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Dive into the research topics where Christine L. Mac Donald is active.

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Featured researches published by Christine L. Mac Donald.


JAMA Neurology | 2014

Prospectively Assessed Clinical Outcomes in Concussive Blast vs Nonblast Traumatic Brain Injury Among Evacuated US Military Personnel

Christine L. Mac Donald; Ann Johnson; Linda Wierzechowski; Elizabeth Kassner; Theresa Stewart; Elliot C. Nelson; Nicole J. Werner; David Zonies; John Oh; Raymond Fang; David L. Brody

IMPORTANCEnBlast injury has been identified as the signature injury in the conflicts in Iraq and Afghanistan. However it remains to be determined whether fundamental differences may exist between blast-related traumatic brain injury (TBI) and TBI due to other mechanisms.nnnOBJECTIVESnTo determine similarities and differences between clinical outcomes in US military personnel with blast-related vs. non-blast-related concussive TBI and to identify the specific domains of impairment that best correlate with overall disability.nnnDESIGN, SETTING, AND PARTICIPANTSnProspective cohort study involving active duty US Military personnel evacuated from Iraq or Afghanistan to Landstuhl Regional Medical Center, in Landstuhl, Germany. Four groups of participants were enrolled from 2010 to 2013: (1) blast plus impact complex TBI (n=53), (2) non-blast related TBI with injury due to other mechanisms (n=29), (3) blast-exposed controls evacuated for other medical reasons (n=27) (4) non-blast-exposed controls evacuated for other medical reasons (n=69). All patients with TBI met Department of Defense criteria for concussive (mild) TBI. The study participants were evaluated 6-12 months after injury at Washington University in St Louis. In total, 255 subjects were enrolled in the study, and 183 participated in follow-up evaluations, 5 of whom were disqualified.nnnMAIN OUTCOMES AND MEASURESnIn-person clinical examinations included evaluation for overall disability, a standardized neurological exam, headache questionnaires, neuropsychological test battery, combat exposure and alcohol use surveys, and structured interview evaluations for post-traumatic stress disorder (PTSD) and depression.nnnRESULTSnGlobal outcomes, headache severity, neuropsychological performance, and surprisingly even PTSD severity and depression were indistinguishable between the two TBI groups, independent of mechanism of injury. Both TBI groups had higher rates of moderate to severe overall disability than the respective control groups: 41/53 (77%) of blast plus impact TBI and 23/29 (79%) of nonblast TBI vs. 16/27 (59%) of blast-exposed controls and 28/69 (41%) of non-blast-exposed controls. In addition, blast-exposed controls had worse headaches and more severe PTSD than non-blast-exposed controls. Self-reported combat exposure intensity was higher in the blast plus impact TBI group than in nonblast TBI group and was higher in blast-exposed controls than in non-blast-exposed controls. However, combat exposure intensity did not correlate with PTSD severity in the TBI groups, but a modest positive correlation was observed in the controls. Overall outcomes were most strongly correlated with depression, headache severity, and number of abnormalities on neuropsychological testing. However a substantial fraction of the variance in overall outcome was not explained by any of the assessed measures.nnnCONCLUSIONS AND RELEVANCEnOne potential interpretation of these results is that TBI itself, independent of injury mechanism and combat exposure intensity, is a primary driver of adverse outcomes. Many other important factors may be as yet unmeasured, and adverse outcomes following war-time injuries are difficult to fully explain.nnnTRIAL REGISTRATIONnclinicaltrials.gov Identifier: NCT01313130.


Neurology | 2015

Clinical and imaging assessment of acute combat mild traumatic brain injury in Afghanistan

Octavian Adam; Christine L. Mac Donald; Dennis Rivet; John Ritter; Todd May; Maria Barefield; Josh Duckworth; Donald LaBarge; Dean Asher; Benjamin Drinkwine; Yvette Woods; Michael Connor; David L. Brody

