Devin McQuaid

717 total citations
12 papers, 562 citations indexed

About

Devin McQuaid is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Devin McQuaid has authored 12 papers receiving a total of 562 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Devin McQuaid's work include Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (3 papers) and Cancer Genomics and Diagnostics (3 papers). Devin McQuaid is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (3 papers) and Cancer Genomics and Diagnostics (3 papers). Devin McQuaid collaborates with scholars based in United States, Canada and Greece. Devin McQuaid's co-authors include Norma J. Nowak, Jeffrey M. Conroy, John K. Cowell, Ravinesh A. Kumar, Camille W. Brune, Jyotsna Sudi, Edwin H. Cook, Samer Karamohamed, Judith A. Badner and Susan L. Christian and has published in prestigious journals such as Biological Psychiatry, British Journal of Cancer and Molecular Cancer Therapeutics.

In The Last Decade

Devin McQuaid

12 papers receiving 551 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Devin McQuaid United States 10 337 312 132 123 99 12 562
I. van der Bürgt Netherlands 16 455 1.4× 728 2.3× 85 0.6× 127 1.0× 137 1.4× 23 1.0k
Martine Doco‐Fenzy France 15 302 0.9× 349 1.1× 44 0.3× 59 0.5× 72 0.7× 29 690
María‐Isabel Tejada Spain 16 581 1.7× 389 1.2× 184 1.4× 69 0.6× 49 0.5× 46 758
Pamela Magini Italy 16 349 1.0× 347 1.1× 35 0.3× 119 1.0× 39 0.4× 38 717
Ruth N. MacKinnon Australia 15 449 1.3× 523 1.7× 136 1.0× 45 0.4× 25 0.3× 31 739
Peter B. Jacky United States 11 421 1.2× 274 0.9× 196 1.5× 40 0.3× 25 0.3× 23 594
Donna M. Muzny United States 15 456 1.4× 551 1.8× 103 0.8× 40 0.3× 23 0.2× 20 854
Ewa Bocian Poland 16 479 1.4× 346 1.1× 59 0.4× 62 0.5× 35 0.4× 51 683
Gordana Raca United States 12 235 0.7× 421 1.3× 29 0.2× 61 0.5× 59 0.6× 28 667
Eva Pipiras France 15 424 1.3× 475 1.5× 28 0.2× 80 0.7× 79 0.8× 26 744

Countries citing papers authored by Devin McQuaid

Since Specialization
Citations

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

Fields of papers citing papers by Devin McQuaid

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Devin McQuaid. 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 Devin McQuaid. The network helps show where Devin McQuaid may publish in the future.

Co-authorship network of co-authors of Devin McQuaid

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

All Works

12 of 12 papers shown
1.
Christian, Susan L., Camille W. Brune, Jyotsna Sudi, et al.. (2008). Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder. Biological Psychiatry. 63(12). 1111–1117. 216 indexed citations
2.
Miliaras, Dimosthenis, et al.. (2007). Karyotypic changes detected by comparative genomic hybridization in a stillborn infant with chorioangioma and liver hemangioma. Birth Defects Research Part A Clinical and Molecular Teratology. 79(3). 236–241. 10 indexed citations
3.
Gaile, Daniel P., Alan D. Hutson, Jeffrey M. Conroy, et al.. (2007). Errors in centering of array data can induce biases in correlation estimates. Journal of Statistical Planning and Inference. 137(11). 3446–3461. 2 indexed citations
4.
Swede, Helen, Jeremy D. Bartos, Neng Chen, et al.. (2006). Genomic profiles of colorectal cancers differ based on patient smoking status. Cancer Genetics and Cytogenetics. 168(2). 98–104. 7 indexed citations
5.
Varma, Rajesh, Huayi Huang, Norma J. Nowak, et al.. (2005). Array comparative genomic hybridisation (aCGH) analysis of premenopausal breast cancers from a nuclear fallout area and matched cases from Western New York. British Journal of Cancer. 93(6). 699–708. 23 indexed citations
6.
Rossi, Michael R., Jeffrey M. Conroy, Devin McQuaid, et al.. (2005). Array CGH analysis of pediatric medulloblastomas. Genes Chromosomes and Cancer. 45(3). 290–303. 46 indexed citations
7.
Rossi, Michael R., Daniel P. Gaile, Jeffrey R. LaDuca, et al.. (2005). Identification of consistent novel submegabase deletions in low‐grade oligodendrogliomas using array‐based comparative genomic hybridization. Genes Chromosomes and Cancer. 44(1). 85–96. 30 indexed citations
8.
Nowak, Norma J., Daniel P. Gaile, Jeffrey M. Conroy, et al.. (2005). Genome-wide aberrations in pancreatic adenocarcinoma. Cancer Genetics and Cytogenetics. 161(1). 36–50. 95 indexed citations
9.
Minderman, Hans, Jeffrey M. Conroy, Kieran L. O’Loughlin, et al.. (2005). In vitro and in vivo irinotecan-induced changes in expression profiles of cell cycle and apoptosis-associated genes in acute myeloid leukemia cells. Molecular Cancer Therapeutics. 4(6). 885–900. 34 indexed citations
10.
Cowell, John K., et al.. (2004). Identification and characterisation of constitutional chromosome abnormalities using arrays of bacterial artificial chromosomes. British Journal of Cancer. 90(4). 860–865. 30 indexed citations
11.
Cowell, John K., Sei‐Ichi Matsui, Jeffrey R. LaDuca, et al.. (2004). Application of bacterial artificial chromosome array-based comparative genomic hybridization and spectral karyotyping to the analysis of glioblastoma multiforme. Cancer Genetics and Cytogenetics. 151(1). 36–51. 55 indexed citations
12.
Collins, Yvonne, Tanja Pejović, Gil Mor, et al.. (2004). Identification of differentially expressed genes in clinically distinct groups of serous ovarian carcinomas using cDNA microarray. International Journal of Molecular Medicine. 14(1). 43–53. 14 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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