Sheila A. Shurtleff

29.3k citations
129 papers · 22.4k · 14 hit papers · h-index 62

Impact in

  • Hematology top 0.05%
    • Acute Myeloid Leukemia Research
    • Chronic Myeloid Leukemia Treatments
  • Genetics top 0.2%
    • Glioma Diagnosis and Treatment

Papers in

Sheila A. Shurtleff

123 papers receiving 21.7k citations

Sheila A. Shurtleff's Hit Papers

Germline Mutations in Predisposition Genes in Pediatric Cancer 2015 · 984 citations
9840+10+21Years since publication50010001.5k

Peers

Sheila A. Shurtleff
Comparison fields: 5 of 143
  • Hematology 8.0k
  • Genetics 3.1k
  • Public Health, Environmental and Occupational Health 7.7k
  • Cancer Research 2.9k
  • Oncology 3.9k
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Brigitte Schlegelberger Germany
Jeffery Lorne Kutok United States
Timothy Aaron Graubert United States
Birgit Burkhardt Germany
Lars Bullinger Germany
Hiroko Tanaka Japan
T. Andrew Lister United Kingdom
Sheila A. Shurtleff relative to Stanley B Pounds United States Stanley B Pounds's profile →
Citations per field
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Citations per year

Countries citing papers authored by Sheila A. Shurtleff

Since Specialization
Citations

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

Fields of papers citing papers by Sheila A. Shurtleff

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Sheila A. Shurtleff, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Sheila A. Shurtleff Line = papers co-authored together Sheila A. Shurtleff links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 129 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Classification, subtype discovery, and prediction of outcome in pediatric acute lymphoblastic leukemia by gene expression profiling
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20021560
2
Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia
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20071480
3
The genetic basis of early T-cell precursor acute lymphoblastic leukaemia
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20121318
4
Deletion of IKZF1 and Prognosis in Acute Lymphoblastic Leukemia
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20091174
5
Germline Mutations in Predisposition Genes in Pediatric Cancer
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2015984
6
D-type cyclin-dependent kinase activity in mammalian cells.
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1994965
7
BCR–ABL1 lymphoblastic leukaemia is characterized by the deletion of Ikaros
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2008871
8
Whole-genome sequencing identifies genetic alterations in pediatric low-grade gliomas
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2013679
9
Genomic Analysis of the Clonal Origins of Relapsed Acute Lymphoblastic Leukemia
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2008665
10
Recurrent Somatic Structural Variations Contribute to Tumorigenesis in Pediatric Osteosarcoma
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2014598
11
The genomic landscape of hypodiploid acute lymphoblastic leukemia
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2013556
12
Clinical Utility of Microarray-Based Gene Expression Profiling in the Diagnosis and Subclassification of Leukemia: Report From the International Microarray Innovations in Leukemia Study Group
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2010542
13
C11orf95–RELA fusions drive oncogenic NF-κB signalling in ependymoma
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2014522
14
TEL/AML1 fusion resulting from a cryptic t(12;21) is the most common genetic lesion in pediatric ALL and defines a subgroup of patients with an excellent prognosis.
1995475
15 2003469
16
Genomic Landscape of Ewing Sarcoma Defines an Aggressive Subtype with Co-Association of STAG2 and TP53 Mutations
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2014419
17 2012411
18 2015400
19 2004377
20 2009313

About Sheila A. Shurtleff

Sheila A. Shurtleff is a scholar working on Hematology, Public Health, Environmental and Occupational Health, Genetics, Cancer Research and Oncology, having authored 129 papers that have together received 22.4k indexed citations. Recurring topics across this work include Acute Myeloid Leukemia Research (43 papers), Acute Lymphoblastic Leukemia research (36 papers), Chronic Myeloid Leukemia Treatments (21 papers), Cancer Genomics and Diagnostics (18 papers), Sarcoma Diagnosis and Treatment (11 papers), Glioma Diagnosis and Treatment (11 papers), Protein Degradation and Inhibitors (8 papers) and CAR-T cell therapy research (7 papers). The work is most often cited by research in Hematology (8.0k citations), Genetics (3.1k citations), Public Health, Environmental and Occupational Health (7.7k citations), Cancer Research (2.9k citations) and Oncology (3.9k citations). Sheila A. Shurtleff has collaborated with scholars based in United States, Singapore and Australia. Frequent co-authors include James R. Downing, Ching‐Hon Pui, Charles J. Sherr, Charles Grenfell Mullighan, Jing Ma, Christopher B. Miller, Susana Catalina Raimondi, Xiaoping Su, Jun‐ya Kato and Dawn E. Quelle. Their work appears in journals such as Blood, Nature, Nature Genetics, Journal of Clinical Oncology and Molecular and Cellular Biology.

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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