Vicki Huff

7.8k total citations
85 papers, 4.5k citations indexed

About

Vicki Huff is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Vicki Huff has authored 85 papers receiving a total of 4.5k indexed citations (citations by other indexed papers that have themselves been cited), including 76 papers in Molecular Biology, 20 papers in Pulmonary and Respiratory Medicine and 15 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Vicki Huff's work include Renal and related cancers (66 papers), Renal cell carcinoma treatment (20 papers) and Ethics and Legal Issues in Pediatric Healthcare (10 papers). Vicki Huff is often cited by papers focused on Renal and related cancers (66 papers), Renal cell carcinoma treatment (20 papers) and Ethics and Legal Issues in Pediatric Healthcare (10 papers). Vicki Huff collaborates with scholars based in United States, Canada and China. Vicki Huff's co-authors include Louise C. Strong, E. Cristy Ruteshouser, Fei Gao, Paul E. Grundy, Sourindra Maiti, Grady F. Saunders, Richard R. Behringer, Rita Alam, Lian-Yu Chao and Elizabeth J. Perlman and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Vicki Huff

85 papers receiving 4.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vicki Huff United States 39 3.6k 1.3k 845 834 431 85 4.5k
Caryn Y. Ito Canada 18 2.1k 0.6× 444 0.3× 368 0.4× 274 0.3× 175 0.4× 27 2.8k
Kankatsu Yun New Zealand 25 1.5k 0.4× 317 0.2× 837 1.0× 477 0.6× 388 0.9× 68 2.7k
David Walterhouse United States 33 1.7k 0.5× 1.2k 0.9× 417 0.5× 139 0.2× 622 1.4× 91 3.2k
Hans Stoop Netherlands 44 4.2k 1.2× 879 0.7× 1.7k 2.0× 198 0.2× 3.1k 7.1× 92 6.3k
Alex Koufos United States 9 1.4k 0.4× 523 0.4× 601 0.7× 296 0.4× 143 0.3× 9 2.3k
Katharina Biermann Netherlands 41 1.7k 0.5× 1.3k 1.0× 544 0.6× 115 0.1× 2.1k 4.8× 121 4.8k
Ad Gillis Netherlands 39 3.6k 1.0× 916 0.7× 990 1.2× 147 0.2× 2.8k 6.5× 84 5.5k
Daynna J. Wolff United States 24 1.0k 0.3× 462 0.3× 1.2k 1.4× 222 0.3× 274 0.6× 80 2.8k
Roland P. Kuiper Netherlands 35 2.6k 0.7× 513 0.4× 758 0.9× 756 0.9× 275 0.6× 123 5.4k
Philip J. Fialkow United States 36 1.3k 0.4× 290 0.2× 970 1.1× 206 0.2× 186 0.4× 84 5.2k

Countries citing papers authored by Vicki Huff

Since Specialization
Citations

This map shows the geographic impact of Vicki Huff'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 Vicki Huff with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Vicki Huff more than expected).

Fields of papers citing papers by Vicki Huff

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Vicki Huff. 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 Vicki Huff. The network helps show where Vicki Huff may publish in the future.

