Stephanie Hallam

839 total citations
18 papers, 630 citations indexed

About

Stephanie Hallam is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Stephanie Hallam has authored 18 papers receiving a total of 630 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 7 papers in Molecular Biology and 5 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Stephanie Hallam's work include Genomics and Rare Diseases (6 papers), Cystic Fibrosis Research Advances (4 papers) and Genomics and Phylogenetic Studies (3 papers). Stephanie Hallam is often cited by papers focused on Genomics and Rare Diseases (6 papers), Cystic Fibrosis Research Advances (4 papers) and Genomics and Phylogenetic Studies (3 papers). Stephanie Hallam collaborates with scholars based in United States and United Kingdom. Stephanie Hallam's co-authors include David A. Hopwood, Francisco Malpartida, Amy Cronister, Alan E. Donnenfeld, Michael J. Butler, Jamie McDonald, Kenneth J. Ward, Helen M. Kieser, David Sugden and G. O. Humphreys and has published in prestigious journals such as Nature, Gene and Fertility and Sterility.

In The Last Decade

Stephanie Hallam

17 papers receiving 613 citations

Peers

Stephanie Hallam

PHARM

GENET

PRM

Danijela Drakulić Serbia

Xiaodan Yu China

Catherine A. Taylor Canada

Xiao Ji China

Gagan B. Panigrahi Canada

George Stratigopoulos United States

Sagar Ghosh United States

Tri M. Bui Nguyen United States

Yali Xie China

Maria Grazia Mascolo Italy

Danijela Drakulić Serbia

Stephanie Hallam

296 ×1.0

29 ×0.1

PHARM

85 ×0.4

GENET

53 ×0.5

PRM

94 ×1.0

Citations per year, relative to Stephanie Hallam Stephanie Hallam (= 1×) peers Danijela Drakulić

Countries citing papers authored by Stephanie Hallam

Since Specialization

Citations

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

Fields of papers citing papers by Stephanie Hallam

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stephanie Hallam

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

All Works

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18 of 18 papers shown

Hallam, Stephanie, et al.. (2025). Exploring Student Perceptions and the Potential Impact of OER in a Textbook Rental Environment. 1(1). 58–91.

Hallam, Stephanie, et al.. (2021). Overdue: Collection development and deselection projects for a faculty-selected collection. College & Undergraduate Libraries. 28(1). 51–66. 1 indexed citations

Hallam, Stephanie, et al.. (2021). Using government documents in open pedagogy: A method for engagement and building skills. MethodsX. 9. 101612–101612. 1 indexed citations

Hallam, Stephanie, et al.. (2021). A process of engagement: Using government documents in open pedagogy. The Journal of Academic Librarianship. 47(3). 102358–102358. 2 indexed citations

Joseph, Loren, Milena Cankovic, Pranil Chandra, et al.. (2016). The Spectrum of Clinical Utilities in Molecular Pathology Testing Procedures for Inherited Conditions and Cancer. Journal of Molecular Diagnostics. 18(5). 605–619. 44 indexed citations

Perreault-Micale, Cynthia L., et al.. (2015). A rigorous approach for selection of optimal variant sets for carrier screening with demonstration of clinical utility. Molecular Genetics & Genomic Medicine. 3(4). 363–373. 7 indexed citations

Hallam, Stephanie, Heather H. Nelson, Valerie Greger, et al.. (2014). Validation for Clinical Use of, and Initial Clinical Experience with, a Novel Approach to Population-Based Carrier Screening using High-Throughput, Next-Generation DNA Sequencing. Journal of Molecular Diagnostics. 16(2). 180–189. 31 indexed citations

Perreault-Micale, Cynthia L., Caleb J. Kennedy, Dana Neitzel, et al.. (2014). Truncating Variants in the Majority of the Cytoplasmic Domain of PCDH15 Are Unlikely to Cause Usher Syndrome 1F. Journal of Molecular Diagnostics. 16(6). 673–678. 10 indexed citations

Hallam, Stephanie, et al.. (2013). Carrier screening of 8,500 IVF patients utilizing next generation DNA sequencing detects common, rare and otherwise undetectable mutations across society-recommended diseases. Fertility and Sterility. 100(3). S479–S480. 1 indexed citations

10.

Umbarger, Mark A., Caleb J. Kennedy, Niru Chennagiri, et al.. (2013). Next-generation carrier screening. Genetics in Medicine. 16(2). 132–140. 30 indexed citations

11.

Hoffman, Jodi D., Valerie Greger, Erin T. Strovel, et al.. (2013). Next‐generation DNA sequencing of HEXA: a step in the right direction for carrier screening. Molecular Genetics & Genomic Medicine. 1(4). 260–268. 19 indexed citations

12.

Cronister, Amy, et al.. (2008). Prevalence and Instability of Fragile X Alleles. Obstetrics and Gynecology. 111(3). 596–601. 55 indexed citations

13.

Cronister, Amy, Miriam S. DiMaio, Maurice J. Mahoney, Alan E. Donnenfeld, & Stephanie Hallam. (2005). Fragile X syndrome carrier screening in the prenatal genetic counseling setting. Genetics in Medicine. 7(4). 246–250. 44 indexed citations

14.

McDonald, Jamie, Franklin J. Miller, Stephanie Hallam, et al.. (2000). Clinical manifestations in a large hereditary hemorrhagic telangiectasia (HHT) type 2 kindred. American Journal of Medical Genetics. 93(4). 320–327. 68 indexed citations

15.

Hoffman, Jodi D., Stephanie Hallam, Vickie L. Venne, Elaine Lyon, & Kenneth Ward. (1998). Implications of a novel cryptic splice site in the BRCA1 gene. American Journal of Medical Genetics. 80(2). 140–144. 26 indexed citations

16.

Hoffman, Jodi D., et al.. (1998). Implications of a novel cryptic splice site in the BRCA1 gene. American Journal of Medical Genetics. 80(2). 140–144. 4 indexed citations

17.

Hallam, Stephanie, Francisco Malpartida, & David A. Hopwood. (1988). Nucleotide sequence, transcription and deduced function of a gene involved in polyketide antibiotic synthesis in Streptomyces coelicolor. Gene. 74(2). 305–320. 153 indexed citations

18.

Malpartida, Francisco, Stephanie Hallam, Helen M. Kieser, et al.. (1987). Homology between Streptomyces genes coding for synthesis of different polyketides used to clone antibiotic biosynthetic genes. Nature. 325(6107). 818–821. 134 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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