Denise I. Quigley

1.2k total citations
19 papers, 807 citations indexed

About

Denise I. Quigley is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Denise I. Quigley has authored 19 papers receiving a total of 807 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Denise I. Quigley's work include Genomic variations and chromosomal abnormalities (4 papers), Receptor Mechanisms and Signaling (4 papers) and Genomics and Rare Diseases (3 papers). Denise I. Quigley is often cited by papers focused on Genomic variations and chromosomal abnormalities (4 papers), Receptor Mechanisms and Signaling (4 papers) and Genomics and Rare Diseases (3 papers). Denise I. Quigley collaborates with scholars based in United States, Japan and Canada. Denise I. Quigley's co-authors include David K. Grandy, Tristan Darland, Seksiri Arttamangkul, R. Ellen Magenis, Susan Amara, Susan B. Olson, Mark S. Sonders, Laura M. Harrison, Ge Zhang and James R. Bunzow and has published in prestigious journals such as Journal of Neuroscience, Molecular Pharmacology and Peptides.

In The Last Decade

Denise I. Quigley

18 papers receiving 776 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Denise I. Quigley United States 9 436 426 75 71 69 19 807
Ajay Ravindranathan United States 12 351 0.8× 409 1.0× 50 0.7× 105 1.5× 80 1.2× 17 927
Motohiko Takemura Japan 20 520 1.2× 650 1.5× 22 0.3× 108 1.5× 53 0.8× 70 1.3k
Nobue Kitanaka Japan 18 473 1.1× 446 1.0× 24 0.3× 105 1.5× 21 0.3× 63 1.0k
S. Huang United States 16 582 1.3× 376 0.9× 28 0.4× 65 0.9× 15 0.2× 21 882
Pierre Hickel France 7 255 0.6× 366 0.9× 25 0.3× 75 1.1× 51 0.7× 7 750
Daniel S. Cowen United States 22 569 1.3× 789 1.9× 17 0.2× 171 2.4× 86 1.2× 31 1.5k
Paul M. Sweetnam United States 21 569 1.3× 616 1.4× 20 0.3× 167 2.4× 24 0.3× 30 1.2k
Elías Utreras Chile 18 185 0.4× 379 0.9× 25 0.3× 223 3.1× 73 1.1× 27 806
Karin da Costa Calaza Brazil 19 291 0.7× 462 1.1× 9 0.1× 93 1.3× 48 0.7× 55 900
Peter Vanhoenacker Belgium 14 401 0.9× 578 1.4× 23 0.3× 85 1.2× 137 2.0× 25 971

Countries citing papers authored by Denise I. Quigley

Since Specialization
Citations

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

Fields of papers citing papers by Denise I. Quigley

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Denise I. Quigley. 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 Denise I. Quigley. The network helps show where Denise I. Quigley may publish in the future.

