Theodore D. Satterthwaite

Dr. Theodore D. Satterthwaite


Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2013 in NeuroImage
Verified
Journal Article
Closed access
TSTheodore D. Satterthwaite
Theodore D. Satterthwaite
MEMark A. Elliott
Mark A. Elliott
RGRaphael T. Gerraty
Raphael T. Gerraty
KRKosha Ruparel
Kosha Ruparel
JLJames Loughead
James Loughead
DWDaniel H. Wolf
Daniel H. Wolf

1 July 2017 in NeuroImage
Verified
Journal Article
Open access
RCRastko Ciric
Rastko Ciric
DWDaniel H. Wolf
Daniel H. Wolf
JPJonathan D. Power
Jonathan D. Power
DRDavid R. Roalf
David R. Roalf
GBGraham L. Baum
Graham L. Baum
TSTheodore D. Satterthwaite
Theodore D. Satterthwaite
Since initial reports regarding the impact of motion artifact on measures of functional connectivity, there has been a proliferation of participant-level confound regression methods to limit its impact. However, many of the most commonly used techniques have not been systematically evaluated using a broad range of outcome measures. Here, we provide a systematic evaluation of 14 participant-level confound regression methods in 393 youths. Specifically, we compare methods according to four benchmarks, including the residual relationship between motion and connectivity, distance-dependent effects of motion on connectivity, network identifiability, and additional degrees of freedom lost in confound regression. Our results delineate two clear trade-offs among methods. First, methods that include global signal regression minimize the relationship between connectivity and motion, but result in distance-dependent artifact. In contrast, censoring methods mitigate both motion artifact and distance-dependence, but use additional degrees of freedom. Importantly, less effective de-noising methods are also unable to identify modular network structure in the connectome. Taken together, these results emphasize the heterogeneous efficacy of existing methods, and suggest that different confound regression strategies may be appropriate in the context of specific scientific goals.

1 March 2012 in NeuroImage
Verified
Journal Article
Closed access
TSTheodore D. Satterthwaite
Theodore D. Satterthwaite
DWDaniel H. Wolf
Daniel H. Wolf
JLJames Loughead
James Loughead
KRKosha Ruparel
Kosha Ruparel
MEMark A. Elliott
Mark A. Elliott
RGRaquel E. Gur
Raquel E. Gur

2 December 2013 in Proceedings of the National Academy of Sciences
Verified
Journal Article
Open access
PDF file
MIMadhura Ingalhalikar
Madhura Ingalhalikar
ASAlex Smith
Alex Smith
DPDrew Parker
Drew Parker
TSTheodore D. Satterthwaite
Theodore D. Satterthwaite
MEMark A. Elliott
Mark A. Elliott
RVRagini Verma
Ragini Verma
Significance: Sex differences are of high scientific and societal interest because of their prominence in behavior of humans and nonhuman species. This work is highly significant because it studies a very large population of 949 youths (8–22 y, 428 males and 521 females) using the diffusion-based structural connectome of the brain, identifying novel sex differences. The results establish that male brains are optimized for intrahemispheric and female brains for interhemispheric communication. The developmental trajectories of males and females separate at a young age, demonstrating wide differences during adolescence and adulthood. The observations suggest that male brains are structured to facilitate connectivity between perception and coordinated action, whereas female brains are designed to facilitate communication between analytical and intuitive processing modes.

1 September 2021 in Neuron
Verified
Journal Article
Closed access
VSValerie J. Sydnor
Valerie J. Sydnor
BLBart Larsen
Bart Larsen
DBDanielle S. Bassett
Danielle S. Bassett
AAAaron Alexander-Bloch
Aaron Alexander-Bloch
DFDamien A. Fair
Damien A. Fair
TSTheodore D. Satterthwaite
Theodore D. Satterthwaite

8 January 2014 in Brain Imaging and Behavior
Verified
Journal Article
Open access
PDF file
PTPaul M. Thompson
Paul M. Thompson
JSJason L. Stein
Jason L. Stein
SMSarah E. Medland
Sarah E. Medland
DHDerrek P. Hibar
Derrek P. Hibar
AVAlejandro Arias Vasquez
Alejandro Arias Vasquez
WDWayne Drevets
Wayne Drevets
The Enhancing NeuroImaging Genetics through Meta-Analysis (ENIGMA) Consortium is a collaborative network of researchers working together on a range of large-scale studies that integrate data from 70 institutions worldwide. Organized into Working Groups that tackle questions in neuroscience, genetics, and medicine, ENIGMA studies have analyzed neuroimaging data from over 12,826 subjects. In addition, data from 12,171 individuals were provided by the CHARGE consortium for replication of findings, in a total of 24,997 subjects. By meta-analyzing results from many sites, ENIGMA has detected factors that affect the brain that no individual site could detect on its own, and that require larger numbers of subjects than any individual neuroimaging study has currently collected. ENIGMA’s first project was a genome-wide association study identifying common variants in the genome associated with hippocampal volume or intracranial volume. Continuing work is exploring genetic associations with subcortical volumes (ENIGMA2) and white matter microstructure (ENIGMA-DTI). Working groups also focus on understanding how schizophrenia, bipolar illness, major depression and attention deficit/hyperactivity disorder (ADHD) affect the brain. We review the current progress of the ENIGMA Consortium, along with challenges and unexpected discoveries made on the way.