A J Carroll

2.6k total citations
32 papers, 1.8k citations indexed

About

A J Carroll is a scholar working on Public Health, Environmental and Occupational Health, Genetics and Molecular Biology. According to data from OpenAlex, A J Carroll has authored 32 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Public Health, Environmental and Occupational Health, 12 papers in Genetics and 11 papers in Molecular Biology. Recurrent topics in A J Carroll's work include Acute Lymphoblastic Leukemia research (13 papers), Acute Myeloid Leukemia Research (10 papers) and Genomic variations and chromosomal abnormalities (9 papers). A J Carroll is often cited by papers focused on Acute Lymphoblastic Leukemia research (13 papers), Acute Myeloid Leukemia Research (10 papers) and Genomic variations and chromosomal abnormalities (9 papers). A J Carroll collaborates with scholars based in United States, Canada and France. A J Carroll's co-authors include WM Crist, F G Behm, Josef T. Prchal, Jaroslav F. Prchal, E W Fuson, Richard A. Gams, Jonathan J. Shuster, Yaddanapudi Ravindranath, Brad Ozanne and Jiin‐Tsuey Cheng and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Clinical Oncology.

In The Last Decade

A J Carroll

32 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
A J Carroll United States	17	873	703	635	283	281	32	1.8k
DG Gilliland United States	15	1.2k 1.3×	744 1.1×	484 0.8×	473 1.7×	381 1.4×	19	2.0k
MJ Borowitz United States	20	995 1.1×	334 0.5×	864 1.4×	322 1.1×	170 0.6×	30	1.6k
Y Hayashi Japan	26	1.2k 1.4×	926 1.3×	754 1.2×	292 1.0×	199 0.7×	47	2.3k
K Michalová Czechia	26	1.1k 1.2×	844 1.2×	394 0.6×	514 1.8×	262 0.9×	171	2.1k
AJ Carroll United States	24	1.4k 1.6×	855 1.2×	1.4k 2.2×	309 1.1×	216 0.8×	37	2.3k
SC Raimondi United States	21	1.4k 1.6×	751 1.1×	1.4k 2.3×	344 1.2×	233 0.8×	46	2.2k
FG Behm United States	15	848 1.0×	505 0.7×	821 1.3×	185 0.7×	124 0.4×	15	1.4k
DK Kalwinsky United States	18	1.1k 1.3×	350 0.5×	962 1.5×	246 0.9×	173 0.6×	30	1.5k
D Arthur United States	19	1.5k 1.8×	785 1.1×	755 1.2×	439 1.6×	192 0.7×	29	2.0k
JW Janssen Germany	14	951 1.1×	552 0.8×	544 0.9×	248 0.9×	123 0.4×	18	1.4k

Countries citing papers authored by A J Carroll

Since Specialization

Citations

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

Fields of papers citing papers by A J Carroll

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A J Carroll. 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 A J Carroll. The network helps show where A J Carroll may publish in the future.

Co-authorship network of co-authors of A J Carroll

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

All Works

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20 of 20 papers shown

Mrózek, Krzysztof, Jessica Kohlschmidt, Deedra Nicolet, et al.. (2017). The mutational oncoprint of recurrent cytogenetic abnormalities in adult patients with de novo acute myeloid leukemia. Leukemia. 31(10). 2211–2218. 48 indexed citations

Wetzler, Meir, Krzysztof Mrózek, Jessica Kohlschmidt, et al.. (2013). Intensive induction is effective in selected octogenarian acute myeloid leukemia patients: prognostic significance of karyotype and selected molecular markers used in the European LeukemiaNet classification. Haematologica. 99(2). 308–313. 28 indexed citations

Becker, Heiko, Kati Maharry, Michael D. Radmacher, et al.. (2011). Clinical outcome and gene- and microRNA-expression profiling according to the Wilms tumor 1 (WT1) single nucleotide polymorphism rs16754 in adult de novo cytogenetically normal acute myeloid leukemia: a Cancer and Leukemia Group B study. Haematologica. 96(10). 1488–1495. 18 indexed citations

Burnside, Rachel D., Romela Pasion, Inder Gadi, et al.. (2011). Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay Rachel D. BurnsideRomela PasionFady M. MikhailAndrew J. CarrollNathaniel H. Robin • Erin L. YoungsInder K. GadiElizabeth KeitgesVikram L. JaswaneyPeter R. Papenhausen • Venkateswara R. PotluriHiba RishegBrooke RushJanice L. SmithStuart Schwartz •. 3 indexed citations