Objective: To evaluate whether diffusion tensor imaging (DTI) will noninvasively reveal white matter changes not present on conventional MRI in acute blast-related mild traumatic brain injury (mTBI) and to determine correlations with clinical measures and recovery. Methods: Prospective observational study of 95 US military service members with mTBI enrolled within 7 days from injury in Afghanistan and 101 healthy controls. Assessments included Rivermead Post-Concussion Symptoms Questionnaire (RPCSQ), Post-Traumatic Stress Disorder Checklist Military (PCLM), Beck Depression Inventory (BDI), Balance Error Scoring System (BESS), Automated Neuropsychological Assessment Metrics (ANAM), conventional MRI, and DTI. Results: Significantly greater impairment was observed in participants with mTBI vs controls: RPCSQ (19.7 ± 12.9 vs 3.6 ± 7.1, p < 0.001), PCLM (32 ± 13.2 vs 20.9 ± 7.1, p < 0.001), BDI (7.4 ± 6.8 vs 2.5 ± 4.9, p < 0.001), and BESS (18.2 ± 8.4 vs 15.1 ± 8.3, p = 0.01). The largest effect size in ANAM performance decline was in simple reaction time (mTBI 74.5 ± 148.4 vs control −11 ± 46.6 milliseconds, p < 0.001). Fractional anisotropy was significantly reduced in mTBI compared with controls in the right superior longitudinal fasciculus (0.393 ± 0.022 vs 0.405 ± 0.023, p < 0.001). No abnormalities were detected with conventional MRI. Time to return to duty correlated with RPCSQ (r = 0.53, p < 0.001), ANAM simple reaction time decline (r = 0.49, p < 0.0001), PCLM (r = 0.47, p < 0.0001), and BDI (r = 0.36 p = 0.0005). Conclusions: Somatic, behavioral, and cognitive symptoms and performance deficits are substantially elevated in acute blast-related mTBI. Postconcussive symptoms and performance on measures of posttraumatic stress disorder, depression, and neurocognitive performance at initial presentation correlate with return-to-duty time. Although changes in fractional anisotropy are uncommon and subtle, DTI is more sensitive than conventional MRI in imaging white matter integrity in blast-related mTBI acutely.


JAMA Neurology | 2017

Early Clinical Predictors of 5-Year Outcome After Concussive Blast Traumatic Brain Injury

Christine L. Mac Donald; Jason Barber; Mary Jordan; Ann Johnson; Sureyya Dikmen; Jesse R. Fann; Nancy Temkin

Importance The long-term clinical effects of wartime traumatic brain injuries (TBIs), most of which are mild, remain incompletely described. Current medical disability cost estimates from world conflicts continually surpass projections. Additional information regarding long-term functional trajectory is needed to reduce this extensive public health burden. Objectives To examine 5-year clinical outcomes leveraging existing clinical data collected at 1 year after injury in the same patients and to identify early risk factors for long-term disability. Design, Setting, and Participants This prospective, longitudinal study enrolled active-duty US military after concussive blast injury (nu2009=u200950) in the acute to subacute stage and combat-deployed control individuals (nu2009=u200944) in Afghanistan or after medical evacuation to Germany from November 1, 2008, through July 1, 2013. One- and 5-year clinical evaluations were completed in the United States. All concussive blast injuries met the Department of Defense definition of mild, uncomplicated TBI. In-person clinical evaluations included standardized evaluations for neurobehavior, neuropsychological performance, and mental health burden that were essentially identical to the evaluations completed at 1-year follow-up. Data were analyzed from October 1 through November 30, 2016. Main Outcomes and Measures Changes in the in-person standardized evaluations for neurobehavior, neuropsychological performance, and mental health burden from the 1- to 5-year follow-up. Predictive modeling was used to identify early risk factors for long-term disability. Results Among the 94 participants (87 men [93%] and 7 women [7%]; mean [SD] age, 34 [8] years), global disability, satisfaction with life, neurobehavioral symptom severity, psychiatric symptom severity, and sleep impairment were significantly worse in patients with concussive blast TBI compared with combat-deployed controls, whereas performance on cognitive measures was no different between groups at the 5-year evaluation. Logistic regression on the dichotomized Extended Glasgow Outcome Scale (GOS-E) at 5 years as a measure of overall disability identified brain injury diagnosis, preinjury intelligence, motor strength, verbal fluency, and neurobehavioral symptom severity at 1 year as risk factors for a poor outcome at 5 years, with an area under the curve of 0.92 indicating excellent prediction strength. Thirty-six of 50 patients with concussive blast TBI (72%) had a decline in the GOS-E from the 1- to 5-year evaluations, in contrast with only 5 of 44 combat-deployed controls (11%). Worsening of symptoms in concussive blast TBI was also observed on measures of posttraumatic stress disorder and depression. Service members with concussive blast TBI experienced evolution, not resolution, of symptoms from the 1- to 5-year outcomes. Conclusions and Relevance Considerable decline was observed in military service members with concussive blast TBI when comparing 1- and 5-year clinical outcomes. These results advocate for new treatment strategies to combat the long-term and extremely costly effect of these wartime injuries.


