Hailey Pinz

415 total citations
5 papers, 68 citations indexed

About

Hailey Pinz is a scholar working on Surgery, Molecular Biology and Genetics. According to data from OpenAlex, Hailey Pinz has authored 5 papers receiving a total of 68 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Surgery, 3 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in Hailey Pinz's work include RNA modifications and cancer (3 papers), Infant Health and Development (1 paper) and Plant nutrient uptake and metabolism (1 paper). Hailey Pinz is often cited by papers focused on RNA modifications and cancer (3 papers), Infant Health and Development (1 paper) and Plant nutrient uptake and metabolism (1 paper). Hailey Pinz collaborates with scholars based in United States and Saudi Arabia. Hailey Pinz's co-authors include Stephen R. Braddock, Kosuke Izumi, Elaine H. Zackai, Elizabeth Bhoj, Dong Li, Jennifer Tarpinian, Dhiren Patel, Aida Telegrafi, Kristin G. Monaghan and Louise C. Pyle and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Journal of Pediatric Gastroenterology and Nutrition.

In The Last Decade

Hailey Pinz

5 papers receiving 67 citations

Peers

Hailey Pinz

MB

SURGE

GENET

BIOCH

PRM

Soroush Hajizadeh United States

W Rayner United Kingdom

Sapna Vyas United Kingdom

Tatiana Krylova Russia

Jin Fang Chai China

Debarati Sethi United Kingdom

H. Hsu United States

Yoann Vial France

Lucia Laugwitz Germany

Soroush Hajizadeh United States

Hailey Pinz

34 ×0.8

MB

19 ×0.8

SURGE

7 ×0.3

GENET

2 ×0.3

BIOCH

7 ×1.0

PRM

Citations per year, relative to Hailey Pinz Hailey Pinz (= 1×) peers Soroush Hajizadeh

Countries citing papers authored by Hailey Pinz

Since Specialization

Citations

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

Fields of papers citing papers by Hailey Pinz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hailey Pinz

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

All Works

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5 of 5 papers shown

1.

Guzmán, Miguel A., et al.. (2021). Hirschsprung Disease in an Infant with L1 syndrome: Report of a New Case and a novel L1CAM variant. SHILAP Revista de lepidopterología. 9(3). 1518–1523. 4 indexed citations

2.

Almannai, Mohammed, Eissa Faqeih, Ali Alasmari, et al.. (2020). Further delineation of METTL23‐associated intellectual disability. American Journal of Medical Genetics Part A. 182(4). 785–791. 7 indexed citations

3.

Johnson, Tyler B., Jacob T. Cain, Stephen R. Braddock, et al.. (2018). Characterization of a recurrent missense mutation in the forkhead DNA-binding domain of FOXP1. Scientific Reports. 8(1). 16161–16161. 6 indexed citations

4.

Pinz, Hailey, Louise C. Pyle, Dong Li, et al.. (2018). De novo variants in Myelin regulatory factor (MYRF) as candidates of a new syndrome of cardiac and urogenital anomalies. American Journal of Medical Genetics Part A. 176(4). 969–972. 38 indexed citations

5.

Pinz, Hailey, et al.. (2017). Congenital Diarrhea From DGAT1 Mutation Leading to Electrolyte Derangements, Protein‐losing Enteropathy, and Rickets. Journal of Pediatric Gastroenterology and Nutrition. 66(3). e82–e83. 13 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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