Amber Hogart

2.1k total citations
10 papers, 1.5k citations indexed

About

Amber Hogart is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Amber Hogart has authored 10 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Molecular Biology and 4 papers in Cognitive Neuroscience. Recurrent topics in Amber Hogart's work include Genetics and Neurodevelopmental Disorders (7 papers), Genomic variations and chromosomal abnormalities (5 papers) and Autism Spectrum Disorder Research (4 papers). Amber Hogart is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Genomic variations and chromosomal abnormalities (5 papers) and Autism Spectrum Disorder Research (4 papers). Amber Hogart collaborates with scholars based in United States and France. Amber Hogart's co-authors include Janine M. LaSalle, Rodney C. Samaco, David Wu, N. Carolyn Schanen, Dag H. Yasui, Raman P. Nagarajan, Michelle Martin, Raman P. Nagarajan, Roxanne O. Vallero and Peggy Farnham and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Genome Research and Human Molecular Genetics.

In The Last Decade

Amber Hogart

10 papers receiving 1.5k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Amber Hogart United States 10 1.2k 972 627 125 115 10 1.5k
Richard J. Simensen United States 21 1.2k 1.0× 912 0.9× 638 1.0× 137 1.1× 82 0.7× 50 1.9k
Richard J. Schroer United States 24 1.3k 1.1× 976 1.0× 795 1.3× 228 1.8× 208 1.8× 39 2.0k
Gokul Ramaswami United States 15 1.2k 1.0× 1.4k 1.5× 426 0.7× 142 1.1× 109 0.9× 16 2.0k
Melissa B. Ramocki United States 19 1.2k 1.0× 1.1k 1.1× 497 0.8× 161 1.3× 222 1.9× 29 1.9k
Elisabetta Tabolacci Italy 21 848 0.7× 850 0.9× 394 0.6× 54 0.4× 174 1.5× 49 1.3k
Béatrice Laudier France 10 675 0.6× 559 0.6× 477 0.8× 168 1.3× 204 1.8× 16 1.7k
Yong-hui Jiang United States 10 854 0.7× 823 0.8× 406 0.6× 134 1.1× 174 1.5× 11 1.3k
Sabrina Buoni Italy 20 745 0.6× 611 0.6× 312 0.5× 174 1.4× 165 1.4× 56 1.4k
Holly N. Cukier United States 16 518 0.4× 525 0.5× 403 0.6× 45 0.4× 147 1.3× 26 1.0k
Gregory J. Pelka Australia 14 783 0.7× 597 0.6× 347 0.6× 31 0.2× 101 0.9× 14 1.0k

Countries citing papers authored by Amber Hogart

Since Specialization
Citations

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

Fields of papers citing papers by Amber Hogart

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amber Hogart

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

All Works

10 of 10 papers shown
1.
Hogart, Amber, Jens Lichtenberg, Subramanian S. Ajay, et al.. (2012). Genome-wide DNA methylation profiles in hematopoietic stem and progenitor cells reveal overrepresentation of ETS transcription factor binding sites. Genome Research. 22(8). 1407–1418. 87 indexed citations
2.
Hogart, Amber, Karen Leung, David Wu, et al.. (2008). Chromosome 15q11–13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy number. Journal of Medical Genetics. 46(2). 86–93. 107 indexed citations
3.
Hogart, Amber, David Wu, Janine M. LaSalle, & N. Carolyn Schanen. (2008). The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13. Neurobiology of Disease. 38(2). 181–191. 226 indexed citations
4.
Hogart, Amber, et al.. (2008). Gender influences monoallelic expression of ATP10A in human brain. Human Genetics. 124(3). 235–242. 29 indexed citations
5.
Hogart, Amber, et al.. (2007). 15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders. Human Molecular Genetics. 16(6). 691–703. 170 indexed citations
6.
Yasui, Dag H., Sailaja Peddada, Mark Bieda, et al.. (2007). Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes. Proceedings of the National Academy of Sciences. 104(49). 19416–19421. 291 indexed citations
7.
Nagarajan, Raman P., et al.. (2006). Reduced MeCP2 Expression is Frequent in Autism Frontal Cortex and Correlates with Aberrant MECP2 Promoter Methylation. Epigenetics. 1(4). 172–182. 265 indexed citations
8.
LaSalle, Janine M., et al.. (2005). Rett Syndrome: A Rosetta Stone for Understanding the Molecular Pathogenesis of Autism. International review of neurobiology. 71. 131–165. 17 indexed citations
9.
Samaco, Rodney C., Amber Hogart, & Janine M. LaSalle. (2004). Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3. Human Molecular Genetics. 14(4). 483–492. 313 indexed citations
10.
Hilton, Matthew J., et al.. (2002). Analysis of novel and recurrent mutations responsible for the tricho-rhino-phalangeal syndromes. Journal of Human Genetics. 47(3). 103–106. 31 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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