Linda Warwick

747 total citations
16 papers, 369 citations indexed

About

Linda Warwick is a scholar working on Genetics, Molecular Biology and Clinical Biochemistry. According to data from OpenAlex, Linda Warwick has authored 16 papers receiving a total of 369 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 6 papers in Molecular Biology and 5 papers in Clinical Biochemistry. Recurrent topics in Linda Warwick's work include BRCA gene mutations in cancer (7 papers), Metabolism and Genetic Disorders (5 papers) and Mitochondrial Function and Pathology (3 papers). Linda Warwick is often cited by papers focused on BRCA gene mutations in cancer (7 papers), Metabolism and Genetic Disorders (5 papers) and Mitochondrial Function and Pathology (3 papers). Linda Warwick collaborates with scholars based in Australia, United States and Netherlands. Linda Warwick's co-authors include Kathy Tucker, Judy Kirk, Elvira Zilliacus, Elizabeth Lobb, Bettina Meiser, Lee Coleman, Avihu Boneh, Stephen J. Wood, Peter J. Anderson and Vicki Anderson and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and British Journal of Haematology.

In The Last Decade

Linda Warwick

14 papers receiving 364 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Linda Warwick Australia 11 182 113 107 64 60 16 369
Karen Fieggen South Africa 13 125 0.7× 146 1.3× 24 0.2× 70 1.1× 50 0.8× 42 390
Loren Peña United States 11 205 1.1× 219 1.9× 261 2.4× 86 1.3× 26 0.4× 25 601
Biruté Tumiene Lithuania 13 142 0.8× 81 0.7× 20 0.2× 34 0.5× 21 0.3× 25 363
Melissa Martyn Australia 14 415 2.3× 111 1.0× 25 0.2× 89 1.4× 100 1.7× 40 647
Susan Hiraki United States 14 315 1.7× 72 0.6× 11 0.1× 61 1.0× 111 1.9× 21 532
L. F. Ross United States 3 208 1.1× 54 0.5× 20 0.2× 122 1.9× 70 1.2× 4 336
Rachel Horton United Kingdom 10 186 1.0× 90 0.8× 9 0.1× 57 0.9× 104 1.7× 31 440
K Stephens United States 7 52 0.3× 79 0.7× 15 0.1× 27 0.4× 43 0.7× 133 296
Lisette Curnow Australia 10 140 0.8× 24 0.2× 16 0.1× 77 1.2× 33 0.6× 15 338
Jennefer N. Kohler United States 8 245 1.3× 83 0.7× 7 0.1× 55 0.9× 59 1.0× 15 362

Countries citing papers authored by Linda Warwick

Since Specialization
Citations

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

Fields of papers citing papers by Linda Warwick

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Linda Warwick

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

All Works

16 of 16 papers shown
1.
Warwick, Linda, Paul Craft, Bruce Ashford, et al.. (2023). Myelodysplastic syndrome and multiple solid tumours in an individual with compound heterozygous deleterious FANCM variants: A case report and review of the literature. British Journal of Haematology. 203(3). 481–484.
2.
Taylor, Natalie, April Morrow, Sian Greening, et al.. (2020). Aligning intuition and theory: enhancing the replicability of behaviour change interventions in cancer genetics. SHILAP Revista de lepidopterología. 1(1). 90–90. 22 indexed citations
3.
Taylor, Natalie, Sian Greening, Claire E. Wakefield, et al.. (2017). Quantifying family dissemination and identifying barriers to communication of risk information in Australian BRCA families. Genetics in Medicine. 19(12). 1323–1331. 38 indexed citations
4.
Warwick, Linda, et al.. (2016). Breast and ovarian cancer referrals to the ACT Genetic Service: are we meeting guidelines?. Internal Medicine Journal. 47(3). 311–317. 5 indexed citations
5.
Warwick, Linda, et al.. (2016). A Relational Approach to Genetic Counseling for Hereditary Breast and Ovarian Cancer. Journal of Genetic Counseling. 26(2). 283–299. 15 indexed citations
6.
Whiley, Phillip J, Michael T. Parsons, Jennifer Leary, et al.. (2014). Multifactorial Likelihood Assessment of BRCA1 and BRCA2 Missense Variants Confirms That BRCA1:c.122A>G(p.His41Arg) Is a Pathogenic Mutation. PLoS ONE. 9(1). e86836–e86836. 20 indexed citations
7.
8.
9.
Zilliacus, Elvira, Bettina Meiser, Elizabeth Lobb, et al.. (2011). Are videoconferenced consultations as effective as face-to-face consultations for hereditary breast and ovarian cancer genetic counseling?. Genetics in Medicine. 13(11). 933–941. 60 indexed citations
10.
Zilliacus, Elvira, Bettina Meiser, Elizabeth Lobb, et al.. (2010). Women's Experience of Telehealth Cancer Genetic Counseling. Journal of Genetic Counseling. 19(5). 463–472. 57 indexed citations
11.
Anderson, Peter J., Stephen J. Wood, Dorothy Francis, et al.. (2004). Neuropsychological functioning in children with early-treated phenylketonuria: impact of white matter abnormalities. Developmental Medicine & Child Neurology. 46(4). 230–8. 50 indexed citations
12.
Anderson, Peter J., Stephen J. Wood, Dorothy Francis, et al.. (2004). Neuropsychological functioning in children with early‐treated phenylketonuria: impact of white matter abnormalities. Developmental Medicine & Child Neurology. 46(4). 230–238. 32 indexed citations
13.
Boneh, Avihu, et al.. (2001). Splenectomy in two siblings with G‐CSF‐dependent glycogen storage disease type Ib. Journal of Inherited Metabolic Disease. 24(3). 419–422. 1 indexed citations
14.
White, S. L., et al.. (1999). Two cases of prenatal analysis for the pathogenic T to G substitution at nucleotide 8993 in mitochondrial DNA. Prenatal Diagnosis. 19(12). 1165–1168. 2 indexed citations
15.
White, S. L., et al.. (1999). Two cases of prenatal analysis for the pathogenic T to G substitution at nucleotide 8993 in mitochondrial DNA. Prenatal Diagnosis. 19(12). 1165–1168. 38 indexed citations
16.
Pitt, James, et al.. (1997). Succinic semialdehyde dehydrogenase deficiency: low excretion of metabolites in a neonate. Journal of Inherited Metabolic Disease. 20(1). 39–42. 11 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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