Loris McGavran

3.8k total citations · 1 hit paper
61 papers, 2.7k citations indexed

About

Loris McGavran is a scholar working on Molecular Biology, Hematology and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Loris McGavran has authored 61 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 18 papers in Hematology and 14 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Loris McGavran's work include Acute Myeloid Leukemia Research (15 papers), Acute Lymphoblastic Leukemia research (14 papers) and Genomic variations and chromosomal abnormalities (8 papers). Loris McGavran is often cited by papers focused on Acute Myeloid Leukemia Research (15 papers), Acute Lymphoblastic Leukemia research (14 papers) and Genomic variations and chromosomal abnormalities (8 papers). Loris McGavran collaborates with scholars based in United States, Canada and Tunisia. Loris McGavran's co-authors include Lynne Meltesen, Stephen P. Hunger, John M. Opitz, Lorrie F. Odom, Ann C. M. Smith, Natalie B. Parker, Bette K. Kleinschmidt‐DeMasters, James M. Sikela, James F. Reynolds and Janet K. Stephens and has published in prestigious journals such as Science, Journal of Clinical Oncology and Blood.

In The Last Decade

Loris McGavran

61 papers receiving 2.6k 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.

Increased Epidermal Growth Factor Receptor Gene Copy Number Is Associated With Poor Prognosis in Head and Neck Squamous Cell Carcinomas

2006 448 citations Loris McGavran, Natalie B. Parker et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Loris McGavran United States	24	1.2k	670	579	427	412	61	2.7k
E N Geissler United States	17	1.9k 1.6×	658 1.0×	443 0.8×	461 1.1×	310 0.8×	19	4.5k
John R.W. Yates United Kingdom	33	2.2k 1.9×	1.5k 2.2×	495 0.9×	563 1.3×	494 1.2×	82	5.4k
Erik C. Thorland United States	28	1.8k 1.5×	2.1k 3.2×	542 0.9×	185 0.4×	288 0.7×	61	4.2k
Ken-ichiro Kosai Japan	23	1.1k 0.9×	466 0.7×	257 0.4×	66 0.2×	415 1.0×	47	2.2k
Omar A. Ibrahimi United States	24	3.3k 2.8×	1.1k 1.7×	394 0.7×	212 0.5×	410 1.0×	54	4.6k
Herzl Ben‐Hur Israel	19	947 0.8×	281 0.4×	1.1k 1.8×	156 0.4×	309 0.8×	80	3.2k
María P. De Miguel Spain	31	1.1k 0.9×	427 0.6×	250 0.4×	214 0.5×	559 1.4×	101	3.1k
Ralf Dressel Germany	32	2.5k 2.1×	440 0.7×	387 0.7×	114 0.3×	513 1.2×	107	4.1k
Tomoko Nakanishi Japan	4	1.3k 1.1×	494 0.7×	215 0.4×	82 0.2×	351 0.9×	9	2.5k
Maria Cristina Magli Italy	29	2.2k 1.9×	814 1.2×	296 0.5×	105 0.2×	385 0.9×	63	3.9k

Countries citing papers authored by Loris McGavran

Since Specialization

Citations

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

Fields of papers citing papers by Loris McGavran

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Loris McGavran

This figure shows the co-authorship network connecting the top 25 collaborators of Loris McGavran. A scholar is included among the top collaborators of Loris McGavran 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 Loris McGavran. Loris McGavran 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

Taylor, Matthew R.G., et al.. (2010). High prevalence of array comparative genomic hybridization abnormalities in adults with unexplained intellectual disability. Genetics in Medicine. 12(1). 32–38. 9 indexed citations

Myers, Jeremy B., et al.. (2007). Teratoid Wilms’ tumor, an important variant of nephroblastoma. Journal of Pediatric Urology. 3(4). 282–286. 17 indexed citations

Kleinschmidt‐DeMasters, Bette K., Lynne Meltesen, Loris McGavran, & Kevin O. Lillehei. (2006). Characterization of Glioblastomas in Young Adults. Brain Pathology. 16(4). 273–286. 42 indexed citations

Trobaugh‐Lotrario, Angela D., Morris Kletzel, Ralph Quinones, et al.. (2004). Monosomy 7 associated with pediatric acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS): successful management by allogeneic hematopoietic stem cell transplant (HSCT). Bone Marrow Transplantation. 35(2). 143–149. 22 indexed citations

