Emily R. Soper

515 total citations
13 papers, 195 citations indexed

About

Emily R. Soper is a scholar working on Genetics, Oncology and Molecular Biology. According to data from OpenAlex, Emily R. Soper has authored 13 papers receiving a total of 195 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Oncology and 4 papers in Molecular Biology. Recurrent topics in Emily R. Soper's work include BRCA gene mutations in cancer (5 papers), Genomics and Rare Diseases (4 papers) and Genetic factors in colorectal cancer (3 papers). Emily R. Soper is often cited by papers focused on BRCA gene mutations in cancer (5 papers), Genomics and Rare Diseases (4 papers) and Genetic factors in colorectal cancer (3 papers). Emily R. Soper collaborates with scholars based in United States, France and Italy. Emily R. Soper's co-authors include Eimear E. Kenny, Noura S. Abul‐Husn, Sabrina A. Suckiel, Gillian M. Belbin, Sinéad Cullina, Judy H. Cho, Jessica Rodriguez, Arden Moscati, Ruth J. F. Loos and Dean Bobo and has published in prestigious journals such as Gastroenterology, Clinical Gastroenterology and Hepatology and Genetics in Medicine.

In The Last Decade

Emily R. Soper

13 papers receiving 193 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Emily R. Soper United States	7	110	64	47	38	24	13	195
Mae Zakhour United States	6	57 0.5×	46 0.7×	36 0.8×	35 0.9×	56 2.3×	17	237
James G. Dowty Australia	8	74 0.7×	59 0.9×	33 0.7×	48 1.3×	40 1.7×	18	161
Sinéad Cullina United States	5	94 0.9×	40 0.6×	27 0.6×	32 0.8×	14 0.6×	8	137
Iva Petrovchich United States	4	118 1.1×	65 1.0×	52 1.1×	51 1.3×	41 1.7×	8	217
Serena Maria Boccia Italy	8	79 0.7×	41 0.6×	25 0.5×	40 1.1×	83 3.5×	25	230
Julyann Pérez‐Mayoral Puerto Rico	7	65 0.6×	32 0.5×	50 1.1×	28 0.7×	71 3.0×	13	172
Mateja Krajc Slovenia	11	203 1.8×	123 1.9×	66 1.4×	58 1.5×	73 3.0×	47	308
Maruta A. Blatchins United States	6	64 0.6×	73 1.1×	26 0.6×	35 0.9×	41 1.7×	10	228
Marit Arnes Norway	12	120 1.1×	56 0.9×	21 0.4×	26 0.7×	40 1.7×	22	560
Marcie Steeves United States	6	106 1.0×	36 0.6×	17 0.4×	16 0.4×	21 0.9×	8	195

Countries citing papers authored by Emily R. Soper

Since Specialization

Citations

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

Fields of papers citing papers by Emily R. Soper

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Emily R. Soper. 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 Emily R. Soper. The network helps show where Emily R. Soper may publish in the future.

Co-authorship network of co-authors of Emily R. Soper

This figure shows the co-authorship network connecting the top 25 collaborators of Emily R. Soper. A scholar is included among the top collaborators of Emily R. Soper 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 Emily R. Soper. Emily R. Soper 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

Zawatsky, Carrie L. Blout, David Bick, Louise Bier, et al.. (2023). Elective genomic testing: Practice resource of the National Society of Genetic Counselors. Journal of Genetic Counseling. 32(2). 281–299. 8 indexed citations

Rutledge, Stephanie, Emily R. Soper, Vikas Pejaver, et al.. (2023). Association of HSD17B13 and PNPLA3 With Liver Enzymes and Fibrosis in Hispanic/Latino Individuals of Diverse Genetic Ancestries. Clinical Gastroenterology and Hepatology. 21(10). 2578–2587.e11. 13 indexed citations

Suckiel, Sabrina A., et al.. (2022). Elective genetic testing: Genetics professionals’ perspectives and practices. Journal of Genetic Counseling. 32(3). 607–617. 1 indexed citations

Soper, Emily R., Sinéad Cullina, Gillian M. Belbin, et al.. (2021). CDH1 pathogenic variants and cancer risk in an unselected patient population. Familial Cancer. 21(2). 235–239. 6 indexed citations

Abul‐Husn, Noura S., Emily R. Soper, Jessica Rodriguez, et al.. (2021). Implementing genomic screening in diverse populations. Genome Medicine. 13(1). 17–17. 39 indexed citations

Zhu, Huili, et al.. (2021). Genetic Variants in Patients With a Family History of Pancreatic Cancer. Pancreas. 50(4). 602–606. 2 indexed citations

Soper, Emily R., et al.. (2021). Genomic Screening Identifies Individuals at High Risk for Hereditary Transthyretin Amyloidosis. Journal of Personalized Medicine. 11(1). 49–49. 11 indexed citations

Soper, Emily R., et al.. (2021). Genomic screening identifies individuals at high risk for hereditary transthyretin amyloidosis. Molecular Genetics and Metabolism. 132. S348–S349. 2 indexed citations

Ang, Celina, Sabrina A. Suckiel, Emily R. Soper, et al.. (2020). Lynch Syndrome–Associated Variants and Cancer Rates in an Ancestrally Diverse Biobank. JCO Precision Oncology. 4(4). 1429–1444. 13 indexed citations

10.

Clark, Dana, Scott T. Michalski, Rashmi Tondon, et al.. (2020). Loss-of-function variants in CTNNA1 detected on multigene panel testing in individuals with gastric or breast cancer. Genetics in Medicine. 22(5). 840–846. 27 indexed citations

11.

Abul‐Husn, Noura S., Emily R. Soper, Jacqueline A. Odgis, et al.. (2019). Exome sequencing reveals a high prevalence of BRCA1 and BRCA2 founder variants in a diverse population-based biobank. Genome Medicine. 12(1). 2–2. 70 indexed citations

12.

Jandorf, Lina, et al.. (2017). Co-Care: A Registry for Individuals at Increased Risk for Colorectal Cancer.. PubMed. 44(1). 11–6. 2 indexed citations

13.

Becker, Andrew, et al.. (2016). 1144 No Increase in Prevalence of Pancreatic Cysts in BRCA1 or BRCA2 Mutation Carriers with Breast Cancer. Gastroenterology. 150(4). S233–S233. 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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