Luanne Wainwright

2.1k total citations · 1 hit paper
15 papers, 1.6k citations indexed

About

Luanne Wainwright is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, Luanne Wainwright has authored 15 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 7 papers in Pathology and Forensic Medicine and 4 papers in Genetics. Recurrent topics in Luanne Wainwright's work include Chromatin Remodeling and Cancer (9 papers), Cancer Mechanisms and Therapy (6 papers) and Cancer Genomics and Diagnostics (3 papers). Luanne Wainwright is often cited by papers focused on Chromatin Remodeling and Cancer (9 papers), Cancer Mechanisms and Therapy (6 papers) and Cancer Genomics and Diagnostics (3 papers). Luanne Wainwright collaborates with scholars based in United States and Canada. Luanne Wainwright's co-authors include Jaclyn A. Biegel, Lucy B. Rorke, Benjamin Fogelgren, Junying Zhou, Laura Tooke, Lu Tan, Alexander R. Judkins, Pierre Russo, Fan Zhang and Alan W. Flake and has published in prestigious journals such as Molecular Therapy, Human Pathology and Human Genetics.

In The Last Decade

Luanne Wainwright

14 papers receiving 1.5k citations

Hit Papers

Germ-line and acquired mutations of INI1 in atypical tera... 1999 2026 2008 2017 1999 200 400 600
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Germ-line and acquired mutations of INI1 in atypical teratoid and rhabdoid tumors.
    1999 629 citations Jaclyn A. Biegel, Junying Zhou et al. PubMed profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Luanne Wainwright United States 12 1.3k 812 240 199 194 15 1.6k
Florian Oyen Germany 20 708 0.5× 484 0.6× 130 0.5× 85 0.4× 112 0.6× 52 1.4k
Blanca Sánchez‐González Spain 20 721 0.5× 381 0.5× 161 0.7× 93 0.5× 101 0.5× 70 1.5k
Y Hayashi Japan 26 926 0.7× 187 0.2× 406 1.7× 237 1.2× 754 3.9× 47 2.3k
Chrystelle Colas France 23 577 0.4× 1.1k 1.4× 130 0.5× 203 1.0× 38 0.2× 72 1.7k
Michael Neat United Kingdom 18 493 0.4× 298 0.4× 50 0.2× 104 0.5× 188 1.0× 38 1.1k
Markus Kreuz Germany 19 392 0.3× 601 0.7× 134 0.6× 95 0.5× 62 0.3× 50 1.0k
Mitchell A. Bitter United States 14 301 0.2× 398 0.5× 117 0.5× 139 0.7× 186 1.0× 23 1.1k
Pierre Heimann Belgium 16 543 0.4× 180 0.2× 223 0.9× 224 1.1× 27 0.1× 49 1.2k
Diane L. Pickering United States 16 271 0.2× 490 0.6× 123 0.5× 308 1.5× 37 0.2× 29 1.3k
Raoul Hinze Germany 21 579 0.4× 183 0.2× 225 0.9× 263 1.3× 35 0.2× 58 2.0k

Countries citing papers authored by Luanne Wainwright

Since Specialization
Citations

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

Fields of papers citing papers by Luanne Wainwright

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luanne Wainwright

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

All Works

15 of 15 papers shown
1.
2.
Zhong, Yiming, Fumin Lin, Feng Xu, et al.. (2020). Genomic characterization of a PPP1CB-ALK fusion with fusion gene amplification in a congenital glioblastoma. Cancer Genetics. 252-253. 37–42. 5 indexed citations
3.
4.
Dougherty, Margaret, Laura Tooke, Lisa Sullivan, et al.. (2012). Clinical utilization of high-resolution single nucleotide polymorphism based oligonucleotide arrays in diagnostic studies of pediatric patients with solid tumors. Cancer Genetics. 205(1-2). 42–54. 15 indexed citations
5.
Tooke, Laura, et al.. (2010). Spectrum of SMARCB1/INI1 mutations in familial and sporadic rhabdoid tumors. Pediatric Blood & Cancer. 56(1). 7–15. 246 indexed citations
6.
Biegel, Jaclyn A., Cheryl M. Coffin, Frederic G. Barr, et al.. (2008). ALK Expression in Rhabdomyosarcomas: Correlation with Histologic Subtype and Fusion Status. Pediatric and Developmental Pathology. 12(4). 275–283. 50 indexed citations
7.
Jackson, Eric M., Tamim H. Shaikh, Fan Zhang, et al.. (2007). Atypical teratoid/rhabdoid tumor in a patient with Beckwith–Wiedemann syndrome. American Journal of Medical Genetics Part A. 143A(15). 1767–1770. 5 indexed citations
8.
Donner, Ludvik R., Luanne Wainwright, Fan Zhang, & Jaclyn A. Biegel. (2007). Mutation of the INI1 gene in composite rhabdoid tumor of the endometrium. Human Pathology. 38(6). 935–939. 31 indexed citations
9.
Jackson, Eric M., Tamim H. Shaikh, Sridharan Gururangan, et al.. (2007). High-density single nucleotide polymorphism array analysis in patients with germline deletions of 22q11.2 and malignant rhabdoid tumor. Human Genetics. 122(2). 117–127. 44 indexed citations
10.
Zhang, Fan, Lu Tan, Luanne Wainwright, Marisa S. Bartolomei, & Jaclyn A. Biegel. (2002). No evidence for hypermethylation of the hSNF5/INI1 promoter in pediatric rhabdoid tumors. Genes Chromosomes and Cancer. 34(4). 398–405. 23 indexed citations
11.
Biegel, Jaclyn A., Lu Tan, Fan Zhang, et al.. (2002). Alterations of the hSNF5/INI1 gene in central nervous system atypical teratoid/rhabdoid tumors and renal and extrarenal rhabdoid tumors.. PubMed. 8(11). 3461–7. 275 indexed citations
12.
Arruda, Valder R., Paul Fields, Ross Milner, et al.. (2001). Lack of Germline Transmission of Vector Sequences Following Systemic Administration of Recombinant AAV-2 Vector in Males. Molecular Therapy. 4(6). 586–592. 124 indexed citations
13.
Biegel, Jaclyn A., et al.. (2000). GermlineINI1 mutation in a patient with a central nervous system atypical teratoid tumor and renal rhabdoid tumor. Genes Chromosomes and Cancer. 28(1). 31–37. 84 indexed citations
14.
Biegel, Jaclyn A., et al.. (1999). Germ-line and acquired mutations of INI1 in atypical teratoid and rhabdoid tumors.. PubMed. 59(1). 74–9. 629 indexed citations breakdown →
15.
Wainwright, Luanne, et al.. (1998). Establishment and molecular characterization of five cell lines derived from renal and extrarenal malignant rhabdoid tumors.. PubMed. 11(12). 1228–37. 14 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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