Betty Doan

740 total citations
16 papers, 418 citations indexed

About

Betty Doan is a scholar working on Genetics, Molecular Biology and Epidemiology. According to data from OpenAlex, Betty Doan has authored 16 papers receiving a total of 418 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Epidemiology. Recurrent topics in Betty Doan's work include Genetic Associations and Epidemiology (5 papers), Genetic Mapping and Diversity in Plants and Animals (5 papers) and Genetic and phenotypic traits in livestock (2 papers). Betty Doan is often cited by papers focused on Genetic Associations and Epidemiology (5 papers), Genetic Mapping and Diversity in Plants and Animals (5 papers) and Genetic and phenotypic traits in livestock (2 papers). Betty Doan collaborates with scholars based in United States, France and Italy. Betty Doan's co-authors include Yin Yao Shugart, Aravinda Chakravarti, Dan E. Arking, Joan E. Bailey‐Wilson, Josef Coresh, P. Ellen Grant, Eric Boerwinkle, Kim Doheny, Elizabeth Pugh and Rachel Straussberg and has published in prestigious journals such as Circulation, The American Journal of Human Genetics and Experimental Gerontology.

In The Last Decade

Betty Doan

16 papers receiving 400 citations

Peers

Betty Doan

CCM

GENET

EPIDE

Zujia Wen China

Evelise Regina Polina Brazil

Jes Fagerness United States

Benjamin M. Neale United States

Andrea Christoforou United States

C. Nuttin France

Miri Carmel Israel

Hilde M. H. Braakman Netherlands

Cristian Tornador Spain

Amy Schneider Australia

Zujia Wen China

Betty Doan

157 ×1.1

37 ×0.3

CCM

133 ×1.3

GENET

8 ×0.2

27 ×0.6

EPIDE

Citations per year, relative to Betty Doan Betty Doan (= 1×) peers Zujia Wen

Countries citing papers authored by Betty Doan

Since Specialization

Citations

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

Fields of papers citing papers by Betty Doan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Betty Doan

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

All Works

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16 of 16 papers shown

Fernandez, Raquel, Marta Bleda, Berta Luzón‐Toro, et al.. (2013). Pathways systematically associated to Hirschsprung’s disease. Orphanet Journal of Rare Diseases. 8(1). 187–187. 14 indexed citations

Benke, Kelly S., Michelle C. Carlson, Betty Doan, et al.. (2011). The association of genetic variants in interleukin-1 genes with cognition: Findings from the cardiovascular health study. Experimental Gerontology. 46(12). 1010–1019. 26 indexed citations

Scharpf, Robert B., Ingo Ruczinski, Benilton S. Carvalho, et al.. (2010). A multilevel model to address batch effects in copy number estimation using SNP arrays. Biostatistics. 12(1). 33–50. 30 indexed citations

Kao, W.H. Linda, Dan E. Arking, Wendy S. Post, et al.. (2009). Genetic Variations in Nitric Oxide Synthase 1 Adaptor Protein Are Associated With Sudden Cardiac Death in US White Community-Based Populations. Circulation. 119(7). 940–951. 128 indexed citations

Kim, Yoonhee, Betty Doan, Priya Duggal, & Joan E. Bailey‐Wilson. (2007). Normalization of microarray expression data using within-pedigree pool and its effect on linkage analysis. BMC Proceedings. 1(S1). S152–S152. 9 indexed citations

Doan, Betty, Alexa J.M. Sorant, Constantine Frangakis, Joan E. Bailey‐Wilson, & Yin Yao Shugart. (2006). Covariate-based linkage analysis: application of a propensity score as the single covariate consistently improves power to detect linkage. European Journal of Human Genetics. 14(9). 1018–1026. 8 indexed citations

Daw, E. Warwick, Betty Doan, & Robert C. Elston. (2005). Linkage mapping methods applied to the COGA data set: Presentation Group 4 of Genetic Analysis Workshop 14. Genetic Epidemiology. 29(S1). S29–S34. 2 indexed citations

Duggal, Priya, Elizabeth M. Gillanders, Rasika A. Mathias, et al.. (2005). Identification of tag single-nucleotide polymorphisms in regions with varying linkage disequilibrium. BMC Genetics. 6(S1). S73–S73. 7 indexed citations

Doan, Betty, Constantine Frangakis, Yin Yao Shugart, & Joan E. Bailey‐Wilson. (2005). Application of the propensity score in a covariate-based linkage analysis of the Collaborative Study on the Genetics of Alcoholism. BMC Genetics. 6(S1). S33–S33. 6 indexed citations

10.

Ibay, Grace, Betty Doan, Taura N. Holmes, et al.. (2004). Candidate high myopia loci on chromosomes 18p and 12q do not play a major role in susceptibility to common myopia. BMC Medical Genetics. 5(1). 20–20. 35 indexed citations

11.

Stambolian, Dwight, Grace Ibay, Betty Doan, et al.. (2004). Genomic Wide Linkage of Familial Myopia and evidence for a locus on chromosome 22. 45(13). 3723–3723. 2 indexed citations

12.

Klein, Alison P., Alexa J.M. Sorant, Agnes Baffoe‐Bonnie, et al.. (2003). Importance sampling method of correction for multiple testing in affected sib-pair linkage analysis. BMC Genetics. 4(Suppl 1). S73–S73. 7 indexed citations

13.

Shugart, Yin Yao, et al.. (2003). Results of a genome‐wide linkage scan for stuttering. American Journal of Medical Genetics Part A. 124A(2). 133–135. 55 indexed citations

14.

Piao, Xianhua, Lina Basel‐Vanagaite, Rachel Straussberg, et al.. (2002). An Autosomal Recessive Form of Bilateral Frontoparietal Polymicrogyria Maps to Chromosome 16q12.2-21. The American Journal of Human Genetics. 70(4). 1028–1033. 84 indexed citations

15.

Shugart, Yin Yao, Claudia Specchia, Huihua Li, et al.. (2001). Comparison of Sib Pair‐Based Approaches for Identifying Quantitative Trait Loci Underlying Asthma in the Busselton Families. Genetic Epidemiology. 21(S1). S198–203. 3 indexed citations

16.

Voisin, M C, et al.. (1989). [Extracardiac malformations in tetralogy of Fallot].. PubMed. 82(5). 689–92. 2 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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