Sarah Bertelsen

10.4k total citations
42 papers, 1.6k citations indexed

About

Sarah Bertelsen is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Sarah Bertelsen has authored 42 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 16 papers in Genetics and 14 papers in Physiology. Recurrent topics in Sarah Bertelsen's work include Genetic Associations and Epidemiology (12 papers), Alzheimer's disease research and treatments (12 papers) and Genetic Mapping and Diversity in Plants and Animals (5 papers). Sarah Bertelsen is often cited by papers focused on Genetic Associations and Epidemiology (12 papers), Alzheimer's disease research and treatments (12 papers) and Genetic Mapping and Diversity in Plants and Animals (5 papers). Sarah Bertelsen collaborates with scholars based in United States, Türkiye and United Kingdom. Sarah Bertelsen's co-authors include Alison Goate, Carlos Cruchaga, Anthony L. Hinrichs, John C. Morris, Celeste M. Karch, David M. Holtzman, Kevin H. Mayo, Anne M. Fagan, Laura J. Bierut and Oscar Harari and has published in prestigious journals such as Proceedings of the National Academy of Sciences, PLoS ONE and Biological Psychiatry.

In The Last Decade

Sarah Bertelsen

40 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sarah Bertelsen United States 21 667 601 347 315 216 42 1.6k
Jarek Wegiel United States 19 830 1.2× 665 1.1× 566 1.6× 449 1.4× 316 1.5× 45 2.0k
Silvia Bagnoli Italy 29 1.0k 1.5× 814 1.4× 342 1.0× 187 0.6× 363 1.7× 135 2.4k
M. Axel Wollmer Germany 25 1.3k 1.9× 954 1.6× 474 1.4× 307 1.0× 474 2.2× 56 2.9k
M. Florencia Iulita Canada 26 969 1.5× 554 0.9× 503 1.4× 122 0.4× 413 1.9× 47 2.2k
Hassan Rahmoune United Kingdom 30 317 0.5× 864 1.4× 227 0.7× 394 1.3× 248 1.1× 61 2.4k
Annerieke Sierksma Belgium 19 695 1.0× 929 1.5× 514 1.5× 159 0.5× 281 1.3× 26 2.0k
Mary E. Hamby United States 16 306 0.5× 541 0.9× 569 1.6× 168 0.5× 466 2.2× 25 1.9k
Daniel Felsky Canada 22 496 0.7× 582 1.0× 283 0.8× 265 0.8× 232 1.1× 79 1.9k
Pascual Sánchez‐Juan Spain 30 758 1.1× 1.3k 2.2× 554 1.6× 185 0.6× 337 1.6× 124 2.7k
Rebecca Sims United Kingdom 22 722 1.1× 570 0.9× 234 0.7× 371 1.2× 121 0.6× 51 1.5k

Countries citing papers authored by Sarah Bertelsen

Since Specialization
Citations

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

Fields of papers citing papers by Sarah Bertelsen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sarah Bertelsen

