Wayne S. Stanley

1.2k total citations
41 papers, 954 citations indexed

About

Wayne S. Stanley is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Wayne S. Stanley has authored 41 papers receiving a total of 954 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 9 papers in Genetics and 7 papers in Clinical Biochemistry. Recurrent topics in Wayne S. Stanley's work include Peroxisome Proliferator-Activated Receptors (10 papers), Genomic variations and chromosomal abnormalities (8 papers) and Metabolism and Genetic Disorders (7 papers). Wayne S. Stanley is often cited by papers focused on Peroxisome Proliferator-Activated Receptors (10 papers), Genomic variations and chromosomal abnormalities (8 papers) and Metabolism and Genetic Disorders (7 papers). Wayne S. Stanley collaborates with scholars based in United States, Australia and Japan. Wayne S. Stanley's co-authors include Inderjit Singh, Miguel Á. Contreras, Oscar Lazo, Mazzaz Hashmi, Carlos E. Irazú, A. Julian Garvin, Donald A. Sens, G. Shashidhar Pai, J L Sullivan and Daniel Bennett and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Neurology and Journal of Cell Science.

In The Last Decade

Wayne S. Stanley

41 papers receiving 916 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Wayne S. Stanley United States 18 685 251 241 150 102 41 954
Dominique Cottreau France 18 468 0.7× 103 0.4× 306 1.3× 110 0.7× 37 0.4× 47 929
Deborah A. Granger United States 9 724 1.1× 60 0.2× 106 0.4× 48 0.3× 63 0.6× 11 941
Lídia Feliubadaló Spain 15 463 0.7× 230 0.9× 31 0.1× 375 2.5× 107 1.0× 42 1.0k
Yoshihiro Horii Japan 17 434 0.6× 46 0.2× 49 0.2× 58 0.4× 76 0.7× 32 739
Susan C. Evans United States 19 739 1.1× 57 0.2× 39 0.2× 134 0.9× 88 0.9× 28 1.1k
S.A. Whitmore Australia 18 536 0.8× 18 0.1× 153 0.6× 255 1.7× 78 0.8× 26 1.3k
Barbára Giglioni Italy 29 1.1k 1.6× 22 0.1× 350 1.5× 215 1.4× 22 0.2× 68 1.9k
Chi‐Jiunn Pan United States 21 420 0.6× 60 0.2× 401 1.7× 619 4.1× 14 0.1× 34 1.5k
Yuichiro Saito Japan 15 757 1.1× 27 0.1× 84 0.3× 297 2.0× 41 0.4× 35 1.2k
Judith M. Podskalny United States 15 665 1.0× 16 0.1× 171 0.7× 134 0.9× 45 0.4× 28 1.0k

