Elizabeth M. Gillanders

11.9k total citations
58 papers, 2.0k citations indexed

About

Elizabeth M. Gillanders is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Elizabeth M. Gillanders has authored 58 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Genetics, 19 papers in Molecular Biology and 16 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Elizabeth M. Gillanders's work include Genetic Associations and Epidemiology (24 papers), Prostate Cancer Treatment and Research (15 papers) and BRCA gene mutations in cancer (14 papers). Elizabeth M. Gillanders is often cited by papers focused on Genetic Associations and Epidemiology (24 papers), Prostate Cancer Treatment and Research (15 papers) and BRCA gene mutations in cancer (14 papers). Elizabeth M. Gillanders collaborates with scholars based in United States, Finland and Norway. Elizabeth M. Gillanders's co-authors include Joan E. Bailey‐Wilson, Jeffrey M. Trent, Priya Duggal, Taura N. Holmes, Leah E. Mechanic, Sheri D. Schully, Diana Freas‐Lutz, Stephen B. Gruber, Lucia A. Hindorff and Teri A. Manolio and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Bioinformatics.

In The Last Decade

Elizabeth M. Gillanders

57 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elizabeth M. Gillanders United States 24 970 896 410 280 226 58 2.0k
C. Sue Richards United States 20 913 0.9× 934 1.0× 394 1.0× 386 1.4× 274 1.2× 41 2.3k
Þórunn Rafnar Iceland 20 462 0.5× 538 0.6× 182 0.4× 181 0.6× 141 0.6× 39 1.7k
Rachel Butler United Kingdom 24 652 0.7× 1.2k 1.4× 426 1.0× 374 1.3× 395 1.7× 61 2.5k
C. Sue Richards United States 22 2.1k 2.1× 1.4k 1.5× 430 1.0× 499 1.8× 420 1.9× 45 3.8k
Karen E. Heath Spain 28 1.1k 1.1× 1.3k 1.4× 232 0.6× 273 1.0× 131 0.6× 106 2.6k
Juliane Hoyer Germany 21 1.1k 1.2× 1.1k 1.2× 126 0.3× 151 0.5× 155 0.7× 43 1.9k
Anna González‐Neira Spain 28 843 0.9× 1.1k 1.2× 166 0.4× 359 1.3× 97 0.4× 80 2.2k
Vasily Ramensky Russia 15 986 1.0× 1.7k 1.8× 109 0.3× 199 0.7× 131 0.6× 39 2.5k
Lukas Habegger United States 17 840 0.9× 1.5k 1.7× 143 0.3× 538 1.9× 99 0.4× 21 2.3k
Noriko Hosoya Japan 22 435 0.4× 1.2k 1.3× 135 0.3× 271 1.0× 172 0.8× 53 2.2k

Countries citing papers authored by Elizabeth M. Gillanders

Since Specialization
Citations

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

Fields of papers citing papers by Elizabeth M. Gillanders

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Elizabeth M. Gillanders. 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 Elizabeth M. Gillanders. The network helps show where Elizabeth M. Gillanders may publish in the future.

