Craig Luccarini

12.7k total citations
23 papers, 948 citations indexed

About

Craig Luccarini is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Craig Luccarini has authored 23 papers receiving a total of 948 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 9 papers in Molecular Biology and 4 papers in Cancer Research. Recurrent topics in Craig Luccarini's work include BRCA gene mutations in cancer (11 papers), Genetic Associations and Epidemiology (5 papers) and Cancer Genomics and Diagnostics (4 papers). Craig Luccarini is often cited by papers focused on BRCA gene mutations in cancer (11 papers), Genetic Associations and Epidemiology (5 papers) and Cancer Genomics and Diagnostics (4 papers). Craig Luccarini collaborates with scholars based in United Kingdom, United States and Singapore. Craig Luccarini's co-authors include Alison M. Dunning, Paul D.P. Pharoah, Douglas F. Easton, Caroline Baynes, Robert Luben, Carlos Caldas, Jean Abraham, Helena Earl, Mel Maranian and Susan Ingle and has published in prestigious journals such as Journal of Molecular Biology, The Journal of Clinical Endocrinology & Metabolism and Cancer Research.

In The Last Decade

Craig Luccarini

23 papers receiving 929 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Craig Luccarini United Kingdom	13	435	296	225	167	164	23	948
Bo Lin China	14	215 0.5×	258 0.9×	264 1.2×	219 1.3×	144 0.9×	36	753
Teresa Ramón y Cajal Spain	19	360 0.8×	434 1.5×	357 1.6×	54 0.3×	243 1.5×	59	956
L. Demers United States	12	283 0.7×	208 0.7×	504 2.2×	162 1.0×	132 0.8×	18	1.0k
Ritva Valavaara Finland	14	126 0.3×	406 1.4×	293 1.3×	121 0.7×	223 1.4×	29	900
Joanna Sawicka United States	15	135 0.3×	219 0.7×	282 1.3×	267 1.6×	138 0.8×	23	899
Ricardo Chirino Spain	16	183 0.4×	210 0.7×	103 0.5×	203 1.2×	98 0.6×	36	587
M. De Jong‐Bakker Netherlands	12	376 0.9×	260 0.9×	591 2.6×	245 1.5×	206 1.3×	18	1.0k
S. Fleming United Kingdom	22	687 1.6×	219 0.7×	107 0.5×	45 0.3×	166 1.0×	59	1.3k
Patricia A. Smanik United States	12	437 1.0×	205 0.7×	130 0.6×	640 3.8×	73 0.4×	16	1.2k
W. Mark Brown United States	21	345 0.8×	347 1.2×	97 0.4×	92 0.6×	84 0.5×	49	1.3k

Countries citing papers authored by Craig Luccarini

Since Specialization

Citations

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

Fields of papers citing papers by Craig Luccarini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Craig Luccarini

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

All Works

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20 of 20 papers shown

Li, Shuai, Robert J. MacInnis, Andrew Lee, et al.. (2022). Segregation analysis of 17,425 population-based breast cancer families: Evidence for genetic susceptibility and risk prediction. The American Journal of Human Genetics. 109(10). 1777–1788. 8 indexed citations

Li, Jingmei, Wei Wen, Brennan Decker, et al.. (2018). Differential Burden of Rare and Common Variants on Tumor Characteristics, Survival, and Mode of Detection in Breast Cancer. Cancer Research. 78(21). 6329–6338. 16 indexed citations

Eccles, Diana, Tom Maishman, William Tapper, et al.. (2017). Abstract S2-03: Does BRCA status affect outcome in young breast cancer patients? Results from the prospective study of outcomes in sporadic and hereditary breast cancer (POSH). Cancer Research. 77(4_Supplement). S2–3. 3 indexed citations

Decker, Brennan, Jamie Allen, Craig Luccarini, et al.. (2016). Abstract 4309: Rare protein truncating and missense variants in ATM, CHEK2, PALB2, but not XRCC2, confer increased breast cancer risks. Cancer Research. 76(14_Supplement). 4309–4309. 2 indexed citations

Abraham, Jean, Mel Maranian, Inmaculada Spiteri, et al.. (2012). Saliva samples are a viable alternative to blood samples as a source of DNA for high throughput genotyping. BMC Medical Genomics. 5(1). 19–19. 120 indexed citations

