Jessica Aldrich

1.7k total citations
22 papers, 359 citations indexed

About

Jessica Aldrich is a scholar working on Cancer Research, Molecular Biology and Oncology. According to data from OpenAlex, Jessica Aldrich has authored 22 papers receiving a total of 359 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Cancer Research, 10 papers in Molecular Biology and 8 papers in Oncology. Recurrent topics in Jessica Aldrich's work include Cancer Genomics and Diagnostics (14 papers), Multiple Myeloma Research and Treatments (5 papers) and Genetic factors in colorectal cancer (4 papers). Jessica Aldrich is often cited by papers focused on Cancer Genomics and Diagnostics (14 papers), Multiple Myeloma Research and Treatments (5 papers) and Genetic factors in colorectal cancer (4 papers). Jessica Aldrich collaborates with scholars based in United States and Ghana. Jessica Aldrich's co-authors include David W. Craig, Winnie S. Liang, Ahmet Kurdoglu, Jacquelyn McDonald, Geidy E. Serrano, J. Valla, Thomas G. Beach, Shobana Sekar, Jonathan Adkins and Lori Cuyugan and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Oncology and Blood.

In The Last Decade

Jessica Aldrich

21 papers receiving 351 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jessica Aldrich United States	10	179	97	86	74	62	22	359
Michael S. Lam United States	9	152 0.8×	103 1.1×	44 0.5×	70 0.9×	45 0.7×	13	365
Pardis Azmoon United States	11	164 0.9×	86 0.9×	38 0.4×	52 0.7×	52 0.8×	18	389
Amy C. Ladd United States	12	306 1.7×	100 1.0×	49 0.6×	80 1.1×	22 0.4×	22	507
Shenyi Jiang China	12	149 0.8×	54 0.6×	101 1.2×	44 0.6×	28 0.5×	22	371
Ribal Bassil United States	10	256 1.4×	40 0.4×	85 1.0×	54 0.7×	110 1.8×	10	689
Guofeng Meng China	12	247 1.4×	63 0.6×	28 0.3×	49 0.7×	31 0.5×	24	377
Zhi Fang China	14	188 1.1×	70 0.7×	81 0.9×	49 0.7×	11 0.2×	22	395
Teh‐Wei Wang Japan	7	134 0.7×	71 0.7×	78 0.9×	138 1.9×	33 0.5×	8	407
Nagarajan Paramasivam Germany	13	239 1.3×	43 0.4×	56 0.7×	23 0.3×	32 0.5×	41	408
Federica Storti Switzerland	11	180 1.0×	75 0.8×	28 0.3×	44 0.6×	40 0.6×	20	362

Countries citing papers authored by Jessica Aldrich

Since Specialization

Citations

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

Fields of papers citing papers by Jessica Aldrich

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jessica Aldrich

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

All Works

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20 of 20 papers shown

Szelinger, Szabolcs, Janine LoBello, Jessica Aldrich, et al.. (2021). Analytic validation and clinical utilization of the comprehensive genomic profiling test, GEM ExTra®. Oncotarget. 12(8). 726–739. 16 indexed citations

Skerget, Sheri, Jessica Aldrich, Christophe Legendre, et al.. (2019). Unsupervised Clustering of DNA Copy Number Profiles Identifies a High-Risk Subtype of Hyperdiploid Multiple Myeloma: An Mmrf Commpass Analysis. Blood. 134(Supplement_1). 1805–1805. 2 indexed citations

Skerget, Sheri, Jessica Aldrich, Sara Nasser, et al.. (2018). Analysis of Sequential Patient Samples from the Mmrf Commpass Study Identifies a High Risk Progression Phenotype. Blood. 132(Supplement 1). 111–111. 2 indexed citations

Pierobon, Mariaelena, Nicholas J. Robert, Donald W. Northfelt, et al.. (2018). Multi-omic profiling of metastatic lesions to guide treatment selection: The Side Out 2 trial experience.. Journal of Clinical Oncology. 36(15_suppl). 1077–1077. 3 indexed citations

Skerget, Sheri, Christophe Legendre, Jessica Aldrich, et al.. (2017). A Molecular Analysis of Cereblon-Related Immunomodulatory Drug Resistance in Commpass Multiple Myeloma Patients. Blood. 130. 1754–1754. 2 indexed citations

