Janelle E. Collinge

1.9k total citations · 1 hit paper
19 papers, 1.4k citations indexed

About

Janelle E. Collinge is a scholar working on Molecular Biology, Immunology and Physiology. According to data from OpenAlex, Janelle E. Collinge has authored 19 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Immunology and 4 papers in Physiology. Recurrent topics in Janelle E. Collinge's work include Erythrocyte Function and Pathophysiology (4 papers), Physiological and biochemical adaptations (3 papers) and Hemoglobinopathies and Related Disorders (3 papers). Janelle E. Collinge is often cited by papers focused on Erythrocyte Function and Pathophysiology (4 papers), Physiological and biochemical adaptations (3 papers) and Hemoglobinopathies and Related Disorders (3 papers). Janelle E. Collinge collaborates with scholars based in Australia, United States and United Kingdom. Janelle E. Collinge's co-authors include Benjamin T. Kile, Donald Metcalf, Adrienne A. Hilton, Sarah Ellis, Priscilla N. Kelly, Andrew W. Roberts, Marina R. Carpinelli, Kylie D. Mason, Jamie I. Fletcher and David C.S. Huang and has published in prestigious journals such as Cell, Proceedings of the National Academy of Sciences and Blood.

In The Last Decade

Janelle E. Collinge

19 papers receiving 1.4k citations

Hit Papers

Programmed Anuclear Cell Death Delimits Platelet Life Span 2007 2026 2013 2019 2007 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Janelle E. Collinge Australia 12 768 351 287 179 174 19 1.4k
Thomas J. Schneider United States 15 640 0.8× 212 0.6× 267 0.9× 175 1.0× 95 0.5× 26 1.3k
Heather M. Bond Italy 23 621 0.8× 143 0.4× 139 0.5× 149 0.8× 165 0.9× 62 1.2k
Pradeep Sathyanarayana United States 22 1.1k 1.4× 188 0.5× 222 0.8× 81 0.5× 194 1.1× 36 1.6k
Natalie J. Foot Australia 19 677 0.9× 230 0.7× 135 0.5× 100 0.6× 139 0.8× 29 1.2k
Michael Kline United States 13 1.3k 1.7× 252 0.7× 478 1.7× 66 0.4× 417 2.4× 24 1.9k
D E Woods United States 18 852 1.1× 261 0.7× 511 1.8× 244 1.4× 144 0.8× 26 1.6k
Ania Wilczynska United Kingdom 26 2.0k 2.6× 159 0.5× 175 0.6× 182 1.0× 176 1.0× 44 2.6k
Holly Evans United Kingdom 18 591 0.8× 215 0.6× 105 0.4× 88 0.5× 416 2.4× 42 1.2k
Yves Courty France 24 549 0.7× 179 0.5× 128 0.4× 85 0.5× 288 1.7× 66 1.4k
Jennifer Whangbo United States 18 818 1.1× 335 1.0× 492 1.7× 122 0.7× 224 1.3× 44 1.7k

