Zandra A. Jenkins

1.6k total citations
14 papers, 467 citations indexed

About

Zandra A. Jenkins is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Zandra A. Jenkins has authored 14 papers receiving a total of 467 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Cell Biology and 5 papers in Genetics. Recurrent topics in Zandra A. Jenkins's work include Cellular transport and secretion (4 papers), Nuclear Structure and Function (4 papers) and Genomics and Rare Diseases (3 papers). Zandra A. Jenkins is often cited by papers focused on Cellular transport and secretion (4 papers), Nuclear Structure and Function (4 papers) and Genomics and Rare Diseases (3 papers). Zandra A. Jenkins collaborates with scholars based in New Zealand, Australia and United States. Zandra A. Jenkins's co-authors include Hans E. Johansson, Petra Hååg, Stephen P. Robertson, Paul M. Clément, Myung Hee Park, Edith C. Wolff, Zeljka Smit‐McBride, John W.B. Hershey, Jacques Baudier and Adam C. O’Neill and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Journal of Clinical Endocrinology & Metabolism and Journal of Cell Science.

In The Last Decade

Zandra A. Jenkins

13 papers receiving 460 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Zandra A. Jenkins New Zealand	10	349	69	57	50	49	14	467
Julia Procter United Kingdom	8	393 1.1×	100 1.4×	35 0.6×	28 0.6×	57 1.2×	9	601
Ying Xia China	9	285 0.8×	95 1.4×	22 0.4×	16 0.3×	34 0.7×	20	434
Robert A. Policastro United States	10	284 0.8×	91 1.3×	37 0.6×	13 0.3×	11 0.2×	16	399
Dżamila M. Bogusławska Poland	10	315 0.9×	153 2.2×	25 0.4×	9 0.2×	31 0.6×	19	526
E. Natt Germany	10	314 0.9×	59 0.9×	84 1.5×	43 0.9×	19 0.4×	13	510
Karen L. Yager United States	8	351 1.0×	39 0.6×	117 2.1×	30 0.6×	29 0.6×	8	493
Michela Mazzocco Italy	10	516 1.5×	304 4.4×	44 0.8×	10 0.2×	49 1.0×	14	668
Anita M. Quintana United States	12	384 1.1×	56 0.8×	212 3.7×	9 0.2×	71 1.4×	24	665
M. Victoria Simón Argentina	10	362 1.0×	32 0.5×	14 0.2×	10 0.2×	17 0.3×	12	495
Elżbieta Heger Poland	6	215 0.6×	89 1.3×	21 0.4×	8 0.2×	23 0.5×	8	344

Countries citing papers authored by Zandra A. Jenkins

Since Specialization

Citations

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

Fields of papers citing papers by Zandra A. Jenkins

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zandra A. Jenkins

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

All Works

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14 of 14 papers shown

Morgan, Tim, Grégory Gimenez, Zandra A. Jenkins, et al.. (2024). Pathogenic FLNA variants affecting the hinge region of filamin A are associated with male survival. American Journal of Medical Genetics Part A. 194(10). e63779–e63779.

Jenkins, Zandra A., Tim Morgan, Grégory Gimenez, et al.. (2021). Exon skip‐inducing variants in FLNA in an attenuated form of frontometaphyseal dysplasia. American Journal of Medical Genetics Part A. 185(12). 3675–3682. 1 indexed citations

Jenkins, Zandra A., et al.. (2020). The X‐linked filaminopathies: Synergistic insights from clinical and molecular analysis. Human Mutation. 41(5). 865–883. 29 indexed citations

Peng, Hui, Zandra A. Jenkins, Ruby White, et al.. (2020). An Activating Variant inCTNNB1is Associated with a Sclerosing Bone Dysplasia and Adrenocortical Neoplasia. The Journal of Clinical Endocrinology & Metabolism. 105(3). 688–695. 8 indexed citations

O’Neill, Adam C., Christina Kyrousi, Richard J. Leventer, et al.. (2018). A Primate-Specific Isoform of PLEKHG6 Regulates Neurogenesis and Neuronal Migration. Cell Reports. 25(10). 2729–2741.e6. 34 indexed citations

Cameron‐Christie, Sophia, Constance Wells, Marleen Simon, et al.. (2018). Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3. The American Journal of Human Genetics. 102(6). 1115–1125. 22 indexed citations

Baudier, Jacques, Zandra A. Jenkins, & Stephen P. Robertson. (2018). The filamin-B–refilin axis – spatiotemporal regulators of the actin-cytoskeleton in development and disease. Journal of Cell Science. 131(8). 13 indexed citations

Jenkins, Zandra A., Margriet van Kogelenberg, Tim Morgan, et al.. (2017). Differential regulation of twoFLNAtranscripts explains some of the phenotypic heterogeneity in the loss-of-function filaminopathies. Human Mutation. 39(1). 103–113. 21 indexed citations

Kogelenberg, Margriet van, Alice R. Clark, Zandra A. Jenkins, et al.. (2015). Diverse phenotypic consequences of mutations affecting the C-terminus of FLNA. Journal of Molecular Medicine. 93(7). 773–782. 9 indexed citations

10.

Jenkins, Zandra A., Mary Jane Gray, Sophia Cameron‐Christie, et al.. (2013). Dysregulation of FHL1 spliceforms due to an indel mutation produces an Emery–Dreifuss muscular dystrophy plus phenotype. Neurogenetics. 14(2). 113–121. 15 indexed citations

11.

Gilquin, Benoît, Fumihiko Nakamura, Zandra A. Jenkins, et al.. (2011). RefilinB (FAM101B) targets FilaminA to organize perinuclear actin networks and regulates nuclear shape. Proceedings of the National Academy of Sciences. 108(28). 11464–11469. 65 indexed citations

12.

Jenkins, Zandra A., Ward Hagar, Christopher L. Bowlus, et al.. (2007). IRON HOMEOSTASIS DURING TRANSFUSIONAL IRON OVERLOAD IN β-THALASSEMIA AND SICKLE CELL DISEASE: Changes in Iron Regulatory Protein, Hepcidin, and Ferritin Expression. Pediatric Hematology and Oncology. 24(4). 237–243. 30 indexed citations

13.

Clément, Paul M., Zandra A. Jenkins, Zeljka Smit‐McBride, et al.. (2003). Identification and characterization of eukaryotic initiation factor 5A‐2. European Journal of Biochemistry. 270(21). 4254–4263. 101 indexed citations

14.

Jenkins, Zandra A., Petra Hååg, & Hans E. Johansson. (2001). Human EIF5A2 on Chromosome 3q25–q27 Is a Phylogenetically Conserved Vertebrate Variant of Eukaryotic Translation Initiation Factor 5A with Tissue-Specific Expression. Genomics. 71(1). 101–109. 119 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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