Stephen T. Reeders

7.4k total citations · 2 hit papers
83 papers, 5.7k citations indexed

About

Stephen T. Reeders is a scholar working on Genetics, Molecular Biology and Immunology and Allergy. According to data from OpenAlex, Stephen T. Reeders has authored 83 papers receiving a total of 5.7k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Genetics, 49 papers in Molecular Biology and 16 papers in Immunology and Allergy. Recurrent topics in Stephen T. Reeders's work include Genetic and Kidney Cyst Diseases (41 papers), Renal and related cancers (28 papers) and Genetic Syndromes and Imprinting (17 papers). Stephen T. Reeders is often cited by papers focused on Genetic and Kidney Cyst Diseases (41 papers), Renal and related cancers (28 papers) and Genetic Syndromes and Imprinting (17 papers). Stephen T. Reeders collaborates with scholars based in United States, United Kingdom and Netherlands. Stephen T. Reeders's co-authors include Karl Tryggvason, Richard A. Wells, Jacob W. IJdo, Antonio Baldini, Billy G. Hudson, Mariko Mariyama, D. J. Weatherall, Toshio Mochizuki, Kay E. Davies and Douglas R. Higgs and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Stephen T. Reeders

80 papers receiving 5.6k 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.

A highly polymorphic DNA marker linked to adult polycystic kidney disease on chromosome 16

1985 518 citations Stephen T. Reeders, M.H. Breuning et al. Nature profile →
Improved telomere detection using a telomere repeat probe (TTAGGG)_ngenerated by PCR

1991 517 citations Jacob W. IJdo, Richard A. Wells et al. Nucleic Acids Research profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stephen T. Reeders United States	37	2.9k	2.9k	1.2k	849	537	83	5.7k
Bernhard Zabel Germany	50	7.2k 2.5×	4.7k 1.6×	620 0.5×	391 0.5×	329 0.6×	166	11.0k
Dominique Weil France	53	6.7k 2.3×	1.4k 0.5×	617 0.5×	362 0.4×	61 0.1×	184	9.8k
Daniel H. Cohn United States	47	3.9k 1.4×	4.1k 1.4×	937 0.8×	106 0.1×	73 0.1×	142	7.3k
Thomas Gridley United States	68	12.8k 4.4×	2.6k 0.9×	674 0.6×	218 0.3×	77 0.1×	146	17.7k
Roger A. Pedersen United States	63	12.5k 4.3×	3.2k 1.1×	592 0.5×	346 0.4×	51 0.1×	156	16.0k
Jordan A. Kreidberg United States	52	6.4k 2.2×	1.8k 0.6×	2.2k 1.9×	64 0.1×	1.3k 2.5×	89	10.1k
Veronica van Heyningen United Kingdom	64	12.3k 4.3×	5.0k 1.7×	210 0.2×	680 0.8×	90 0.2×	212	15.9k
Yasuhide Furuta Japan	37	5.6k 2.0×	1.4k 0.5×	1.5k 1.3×	138 0.2×	75 0.1×	85	8.2k
Michel Goossens France	50	3.5k 1.2×	2.2k 0.8×	153 0.1×	181 0.2×	76 0.1×	170	8.1k
Antonio Baldini United States	50	8.5k 2.9×	3.4k 1.2×	98 0.1×	1.4k 1.7×	160 0.3×	191	10.8k

Countries citing papers authored by Stephen T. Reeders

Since Specialization

Citations

This map shows the geographic impact of Stephen T. Reeders'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 Stephen T. Reeders with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephen T. Reeders more than expected).

Fields of papers citing papers by Stephen T. Reeders

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephen T. Reeders. 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 Stephen T. Reeders. The network helps show where Stephen T. Reeders may publish in the future.

Co-authorship network of co-authors of Stephen T. Reeders

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Zhou, Jing & Stephen T. Reeders. (2015). The a Chains of Type IV Collagen. Contributions to nephrology. 117. 80–104. 3 indexed citations

Chen, Xing-Zhen, Peter Vassilev, Nùria Basora, et al.. (1999). Polycystin-L is a calcium-regulated cation channel permeable to calcium ions. Nature. 401(6751). 383–386. 182 indexed citations

Schneider, Michael, Hideki Nomura, Jing Zhou, et al.. (1996). A Gene Similar to PKD1 Maps to Chromosome 4q22: A Candidate Gene for PKD2. Genomics. 38(1). 1–4. 20 indexed citations

Duyk, Geoffrey M., et al.. (1996). Structural motifs of the PKD1 protein. Nephrology Dialysis Transplantation. 11(supp6). 2–4. 16 indexed citations