Countries citing papers authored by Janelle E. Collinge

Since Specialization
Citations

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

Fields of papers citing papers by Janelle E. Collinge

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Janelle E. Collinge

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

All Works

19 of 19 papers shown
1.
Brown, Fiona C., Loretta Cerruti, Janelle E. Collinge, et al.. (2015). Activation of the erythroid K-Cl cotransporter Kcc1 enhances sickle cell disease pathology in a humanized mouse model. Blood. 126(26). 2863–2870. 16 indexed citations
2.
Brown, Fiona C., Nicholas A. Scott, Gerhard Rank, et al.. (2012). ENU mutagenesis identifies the first mouse mutants reproducing human β-thalassemia at the genomic level. Blood Cells Molecules and Diseases. 50(2). 86–92. 15 indexed citations
3.
Masters, Seth L., Motti Gerlic, Donald Metcalf, et al.. (2012). NLRP1 Inflammasome Activation Induces Pyroptosis of Hematopoietic Progenitor Cells. Immunity. 37(6). 1009–1023. 238 indexed citations
4.
Kauppi, Maria, Adrienne A. Hilton, Donald Metcalf, et al.. (2011). Thrombocytopenia and erythrocytosis in mice with a mutation in the gene encoding the hemoglobin β minor chain. Proceedings of the National Academy of Sciences. 109(2). 576–581. 3 indexed citations
5.
Maxwell, Mhairi J., Lisa M. Ooms, Elizabeth M. Davies, et al.. (2011). An ENU-induced mouse mutant of SHIP1 reveals a critical role of the stem cell isoform for suppression of macrophage activation. Blood. 117(20). 5362–5371. 15 indexed citations
6.
Verhagen, Anne M., Carolyn A. de Graaf, Tracey M. Baldwin, et al.. (2011). Reduced Lymphocyte Longevity and Homeostatic Proliferation in Lamin B Receptor-Deficient Mice Results in Profound and Progressive Lymphopenia. The Journal of Immunology. 188(1). 122–134. 9 indexed citations
7.
Mead, Simon, Diana Caine, Jonathan D. F. Wadsworth, et al.. (2010). PATU2 Novel truncation mutation of PRNP causes chronic diarrhoea, sensory neuropathy and autonomic failure associated with prion protein deposition in the cerebral blood vessels and small bowel. Journal of Neurology Neurosurgery & Psychiatry. 81(11). e24–e24. 2 indexed citations
8.
Verhagen, Anne M., Morgan E. Wallace, Sarah A. Jones, et al.. (2009). A Kinase-Dead Allele of Lyn Attenuates Autoimmune Disease Normally Associated with Lyn Deficiency. The Journal of Immunology. 182(4). 2020–2029. 15 indexed citations
9.
Collinge, Janelle E., Alisha Anderson, Andrew R. Weeks, Travis K. Johnson, & Stephen W. McKechnie. (2008). Latitudinal and cold-tolerance variation associate with DNA repeat-number variation in the hsr-omega RNA gene of Drosophila melanogaster. Heredity. 101(3). 260–270. 20 indexed citations
10.
Smyth, Ian, Douglas F. Hacking, Adrienne A. Hilton, et al.. (2008). A Mouse Model of Harlequin Ichthyosis Delineates a Key Role for Abca12 in Lipid Homeostasis. PLoS Genetics. 4(9). e1000192–e1000192. 87 indexed citations
11.
Smyth, Ian, Douglas F. Hacking, Adrienne A. Hilton, et al.. (2008). Correction: A Mouse Model of Harlequin Ichthyosis Delineates a Key Role for Abca12 in Lipid Homeostasis. PLoS Genetics. 4(10). 16 indexed citations
12.
Mason, Kylie D., Marina R. Carpinelli, Jamie I. Fletcher, et al.. (2007). Programmed Anuclear Cell Death Delimits Platelet Life Span. Cell. 128(6). 1173–1186. 767 indexed citations breakdown →
13.
Mason, Kylie D., Marina R. Carpinelli, Janelle E. Collinge, et al.. (2006). The Bcl-2 Protein Family Is Essential for Platelet Survival In Vivo.. Blood. 108(11). 697–697. 1 indexed citations
14.
Collinge, Janelle E., Ary A. Hoffmann, & Stephen W. McKechnie. (2005). Altitudinal patterns for latitudinally varying traits and polymorphic markers in Drosophila melanogaster from eastern Australia. Journal of Evolutionary Biology. 19(2). 473–482. 53 indexed citations
15.
Anderson, Alisha, Janelle E. Collinge, Ary A. Hoffmann, Mark Kellett, & Stephen W. McKechnie. (2003). Thermal tolerance trade-offs associated with the right arm of chromosome 3 and marked by the hsr-omega gene in Drosophila melanogaster. Heredity. 90(2). 195–202. 90 indexed citations
16.
Gydesen, Susanne, A. Brun, Lisa Chakrabarti, et al.. (2002). Chromosome 3 linked frontotemporal dementia (FTD-3). UCL Discovery (University College London). 6 indexed citations
17.
Yuluğ, Işık G., et al.. (1995). AN IMPROVED PROTOCOL FOR THE ANALYSIS OF SOD1 GENE-MUTATIONS, AND A NEW MUTATION IN EXON-4 (VOL 4, PG 1101, 1995). UCL Discovery (University College London). 3 indexed citations
18.
Palmer, Mark S., Katie Sidle, Tracy Campbell, et al.. (1992). Absence of PRP gene mutation in patient showing PRP immunostaining. Neurobiology of Aging. 13. S94–S94. 2 indexed citations
19.
Collinge, Janelle E., Lynn E. DeLisi, A. Boccio, et al.. (1991). Evidence for a Pseudo-autosomal Locus for Schizophrenia Using the Method of Affected Sibling Pairs. The British Journal of Psychiatry. 158(5). 624–629. 49 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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