George Santangelo | Academic Influence

George Santangelo's AcademicInfluence.com Rankings

George Santangelo

Computer Science

#12763

World Rank

#13670

Historical Rank

#2355

USA Rank

Data Science

#376

World Rank

#385

Historical Rank

#41

USA Rank

computer-science Degrees

George Santangelo

Biology

#16088

World Rank

#20204

Historical Rank

#3139

USA Rank

Computational Biology

#397

World Rank

#399

Historical Rank

#51

USA Rank

biology Degrees

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Computer Science
Biology

George Santangelo's Degrees

PhD Genomics Stanford University

Why Is George Santangelo Influential?

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According to Wikipedia, George M. Santangelo is an American genomicist and data scientist. He is the director of the Office of Portfolio Analysis at the National Institutes of Health. Education and career Santangelo received his bachelor's degree from the University of Pennsylvania, and his Ph.D. from Yale University. In 2011, he was appointed as director of the newly formed Office of Portfolio Analysis at the National Institutes of Health. Santangelo oversees a team of analysts, data scientists, and software developers to enable data-driven decision-making.

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George Santangelo's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Glucose Signaling in Saccharomyces cerevisiae (2006) (539)
Reverse recruitment: the Nup84 nuclear pore subcomplex mediates Rap1/Gcr1/Gcr2 transcriptional activation. (2005) (144)
GCR1, a transcriptional activator in Saccharomyces cerevisiae, complexes with RAP1 and can function without its DNA binding domain. (1993) (90)
Two separable functional domains of simian virus 40 large T antigen: carboxyl-terminal region of simian virus 40 large T antigen is required for efficient capsid protein synthesis (1985) (69)
Efficient transcription of the glycolytic gene ADH1 and three translational component genes requires the GCR1 product, which can act through TUF/GRF/RAP binding sites (1990) (65)
Glucose-Responsive Regulators of Gene Expression in Saccharomyces cerevisiae Function at the Nuclear Periphery via a Reverse Recruitment Mechanism (2007) (63)
Efficient expression of the Saccharomyces cerevisiae glycolytic gene ADH1 is dependent upon a cis-acting regulatory element (UASRPG) found initially in genes encoding ribosomal proteins. (1990) (62)
Rap1p requires Gcr1p and Gcr2p homodimers to activate ribosomal protein and glycolytic genes, respectively. (2001) (61)
Properties of promoters cloned randomly from the Saccharomyces cerevisiae genome (1988) (51)
The Nuclear Pore Complex Mediates Binding of the Mig1 Repressor to Target Promoters (2011) (38)
Unigenic evolution: a novel genetic method localizes a putative leucine zipper that mediates dimerization of the Saccharomyces cerevisiae regulator Gcr1p. (1995) (36)
The transcription factor Gcr1 stimulates cell growth by participating in nutrient-responsive gene expression on a global level (2007) (35)
Dependence of Escherichia coli hyperbaric oxygen toxicity on the lipid acyl chain composition (1978) (35)
Specialized Rap1p/Gcr1p transcriptional activation through Gcr1p DNA contacts requires Gcr2p, as does hyperphosphorylation of Gcr1p. (1997) (31)
Analysis in Cos-1 cells of processing and polyadenylation signals by using derivatives of the herpes simplex virus type 1 thymidine kinase gene (1983) (31)
Chemical inhibition of CaaX protease activity disrupts yeast Ras localization (2010) (25)
Reverse recruitment : The Nup 84 nuclear pore subcomplex mediates Rap 1 Gcr 1 Gcr 2 transcriptional activation (2005) (24)
Heterologous Expression Studies of Saccharomyces cerevisiae Reveal Two Distinct Trypanosomatid CaaX Protease Activities and Identify Their Potential Targets (2009) (18)
Coiled coil structures and transcription: an analysis of the S. cerevisiae coilome (2007) (17)
The global transcriptional activator of Saccharomyces cerevisiae, Gcr1p, mediates the response to glucose by stimulating protein synthesis and CLN-dependent cell cycle progression. (2003) (16)
Preparation of a "functional library" of African green monkey DNA fragments which substitute for the processing/polyadenylation signal in the herpes simplex virus type 1 thymidine kinase gene (1983) (11)
Saccharomyces cerevisiae ribosomal protein L37 is encoded by duplicate genes that are differentially expressed (1994) (11)
The GCR1 gene of Saccharomyces cerevisiae is a split gene with an unusually long intron. (1994) (10)
Cloning of open reading frames and promoters from the Saccharomyces cerevisiae genome: construction of genomic libraries of random small fragments. (1986) (9)
Screening a yeast promoter library leads to the isolation of the RP29/L32 and SNR17B/RPL37A divergent promoters and the discovery of a gene encoding ribosomal protein L37. (1991) (8)
A Saccharomyces cerevisiae mitochondrial DNA fragment activates Reg1p-dependent glucose-repressible transcription in the nucleus (1997) (3)
Global Climate Change and the ecology of the next decade (2008) (2)
TwoSeparable Functional DomainsofSimian Virus40LargeT Antigen: Carboxyl-Terminal Region ofSimian Virus40LargeT Antigen IsRequired forEfficient Capsid Protein Synthesis (1985) (0)

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