Sarah D. Isaacs

9.7k total citations
57 papers, 2.5k citations indexed

About

Sarah D. Isaacs is a scholar working on Pulmonary and Respiratory Medicine, Genetics and Molecular Biology. According to data from OpenAlex, Sarah D. Isaacs has authored 57 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Pulmonary and Respiratory Medicine, 30 papers in Genetics and 25 papers in Molecular Biology. Recurrent topics in Sarah D. Isaacs's work include Prostate Cancer Treatment and Research (37 papers), Genetic Associations and Epidemiology (16 papers) and Prostate Cancer Diagnosis and Treatment (15 papers). Sarah D. Isaacs is often cited by papers focused on Prostate Cancer Treatment and Research (37 papers), Genetic Associations and Epidemiology (16 papers) and Prostate Cancer Diagnosis and Treatment (15 papers). Sarah D. Isaacs collaborates with scholars based in United States, Sweden and United Kingdom. Sarah D. Isaacs's co-authors include Patrick C. Walsh, William B. Isaacs, Deborah A. Meyers, Siqun L. Zheng, Jianfeng Xu, Kathleen E. Wiley, Aubrey R. Turner, John D. Carpten, Gregory A. Hawkins and Kathy E. Wiley and has published in prestigious journals such as Proceedings of the National Academy of Sciences, JNCI Journal of the National Cancer Institute and Cancer Research.

In The Last Decade

Sarah D. Isaacs

57 papers receiving 2.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sarah D. Isaacs United States 34 1.2k 1.1k 944 576 342 57 2.5k
Miguel Ángel Pujana Spain 29 297 0.2× 2.1k 1.9× 496 0.5× 556 1.0× 184 0.5× 78 3.0k
Bernard Kwabi‐Addo United States 20 525 0.4× 2.1k 1.9× 368 0.4× 522 0.9× 95 0.3× 47 2.7k
Tin Htwe Thin United States 18 475 0.4× 906 0.8× 402 0.4× 233 0.4× 103 0.3× 25 1.7k
David E. Goldgar France 37 483 0.4× 2.1k 1.9× 3.2k 3.4× 1.1k 1.9× 820 2.4× 72 4.9k
Vei Mah United States 20 390 0.3× 927 0.8× 250 0.3× 236 0.4× 84 0.2× 38 1.7k
Todd D. Shuster United States 7 969 0.8× 434 0.4× 357 0.4× 314 0.5× 43 0.1× 9 1.3k
Zsofia Kote‐Jarai United Kingdom 31 1.3k 1.0× 1.4k 1.3× 1.1k 1.2× 649 1.1× 364 1.1× 92 3.0k
Susan Minton United States 22 351 0.3× 1.4k 1.3× 348 0.4× 563 1.0× 276 0.8× 41 2.9k
Joel Skoletsky United States 10 457 0.4× 702 0.6× 227 0.2× 462 0.8× 635 1.9× 13 1.7k
Eva Tomiak Canada 22 507 0.4× 293 0.3× 206 0.2× 339 0.6× 122 0.4× 59 1.6k

Countries citing papers authored by Sarah D. Isaacs

Since Specialization
Citations

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

Fields of papers citing papers by Sarah D. Isaacs

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sarah D. Isaacs. 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 Sarah D. Isaacs. The network helps show where Sarah D. Isaacs may publish in the future.