Brain | 2015

Quantitative assessments of traumatic axonal injury in human brain: concordance of microdialysis and advanced MRI

Sandra Magnoni; Christine L. Mac Donald; Thomas J. Esparza; Valeria Conte; James Sorrell; Mario Macrì; Giulio Bertani; Riccardo Biffi; Antonella Costa; Brian Sammons; Abraham Z. Snyder; Joshua S. Shimony; Fabio Triulzi; Nino Stocchetti; David L. Brody

Axonal injury is a major contributor to adverse outcomes following brain trauma. However, the extent of axonal injury cannot currently be assessed reliably in living humans. Here, we used two experimental methods with distinct noise sources and limitations in the same cohort of 15 patients with severe traumatic brain injury to assess axonal injury. One hundred kilodalton cut-off microdialysis catheters were implanted at a median time of 17 h (13-29 h) after injury in normal appearing (on computed tomography scan) frontal white matter in all patients, and samples were collected for at least 72 h. Multiple analytes, such as the metabolic markers glucose, lactate, pyruvate, glutamate and tau and amyloid-β proteins, were measured every 1-2 h in the microdialysis samples. Diffusion tensor magnetic resonance imaging scans at 3 T were performed 2-9 weeks after injury in 11 patients. Stability of diffusion tensor imaging findings was verified by repeat scans 1-3 years later in seven patients. An additional four patients were scanned only at 1-3 years after injury. Imaging abnormalities were assessed based on comparisons with five healthy control subjects for each patient, matched by age and sex (32 controls in total). No safety concerns arose during either microdialysis or scanning. We found that acute microdialysis measurements of the axonal cytoskeletal protein tau in the brain extracellular space correlated well with diffusion tensor magnetic resonance imaging-based measurements of reduced brain white matter integrity in the 1-cm radius white matter-masked region near the microdialysis catheter insertion sites. Specifically, we found a significant inverse correlation between microdialysis measured levels of tau 13-36 h after injury and anisotropy reductions in comparison with healthy controls (Spearmans r = -0.64, P = 0.006). Anisotropy reductions near microdialysis catheter insertion sites were highly correlated with reductions in multiple additional white matter regions. We interpret this result to mean that both microdialysis and diffusion tensor magnetic resonance imaging accurately reflect the same pathophysiological process: traumatic axonal injury. This cross-validation increases confidence in both methods for the clinical assessment of axonal injury. However, neither microdialysis nor diffusion tensor magnetic resonance imaging have been validated versus post-mortem histology in humans. Furthermore, future work will be required to determine the prognostic significance of these assessments of traumatic axonal injury when combined with other clinical and radiological measures.


NeuroImage: Clinical | 2017

5-Year imaging sequelae of concussive blast injury and relation to early clinical outcome

Christine L. Mac Donald; Jason Barber; Jalal B. Andre; Nicole Evans; Chris Panks; Samantha Sun; Kody Zalewski; R. Elizabeth Sanders; Nancy Temkin

