Jason Carmichael

597 total citations
6 papers, 103 citations indexed

About

Jason Carmichael is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Jason Carmichael has authored 6 papers receiving a total of 103 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 3 papers in Molecular Biology and 1 paper in Cognitive Neuroscience. Recurrent topics in Jason Carmichael's work include Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Nutrition, Genetics, and Disease (1 paper). Jason Carmichael is often cited by papers focused on Genomics and Rare Diseases (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Nutrition, Genetics, and Disease (1 paper). Jason Carmichael collaborates with scholars based in United States, Mexico and Israel. Jason Carmichael's co-authors include Megan T. Cho, Kyle Retterer, Jeffrey W. Innis, Linshan Shang, Wendy K. Chung, Katrina Haude, Margaret A. Pearson, Chin-To Fong, Lindsay B. Henderson and Kristin G. Monaghan and has published in prestigious journals such as American Journal of Medical Genetics Part A, Neurogenetics and Journal of Genetic Counseling.

In The Last Decade

Jason Carmichael

6 papers receiving 101 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Jason Carmichael United States	5	61	58	14	11	6	6	103
Katrina Haude United States	5	81 1.3×	41 0.7×	15 1.1×	10 0.9×	6 1.0×	6	118
Stefanie Beck‐Woedl Germany	7	67 1.1×	68 1.2×	25 1.8×	14 1.3×	4 0.7×	10	118
M.P. Botella Spain	5	80 1.3×	79 1.4×	10 0.7×	33 3.0×	7 1.2×	7	135
Elise Fiala United States	5	46 0.8×	72 1.2×	14 1.0×	4 0.4×	5 0.8×	10	110
Jessica Sebastian United States	6	64 1.0×	92 1.6×	9 0.6×	13 1.2×	12 2.0×	11	146
Tammy Kammin United Kingdom	5	58 1.0×	54 0.9×	6 0.4×	6 0.5×	6 1.0×	5	115
Alessandro Calcia Italy	5	41 0.7×	60 1.0×	4 0.3×	19 1.7×	6 1.0×	8	100
Eloi Mercier Canada	7	89 1.5×	76 1.3×	5 0.4×	7 0.6×	3 0.5×	9	152
Meron Azage United States	4	81 1.3×	91 1.6×	5 0.4×	11 1.0×	7 1.2×	6	129
Fathiya Al Murshedi Oman	6	45 0.7×	56 1.0×	10 0.7×	11 1.0×	7 1.2×	14	114

Countries citing papers authored by Jason Carmichael

Since Specialization

Citations

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

Fields of papers citing papers by Jason Carmichael

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jason Carmichael

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

All Works

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6 of 6 papers shown

Freeman, Rebecca, Adriana Backx Noronha Viana, Jason Carmichael, et al.. (2024). Applying data science methodologies with artificial intelligence variant reinterpretation to map and estimate genetic disorder prevalence utilizing clinical data. American Journal of Medical Genetics Part A. 194(5). e63505–e63505. 5 indexed citations

Galarreta, Carolina I., Karen Wong, Jason Carmichael, et al.. (2023). A homozygous Gly470Ala variant in PEX6 causes severe Zellweger spectrum disorder. American Journal of Medical Genetics Part A. 191(8). 2057–2063. 4 indexed citations

Carmichael, Jason, et al.. (2021). Hemimegalencephaly and intractable seizures associated with the NPRL3 gene variant in a newborn: A case report. American Journal of Medical Genetics Part A. 185(7). 2126–2130. 12 indexed citations

Douglas, Ganka, Megan T. Cho, Aida Telegrafi, et al.. (2018). De novo missense variants in MEIS2 recapitulate the microdeletion phenotype of cardiac and palate abnormalities, developmental delay, intellectual disability and dysmorphic features. American Journal of Medical Genetics Part A. 176(9). 1845–1851. 23 indexed citations

Shen, Joseph, et al.. (2018). Identifying and Addressing Genetic Counseling Challenges among Indigenous People of Oaxaca—One Center's Experience with Two Immigrant Farmworker Families in the Central Valley of California. Journal of Genetic Counseling. 27(4). 996–1004. 7 indexed citations

Shang, Linshan, Lindsay B. Henderson, Megan T. Cho, et al.. (2015). De novo missense variants in PPP2R5D are associated with intellectual disability, macrocephaly, hypotonia, and autism. Neurogenetics. 17(1). 43–49. 52 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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