Justine E. Marum

1.1k total citations
14 papers, 302 citations indexed

About

Justine E. Marum is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Justine E. Marum has authored 14 papers receiving a total of 302 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Justine E. Marum's work include Genomics and Rare Diseases (5 papers), Chronic Lymphocytic Leukemia Research (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Justine E. Marum is often cited by papers focused on Genomics and Rare Diseases (5 papers), Chronic Lymphocytic Leukemia Research (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). Justine E. Marum collaborates with scholars based in Australia, United Kingdom and United States. Justine E. Marum's co-authors include Susan Branford, Alison G. Compton, David R. Thorburn, Sze Chern Lim, Elena J. Tucker, John Christodoulou, Belinda Chong, Michael Springer, Silke Leimkühler and Zornitza Stark and has published in prestigious journals such as Blood, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Justine E. Marum

14 papers receiving 299 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Justine E. Marum Australia 8 152 101 59 45 38 14 302
Zahra Assouline France 13 357 2.3× 63 0.6× 141 2.4× 71 1.6× 8 0.2× 26 505
Arthavan Selvanathan Australia 7 88 0.6× 32 0.3× 32 0.5× 98 2.2× 5 0.1× 22 290
Concetta Aloi Italy 9 209 1.4× 90 0.9× 10 0.2× 11 0.2× 28 0.7× 21 411
Patroula Smpokou United States 9 195 1.3× 29 0.3× 23 0.4× 8 0.2× 12 0.3× 12 279
Birgit Haberberger Germany 5 432 2.8× 64 0.6× 243 4.1× 7 0.2× 39 1.0× 5 504
Angela Sun United States 10 160 1.1× 121 1.2× 18 0.3× 7 0.2× 1 0.0× 35 417
Alan Stuart Canada 7 95 0.6× 96 1.0× 15 0.3× 30 0.7× 16 224
Francisco Laranjeira Portugal 9 104 0.7× 32 0.3× 30 0.5× 22 0.5× 23 269
Ahmad Alodaib Saudi Arabia 9 160 1.1× 39 0.4× 86 1.5× 13 0.3× 1 0.0× 13 257
Yaser Heshmati Sweden 9 103 0.7× 36 0.4× 10 0.2× 38 0.8× 15 201

Countries citing papers authored by Justine E. Marum

Since Specialization
Citations

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

Fields of papers citing papers by Justine E. Marum

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Justine E. Marum. 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 Justine E. Marum. The network helps show where Justine E. Marum may publish in the future.

Co-authorship network of co-authors of Justine E. Marum

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

All Works

14 of 14 papers shown
1.
Lee, Ling, Fiona Lynch, Melissa Martyn, et al.. (2023). Two-step offer and return of multiple types of additional genomic findings to families after ultrarapid trio genomic testing in the acute care setting: a study protocol. BMJ Open. 13(6). e072999–e072999. 7 indexed citations
2.
Akesson, Lauren, Rocío Rius, Natasha J. Brown, et al.. (2022). Distinct diagnostic trajectories in NBAS‐associated acute liver failure highlights the need for timely functional studies. JIMD Reports. 63(3). 240–249. 2 indexed citations
3.
Scheffer, Ingrid E., Caitlin A. Bennett, Deepak Gill, et al.. (2022). Exome sequencing for patients with developmental and epileptic encephalopathies in clinical practice. Developmental Medicine & Child Neurology. 65(1). 50–57. 20 indexed citations
4.
Yaplito‐Lee, Joy, et al.. (2020). Successful treatment of lathosterolosis: A rare defect in cholesterol biosynthesis—A case report and review of literature. JIMD Reports. 56(1). 14–19. 8 indexed citations
5.
Tan, Natalie B., Rachel Stapleton, Zornitza Stark, et al.. (2020). Evaluating systematic reanalysis of clinical genomic data in rare disease from single center experience and literature review. Molecular Genetics & Genomic Medicine. 8(11). e1508–e1508. 44 indexed citations
6.
Tan, Tiong Yang, Sebastian Lunke, Belinda Chong, et al.. (2019). A head-to-head evaluation of the diagnostic efficacy and costs of trio versus singleton exome sequencing analysis. European Journal of Human Genetics. 27(12). 1791–1799. 35 indexed citations
7.
Slade, C, Samar Ojaimi, Sara Barnes, et al.. (2018). Pitfalls of immunotherapy: lessons from a patient with CTLA-4 haploinsufficiency. Allergy Asthma and Clinical Immunology. 14(1). 65–65. 7 indexed citations
8.
Marum, Justine E., David T Yeung, Leanne Purins, et al.. (2017). ASXL1 and BIM germ line variants predict response and identify CML patients with the greatest risk of imatinib failure. Blood Advances. 1(18). 1369–1381. 18 indexed citations
9.
10.
Marum, Justine E. & Susan Branford. (2016). Current developments in molecular monitoring in chronic myeloid leukemia. Therapeutic Advances in Hematology. 7(5). 237–251. 20 indexed citations
11.
12.
Branford, Susan, Paul Wang, Wendy T Parker, et al.. (2015). High Incidence of Mutated Cancer-Associated Genes at Diagnosis in CML Patients with Early Transformation to Blast Crisis. Blood. 126(23). 600–600. 3 indexed citations
13.
Lim, Sze Chern, Katherine R. Smith, David A. Stroud, et al.. (2014). A Founder Mutation in PET100 Causes Isolated Complex IV Deficiency in Lebanese Individuals with Leigh Syndrome. The American Journal of Human Genetics. 94(2). 209–222. 54 indexed citations
14.
Lim, Sze Chern, Justine E. Marum, Elena J. Tucker, et al.. (2013). Mutations in LYRM4, encoding iron–sulfur cluster biogenesis factor ISD11, cause deficiency of multiple respiratory chain complexes. Human Molecular Genetics. 22(22). 4460–4473. 81 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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