Current imaging diagnostic techniques are often insensitive to the underlying pathological changes following mild traumatic brain injury (TBI) or concussion so much so that the explicit definition of these uncomplicated mild brain injuries includes the absence of radiological findings. In the US military, this is complicated by the natural tendency of service members to down play symptoms for fear of removal from their unit particularly in combat making it challenging for clinicians to definitively diagnose and determine course of treatment. Questions remain regarding the long-term impact of these war-time brain injuries. The objective of the current study was to evaluate the long-term imaging sequelae of blast concussion in active-duty US military and leverage previous longitudinal data collected in these same patients to identify predictors of sustained DTI signal change indicative of chronic neurodegeneration. In total, 50 blast TBI and 44 combat-deployed controls were evaluated at this 5-year follow up by advanced neuroimaging techniques including diffusion tensor imaging and quantitative volumetry. While cross-sectional analysis of regions of white matter on DTI images did not reveal significant differences across groups after statistical correction, an approach flexible to the heterogeneity of brain injury at the single-subject level identified 74% of the concussive blast TBI cohort to have reductions in fractional anisotropy indicative of chronic brain injury. Logistic regression leveraging clinical and demographic data collected in the acute/sub-acute and 1-year follow up to determine predictors of these long-term imaging changes determined that brain injury diagnosis, older age, verbal memory and verbal fluency best predicted the presence of DTI abnormalities 5 years post injury with an AUC of 0.78 indicating good prediction strength. These results provide supporting evidence for the evolution not resolution of this brain injury pathology, adding to the growing body of literature describing imaging signatures of chronic neurodegeneration even after mild TBI and concussion.


Journal of Child Neurology | 2016

Head Impact Exposure During a Weekend Youth Soccer Tournament

Sara P. Chrisman; Christine L. Mac Donald; Seth D. Friedman; Jalal B. Andre; Ali Rowhani-Rahbar; Sara Drescher; Elizabeth Stein; Matthew Holm; Nicole Evans; Andrew Poliakov; Randal P. Ching; Christina C. Schwien; Monica S. Vavilala; Frederick P. Rivara

Concussion is a known risk in youth soccer, but little is known about subconcussive head impacts. The authors provided a prospective cohort study measuring frequency and magnitude of subconcussive head impacts using accelerometry in a middle school–age soccer tournament, and association between head impacts and changes in (1) symptoms, (2) cognitive testing, and (3) advanced neuroimaging. A total of 17 youth completed the study (41% female, mean 12.6 years). There were 73 head impacts >15g measured (45% headers) and only 2 had a maximum peak linear acceleration >50g. No youth reported symptoms consistent with concussion. After correction for multiple comparisons and a sensitivity analysis excluding clear outliers, no significant associations were found between head impact exposure and neuropsychological testing or advanced neuroimaging. The authors conclude that head impacts were relatively uncommon and low in acceleration in youth playing a weekend soccer tournament. This study adds to the limited data regarding head impacts in youth soccer.


Journal of Neurotrauma | 2017

Outcome Trends after US Military Concussive Traumatic Brain Injury

Christine L. Mac Donald; Ann Johnson; Linda Wierzechowski; Elizabeth Kassner; Theresa Stewart; Elliot C. Nelson; Nicole J. Werner; Octavian R. Adam; Dennis Rivet; Stephen F. Flaherty; John S. Oh; David Zonies; Raymond Fang; David L. Brody

Care for US military personnel with combat-related concussive traumatic brain injury (TBI) has substantially changed in recent years, yet trends in clinical outcomes remain largely unknown. Our prospective longitudinal studies of US military personnel with concussive TBI from 2008-2013 at Landstuhl Regional Medical Center in Germany and twp sites in Afghanistan provided an opportunity to assess for changes in outcomes over time and analyze correlates of overall disability. We enrolled 321 active-duty US military personnel who sustained concussive TBI in theater and 254 military controls. We prospectively assessed clinical outcomes 6-12 months later in 199 with concussive TBI and 148 controls. Global disability, neurobehavioral impairment, depression severity, and post-traumatic stress disorder (PTSD) severity were worse in concussive TBI groups in comparison with controls in all cohorts. Global disability primarily reflected a combination of work-related and nonwork-related disability. There was a modest but statistically significant trend toward less PTSD in later cohorts. Specifically, there was a decrease of 5.9 points of 136 possible on the Clinician Administered PTSD Scale (-4.3%) per year (95% confidence interval, 2.8-9.0 points, pu2009=u20090.0037 linear regression, pu2009=u20090.03 including covariates in generalized linear model). No other significant trends in outcomes were found. Global disability was more common in those with TBI, those evacuated from theater, and those with more severe depression and PTSD. Disability was not significantly related to neuropsychological performance, age, education, self-reported sleep deprivation, injury mechanism, or date of enrollment. Thus, across multiple cohorts of US military personnel with combat-related concussion, 6-12 month outcomes have improved only modestly and are often poor. Future focus on early depression and PTSD after concussive TBI appears warranted. Adverse outcomes are incompletely explained, however, and additional studies with prospective collection of data on acute injury severity and polytrauma, as well as reduced attrition before follow-up will be required to fully address the root causes of persistent disability after wartime injury.


