Jennifer Tarpinian

653 total citations
5 papers, 117 citations indexed

About

Jennifer Tarpinian is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Jennifer Tarpinian has authored 5 papers receiving a total of 117 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 2 papers in Pediatrics, Perinatology and Child Health and 2 papers in Genetics. Recurrent topics in Jennifer Tarpinian's work include Hearing, Cochlea, Tinnitus, Genetics (1 paper), Cystic Fibrosis Research Advances (1 paper) and Genetic Syndromes and Imprinting (1 paper). Jennifer Tarpinian is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (1 paper), Cystic Fibrosis Research Advances (1 paper) and Genetic Syndromes and Imprinting (1 paper). Jennifer Tarpinian collaborates with scholars based in United States and Germany. Jennifer Tarpinian's co-authors include Kosuke Izumi, Elaine H. Zackai, Cara Skraban, Hailey Pinz, Dong Li, Elizabeth Bhoj, Jorune Balciuniene, Aida Telegrafi, Kristin G. Monaghan and Louise C. Pyle and has published in prestigious journals such as Genetics in Medicine, Epilepsy Research and Prenatal Diagnosis.

In The Last Decade

Jennifer Tarpinian

5 papers receiving 117 citations

Peers

Jennifer Tarpinian

GENET

MB

PRM

PPCH

SS

Fabio Sirchia Italy

Jiddeke van de Kamp Netherlands

Radka Kremlíková Pourová Czechia

María de la Luz Arenas‐Sordo Mexico

Faezeh Mojahedi Iran

Stefania Lenarduzzi Italy

Yoko Hiraki Japan

Masato Yokozawa Japan

Molly B. Sheridan United States

Rebecca Willaert United States

Fabio Sirchia Italy

Jennifer Tarpinian

108 ×2.0

GENET

103 ×2.0

MB

8 ×0.4

PRM

33 ×1.6

PPCH

18 ×0.9

SS

Citations per year, relative to Jennifer Tarpinian Jennifer Tarpinian (= 1×) peers Fabio Sirchia

Countries citing papers authored by Jennifer Tarpinian

Since Specialization

Citations

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

Fields of papers citing papers by Jennifer Tarpinian

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jennifer Tarpinian

This figure shows the co-authorship network connecting the top 25 collaborators of Jennifer Tarpinian. A scholar is included among the top collaborators of Jennifer Tarpinian 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 Jennifer Tarpinian. Jennifer Tarpinian 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.

Grand, Katheryn, Cara Skraban, Jennifer L. Cohen, et al.. (2021). Nonlethal presentations of CYP26B1‐related skeletal anomalies and multiple synostoses syndrome. American Journal of Medical Genetics Part A. 185(9). 2766–2775. 7 indexed citations

2.

Torres, Raúl, Rotem Ben‐Shachar, Jodi D. Hoffman, et al.. (2020). Evaluation and classification of severity for 176 genes on an expanded carrier screening panel. Prenatal Diagnosis. 40(10). 1246–1257. 28 indexed citations

3.

Guan, Qiaoning, Jorune Balciuniene, Kajia Cao, et al.. (2018). AUDIOME: a tiered exome sequencing–based comprehensive gene panel for the diagnosis of heterogeneous nonsyndromic sensorineural hearing loss. Genetics in Medicine. 20(12). 1600–1608. 27 indexed citations

4.

Romasko, Edward J., Elizabeth T. DeChene, Jorune Balciuniene, et al.. (2018). PCDH19-related epilepsy in a male with Klinefelter syndrome: Additional evidence supporting PCDH19 cellular interference disease mechanism. Epilepsy Research. 145. 89–92. 17 indexed citations

5.

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

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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