Heather M. Stringham

61.1k total citations
19 papers, 833 citations indexed

About

Heather M. Stringham is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Heather M. Stringham has authored 19 papers receiving a total of 833 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 11 papers in Genetics and 5 papers in Ophthalmology. Recurrent topics in Heather M. Stringham's work include Genetic Associations and Epidemiology (8 papers), Genetic Mapping and Diversity in Plants and Animals (5 papers) and Genetic and phenotypic traits in livestock (3 papers). Heather M. Stringham is often cited by papers focused on Genetic Associations and Epidemiology (8 papers), Genetic Mapping and Diversity in Plants and Animals (5 papers) and Genetic and phenotypic traits in livestock (3 papers). Heather M. Stringham collaborates with scholars based in United States, Finland and United Kingdom. Heather M. Stringham's co-authors include Michael Boehnke, Julia E. Richards, Catherine A. Downs, Paul R. Lichter, Karen L. Mohlke, Francis S. Collins, Anne Jackson, Timo T. Valle, Jaakko Tuomilehto and Richard N. Bergman and has published in prestigious journals such as Diabetes, Ophthalmology and The American Journal of Human Genetics.

In The Last Decade

Heather M. Stringham

19 papers receiving 806 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 M. Stringham United States 13 447 346 211 125 121 19 833
Vedam L. Ramprasad India 18 534 1.2× 207 0.6× 382 1.8× 90 0.7× 42 0.3× 61 1.1k
A Munnich France 14 685 1.5× 347 1.0× 83 0.4× 56 0.4× 254 2.1× 37 1.1k
Matthias Klaften Germany 13 255 0.6× 115 0.3× 39 0.2× 93 0.7× 136 1.1× 22 460
Manuela Fanciulli Italy 11 241 0.5× 367 1.1× 44 0.2× 27 0.2× 21 0.2× 13 726
Catherine Schwesinger United States 10 573 1.3× 90 0.3× 152 0.7× 104 0.8× 106 0.9× 11 813
Yusaku Yoshida Japan 12 223 0.5× 60 0.2× 29 0.1× 187 1.5× 268 2.2× 30 718
L Dralands Belgium 12 258 0.6× 39 0.1× 553 2.6× 35 0.3× 86 0.7× 41 828
Natalie Hauser United States 13 293 0.7× 228 0.7× 17 0.1× 74 0.6× 42 0.3× 26 562
Mehdi Motallebipour Sweden 7 339 0.8× 108 0.3× 357 1.7× 48 0.4× 34 0.3× 7 659
Tie Ke China 16 704 1.6× 117 0.3× 49 0.2× 62 0.5× 35 0.3× 35 913

Countries citing papers authored by Heather M. Stringham

Since Specialization
Citations

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

Fields of papers citing papers by Heather M. Stringham

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Heather M. Stringham

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

All Works

19 of 19 papers shown
1.
Xia, Lu, Seunggeun Lee, Xiang Zhou, et al.. (2018). Subset-Based Analysis Using Gene-Environment Interactions for Discovery of Genetic Associations across Multiple Studies or Phenotypes. Human Heredity. 83(6). 283–314. 5 indexed citations
2.
Davis, James P., Jeroen R. Huyghe, Adam E. Locke, et al.. (2017). Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study. PLoS Genetics. 13(10). e1007079–e1007079. 31 indexed citations
3.
4.
Kim, Daniel Seung, Anne Jackson, Heather M. Stringham, et al.. (2017). Novel association of TM6SF2 rs58542926 genotype with increased serum tyrosine levels and decreased apoB-100 particles in Finns. Journal of Lipid Research. 58(7). 1471–1481. 43 indexed citations
5.
Rice, John D., et al.. (2017). Meta‐analysis of gene‐environment interaction exploiting gene‐environment independence across multiple case‐control studies. Statistics in Medicine. 36(24). 3895–3909. 1 indexed citations
6.
Shi, Li, Bhramar Mukherjee, Jeremy M. G. Taylor, et al.. (2014). The Role of Environmental Heterogeneity in Meta-Analysis of Gene-Environment Interactions With Quantitative Traits. Genetic Epidemiology. 38(5). 416–429. 10 indexed citations
7.
Li, Xia, Yu‐Hsiang Shu, Anny H. Xiang, et al.. (2009). Additive Effects of Genetic Variation in GCK and G6PC2 on Insulin Secretion and Fasting Glucose. Diabetes. 58(12). 2946–2953. 28 indexed citations
8.
Scott, Laura J., Lori L. Bonnycastle, Cristen J. Willer, et al.. (2006). Association of Transcription Factor 7-Like 2 (TCF7L2) Variants With Type 2 Diabetes in a Finnish Sample. Diabetes. 55(9). 2649–2653. 186 indexed citations
9.
Stringham, Heather M., et al.. (2002). X-Linked Macular Degeneration Associated with a RPGR Nonsense Mutation Causing Premature Termination. Investigative Ophthalmology & Visual Science. 43(13). 803–803. 1 indexed citations
10.
Ayyagari, Radha, F. Yesim Demirci, Jiafan Liu, et al.. (2002). X-Linked Recessive Atrophic Macular Degeneration from RPGR Mutation. Genomics. 80(2). 166–171. 112 indexed citations
11.
Fingerlin, Tasha E., Michael R. Erdos, Richard M. Watanabe, et al.. (2002). Variation in Three Single Nucleotide Polymorphisms in the Calpain-10 Gene Not Associated With Type 2 Diabetes in a Large Finnish Cohort. Diabetes. 51(5). 1644–1648. 52 indexed citations
12.
Stringham, Heather M. & Michael Boehnke. (2001). Lod scores for gene mapping in the presence of marker map uncertainty. Genetic Epidemiology. 21(1). 31–39. 7 indexed citations
13.
Cerosaletti, Karen, Ethan M. Lange, Heather M. Stringham, et al.. (1998). Fine Localization of the Nijmegen Breakage Syndrome Gene to 8q21: Evidence for a Common Founder Haplotype. The American Journal of Human Genetics. 63(1). 125–134. 46 indexed citations
14.
Othman, Mohammad, Scot A. Sullivan, Gregory L. Skuta, et al.. (1998). Autosomal Dominant Nanophthalmos (NNO1) with High Hyperopia and Angle-Closure Glaucoma Maps to Chromosome 11. The American Journal of Human Genetics. 63(5). 1411–1418. 94 indexed citations
15.
Lichter, Paul R., Julia E. Richards, Catherine A. Downs, et al.. (1997). Cosegregation of Open-angle Glaucoma and the Nail-Patella Syndrome. American Journal of Ophthalmology. 124(4). 506–515. 76 indexed citations
16.
Lichter, Paul R., Julia E. Richards, Michael Boehnke, et al.. (1997). Juvenile Glaucoma Linked to the GLC1A Gene on Chromosome 1q in a Panamanian Family. American Journal of Ophthalmology. 123(3). 413–416. 13 indexed citations
17.
Johnson, A. Tim, Julia E. Richards, Michael Boehnke, et al.. (1996). Clinical Phenotype of Juvenile-onset Primary Open-angle Glaucoma Linked to Chromosome 1q. Ophthalmology. 103(5). 808–814. 51 indexed citations
18.
Stringham, Heather M. & Michael Boehnke. (1996). Identifying marker typing incompatibilities in linkage analysis.. PubMed. 59(4). 946–50. 36 indexed citations
19.
Lichter, Paul R., Julia E. Richards, Michael Boehnke, et al.. (1996). Juvenile glaucoma linked to GLCIA in a Panamanian family.. PubMed. 94. 335–46; discussion 347. 3 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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