Lisowsky, Thomas, Debra Weinstat‐Saslow, N.J. Barton, Stephen T. Reeders, & Michael Schneider. (1995). A New Human Gene Located in thePKD1Region of Chromosome 16 Is a Functional Homologue toERV1of Yeast. Genomics. 29(3). 690–697. 48 indexed citations

Liu, P., Julio C. Siciliano, Randy J. Legerski, et al.. (1993). Regional mapping of human DNA excision repair gene ERCC4 to chromosome 16pl3.13–pl3.2. Mutagenesis. 8(3). 199–205. 18 indexed citations

Weinstat‐Saslow, Debra, Gregory G. Germino, Stefan Somlo, & Stephen T. Reeders. (1993). A transducin-like gene maps to the autosomal dominant polycystic kidney disease gene region. Genomics. 18(3). 709–711. 5 indexed citations

Germino, Gregory G., Debra Weinstat‐Saslow, Heinz Himmelbauer, et al.. (1992). The gene for autosomal dominant polycystic kidney disease lies in a 750-kb CpG-rich region. Genomics. 13(1). 144–151. 65 indexed citations

Somlo, Stefan, Brunhilde Wirth, Gregory G. Germino, et al.. (1992). Fine genetic localization of the gene for autosomal dominant polycystic kidney disease (PKD1) with respect to physically mapped markers. Genomics. 13(1). 152–158. 29 indexed citations

10.

IJdo, Jacob W., Antonio Baldini, Richard A. Wells, David C. Ward, & Stephen T. Reeders. (1992). FRA2B is distinct from inverted telomere repeat arrays at 2q13. Genomics. 12(4). 833–835. 20 indexed citations

11.

Mariyama, Mariko, et al.. (1992). Colocalization of the genes for the α3(IV) and α4(IV) chains of type IV collagen to chromosome 2 bands q35–q37. Genomics. 13(3). 809–813. 81 indexed citations

12.

Himmelbauer, Heinz, Gregory G. Germino, Debra Weinstat‐Saslow, et al.. (1992). Human-mouse homologies in the region of the polycystic kidney disease gene (PKD1). Genomics. 13(1). 35–38. 22 indexed citations

13.

IJdo, Jacob W., Richard A. Wells, Antonio Baldini, & Stephen T. Reeders. (1991). Improved telomere detection using a telomere repeat probe (TTAGGG)_ngenerated by PCR. Nucleic Acids Research. 19(17). 4780–4780. 517 indexed citations breakdown →

14.

Gillespie, Gerald A.J., Stefan Somlo, Gregory G. Germino, Debra Weinstat‐Saslow, & Stephen T. Reeders. (1991). CpG island in the region of an autosomal dominant polycystic kidney disease locus defines the 5' end of a gene encoding a putative proton channel.. Proceedings of the National Academy of Sciences. 88(10). 4289–4293. 47 indexed citations

15.

Lamb, Janette, R H Lindenbaum, Stephen T. Reeders, et al.. (1989). DETECTION OF BREAKPOINTS IN SUBMICROSCOPIC CHROMOSOMAL TRANSLOCATION, ILLUSTRATING AN IMPORTANT MECHANISM FOR GENETIC DISEASE. The Lancet. 334(8667). 819–824. 71 indexed citations

16.

Ramsay, Michèle, Stephen T. Reeders, Peter D. Thomson, et al.. (1988). Mutations for the autosomal recessive and autosomal dominant forms of polycystic kidney disease are not allelic. Human Genetics. 79(1). 73–75. 10 indexed citations

17.

Reeders, Stephen T., M.H. Breuning, G. CORNEY, et al.. (1986). Two genetic markers closely linked to adult polycystic kidney disease on chromosome 16.. BMJ. 292(6524). 851–853. 74 indexed citations

18.

Reeders, Stephen T., M.H. Breuning, G. CORNEY, et al.. (1986). Two Genetic Markers Closely Linked to Adult Polycystic Kidney Disease on Chromosome 16. The Journal of Urology. 136(4). 987–987. 13 indexed citations

19.

Swann, R A, Sharne Foulkes, B. Holmes, et al.. (1985). "Agrobacterium yellow group" and Pseudomonas paucimobilis causing peritonitis in patients receiving continuous ambulatory peritoneal dialysis.. Journal of Clinical Pathology. 38(11). 1293–1299. 28 indexed citations

20.

Ratcliffe, Peter J., Stephen T. Reeders, & J M Theaker. (1984). Bleeding oesophageal varices and hepatic dysfunction in adult polycystic kidney disease.. BMJ. 288(6427). 1330–1331. 33 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.

Explore authors with similar magnitude of impact