Stacey Gabriel

400.6k total citations · 15 hit papers
100 papers, 57.8k citations indexed

About

Stacey Gabriel is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Stacey Gabriel has authored 100 papers receiving a total of 57.8k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Molecular Biology, 35 papers in Genetics and 21 papers in Cancer Research. Recurrent topics in Stacey Gabriel's work include Cancer Genomics and Diagnostics (19 papers), Genetic Associations and Epidemiology (18 papers) and Genomics and Phylogenetic Studies (12 papers). Stacey Gabriel is often cited by papers focused on Cancer Genomics and Diagnostics (19 papers), Genetic Associations and Epidemiology (18 papers) and Genomics and Phylogenetic Studies (12 papers). Stacey Gabriel collaborates with scholars based in United States, United Kingdom and Germany. Stacey Gabriel's co-authors include David Altshuler, Mark J. Daly, Mark A. DePristo, Kiran Garimella, Eric Banks, Kristian Cibulskis, Andrew Kernytsky, Aaron McKenna, Andrey Sivachenko and Matthew G. Hanna and has published in prestigious journals such as Nature, Science and New England Journal of Medicine.

In The Last Decade

Stacey Gabriel

100 papers receiving 57.0k citations

Hit Papers

5 papers align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

2010 17.4k citations Aaron McKenna, Matthew G. Hanna et al. Genome Research profile →
EGFR Mutations in Lung Cancer: Correlation with Clinical Response to Gefitinib Therapy

2004 7.5k citations J. Guillermo Paez, Pasi A. Jänne et al. Science profile →
A framework for variation discovery and genotyping using next-generation DNA sequencing data

2011 7.3k citations Mark A. DePristo, Eric Banks et al. Nature Genetics profile →
The Structure of Haplotype Blocks in the Human Genome

2002 4.5k citations Stacey Gabriel, Brendan Blumenstiel et al. Science profile →
From FastQ Data to High‐Confidence Variant Calls: The Genome Analysis Toolkit Best Practices Pipeline

2013 4.3k citations Eric Banks, Kiran Garimella et al. profile →
Discovery and saturation analysis of cancer genes across 21 tumour types

2014 2.1k citations Levi A. Garraway, Todd R. Golub et al. Nature profile →
Detecting recent positive selection in the human genome from haplotype structure

2002 1.4k citations David Reich, Daniel J. Richter et al. Nature profile →
Efficiency and power in genetic association studies

2005 1.4k citations Stacey Gabriel, Mark J. Daly et al. Nature Genetics profile →
Pan-cancer patterns of somatic copy number alteration

2013 1.2k citations Stacey Gabriel, Matthew Meyerson et al. Nature Genetics profile →
Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing

2009 983 citations Stacey Gabriel, Eric S. Lander et al. profile →
Integrative Transcriptome Analysis Reveals Common Molecular Subclasses of Human Hepatocellular Carcinoma

2009 872 citations Yujin Hoshida, Sebastian Nijman et al. Cancer Research profile →
Advances in understanding cancer genomes through second-generation sequencing

2010 798 citations Matthew Meyerson, Stacey Gabriel et al. profile →
Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants

2012 620 citations Stacey Gabriel, David Altshuler et al. Nature profile →
Assessing the impact of population stratification on genetic association studies

2004 546 citations David Reich, Gavin J. McDonald et al. Nature Genetics profile →
Genetic Interleukin 6 Signaling Deficiency Attenuates Cardiovascular Risk in Clonal Hematopoiesis

2019 267 citations Alexander G. Bick, James P. Pirruccello et al. Circulation profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stacey Gabriel United States	54	27.2k	20.1k	10.5k	9.0k	8.5k	100	57.8k
Joe W. Gray United States	99	26.8k 1.0×	12.1k 0.6×	10.8k 1.0×	11.5k 1.3×	3.4k 0.4×	487	46.4k
Steve Horvath United States	106	44.2k 1.6×	11.1k 0.6×	8.3k 0.8×	4.3k 0.5×	7.1k 0.8×	447	70.9k
Myles Brown United States	101	35.8k 1.3×	12.2k 0.6×	10.2k 1.0×	10.3k 1.1×	8.2k 1.0×	286	50.4k
Elaine R. Mardis United States	76	24.5k 0.9×	7.1k 0.4×	9.8k 0.9×	10.2k 1.1×	5.8k 0.7×	305	44.2k
Andrew P. Feinberg United States	92	45.0k 1.7×	15.5k 0.8×	6.8k 0.6×	5.9k 0.7×	2.9k 0.3×	235	62.2k
David Altshuler United States	80	29.7k 1.1×	30.5k 1.5×	7.1k 0.7×	3.5k 0.4×	2.7k 0.3×	150	63.8k
Rafael A. Irizarry United States	74	38.9k 1.4×	8.1k 0.4×	8.1k 0.8×	4.7k 0.5×	3.9k 0.5×	191	57.2k
Brad T. Sherman United States	23	37.7k 1.4×	7.7k 0.4×	11.4k 1.1×	5.1k 0.6×	4.8k 0.6×	43	59.6k
Jay Shendure United States	115	36.0k 1.3×	17.1k 0.9×	8.2k 0.8×	2.9k 0.3×	2.6k 0.3×	297	52.4k
Christian von Mering Switzerland	68	45.6k 1.7×	6.3k 0.3×	7.5k 0.7×	4.3k 0.5×	5.7k 0.7×	134	69.7k

Countries citing papers authored by Stacey Gabriel

Since Specialization

Citations

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

Fields of papers citing papers by Stacey Gabriel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stacey Gabriel. 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 Stacey Gabriel. The network helps show where Stacey Gabriel may publish in the future.

