Richard S. Spielman

17.0k total citations · 2 hit papers
119 papers, 11.9k citations indexed

About

Richard S. Spielman is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Richard S. Spielman has authored 119 papers receiving a total of 11.9k indexed citations (citations by other indexed papers that have themselves been cited), including 62 papers in Genetics, 46 papers in Molecular Biology and 16 papers in Surgery. Recurrent topics in Richard S. Spielman's work include Genetic Associations and Epidemiology (22 papers), Diabetes and associated disorders (18 papers) and Genetic Mapping and Diversity in Plants and Animals (16 papers). Richard S. Spielman is often cited by papers focused on Genetic Associations and Epidemiology (22 papers), Diabetes and associated disorders (18 papers) and Genetic Mapping and Diversity in Plants and Animals (16 papers). Richard S. Spielman collaborates with scholars based in United States, United Kingdom and Brazil. Richard S. Spielman's co-authors include Warren J. Ewens, Ralph McGinnis, Vivian G. Cheung, Michael P. Morley, Kathryn G. Ewens, Teresa M. Weber, Joshua Burdick, Cliona Molony, Patrick Concannon and Richard S. Legro and has published in prestigious journals such as Nature, Science and Proceedings of the National Academy of Sciences.

In The Last Decade

Richard S. Spielman

118 papers receiving 11.4k citations

Hit Papers

align trajectories

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.

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM).

1993 2.9k citations Richard S. Spielman, Ralph McGinnis et al. profile →
Genetic analysis of genome-wide variation in human gene expression

2004 946 citations Michael P. Morley, Kathryn G. Ewens et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Richard S. Spielman United States	46	6.1k	4.5k	1.5k	1.3k	1.1k	119	11.9k
Marianne LeMeur France	39	3.9k 0.6×	8.2k 1.8×	2.3k 1.5×	1.9k 1.5×	789 0.7×	55	13.4k
Joseph H. Nadeau United States	54	5.9k 1.0×	7.3k 1.6×	1.0k 0.7×	1.3k 1.0×	681 0.6×	244	13.1k
Kāri Stefánsson Iceland	80	6.1k 1.0×	6.5k 1.4×	1.5k 1.0×	799 0.6×	381 0.4×	246	17.8k
Dale D. Dykes United States	17	4.9k 0.8×	6.7k 1.5×	2.4k 1.6×	1.6k 1.3×	1.3k 1.2×	47	18.2k
Christine M. Distèche United States	67	6.9k 1.1×	10.6k 2.3×	2.3k 1.5×	718 0.6×	350 0.3×	226	17.3k
Andrew P. Morris United Kingdom	54	4.8k 0.8×	4.3k 1.0×	1.0k 0.7×	744 0.6×	446 0.4×	229	11.4k
P. Pearson Netherlands	55	4.7k 0.8×	6.3k 1.4×	464 0.3×	578 0.5×	388 0.4×	209	10.7k
Daniel Cohen France	48	3.2k 0.5×	5.6k 1.2×	1.2k 0.8×	2.3k 1.8×	1.4k 1.3×	174	11.9k
Daniel E. Weeks United States	53	4.6k 0.8×	3.4k 0.8×	1.1k 0.7×	694 0.6×	426 0.4×	214	10.7k
Herbert F. Polesky United States	25	5.1k 0.8×	6.8k 1.5×	2.6k 1.7×	1.7k 1.3×	1.3k 1.2×	135	19.7k

Countries citing papers authored by Richard S. Spielman

Since Specialization

Citations

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

Fields of papers citing papers by Richard S. Spielman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Richard S. Spielman. 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 Richard S. Spielman. The network helps show where Richard S. Spielman may publish in the future.

Co-authorship network of co-authors of Richard S. Spielman

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

All Works

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20 of 20 papers shown

Cheung, Vivian G., Renuka R. Nayak, Isabel X. Wang, et al.. (2010). Polymorphic Cis- and Trans-Regulation of Human Gene Expression. PLoS Biology. 8(9). e1000480–e1000480. 122 indexed citations

Cheung, Vivian G. & Richard S. Spielman. (2009). Genetics of human gene expression: mapping DNA variants that influence gene expression. Nature Reviews Genetics. 10(9). 595–604. 166 indexed citations

