Elly Brokamp

1.6k total citations
9 papers, 177 citations indexed

About

Elly Brokamp is a scholar working on Genetics, Cognitive Neuroscience and Surgery. According to data from OpenAlex, Elly Brokamp has authored 9 papers receiving a total of 177 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 2 papers in Cognitive Neuroscience and 1 paper in Surgery. Recurrent topics in Elly Brokamp's work include Genomics and Rare Diseases (4 papers), BRCA gene mutations in cancer (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Elly Brokamp is often cited by papers focused on Genomics and Rare Diseases (4 papers), BRCA gene mutations in cancer (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Elly Brokamp collaborates with scholars based in United States, Australia and Italy. Elly Brokamp's co-authors include Jessica Duis, Ashley H. Shoemaker, Pieter Joost van Wattum, Anna K. Childers, Althea Robinson Shelton, Jennifer L. Miller, Ann Scheimann, Parisa Salehi, Nathan C. Bingham and Rizwan Hamid and has published in prestigious journals such as Arthritis Research & Therapy, Genetics in Medicine and American Journal of Medical Genetics Part A.

In The Last Decade

Elly Brokamp

8 papers receiving 172 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elly Brokamp United States	6	132	62	25	19	18	9	177
Grace E. VanNoy United States	8	155 1.2×	72 1.2×	47 1.9×	17 0.9×	13 0.7×	15	232
Lily Hoffman‐Andrews United States	5	119 0.9×	99 1.6×	24 1.0×	23 1.2×	21 1.2×	11	240
Salima El Chehadeh-Djebbar France	4	154 1.2×	72 1.2×	23 0.9×	12 0.6×	10 0.6×	4	222
Elaine M. Pereira United States	8	100 0.8×	68 1.1×	35 1.4×	9 0.5×	8 0.4×	24	191
Lee Zellmer United States	7	203 1.5×	88 1.4×	32 1.3×	27 1.4×	39 2.2×	8	257
Yannis Duffourd France	7	201 1.5×	125 2.0×	38 1.5×	10 0.5×	14 0.8×	8	266
Lea Velsher Canada	8	91 0.7×	61 1.0×	16 0.6×	22 1.2×	43 2.4×	18	181
Fabio Sirchia Italy	9	108 0.8×	103 1.7×	33 1.3×	16 0.8×	8 0.4×	35	208
Kristen Rasmussen United States	8	163 1.2×	114 1.8×	33 1.3×	20 1.1×	33 1.8×	10	263
Frances Elmslie United Kingdom	10	99 0.8×	117 1.9×	43 1.7×	13 0.7×	20 1.1×	16	291

Countries citing papers authored by Elly Brokamp

Since Specialization

Citations

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

Fields of papers citing papers by Elly Brokamp

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elly Brokamp

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

All Works

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9 of 9 papers shown

1.

Brokamp, Elly, Tyne W. Miller‐Fleming, Gillian W. Hooker, et al.. (2025). Systematic method for classifying multiple congenital anomaly cases in electronic health records. Genetics in Medicine. 27(6). 101415–101415.

2.

Appelbaum, Paul S., Karolynn Siegel, Julia Wynn, et al.. (2022). Challenges of variant reinterpretation: Opinions of stakeholders and need for guidelines. Genetics in Medicine. 24(9). 1878–1887. 19 indexed citations

3.

Briere, Lauren C., Melissa Walker, Frances A. High, et al.. (2021). A description of novel variants and review of phenotypic spectrum in UBA5-related early epileptic encephalopathy. Molecular Case Studies. 7(3). a005827–a005827. 15 indexed citations

4.

Cogan, Joy D., Lynette Rives, Amy K. Robertson, et al.. (2020). Limitations of exome sequencing in detecting rare and undiagnosed diseases. American Journal of Medical Genetics Part A. 182(6). 1400–1406. 53 indexed citations

5.

Wang, Wei, et al.. (2019). Juvenile idiopathic arthritis associated with a mutation in GATA3. Arthritis Research & Therapy. 21(1). 156–156. 4 indexed citations

6.

Duis, Jessica, Pieter Joost van Wattum, Ann Scheimann, et al.. (2019). A multidisciplinary approach to the clinical management of Prader–Willi syndrome. Molecular Genetics & Genomic Medicine. 7(3). e514–e514. 55 indexed citations

7.

Macnamara, Ellen F., Kelly Schoch, Emily Glanton, et al.. (2019). Cases from the Undiagnosed Diseases Network: The continued value of counseling skills in a new genomic era. Journal of Genetic Counseling. 28(2). 194–201. 19 indexed citations

8.

Palmer, Christina G.S., Allyn McConkie‐Rosell, Ingrid A. Holm, et al.. (2018). Understanding Adult Participant and Parent Empowerment Prior to Evaluation in the Undiagnosed Diseases Network. Journal of Genetic Counseling. 27(5). 1087–1101. 11 indexed citations

9.

Brokamp, Elly, et al.. (2016). The Utility of Genomic Variant Databases in Genetic Counseling. 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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