Hannah C. Happ

467 total citations
7 papers, 256 citations indexed

About

Hannah C. Happ is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Hannah C. Happ has authored 7 papers receiving a total of 256 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in Hannah C. Happ's work include Ocular Disorders and Treatments (3 papers), Corneal Surgery and Treatments (2 papers) and MicroRNA in disease regulation (2 papers). Hannah C. Happ is often cited by papers focused on Ocular Disorders and Treatments (3 papers), Corneal Surgery and Treatments (2 papers) and MicroRNA in disease regulation (2 papers). Hannah C. Happ collaborates with scholars based in United States, France and Germany. Hannah C. Happ's co-authors include Gemma L. Carvill, K. Mark Ansel, Heather H. Pua, Linda M. Reis, Eric Weh, Elena V. Semina, Dirk Baumjohann, Christoph Schneider, Richard M. Locksley and Jakob von Moltke and has published in prestigious journals such as The Journal of Experimental Medicine, Cell Reports and Human Genetics.

In The Last Decade

Hannah C. Happ

7 papers receiving 253 citations

Peers

Hannah C. Happ

MB

GENET

CR

IMMUN

RNMI

Margherita Baldassarri Italy

Carolina Courage Finland

Pamela Trapane United States

Masafumi Kanno Japan

Kimihiko Banno Japan

Mitja Mitrovič United States

Sofia M. Calado Portugal

Katherine S. Elliott United Kingdom

Andrew E. Blum United States

Sofie Ingvast Sweden

Margherita Baldassarri Italy

Hannah C. Happ

120 ×0.9

MB

91 ×1.2

GENET

30 ×0.5

CR

15 ×0.3

IMMUN

9 ×0.3

RNMI

Citations per year, relative to Hannah C. Happ Hannah C. Happ (= 1×) peers Margherita Baldassarri

Countries citing papers authored by Hannah C. Happ

Since Specialization

Citations

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

Fields of papers citing papers by Hannah C. Happ

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hannah C. Happ. 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 Hannah C. Happ. The network helps show where Hannah C. Happ may publish in the future.

Co-authorship network of co-authors of Hannah C. Happ

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

All Works

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7 of 7 papers shown

1.

Zhang, Daniel Y., Andrew Gould, Hannah C. Happ, et al.. (2021). Ultrasound-mediated blood–brain barrier opening increases cell-free DNA in a time-dependent manner. Neuro-Oncology Advances. 3(1). vdab165–vdab165. 10 indexed citations

2.

Happ, Hannah C. & Gemma L. Carvill. (2020). A 2020 View on the Genetics of Developmental and Epileptic Encephalopathies. Epiliepsy currents. 20(2). 90–96. 45 indexed citations

3.

Pua, Heather H., et al.. (2019). Increased Hematopoietic Extracellular RNAs and Vesicles in the Lung during Allergic Airway Responses. Cell Reports. 26(4). 933–944.e4. 58 indexed citations

4.

Pua, Heather H., Hannah C. Happ, Christoph Schneider, et al.. (2017). MicroRNA regulation of type 2 innate lymphoid cell homeostasis and function in allergic inflammation. The Journal of Experimental Medicine. 214(12). 3627–3643. 68 indexed citations

5.

Happ, Hannah C., Kala F. Schilter, Eric Weh, Linda M. Reis, & Elena V. Semina. (2016). 8q21.11 microdeletion in two patients with syndromic peters anomaly. American Journal of Medical Genetics Part A. 170(9). 2471–2475. 16 indexed citations

6.

Happ, Hannah C., Eric Weh, Deborah M. Costakos, Linda M. Reis, & Elena V. Semina. (2016). Case report of homozygous deletion involving the first coding exons of GCNT2 isoforms A and B and part of the upstream region of TFAP2A in congenital cataract. BMC Medical Genetics. 17(1). 64–64. 6 indexed citations

7.

Weh, Eric, Linda M. Reis, Hannah C. Happ, et al.. (2014). Whole exome sequence analysis of Peters anomaly. Human Genetics. 133(12). 1497–1511. 53 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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