Kath Smith

3.6k total citations · 1 hit paper
23 papers, 1.8k citations indexed

About

Kath Smith is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Kath Smith has authored 23 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 12 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Kath Smith's work include Genomic variations and chromosomal abnormalities (9 papers), Congenital heart defects research (5 papers) and Genomics and Rare Diseases (4 papers). Kath Smith is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Congenital heart defects research (5 papers) and Genomics and Rare Diseases (4 papers). Kath Smith collaborates with scholars based in United Kingdom, United States and Austria. Kath Smith's co-authors include Peter W. Andrews, Edna L. Maltby, H. D. M. Moore, Paul J. Gokhale, Jonathan S. Draper, James A. Thomson, Julie A. Johnson, Lorraine F. Meisner, Thomas P. Zwaka and Duncan Baker and has published in prestigious journals such as Nature Biotechnology, Human Molecular Genetics and Journal of Psychosomatic Research.

In The Last Decade

Kath Smith

22 papers receiving 1.7k citations

Hit Papers

Recurrent gain of chromosomes 17q and 12 in cultured huma... 2003 2026 2010 2018 2003 250 500 750
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Recurrent gain of chromosomes 17q and 12 in cultured human embryonic stem cells
    2003 759 citations Jonathan S. Draper, Kath Smith et al. Nature Biotechnology profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kath Smith United Kingdom 12 1.5k 367 347 273 163 23 1.8k
Milla Mikkola Finland 12 1.2k 0.8× 242 0.7× 203 0.6× 281 1.0× 162 1.0× 13 1.5k
Eungi Yang United States 14 1.5k 1.1× 194 0.5× 222 0.6× 271 1.0× 245 1.5× 14 1.8k
Shunping Wang United States 5 1.6k 1.1× 307 0.8× 256 0.7× 396 1.5× 249 1.5× 7 1.8k
Jin Young Joo South Korea 14 2.3k 1.6× 259 0.7× 415 1.2× 406 1.5× 297 1.8× 18 2.5k
Sarah Eminli United States 9 2.8k 1.9× 386 1.1× 337 1.0× 471 1.7× 375 2.3× 12 3.0k
Karolina Lundin Finland 16 1.2k 0.8× 302 0.8× 174 0.5× 394 1.4× 158 1.0× 29 1.5k
Daisy A. Robinton United States 8 1.6k 1.1× 162 0.4× 289 0.8× 235 0.9× 159 1.0× 9 2.0k
Warakorn Kulalert United States 5 1.7k 1.2× 137 0.4× 213 0.6× 271 1.0× 264 1.6× 6 1.8k
Samer M. I. Hussein Canada 16 1.4k 1.0× 173 0.5× 173 0.5× 199 0.7× 330 2.0× 33 1.8k
Frances A. Brook United Kingdom 17 2.8k 1.9× 524 1.4× 299 0.9× 501 1.8× 163 1.0× 26 3.3k

