Thomas Arbogast

498 total citations
7 papers, 208 citations indexed

About

Thomas Arbogast is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Thomas Arbogast has authored 7 papers receiving a total of 208 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Genetics and 2 papers in Cognitive Neuroscience. Recurrent topics in Thomas Arbogast's work include Congenital heart defects research (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Thomas Arbogast is often cited by papers focused on Congenital heart defects research (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Thomas Arbogast collaborates with scholars based in France, United States and Canada. Thomas Arbogast's co-authors include Yann Hérault, Claire Chevalier, Nurudeen O. Afinowi, Maksym V. Kopanitsa, Marie‐Christine Birling, Eugenia Migliavacca, Belinda S. Cowling, Marie‐France Champy, Abdel‐Mouttalib Ouagazzal and Alexandre Reymond and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and PLoS Genetics.

In The Last Decade

Thomas Arbogast

7 papers receiving 207 citations

Peers

Thomas Arbogast

MB

GENET

CN

IMMUN

CMN

Alicia Hawes United States

Lina Lu China

Gloria Negri Italy

Christoph Dotter Austria

Craig Chinault United States

Arjan PM de Brouwer Netherlands

Nathalie Fieremans Belgium

Antonella Fabretto Italy

Katrin Männik Estonia

Alisdair McNeill United Kingdom

Alicia Hawes United States

Thomas Arbogast

98 ×0.7

MB

128 ×1.0

GENET

65 ×1.2

CN

10 ×0.7

IMMUN

13 ×1.3

CMN

Citations per year, relative to Thomas Arbogast Thomas Arbogast (= 1×) peers Alicia Hawes

Countries citing papers authored by Thomas Arbogast

Since Specialization

Citations

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

Fields of papers citing papers by Thomas Arbogast

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thomas Arbogast

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

Harel, Tamar, John N. Griffin, Thomas Arbogast, et al.. (2020). Loss of function mutations in CCDC32 cause a congenital syndrome characterized by craniofacial, cardiac and neurodevelopmental anomalies. Human Molecular Genetics. 29(9). 1489–1497. 7 indexed citations

2.

Niihori, Tetsuya, Atsushi Fujita, Hirofumi Ohashi, et al.. (2019). Germline-Activating RRAS2 Mutations Cause Noonan Syndrome. The American Journal of Human Genetics. 104(6). 1233–1240. 35 indexed citations

3.

Qiu, Yuqi, Thomas Arbogast, Hongying Li, et al.. (2019). Oligogenic Effects of 16p11.2 Copy-Number Variation on Craniofacial Development. Cell Reports. 28(13). 3320–3328.e4. 25 indexed citations

4.

Arbogast, Thomas, Jacob Ellegood, Spencer U. McKinstry, et al.. (2018). Kctd13-deficient mice display short-term memory impairment and sex-dependent genetic interactions. Human Molecular Genetics. 28(9). 1474–1486. 26 indexed citations

5.

Arbogast, Thomas, Giovanni Iacono, Claire Chevalier, et al.. (2017). Mouse models of 17q21.31 microdeletion and microduplication syndromes highlight the importance of Kansl1 for cognition. PLoS Genetics. 13(7). e1006886–e1006886. 20 indexed citations

6.

Arbogast, Thomas, Abdel‐Mouttalib Ouagazzal, Claire Chevalier, et al.. (2016). Reciprocal Effects on Neurocognitive and Metabolic Phenotypes in Mouse Models of 16p11.2 Deletion and Duplication Syndromes. PLoS Genetics. 12(2). e1005709–e1005709. 83 indexed citations

7.

Arbogast, Thomas, Matthieu Raveau, Claire Chevalier, et al.. (2015). Deletion of the App-Runx1 region in mice models human partial monosomy 21. Disease Models & Mechanisms. 8(6). 623–634. 12 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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