Co-authorship network of co-authors of Denise I. Quigley

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

All Works

19 of 19 papers shown
1.
Wen, Ting, Janice C. Palumbos, Betsy Ostrander, et al.. (2025). Vertical inheritance and unique differential phenotypes of reciprocal recombinant chromosome 18 within a multi-generation family. European Journal of Human Genetics. 34(1). 128–133.
2.
Mao, Rong, et al.. (2022). Atypical presentation of Angelman syndrome with intact expressive language due to low‐level mosaicism. Molecular Genetics & Genomic Medicine. 10(10). e2018–e2018. 2 indexed citations
3.
Leo, Michael C., Carmit K. McMullen, Benjamin S. Wilfond, et al.. (2016). Patients' ratings of genetic conditions validate a taxonomy to simplify decisions about preconception carrier screening via genome sequencing. American Journal of Medical Genetics Part A. 170(3). 574–582. 20 indexed citations
4.
Mascarello, James T., Betsy Hirsch, Hutton M. Kearney, et al.. (2011). Section E9 of the American College of Medical Genetics technical standards and guidelines: Fluorescence in situ hybridization. Genetics in Medicine. 13(7). 667–675. 58 indexed citations
5.
Foley, Kevin F & Denise I. Quigley. (2010). Pharmacogenomic potential of psychiatric medications and CYP2D6.. PubMed. 42(1). 32–4. 7 indexed citations
6.
Day, Stephen, Angela Hudson, Andrea Mast, et al.. (2009). Analytical performance of the Investigational Use Only Cervista™ HPV HR test as determined by a multi-center study. Journal of Clinical Virology. 45. S63–S72. 51 indexed citations
7.
Stuart, Robert K., et al.. (2008). Tetraploidy and 5q deletion in myelodysplastic syndrome: A case report. Cancer Genetics and Cytogenetics. 183(1). 64–68. 4 indexed citations
8.
Quigley, Denise I., Jessica K. Booker, & Daynna J. Wolff. (2007). The Prothrombin 20209C>T Sequence Variant: To Test or Not to Test.. PubMed. 33(2). 1–3. 1 indexed citations
9.
Laudadio, Jennifer, Denise I. Quigley, Raymond Tubbs, & Daynna J. Wolff. (2006). HER2 testing: a review of detection methodologies and their clinical performance. Expert Review of Molecular Diagnostics. 7(1). 53–64. 29 indexed citations
10.
Quigley, Denise I. & Daynna J. Wolff. (2006). Pediatric T-cell acute lymphoblastic leukemia with aberrations of both MLL loci. Cancer Genetics and Cytogenetics. 168(1). 77–79. 2 indexed citations
11.
Quigley, Denise I., Marie McDonald, Priya S. Kishnani, et al.. (2005). Triploid mosaicism in a 45,X/69,XXY infant. American Journal of Medical Genetics Part A. 138A(2). 171–174. 21 indexed citations
12.
Quigley, Denise I., et al.. (2004). A clinical report of a patient with two abnormal cell lines: 46,XX,del(21)(q22.1) and 47,XX,+3. American Journal of Medical Genetics Part A. 132A(1). 101–105. 1 indexed citations
13.
Quigley, Denise I., Kathleen Kaiser‐Rogers, Arthur S. Aylsworth, & Kathleen W. Rao. (2003). Submicroscopic deletion 9(q34.4) and duplication 19(p13.3): Identified by subtelomere specific FISH probes. American Journal of Medical Genetics Part A. 125A(1). 67–72. 8 indexed citations
14.
Bunzow, James R., Mark S. Sonders, Seksiri Arttamangkul, et al.. (2001). Amphetamine, 3,4-Methylenedioxymethamphetamine, Lysergic Acid Diethylamide, and Metabolites of the Catecholamine Neurotransmitters Are Agonists of a Rat Trace Amine Receptor. Molecular Pharmacology. 60(6). 1181–1188. 497 indexed citations
15.
Quigley, Denise I., Seksiri Arttamangkul, Richard G. Allen, & David K. Grandy. (2000). Integrity of tritiated orphanin FQ/Nociceptin: implications for establishing a reliable binding assay. Peptides. 21(7). 1111–1118. 4 indexed citations
16.
Allen, Charles N., Zhi‐Gen Jiang, Koji Teshima, et al.. (1999). Orphanin-FQ/Nociceptin (OFQ/N) Modulates the Activity of Suprachiasmatic Nucleus Neurons. Journal of Neuroscience. 19(6). 2152–2160. 62 indexed citations
17.
Quigley, Denise I., John G. McDougall, Tristan Darland, et al.. (1998). Orphanin FQ is the Major OFQ1–17-Containing Peptide Produced in the Rodent and Monkey Hypothalamus. Peptides. 19(1). 133–139. 24 indexed citations
18.
Goodwin, Edwin H., Julianne Meyne, Susan M. Bailey, & Denise I. Quigley. (1996). On the origin of lateral asymmetry. Chromosoma. 104(5). 345–347. 15 indexed citations
19.
Goodwin, Edwin H., Julianne Meyne, Susan M. Bailey, & Denise I. Quigley. (1996). On the origin of lateral asymmetry. Chromosoma. 104(5). 345–347. 1 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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