Stacey B. Gabriel

27.7k total citations · 4 hit papers
13 papers, 3.6k citations indexed

About

Stacey B. Gabriel is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Stacey B. Gabriel has authored 13 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Genetics and 2 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Stacey B. Gabriel's work include Genetic Associations and Epidemiology (4 papers), Genomics and Rare Diseases (3 papers) and RNA and protein synthesis mechanisms (3 papers). Stacey B. Gabriel is often cited by papers focused on Genetic Associations and Epidemiology (4 papers), Genomics and Rare Diseases (3 papers) and RNA and protein synthesis mechanisms (3 papers). Stacey B. Gabriel collaborates with scholars based in United States, Australia and United Kingdom. Stacey B. Gabriel's co-authors include Liuda Ziaugra, Diana Tabbaa, David Altshuler, Mark J. Daly, Steven A. McCarroll, Charles Lee, George H. Perry, Michael C. Zody, Stephanie Dallaire and Jeffrey C. Barrett and has published in prestigious journals such as Circulation, Nature Genetics and Journal of Clinical Oncology.

In The Last Decade

Stacey B. Gabriel

13 papers receiving 3.6k citations

Hit Papers

SNP Genotyping Using the Sequenom MassARRAY iPLEX Platform 2005 2026 2012 2019 2009 2005 2008 2012 250 500 750
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.

  1. SNP Genotyping Using the Sequenom MassARRAY iPLEX Platform
    2009 814 citations Stacey B. Gabriel, Liuda Ziaugra et al. Current Protocols in Human Genetics profile →
  2. Common deletion polymorphisms in the human genome
    2005 527 citations Steven A. McCarroll, Tracy N. Hadnott et al. Nature Genetics profile →
  3. Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs
    2008 507 citations Joshua M. Korn, Finny G. Kuruvilla et al. Nature Genetics profile →
  4. De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly
    2012 463 citations Jeong Ho Lee, My N. Huynh et al. Nature Genetics profile →

Peers

Stacey B. Gabriel
Arif B. Ekici Germany
Jennifer L. Moran United States
Hossein Najmabadi Iran
Е. И. Рогаев Russia
Kathrin Saar Germany
Luis A. Pérez‐Jurado Spain
Yoichi Gondo Japan
Daniela S. Gerhard United States
Lluı́s Armengol Spain
Kimberly F. Doheny United States
Arif B. Ekici Germany
Stacey B. Gabriel
Citations per year, relative to Stacey B. Gabriel Stacey B. Gabriel (= 1×) peers Arif B. Ekici

Countries citing papers authored by Stacey B. Gabriel

Since Specialization
Citations

This map shows the geographic impact of Stacey B. 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 B. 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 B. Gabriel more than expected).

Fields of papers citing papers by Stacey B. Gabriel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stacey B. Gabriel

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

All Works

13 of 13 papers shown
1.
Li, Hongda, Stephanie Bielas, Maha S. Zaki, et al.. (2016). Biallelic Mutations in Citron Kinase Link Mitotic Cytokinesis to Human Primary Microcephaly. The American Journal of Human Genetics. 99(2). 501–510. 59 indexed citations
2.
Wilson, Frederick H., Cory M. Johannessen, Federica Piccioni, et al.. (2015). A Functional Landscape of Resistance to ALK Inhibition in Lung Cancer. Cancer Cell. 27(3). 397–408. 130 indexed citations
3.
Schuberth, Christian, Hong‐Hee Won, Peter Blattmann, et al.. (2015). Systematic Cell-Based Phenotyping of Missense Alleles Empowers Rare Variant Association Studies: A Case for LDLR and Myocardial Infarction. PLoS Genetics. 11(2). e1004855–e1004855. 2 indexed citations
4.
Wagle, Nikhil, Nancy U. Lin, Andrea L. Richardson, et al.. (2014). Whole-exome sequencing (WES) of HER2+ metastatic breast cancer (MBC) from patients (pts) treated with prior trastuzumab (T): A correlative analysis of TBCRC003.. Journal of Clinical Oncology. 32(15_suppl). 536–536. 2 indexed citations
5.
Lee, Jeong Ho, My N. Huynh, Jennifer L. Silhavy, et al.. (2012). De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly. Nature Genetics. 44(8). 941–945. 463 indexed citations breakdown →
6.
Calvo, Sarah E., Elena J. Tucker, Alison G. Compton, et al.. (2010). High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency. Nature Genetics. 42(10). 851–858. 279 indexed citations
7.
Gabriel, Stacey B., Liuda Ziaugra, & Diana Tabbaa. (2009). SNP Genotyping Using the Sequenom MassARRAY iPLEX Platform. Current Protocols in Human Genetics. 60(1). Unit 2.12–Unit 2.12. 814 indexed citations breakdown →
8.
Korn, Joshua M., Finny G. Kuruvilla, Steven A. McCarroll, et al.. (2008). Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs. Nature Genetics. 40(10). 1253–1260. 507 indexed citations breakdown →
9.
McCarroll, Steven A., Tracy N. Hadnott, George H. Perry, et al.. (2005). Common deletion polymorphisms in the human genome. Nature Genetics. 38(1). 86–92. 527 indexed citations breakdown →
10.
Gabriel, Stacey B. & Liuda Ziaugra. (2004). SNP Genotyping using Sequenom MassARRAY 7K Platform. Current Protocols in Human Genetics. 42(1). Unit 2.12–Unit 2.12. 22 indexed citations
11.
Reich, David, Stacey B. Gabriel, & David Altshuler. (2003). Quality and completeness of SNP databases. Nature Genetics. 33(4). 457–458. 142 indexed citations
12.
Sklar, Pamela, Stacey B. Gabriel, Melvin G. McInnis, et al.. (2002). Family-based association study of 76 candidate genes in bipolar disorder: BDNF is a potential risk locus. Molecular Psychiatry. 7(6). 579–593. 468 indexed citations
13.
Topol, Eric J., Jeanette McCarthy, Stacey B. Gabriel, et al.. (2001). Single Nucleotide Polymorphisms in Multiple Novel Thrombospondin Genes May Be Associated With Familial Premature Myocardial Infarction. Circulation. 104(22). 2641–2644. 219 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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