Countries citing papers authored by Kath Smith

Since Specialization
Citations

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

Fields of papers citing papers by Kath Smith

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kath Smith

This figure shows the co-authorship network connecting the top 25 collaborators of Kath Smith. A scholar is included among the top collaborators of Kath Smith 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 Kath Smith. Kath Smith 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.
Smith, Kath, Martin Christian, Talat Mushtaq, et al.. (2019). Phenotypic diversity and correlation with the genotypes of pseudohypoaldosteronism type 1. Journal of Pediatric Endocrinology and Metabolism. 32(9). 959–967. 17 indexed citations
2.
Balasubramanian, Meena, Nadja Fratzl‐Zelman, Nicola Peel, et al.. (2018). Novel PLS3 variants in X‐linked osteoporosis: Exploring bone material properties. American Journal of Medical Genetics Part A. 176(7). 1578–1586. 23 indexed citations
3.
Balasubramanian, Meena, Rebecca M. Jones, Elizabeth Milne, et al.. (2018). Autism and heritable bone fragility: A true association?. Bone Reports. 8. 156–162. 9 indexed citations
4.
Wakeling, Emma, et al.. (2018). Expanding the molecular basis and phenotypic spectrum of ZDHHC9 ‐associated X‐linked intellectual disability. American Journal of Medical Genetics Part A. 176(5). 1238–1244. 10 indexed citations
5.
Smith, Kath, et al.. (2016). Short case report: Xq23 deletion involving PAK3 as a novel cause of developmental delay in a 6-year-old boy. Clinical Dysmorphology. 26(1). 38–40. 6 indexed citations
6.
Balasubramanian, Meena, et al.. (2015). Inherited duplication of the short arm of chromosome 18p11.32–p11.31 associated with developmental delay/intellectual disability. Clinical Dysmorphology. 25(1). 19–22. 20 indexed citations
7.
Balasubramanian, Meena, et al.. (2015). A novel de novo 20q13.32–q13.33 deletion in a 2-year-old child with poor growth, feeding difficulties and low bone mass. Journal of Human Genetics. 60(6). 313–317. 17 indexed citations
8.
Smith, Kath, et al.. (2015). Clinical report. Clinical Dysmorphology. 24(4). 151–155. 2 indexed citations
9.
Smith, Kath, et al.. (2014). A Novel (Paternally Inherited) Duplication 13q31.3q32.3 in a 12-Year-Old Patient with Facial Dysmorphism and Developmental Delay. Molecular Syndromology. 5(5). 245–250. 3 indexed citations
10.
Balasubramanian, Meena, Emma Shearing, Kath Smith, et al.. (2014). Pneumothorax from subpleural blebs—A new association of sotos syndrome?. American Journal of Medical Genetics Part A. 164(5). 1222–1226. 2 indexed citations
11.
Mudhar, Hardeep Singh, et al.. (2012). Fluorescence in situ hybridisation (FISH) in histologically challenging conjunctival melanocytic lesions. British Journal of Ophthalmology. 97(1). 40–46. 17 indexed citations
12.
Balasubramanian, Meena, Kath Smith, Santosh Mordekar, & Michael Parker. (2011). Clinical report: An interstitial deletion of 16p13.11 detected by array CGH in a patient with infantile spasms. European Journal of Medical Genetics. 54(3). 314–318. 18 indexed citations
13.
Balasubramanian, Meena, Kath Smith, Lina Basel‐Vanagaite, et al.. (2011). Case series: 2q33.1 microdeletion syndrome—further delineation of the phenotype. Journal of Medical Genetics. 48(5). 290–298. 64 indexed citations
14.
Smith, Kath, et al.. (2011). Sensory processing and everyday life. ORCA Online Research @Cardiff. 1 indexed citations
15.
Baker, Duncan, Neil J. Harrison, Edna L. Maltby, et al.. (2007). Adaptation to culture of human embryonic stem cells and oncogenesis in vivo. Nature Biotechnology. 25(2). 207–215. 480 indexed citations
16.
Enver, Tariq, Shamit Soneji, Chirag Joshi, et al.. (2005). Cellular differentiation hierarchies in normal and culture-adapted human embryonic stem cells. Human Molecular Genetics. 14(21). 3129–3140. 220 indexed citations
17.
Kotula, Paul G., John Henry J. Scott, Mah Lee Ng, et al.. (2005). WELCOME FROM THE PROGRAM COMMITTEE. Microscopy and Microanalysis. 11(I1). 44–44. 1 indexed citations
18.
Flasza, Marzena, et al.. (2003). Reprogramming in Inter-Species Embryonal Carcinoma–Somatic Cell Hybrids Induces Expression of Pluripotency and Differentiation Markers. Cloning and Stem Cells. 5(4). 339–354. 55 indexed citations
19.
Draper, Jonathan S., Kath Smith, Paul J. Gokhale, et al.. (2003). Recurrent gain of chromosomes 17q and 12 in cultured human embryonic stem cells. Nature Biotechnology. 22(1). 53–54. 759 indexed citations breakdown →
20.
Evans, Philip D., et al.. (1988). Minor infection, minor life events and the four day desirability dip. Journal of Psychosomatic Research. 32(4-5). 533–539. 24 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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