Stacey Bolk

5.2k total citations · 2 hit papers
15 papers, 3.6k citations indexed

About

Stacey Bolk is a scholar working on Surgery, Molecular Biology and Endocrine and Autonomic Systems. According to data from OpenAlex, Stacey Bolk has authored 15 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Surgery, 8 papers in Molecular Biology and 3 papers in Endocrine and Autonomic Systems. Recurrent topics in Stacey Bolk's work include Congenital gastrointestinal and neural anomalies (7 papers), Neuroscience of respiration and sleep (3 papers) and Intestinal Malrotation and Obstruction Disorders (2 papers). Stacey Bolk is often cited by papers focused on Congenital gastrointestinal and neural anomalies (7 papers), Neuroscience of respiration and sleep (3 papers) and Intestinal Malrotation and Obstruction Disorders (2 papers). Stacey Bolk collaborates with scholars based in United States, Netherlands and France. Stacey Bolk's co-authors include Eric S. Lander, Aravinda Chakravarti, Shelli Farhadian, Daniel J. Richter, David Reich, James Ireland, Ryk Ward, Michele Cargill, Pardis C. Sabeti and Misha Angrist and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nature Genetics.

In The Last Decade

Stacey Bolk

15 papers receiving 3.5k citations

Hit Papers

The common PPARγ Pro12Ala polymorphism is associated with... 2000 2026 2008 2017 2000 2001 400 800 1.2k
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. The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes
    2000 1.3k citations David Altshuler, Joel N. Hirschhorn et al. Nature Genetics profile →
  2. Linkage disequilibrium in the human genome
    2001 1.3k citations David Reich, Michele Cargill et al. Nature profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stacey Bolk United States 13 1.8k 1.7k 903 438 306 15 3.6k
Charles R. Lane United States 10 1.1k 0.6× 1.7k 1.0× 463 0.5× 511 1.2× 294 1.0× 22 2.9k
Derek Gordon United States 32 1.5k 0.8× 1.3k 0.7× 401 0.4× 233 0.5× 196 0.6× 129 3.5k
Anne E. Kwitek United States 34 1.5k 0.8× 2.0k 1.2× 346 0.4× 651 1.5× 370 1.2× 125 4.5k
Colette Rossier Switzerland 35 1.1k 0.6× 2.6k 1.5× 277 0.3× 1.0k 2.4× 169 0.6× 62 4.8k
Eduard Ayuso Spain 34 1.5k 0.9× 1.9k 1.1× 626 0.7× 730 1.7× 318 1.0× 61 3.3k
Soumitra Ghosh United States 25 836 0.5× 912 0.5× 392 0.4× 369 0.8× 304 1.0× 44 2.6k
Claude Szpirer Belgium 39 1.8k 1.0× 3.0k 1.7× 327 0.4× 543 1.2× 661 2.2× 190 5.3k
Matthew DeFelice United States 5 2.4k 1.4× 2.0k 1.1× 314 0.3× 403 0.9× 262 0.9× 7 5.1k
Brendan Blumenstiel United States 8 2.4k 1.4× 2.1k 1.2× 315 0.3× 406 0.9× 262 0.9× 12 5.4k
Ohad S. Birk Israel 33 1.2k 0.7× 2.1k 1.2× 405 0.4× 175 0.4× 228 0.7× 121 3.7k

Countries citing papers authored by Stacey Bolk

Since Specialization
Citations

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

Fields of papers citing papers by Stacey Bolk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stacey Bolk

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

All Works

15 of 15 papers shown
1.
Altshuler, David, Mia Klannemark, Cecilia M. Lindgren, et al.. (2005). et Lander ES. 2000. The common PPARgamma Prol2Ala polymorphism is associated with decreased risk of type 2 diabetes. Nat Genet Sep; 26 (l): 76-80. American Thoracic Society. 1987. Standards for the diagnosis and care of patients with chronic obstructive pulmonary disease (COPD) and asthma. Am Rev Respir Dis. 2 indexed citations
2.
Weese‐Mayer, Debra E., Stacey Bolk, Jean M. Silvestri, & Aravinda Chakravarti. (2002). Idiopathic congenital central hypoventilation syndrome: Evaluation of brain‐derived neurotrophic factor genomic DNA sequence variation. American Journal of Medical Genetics. 107(4). 306–310. 55 indexed citations
3.
Reich, David, Michele Cargill, Stacey Bolk, et al.. (2001). Linkage disequilibrium in the human genome. Nature. 411(6834). 199–204. 1251 indexed citations breakdown →
4.
Silverman, Eric S., Stephen B. Liggett, Erwin W. Gelfand, et al.. (2001). The pharmacogenetics of asthma: a candidate gene approach. The Pharmacogenomics Journal. 1(1). 27–37. 23 indexed citations
5.
Reich, David, Michele Cargill, Stacey Bolk, et al.. (2001). Reich, D. E., Cargill, M. and Bolk, S. et al.. Linkage disequilibrium in the human genome. Nature, 411: 199-204. 55 indexed citations
6.
Altshuler, David, Joel N. Hirschhorn, Mia Klannemark, et al.. (2000). The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes. Nature Genetics. 26(1). 76–80. 1310 indexed citations breakdown →
7.
Hirschhorn, Joel N., Pamela Sklar, Kerstin Lindblad‐Toh, et al.. (2000). SBE-TAGS: An array-based method for efficient single-nucleotide polymorphism genotyping. Proceedings of the National Academy of Sciences. 97(22). 12164–12169. 143 indexed citations
8.
Bolk, Stacey, Anna Pelet, Robert M.W. Hofstra, et al.. (2000). A human model for multigenic inheritance: Phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus. Proceedings of the National Academy of Sciences. 97(1). 268–273. 156 indexed citations
9.
Angrist, Misha, Shuqian Jing, Stacey Bolk, et al.. (1998). HumanGFRA1: Cloning, Mapping, Genomic Structure, and Evaluation as a Candidate Gene for Hirschsprung Disease Susceptibility. Genomics. 48(3). 354–362. 42 indexed citations
10.
11.
Angrist, Misha, Stacey Bolk, Marc K. Halushka, Paul A. Lapchak, & Aravinda Chakravarti. (1996). Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient. Nature Genetics. 14(3). 341–344. 199 indexed citations
12.
Bolk, Stacey, Misha Angrist, Stuart Schwartz, et al.. (1996). Congenital central hypoventilation syndrome: Mutation analysis of the receptor tyrosine kinase RET. American Journal of Medical Genetics. 63(4). 603–609. 35 indexed citations
13.
Bolk, Stacey, Misha Angrist, Stuart Schwartz, et al.. (1996). Congenital central hypoventilation syndrome: Mutation analysis of the receptor tyrosine kinase RET. American Journal of Medical Genetics. 63(4). 603–609. 3 indexed citations
14.
Angrist, Misha, Stacey Bolk, Bonnie Thiel, et al.. (1995). Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease. Human Molecular Genetics. 4(5). 821–830. 180 indexed citations
15.
Puffenberger, Erik G., Stacey Bolk, Tara C. Matise, et al.. (1994). Identity-by-descent and association mapping of a recessive gene for Hirschsprung disease on human chromosome 13q22. Human Molecular Genetics. 3(8). 1217–1225. 175 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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