Sara A. Wirth

481 total citations
4 papers, 136 citations indexed

About

Sara A. Wirth is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Sara A. Wirth has authored 4 papers receiving a total of 136 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 1 paper in Cellular and Molecular Neuroscience and 1 paper in Pediatrics, Perinatology and Child Health. Recurrent topics in Sara A. Wirth's work include Zebrafish Biomedical Research Applications (1 paper), Hereditary Neurological Disorders (1 paper) and CRISPR and Genetic Engineering (1 paper). Sara A. Wirth is often cited by papers focused on Zebrafish Biomedical Research Applications (1 paper), Hereditary Neurological Disorders (1 paper) and CRISPR and Genetic Engineering (1 paper). Sara A. Wirth collaborates with scholars based in United States, Egypt and Qatar. Sara A. Wirth's co-authors include Valentina Stanley, Joseph G. Gleeson, Wiebke Herzog, Brant M. Weinstein, Damir Musaev, Stephanie Grainger, Karl Willert, Matthew Swift, Maha S. Zaki and Jenna Richter and has published in prestigious journals such as Cell, The American Journal of Human Genetics and Cell Reports.

In The Last Decade

Sara A. Wirth

4 papers receiving 136 citations

Peers

Sara A. Wirth

MB

CB

GENET

PPCH

CR

Christel Thauvin France

Saoud Tahsin Swafiri Spain

Orla Galvin United Kingdom

Tom Rabinowitz Israel

Sarita Rani Patnaik Germany

Samantha Penney United States

Nicole B. Rockweiler United States

Hwajin Jung South Korea

Yanwei Song China

Christina Pyrgaki United States

Christel Thauvin France

Sara A. Wirth

81 ×1.0

MB

40 ×0.8

CB

37 ×1.3

GENET

6 ×0.3

PPCH

14 ×0.9

CR

Citations per year, relative to Sara A. Wirth Sara A. Wirth (= 1×) peers Christel Thauvin

Countries citing papers authored by Sara A. Wirth

Since Specialization

Citations

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

Fields of papers citing papers by Sara A. Wirth

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sara A. Wirth. 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 Sara A. Wirth. The network helps show where Sara A. Wirth may publish in the future.

Co-authorship network of co-authors of Sara A. Wirth

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

All Works

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4 of 4 papers shown

1.

Yang, Xiaoxu, Martin W. Breuss, Danny Antaki, et al.. (2021). Developmental and temporal characteristics of clonal sperm mosaicism. Cell. 184(18). 4772–4783.e15. 26 indexed citations

2.

Breuss, Martin W., An Nguyen, Qiong Song, et al.. (2018). Mutations in LNPK, Encoding the Endoplasmic Reticulum Junction Stabilizer Lunapark, Cause a Recessive Neurodevelopmental Syndrome. The American Journal of Human Genetics. 103(2). 296–304. 22 indexed citations

3.

Marin‐Valencia, Isaac, Andreas Gerondopoulos, Maha S. Zaki, et al.. (2017). Homozygous Mutations in TBC1D23 Lead to a Non-degenerative Form of Pontocerebellar Hypoplasia. The American Journal of Human Genetics. 101(3). 441–450. 43 indexed citations

4.

Grainger, Stephanie, Jenna Richter, Claire Pouget, et al.. (2016). Wnt9a Is Required for the Aortic Amplification of Nascent Hematopoietic Stem Cells. Cell Reports. 17(6). 1595–1606. 45 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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