Legendre, Christophe, Jessica Aldrich, Sara Nasser, et al.. (2017). FGFR3 Mutations Are an Adverse Prognostic Factor in Patients with t(4;14)(p16;q32) Multiple Myeloma: An Mmrf Commpass Analysis. Blood. 130. 3027–3027. 6 indexed citations

Weiss, Glen J., Sara A. Byron, Jessica Aldrich, et al.. (2017). A prospective pilot study of genome-wide exome and transcriptome profiling in patients with small cell lung cancer progressing after first-line therapy. PLoS ONE. 12(6). e0179170–e0179170. 8 indexed citations

Zhrebker, Leah, Irene Cherni, Margaret M. Hinshelwood, et al.. (2017). Case report: whole exome sequencing of primary cardiac angiosarcoma highlights potential for targeted therapies. BMC Cancer. 17(1). 17–17. 21 indexed citations

Manojlovic, Zarko, Winnie S. Liang, Jessica Aldrich, et al.. (2017). Comprehensive molecular profiling of 718 Multiple Myelomas reveals significant differences in mutation frequencies between African and European descent cases. PLoS Genetics. 13(11). e1007087–e1007087. 45 indexed citations

10.

Halperin, Rebecca F., John D. Carpten, Zarko Manojlovic, et al.. (2017). A method to reduce ancestry related germline false positives in tumor only somatic variant calling. BMC Medical Genomics. 10(1). 61–61. 19 indexed citations

11.

Basu, Gargi D., Thomas Royce, Janine LoBello, et al.. (2016). Abstract 4493: Germline findings in targeted tumor sequencing using matched normal DNA. Cancer Research. 76(14_Supplement). 4493–4493.

12.

Aldrich, Jessica, Jonathan J. Keats, Winnie S. Liang, John D. Carpten, & David W. Craig. (2016). Abstract 45: Detection of focal somatic copy number variants in whole genome, whole exome, and targeted next-generation sequencing data of tumor/normal pairs. Clinical Cancer Research. 22(1_Supplement). 45–45. 2 indexed citations

13.

LoRusso, Patricia, Sara M. Tolaney, Shukmei Wong, et al.. (2015). Abstract CT325: Combination of the PARP inhibitor veliparib (ABT888) with irinotecan in patients with triple negative breast cancer: Preliminary activity and signature of response. Cancer Research. 75(15_Supplement). CT325–CT325. 5 indexed citations

14.

Borad, Mitesh J., Jan B. Egan, Mia D. Champion, et al.. (2015). Abstract CT112: Implementation of CLIA enabled integrated whole genome (WGS)/exome (WES)/transcriptome (RNAseq) next-gen sequencing to identify therapeutically relevant targets in advanced cancer patients. Cancer Research. 75(15_Supplement). CT112–CT112. 1 indexed citations

15.

Sekar, Shobana, Jacquelyn McDonald, Lori Cuyugan, et al.. (2014). Alzheimer's disease is associated with altered expression of genes involved in immune response and mitochondrial processes in astrocytes. Neurobiology of Aging. 36(2). 583–591. 152 indexed citations

16.

Liang, Winnie S., Jessica Aldrich, Sara Nasser, et al.. (2014). Simultaneous Characterization of Somatic Events and HPV-18 Integration in a Metastatic Cervical Carcinoma Patient Using DNA and RNA Sequencing. International Journal of Gynecological Cancer. 24(2). 1–10. 17 indexed citations

17.

Jiagge, Evelyn, Shukmei Wong, Sean McDermott, et al.. (2014). Abstract LB-59: Distinct pathways differentiate the CD44+ mesenchymal-like from the ALDH+ epithelial-like phenotype of triple negative breast cancer stem cells. Cancer Research. 74(19_Supplement). LB–59. 1 indexed citations

18.

Weiss, Glen J., Winnie S. Liang, Michael J. Demeure, et al.. (2013). A Pilot Study Using Next-Generation Sequencing in Advanced Cancers: Feasibility and Challenges. PLoS ONE. 8(10). e76438–e76438. 22 indexed citations

19.

Liang, Winnie S., Jessica Aldrich, Waibhav Tembe, et al.. (2013). Long insert whole genome sequencing for copy number variant and translocation detection. Nucleic Acids Research. 42(2). e8–e8. 11 indexed citations

20.

Demeure, Michael J., David W. Craig, Shripad Sinari, et al.. (2012). Cancer of the ampulla of Vater: analysis of the whole genome sequence exposes a potential therapeutic vulnerability. Genome Medicine. 4(7). 56–56. 12 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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