This figure shows the co-authorship network connecting the top 25 collaborators of Sarah Bertelsen. A scholar is included among the top collaborators of Sarah Bertelsen 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 Sarah Bertelsen. Sarah Bertelsen 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.
Bowles, Kathryn R., Derian A. Pugh, Yiyuan Liu, et al.. (2022). 17q21.31 sub-haplotypes underlying H1-associated risk for Parkinson’s disease are associated with LRRC37A/2 expression in astrocytes. Molecular Neurodegeneration. 17(1). 48–48. 21 indexed citations
2.
Deming, Yuetiva, Kathleen Black, David Carrell, et al.. (2016). Chitinase-3-like 1 protein (CHI3L1) locus influences cerebrospinal fluid levels of YKL-40. BMC Neurology. 16(1). 217–217. 12 indexed citations
3.
Harari, Oscar, Carlos Cruchaga, John S. K. Kauwe, et al.. (2014). Phosphorylated Tau-Aβ42 Ratio as a Continuous Trait for Biomarker Discovery for Early-Stage Alzheimer’s Disease in Multiplex Immunoassay Panels of Cerebrospinal Fluid. Biological Psychiatry. 75(9). 723–731. 69 indexed citations
4.
Kauwe, John S. K., Matthew H. Bailey, Perry G. Ridge, et al.. (2014). Genome-Wide Association Study of CSF Levels of 59 Alzheimer's Disease Candidate Proteins: Significant Associations with Proteins Involved in Amyloid Processing and Inflammation. PLoS Genetics. 10(10). e1004758–e1004758. 98 indexed citations
5.
Jin, Sheng Chih, Bruno A. Benítez, Celeste M. Karch, et al.. (2014). Coding variants in TREM2 increase risk for Alzheimer's disease. Human Molecular Genetics. 23(21). 5838–5846. 237 indexed citations
6.
Benítez, Bruno A., Celeste M. Karch, Yefei Cai, et al.. (2013). The PSEN1, p.E318G Variant Increases the Risk of Alzheimer's Disease in APOE-ε4 Carriers. PLoS Genetics. 9(8). e1003685–e1003685. 52 indexed citations
7.
Benítez, Bruno A., Celeste M. Karch, Sheng Chih Jin, et al.. (2013). O4–01–05: Rare variants in APP and PSEN1 genes associated with extreme levels of beta‐amyloid 42 and tau protein in cerebrospinal fluid. Alzheimer s & Dementia. 9(4S_Part_17). 1 indexed citations
8.
Cruchaga, Carlos, John S. K. Kauwe, Petra Nowotny, et al.. (2012). Cerebrospinal fluid APOE levels: an endophenotype for genetic studies for Alzheimer's disease. Human Molecular Genetics. 21(20). 4558–4571. 157 indexed citations
9.
Kauwe, John, Carlos Cruchaga, Sarah Bertelsen, et al.. (2010). Validating Predicted Biological Effects of Alzheimer's Disease Associated SNPs Using CSF Biomarker Levels. Journal of Alzheimer s Disease. 21(3). 833–842. 33 indexed citations
10.
Werlauff, Ulla, et al.. (2009). Physical characteristics and applicability of standard assessment methods in a total population of spinal muscular atrophy type II patients. Neuromuscular Disorders. 20(1). 34–43. 17 indexed citations
11.
12.
Dick, Danielle M., Fazil Alıev, Richard A. Grucza, et al.. (2008). Using Dimensional Models of Externalizing Psychopathology to Aid in Gene Identification. Archives of General Psychiatry. 65(3). 310–318. 109 indexed citations
13.
Wang, Jen C., Anthony L. Hinrichs, Sarah Bertelsen, et al.. (2007). Functional Variants in TAS2R38 and TAS2R16 Influence Alcohol Consumption in High‐Risk Families of African‐American Origin. Alcoholism Clinical and Experimental Research. 31(2). 209–215. 93 indexed citations
14.
Dick, Danielle M., Jen C. Wang, Jevon Plunkett, et al.. (2007). Family‐Based Association Analyses of Alcohol Dependence Phenotypes Across DRD2 and Neighboring Gene ANKK1. Alcoholism Clinical and Experimental Research. 31(10). 1645–1653. 93 indexed citations
15.
Dick, Danielle M., Arpana Agrawal, Jen C. Wang, et al.. (2007). Alcohol dependence with comorbid drug dependence: genetic and phenotypic associations suggest a more severe form of the disorder with stronger genetic contribution to risk*. Addiction. 102(7). 1131–1139. 74 indexed citations
16.
Nowotny, Petra, Sarah Bertelsen, Anthony L. Hinrichs, et al.. (2007). Association studies between common variants in prolyl isomerase Pin1 and the risk for late-onset Alzheimer's disease. Neuroscience Letters. 419(1). 15–17. 23 indexed citations
17.
Dick, Danielle M., Fazil Alıev, John R. Kramer, et al.. (2006). Association of CHRM2 with IQ: Converging Evidence for a Gene Influencing Intelligence. Behavior Genetics. 37(2). 265–272. 46 indexed citations
18.
Dunn, G. M., Anthony L. Hinrichs, Sarah Bertelsen, et al.. (2005). Microsatellites versus single-nucleotide polymorphisms in linkage analysis for quantitative and qualitative measures. BMC Genetics. 6(S1). S122–S122. 12 indexed citations
19.
Hinrichs, Anthony L., Sarah Bertelsen, Laura J. Bierut, et al.. (2005). Multipoint identity-by-descent computations for single-point polymorphism and microsatellite maps. BMC Genetics. 6(S1). S34–S34. 8 indexed citations
20.
Ghosh, Saurabh, Sarah Bertelsen, & Theodore Reich. (2003). Linkage mapping of total cholesterol level in a young cohort via nonparametric regression. BMC Genetics. 4(Suppl 1). S92–S92. 1 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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