Co-authorship network of co-authors of Vicki Huff

This figure shows the co-authorship network connecting the top 25 collaborators of Vicki Huff. A scholar is included among the top collaborators of Vicki Huff 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 Vicki Huff. Vicki Huff is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Ruteshouser, E. Cristy, et al.. (2024). Generation of a Wt1 conditional deletion, nuclear red fluorescent protein reporter allele in the mouse. Differentiation. 138. 100791–100791. 1 indexed citations
2.
Gadd, Samantha, Vicki Huff, Andrew D. Skol, et al.. (2022). Genetic changes associated with relapse in favorable histology Wilms tumor: A Children’s Oncology Group AREN03B2 study. Cell Reports Medicine. 3(6). 100644–100644. 12 indexed citations
3.
Mariottini, Chiara, Leonardo Munari, Nikos Tzavaras, et al.. (2019). Wilm’s tumor 1 promotes memory flexibility. Nature Communications. 10(1). 3756–3756. 18 indexed citations
4.
Armstrong, Amy E., Samantha Gadd, Vicki Huff, et al.. (2018). A unique subset of low-risk Wilms tumors is characterized by loss of function of TRIM28 (KAP1), a gene critical in early renal development: A Children’s Oncology Group study. PLoS ONE. 13(12). e0208936–e0208936. 30 indexed citations
5.
Mokkapati, Sharada, Le Huang, E. Cristy Ruteshouser, et al.. (2014). β-Catenin Activation in a Novel Liver Progenitor Cell Type Is Sufficient to Cause Hepatocellular Carcinoma and Hepatoblastoma. Cancer Research. 74(16). 4515–4525. 72 indexed citations
6.
Dome, Jeffrey S. & Vicki Huff. (2013). Wilms Tumor Overview. 357(1). 89–89. 14 indexed citations
7.
Makki, Mohammad Shahidul, E. Cristy Ruteshouser, & Vicki Huff. (2013). Ubiquitin specific protease 18 (Usp18) is a WT1 transcriptional target. Experimental Cell Research. 319(5). 612–622. 20 indexed citations
8.
Gao, Fei, Jun Zhang, Xiaona Wang, et al.. (2013). Wt1 functions in ovarian follicle development by regulating granulosa cell differentiation. Human Molecular Genetics. 23(2). 333–341. 71 indexed citations
9.
Dome, Jeffrey S., Conrad V. Fernandez, Elizabeth A. Mullen, et al.. (2012). Children's Oncology Group's 2013 blueprint for research: Renal tumors. Pediatric Blood & Cancer. 60(6). 994–1000. 120 indexed citations
10.
Perlman, Elizabeth J., Paul E. Grundy, James R. Anderson, et al.. (2010). WT1 Mutation and 11P15 Loss of Heterozygosity Predict Relapse in Very Low-Risk Wilms Tumors Treated With Surgery Alone: A Children's Oncology Group Study. Journal of Clinical Oncology. 29(6). 698–703. 54 indexed citations
11.
Shamberger, Robert C., James R. Anderson, Norman E. Breslow, et al.. (2010). Long-term Outcomes for Infants With Very Low Risk Wilms Tumor Treated With Surgery Alone in National Wilms Tumor Study-5. Annals of Surgery. 251(3). 555–558. 50 indexed citations
12.
Hu, Qianghua, Fei Gao, Weihua Tian, et al.. (2010). Wt1 ablation and Igf2 upregulation in mice result in Wilms tumors with elevated ERK1/2 phosphorylation. Journal of Clinical Investigation. 121(1). 174–183. 86 indexed citations
13.
Vicent, Silvestre, Chen Ron, Leanne C. Sayles, et al.. (2010). Wilms tumor 1 (WT1) regulates KRAS-driven oncogenesis and senescence in mouse and human models. Journal of Clinical Investigation. 120(11). 3940–3952. 101 indexed citations
14.
Drake, Kylie M., E. Cristy Ruteshouser, Rachael Natrajan, et al.. (2009). Loss of Heterozygosity at 2q37 in Sporadic Wilms' Tumor: Putative Role for miR-562. Clinical Cancer Research. 15(19). 5985–5992. 51 indexed citations
15.
Huff, Vicki. (2007). Wilms Tumor Genetics: A New, UnX-pected Twist to the Story. Cancer Cell. 11(2). 105–107. 7 indexed citations
16.
Gao, Fei, Sourindra Maiti, Nargis A. Alam, et al.. (2006). The Wilms tumor gene, Wt1 , is required for Sox9 expression and maintenance of tubular architecture in the developing testis. Proceedings of the National Academy of Sciences. 103(32). 11987–11992. 185 indexed citations
17.
Chao, Lian-Yu, Vicki Huff, Louise C. Strong, & Grady F. Saunders. (2000). Mutation in thePAX6 gene in twenty patients with aniridia. Human Mutation. 15(4). 332–339. 41 indexed citations
18.
El‐Naggar, Adel K., Syeling Lai, Gary L. Clayman, et al.. (1999). Frequent loss of imprinting at the IGF2 and H19 genes in head and neck squamous carcinoma. Oncogene. 18(50). 7063–7069. 41 indexed citations
19.
Huff, Vicki. (1998). Wilms tumor genetics. American Journal of Medical Genetics. 79(4). 260–267. 122 indexed citations
20.
Huff, Vicki, et al.. (1987). AnEcoRl polymorphism associated with a human genomic clone from band 11p13. Nucleic Acids Research. 15(18). 7651–7651. 8 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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