Jacqueline Woolf

470 total citations
8 papers, 264 citations indexed

About

Jacqueline Woolf is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Jacqueline Woolf has authored 8 papers receiving a total of 264 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Pulmonary and Respiratory Medicine and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Jacqueline Woolf's work include Porphyrin Metabolism and Disorders (8 papers), Heme Oxygenase-1 and Carbon Monoxide (5 papers) and Methemoglobinemia and Tumor Lysis Syndrome (4 papers). Jacqueline Woolf is often cited by papers focused on Porphyrin Metabolism and Disorders (8 papers), Heme Oxygenase-1 and Carbon Monoxide (5 papers) and Methemoglobinemia and Tumor Lysis Syndrome (4 papers). Jacqueline Woolf collaborates with scholars based in United Kingdom, France and Switzerland. Jacqueline Woolf's co-authors include Sharon D. Whatley, George H. Elder, Michael N. Badminton, Robert G. Newcombe, A.Y. Finlay, Hervé Puy, Jean‐Charles Deybach, Stuart J. Smyth, X. Schneider‐Yin and Cécile Ged and has published in prestigious journals such as The American Journal of Human Genetics, Clinical Chemistry and British Journal of Dermatology.

In The Last Decade

Jacqueline Woolf

7 papers receiving 256 citations

Peers

Jacqueline Woolf

MB

PPCH

PRM

RHEUM

CB

Doreen Meissner South Africa

X. Schneider‐Yin Switzerland

Amelie T. van der Ven Germany

Aisha Al Shamsi United Arab Emirates

Athanasia Stoupa France

Gianluca Spena Italy

Sabrina Bausenwein Germany

Regan Klatt Canada

Michelle Steinraths Canada

Clara Yujing Cheong Singapore

Doreen Meissner South Africa

Jacqueline Woolf

285 ×1.2

MB

87 ×0.9

PPCH

67 ×0.9

PRM

84 ×1.3

RHEUM

27 ×2.7

CB

Citations per year, relative to Jacqueline Woolf Jacqueline Woolf (= 1×) peers Doreen Meissner

Countries citing papers authored by Jacqueline Woolf

Since Specialization

Citations

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

Fields of papers citing papers by Jacqueline Woolf

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jacqueline Woolf

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

All Works

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8 of 8 papers shown

1.

Woolf, Jacqueline, Joanne Marsden, Sharon D. Whatley, et al.. (2016). Best practice guidelines on first-line laboratory testing for porphyria. Annals of Clinical Biochemistry International Journal of Laboratory Medicine. 54(2). 188–198. 34 indexed citations

2.

Katugampola, Ruwani, Michael N. Badminton, A.Y. Finlay, et al.. (2012). Congenital erythropoietic porphyria: a single-observer clinical study of 29 cases. British Journal of Dermatology. 167(4). 901–913. 47 indexed citations

3.

Anstey, A., A.Y. Finlay, Sharon D. Whatley, et al.. (2012). A management algorithm for congenital erythropoietic porphyria derived from a study of 29 cases. British Journal of Dermatology. 167(4). 888–900. 37 indexed citations

4.

Gucev, Zoran, et al.. (2011). Congenital erythropoietic porphyria with two mutations of the uroporphyrinogen III synthase gene (Cys73Arg, Thr228Met). Indian journal of human genetics. 17(2). 104–104.

5.

Huxley, J.N., et al.. (2009). Congenital erythropoietic porphyria in a longhorn calf. Veterinary Record. 165(23). 694–695. 5 indexed citations

6.

Whatley, Sharon D., et al.. (2009). Diagnostic Strategies for Autosomal Dominant Acute Porphyrias: Retrospective Analysis of 467 Unrelated Patients Referred for Mutational Analysis of the HMBS, CPOX, or PPOX Gene. Clinical Chemistry. 55(7). 1406–1414. 61 indexed citations

7.

Lamoril, J., Hervé Puy, Sharon D. Whatley, et al.. (2001). Characterization of Mutations in the CPO Gene in British Patients Demonstrates Absence of Genotype-Phenotype Correlation and Identifies Relationship between Hereditary Coproporphyria and Harderoporphyria. The American Journal of Human Genetics. 68(5). 1130–1138. 38 indexed citations

8.

Long, Calista, Stuart J. Smyth, Jacqueline Woolf, et al.. (1993). Detection of latent variegate porphyria by fluorescence emission spectroscopy of plasma. British Journal of Dermatology. 129(1). 9–13. 42 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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