Julia Rankin

7.8k total citations
39 papers, 1.7k citations indexed

About

Julia Rankin is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Julia Rankin has authored 39 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 13 papers in Genetics and 11 papers in Cellular and Molecular Neuroscience. Recurrent topics in Julia Rankin's work include Genomic variations and chromosomal abnormalities (8 papers), Genetic Neurodegenerative Diseases (7 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Julia Rankin is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genetic Neurodegenerative Diseases (7 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Julia Rankin collaborates with scholars based in United Kingdom, United States and Germany. Julia Rankin's co-authors include David C. Rubinsztein, Andreas Wyttenbach, Sian Ellard, Y. Narain, Robert A. Furlong, Jina Swartz, Jenny Carmichael, R. A. Furlong, Neil Stoodley and Philip Jardine and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Genes & Development and Brain.

In The Last Decade

Julia Rankin

38 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Julia Rankin United Kingdom 21 1.1k 560 314 282 258 39 1.7k
Helen Griffin United Kingdom 23 1.0k 0.9× 374 0.7× 247 0.8× 174 0.6× 160 0.6× 49 1.5k
Yoshihisa Sakai United States 16 1.2k 1.1× 297 0.5× 465 1.5× 167 0.6× 149 0.6× 37 1.8k
Göknur Haliloğlu Türkiye 23 922 0.8× 224 0.4× 259 0.8× 210 0.7× 183 0.7× 116 1.7k
Saïd Akli United States 24 1.0k 0.9× 287 0.5× 562 1.8× 104 0.4× 238 0.9× 40 1.8k
Angela Abicht Germany 27 1.2k 1.1× 262 0.5× 269 0.9× 864 3.1× 537 2.1× 124 2.1k
Maire Leyne United States 15 689 0.6× 613 1.1× 100 0.3× 92 0.3× 241 0.9× 21 1.3k
Carlo Rinaldi Italy 21 1.2k 1.1× 533 1.0× 148 0.5× 306 1.1× 95 0.4× 47 1.7k
Nobutada Tachi Japan 16 789 0.7× 619 1.1× 150 0.5× 234 0.8× 148 0.6× 86 1.3k
Lyne Bourbonnière Canada 21 792 0.7× 291 0.5× 101 0.3× 168 0.6× 226 0.9× 31 2.1k
Narihiro Minami Japan 21 878 0.8× 329 0.6× 135 0.4× 98 0.3× 294 1.1× 58 1.3k

Countries citing papers authored by Julia Rankin

Since Specialization
Citations

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

Fields of papers citing papers by Julia Rankin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Julia Rankin

