Solveig K. Sieberts

9.5k total citations
23 papers, 946 citations indexed

About

Solveig K. Sieberts is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Solveig K. Sieberts has authored 23 papers receiving a total of 946 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 12 papers in Genetics and 4 papers in Physiology. Recurrent topics in Solveig K. Sieberts's work include Genetic Associations and Epidemiology (11 papers), Bioinformatics and Genomic Networks (9 papers) and Genetic Mapping and Diversity in Plants and Animals (5 papers). Solveig K. Sieberts is often cited by papers focused on Genetic Associations and Epidemiology (11 papers), Bioinformatics and Genomic Networks (9 papers) and Genetic Mapping and Diversity in Plants and Animals (5 papers). Solveig K. Sieberts collaborates with scholars based in United States, United Kingdom and Canada. Solveig K. Sieberts's co-authors include Eric E. Schadt, Philip L. De Jager, E. A. Thompson, Ellen M. Wijsman, Lei Yu, Charles C. White, Jishu Xu, Ellis Patrick, Sara Mostafavi and Chris Gaiteri and has published in prestigious journals such as Nature Communications, Nature Genetics and Nature Neuroscience.

In The Last Decade

Solveig K. Sieberts

23 papers receiving 933 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Solveig K. Sieberts United States 14 541 390 169 70 66 23 946
Tricia A. Thornton‐Wells United States 21 506 0.9× 309 0.8× 204 1.2× 32 0.5× 74 1.1× 41 1.1k
Jean Maurice Delabar France 23 851 1.6× 808 2.1× 214 1.3× 50 0.7× 84 1.3× 48 1.9k
Francesca Telese United States 14 1.1k 2.1× 259 0.7× 169 1.0× 70 1.0× 139 2.1× 31 1.5k
Fayçal Guedj United States 18 318 0.6× 403 1.0× 95 0.6× 23 0.3× 50 0.8× 32 1.0k
Mark Kilgore United States 13 517 1.0× 182 0.5× 200 1.2× 76 1.1× 139 2.1× 36 967
Pamela St. Jean United States 11 409 0.8× 405 1.0× 242 1.4× 38 0.5× 183 2.8× 16 1.0k
Omid Kohannim United States 20 500 0.9× 255 0.7× 219 1.3× 20 0.3× 51 0.8× 35 1.2k
Suk Ling Hong Kong 19 443 0.8× 198 0.5× 326 1.9× 64 0.9× 142 2.2× 65 1.1k
Mette A. Peters United States 17 580 1.1× 286 0.7× 176 1.0× 16 0.2× 86 1.3× 29 1.1k
Amy H. Yang United States 20 1.1k 2.0× 414 1.1× 201 1.2× 161 2.3× 100 1.5× 26 1.8k

Countries citing papers authored by Solveig K. Sieberts

Since Specialization
Citations

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

Fields of papers citing papers by Solveig K. Sieberts

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Solveig K. Sieberts. 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 Solveig K. Sieberts. The network helps show where Solveig K. Sieberts may publish in the future.