Co-authorship network of co-authors of Elizabeth M. Gillanders

This figure shows the co-authorship network connecting the top 25 collaborators of Elizabeth M. Gillanders. A scholar is included among the top collaborators of Elizabeth M. Gillanders 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 Elizabeth M. Gillanders. Elizabeth M. Gillanders 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.
Nelson, Stefanie A., Danielle M. Carrick, Danielle Daee, Ian M. Fingerman, & Elizabeth M. Gillanders. (2024). Variation to biology: optimizing functional analysis of cancer risk variants. JNCI Journal of the National Cancer Institute. 116(12). 1882–1889. 1 indexed citations
2.
Shams‐White, Marissa, Rolando Barajas, Roxanne E. Jensen, et al.. (2021). Systems epidemiology and cancer: A review of the National Institutes of Health extramural grant portfolio 2013–2018. PLoS ONE. 16(4). e0250061–e0250061. 4 indexed citations
3.
Gallicchio, Lisa, Danielle Daee, Melissa Rotunno, et al.. (2021). Epidemiologic Research of Rare Cancers: Trends, Resources, and Challenges. Cancer Epidemiology Biomarkers & Prevention. 30(7). 1305–1311. 14 indexed citations
4.
Zhao, Yongmei, Monika Mehta, Ashley Walton, et al.. (2019). Robustness of RNA sequencing on older formalin-fixed paraffin-embedded tissue from high-grade ovarian serous adenocarcinomas. PLoS ONE. 14(5). e0216050–e0216050. 35 indexed citations
5.
Sonderman, Jennifer S., Traci N. Bethea, Cari M. Kitahara, et al.. (2016). Multiple Myeloma Mortality in Relation to Obesity Among African Americans. JNCI Journal of the National Cancer Institute. 108(10). djw120–djw120. 22 indexed citations
6.
Carrick, Danielle M., et al.. (2014). The Use of Biospecimens in Population-Based Research: A Review of the National Cancer Institute's Division of Cancer Control and Population Sciences Grant Portfolio. Biopreservation and Biobanking. 12(4). 240–245. 14 indexed citations
7.
Amos, Christopher I., Eric DeRycke, Elizabeth M. Gillanders, et al.. (2012). Abstract 78: Genetic Associations and Mechanisms in Oncology (GAME-ON): A network approach to post-GWAS research.. Cancer Epidemiology Biomarkers & Prevention. 21(11_Supplement). 78–78.
8.
Hindorff, Lucia A., Elizabeth M. Gillanders, & Teri A. Manolio. (2011). Genetic architecture of cancer and other complex diseases: lessons learned and future directions. Carcinogenesis. 32(7). 945–954. 75 indexed citations
9.
Khoury, Muin J., Steven B. Clauser, Andrew N. Freedman, et al.. (2011). Population Sciences, Translational Research, and the Opportunities and Challenges for Genomics to Reduce the Burden of Cancer in the 21st Century. Cancer Epidemiology Biomarkers & Prevention. 20(10). 2105–2114. 39 indexed citations
10.
Arason, Aðalgeir, Haukur Gunnarsson, Guðrún Jóhannesdóttir, et al.. (2010). Genome-wide search for breast cancer linkage in large Icelandic non-BRCA1/2 families. Breast Cancer Research. 12(4). R50–R50. 13 indexed citations
11.
Schully, Sheri D., et al.. (2009). Translational Research in Cancer Genetics: The Road Less Traveled. Public Health Genomics. 14(1). 1–8. 54 indexed citations
12.
Snoo, Femke A. de, Jouke‐Jan Hottenga, Elizabeth M. Gillanders, et al.. (2008). Genome-wide linkage scan for atypical nevi in p16-Leiden melanoma families. European Journal of Human Genetics. 16(9). 1135–1141. 10 indexed citations
13.
Rendtorff, Nanna Dahl, Mei Zhu, Toril Fagerheim, et al.. (2006). A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment. European Journal of Human Genetics. 14(10). 1097–1105. 54 indexed citations
14.
Duggal, Priya, Elizabeth M. Gillanders, Rasika A. Mathias, et al.. (2005). Identification of tag single-nucleotide polymorphisms in regions with varying linkage disequilibrium. BMC Genetics. 6(S1). S73–S73. 7 indexed citations
15.
Chang, Bao-Li, Elizabeth M. Gillanders, Sarah D. Isaacs, et al.. (2004). Evidence for a general cancer susceptibility locus at 3p24 in families with hereditary prostate cancer. Cancer Letters. 219(2). 177–182. 1 indexed citations
16.
Xu, Jianfeng, Carl D. Langefeld, S. Lilly Zheng, et al.. (2003). Interaction effect of PTEN and CDKN1B chromosomal regions on prostate cancer linkage. Human Genetics. -1(1). 1–1. 17 indexed citations
17.
18.
Tranebjærg, Lisbeth, Tanya M. Teslovich, MaryPat Jones, et al.. (2003). Genome-wide homozygosity mapping localizes a gene for autosomal recessive non-progressive infantile ataxia to 20q11-q13. Human Genetics. 113(3). 293–295. 13 indexed citations
19.
Wiklund, Fredrik, Elizabeth M. Gillanders, Julie Albertus, et al.. (2003). Genome‐wide scan of Swedish families with hereditary prostate cancer: Suggestive evidence of linkage at 5q11.2 and 19p13.3. The Prostate. 57(4). 290–297. 46 indexed citations
20.
Appukuttan, Binoy, Elizabeth M. Gillanders, Suh-Hang Hank Juo, et al.. (1999). Localization of a Gene for Duane Retraction Syndrome to Chromosome 2q31. The American Journal of Human Genetics. 65(6). 1639–1646. 77 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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