Whitney Neufeld‐Kaiser

655 total citations
13 papers, 315 citations indexed

About

Whitney Neufeld‐Kaiser is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Whitney Neufeld‐Kaiser has authored 13 papers receiving a total of 315 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 5 papers in Pediatrics, Perinatology and Child Health and 4 papers in Molecular Biology. Recurrent topics in Whitney Neufeld‐Kaiser's work include Genomic variations and chromosomal abnormalities (4 papers), BRCA gene mutations in cancer (3 papers) and Congenital heart defects research (3 papers). Whitney Neufeld‐Kaiser is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), BRCA gene mutations in cancer (3 papers) and Congenital heart defects research (3 papers). Whitney Neufeld‐Kaiser collaborates with scholars based in United States, South Africa and Canada. Whitney Neufeld‐Kaiser's co-authors include Yajuan J. Liu, Wendy McKinnon, Kathryn F. Peters, Bonnie Jeanne Baty, Robin L. Bennett, Kwang‐Ting Cheng, Pamela Flodman, Peter H. Byers, Kimberly Martin and Andrew Cheng and has published in prestigious journals such as BMC Medicine, Human Mutation and Frontiers in Genetics.

In The Last Decade

Whitney Neufeld‐Kaiser

12 papers receiving 295 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Whitney Neufeld‐Kaiser United States 9 219 101 84 35 26 13 315
Sabine Hentze Germany 11 139 0.6× 178 1.8× 60 0.7× 63 1.8× 12 0.5× 18 412
Michael T. Gabbett Australia 11 168 0.8× 116 1.1× 59 0.7× 16 0.5× 47 1.8× 25 313
Melissa A. Richard United States 9 96 0.4× 179 1.8× 37 0.4× 24 0.7× 26 1.0× 27 313
Julia Grinshpun‐Cohen Israel 7 247 1.1× 110 1.1× 104 1.2× 35 1.0× 15 0.6× 13 351
Mahmoud Aarabi United States 11 207 0.9× 196 1.9× 214 2.5× 68 1.9× 29 1.1× 20 541
Jadranka Popović United States 10 144 0.7× 245 2.4× 49 0.6× 47 1.3× 56 2.2× 12 522
Tamar Goldwaser United States 6 116 0.5× 56 0.6× 147 1.8× 21 0.6× 30 1.2× 7 297
Gabrielle Christenhusz Belgium 9 258 1.2× 66 0.7× 79 0.9× 139 4.0× 11 0.4× 10 374
Elena Ashkinadze United States 9 115 0.5× 57 0.6× 175 2.1× 54 1.5× 19 0.7× 20 294
Janet Marcadier Canada 6 110 0.5× 119 1.2× 47 0.6× 12 0.3× 37 1.4× 8 244

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
1.
Fang, He, Stephen Eacker, Yu Wu, et al.. (2025). Genetic and functional characterization of inherited complex chromosomal rearrangements in a family with multisystem anomalies. Genetics in Medicine Open. 3. 103423–103423. 1 indexed citations
2.
Liu, Yajuan, et al.. (2023). 11. Evaluation of Hi-C versus optical genome mapping for diagnosing constitutional genomic structural variants. Cancer Genetics. 278-279. 4–4. 1 indexed citations
3.
Deng, Xinxian, He Fang, Whitney Neufeld‐Kaiser, et al.. (2020). Deletion of FUNDC2 and CMC4 on Chromosome Xq28 Is Sufficient to Cause Hypergonadotropic Hypogonadism in Men. Frontiers in Genetics. 11. 557341–557341. 6 indexed citations
4.
Cheng, Andrew, Whitney Neufeld‐Kaiser, Peter H. Byers, & Yajuan J. Liu. (2020). 6q25.1 (TAB2) microdeletion is a risk factor for hypoplastic left heart: a case report that expands the phenotype. BMC Cardiovascular Disorders. 20(1). 137–137. 10 indexed citations
5.
Dines, Jennifer N., Yajuan J. Liu, Whitney Neufeld‐Kaiser, et al.. (2019). Expanding phenotype with severe midline brain anomalies and missense variant supports a causal role for FOXA2 in 20p11.2 deletion syndrome. American Journal of Medical Genetics Part A. 179(9). 1783–1790. 12 indexed citations
6.
Byers, Heather M., et al.. (2018). Discordant sex between fetal screening and postnatal phenotype requires evaluation. Journal of Perinatology. 39(1). 28–33. 18 indexed citations
7.
Cheng, Andrew, Mary Beth Dinulos, Whitney Neufeld‐Kaiser, et al.. (2017). 6q25.1 (TAB2) microdeletion syndrome: Congenital heart defects and cardiomyopathy. American Journal of Medical Genetics Part A. 173(7). 1848–1857. 30 indexed citations
8.
Gallego, Daniel F., Whitney Neufeld‐Kaiser, Sheila R. Weiss, et al.. (2017). Intrauterine Fetal Growth Restriction and Oligohydramnios of Undetermined Etiology. The Journal of Applied Laboratory Medicine. 1(5). 576–580.
9.
10.
Hampel, Heather, Robin E. Grubs, Stéphanie Fox, et al.. (2009). Genetic Counseling Practice Analysis. Journal of Genetic Counseling. 18(3). 205–216. 21 indexed citations
11.
Pagon, Roberta A, Peter Tarczy‐Hornoch, Thomas D. Bird, et al.. (2002). GeneTests-GeneClinics: Genetic testing information for a growing audience. Human Mutation. 19(5). 501–509. 57 indexed citations
12.
Martin, Rick A., Whitney Neufeld‐Kaiser, Pamela Flodman, et al.. (2000). Ultrasonographic detection of orbicularis oris defects in first degree relatives of isolated cleft lip patients. American Journal of Medical Genetics. 90(2). 155–161. 43 indexed citations
13.
McKinnon, Wendy, et al.. (1997). Predisposition genetic testing for late-onset disorders in adults. A position paper of the National Society of Genetic Counselors.. PubMed. 278(15). 1217–20. 86 indexed citations

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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