Jennifer A. Donald

3.5k total citations
66 papers, 2.0k citations indexed

About

Jennifer A. Donald is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, Jennifer A. Donald has authored 66 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Genetics, 26 papers in Molecular Biology and 9 papers in Immunology. Recurrent topics in Jennifer A. Donald's work include Genetic Associations and Epidemiology (15 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Genomic variations and chromosomal abnormalities (9 papers). Jennifer A. Donald is often cited by papers focused on Genetic Associations and Epidemiology (15 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Genomic variations and chromosomal abnormalities (9 papers). Jennifer A. Donald collaborates with scholars based in Australia, United Kingdom and United States. Jennifer A. Donald's co-authors include Philip B. Mitchell, Peter R. Schofield, Anna Scimone, Deborah L. Couldwell, Gwendolyn L. Gilbert, Neisha Jeoffreys, Kaitlin A. Tagg, Renee F. Badenhop, M. J. Moses and Janice M. Fullerton and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Nature Genetics.

In The Last Decade

Jennifer A. Donald

66 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jennifer A. Donald Australia 26 898 687 259 212 172 66 2.0k
Andrew Campbell Australia 20 918 1.0× 423 0.6× 206 0.8× 176 0.8× 123 0.7× 36 2.2k
Banu Anlar Türkiye 28 546 0.6× 181 0.3× 187 0.7× 187 0.9× 172 1.0× 202 2.9k
Venita Jay Canada 31 842 0.9× 350 0.5× 652 2.5× 264 1.2× 176 1.0× 154 3.0k
G Ponsot France 36 1.5k 1.6× 458 0.7× 723 2.8× 132 0.6× 131 0.8× 147 3.8k
Françoise Goutières France 32 1.4k 1.6× 579 0.8× 488 1.9× 107 0.5× 124 0.7× 76 3.2k
Paolo Balestri Italy 30 944 1.1× 835 1.2× 811 3.1× 137 0.6× 117 0.7× 109 2.8k
Jan Wahlström Sweden 38 1.3k 1.5× 1.1k 1.6× 155 0.6× 317 1.5× 307 1.8× 136 4.3k
Moshe Frydman Israel 37 2.4k 2.6× 1.4k 2.0× 70 0.3× 310 1.5× 171 1.0× 132 4.6k
Donald R. Johns United States 31 2.2k 2.5× 334 0.5× 124 0.5× 165 0.8× 86 0.5× 57 3.8k
Dorit Lev Israel 39 2.0k 2.2× 1.0k 1.5× 387 1.5× 334 1.6× 174 1.0× 188 4.9k

Countries citing papers authored by Jennifer A. Donald

Since Specialization
Citations

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

Fields of papers citing papers by Jennifer A. Donald

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jennifer A. Donald. 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 Jennifer A. Donald. The network helps show where Jennifer A. Donald may publish in the future.