This figure shows the co-authorship network connecting the top 25 collaborators of Julia Rankin. A scholar is included among the top collaborators of Julia Rankin 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 Julia Rankin. Julia Rankin 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.
Lord, Jenny, Htoo A. Wai, Elena Arciero, et al.. (2024). Noncoding variants are a rare cause of recessive developmental disorders in trans with coding variants. Genetics in Medicine. 26(12). 101249–101249. 3 indexed citations
2.
Kumar, Ajith, Angela F. Brady, Tessa Homfray, et al.. (2022). Expanding the phenotype of TAB2 variants and literature review. American Journal of Medical Genetics Part A. 188(11). 3331–3342. 6 indexed citations
3.
Parry, David, Paula Carroll, Joseph A. Marsh, et al.. (2020). PRIM1 deficiency causes a distinctive primordial dwarfism syndrome. Genes & Development. 34(21-22). 1520–1533. 18 indexed citations
4.
Proudfoot, Malcolm J., Nick Gutowski, Dieter Edbauer, et al.. (2014). Early dipeptide repeat pathology in a frontotemporal dementia kindred with C9ORF72 mutation and intellectual disability. Acta Neuropathologica. 127(3). 451–458. 51 indexed citations
5.
Fenwick, Aimée L, Jacqueline A.C. Goos, Julia Rankin, et al.. (2014). Apparently synonymous substitutions in FGFR2affect splicing and result in mild Crouzon syndrome. BMC Medical Genetics. 15(1). 95–95. 12 indexed citations
6.
Cushion, Thomas D., William B. Dobyns, Jonathan G.L. Mullins, et al.. (2013). Overlapping cortical malformations and mutations in TUBB2B and TUBA1A. Brain. 136(2). 536–548. 101 indexed citations
7.
Shah, Siddharth, Sian Ellard, Rachel Kneen, et al.. (2012). Childhood presentation of COL4A1 mutations. Developmental Medicine & Child Neurology. 54(6). 569–574. 53 indexed citations
8.
Parker, Michael, Julia Rankin, Louise C. Wilson, et al.. (2011). Type 1 collagenopathy presenting with a Russell–Silver phenotype. American Journal of Medical Genetics Part A. 155(6). 1414–1418. 6 indexed citations
9.
Shah, Siddharth, Y Kumar, Brendan McLean, et al.. (2009). A dominantly inherited mutation in collagen IV A1 (COL4A1) causing childhood onset stroke without porencephaly. European Journal of Paediatric Neurology. 14(2). 182–187. 48 indexed citations
10.
Thomas, N. Simon, John F. Harvey, David J. Bunyan, et al.. (2009). Clinical and molecular characterization of duplications encompassing the human SHOX gene reveal a variable effect on stature. American Journal of Medical Genetics Part A. 149A(7). 1407–1414. 43 indexed citations
11.
Giurgea, Irina, Chantal Missirian, Pierre Cacciagli, et al.. (2008). TCF4Deletions in Pitt-Hopkins Syndrome. Human Mutation. 29(11). E242–E251. 45 indexed citations
12.
Rankin, Julia, Michaela Auer‐Grumbach, Warwick Bagg, et al.. (2008). Extreme phenotypic diversity and nonpenetrance in families with the LMNA gene mutation R644C. American Journal of Medical Genetics Part A. 146A(12). 1530–1542. 80 indexed citations
13.
James, Paul A., Julia Rankin, & Kevin Talbot. (2008). Asymmetrical late onset motor neuropathy associated with a novel mutation in the small heat shock protein HSPB1 (HSP27). Journal of Neurology Neurosurgery & Psychiatry. 79(4). 461–463. 39 indexed citations
14.
Weisfeld‐Adams, James D., Michael R. Carter, Marcus Likeman, & Julia Rankin. (2007). Three Sisters with Chiari I Malformation with and without Associated Syringomyelia. Pediatric Neurosurgery. 43(6). 533–538. 11 indexed citations
15.
Rankin, Julia & Sian Ellard. (2006). The laminopathies: a clinical review. Clinical Genetics. 70(4). 261–274. 131 indexed citations
16.
Vos, Michel De, Bruce E. Hayward, Ruth Charlton, et al.. (2006). PMS2 Mutations in Childhood Cancer. JNCI Journal of the National Cancer Institute. 98(5). 358–361. 63 indexed citations
17.
Ho, Luk, Jenny Carmichael, Jina Swartz, et al.. (2001). The molecular biology of Huntington's disease. Psychological Medicine. 31(1). 3–14. 79 indexed citations
18.
Rankin, Julia, T Strachan, Majlinda Lako, & Susan Lindsay. (1999). Partial cloning and assignment<footref rid="foot01"><sup>1</sup></footref> of WNT6 to human chromosome band 2q35 by in situ hybridization. Cytogenetic and Genome Research. 84(1-2). 50–52. 15 indexed citations
19.
Rubinsztein, David C., Andreas Wyttenbach, & Julia Rankin. (1999). Intracellular inclusions, pathological markers in diseases caused by expanded polyglutamine tracts?. Journal of Medical Genetics. 36(4). 265–270. 45 indexed citations
20.
Rankin, Julia, Kenneth Smith, Emmanuel Huguet, et al.. (1997). A novel human Wnt gene, WNT10B, maps to 12q13 and is expressed in human breast carcinomas. Oncogene. 14(10). 1249–1253. 75 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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