David A. Sweetser

7.5k total citations
62 papers, 3.0k citations indexed

About

David A. Sweetser is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, David A. Sweetser has authored 62 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 22 papers in Genetics and 12 papers in Hematology. Recurrent topics in David A. Sweetser's work include Acute Myeloid Leukemia Research (11 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Metabolism and Genetic Disorders (7 papers). David A. Sweetser is often cited by papers focused on Acute Myeloid Leukemia Research (11 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Metabolism and Genetic Disorders (7 papers). David A. Sweetser collaborates with scholars based in United States, Australia and United Kingdom. David A. Sweetser's co-authors include Jeffrey I. Gordon, E H Birkenmeier, Robert O. Heuckeroth, Irwin D. Bernstein, William G. Woods, Jerald P. Radich, Peter C. Hoppe, Derek L. Stirewalt, Soheil Meshinchi and Jonathan D. Buckley and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

David A. Sweetser

60 papers receiving 3.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David A. Sweetser United States 27 1.9k 599 585 412 340 62 3.0k
Tsukasa Ohmori Japan 26 1.7k 0.9× 774 1.3× 440 0.8× 361 0.9× 262 0.8× 108 3.2k
Francis James Grant United States 22 1.5k 0.8× 742 1.2× 373 0.6× 246 0.6× 335 1.0× 33 3.1k
Frédéric Mazurier France 29 1.6k 0.8× 758 1.3× 299 0.5× 498 1.2× 199 0.6× 67 2.8k
G Grimber France 24 1.2k 0.6× 187 0.3× 312 0.5× 293 0.7× 168 0.5× 48 2.1k
Takayuki Hoshii Japan 23 2.4k 1.3× 644 1.1× 205 0.4× 558 1.4× 156 0.5× 48 3.6k
Mitsuo Nishikawa Japan 24 1.4k 0.8× 272 0.5× 311 0.5× 246 0.6× 484 1.4× 83 2.6k
Eric Campeau United States 17 2.2k 1.2× 168 0.3× 214 0.4× 558 1.4× 118 0.3× 32 3.6k
Venkatesha Basrur United States 30 2.5k 1.3× 334 0.6× 366 0.6× 471 1.1× 82 0.2× 86 3.2k
Tina Garofalo Italy 34 2.1k 1.1× 339 0.6× 205 0.4× 103 0.3× 189 0.6× 112 3.4k
L. Marty France 13 2.4k 1.3× 174 0.3× 441 0.8× 552 1.3× 188 0.6× 19 3.7k

