Caitlin Edwards

1.2k total citations
7 papers, 832 citations indexed

About

Caitlin Edwards is a scholar working on Molecular Biology, Neurology and Oncology. According to data from OpenAlex, Caitlin Edwards has authored 7 papers receiving a total of 832 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 2 papers in Neurology and 2 papers in Oncology. Recurrent topics in Caitlin Edwards's work include Pancreatic and Hepatic Oncology Research (2 papers), Neuroendocrine Tumor Research Advances (2 papers) and Myasthenia Gravis and Thymoma (1 paper). Caitlin Edwards is often cited by papers focused on Pancreatic and Hepatic Oncology Research (2 papers), Neuroendocrine Tumor Research Advances (2 papers) and Myasthenia Gravis and Thymoma (1 paper). Caitlin Edwards collaborates with scholars based in Australia, United Kingdom and United States. Caitlin Edwards's co-authors include Rajesh V. Thakker, G. M. Besser, Julian R. Sampson, JP Monson, C Wooding, S. A. Forbes, A. A. J. Pannett, J. H. Duncan Bassett, Paul T. Christie and Malcolm H. Wheeler and has published in prestigious journals such as The American Journal of Human Genetics, Epilepsia and QJM.

In The Last Decade

Caitlin Edwards

7 papers receiving 805 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Caitlin Edwards Australia	6	557	419	391	218	120	7	832
J T Pang United Kingdom	8	386 0.7×	309 0.7×	290 0.7×	85 0.4×	207 1.7×	15	648
Manuela Albertelli Italy	19	567 1.0×	340 0.8×	478 1.2×	245 1.1×	147 1.2×	66	935
Gerard Walls United Kingdom	14	896 1.6×	595 1.4×	615 1.6×	344 1.6×	219 1.8×	21	1.5k
John V. Verner United States	10	460 0.8×	160 0.4×	292 0.7×	135 0.6×	152 1.3×	17	901
Guido Somers Belgium	13	359 0.6×	226 0.5×	253 0.6×	303 1.4×	358 3.0×	39	968
Mara Boschetti Italy	18	276 0.5×	135 0.3×	153 0.4×	487 2.2×	116 1.0×	56	884
Jijun Shi China	17	301 0.5×	211 0.5×	93 0.2×	27 0.1×	166 1.4×	40	690
Mehtap Çakır Türkiye	14	168 0.3×	81 0.2×	126 0.3×	278 1.3×	141 1.2×	34	633
Kiyoyuki Takahashi Japan	12	298 0.5×	146 0.3×	216 0.6×	82 0.4×	113 0.9×	22	512
Paola Razzore Italy	14	141 0.3×	68 0.2×	50 0.1×	566 2.6×	89 0.7×	22	689

Countries citing papers authored by Caitlin Edwards

Since Specialization

Citations

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

Fields of papers citing papers by Caitlin Edwards

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Caitlin Edwards

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

All Works

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7 of 7 papers shown

1.

Goldblatt, Jack, et al.. (2011). Further evidence for a marfanoid syndrome with neonatal progeroid features and severe generalized lipodystrophy due to frameshift mutations near the 3′ end of the FBN1 gene. American Journal of Medical Genetics Part A. 155(4). 717–720. 30 indexed citations

2.

Phillips, Marianne, et al.. (2011). Perilobar Nephrogenic Rests and Chromosome 22. Pediatric and Developmental Pathology. 14(6). 485–492. 3 indexed citations

3.

Heron, Sarah E., Marta Hernández, Caitlin Edwards, et al.. (2009). Neonatal seizures and long QT Syndrome: A cardiocerebral channelopathy?. Epilepsia. 51(2). 293–296. 56 indexed citations

4.

Bassett, J. H. Duncan, S. A. Forbes, A. A. J. Pannett, et al.. (1998). Characterization of Mutations in Patients with Multiple Endocrine Neoplasia Type 1. The American Journal of Human Genetics. 62(2). 232–244. 295 indexed citations

5.

Trump, Dorothy, Bernadette Farren, C Wooding, et al.. (1996). Clinical studies of multiple endocrine neoplasia type 1 (MEN1). QJM. 89(9). 653–670. 330 indexed citations

6.

Notghi, A., et al.. (1988). 131-I radioiodine therapy for hyperthyroidism in patients with Graves' disease, uninodular goitre and multinodular goitre.. PubMed. 101(858). 784–6. 10 indexed citations

7.

Jeffcoate, William, Lesley Rees, Susan Tomlin, et al.. (1977). Metyrapone in long-term management of Cushing's disease.. BMJ. 2(6081). 215–217. 108 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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