C. Thomas Caskey

Baylor College of Medicine — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

65h-index24.7kcitations214works0.02yr avg
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Research Topics

Biochemical and Molecular Research(52), Genetics and Neurodevelopmental Disorders(28), Genetic Neurodegenerative Diseases(23), Cytomegalovirus and herpesvirus research(22), Muscle Physiology and Disorders(21)

Publications212 total

2021 Allan Award
The American Journal of Human Genetics·2022· 1 citedOpen Access
Stephen T. Warren: Human geneticist who advanced understanding of mutational mechanisms and developmental disorders
Proceedings of the National Academy of Sciences·2021Open Access
Precision medicine integrating whole-genome sequencing, comprehensive metabolomics, and advanced imaging
Proceedings of the National Academy of Sciences·2020· 136 citedOpen Access
An unsupervised learning approach to identify novel signatures of health and disease from multimodal data
Genome Medicine·2020· 53 citedOpen Access
Precision medicine in neurology
Elsevier eBooks·2020· 1 cited
MOESM5 of An unsupervised learning approach to identify novel signatures of health and disease from multimodal data
Figshare·2020Open Access
List of contributors
Elsevier eBooks·2020
MOESM2 of An unsupervised learning approach to identify novel signatures of health and disease from multimodal data
Figshare·2020Open Access
MOESM4 of An unsupervised learning approach to identify novel signatures of health and disease from multimodal data
Figshare·2020Open Access
Predispositional genome sequencing in healthy adults: design, participant characteristics, and early outcomes of the PeopleSeq Consortium
Genome Medicine·2019· 56 citedOpen Access
Response to Whiffin et al.
The American Journal of Human Genetics·2019· 1 citedOpen Access
Unsupervised integration of multimodal dataset identifies novel signatures of health and disease
2018· 2 citedOpen Access
Profound perturbation of the human metabolome by obesity
2018· 9 citedOpen Access
Identification of Misclassified ClinVar Variants via Disease Population Prevalence
The American Journal of Human Genetics·2018· 146 citedOpen Access
Aberrant GlyRS-HDAC6 interaction linked to axonal transport deficits in Charcot-Marie-Tooth neuropathy
Nature Communications·2018· 113 citedOpen Access
Profiling of Short-Tandem-Repeat Disease Alleles in 12,632 Human Whole Genomes
The American Journal of Human Genetics·2017· 205 citedOpen Access
Whole-genome sequencing identifies common-to-rare variants associated with human blood metabolites
Nature Genetics·2017· 481 cited
Structure, expression, and mutation of the hypoxanthine phosphoribosyltransferase gene (intervening sequences/transcriptional initiation/minigene)
2016
Plasma metabolomic profiles enhance precision medicine for volunteers of normal health
Proceedings of the National Academy of Sciences·2015· 172 citedOpen Access
Mendelian, Non-Mendelian, Multigenic Inheritance, and Epigenetics
Elsevier eBooks·2014· 27 cited
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Frequent Co-authors

Richard A. Gibbs(7), Antonio Pizzuti(6), Raymond G. Fenwick(6), David L. Nelson(4), Ying‐Hui Fu(4), Tetsuo Ashizawa(4), J. Craig Venter(4), A. Craig Chinault(4), Jeffrey S. Chamberlain(4), Maura Pieretti(3), Stephen Richards(3), M. Benjamin Perryman(3), Qingyun Liu(3), Zhizhen Zeng(3), Chang Bai(3), Christopher P. Austin(3), Jilly F. Evans(3), Michael L. Metzker(3), Xiangwei Wu(3), Donna M. Muzny(3)