Kath Smith

3.6k citations

23 papers · 1.8k indexed · 1 hit paper · h-index 12

Impact in

Molecular Biology top 5%
- Pluripotent Stem Cells Research
- CRISPR and Genetic Engineering
- Renal and related cancers
Genetics top 10%
- Mesenchymal stem cell research
- Genomic variations and chromosomal abnormalities

Papers in ⓘ

Structural Biology 1
Genetics 14
- Genomic variations and chromosomal abnormalities 9
- Congenital Ear and Nasal Anomalies 4
- Genetics and Neurodevelopmental Disorders 4
- Genomics and Rare Diseases 4
- Connective tissue disorders research 3

Co-authors: Peter W. Andrews (4 shared papers)Edna L. Maltby (3 shared papers)H. D. M. Moore (2 shared papers)Jonathan S. Draper (2 shared papers)Paul J. Gokhale (2 shared papers)Lorraine F. Meisner (1 shared paper)James A. Thomson (1 shared paper)Thomas P. Zwaka (1 shared paper)
Journals: Nature Biotechnology (2 papers)Microscopy and Microanalysis (1 paper)Human Molecular Genetics (1 paper)European Journal of Medical Genetics (1 paper)Journal of Medical Genetics (1 paper)
Partner nations: United Kingdom United States Iran

In The Last Decade

Kath Smith

22 papers receiving 1.7k citations

Hit Papers

align trajectories log scale

Recurrent gain of chromosomes 17q and 12 in cultured human embryonic stem cells 2003 · 759 citations

