Rachel Lorier

1.0k total citations
13 papers, 698 citations indexed

About

Rachel Lorier is a scholar working on Molecular Biology, Oncology and Pharmacology. According to data from OpenAlex, Rachel Lorier has authored 13 papers receiving a total of 698 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Oncology and 4 papers in Pharmacology. Recurrent topics in Rachel Lorier's work include Pharmacogenetics and Drug Metabolism (4 papers), Drug Transport and Resistance Mechanisms (2 papers) and MicroRNA in disease regulation (2 papers). Rachel Lorier is often cited by papers focused on Pharmacogenetics and Drug Metabolism (4 papers), Drug Transport and Resistance Mechanisms (2 papers) and MicroRNA in disease regulation (2 papers). Rachel Lorier collaborates with scholars based in United States, Canada and Qatar. Rachel Lorier's co-authors include Shuang Jia, Martin J. Hessner, Mariko Suchi, Sreelatha T. Reddy, Ulrich Broeckel, Rhonda Geoffrey, James Verbsky, Ulrich Broeckel, Amy Turner and Praful Aggarwal and has published in prestigious journals such as New England Journal of Medicine, The Journal of Immunology and PLoS ONE.

In The Last Decade

Rachel Lorier

13 papers receiving 683 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Rachel Lorier United States	10	363	247	161	124	87	13	698
Tianbo Jin China	16	374 1.0×	130 0.5×	111 0.7×	134 1.1×	19 0.2×	95	882
Agnieszka Zielińska Poland	14	203 0.6×	534 2.2×	39 0.2×	95 0.8×	249 2.9×	40	941
Branka Zukić Serbia	16	217 0.6×	53 0.2×	42 0.3×	93 0.8×	99 1.1×	56	559
Emanuela Campalani United Kingdom	8	165 0.5×	374 1.5×	63 0.4×	38 0.3×	53 0.6×	14	593
Lisa R. Treviño United States	8	457 1.3×	54 0.2×	123 0.8×	126 1.0×	359 4.1×	15	1.2k
Ronald Honchel United States	11	249 0.7×	44 0.2×	41 0.3×	73 0.6×	84 1.0×	15	720
Vanessa S. Silveira Brazil	16	430 1.2×	45 0.2×	29 0.2×	24 0.2×	85 1.0×	32	648
Gwénaëlle Carn France	12	306 0.8×	69 0.3×	44 0.3×	354 2.9×	16 0.2×	22	927
Audrey Weber United States	12	143 0.4×	105 0.4×	33 0.2×	202 1.6×	155 1.8×	30	612
Daniel Klintman Sweden	11	75 0.2×	163 0.7×	48 0.3×	54 0.4×	12 0.1×	16	428

Countries citing papers authored by Rachel Lorier

Since Specialization

Citations

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

Fields of papers citing papers by Rachel Lorier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rachel Lorier

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

All Works

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13 of 13 papers shown

Turner, Amy, Praful Aggarwal, Andrea Matter, et al.. (2021). Donor-specific phenotypic variation in hiPSC cardiomyocyte-derived exosomes impacts endothelial cell function. American Journal of Physiology-Heart and Circulatory Physiology. 320(3). H954–H968. 12 indexed citations

Basel, Donald, David Bick, Rachel Lorier, et al.. (2017). A Rare Combination of Functional Disomy Xp, Deletion Xq13.2-q28 Spanning the XIST Gene, and Duplication 3q25.33-q29 in a Female with der(X)t(X;3)(q13.2;q25.33). Journal of Pediatric Genetics. 7(1). 23–28. 4 indexed citations

Pratt, Victoria M., Robin E. Everts, Praful Aggarwal, et al.. (2016). Characterization of 137 Genomic DNA Reference Materials for 28 Pharmacogenetic Genes: A GeT-RM Collaborative Project. 3 indexed citations

Pratt, Victoria M., Robin E. Everts, Praful Aggarwal, et al.. (2015). Characterization of 137 Genomic DNA Reference Materials for 28 Pharmacogenetic Genes. Journal of Molecular Diagnostics. 18(1). 109–123. 107 indexed citations

Aggarwal, Praful, Amy Turner, Andrea Matter, et al.. (2014). RNA Expression Profiling of Human iPSC-Derived Cardiomyocytes in a Cardiac Hypertrophy Model. PLoS ONE. 9(9). e108051–e108051. 43 indexed citations

Giampietro, Philip F., Linlea Armstrong, Robert D. Blank, et al.. (2014). Whole exome sequencing identifies a POLRID mutation segregating in a father and two daughters with findings of Klippel–Feil and Treacher Collins syndromes. American Journal of Medical Genetics Part A. 167(1). 95–102. 10 indexed citations

Thompson, Patrick, Heather E. Wheeler, Shannon M. Delaney, et al.. (2014). Pharmacokinetics and pharmacogenomics of daunorubicin in children: a report from the Children’s Oncology Group. Cancer Chemotherapy and Pharmacology. 74(4). 831–838. 24 indexed citations

Irvin, Marguerite R., C. Charles Gu, Alexander J. Stoddard, et al.. (2012). Whole-exome Sequencing and an iPSC-Derived Cardiomyocyte Model Provides a Powerful Platform for Gene Discovery in Left Ventricular Hypertrophy. Frontiers in Genetics. 3. 92–92. 16 indexed citations

Fernandez, Christian A., Colton Smith, Wenjian Yang, et al.. (2012). Concordance of DMET Plus Genotyping Results With Those of Orthogonal Genotyping Methods. Clinical Pharmacology & Therapeutics. 92(3). 360–365. 35 indexed citations

10.

Hicks, J. Kevin, Kristine R. Crews, James M. Hoffman, et al.. (2012). A Clinician-Driven Automated System for Integration of Pharmacogenetic Interpretations Into an Electronic Medical Record. Clinical Pharmacology & Therapeutics. 92(5). 563–566. 77 indexed citations

11.

Schmitt, Erica G., Dipica Haribhai, Jason B. Williams, et al.. (2012). IL-10 Produced by Induced Regulatory T Cells (iTregs) Controls Colitis and Pathogenic Ex-iTregs during Immunotherapy. The Journal of Immunology. 189(12). 5638–5648. 74 indexed citations

12.

Wineinger, Nathan E., Nicholas M. Pajewski, Richard Kennedy, et al.. (2011). Characterization of autosomal copy-number variation in African Americans: the HyperGEN Study. European Journal of Human Genetics. 19(12). 1271–1275. 5 indexed citations

13.

Reddy, Sreelatha T., Shuang Jia, Rhonda Geoffrey, et al.. (2009). An Autoinflammatory Disease Due to Homozygous Deletion of the IL1RN Locus. New England Journal of Medicine. 360(23). 2438–2444. 288 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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