Rodney R. Higgins

4.1k total citations · 1 hit paper
19 papers, 1.3k citations indexed

About

Rodney R. Higgins is a scholar working on Genetics, Hematology and Molecular Biology. According to data from OpenAlex, Rodney R. Higgins has authored 19 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 7 papers in Hematology and 6 papers in Molecular Biology. Recurrent topics in Rodney R. Higgins's work include Genomic variations and chromosomal abnormalities (9 papers), Acute Myeloid Leukemia Research (6 papers) and Acute Lymphoblastic Leukemia research (5 papers). Rodney R. Higgins is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Acute Myeloid Leukemia Research (6 papers) and Acute Lymphoblastic Leukemia research (5 papers). Rodney R. Higgins collaborates with scholars based in United States, Israel and Netherlands. Rodney R. Higgins's co-authors include Mark J. Pettenati, Jonathan L. Haines, David D. Weaver, Rebecca S. Wappner, Catherine G. Palmer, Athena M. Cherry, Martin S. Tallman, Gordon W. Dewald, Jacob M. Rowe and Gail H. Vance and has published in prestigious journals such as Blood, Cancer and Cancer Epidemiology Biomarkers & Prevention.

In The Last Decade

Rodney R. Higgins

19 papers receiving 1.2k 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.

Karyotype is an independent prognostic factor in adult acute lymphoblastic leukemia (ALL): analysis of cytogenetic data from patients treated on the Medical Research Council (MRC) UKALLXII/Eastern Cooperative Oncology Group (ECOG) 2993 trial

2006 502 citations Anthony V. Moorman, Christine J. Harrison et al. Blood profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rodney R. Higgins United States	13	576	527	483	481	384	19	1.3k
Marta S. Gallego Argentina	15	317 0.6×	257 0.5×	95 0.2×	95 0.2×	228 0.6×	43	644
Marinella Veltroni Italy	15	549 1.0×	606 1.1×	234 0.5×	46 0.1×	162 0.4×	26	938
W.-D. Ludwig Germany	17	449 0.8×	319 0.6×	90 0.2×	64 0.1×	204 0.5×	37	754
Cécile Brachet Belgium	14	95 0.2×	241 0.5×	171 0.4×	137 0.3×	362 0.9×	36	845
B A Dsupin United States	12	83 0.1×	178 0.3×	294 0.6×	237 0.5×	194 0.5×	14	1.4k
Giorgio Adriano Paskulin Brazil	17	95 0.2×	88 0.2×	190 0.4×	344 0.7×	351 0.9×	89	899
Tahsin Yakut Türkiye	15	76 0.1×	117 0.2×	174 0.4×	191 0.4×	315 0.8×	78	762
P Malet France	15	79 0.1×	142 0.3×	119 0.2×	214 0.4×	336 0.9×	65	768
Nataline B. Kardon United States	13	85 0.1×	103 0.2×	281 0.6×	329 0.7×	232 0.6×	26	640
AM Mauer United States	12	397 0.7×	584 1.1×	234 0.5×	39 0.1×	95 0.2×	19	912

Countries citing papers authored by Rodney R. Higgins

Since Specialization

Citations

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

Fields of papers citing papers by Rodney R. Higgins

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rodney R. Higgins. 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 Rodney R. Higgins. The network helps show where Rodney R. Higgins may publish in the future.

Co-authorship network of co-authors of Rodney R. Higgins

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

All Works

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19 of 19 papers shown

Strickland, Stephen A., Zhuoxin Sun, Rhett P. Ketterling, et al.. (2017). Independent Prognostic Significance of Monosomy 17 and Impact of Karyotype Complexity in Monosomal Karyotype/Complex Karyotype Acute Myeloid Leukemia: Results from Four ECOG-ACRIN Prospective Therapeutic Trials. Leukemia Research. 59. 55–64. 13 indexed citations

Higgins, Rodney R., et al.. (2013). Osteolytic Bone Lesions, Hypercalcemia, and Renal Failure: A Rare Presentation of Childhood Acute Lymphoblastic Leukemia. 1(2). 73–78. 3 indexed citations

Messinger, Yoav H., Rodney R. Higgins, Meenakshi Devidas, et al.. (2012). Pediatric acute lymphoblastic leukemia with a t(8;14)(q11.2;q32): B-cell disease with a high proportion of Down syndrome: a Children's Oncology Group study. Cancer Genetics. 205(9). 453–458. 7 indexed citations