Countries citing papers authored by David A. Sweetser

Since Specialization
Citations

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

Fields of papers citing papers by David A. Sweetser

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David A. Sweetser

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

All Works

20 of 20 papers shown
1.
Stergachis, Andrew B., et al.. (2025). Late-Onset Multiple Acyl-CoA Dehydrogenase Deficiency Presenting as Hyperammonemia and Encephalopathy: Case Series. The Neurohospitalist. 15(4). 372–376. 1 indexed citations
2.
Chung, Daniel C., Douglas S. Micalizzi, Kristen M. Shannon, et al.. (2023). A pooled electronic consultation program to improve access to genetics specialists. SHILAP Revista de lepidopterología. 1(1). 100819–100819. 1 indexed citations
3.
Pan, Xueyang, Mengqi Ma, Shenzhao Lu, et al.. (2023). Allelic strengths of encephalopathy-associated UBA5 variants correlate between in vivo and in vitro assays. eLife. 12. 2 indexed citations
4.
Briere, Lauren C., Melissa Walker, Lance H. Rodan, et al.. (2023). A de novo missense variant in EZH1 associated with developmental delay exhibits functional deficits in Drosophila melanogaster. Genetics. 224(4). 6 indexed citations
5.
Cardenas, Christian L. Lino, Lauren C. Briere, David A. Sweetser, Mark E. Lindsay, & Patricia L. Musolino. (2023). A seed sequence variant in miR-145-5p causes multisystem smooth muscle dysfunction syndrome. Journal of Clinical Investigation. 133(5). 1 indexed citations
6.
Huang, Yan, Gabrielle Lemire, Lauren C. Briere, et al.. (2022). The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability. The American Journal of Human Genetics. 109(10). 1923–1931. 10 indexed citations
7.
Briere, Lauren C., Melissa Walker, Frances A. High, et al.. (2021). A description of novel variants and review of phenotypic spectrum in UBA5-related early epileptic encephalopathy. Molecular Case Studies. 7(3). a005827–a005827. 15 indexed citations
8.
Theodorou, Evangelos A., et al.. (2021). TLE4 Is a Critical Mediator of Osteoblast and Runx2-Dependent Bone Development. Frontiers in Cell and Developmental Biology. 9. 671029–671029. 4 indexed citations
9.
Hennig, Krista M., Daniel M. Fass, Wen‐Ning Zhao, et al.. (2017). WNT/β-Catenin Pathway and Epigenetic Mechanisms Regulate the Pitt-Hopkins Syndrome and Schizophrenia Risk Gene TCF4. PubMed. 3(1). 53–71. 21 indexed citations
10.
Brynczka, Christopher, et al.. (2016). TLE4 regulation of wnt-mediated inflammation underlies its role as a tumor suppressor in myeloid leukemia. Leukemia Research. 48. 46–56. 12 indexed citations
11.
Sweetser, David A., Angela E. Lin, Maria J. Troulis, Teresa C. Chen, & Sjirk J. Westra. (2016). Case 34-2016. New England Journal of Medicine. 375(19). 1879–1890. 3 indexed citations
12.
Wheat, Justin C., Daniela S. Krause, Thomas Shin, et al.. (2014). The Corepressor Tle4 Is a Novel Regulator of Murine Hematopoiesis and Bone Development. PLoS ONE. 9(8). e105557–e105557. 24 indexed citations
13.
Consugar, Mark, Daniel Navarro-Gomez, Emily Place, et al.. (2014). Panel-based genetic diagnostic testing for inherited eye diseases is highly accurate and reproducible, and more sensitive for variant detection, than exome sequencing. Genetics in Medicine. 17(4). 253–261. 179 indexed citations
14.
Giampietro, Philip F., Linlea Armstrong, Robert D. Blank, et al.. (2014). Whole exome sequencing identifies a POLRID mutation segregating in a father and two daughters with findings of Klippel–Feil and Treacher Collins syndromes. American Journal of Medical Genetics Part A. 167(1). 95–102. 10 indexed citations
15.
Sahai, Inderneel, Cheryl Garganta, Jeffrey A. Bailey, et al.. (2013). Newborn Screening for Glutaric Aciduria-II: The New England Experience. JIMD Reports. 13. 1–14. 12 indexed citations
16.
Sweetser, David A., Andrew Peniket, Yuntian Zhang, et al.. (2005). Delineation of the minimal commonly deleted segment and identification of candidate tumor‐suppressor genes in del(9q) acute myeloid leukemia. Genes Chromosomes and Cancer. 44(3). 279–291. 45 indexed citations
17.
Rice, Julie, et al.. (2000). Transgenic rescue of aganglionosis and piebaldism in lethal spotted mice. Developmental Dynamics. 217(1). 120–132. 31 indexed citations
18.
Sweetser, David A., et al.. (1997). Oncogenesis and altered differentiation induced by activated Ras in neuroblasts of transgenic mice. Oncogene. 15(23). 2783–2794. 23 indexed citations
19.
Steiner, Robert D., et al.. (1996). Nonketotic hyperglycinemia: Atypical clinical and biochemical manifestations. The Journal of Pediatrics. 128(2). 243–246. 39 indexed citations
20.
Herman, T E, David A. Sweetser, William H. McAlister, & S. Bruce Dowton. (1993). Schinzel-Giedion syndrome and congenital megacalyces. Pediatric Radiology. 23(2). 111–112. 16 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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