Emily Fassi

1.4k total citations
4 papers, 112 citations indexed

About

Emily Fassi is a scholar working on Pathology and Forensic Medicine, Genetics and Surgery. According to data from OpenAlex, Emily Fassi has authored 4 papers receiving a total of 112 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Pathology and Forensic Medicine, 2 papers in Genetics and 1 paper in Surgery. Recurrent topics in Emily Fassi's work include Genetic factors in colorectal cancer (2 papers), Genomics and Rare Diseases (1 paper) and Cellular transport and secretion (1 paper). Emily Fassi is often cited by papers focused on Genetic factors in colorectal cancer (2 papers), Genomics and Rare Diseases (1 paper) and Cellular transport and secretion (1 paper). Emily Fassi collaborates with scholars based in United States. Emily Fassi's co-authors include Marwan Shinawi, Marcia Willing, Margaret A. Hefner, Dustin Baldridge, Tomi L. Toler, Dorothy K. Grange, Beth A. Kozel, Linda Manwaring, Sarah M. Brown and Charles W. Goss and has published in prestigious journals such as Genetics in Medicine, American Journal of Medical Genetics Part C Seminars in Medical Genetics and Journal of Genetic Counseling.

In The Last Decade

Emily Fassi

4 papers receiving 112 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Emily Fassi United States	4	90	38	16	11	11	4	112
Elise Fiala United States	5	72 0.8×	46 1.2×	14 0.9×	5 0.5×	14 1.3×	10	110
Gabrielle Lemire Canada	7	72 0.8×	91 2.4×	17 1.1×	9 0.8×	10 0.9×	16	165
Yoko Hiraki Japan	10	131 1.5×	97 2.6×	13 0.8×	6 0.5×	10 0.9×	17	219
Jessica Sebastian United States	6	92 1.0×	64 1.7×	9 0.6×	7 0.6×	9 0.8×	11	146
Maria Concetta Cutrupi Italy	5	44 0.5×	50 1.3×	10 0.6×	7 0.6×	5 0.5×	7	124
Jörg Dötsch Germany	5	39 0.4×	76 2.0×	25 1.6×	9 0.8×	13 1.2×	9	131
Monika Weisz Hubshman Israel	6	108 1.2×	79 2.1×	8 0.5×	9 0.8×	15 1.4×	7	165
Berardo Rinaldi Italy	7	90 1.0×	99 2.6×	32 2.0×	5 0.5×	7 0.6×	26	170
François Lecoquierre France	7	57 0.6×	63 1.7×	6 0.4×	10 0.9×	15 1.4×	18	114
Haley Streff United States	9	93 1.0×	100 2.6×	19 1.2×	6 0.5×	8 0.7×	24	188

Countries citing papers authored by Emily Fassi

Since Specialization

Citations

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

Fields of papers citing papers by Emily Fassi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emily Fassi

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

All Works

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4 of 4 papers shown

1.

Fassi, Emily, et al.. (2020). Breast cancer polygenic risk scores in the clinical cancer genetic counseling setting: Current practices and impact on patient management. Journal of Genetic Counseling. 30(2). 588–597. 18 indexed citations

2.

Fassi, Emily, et al.. (2018). Mutations in the PH Domain of DNM1 are associated with a nonepileptic phenotype characterized by developmental delay and neurobehavioral abnormalities. Molecular Genetics & Genomic Medicine. 6(2). 294–300. 20 indexed citations

3.

Baldridge, Dustin, Jennifer Heeley, Linda Manwaring, et al.. (2017). The Exome Clinic and the role of medical genetics expertise in the interpretation of exome sequencing results. Genetics in Medicine. 19(9). 1040–1048. 65 indexed citations

4.

Hefner, Margaret A. & Emily Fassi. (2017). Genetic counseling in CHARGE syndrome: Diagnostic evaluation through follow up. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 175(4). 407–416. 9 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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