Seth Dobrin

1.1k total citations
15 papers, 789 citations indexed

About

Seth Dobrin is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Seth Dobrin has authored 15 papers receiving a total of 789 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 6 papers in Genetics and 2 papers in Surgery. Recurrent topics in Seth Dobrin's work include Genetic Associations and Epidemiology (4 papers), Gene expression and cancer classification (3 papers) and Genomic variations and chromosomal abnormalities (2 papers). Seth Dobrin is often cited by papers focused on Genetic Associations and Epidemiology (4 papers), Gene expression and cancer classification (3 papers) and Genomic variations and chromosomal abnormalities (2 papers). Seth Dobrin collaborates with scholars based in United States, Ireland and United Kingdom. Seth Dobrin's co-authors include Kevin A. Strauss, D. Holmes Morton, Erik G. Puffenberger, Dietrich A. Stephan, Matthew J. Huentelman, David Page, Jan Struyf, S. Roche, Patrick O. McKeon and E. Claffey and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Stroke.

In The Last Decade

Seth Dobrin

14 papers receiving 774 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Seth Dobrin United States 8 441 372 239 89 80 15 789
Polina Bukshpun United States 15 269 0.6× 281 0.8× 334 1.4× 66 0.7× 59 0.7× 16 1.0k
Claudio Toma Spain 21 527 1.2× 359 1.0× 359 1.5× 153 1.7× 151 1.9× 41 1.0k
Ismail Thanseem Japan 15 317 0.7× 462 1.2× 262 1.1× 98 1.1× 63 0.8× 28 877
Sylvia Dobrzeniecka Canada 16 573 1.3× 575 1.5× 127 0.5× 151 1.7× 52 0.7× 17 969
S. Schaeffer France 9 547 1.2× 456 1.2× 272 1.1× 186 2.1× 47 0.6× 14 831
Joel Almajano United States 3 420 1.0× 330 0.9× 456 1.9× 217 2.4× 40 0.5× 3 809
Paolo Alfieri Italy 20 327 0.7× 648 1.7× 187 0.8× 144 1.6× 108 1.4× 69 1.1k
Reymundo Lozano United States 20 819 1.9× 552 1.5× 519 2.2× 100 1.1× 81 1.0× 44 1.1k
Markéta Havlovičová Czechia 14 274 0.6× 244 0.7× 215 0.9× 135 1.5× 92 1.1× 33 643
Holly N. Cukier United States 16 518 1.2× 525 1.4× 403 1.7× 147 1.7× 84 1.1× 26 1.0k

Countries citing papers authored by Seth Dobrin

Since Specialization
Citations

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

Fields of papers citing papers by Seth Dobrin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Seth Dobrin

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

All Works

15 of 15 papers shown
1.
Dobrin, Seth. (2024). AI iQ for a Human-Focused Future. 2 indexed citations
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Raggio, Cathleen, Philip F. Giampietro, Seth Dobrin, et al.. (2009). A novel locus for adolescent idiopathic scoliosis on chromosome 12p. Journal of Orthopaedic Research®. 27(10). 1366–1372. 40 indexed citations
5.
Struyf, Jan, Seth Dobrin, & David Page. (2008). Combining gene expression, demographic and clinical data in modeling disease: a case study of bipolar disorder and schizophrenia. BMC Genomics. 9(1). 531–531. 33 indexed citations
6.
Roche, S., Chunping Zhao, E. Claffey, et al.. (2007). Candidate gene analysis of 21q22: Support for S100B as a susceptibility gene for bipolar affective disorder with psychosis. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(8). 1094–1096. 50 indexed citations
7.
Cassidy, Frederick, et al.. (2007). Genome‐wide scan of bipolar disorder and investigation of population stratification effects on linkage: Support for susceptibility loci at 4q21, 7q36, 9p21, 12q24, 14q24, and 16p13. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(6). 791–801. 31 indexed citations
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Strauss, Kevin A., Erik G. Puffenberger, Matthew J. Huentelman, et al.. (2006). Recessive Symptomatic Focal Epilepsy and Mutant Contactin-Associated Protein-like 2. New England Journal of Medicine. 354(13). 1370–1377. 479 indexed citations
11.
Motsinger‐Reif, Alison A., Marylyn D. Ritchie, & Seth Dobrin. (2006). Clinical applications of whole-genome association studies: future applications at the bedside. Expert Review of Molecular Diagnostics. 6(4). 551–565. 10 indexed citations
12.
Dobrin, Seth, et al.. (2006). Automating Microsatellite Genotyping with Array Tape. JALA Journal of the Association for Laboratory Automation. 11(4). 260–267. 1 indexed citations
13.
Puffenberger, Erik G., Diane Hu‐Lince, David W. Craig, et al.. (2004). Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function. Proceedings of the National Academy of Sciences. 101(32). 11689–11694. 108 indexed citations
14.
Meyer, Jobst, et al.. (2004). No causative DLL4 mutations in periodic catatonia patients from 15q15 linked families. Schizophrenia Research. 75(1). 1–3. 5 indexed citations
15.
Dobrin, Seth & Dietrich Stephan. (2003). Integrating microarrays into disease-gene identification strategies. Expert Review of Molecular Diagnostics. 3(3). 375–385. 7 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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