Co-authorship network of co-authors of Stacey Gabriel

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Kachuri, Linda, Angel C. Y. Mak, Donglei Hu, et al.. (2023). Gene expression in African Americans, Puerto Ricans and Mexican Americans reveals ancestry-specific patterns of genetic architecture. Nature Genetics. 55(6). 952–963. 23 indexed citations

Woolley, Ann E., Scott Dryden‐Peterson, Andy Kim, et al.. (2022). At-home Testing and Risk Factors for Acquisition of SARS-CoV-2 Infection in a Major US Metropolitan Area. Open Forum Infectious Diseases. 9(11). ofac505–ofac505. 1 indexed citations

Lange, Leslie A., François Aguet, Kristin Ardlie, et al.. (2022). Gene expression associations with body mass index in the Multi-Ethnic Study of Atherosclerosis. International Journal of Obesity. 47(2). 109–116. 5 indexed citations

Pollock, Nira R., Jesica R. Jacobs, Claire O’Kane, et al.. (2021). Performance and Operational Evaluation of the Access Bio CareStart Rapid Antigen Test in a High-Throughput Drive-Through Community Testing Site in Massachusetts. Open Forum Infectious Diseases. 8(7). ofab243–ofab243. 20 indexed citations

Sirén, Jouni, Jean Monlong, Xian Chang, et al.. (2021). Pangenomics enables genotyping of known structural variants in 5202 diverse genomes. Science. 374(6574). abg8871–abg8871. 165 indexed citations

Honigberg, Michael C., Seyedeh M. Zekavat, Abhishek Niroula, et al.. (2020). Premature Menopause, Clonal Hematopoiesis, and Coronary Artery Disease in Postmenopausal Women. Circulation. 143(5). 410–423. 96 indexed citations

Abdulhay, Nour J., Claudia Fiorini, Jeffrey M. Verboon, et al.. (2019). Impaired human hematopoiesis due to a cryptic intronic GATA1 splicing mutation. The Journal of Experimental Medicine. 216(5). 1050–1060. 23 indexed citations

Mitt, Mario, Mart Kals, Kalle Pärn, et al.. (2017). Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel. Nature. 20 indexed citations

Ito, Kaoru, Alexander G. Bick, Jason Flannick, et al.. (2013). Increased Burden of Cardiovascular Disease in Carriers of APOL1 Genetic Variants. Circulation Research. 114(5). 845–850. 110 indexed citations

10.

Hoshida, Yujin, Augusto Villanueva, Angelo Sangiovanni, et al.. (2013). Prognostic Gene Expression Signature for Patients With Hepatitis C–Related Early-Stage Cirrhosis. Gastroenterology. 144(5). 1024–1030. 158 indexed citations

11.

Haas, Joel T., Harland S. Winter, Elaine T. Lim, et al.. (2012). DGAT1 mutation is linked to a congenital diarrheal disorder. Journal of Clinical Investigation. 122(12). 4680–4684. 115 indexed citations

12.

Martínez, Fernando J., Jeong Ho Lee, Ji Eun Lee, et al.. (2012). Whole exome sequencing identifies a splicing mutation in NSUN2 as a cause of a Dubowitz-like syndrome. Journal of Medical Genetics. 49(6). 380–385. 183 indexed citations

13.

Yu, Timothy W., Elaine T. Lim, Christine Stevens, et al.. (2012). Whole-Exome Sequencing and Homozygosity Analysis Implicate Depolarization-Regulated Neuronal Genes in Autism. Digital Access to Scholarship at Harvard (DASH) (Harvard University). 131 indexed citations

14.

Wagle, Nikhil, Michael F. Berger, Matthew J. Davis, et al.. (2011). High-Throughput Detection of Actionable Genomic Alterations in Clinical Tumor Samples by Targeted, Massively Parallel Sequencing. Cancer Discovery. 2(1). 82–93. 384 indexed citations

15.

Peloso, Gina M., Serkalem Demissie, Dorothea Collins, et al.. (2010). Common genetic variation in multiple metabolic pathways influences susceptibility to low HDL-cholesterol and coronary heart disease. Journal of Lipid Research. 51(12). 3524–3532. 57 indexed citations

16.

McKenna, Aaron, Matthew G. Hanna, Eric Banks, et al.. (2010). The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data. Genome Research. 20(9). 1297–1303. 17384 indexed citations breakdown →

17.

Hoshida, Yujin, Sebastian Nijman, Masahiro Kobayashi, et al.. (2009). Integrative Transcriptome Analysis Reveals Common Molecular Subclasses of Human Hepatocellular Carcinoma. Cancer Research. 69(18). 7385–7392. 872 indexed citations breakdown →

18.

Goldfeld, Sharon, et al.. (2008). Information for Action: Developing the Victorian Child and Adolescent Monitoring System (VCAMS). 15(3). 19. 2 indexed citations

19.

Winckler, Wendy, Simon Myers, Daniel J. Richter, et al.. (2005). Comparison of Fine-Scale Recombination Rates in Humans and Chimpanzees. Science. 308(5718). 107–111. 280 indexed citations

20.

Paez, J. Guillermo, Pasi A. Jänne, Jeffrey C. Lee, et al.. (2004). EGFR Mutations in Lung Cancer: Correlation with Clinical Response to Gefitinib Therapy. Science. 304(5676). 1497–1500. 7539 indexed citations breakdown →

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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