (3 papers)

In The Last Decade

Whitney Neufeld‐Kaiser

12 papers receiving 295 citations

Peers

Whitney Neufeld‐Kaiser
Comparison fields: 5 of 58
  • Genetics 219
  • Molecular Biology 101
  • Pediatrics, Perinatology and Child Health 84
  • Public Health, Environmental and Occupational Health 35
  • Surgery 26
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Countries citing papers authored by Whitney Neufeld‐Kaiser

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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 of co-authors of Whitney Neufeld‐Kaiser

This figure shows the co-authorship network connecting the top 25 collaborators of Whitney Neufeld‐Kaiser. A scholar is included among the top collaborators of Whitney Neufeld‐Kaiser based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Whitney Neufeld‐Kaiser. Whitney Neufeld‐Kaiser is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

13 of 13 papers shown
#WorkIndexed citations
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Predisposition genetic testing for late-onset disorders in adults. A position paper of the National Society of Genetic Counselors.
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) and Prenatal Screening and Diagnostics (3 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 BMC Medicine, Human Mutation and Frontiers in Genetics.

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.

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