Sue Forrest

506 total citations
12 papers, 395 citations indexed

About

Sue Forrest is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Sue Forrest has authored 12 papers receiving a total of 395 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 3 papers in Clinical Biochemistry and 3 papers in Genetics. Recurrent topics in Sue Forrest's work include Metabolism and Genetic Disorders (3 papers), DNA Repair Mechanisms (2 papers) and Mitochondrial Function and Pathology (2 papers). Sue Forrest is often cited by papers focused on Metabolism and Genetic Disorders (3 papers), DNA Repair Mechanisms (2 papers) and Mitochondrial Function and Pathology (2 papers). Sue Forrest collaborates with scholars based in Australia, United States and Germany. Sue Forrest's co-authors include Richard G.H. Cotton, D. M. Danks, Rowan G. Walker, Robert N. Gibson, Kathryn Friend, David Ravine, P Kincaid-Smith, Robert I. Richards, L. J. Sheffield and H H Dahl and has published in prestigious journals such as The Lancet, Clinical Chemistry and Neuroreport.

In The Last Decade

Sue Forrest

12 papers receiving 385 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sue Forrest Australia	9	293	172	69	66	43	12	395
Daniel R. Carvalho Brazil	11	164 0.6×	84 0.5×	92 1.3×	57 0.9×	43 1.0×	31	343
Dina Marek‐Yagel Israel	12	358 1.2×	78 0.5×	63 0.9×	29 0.4×	14 0.3×	26	507
Patricia Galvin‐Parton United States	11	192 0.7×	84 0.5×	93 1.3×	20 0.3×	45 1.0×	13	313
C R Müller Germany	12	262 0.9×	70 0.4×	132 1.9×	44 0.7×	13 0.3×	17	387
Stephanie Demuth Germany	9	270 0.9×	205 1.2×	32 0.5×	25 0.4×	54 1.3×	11	407
Silvio Ferraris Italy	12	262 0.9×	42 0.2×	198 2.9×	34 0.5×	45 1.0×	12	370
Daniel Beltrán Valero de Bernabé United States	6	469 1.6×	77 0.4×	92 1.3×	84 1.3×	25 0.6×	6	556
Dalia Ghoneim United States	10	277 0.9×	125 0.7×	28 0.4×	31 0.5×	19 0.4×	15	409
L Duprez Belgium	14	271 0.9×	190 1.1×	16 0.2×	43 0.7×	106 2.5×	16	656
Richard L. Mallonee United States	6	191 0.7×	130 0.8×	15 0.2×	9 0.1×	30 0.7×	14	375

Countries citing papers authored by Sue Forrest

Since Specialization

Citations

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

Fields of papers citing papers by Sue Forrest

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sue Forrest

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

All Works

Sort: Min cites: Since: Top N: Style:

12 of 12 papers shown

Chan, Benjamin K., Erin Bromage, Julianne H. Grose, et al.. (2021). The Use of Bacteriophages and Immunological Monitoring for the Treatment of a Case of Chronic Septicemic Cutaneous Ulcerative Disease in a Loggerhead Sea Turtle Caretta caretta. Journal of Aquatic Animal Health. 33(3). 139–154. 8 indexed citations

Bruno, Damien L., Devika Ganesamoorthy, Natalie Thorne, et al.. (2014). Use of Copy Number Deletion Polymorphisms to Assess DNA Chimerism. Clinical Chemistry. 60(8). 1105–1114. 18 indexed citations

Smith, Margaret J., R. J. M. Gardner, Melanie A. Knight, et al.. (1999). Early-onset Alzheimerʼs disease caused by a novel mutation at codon 219 of the presenilin-1 gene. Neuroreport. 10(3). 503–507. 20 indexed citations

O’Neill, Michael J., Warrick J. Brewer, David Copolov, et al.. (1999). Kallmann syndrome gene (KAL-X) is not mutated in schizophrenia. American Journal of Medical Genetics. 88(1). 34–37. 5 indexed citations

Delatycki, M. B., Melanie A. Knight, M. Koenig, et al.. (1999). G130V, a common FRDA point mutation, appears to have arisen from a common founder. Human Genetics. 105(4). 343–346. 5 indexed citations

Cotton, Richard G.H., Edward Edkins, & Sue Forrest. (1998). Mutation detection : a practical approach. Oxford University Press eBooks. 31 indexed citations

Forrest, Sue, Melanie A. Knight, Martin B. Delatycki, et al.. (1998). The correlation of clinical phenotype in Friedreich ataxia with the site of point mutations in the FRDA gene. Neurogenetics. 1(4). 253–257. 56 indexed citations

Sheffield, Leslie J., Amelia H. Osborn, Wendy Hutchison, et al.. (1998). Segregation of mutations in arylsulphatase E and correlation with the clinical presentation of chondrodysplasia punctata.. Journal of Medical Genetics. 35(12). 1004–1008. 19 indexed citations

Ramus, Susan J., Sue Forrest, David Pitt, Jennifer A. Saleeba, & Richard G.H. Cotton. (1993). Comparison of genotype and intellectual phenotype in untreated PKU patients.. Journal of Medical Genetics. 30(5). 401–405. 45 indexed citations

10.

Ravine, David, Sue Forrest, L. J. Sheffield, et al.. (1992). Phenotype and genotype heterogeneity in autosomal dominant polycystic kidney disease. The Lancet. 340(8831). 1330–1333. 135 indexed citations

11.

Dahl, Hans‐Henrik M., Wendy Hutchison, Zheng Guo, Sue Forrest, & Lise Lotte Hansen. (1991). Polymorphisms in the human X-linked pyruvate dehydrogenase E1? gene. Human Genetics. 87(1). 49–53. 10 indexed citations

12.

Howells, David W., Sue Forrest, H H Dahl, & Richard G.H. Cotton. (1990). Insertion of an extra codon for threonine is a cause of dihydropteridine reductase deficiency.. PubMed. 47(2). 279–85. 43 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.

Explore authors with similar magnitude of impact