Co-authorship network of co-authors of Sarah D. Isaacs

This figure shows the co-authorship network connecting the top 25 collaborators of Sarah D. Isaacs. A scholar is included among the top collaborators of Sarah D. Isaacs 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 Sarah D. Isaacs. Sarah D. Isaacs 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.
Lotan, Tamara L., Alba Torres, Miao Zhang, et al.. (2017). Somatic molecular subtyping of prostate tumors from HOXB13 G84E carriers. Oncotarget. 8(14). 22772–22782. 9 indexed citations
2.
Jin, Guangfu, Jielin Sun, Sarah D. Isaacs, et al.. (2011). Human polymorphisms at long non-coding RNAs (lncRNAs) and association with prostate cancer risk. Carcinogenesis. 32(11). 1655–1659. 112 indexed citations
3.
Hsu, Fang‐Chi, Jielin Sun, Fredrik Wiklund, et al.. (2009). A Novel Prostate Cancer Susceptibility Locus at 19q13. Cancer Research. 69(7). 2720–2723. 36 indexed citations
4.
Liu, Wennuan, Jishan Sun, Ge Li, et al.. (2009). Association of a Germ-Line Copy Number Variation at 2p24.3 and Risk for Aggressive Prostate Cancer. Cancer Research. 69(6). 2176–2179. 58 indexed citations
5.
Sun, Jielin, Siqun L. Zheng, Fredrik Wiklund, et al.. (2008). Sequence Variants at 22q13 Are Associated with Prostate Cancer Risk. Cancer Research. 69(1). 10–15. 79 indexed citations
6.
Sun, Jielin, Ethan M. Lange, Sarah D. Isaacs, et al.. (2008). Chromosome 8q24 risk variants in hereditary and non‐hereditary prostate cancer patients. The Prostate. 68(5). 489–497. 28 indexed citations
7.
Zheng, S. Lilly, Bao-Li Chang, Jielin Sun, et al.. (2006). Germ-Line Mutation of NKX3.1 Cosegregates with Hereditary Prostate Cancer and Alters the Homeodomain Structure and Function. Cancer Research. 66(1). 69–77. 35 indexed citations
8.
Xu, Junyan, Jurga Sauvageot, Charles M. Ewing, et al.. (2006). GermlineATBF1 mutations and prostate cancer risk. The Prostate. 66(10). 1082–1085. 18 indexed citations
9.
Brown, W. Mark, Ethan M. Lange, S. Lilly Zheng, et al.. (2004). Hereditary prostate cancer in African American families: linkage analysis using markers that map to five candidate susceptibility loci. British Journal of Cancer. 90(2). 510–514. 28 indexed citations
10.
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
11.
Zheng, Siqun L., Josyf C. Mychaleckyj, Gregory A. Hawkins, et al.. (2003). Evaluation of DLC1 as a prostate cancer susceptibility gene: mutation screen and association study. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 528(1-2). 45–53. 16 indexed citations
12.
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
13.
Chang, B., S. Lilly Zheng, Sarah D. Isaacs, et al.. (2003). Polymorphisms in the CYP1B1 gene are associated with increased risk of prostate cancer. British Journal of Cancer. 89(8). 1524–1529. 55 indexed citations
14.
Chang, Bao‐Li, Siqun L. Zheng, Sarah D. Isaacs, et al.. (2003). Polymorphisms in the CYP1A1 gene are associated with prostate cancer risk. International Journal of Cancer. 106(3). 375–378. 53 indexed citations
15.
Chang, Bao‐Li, S. Lilly Zheng, Sarah D. Isaacs, et al.. (2003). Evaluation of SRD5A2 sequence variants in susceptibility to hereditary and sporadic prostate cancer. The Prostate. 56(1). 37–44. 21 indexed citations
16.
Chang, Bao-Li, Siqun L. Zheng, Gregory A. Hawkins, et al.. (2002). Polymorphic GGC repeats in the androgen receptor gene are associated with hereditary and sporadic prostate cancer risk. Human Genetics. 110(2). 122–129. 64 indexed citations
17.
Zheng, Siqun L., Bao Chang, Dennis Faith, et al.. (2002). Sequence variants of alpha-methylacyl-CoA racemase are associated with prostate cancer risk.. PubMed. 62(22). 6485–8. 47 indexed citations
18.
Hawkins, Gregory A., Josyf C. Mychaleckyj, Siqun L. Zheng, et al.. (2002). Germline sequence variants of the LZTS1 gene are associated with prostate cancer risk. Cancer Genetics and Cytogenetics. 137(1). 1–7. 17 indexed citations
19.
Isaacs, Sarah D., et al.. (2000). Expression of p53 and p21waf1/cip1in gastric carcinoma: lack of inter-relationship or correlation with prognosis. European Journal of Surgical Oncology. 26(1). 39–43. 26 indexed citations
20.
Finucci, Joan M., et al.. (1982). Empirical Validation of Reading and Spelling Quotients. Developmental Medicine & Child Neurology. 24(s45). 733–744. 33 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Miguel Ángel Pujana Breakdown of academic impact, for papers by Bernard Kwabi‐Addo Breakdown of academic impact, for papers by Tin Htwe Thin Breakdown of academic impact, for papers by David E. Goldgar Breakdown of academic impact, for papers by Vei Mah Breakdown of academic impact, for papers by Todd D. Shuster Breakdown of academic impact, for papers by Zsofia Kote‐Jarai Breakdown of academic impact, for papers by Susan Minton Breakdown of academic impact, for papers by Joel Skoletsky Breakdown of academic impact, for papers by Eva Tomiak
Rankless by CCL
2026