Liza L. Cox

1.1k total citations
12 papers, 484 citations indexed

About

Liza L. Cox is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Liza L. Cox has authored 12 papers receiving a total of 484 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 2 papers in Surgery. Recurrent topics in Liza L. Cox's work include Ocular Disorders and Treatments (3 papers), Genetic and rare skin diseases. (2 papers) and melanin and skin pigmentation (2 papers). Liza L. Cox is often cited by papers focused on Ocular Disorders and Treatments (3 papers), Genetic and rare skin diseases. (2 papers) and melanin and skin pigmentation (2 papers). Liza L. Cox collaborates with scholars based in Australia, United States and Italy. Liza L. Cox's co-authors include Timothy C. Cox, Andrea Ballabio, Loris Bernard, Marinella Gebbia, Christine Petit, Leslie J. Sheffield, Jacqueline Levilliers, Giancarlo Parenti, Brunella Franco and P Maroteaux and has published in prestigious journals such as Cell, Development and Developmental Biology.

In The Last Decade

Liza L. Cox

12 papers receiving 478 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Liza L. Cox Australia	10	292	198	56	48	34	12	484
Hirofumi Kodera Japan	9	277 0.9×	123 0.6×	57 1.0×	42 0.9×	24 0.7×	12	381
Sika Ristevski Australia	11	359 1.2×	135 0.7×	44 0.8×	31 0.6×	25 0.7×	15	541
Barry L. Barnoski United States	10	422 1.4×	132 0.7×	27 0.5×	26 0.5×	23 0.7×	16	568
Gandham SriLakshmi Bhavani India	13	277 0.9×	304 1.5×	61 1.1×	61 1.3×	47 1.4×	45	542
W. J. Craigen United States	15	635 2.2×	160 0.8×	47 0.8×	17 0.4×	35 1.0×	17	782
M. Lutz Germany	10	475 1.6×	185 0.9×	19 0.3×	38 0.8×	21 0.6×	10	542
Mika Kikkawa Japan	13	284 1.0×	102 0.5×	184 3.3×	54 1.1×	45 1.3×	22	620
Fumio Takada Japan	12	406 1.4×	151 0.8×	38 0.7×	41 0.9×	34 1.0×	33	624
M. Rivière Belgium	15	588 2.0×	238 1.2×	33 0.6×	51 1.1×	19 0.6×	42	775
Michelle M. Thiaville United States	11	422 1.4×	93 0.5×	45 0.8×	137 2.9×	30 0.9×	14	534

Countries citing papers authored by Liza L. Cox

Since Specialization

Citations

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

Fields of papers citing papers by Liza L. Cox

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Liza L. Cox. 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 Liza L. Cox. The network helps show where Liza L. Cox may publish in the future.

Co-authorship network of co-authors of Liza L. Cox

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

All Works

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12 of 12 papers shown

Chu, Emily Y., et al.. (2017). Disrupted IRF6-NME1/2 Complexes as a Cause of Cleft Lip/Palate. Journal of Dental Research. 96(11). 1330–1338. 19 indexed citations

Rosin, Jessica M., Wenjie Li, Liza L. Cox, et al.. (2016). A distal 594bp ECR specifies Hmx1 expression in pinna and lateral facial morphogenesis and is regulated by Hox-Pbx-Meis. Development. 143(14). 2582–92. 10 indexed citations

Hadsell, Darryl L., Monique Rijnkels, Chad J. Creighton, et al.. (2014). In-silico QTL mapping of postpubertal mammary ductal development in the mouse uncovers potential human breast cancer risk loci. Mammalian Genome. 26(1-2). 57–79. 13 indexed citations

Siebert, Joseph R., Kenneth J. Smith, Liza L. Cox, Ian A. Glass, & Timothy C. Cox. (2013). Microtomographic Analysis of Lower Urinary Tract Obstruction. Pediatric and Developmental Pathology. 16(6). 405–414. 7 indexed citations

Rolfe, Sara, Linda G. Shapiro, Timothy C. Cox, A. Murat Maga, & Liza L. Cox. (2011). A landmark-free framework for the detection and description of shape differences in embryos. PubMed. 2011. 5153–5156. 6 indexed citations

Ashe, Alyson, Nadia Whitelaw, Timothy J. C. Bruxner, et al.. (2008). A genome-wide screen for modifiers of transgene variegation identifies genes with critical roles in development. Genome biology. 9(12). R182–R182. 82 indexed citations

Cox, Timothy C., Timothy Sadlon, Quenten Schwarz, et al.. (2003). The major splice variant of human 5-aminolevulinate synthase-2 contributes significantly to erythroid heme biosynthesis. The International Journal of Biochemistry & Cell Biology. 36(2). 281–295. 20 indexed citations

Richman, Joy M., et al.. (2002). Isolation and characterisation of the chick orthologue of the Opitz syndrome gene, Mid1, supports a conserved role in vertebrate development. The International Journal of Developmental Biology. 46(4). 441–448. 20 indexed citations

Kayserili, Hülya, Timothy C. Cox, Liza L. Cox, et al.. (2001). Molecular characterisation of a new case of microphthalmia with linear skin defects (MLS). Journal of Medical Genetics. 38(6). 411–417. 15 indexed citations

10.

Hargrave, Murray, Asanka Karunaratne, Liza L. Cox, et al.. (2000). The HMG Box Transcription Factor Gene Sox14 Marks a Novel Subset of Ventral Interneurons and Is Regulated by Sonic Hedgehog. Developmental Biology. 219(1). 142–153. 50 indexed citations

11.

Cox, Timothy C., Liza L. Cox, & Andrea Ballabio. (1998). A very high density microsatellite map (1 STR / 41 kb) of 1.7 Mb on Xp22 spanning the microphthalmia with linear skin defects (MLS) syndrome critical region. European Journal of Human Genetics. 6(4). 406–412. 9 indexed citations

12.

Franco, Brunella, Germana Meroni, Giancarlo Parenti, et al.. (1995). A cluster of sulfatase genes on Xp22.3: Mutations in chondrodysplasia punctata (CDPX) and implications for warfarin embryopathy. Cell. 81(1). 15–25. 233 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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