Co-authorship network of co-authors of Jennifer A. Donald

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

All Works

20 of 20 papers shown
1.
Donald, Jennifer A.. (2012). A Review of Childhood Abuse Questionnaires and Suggested Treatment Approaches. InTech eBooks. 6 indexed citations
2.
Chiu, Christine L., Richard D. Bagnall, Jodie Ingles, et al.. (2009). Mutations in Alpha-Actinin-2 Cause Hypertrophic Cardiomyopathy. Journal of the American College of Cardiology. 55(11). 1127–1135. 138 indexed citations
3.
Fullerton, Janice M., et al.. (2009). Association between the serotonin 2A receptor gene and bipolar affective disorder in an Australian cohort. Psychiatric Genetics. 19(5). 244–252. 17 indexed citations
4.
Roscioli, Tony, Donald B. Bloch, Christopher G. Bell, et al.. (2006). Mutations in the gene encoding the PML nuclear body protein Sp110 are associated with immunodeficiency and hepatic veno-occlusive disease. Nature Genetics. 38(6). 620–622. 60 indexed citations
5.
Blair, Ian P., Renee F. Badenhop, Anna Scimone, et al.. (2005). Identification, characterization, and association analysis of novel genes from the bipolar disorder susceptibility locus on chromosome 4q35. Psychiatric Genetics. 15(3). 199–204. 2 indexed citations
6.
Blair, Ian P., Renee F. Badenhop, Anna Scimone, et al.. (2005). Association analysis of transcripts from the bipolar susceptibility locus on chromosome 4q35, exclusion of a pathogenic role for eight positional candidate genes. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 134B(1). 56–59. 3 indexed citations
7.
Cheung, Carol C., I.C.A. Martin, Kyall R. Zenger, et al.. (2004). Quantitative trait loci for steady-state platelet count in mice. Mammalian Genome. 15(10). 784–797. 15 indexed citations
8.
Cheung, Carol C., et al.. (2003). Quantitative trait loci for steady-state platelet count in mice. The American Journal of Human Genetics. 73(5). 1 indexed citations
9.
Roscioli, Tony, Peter J. Taylor, Jennifer A. Donald, et al.. (2003). The 10q24‐linked split hand/split foot syndrome (SHFM3): Narrowing of the critical region and confirmation of the clinical phenotype. American Journal of Medical Genetics Part A. 124A(2). 136–141. 12 indexed citations
10.
Donald, Jennifer A., et al.. (2002). Flow cytometry in the study of mitochondrial respiratory chain disorders. Mitochondrion. 1(5). 437–445. 8 indexed citations
11.
Blair, Ian P., Renee F. Badenhop, M. J. Moses, et al.. (2002). A transcript map encompassing a susceptibility locus for bipolar affective disorder on chromosome 4q35. Molecular Psychiatry. 7(8). 867–873. 9 indexed citations
12.
Badenhop, Renee F., M. J. Moses, Anna Scimone, et al.. (2002). A genome screen of 13 bipolar affective disorder pedigrees provides evidence for susceptibility loci on chromosome 3 as well as chromosomes 9, 13 and 19. Molecular Psychiatry. 7(8). 851–859. 52 indexed citations
13.
Ryan, Monique M., Peter Taylor, Jennifer A. Donald, et al.. (1999). A Novel Syndrome of Episodic Muscle Weakness Maps to Xp22.3. The American Journal of Human Genetics. 65(4). 1104–1113. 8 indexed citations
14.
Adams, Linda J., et al.. (1996). Nonlinkage of D6S260, a putative schizophrenia locus, to bipolar affective disorder. American Journal of Medical Genetics. 67(5). 485–487. 2 indexed citations
15.
Mitchell, Philip B., Brent Waters, Jennifer A. Donald, et al.. (1994). Exclusion of close linkage of bipolar disorder to the Gs-α subunit gene in nine Australian pedigrees. Journal of Affective Disorders. 32(3). 187–195. 29 indexed citations
16.
Donald, Jennifer A., et al.. (1992). Progression of HIV‐related disease is associated with HLA DQ and DR alleles defined by restriction fragment length polymorphisms. Tissue Antigens. 39(5). 241–247. 18 indexed citations
17.
Kefford, Richard, et al.. (1991). Hereditary melanoma in Australia variable association with dysplastic nevi and. Cancer Genetics and Cytogenetics. 51(1). 45–55. 55 indexed citations
18.
Wilton, Alan N., W. Barendse, Jennifer A. Donald, et al.. (1991). HLA‐DRB types in pre‐eclampsia and eclampsia. Tissue Antigens. 38(1). 137–141. 15 indexed citations
19.
Donald, Jennifer A., et al.. (1988). Hemoglobin F production in heterocellular hereditary persistence of fetal hemoglobin and its linkage to the ? globin gene complex. Human Genetics. 80(1). 69–74. 5 indexed citations
20.
Denton, Michael J., et al.. (1988). Analysis of linkage relationships of X-linked retinitis pigmentosa with the following Xp loci: L1.28, OTC, 754, XJ-1.1, pERT87, and C7. Human Genetics. 78(1). 60–64. 48 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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