Countries citing papers authored by Wayne S. Stanley

Since Specialization
Citations

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

Fields of papers citing papers by Wayne S. Stanley

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Wayne S. Stanley

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

All Works

20 of 20 papers shown
1.
Mariani, Brian D., et al.. (2014). Comparison of array CGH and next generation sequencing for detection of a cryptic translocation identified by PGD. Fertility and Sterility. 102(3). e178–e179. 1 indexed citations
2.
Novik, Veronica, et al.. (2014). The accuracy of chromosomal microarray testing for identification of embryonic mosaicism in human blastocysts. Molecular Cytogenetics. 7(1). 18–18. 24 indexed citations
3.
Novik, Veronica, Erin Morris, Khoa D. Tran, et al.. (2012). Clinical validation for mosaicism detected in trophectoderm biopsy samples analyzed by chromosomal microarrays. Fertility and Sterility. 98(3). S136–S136. 1 indexed citations
4.
Stanley, Wayne S., et al.. (2002). Sensitivity of detection of B-cell lymphoma in bone marrow by fluorescence in situ hybridization. Cancer Genetics and Cytogenetics. 138(2). 174–176. 3 indexed citations
5.
Li, Marilyn M., et al.. (2000). Characterization and clinical implications of marker chromosomes identified at prenatal diagnosis. Prenatal Diagnosis. 20(2). 138–143. 6 indexed citations
6.
Stanley, Wayne S., Sandra Burkett, Albert Quiery, et al.. (1997). Constitutional inversion of chromosome 7 and hematologic cancers. Cancer Genetics and Cytogenetics. 96(1). 46–49. 12 indexed citations
7.
Saal, Howard M., et al.. (1996). Loss of the N-myc oncogene in a patient with a small interstitial deletion of the short arm of chromosome 2. American Journal of Medical Genetics. 66(4). 373–377. 10 indexed citations
8.
Stanley, Wayne S., et al.. (1993). Mosaic 5p tetrasomy. American Journal of Medical Genetics. 45(6). 774–776. 24 indexed citations
9.
Pagliaro, Lance C. & Wayne S. Stanley. (1993). Interphase FISH and morphologic analysis of AML. Cancer Genetics and Cytogenetics. 67(2). 95–100. 3 indexed citations
10.
Stanley, Wayne S., et al.. (1992). Longitudinal cytogenetic study of metaphase and interphase cells in childhood monosomy 7 syndrome. Cancer Genetics and Cytogenetics. 62(2). 160–165. 6 indexed citations
11.
Kremser, K, et al.. (1992). Complementation in Zellweger Syndrome: Biochemical Analysis of Newly Generated Peroxisomes. Human Heredity. 42(3). 172–178. 1 indexed citations
12.
Singh, Inderjit, Wayne S. Stanley, Takashi Hashimoto, Oscar Lazo, & Miguel Á. Contreras. (1991). Rhizomelic chondrodysplasia punctata: Biochemical studies of peroxisomes isolated from cultured skin fibroblasts. Archives of Biochemistry and Biophysics. 286(1). 277–283. 22 indexed citations
13.
Stanley, Wayne S., et al.. (1990). Infantile Fibrosarcoma—a Misnomer?. Pediatric Pathology. 10(6). 901–907. 26 indexed citations
14.
Lazo, Oscar, Miguel Á. Contreras, Alok Bhushan, Wayne S. Stanley, & Inderjit Singh. (1989). Adrenoleukodystrophy: Impaired oxidation of fatty acids due to peroxisomal lignoceroyl-CoA ligase deficiency. Archives of Biochemistry and Biophysics. 270(2). 722–728. 65 indexed citations
15.
Pai, G. Shashidhar, et al.. (1989). Bleomycin hypersensitivity in dyskeratosis congenita fibroblasts, lymphocytes, and transformed lymphoblasts. Cytogenetic and Genome Research. 52(3-4). 186–189. 21 indexed citations
16.
Hayward, Nicholas K., et al.. (1989). Spontaneous and 4-nitroquinoline 1-oxide-induced G2 chromosome aberrations in lymphoblasts from familial melanoma patients. Cancer Genetics and Cytogenetics. 39(2). 233–243. 4 indexed citations
17.
Stanley, Wayne S., et al.. (1988). Incidental detection of premature centromere separation in amniocytes associated with a mild form of Roberts syndrome. Prenatal Diagnosis. 8(8). 565–569. 13 indexed citations
18.
Stanley, Wayne S., et al.. (1987). Generation of phenotypically distinct macrophagehepatoma hybrid clones. Immunobiology. 174(4-5). 444–459. 4 indexed citations
19.
Garvin, A. Julian, Wayne S. Stanley, Daniel Bennett, J L Sullivan, & Donald A. Sens. (1986). The in vitro growth, heterotransplantation, and differentiation of a human rhabdomyosarcoma cell line.. PubMed. 125(1). 208–17. 60 indexed citations
20.
Stanley, Wayne S., et al.. (1985). Combined Phenotypic and Genotypic Analysis of Ringed Sideroblasts in Acquired Idiopathic Sideroblastic Anemia. Acta Haematologica. 73(4). 235–238. 2 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

Breakdown of academic impact, for papers by Dominique Cottreau Breakdown of academic impact, for papers by Deborah A. Granger Breakdown of academic impact, for papers by Lídia Feliubadaló Breakdown of academic impact, for papers by Yoshihiro Horii Breakdown of academic impact, for papers by Susan C. Evans Breakdown of academic impact, for papers by S.A. Whitmore Breakdown of academic impact, for papers by Barbára Giglioni Breakdown of academic impact, for papers by Chi‐Jiunn Pan Breakdown of academic impact, for papers by Yuichiro Saito Breakdown of academic impact, for papers by Judith M. Podskalny
Rankless by CCL
2026