Emily Fleming

966 total citations
10 papers, 489 citations indexed

About

Emily Fleming is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Emily Fleming has authored 10 papers receiving a total of 489 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Surgery. Recurrent topics in Emily Fleming's work include Congenital heart defects research (3 papers), Craniofacial Disorders and Treatments (2 papers) and Genomics and Rare Diseases (1 paper). Emily Fleming is often cited by papers focused on Congenital heart defects research (3 papers), Craniofacial Disorders and Treatments (2 papers) and Genomics and Rare Diseases (1 paper). Emily Fleming collaborates with scholars based in United States. Emily Fleming's co-authors include Thomas F. Cash, Laura Steadman, James Shelton, Matthew Withiam‐Leitch, Susan Hughes, Joseph T. Alaimo, Jennifer Hanson, Shivarajan Amudhavalli, Benjamin J. Landis and Dihong Zhou and has published in prestigious journals such as SHILAP Revista de lepidopterología, Clinical Genetics and Birth.

In The Last Decade

Emily Fleming

7 papers receiving 465 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Emily Fleming United States	5	390	90	75	71	56	10	489
Steffanie Sperry United States	9	283 0.7×	71 0.8×	34 0.5×	64 0.9×	44 0.8×	13	417
Hannah L. Quittkat Germany	4	290 0.7×	39 0.4×	72 1.0×	63 0.9×	45 0.8×	6	383
Ross Krawczyk United States	5	230 0.6×	48 0.5×	42 0.6×	35 0.5×	31 0.6×	12	273
Nicole Paraskeva United Kingdom	11	237 0.6×	43 0.5×	60 0.8×	20 0.3×	75 1.3×	27	379
Danielle A. Gagne United States	6	343 0.9×	44 0.5×	117 1.6×	44 0.6×	91 1.6×	7	409
Tejal A. Jakatdar United States	5	315 0.8×	24 0.3×	50 0.7×	184 2.6×	34 0.6×	7	421
Elayne Saltzberg United States	4	411 1.1×	49 0.5×	79 1.1×	54 0.8×	51 0.9×	5	447
Tracy Lo United States	8	314 0.8×	18 0.2×	35 0.5×	82 1.2×	94 1.7×	12	471
Madison F. Vani Canada	9	245 0.6×	16 0.2×	52 0.7×	25 0.4×	56 1.0×	27	440
Zachary A. Soulliard United States	12	306 0.8×	13 0.1×	85 1.1×	23 0.3×	46 0.8×	28	432

Countries citing papers authored by Emily Fleming

Since Specialization

Citations

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

Fields of papers citing papers by Emily Fleming

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emily Fleming

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

All Works

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10 of 10 papers shown

1.

Viso, Florencia Del, et al.. (2024). SF3B2 Haploinsufficiency Associated With Hirschprung Disease and Complex Cardiac Defect Without Craniofacial Microsomia. American Journal of Medical Genetics Part A. 197(2). e63886–e63886.

2.

Viso, Florencia Del, et al.. (2023). P448: SF3B2-Related cardiac defects and Hirschsprung disease without craniofacial microsomia. SHILAP Revista de lepidopterología. 1(1). 100495–100495.

3.

Hanson, Jennifer, Susan Hughes, Shivarajan Amudhavalli, et al.. (2021). TAB2 variants cause cardiovascular heart disease, connective tissue disorder, and developmental delay. Clinical Genetics. 101(2). 214–220. 7 indexed citations

4.

Fleming, Emily, et al.. (2021). Second patient with GNB2-related neurodevelopmental disease: Further evidence for a gene-disease association. European Journal of Medical Genetics. 64(7). 104243–104243.

5.

Fleming, Emily, et al.. (2020). Adolescents with congenital heart defects: a patient and parental perspective of genetic information and genetic risk. Cardiology in the Young. 30(2). 219–226. 6 indexed citations

6.

Fleming, Emily, et al.. (2020). 37-year-old Transgender Man with Fevers, Dysuria, and Sudden Decompensation. SHILAP Revista de lepidopterología. 4(3). 277–282. 1 indexed citations

7.

Grote, Lauren, Isabelle Thiffault, Emily Farrow, et al.. (2018). Incidental diagnosis of tuberous sclerosis complex by exome sequencing in three families with subclinical findings. Neurogenetics. 19(3). 205–213. 6 indexed citations

8.

Fleming, Emily, et al.. (2012). Objective structured clinical examinations and reliability: are we there yet?. The Clinical Teacher. 9(3). 193–194. 1 indexed citations

9.

Withiam‐Leitch, Matthew, James Shelton, & Emily Fleming. (2006). Central Fetal Monitoring: Effect on Perinatal Outcomes and Cesarean Section Rate. Birth. 33(4). 284–288. 16 indexed citations

10.

Cash, Thomas F., et al.. (2002). Beyond Body Image as a Trait: The Development and Validation of the Body Image States Scale. Eating Disorders. 10(2). 103–113. 452 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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