NeuroImage: Clinical | 2016

Longitudinal cerebellar diffusion tensor imaging changes in posterior fossa syndrome.

Sean D. McEvoy; Amy Lee; Andrew Poliakov; Seth D. Friedman; Dennis W. W. Shaw; Samuel R. Browd; Richard G. Ellenbogen; Jeffrey G. Ojemann; Christine L. Mac Donald

Posterior fossa syndrome is a severe transient loss of language that frequently complicates resection of tumors of the cerebellum. The associated pathophysiology and relevant anatomy to this language deficit remains controversial. We performed a retrospective analysis of all cerebellar tumor resections at Seattle Childrens Hospital from 2010 to 2015. Diffusion tensor imaging was performed on each of the patients as part of their clinical scan. Patients included in the study were divided into groups based on language functioning following resection: intact (N = 19), mild deficit (N = 19), and posterior fossa syndrome (N = 9). Patients with posterior fossa syndrome showed white matter changes evidenced by reductions in fractional anisotropy in the left and right superior cerebellar peduncle following resection, and these changes were still evident 1-year after surgery. These changes were greater in the superior cerebellar peduncle than elsewhere in the cerebellum. Prior to surgery, posterior fossa patients did not show changes in fractional anisotropy however differences were observed in mean and radial diffusivity measures in comparison to other groups which may provide a radiographic marker of those at greatest risk of developing post-operative language loss.


Acta Neuropathologica | 2018

First confirmed case of chronic traumatic encephalopathy in a professional bull rider

C. Dirk Keene; Caitlin S. Latimer; Lisa Steele; Christine L. Mac Donald

There is increased concern regarding the prevalence of chronic traumatic encephalopathy [5] following repeated head impact exposure in a variety of sports [2, 4, 6, 7] and the military [3] but the existence in other populations is unknown. We present the first-confirmed case of a professional bull rider with CTE. Following sustainment of at least 15 head injuries over a 10-year period confirmed by collateral sources, records review, and ante-mortem imaging studies, the majority witnessed and documented on videotape, he committed suicide. Unique to this case, we performed imaging-guided brain tissue sampling for neuropathological investigation. This approach may provide for more focused tissue sampling that is sensitive and flexible to the heterogeneity of brain injury complementing standard neuropathological evaluation strategies. Past medical history identified first-diagnosed concussion at age 16 with confirmed loss of consciousness (LOC) and additional exposures approximately biennially until age 21 when he sustained five head injuries over the course of a 12-month period. Each incident involved LOC for minutes followed by disorientation, confusion, ocular disturbance including photophobia, and periods of anterograde amnesia lasting hours to days. The decedent was evaluated by onsite medical personnel and/or admitted to a hospital for observation with radiographic CT examination, noted as unremarkable each time. At age 23, he sustained a blow to the head after being stepped on by a rearing bull crushing his helmet with LOC for 1 h, meeting criteria for moderate brain injury [8]. Initial Glasgow Coma Scale (GCS) at hospital presentation was 10, and remained 10 for 24 h before returning to 14 out of 15 by day 2. CT evaluation again was negative for pathoanatomical brain injury lesions. MRI evaluation completed 3 months later identified multiple regions of hemorrhagic foci bilaterally in the frontal lobes, right temporal lobe, left hippocampus, and left brainstem, consistent with microhemorrhage following shear injury meeting radiographic criteria for diffuse axonal injury [1]. Following these exposures, the decedent was noted to have post-traumatic headache, memory loss, concentration problems, attentional dysfunction, mood lability, disinhibition, diplopia, photophobia, phonophobia, vestibular dysfunction, insomnia, irritability, explosivity, depression, anxiety, dysarthria with mild aphasia, difficulty with mental flexibility and planning, motor slowing, exaggerated somatic concern, hostility, and conceptual disorganization. Family members described a very bright, jovial, and affable young man who was conscientious and loving but in the last 6–9 months of life rapidly deteriorated, becoming reclusive and hypervigilant with paralyzing panic attacks, and displaying significant behavioral changes characterized by erratic and impulsive decisions until his death at 25. Following consent for brain donation, familial consent was provided for review of medical records, clinical CT, and MRI scans collected on the decedent prior to death in accordance with regulations. The decedent’s fixed brain was examined for gross findings and then imaged ex vivo with high-resolution MRI for co-registration to the ante-mortem scans. This allowed imaged-guided tissue sectioning for pathoanatomic lesions visible on the ante-mortem MRI that may be grossly unremarkable. Standard sampling was performed to evaluate for traumatic brain injury, CTE [5], and other neurodegenerative processes. Sampled regions included bilateral superior and middle frontal gyri, orbitofrontal cortex, superior and middle temporal gyri, anterior temporal lobes, inferior parietal lobules, hippocampi and entorhinal cortex at two levels, amygdalae, thalami, * Christine L. Mac Donald [email protected]