Peers

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-authors

The 25 scholars most cited alongside Kath Smith, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Kath Smith Line = papers co-authored together Kath Smith links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 23 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Recurrent gain of chromosomes 17q and 12 in cultured human embryonic stem cells Nature Biotechnology ·Jonathan S. Draper, Kath Smith, Paul J. Gokhale, H. D. M. Moore, Edna L. Maltby, Julie A. Johnson, Lorraine F. Meisner, Thomas P. Zwaka, James A. Thomson, Peter W. Andrews Hit paper breakdown →	2003	759
2	Adaptation to culture of human embryonic stem cells and oncogenesis in vivo Nature Biotechnology ·Duncan Baker, Neil J. Harrison, Edna L. Maltby, Kath Smith, H. D. M. Moore, Pamela J. Shaw, Paul R. Heath, Hazel M. Holden, Peter W. Andrews	2007	480
3	Cellular differentiation hierarchies in normal and culture-adapted human embryonic stem cells Human Molecular Genetics ·Tariq Enver, Shamit Soneji, Chirag Joshi, John Brown, Francisco J. Iborra, Torben Ørntoft, Thomas Thykjær, Edna L. Maltby, Kath Smith, Raed Abu Dawud, Mark Jones, Maryam Moghaddam Matin, Paul J. Gokhale, Jonathan S. Draper, Peter W. Andrews	2005	220
4	Case series: 2q33.1 microdeletion syndrome—further delineation of the phenotype Journal of Medical Genetics ·Meena Balasubramanian, Kath Smith, Lina Basel‐Vanagaite, Murray Feingold, Pamela Brock, Gordon C. Gowans, Pradeep Vasudevan, Lara Cresswell, Emma‐Jane Taylor, Civonnia Harris, Neil Friedman, Rocio Moran, Holly Feret, Elaine H. Zackai, Aaron Theisen, Jill A. Rosenfeld, Michael Parker	2011	64
5	Reprogramming in Inter-Species Embryonal Carcinoma–Somatic Cell Hybrids Induces Expression of Pluripotency and Differentiation Markers Cloning and Stem Cells ·Marzena Flasza, Andrew F. Shering, Kath Smith, Peter W. Andrews, Polly Talley, Peter Johnson	2003	55
6	Minor infection, minor life events and the four day desirability dip Journal of Psychosomatic Research ·Philip D. Evans, Marian K. Pitts, Kath Smith	1988	24
7	Novel PLS3 variants in X‐linked osteoporosis: Exploring bone material properties American Journal of Medical Genetics Part A ·Meena Balasubramanian, Nadja Fratzl‐Zelman, Rory O’Sullivan, Mary Bull, Nicola Peel, Rebecca C. Pollitt, Rebecca Jones, Elizabeth Milne, Kath Smith, Paul Roschger, Klaus Klaushofer, Nicholas Bishop	2018	23
8	Inherited duplication of the short arm of chromosome 18p11.32–p11.31 associated with developmental delay/intellectual disability Clinical Dysmorphology ·Meena Balasubramanian, Sivagamy Sithambaram, Kath Smith	2015	20
9	Clinical report: An interstitial deletion of 16p13.11 detected by array CGH in a patient with infantile spasms European Journal of Medical Genetics ·Meena Balasubramanian, Kath Smith, Santosh Mordekar, Michael Parker	2011	18
10	Fluorescence in situ hybridisation (FISH) in histologically challenging conjunctival melanocytic lesions British Journal of Ophthalmology ·Hardeep Singh Mudhar, Kath Smith, Polly Talley, Abigail Whitworth, Neil Atkey, I G Rennie	2012	17
11	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 ·Meena Balasubramanian, Edward Atack, Kath Smith, Michael Parker	2015	17
12	Phenotypic diversity and correlation with the genotypes of pseudohypoaldosteronism type 1 Journal of Pediatric Endocrinology and Metabolism ·Jaya Sujatha Gopal‐Kothandapani, Arpan B. Doshi, Kath Smith, Martin Christian, Talat Mushtaq, Indraneel Banerjee, Raja Padidela, Renuka Ramakrishnan, Catherine Owen, Timothy Cheetham, Paul Dimitri	2019	17
13	Expanding the molecular basis and phenotypic spectrum of ZDHHC9 ‐associated X‐linked intellectual disability American Journal of Medical Genetics Part A ·Schaida Schirwani, Emma Wakeling, Kath Smith, (unknown), (unknown)	2018	10
14	Autism and heritable bone fragility: A true association? Bone Reports ·Meena Balasubramanian, Rebecca M. Jones, Elizabeth Milne, Charlotte J. Marshall, Paul Arundel, Kath Smith, Nicholas Bishop	2018	9
15	Short case report: Xq23 deletion involving PAK3 as a novel cause of developmental delay in a 6-year-old boy Clinical Dysmorphology ·Ashley Cartwright, Kath Smith, Meena Balasubramanian	2016	6
16	Tigroid pattern of cerebral white matter involvement in chromosome 6p25 deletion syndrome with concomitant 5p15 duplication Journal of Pediatric Genetics ·Kath Smith, Steven Williams, Paul D. Griffiths, Michael Parker, Santosh Mordekar, Meena Balasubramanian	2015	5
17	Copy number variants in association with type 1 collagenopathy: Atypical osteogenesis imperfecta American Journal of Medical Genetics Part A ·Meena Balasubramanian, Ashley Cartwright, Kath Smith, Paul Arundel, Nicholas Bishop	2015	4
18	A Novel (Paternally Inherited) Duplication 13q31.3q32.3 in a 12-Year-Old Patient with Facial Dysmorphism and Developmental Delay Molecular Syndromology ·Edward Atack, Helen Fairtlough, Kath Smith, Meena Balasubramanian	2014	3
19	Clinical and molecular characterization of the first familial report of 1p32 microdeletion Clinical Dysmorphology ·Schaida Schirwani, Kath Smith, Meena Balasubramanian	2017	3
20	Pneumothorax from subpleural blebs—A new association of sotos syndrome? American Journal of Medical Genetics Part A ·Meena Balasubramanian, Emma Shearing, Kath Smith, R. Chavasse, Robert W. Taylor, Katrina Tatton‐Brown, Robert Primhak, Kelechi Ugonna, Michael Parker	2014	2

About Kath Smith

Kath Smith is a scholar working on Structural Biology, Genetics, Genetics, Applied Psychology and Molecular Biology, having authored 23 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Congenital heart defects research (5 papers), Congenital Ear and Nasal Anomalies (4 papers), CRISPR and Genetic Engineering (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), Genomics and Rare Diseases (4 papers), Pluripotent Stem Cells Research (4 papers) and Connective tissue disorders research (3 papers). The work is most often cited by research in Molecular Biology (1.5k citations), Genetics (152 citations), Genetics (367 citations), Developmental Neuroscience (53 citations) and Biomedical Engineering (347 citations). Kath Smith has collaborated with scholars based in United Kingdom, United States and Iran. Frequent co-authors include Peter W. Andrews, Edna L. Maltby, H. D. M. Moore, Jonathan S. Draper, Paul J. Gokhale, Lorraine F. Meisner, James A. Thomson, Thomas P. Zwaka, Julie A. Johnson and Neil J. Harrison. Their work appears in journals such as Nature Biotechnology, Microscopy and Microanalysis, Human Molecular Genetics, European Journal of Medical Genetics and Journal of Medical Genetics.

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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