Co-authorship network of co-authors of Solveig K. Sieberts

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

All Works

20 of 20 papers shown
1.
Neto, Elias Chaibub, et al.. (2024). A novel estimator for the two-way partial AUC. BMC Medical Informatics and Decision Making. 24(1). 57–57. 1 indexed citations
2.
Fernandes, Blossom, Pamela Y. Collins, Jennifer Velloza, et al.. (2023). Evidencing the Impact of Web-Based Coproduction With Youth on Mental Health Research: Qualitative Findings From the MindKind Study. JMIR Public Health and Surveillance. 9. e42963–e42963. 7 indexed citations
3.
Hoffman, Gabriel E., Andrew E. Jaffe, Michael J. Gandal, et al.. (2022). Comment on: What genes are differentially expressed in individuals with schizophrenia? A systematic review. Molecular Psychiatry. 28(2). 523–525. 7 indexed citations
4.
Gockley, Jake, Kelsey S. Montgomery, William L. Poehlman, et al.. (2021). Multi-tissue neocortical transcriptome-wide association study implicates 8 genes across 6 genomic loci in Alzheimer’s disease. Genome Medicine. 13(1). 76–76. 42 indexed citations
5.
Greenwood, Anna K., Kelsey S. Montgomery, Kara Woo, et al.. (2020). The AD Knowledge Portal: A Repository for Multi‐Omic Data on Alzheimer's Disease and Aging. Current Protocols in Human Genetics. 108(1). e105–e105. 52 indexed citations
6.
Mukherjee, Sumit, Christoph Preuß, Suman Jayadev, et al.. (2020). Molecular estimation of neurodegeneration pseudotime in older brains. Nature Communications. 11(1). 5781–5781. 31 indexed citations
7.
Mukherjee, Sumit, Thanneer M. Perumal, Kenneth Daily, et al.. (2019). Identifying and ranking potential driver genes of Alzheimer’s disease using multiview evidence aggregation. Bioinformatics. 35(14). i568–i576. 13 indexed citations
8.
Hauberg, Mads E., John F. Fullard, Lingxue Zhu, et al.. (2018). Differential activity of transcribed enhancers in the prefrontal cortex of 537 cases with schizophrenia and controls. Molecular Psychiatry. 24(11). 1685–1695. 29 indexed citations
9.
Huckins, Laura M., Amanda Dobbyn, Douglas M. Ruderfer, et al.. (2017). Novel Bipolar And Schizophrenia Risk Genes Identified Through Genic Associations In Transcriptome Imputation. European Neuropsychopharmacology. 27. S487–S487. 1 indexed citations
10.
Ng, Bernard, Charles C. White, Hans‐Ulrich Klein, et al.. (2017). An xQTL map integrates the genetic architecture of the human brain's transcriptome and epigenome. Nature Neuroscience. 20(10). 1418–1426. 230 indexed citations
11.
Ferté, Charles, Andrew D. Trister, Erich Huang, et al.. (2013). Impact of Bioinformatic Procedures in the Development and Translation of High-Throughput Molecular Classifiers in Oncology. Clinical Cancer Research. 19(16). 4315–4325. 33 indexed citations
12.
Derry, Jonathan M.J., Lara M. Mangravite, Christine Suver, et al.. (2012). Developing predictive molecular maps of human disease through community-based modeling. Nature Genetics. 44(2). 127–130. 36 indexed citations
13.
Greenawalt, Danielle M., Solveig K. Sieberts, Cynthia J. Girman, et al.. (2012). Integrating Genetic Association, Genetics of Gene Expression, and Single Nucleotide Polymorphism Set Analysis to Identify Susceptibility Loci for Type 2 Diabetes Mellitus. American Journal of Epidemiology. 176(5). 423–430. 31 indexed citations
14.
Greenawalt, Danielle M., Radu Dobrin, Eugene Chudin, et al.. (2011). A survey of the genetics of stomach, liver, and adipose gene expression from a morbidly obese cohort. Genome Research. 21(7). 1008–1016. 99 indexed citations
15.
Su, Wan‐Lin, Solveig K. Sieberts, Robert Kleinhanz, et al.. (2010). Assessing the prospects of genome-wide association studies performed in inbred mice. Mammalian Genome. 21(3-4). 143–152. 16 indexed citations
16.
Aronne, Louis J., Serena Tonstad, Manuel Moreno, et al.. (2010). A clinical trial assessing the safety and efficacy of taranabant, a CB1R inverse agonist, in obese and overweight patients: a high-dose study. International Journal of Obesity. 34(5). 919–935. 73 indexed citations
17.
Murua, Alejandro, Werner Stuetzle, Jeremy Tantrum, & Solveig K. Sieberts. (2008). Model Based Document Classification and Clustering. 8. 1–24. 3 indexed citations
18.
Sieberts, Solveig K. & Eric E. Schadt. (2007). Moving toward a system genetics view of disease. Mammalian Genome. 18(6-7). 389–401. 131 indexed citations
19.
George, Andrew W., Saonli Basu, Na Li, et al.. (2003). Approaches to mapping genetically correlated complex traits. BMC Genetics. 4(S1). S71–S71. 6 indexed citations
20.
Sieberts, Solveig K., Ellen M. Wijsman, & E. A. Thompson. (2002). Relationship Inference from Trios of Individuals, in the Presence of Typing Error. The American Journal of Human Genetics. 70(1). 170–180. 57 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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