Paul K. Lovelock

878 total citations
14 papers, 532 citations indexed

About

Paul K. Lovelock is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Paul K. Lovelock has authored 14 papers receiving a total of 532 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Surgery. Recurrent topics in Paul K. Lovelock's work include BRCA gene mutations in cancer (3 papers), Cystic Fibrosis Research Advances (3 papers) and RNA Research and Splicing (3 papers). Paul K. Lovelock is often cited by papers focused on BRCA gene mutations in cancer (3 papers), Cystic Fibrosis Research Advances (3 papers) and RNA Research and Splicing (3 papers). Paul K. Lovelock collaborates with scholars based in Australia, France and United States. Paul K. Lovelock's co-authors include Brandon J. Wainwright, Janine Kesting, Joanne T.E. Shaw, David L. Duffy, Stephen J. Delaney, Scott Thomson, David A. Good, Frances Busfield, Murray Hargrave and Devra P. Rich and has published in prestigious journals such as Nature Genetics, The EMBO Journal and Diabetes.

In The Last Decade

Paul K. Lovelock

14 papers receiving 523 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Paul K. Lovelock Australia	11	259	176	164	97	81	14	532
Chelsea C. Estrada United States	10	189 0.7×	90 0.5×	80 0.5×	42 0.4×	35 0.4×	15	436
D. P. S. SANDHU United Kingdom	12	156 0.6×	32 0.2×	220 1.3×	125 1.3×	64 0.8×	22	472
Sonja Vogl Austria	7	163 0.6×	95 0.5×	54 0.3×	72 0.7×	84 1.0×	11	376
Angela M. Jones United Kingdom	11	169 0.7×	86 0.5×	72 0.4×	92 0.9×	75 0.9×	14	472
Yoshitaka Akagi Japan	10	253 1.0×	86 0.5×	52 0.3×	30 0.3×	55 0.7×	15	440
Patricia N. Konrad United States	12	194 0.7×	66 0.4×	48 0.3×	36 0.4×	44 0.5×	20	610
M.R. Persey United Kingdom	6	563 2.2×	96 0.5×	39 0.2×	88 0.9×	130 1.6×	13	658
S.S. Papiha United Kingdom	14	194 0.7×	162 0.9×	45 0.3×	32 0.3×	15 0.2×	26	515
Rachel Morissette United States	9	229 0.9×	211 1.2×	88 0.5×	25 0.3×	51 0.6×	12	414
Renée S. Suen Canada	6	164 0.6×	57 0.3×	315 1.9×	27 0.3×	79 1.0×	7	544

Countries citing papers authored by Paul K. Lovelock

Since Specialization

Citations

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

Fields of papers citing papers by Paul K. Lovelock

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Paul K. Lovelock. 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 Paul K. Lovelock. The network helps show where Paul K. Lovelock may publish in the future.

Co-authorship network of co-authors of Paul K. Lovelock

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

All Works

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14 of 14 papers shown

Wronski, Ania, et al.. (2007). Colocalisation of predicted exonic splicing enhancers in BRCA2 with reported sequence variants. Breast Cancer Research and Treatment. 110(2). 227–234. 14 indexed citations

Lovelock, Paul K., Amanda B. Spurdle, Myth T.S. Mok, et al.. (2007). Identification of BRCA1 missense substitutions that confer partial functional activity: potential moderate risk variants?. Breast Cancer Research. 9(6). R82–R82. 46 indexed citations

Lose, Felicity, Paul K. Lovelock, Georgia Chenevix‐Trench, et al.. (2006). Variation in the RAD51 gene and familial breast cancer. Breast Cancer Research. 8(3). R26–R26. 26 indexed citations

Lovelock, Paul K., Ee Ming Wong, Carl N. Sprung, et al.. (2006). Prediction of BRCA1 and BRCA2 mutation status using post-irradiation assays of lymphoblastoid cell lines is compromised by inter-cell-line phenotypic variability. Breast Cancer Research and Treatment. 104(3). 257–266. 5 indexed citations

Lovelock, Paul K., et al.. (2005). Evolutionary conservation analysis increases the colocalization of predicted exonic splicing enhancers in the BRCA1gene with missense sequence changes and in-frame deletions, but not polymorphisms. Breast Cancer Research. 7(6). R929–39. 22 indexed citations

Good, David A., Frances Busfield, Paul K. Lovelock, et al.. (2004). Identification of SQSTM1 mutations in familial Paget's disease in Australian pedigrees. Bone. 35(1). 277–282. 48 indexed citations

Busfield, Frances, David L. Duffy, Janine Kesting, et al.. (2002). A Genomewide Search for Type 2 Diabetes–Susceptibility Genes in Indigenous Australians. The American Journal of Human Genetics. 70(2). 349–357. 68 indexed citations

Tate, Jillian R., Michael M. Hoffmann, Paul K. Lovelock, Janine Kesting, & Joanne T.E. Shaw. (2001). Identification of an apolipoprotein(e) variant associated with type III hyperlipoproteinaemia in an indigenous Australian. Annals of Clinical Biochemistry International Journal of Laboratory Medicine. 38(1). 46–53. 6 indexed citations

Good, David A., Frances Busfield, David L. Duffy, et al.. (2001). Familial Paget's Disease of Bone: Nonlinkage to the PDB1 and PDB2 Loci on Chromosomes 6p and 18q in a Large Pedigree. Journal of Bone and Mineral Research. 16(1). 33–38. 30 indexed citations

10.

Tate, Jill, et al.. (1999). Apolipoprotein E polymorphism in indigenous Australians: allelic frequencies and relationship with dyslipidaemia. The Medical Journal of Australia. 170(4). 161–164. 11 indexed citations

11.

Shaw, Joanne T.E., Paul K. Lovelock, Janine Kesting, et al.. (1998). Novel susceptibility gene for late-onset NIDDM is localized to human chromosome 12q.. Diabetes. 47(11). 1793–1796. 61 indexed citations

12.

Delaney, Stephen J., Eric W.F.W. Alton, S.N. Smith, et al.. (1996). Cystic fibrosis mice carrying the missense mutation G551D replicate human genotype-phenotype correlations.. The EMBO Journal. 15(5). 955–963. 96 indexed citations

13.

Delaney, Stephen J., Peter Koopman, Paul K. Lovelock, & Brandon J. Wainwright. (1994). Alternative Splicing of the First Nucleotide Binding Fold of CFTR in Mouse Testes Is Associated with Specific Stages of Spermatogenesis. Genomics. 20(3). 517–518. 10 indexed citations

14.

Delaney, Stephen J., Devra P. Rich, Scott Thomson, et al.. (1993). Cystic fibrosis transmembrane conductance regulator splice variants are not conserved and fail to produce chloride channels. Nature Genetics. 4(4). 426–430. 89 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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