Scollen, Serena, Craig Luccarini, Caroline Baynes, et al.. (2011). TGF-β Signaling Pathway and Breast Cancer Susceptibility. Cancer Epidemiology Biomarkers & Prevention. 20(6). 1112–1119. 47 indexed citations

Barnett, Gillian C., Charlotte E. Coles, Rebecca Elliott, et al.. (2011). Independent validation of genes and polymorphisms reported to be associated with radiation toxicity: a prospective analysis study. The Lancet Oncology. 13(1). 65–77. 160 indexed citations

Abraham, Jean, Mel Maranian, Kristy Driver, et al.. (2011). CYP2D6 Gene Variants and Their Association with Breast Cancer Susceptibility. Cancer Epidemiology Biomarkers & Prevention. 20(6). 1255–1258. 9 indexed citations

Abraham, Jean, Mel Maranian, Kristy Driver, et al.. (2010). CYP2D6 gene variants: association with breast cancer specific survival in a cohort of breast cancer patients from the United Kingdom treated with adjuvant tamoxifen. Breast Cancer Research. 12(4). R64–R64. 70 indexed citations

10.

Field, Helen I., Serena Scollen, Craig Luccarini, et al.. (2009). Seq4SNPs: new software for retrieval of multiple, accurately annotated DNA sequences, ready formatted for SNP assay design. BMC Bioinformatics. 10(1). 180–180. 4 indexed citations

11.

Cebrián, Arancha, Paul D.P. Pharoah, Shahana Ahmed, et al.. (2006). Tagging Single-Nucleotide Polymorphisms in Antioxidant Defense Enzymes and Susceptibility to Breast Cancer. Cancer Research. 66(2). 1225–1233. 68 indexed citations

12.

Lesueur, Fabienne, Honglin Song, Shahana Ahmed, et al.. (2006). Single-nucleotide polymorphisms in the RB1 gene and association with breast cancer in the British population. British Journal of Cancer. 94(12). 1921–1926. 10 indexed citations

13.

Alzahrani, Ali, Manjinder S. Sandhu, Robert Luben, et al.. (2005). IGF1 and IGFBP3 tagging polymorphisms are associated with circulating levels of IGF1, IGFBP3 and risk of breast cancer. Human Molecular Genetics. 15(1). 1–10. 142 indexed citations

14.

Benusiglio, Patrick R., Fabienne Lesueur, Craig Luccarini, et al.. (2005). Common ERBB2 polymorphisms and risk of breast cancer in a white British population: a case–control study. Breast Cancer Research. 7(2). R204–9. 49 indexed citations

15.

Benusiglio, Patrick R., Fabienne Lesueur, Craig Luccarini, et al.. (2005). Common variation in EMSYand risk of breast and ovarian cancer: a case-control study using HapMap tagging SNPs. BMC Cancer. 5(1). 81–81. 14 indexed citations

16.

Cebrián, Arancha, Fabienne Lesueur, Sam Martin, et al.. (2005). Polymorphisms in the Initiators of RET (Rearranged during Transfection) Signaling Pathway and Susceptibility to Sporadic Medullary Thyroid Carcinoma. The Journal of Clinical Endocrinology & Metabolism. 90(11). 6268–6274. 64 indexed citations

17.

Cebrián, Arancha, et al.. (2005). The search for low-penetrance breast cancer genes. Breast Cancer Research. 7(S2). 2 indexed citations

18.

Burrows, Nigel, A C Nicholls, Allan J. Richards, et al.. (1998). A Point Mutation in an Intronic Branch Site Results in Aberrant Splicing of COL5A1 and in Ehlers-Danlos Syndrome Type II in Two British Families. The American Journal of Human Genetics. 63(2). 390–398. 69 indexed citations

19.

Richards, Allan J., Craig Luccarini, & F M Pope. (1997). The Structural Organisation of LAMA4, the Gene Encoding Laminin αL4. European Journal of Biochemistry. 248(1). 15–23. 6 indexed citations

20.

Wright, Stephanie C. & Craig Luccarini. (1996). Effect of the Position of TAR on Transcriptional Activation by HIV-1 Tatin Vivo. Journal of Molecular Biology. 263(1). 1–7. 4 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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