Sandra D. Dreyer

1.2k total citations
11 papers, 818 citations indexed

About

Sandra D. Dreyer is a scholar working on Molecular Biology, Genetics and Nephrology. According to data from OpenAlex, Sandra D. Dreyer has authored 11 papers receiving a total of 818 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Nephrology. Recurrent topics in Sandra D. Dreyer's work include RNA Research and Splicing (4 papers), Renal and related cancers (3 papers) and Connective tissue disorders research (3 papers). Sandra D. Dreyer is often cited by papers focused on RNA Research and Splicing (4 papers), Renal and related cancers (3 papers) and Connective tissue disorders research (3 papers). Sandra D. Dreyer collaborates with scholars based in United States, Germany and Canada. Sandra D. Dreyer's co-authors include Brendan Lee, Andreas Winterpacht, Bernhard Zabel, William G. Cole, Guang Zhou, Randy L. Johnson, Antonio Baldini, Kerby C. Oberg, Roy Morello and Yoshifumi Ninomiya and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and The American Journal of Human Genetics.

In The Last Decade

Sandra D. Dreyer

11 papers receiving 799 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sandra D. Dreyer United States 10 499 285 276 94 77 11 818
Carmen V. Pepicelli United States 7 1.2k 2.5× 248 0.9× 81 0.3× 88 0.9× 64 0.8× 8 1.6k
C McKeown United Kingdom 13 735 1.5× 551 1.9× 122 0.4× 139 1.5× 59 0.8× 25 1.3k
Katherine Holman Australia 15 529 1.1× 522 1.8× 66 0.2× 41 0.4× 28 0.4× 31 911
M. Le Merrer France 23 983 2.0× 919 3.2× 52 0.2× 84 0.9× 135 1.8× 93 1.8k
C. Pressman United States 7 533 1.1× 196 0.7× 27 0.1× 51 0.5× 17 0.2× 7 680
Carol A. Crowe United States 17 582 1.2× 318 1.1× 23 0.1× 100 1.1× 70 0.9× 28 904
Christelle Arrondel France 13 457 0.9× 271 1.0× 397 1.4× 54 0.6× 139 1.8× 17 980
A E Broadus United States 8 636 1.3× 137 0.5× 79 0.3× 64 0.7× 21 0.3× 8 968
Annegret Buske Germany 13 327 0.7× 227 0.8× 32 0.1× 82 0.9× 37 0.5× 18 908
David Bourn United Kingdom 13 132 0.3× 60 0.2× 107 0.4× 18 0.2× 41 0.5× 33 604

Countries citing papers authored by Sandra D. Dreyer

Since Specialization
Citations

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

Fields of papers citing papers by Sandra D. Dreyer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sandra D. Dreyer. 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 Sandra D. Dreyer. The network helps show where Sandra D. Dreyer may publish in the future.

Co-authorship network of co-authors of Sandra D. Dreyer

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

All Works

11 of 11 papers shown
1.
Dreyer, Sandra D., Takuji Naruse, Roy Morello, et al.. (2004). Lmx1b expression during joint and tendon formation: localization and evaluation of potential downstream targets. Gene Expression Patterns. 4(4). 397–405. 24 indexed citations
2.
Morello, Roy, Guang Zhou, Sandra D. Dreyer, et al.. (2001). Regulation of glomerular basement membrane collagen expression by LMX1B contributes to renal disease in nail patella syndrome. Nature Genetics. 27(2). 205–208. 141 indexed citations
3.
Dreyer, Sandra D.. (2000). LMX1B transactivation and expression in nail-patella syndrome. Human Molecular Genetics. 9(7). 1067–1074. 78 indexed citations
4.
Dreyer, Sandra D., Qiping Zheng, Bernhard Zabel, Andreas Winterpacht, & Brendan Lee. (1999). Isolation, Characterization, and Mapping of a Zinc Finger Gene, ZFP95, Containing Both a SCAN Box and an Alternatively Spliced KRAB A Domain. Genomics. 62(1). 119–122. 25 indexed citations
5.
Seri, Marco, Salvatore Melchionda, Sandra D. Dreyer, et al.. (1999). Identification of LMX1B gene point mutations in italian patients affected with Nail-Patella syndrome.. International Journal of Molecular Medicine. 4(3). 285–90. 23 indexed citations
6.
Dreyer, Sandra D., Guang Zhou, & Brendan Lee. (1999). The long and the short of it: developmental genetics of the skeletal dysplasias. Clinical Genetics. 57(s1). 50–59. 2 indexed citations
7.
Dreyer, Sandra D., Guang Zhou, & Brendan Lee. (1998). The long and the short of it: developmental genetics of the skeletal dysplasias. Clinical Genetics. 54(6). 464–473. 18 indexed citations
8.
Dreyer, Sandra D., Mark V. Clough, Wafaa Eyaid, et al.. (1998). Mutation Analysis of LMX1B Gene in Nail-Patella Syndrome Patients. The American Journal of Human Genetics. 63(6). 1651–1658. 117 indexed citations
9.
Payen, Emmanuel, David Michalovich, Sandra D. Dreyer, et al.. (1998). The Centromeric/Nucleolar Chromatin Protein ZFP-37 May Function to Specify Neuronal Nuclear Domains. Journal of Biological Chemistry. 273(15). 9099–9109. 29 indexed citations
10.
Dreyer, Sandra D., Guang Zhou, Antonio Baldini, et al.. (1998). Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome. Nature Genetics. 19(1). 47–50. 342 indexed citations
11.
Dreyer, Sandra D., Mirta A. Machado, William A. Horton, et al.. (1998). Cloning, characterization, and chromosomal assignment of the human ortholog of murine Zfp-37, a candidate gene for Nager syndrome. Mammalian Genome. 9(6). 458–462. 19 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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