Anne W. Higgins

2.5k total citations
17 papers, 885 citations indexed

About

Anne W. Higgins is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Anne W. Higgins has authored 17 papers receiving a total of 885 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Hematology and 7 papers in Genetics. Recurrent topics in Anne W. Higgins's work include Acute Myeloid Leukemia Research (6 papers), Chromosomal and Genetic Variations (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Anne W. Higgins is often cited by papers focused on Acute Myeloid Leukemia Research (6 papers), Chromosomal and Genetic Variations (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Anne W. Higgins collaborates with scholars based in United States, Japan and Germany. Anne W. Higgins's co-authors include Huntington F. Willard, Karen M. Gustashaw, Mary G. Schueler, M. Katharine Rudd, Sarah T. South, Charles Lee, Hutton M. Kearney, Allen N. Lamb, Patricia M. Miron and Lloyd Hutchinson and has published in prestigious journals such as Science, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Anne W. Higgins

16 papers receiving 871 citations

Peers

Anne W. Higgins

GENET

PPCH

HEMAT

James Tepperberg United States

Stephen Laderman United States

Vida Petrovic Australia

D E Rooney United Kingdom

Patricia Emmerich Germany

Herman E. Wyandt United States

Atsuko Fujimoto United States

Christa M. Lese United States

Judith Stamberg United States

E.P.J. Arnoldus Netherlands

James Tepperberg United States

Anne W. Higgins

362 ×0.7

149 ×0.4

532 ×1.5

GENET

284 ×2.0

PPCH

86 ×0.9

HEMAT

Citations per year, relative to Anne W. Higgins Anne W. Higgins (= 1×) peers James Tepperberg

Countries citing papers authored by Anne W. Higgins

Since Specialization

Citations

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

Fields of papers citing papers by Anne W. Higgins

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anne W. Higgins

This figure shows the co-authorship network connecting the top 25 collaborators of Anne W. Higgins. A scholar is included among the top collaborators of Anne W. 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 Anne W. Higgins. Anne W. 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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17 of 17 papers shown

Yuan, Robert, et al.. (2026). Clinico-genomic characterization of RAS-mutant acute myeloid leukemia. Annals of Hematology. 105(3). 99–99.

Patel, Shyam A., Rena Zheng, Lloyd Hutchinson, et al.. (2024). Natural history of clonal haematopoiesis seen in real‐world haematology settings. British Journal of Haematology. 204(5). 1844–1855. 8 indexed citations

Patel, Shyam A., Rena Zheng, Lloyd Hutchinson, et al.. (2023). Sole DNMT3A/TET2/ASXL1 Mutations Define a Distinct Clinical Trajectory for Patients with Clonal Hematopoiesis. Blood. 142(Supplement 1). 4068–4068. 2 indexed citations

Patel, Shyam A., Jan Černý, Muthalagu Ramanathan, et al.. (2023). Prognostic heterogeneity and clonal dynamics within distinct subgroups of myelodysplastic syndrome and acute myeloid leukemia with TP53 disruptions. SHILAP Revista de lepidopterología. 4(4). 1059–1070. 18 indexed citations

Patel, Shyam A., Jacob R. Bledsoe, Anne W. Higgins, Lloyd Hutchinson, & Jonathan M. Gerber. (2021). Rapid and Deep Remission Induced by Blinatumomab for CD19-Positive Chronic Myeloid Leukemia in Lymphoid Blast Phase. JCO Precision Oncology. 5(5). 1141–1146. 5 indexed citations

Patel, Shyam A., Maxwell R. Lloyd, Jan Černý, et al.. (2021). Clinico-genomic profiling and clonal dynamic modeling of TP53-aberrant myelodysplastic syndrome and acute myeloid leukemia. Leukemia & lymphoma. 62(14). 3348–3360. 24 indexed citations

South, Sarah T., Charles Lee, Allen N. Lamb, Anne W. Higgins, & Hutton M. Kearney. (2013). ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013. Genetics in Medicine. 15(11). 901–909. 232 indexed citations

Shi, Min, et al.. (2013). Improved Detection Rate of Cytogenetic Abnormalities in Chronic Lymphocytic Leukemia and Other Mature B-Cell Neoplasms With Use of CpG-Oligonucleotide DSP30 and Interleukin 2 Stimulation. American Journal of Clinical Pathology. 139(5). 662–669. 18 indexed citations

Zhang, Haojian, Cong Peng, Yiguo Hu, et al.. (2012). The Blk pathway functions as a tumor suppressor in chronic myeloid leukemia stem cells. Nature Genetics. 44(8). 861–871. 62 indexed citations

10.

Lachke, Salil A., Anne W. Higgins, Maiko Inagaki, et al.. (2011). The cell adhesion gene PVRL3 is associated with congenital ocular defects. Human Genetics. 131(2). 235–250. 42 indexed citations

11.

Kim, Hyung‐Goo, M Stefanova, Anne W. Higgins, et al.. (2007). Extensive molecular genetic analysis of the 3p14.3 region in patients with Zimmermann–Laband syndrome. American Journal of Medical Genetics Part A. 143A(22). 2668–2674. 9 indexed citations

12.

Kim, Hyung‐Goo, Anne W. Higgins, Shotaro Kishikawa, et al.. (2006). Candidate loci for Zimmermann–Laband syndrome at 3p14.3. American Journal of Medical Genetics Part A. 143A(2). 107–111. 15 indexed citations

13.

Higgins, Anne W., Karen M. Gustashaw, & Huntington F. Willard. (2005). Engineered human dicentric chromosomes show centromere plasticity. Chromosome Research. 13(8). 745–762. 36 indexed citations

14.

Schueler, Mary G., Anne W. Higgins, M. Katharine Rudd, Karen M. Gustashaw, & Huntington F. Willard. (2001). Genomic and Genetic Definition of a Functional Human Centromere. Science. 294(5540). 109–115. 376 indexed citations

15.

Schueler, Mary G., Anne W. Higgins, Ramaiah Nagaraja, et al.. (2000). Large-Insert Clone/STS Contigs in Xq11–q12, Spanning Deletions in Patients with Androgen Insensitivity and Mental Retardation. Genomics. 66(1). 104–109. 12 indexed citations

16.

Higgins, Anne W., Mary G. Schueler, & Huntington F. Willard. (1999). Chromosome engineering: generation of mono- and dicentric isochromosomes in a somatic cell hybrid system. Chromosoma. 108(4). 256–265. 20 indexed citations

17.

Lebo, Roger V., et al.. (1999). Symmetric replication of an unstable isodicentric Xq chromosome derived from isolocal maternal sister chromatid recombination. American Journal of Medical Genetics. 85(5). 429–437. 6 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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