Liu, Lanting, et al.. (2004). Nonpositive Terminal Deoxynucleotidyl Transferase in Pediatric Precursor B-Lymphoblastic Leukemia. American Journal of Clinical Pathology. 121(6). 810–815. 15 indexed citations

Tsai, Anne Chun‐Hui, et al.. (2003). A child with Angelman syndrome and trisomy 13 findings due to associated paternal UPD 15 and segmental UPD 13. American Journal of Medical Genetics Part A. 126A(2). 208–212. 18 indexed citations

Lear-Kaul, Kelly C., et al.. (2003). Her-2/neu status in breast cancer metastases to the central nervous system.. PubMed. 127(11). 1451–7. 48 indexed citations

Thomas, James A., John P. Johnson, Rebecca L. Wilson, et al.. (2003). Genetic and clinical characterization of patients with an interstitial duplication 15q11‐q13, emphasizing behavioral phenotype and response to treatment. American Journal of Medical Genetics Part A. 119A(2). 111–120. 49 indexed citations

Fleitz, Julie, Sandra L. Wootton‐Gorges, Josephine Wyatt‐Ashmead, et al.. (2003). Renal cell carcinoma in long-term survivors of advanced stage neuroblastoma in early childhood. Pediatric Radiology. 33(8). 540–545. 35 indexed citations

10.

Wyatt‐Ashmead, Josephine, Bette K. Kleinschmidt‐DeMasters, Gary W. Mierau, et al.. (2001). Choroid Plexus Carcinomas and Rhabdoid Tumors: Phenotypic and Genotypic Overlap. Pediatric and Developmental Pathology. 4(6). 545–549. 21 indexed citations

11.

Kadan‐Lottick, Nina S., Linda C. Stork, Stephanie Z. Ruyle, et al.. (2000). Cytogenetic abnormalities in a case of botryoid rhabdomyosarcoma. Medical and Pediatric Oncology. 34(4). 293–295. 5 indexed citations

12.

McGavran, Loris, et al.. (1999). TEL-AML1 fusion identifies a subset of children with standard risk acute lymphoblastic leukemia who have an excellent prognosis when treated with therapy that includes a single delayed intensification. Leukemia. 13(11). 1708–1712. 35 indexed citations

13.

McGavran, Loris, et al.. (1998). Alternative splicing in wild-type AF10 and CALM cDNAs and in AF10-CALM and CALM-AF10 fusion cDNAs produced by the t(10;11)(p13–14;q14–q21) suggests a potential role for truncated AF10 polypeptides. Leukemia. 12(9). 1404–1410. 26 indexed citations

14.

Hunger, Stephen P., et al.. (1997). Hyperdiploidy andE2A-PBX1 fusion in an adult with t(1;19)+ acute lymphoblastic leukemia: Case report and review of the literature. Genes Chromosomes and Cancer. 20(4). 392–398. 19 indexed citations

15.

Wachtel, S S, David W. Sammons, Michael W. Manley, et al.. (1996). Fetal cells in maternal blood: recovery by charge flow separation. Human Genetics. 98(2). 162–166. 50 indexed citations

16.

McGavran, Loris, et al.. (1995). Intracranial Malignant Germ Cell Tumor and the Klinefelter Syndrome. Pediatric Neurosurgery. 23(4). 219–224. 17 indexed citations

17.

Poole, Steven R., Ann C. M. Smith, Taru Hays, Loris McGavran, & Arleen D. Auerbach. (1992). Monozygotic twin girls with congenital malformations resembling Fanconi anemia. American Journal of Medical Genetics. 42(6). 780–784. 16 indexed citations

18.

McGavran, Loris, et al.. (1990). Sister Chromatid Exchanges and Chromosome Aberration Frequencies in Plutonium Workers. International Journal of Radiation Biology. 58(1). 195–207. 22 indexed citations

19.

Timmons, Charles F., et al.. (1989). Hyperdiploidy including trisomy 8 in a cystic partially differentiated nephroblastoma. Cancer Genetics and Cytogenetics. 41(1). 79–85. 9 indexed citations

20.

Heideman, Richard L., Loris McGavran, & Gail Waldstein. (1986). Nephroblastomatosis and Deletion of lip. Journal of Pediatric Hematology/Oncology. 8(3). 231–234. 7 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