Ross, Julie A., Cindy K. Blair, James R. Cerhan, et al.. (2011). Nonsteroidal Anti-inflammatory Drug and Acetaminophen Use and Risk of Adult Myeloid Leukemia. Cancer Epidemiology Biomarkers & Prevention. 20(8). 1741–1750. 26 indexed citations

Fink, James M., et al.. (2011). 22q13.32 Deletion and Duplication and Inversion in the Same Family: A Rare Occurrence. PubMed. 2011. 1–4. 9 indexed citations

McCormick, Stanley R., et al.. (2010). FLT3 mutations at diagnosis and relapse in acute myeloid leukemia: cytogenetic and pathologic correlations, including cuplike blast morphology.. Archives of Pathology & Laboratory Medicine. 134(8). 1143–51. 38 indexed citations

McCormick, Stanley R., et al.. (2010). FLT3 Mutations at Diagnosis and Relapse in Acute Myeloid Leukemia: Cytogenetic and Pathologic Correlations, Including Cuplike Blast Morphology. Archives of Pathology & Laboratory Medicine. 134(8). 1143–1151. 38 indexed citations

Klaassens, Merel, R. J. H. Galjaard, Daryl A. Scott, et al.. (2007). Prenatal detection and outcome of congenital diaphragmatic hernia (CDH) associated with deletion of chromosome 15q26: Two patients and review of the literature. American Journal of Medical Genetics Part A. 143A(18). 2204–2212. 42 indexed citations

Moorman, Anthony V., Christine J. Harrison, Georgina Buck, et al.. (2006). Karyotype is an independent prognostic factor in adult acute lymphoblastic leukemia (ALL): analysis of cytogenetic data from patients treated on the Medical Research Council (MRC) UKALLXII/Eastern Cooperative Oncology Group (ECOG) 2993 trial. Blood. 109(8). 3189–3197. 502 indexed citations breakdown →

10.

Vance, Gail H., Haesook Kim, Athena M. Cherry, et al.. (2006). Utility of interphase FISH to stratify patients into cytogenetic risk categories at diagnosis of AML in an Eastern Cooperative Oncology Group (ECOG) clinical trial (E1900). Leukemia Research. 31(5). 605–609. 14 indexed citations

11.

Cherry, Athena M., Stephanie R. Brockman, Sarah F. Paternoster, et al.. (2003). Comparison of interphase FISH and metaphase cytogenetics to study myelodysplastic syndrome: an Eastern Cooperative Oncology Group (ECOG) study. Leukemia Research. 27(12). 1085–1090. 54 indexed citations

12.

Higgins, Rodney R., et al.. (1998). Duplication 6q22?qter: Definition of the phenotype. American Journal of Medical Genetics. 78(2). 123–126. 5 indexed citations

13.

Hsu, Lillian Y. F., Richard L. Neu, Daniel L. Van Dyke, et al.. (1997). RARE TRISOMY MOSAICISM DIAGNOSED IN AMNIOCYTES, INVOLVING AN AUTOSOME OTHER THAN CHROMOSOMES 13, 18, 20, AND 21: KARYOTYPE/PHENOTYPE CORRELATIONS. Prenatal Diagnosis. 17(3). 201–242. 143 indexed citations

14.

Schimmenti, Lisa A., Rodney R. Higgins, Nancy J. Mendelsohn, et al.. (1995). Monosomy 9p24→pter and trisomy 5q31→qter: Case report and review of two cases. American Journal of Medical Genetics. 57(1). 52–56. 9 indexed citations

15.

Pettenati, Mark J., P. Nagesh Rao, Mary C. Phelan, et al.. (1995). Paracentric inversions in humans: A review of 446 paracentric inversions with presentation of 120 new cases. American Journal of Medical Genetics. 55(2). 171–187. 82 indexed citations

16.

Higgins, Rodney R., et al.. (1992). Trisomy 16p in a liveborn infant and review of trisomy 16p. American Journal of Medical Genetics. 42(3). 316–319. 17 indexed citations

17.

Kinney, Janet S., et al.. (1992). X;6 translocation in a child with congenital acute lymphocytic leukemia. Cancer. 69(3). 799–803. 9 indexed citations

18.

Higgins, Rodney R., et al.. (1990). Ectro‐amelia syndrome associated with an interstitial deletion of 7q. American Journal of Medical Genetics. 35(1). 95–99. 51 indexed citations

19.

Pettenati, Mark J., Jonathan L. Haines, Rodney R. Higgins, et al.. (1986). Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature. Human Genetics. 74(2). 143–154. 224 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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