Heather Pierce

1.2k total citations
16 papers, 728 citations indexed

About

Heather Pierce is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Heather Pierce has authored 16 papers receiving a total of 728 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Genetics and 5 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Heather Pierce's work include BRCA gene mutations in cancer (6 papers), Sarcoma Diagnosis and Treatment (3 papers) and Genomics and Rare Diseases (2 papers). Heather Pierce is often cited by papers focused on BRCA gene mutations in cancer (6 papers), Sarcoma Diagnosis and Treatment (3 papers) and Genomics and Rare Diseases (2 papers). Heather Pierce collaborates with scholars based in United States, United Kingdom and Italy. Heather Pierce's co-authors include Andrew J. Pierce, Dawn Michelle Stults, Michael W. Killen, John P. O’Bryan, Checo J. Rorie, Bernard E. Weissman, Khédoudja Nafa, Prema Kolachana, Jaya M. Satagopan and Nathan A. Ellis and has published in prestigious journals such as Journal of Biological Chemistry, Cancer Research and Genome Research.

In The Last Decade

Heather Pierce

15 papers receiving 707 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Heather Pierce United States 11 512 247 134 102 99 16 728
Marieke Levitus Netherlands 10 973 1.9× 307 1.2× 338 2.5× 66 0.6× 127 1.3× 12 1.1k
Jonas Carlsson Almlöf Sweden 12 329 0.6× 150 0.6× 120 0.9× 46 0.5× 82 0.8× 16 681
Ulrike Schwarz‐Boeger Germany 10 401 0.8× 215 0.9× 167 1.2× 81 0.8× 172 1.7× 23 739
Gönül Oğur Türkiye 13 468 0.9× 210 0.9× 38 0.3× 26 0.3× 27 0.3× 51 700
Jonathan P. Park United States 19 462 0.9× 267 1.1× 83 0.6× 203 2.0× 177 1.8× 36 898
Tuomo Mantere Finland 12 330 0.6× 243 1.0× 133 1.0× 67 0.7× 57 0.6× 22 605
Simon McBride United Kingdom 5 310 0.6× 230 0.9× 41 0.3× 106 1.0× 148 1.5× 9 635
Dominiek Smeets Belgium 13 283 0.6× 87 0.4× 235 1.8× 122 1.2× 308 3.1× 19 719
Jennifer L. Geurts United States 9 245 0.5× 290 1.2× 102 0.8× 41 0.4× 136 1.4× 27 505
E. Cristy Ruteshouser United States 19 886 1.7× 206 0.8× 121 0.9× 26 0.3× 100 1.0× 23 1.0k

Countries citing papers authored by Heather Pierce

Since Specialization
Citations

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

Fields of papers citing papers by Heather Pierce

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Heather Pierce

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

All Works

16 of 16 papers shown
1.
Roberts, John E., Laura Monje‐Garcia, Robert J. Theobald, et al.. (2025). Putting the patient at the centre: a call for research involvement of nurses, midwives and allied health professionals working in genomics. BMJ Open. 15(8). e086962–e086962.
2.
Izatt, Louise, Martina Owens, Heather Pierce, Sarah Wilcox, & Soo‐Mi Park. (2021). A practical guide to genetic testing in endocrinology. Clinical Endocrinology. 97(4). 388–399. 1 indexed citations
3.
Andrews, Katrina, Edward H. Thompson, Ben Challis, et al.. (2020). Genetic testing for hereditary hyperparathyroidism and familial hypocalciuric hypercalcaemia in a large UK cohort. Clinical Endocrinology. 93(4). 409–418. 25 indexed citations
4.
Slavotinek, Anne, Julie Kaylor, Heather Pierce, et al.. (2014). CRB2 Mutations Produce a Phenotype Resembling Congenital Nephrosis, Finnish Type, with Cerebral Ventriculomegaly and Raised Alpha-Fetoprotein. The American Journal of Human Genetics. 96(1). 162–169. 59 indexed citations
5.
McDonald, John, Rouzan G. Karabakhtsian, Heather Pierce, et al.. (2012). Small cell carcinoma of the ovary of hypercalcemic type: a case report. Journal of Pediatric Surgery. 47(3). 588–592. 21 indexed citations
6.
Eble, John N., Heather Pierce, Paul L. Crispen, et al.. (2012). Bilateral Ovarian Steroid Cell Tumors and Massive Macronodular Adrenocortical Disease in a Patient With Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome. American Journal of Clinical Pathology. 138(suppl_1). A203–A203. 2 indexed citations
7.
Stults, Dawn Michelle, Michael W. Killen, Heather Pierce, & Andrew J. Pierce. (2007). Genomic architecture and inheritance of human ribosomal RNA gene clusters. Genome Research. 18(1). 13–18. 230 indexed citations
8.
Rosenthal, M. Sara & Heather Pierce. (2005). Inherited Medullary Thyroid Cancer and the Duty to Warn: Revisiting Pate v. Threlkel in Light of HIPAA. Thyroid. 15(2). 140–145. 14 indexed citations
9.
Rorie, Checo J., et al.. (2004). TheEws/Fli-1Fusion Gene Switches the Differentiation Program of Neuroblastomas to Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumors. Cancer Research. 64(4). 1266–1277. 73 indexed citations
10.
Offit, Kenneth, Heather Pierce, Tomas Kirchhoff, et al.. (2003). Frequency of CHEK2*1100delC in New York breast cancer cases and controls. BMC Medical Genetics. 4(1). 1–1. 105 indexed citations
11.
Offit, Kenneth, Shlomit Gilad, Shoshana Paglin, et al.. (2002). Rare variants of ATM and risk for Hodgkin's disease and radiation-associated breast cancers.. PubMed. 8(12). 3813–9. 29 indexed citations
12.
Spurdle, Amanda B., P Kolachana, Betsy Bove, et al.. (2001). A single nucleotide polymorphism in the 5' untranslated region of RAD51 and risk of cancer among BRCA1/2 mutation carriers.. PubMed. 10(9). 955–60. 118 indexed citations
13.
Martignetti, John A., Bruce D. Gelb, Heather Pierce, Piero Picci, & Robert J. Desnick. (2000). Malignant fibrous histiocytoma: Inherited and sporadic forms have loss of heterozygosity at chromosome bands 9p21–22—evidence for a common genetic defect. Genes Chromosomes and Cancer. 27(2). 191–195. 2 indexed citations
14.
Martignetti, John A., Bruce D. Gelb, Heather Pierce, Piero Picci, & Robert J. Desnick. (2000). Malignant fibrous histiocytoma: Inherited and sporadic forms have loss of heterozygosity at chromosome bands 9p21-22?evidence for a common genetic defect. Genes Chromosomes and Cancer. 27(2). 191–195. 30 indexed citations
15.
Pierce, Heather, Fred Schachat, Philip W. Brandt, Christian R. Lombardo, & Brian K. Kay. (1998). Identification of Troponin C Antagonists from a Phage-displayed Random Peptide Library. Journal of Biological Chemistry. 273(36). 23448–23453. 8 indexed citations
16.
Pierce, Heather, Nils B. Adey, & Brian K. Kay. (1996). Identification of cyclized calmodulin antagonists from a phage display random peptide library. Molecular Diversity. 1(4). 259–265. 11 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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