Cheung, Vivian G. & Richard S. Spielman. (2007). Data for Genetic Analysis Workshop (GAW) 15, Problem 1: genetics of gene expression variation in humans. BMC Proceedings. 1(S1). S2–S2. 15 indexed citations

Werner, Petra, M Raducha, Elaine A. Ostrander, et al.. (2005). The keeshond defect in cardiac conotruncal development is oligogenic1. Human Genetics. 116(5). 368–377. 22 indexed citations

Ewens, Warren J. & Richard S. Spielman. (2004). Reply to Wittkowski and Liu (Beyond the TDT: Rejoinder to Ewens and Spielman). Human Heredity. 58(1). 61–62. 1 indexed citations

Önengüt-Gümüşcü, Suna, Kathryn G. Ewens, Richard S. Spielman, & Patrick Concannon. (2004). A functional polymorphism (1858C/T) in the PTPN22 gene is linked and associated with type I diabetes in multiplex families. Genes and Immunity. 5(8). 678–680. 107 indexed citations

Williams, Sloan R., Napoleon A. Chagnon, & Richard S. Spielman. (2002). Nuclear and mitochondrial genetic variation in the Yanomamö: A test case for ancient DNA studies of prehistoric populations. American Journal of Physical Anthropology. 117(3). 246–246.

Watts, Jason A., Michael P. Morley, Joshua Burdick, et al.. (2002). Gene Expression Phenotype in Heterozygous Carriers of Ataxia Telangiectasia. The American Journal of Human Genetics. 71(4). 791–800. 38 indexed citations

Cox, Nancy J., Beth Wapelhorst, Victoria Morrison, et al.. (2001). Seven Regions of the Genome Show Evidence of Linkage to Type 1 Diabetes in a Consensus Analysis of 767 Multiplex Families. The American Journal of Human Genetics. 69(4). 820–830. 203 indexed citations

10.

Ewens, Warren J. & Richard S. Spielman. (1998). Reply to Laird et al.. The American Journal of Human Genetics. 63(6). 1915–1915. 3 indexed citations

11.

Concannon, Patrick, K J Gogolin-Ewens, David A. Hinds, et al.. (1998). A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus. Nature Genetics. 19(3). 292–296. 265 indexed citations

12.

Yamagata, Kazuya, Jun Takeda, Stephan Menzel, et al.. (1996). Searching for NIDDM susceptibility genes: studies of genes with triplet repeats expressed in skeletal muscle. Diabetologia. 39(6). 725–730. 2 indexed citations

13.

McGinnis, Ralph & Richard S. Spielman. (1995). Insulin Gene 5′ Flanking Polymorphism: Length of Class 1 Alleles in Number of Repeat Units. Diabetes. 44(11). 1296–1302. 35 indexed citations

14.

Stirling, Brigid, Nancy J. Cox, Graeme I. Bell, et al.. (1995). Linkage studies in NIDDM with markers near the sulphonylurea receptor gene. Diabetologia. 38(12). 1479–1481. 18 indexed citations

15.

Stirling, Brigid, Nancy J. Cox, Graeme I. Bell, et al.. (1995). Identification of Microsatellite Markers Near the Human ob Gene and Linkage Studies in NIDDM-Affected Sib Pairs. Diabetes. 44(8). 999–1001. 29 indexed citations

16.

Blanché, Hélène, Gilles Vergnaud, Béatrice Gouyon, et al.. (1992). Genetic mapping of three human homologues of murine t-complex genes localizes TCP10 to 6q27, 15 cM distal to TCP1 and PLG. Genomics. 12(4). 826–828. 7 indexed citations

17.

Spielman, Richard S., Max P. Baur, & Françoise Clerget‐Darpoux. (1989). Genetic analysis of IDDM: Summary of GAW5 IDDM results. Genetic Epidemiology. 6(1). 43–58. 45 indexed citations

18.

Cox, Nancy J., et al.. (1989). Four RFLPs of the human insulin receptor gene: Pstl, Kpnl, Rsal (2 RFLPs). Nucleic Acids Research. 17(2). 820–820. 1 indexed citations

19.

Cox, Nancy J., et al.. (1988). Four RFLPS of the human insulin receptor gene: PstI, KpnI, RsaI (2 RFLPs). Nucleic Acids Research. 16(16). 8204–8204. 4 indexed citations

20.

Spielman, Richard S.. (1977). Registers for the detection and prevention of genetic disease. The American Journal of Human Genetics. 29(4). 411–412. 13 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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