Conrad Smith

635 total citations
6 papers, 170 citations indexed

About

Conrad Smith is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Conrad Smith has authored 6 papers receiving a total of 170 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Clinical Biochemistry and 2 papers in Genetics. Recurrent topics in Conrad Smith's work include Mitochondrial Function and Pathology (4 papers), Metabolism and Genetic Disorders (4 papers) and ATP Synthase and ATPases Research (3 papers). Conrad Smith is often cited by papers focused on Mitochondrial Function and Pathology (4 papers), Metabolism and Genetic Disorders (4 papers) and ATP Synthase and ATPases Research (3 papers). Conrad Smith collaborates with scholars based in United Kingdom and Australia. Conrad Smith's co-authors include Carl Fratter, Joanna Poulton, A O'Rourke, Vasantha Gowda, Julie Evans, Neil Ashley, Susan M. Adams, Charlotte L. Alston, Emma L. Blakely and Garry K. Brown and has published in prestigious journals such as Neurology, Human Molecular Genetics and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Conrad Smith

5 papers receiving 164 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Conrad Smith United Kingdom	5	152	101	26	13	10	6	170
Taro Yamazaki Japan	6	175 1.2×	136 1.3×	29 1.1×	7 0.5×	5 0.5×	11	196
Marie‐Aude Spitz France	7	99 0.7×	29 0.3×	53 2.0×	21 1.6×	16 1.6×	11	136
Yngve Thomas Bliksrud Norway	7	87 0.6×	111 1.1×	14 0.5×	5 0.4×	7 0.7×	17	165
Karit Reinson Estonia	8	122 0.8×	80 0.8×	67 2.6×	36 2.8×	15 1.5×	14	198
Ilya Kanivets Russia	7	91 0.6×	29 0.3×	61 2.3×	11 0.8×	12 1.2×	39	162
Varunvenkat M. Srinivasan India	8	51 0.3×	39 0.4×	13 0.5×	7 0.5×	5 0.5×	36	113
Alexandra Bright United Kingdom	5	250 1.6×	173 1.7×	29 1.1×	25 1.9×	2 0.2×	8	276
Sanna Puusepp Estonia	6	84 0.6×	30 0.3×	77 3.0×	36 2.8×	14 1.4×	8	149
Michela Stagnaro Italy	5	66 0.4×	29 0.3×	38 1.5×	7 0.5×	18 1.8×	9	99
Anaïs Begemann Switzerland	3	51 0.3×	36 0.4×	47 1.8×	10 0.8×	26 2.6×	4	108

Countries citing papers authored by Conrad Smith

Since Specialization

Citations

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

Fields of papers citing papers by Conrad Smith

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Conrad Smith

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

All Works

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6 of 6 papers shown

1.

Labrum, Robyn, Charlotte L. Alston, Cathy E. Woodward, et al.. (2022). Genetic testing for mitochondrial disease: the United Kingdom best practice guidelines. European Journal of Human Genetics. 31(2). 148–163. 33 indexed citations

2.

Uusimaa, Johanna, Vasantha Gowda, Conrad Smith, et al.. (2013). Prospective study of POLG mutations presenting in children with intractable epilepsy: Prevalence and clinical features. Epilepsia. 54(6). 1002–1011. 34 indexed citations

3.

Pitceathly, Robert D. S., Susan E Tomlinson, Iain P. Hargreaves, et al.. (2012). Distal myopathy with cachexia: an unrecognised phenotype caused by dominantly-inherited mitochondrial polymerase γ mutations. Journal of Neurology Neurosurgery & Psychiatry. 84(1). 107–110. 13 indexed citations

4.

Fratter, Carl, Charlotte L. Alston, Emma L. Blakely, et al.. (2011). RRM2B mutations are frequent in familial PEO with multiple mtDNA deletions. Neurology. 76(23). 2032–2034. 45 indexed citations

5.

Ashley, Neil, A O'Rourke, Conrad Smith, et al.. (2008). Depletion of mitochondrial DNA in fibroblast cultures from patients with POLG1 mutations is a consequence of catalytic mutations. Human Molecular Genetics. 17(16). 2496–2506. 45 indexed citations

6.

Smith, Conrad, et al.. (2003). Educating the Masses: The Unfolding History of Black School Administrators in Arkansas, 1900–2000.

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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