Byer, Stephanie J., Buffie Clodfelder‐Miller, A J Carroll, et al.. (2010). Tamoxifen inhibits malignant peripheral nerve sheath tumor growth in an estrogen receptor-independent manner. Neuro-Oncology. 13(1). 28–41. 33 indexed citations

Maloney, Kelly W., William L. Carroll, A J Carroll, et al.. (2008). Comparison of the biology of Down syndrome (DS) acute lymphoblastic leukemia (ALL) and non-DS ALL: Children’s Oncology Group (COG) study P9900. Journal of Clinical Oncology. 26(15_suppl). 10003–10003. 2 indexed citations

Moorman, Anthony V., S Raimondi, C-H Pui, et al.. (2005). No prognostic effect of additional chromosomal abnormalities in children with acute lymphoblastic leukemia and 11q23 abnormalities. Leukemia. 19(4). 557–563. 15 indexed citations

Descartes, Maria, et al.. (1997). Identification of a recombination event narrowing the Lafora disease gene region.. Journal of Medical Genetics. 34(7). 590–591. 5 indexed citations

Bowman, W. Paul, Jonathan J. Shuster, B. Cook, et al.. (1996). Improved survival for children with B-cell acute lymphoblastic leukemia and stage IV small noncleaved-cell lymphoma: a pediatric oncology group study.. Journal of Clinical Oncology. 14(4). 1252–1261. 126 indexed citations

10.

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

11.

Gallego, Marta S., A J Carroll, Alberto S. Pappo, et al.. (1994). Variant t(8;21) rearrangements in acute myeloblastic leukemia of childhood. Cancer Genetics and Cytogenetics. 75(2). 139–144. 29 indexed citations

12.

Trueworthy, Robert C., Jonathan J. Shuster, Thomas Look, et al.. (1992). Ploidy of lymphoblasts is the strongest predictor of treatment outcome in B-progenitor cell acute lymphoblastic leukemia of childhood: a Pediatric Oncology Group study.. Journal of Clinical Oncology. 10(4). 606–613. 168 indexed citations

13.

Crist, W M, A J Carroll, & Ching‐Hon Pui. (1990). Pre-B-Cell Acute Lymphoblastic Leukemia in Childhood. Leukemia & lymphoma. 3(1). 1–6. 16 indexed citations

14.

Cheng, Jiin‐Tsuey, Ta-si Liu, N Schneider, et al.. (1990). The tal gene undergoes chromosome translocation in T cell leukemia and potentially encodes a helix-loop-helix protein.. The EMBO Journal. 9(2). 415–424. 296 indexed citations

15.

Borowitz, M, Jonathan J. Shuster, Curt I. Civin, et al.. (1990). Prognostic significance of CD34 expression in childhood B-precursor acute lymphocytic leukemia: a Pediatric Oncology Group study.. Journal of Clinical Oncology. 8(8). 1389–1398. 77 indexed citations

16.

Münke, M., Bernhard Föllmer, Paul C. Watkins, et al.. (1988). Regional assignment of six polymorphic DNA sequences on chromosome 21 by in situ hybridization to normal and rearranged chromosomes.. PubMed. 42(4). 542–9. 10 indexed citations

17.

Pistoia, Vito, A J Carroll, Arabella B. Tilden, et al.. (1986). Establishment of Tac-negative, interleukin-2-dependent cytotoxic cell lines from large granular lymphocytes (LGL) of patients with expanded LGL populations. Journal of Clinical Immunology. 6(6). 457–466. 16 indexed citations

18.

Daw, Jessica, et al.. (1984). An unbalanced (6q;13q) translocation in a male with clinical features of Ehlers-Danlos type II syndrome.. Journal of Medical Genetics. 21(3). 226–228. 6 indexed citations

19.

Prchal, J T, et al.. (1979). A study of a patient with chronic lymphocytic leukemia (CLL) which demonstrates that proliferation of the lymphocytic clone in CLL does not include T lymphocytes. Clinical Immunology and Immunopathology. 13(2). 231–236. 15 indexed citations

20.

Prchal, Josef T., et al.. (1978). A common progenitor for human myeloid and lymphoid cells. Nature. 274(5671). 590–591. 226 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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