bioRxiv | 2018

The Evolution of White Matter Microstructural Changes After Mild Traumatic Brain Injury: A Longitudinal DTI and NODDI Study

Eva M. Palacios; Julia P Owen; Esther L. Yuh; Maxwell B. Wang; Mary J Vassar; Adam R. Ferguson; Ramon Diaz-Arrastia; Joseph T. Giacino; David O. Okonkwo; Claudia S. Robertson; Murray B. Stein; Nancy Temkin; Sonia Jain; Michael McCrea; Christine L. Mac Donald; Harvey S. Levin; Geoffrey T. Manley; Pratik Mukherjee; Track-Tbi Investigators

Neuroimaging biomarkers show promise for improving precision diagnosis and prognosis after mild traumatic brain injury (mTBI), but none has yet been adopted in routine clinical practice. Biophysical modeling of multishell diffusion MRI, using the neurite orientation dispersion and density imaging (NODDI) framework, may improve upon conventional diffusion tensor imaging (DTI) in revealing subtle patterns of underlying white matter microstructural pathology, such as diffuse axonal injury (DAI) and neuroinflammation, that are important for detecting mTBI and determining patient outcome. With a cross-sectional and longitudinal design, we assessed structural MRI, DTI and NODDI in 40 mTBI patients at 2 weeks and 6 months after injury and 14 matched control participants with orthopedic trauma but not suffering from mTBI at 2 weeks. Self-reported and performance-based cognitive measures assessing postconcussive symptoms, memory, executive functions and processing speed were investigated in post-acute and chronic phase after injury for the mTBI subjects. Machine learning analysis was used to identify mTBI patients with the best neuropsychological improvement over time and relate this outcome to DTI and NODDI biomarkers. In the cross-sectional comparison with the trauma control group at 2 weeks post-injury, mTBI patients showed decreased fractional anisotropy (FA) and increased mean diffusivity (MD) on DTI mainly in anterior tracts that corresponded to white matter regions of elevated free water fraction (FISO) on NODDI, signifying vasogenic edema. Patients showed decreases from 2 weeks to 6 months in white matter neurite density on NODDI, predominantly in posterior tracts. No significant longitudinal changes in DTI metrics were observed. The machine learning analysis divided the mTBI patients into two groups based on their recovery. Voxel-wise group comparison revealed associations between white matter orientation dispersion index (ODI) and FISO with degree and trajectory of improvement within the mTBI group. In conclusion, white matter FA and MD alterations early after mTBI might reflect vasogenic edema, as shown by elevated free water on NODDI. Longer-term declines in neurite density on NODDI suggest progressive axonal degeneration due to DAI, especially in tracts known to be integral to the structural connectome. Overall, these results show that the NODDI parameters appear to be more sensitive to longitudinal changes than DTI metrics. Thus, NODDI merits further study in larger cohorts for mTBI diagnosis, prognosis and treatment monitoring.

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Nancy Temkin

University of Washington

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David L. Brody

Washington University in St. Louis

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Ann Johnson

Washington University in St. Louis

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Jason Barber

University of Washington

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Kody Zalewski

University of Washington

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Paul K. Crane

University of Washington

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C. Dirk Keene

University of Washington

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Chris Panks

University of Washington

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