Janson J. White

1.6k total citations
7 papers, 251 citations indexed

About

Janson J. White is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Janson J. White has authored 7 papers receiving a total of 251 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Cognitive Neuroscience. Recurrent topics in Janson J. White's work include Cancer-related gene regulation (3 papers), Wnt/β-catenin signaling in development and cancer (2 papers) and Autism Spectrum Disorder Research (2 papers). Janson J. White is often cited by papers focused on Cancer-related gene regulation (3 papers), Wnt/β-catenin signaling in development and cancer (2 papers) and Autism Spectrum Disorder Research (2 papers). Janson J. White collaborates with scholars based in United States, Brazil and Poland. Janson J. White's co-authors include James R. Lupski, Shalini N. Jhangiani, Richard A. Gibbs, Claudia M.B. Carvalho, Yavuz Bayram, Tomasz Gambin, Zeynep Coban‐Akdemir, Jawid M. Fatih, Eric Boerwinkle and Jaya Punetha and has published in prestigious journals such as The American Journal of Human Genetics, Journal of Affective Disorders and Journal of Child and Adolescent Psychopharmacology.

In The Last Decade

Janson J. White

7 papers receiving 249 citations

Peers

Janson J. White

MB

GENET

CB

IMMUN

CR

Paul Ling-Fung Tang United States

Barbara Oehl‐Jaschkowitz Germany

Anneke T. Vulto‐van Silfhout Netherlands

Sebastian Röner Germany

Volkan Okur United States

Lucas Fares‐Taie France

Julie Kaylor United States

Arjan PM de Brouwer Netherlands

Hagar Mor‐Shaked Israel

Amjad Khan Pakistan

Paul Ling-Fung Tang United States

Janson J. White

143 ×0.7

MB

111 ×1.2

GENET

22 ×0.9

CB

12 ×1.1

IMMUN

10 ×0.9

CR

Citations per year, relative to Janson J. White Janson J. White (= 1×) peers Paul Ling-Fung Tang

Countries citing papers authored by Janson J. White

Since Specialization

Citations

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

Fields of papers citing papers by Janson J. White

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Janson J. White. 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 Janson J. White. The network helps show where Janson J. White may publish in the future.

Co-authorship network of co-authors of Janson J. White

This figure shows the co-authorship network connecting the top 25 collaborators of Janson J. White. A scholar is included among the top collaborators of Janson J. White 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 Janson J. White. Janson J. White 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.

Patel, Nisha, John M. Graham, Michael J. Bamshad, et al.. (2021). Further delineation of van den Ende‐Gupta syndrome: Genetic heterogeneity and overlap with congenital heart defects and skeletal malformations syndrome. American Journal of Medical Genetics Part A. 185(7). 2136–2149. 3 indexed citations

2.

Zhang, Chaofan, Juliana F. Mazzeu, Jesper Eisfeldt, et al.. (2020). Novel pathogenic genomic variants leading to autosomal dominant and recessive Robinow syndrome. American Journal of Medical Genetics Part A. 185(12). 3593–3600. 14 indexed citations

3.

Gillentine, Madelyn A., Jiani Yin, Christopher M. Grochowski, et al.. (2018). CHRNA7 copy number gains are enriched in adolescents with major depressive and anxiety disorders. Journal of Affective Disorders. 239. 247–252. 12 indexed citations

4.

Coban‐Akdemir, Zeynep, Janson J. White, Xiaofei Song, et al.. (2018). Identifying Genes Whose Mutant Transcripts Cause Dominant Disease Traits by Potential Gain-of-Function Alleles. The American Journal of Human Genetics. 103(2). 171–187. 120 indexed citations

5.

Gillentine, Madelyn A., Janson J. White, Christopher M. Grochowski, et al.. (2017). CHRNA7 Deletions are Enriched in Risperidone-Treated Children and Adolescents. Journal of Child and Adolescent Psychopharmacology. 27(10). 908–915. 8 indexed citations

6.

White, Janson J., Juliana F. Mazzeu, Alexander Hoischen, et al.. (2016). DVL3 Alleles Resulting in a −1 Frameshift of the Last Exon Mediate Autosomal-Dominant Robinow Syndrome. The American Journal of Human Genetics. 98(3). 553–561. 69 indexed citations

7.

Boone, Philip M., Bo Yuan, Shen Gu, et al.. (2015). Hutterite‐type cataract maps to chromosome 6p21.32‐p21.31, cosegregates with a homozygous mutation in LEMD2, and is associated with sudden cardiac death. Molecular Genetics & Genomic Medicine. 4(1). 77–94. 25 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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