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Author Details

Ashok Veeraraghavan
Rice University
2005
91
29
PMIDPaper TitleJournal TitlePublished Year
36798295Subdural CMOS optical probe (SCOPe) for bidirectional neural interfacing.bioRxiv2023
37561613CoIR: Compressive Implicit Radar.IEEE Trans Pattern Anal Mach Intell2023
37799697Real-time, deep-learning aided lensless microscope.Biomed Opt Express2023
37854569SpeckleCam: high-resolution computational speckle contrast tomography for deep blood flow imaging.Biomed Opt Express2023
37456517High-Speed Time-Domain Diffuse Optical Tomography with a Sensitivity Equation-based Neural Network.IEEE Trans Comput Imaging2023
37379386NeuWS: Neural wavefront shaping for guidestar-free imaging through static and dynamic scattering media.Sci Adv2023
37267897Response to Grosse et al.Am J Hum Genet2023
36788231Scalable, high quality, whole genome sequencing from archived, newborn, dried blood spots.NPJ Genom Med2023
36908760Unrolled-DOT: an interpretable deep network for diffuse optical tomography.J Biomed Opt2023
33104508FlatNet: Towards Photorealistic Scene Reconstruction From Lensless Measurements.IEEE Trans Pattern Anal Mach Intell2022
36212271Evolution of Mood Symptomatology Through the COVID-19 Pandemic: Findings From the CovidSense Longitudinal Study.Cureus2022
36338918Recent Advances in Lensless Imaging.Optica2022
36242441Snapshot polarimetric diffuse-specular separation.Opt Express2022
36037460PS <sup>2</sup> F: Polarized Spiral Point Spread Function for Single-Shot 3D Sensing.IEEE Trans Pattern Anal Mach Intell2022
36269651The Family Level Assessment of Screen Use-Mobile Approach: Development of an Approach to Measure Children's Mobile Device Use.JMIR Form Res2022
35882841An automated 13.5â¿¿hour system for scalable diagnosis and acute management guidance for genetic diseases.Nat Commun2022
36007526A genome sequencing system for universal newborn screening, diagnosis, and precision medicine for severe genetic diseases.Am J Hum Genet2022
36215563FlatNet3D: intensity and absolute depth from single-shot lensless capture.J Opt Soc Am A Opt Image Sci Vis2022
35256759In vivo lensless microscopy via a phase mask generating diffraction patterns with high-contrast contours.Nat Biomed Eng2022
35323113An Objective System for Quantitative Assessment of Television Viewing Among Children (Family Level Assessment of Screen Use in the Home-Television): System Development Study.JMIR Pediatr Parent2022
34039980Publisher Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease.NPJ Genom Med2021
33569935HRVCam: robust camera-based measurement of heart rate variability.J Biomed Opt2021
33891548High Resolution, Deep Imaging Using Confocal Time-of-Flight Diffuse Optical Tomography.IEEE Trans Pattern Anal Mach Intell2021
33891546SASSI - Super-Pixelated Adaptive Spatio-Spectral Imaging.IEEE Trans Pattern Anal Mach Intell2021
33888711Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease.NPJ Genom Med2021
34951854A Mechanically Flexible, Implantable Neural Interface for Computational Imaging and Optogenetic Stimulation Over 5.4ÿ5.4mm<sup>2</sup> FoV.IEEE Trans Biomed Circuits Syst2021
35154871Deep-3D microscope: 3D volumetric microscopy of thick scattering samples using a wide-field microscope and machine learning.Biomed Opt Express2021
34966190Ultrafast and Ultrahigh-Resolution Diffuse Optical Tomography for Brain Imaging with Sensitivity Equation based Noniterative Sparse Optical Reconstruction (SENSOR).J Quant Spectrosc Radiat Transf2021
34645491Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases.Genome Med2021
34808905EDoF-ToF: extended depth of field time-of-flight imaging.Opt Express2021
34077649Rapid Sequencing-Based Diagnosis of Thiamine Metabolism Dysfunction Syndrome.N Engl J Med2021
34039997Author Correction: Rapid whole genome sequencing impacts care and resource utilization in infants with congenital heart disease.NPJ Genom Med2021
32324539PhlatCam: Designed Phase-Mask Based Thin Lensless Camera.IEEE Trans Pattern Anal Mach Intell2020
33659085Systematic analysis of video-based pulse measurement from compressed videos.Biomed Opt Express2020
33167411Vision and Deep Learning-Based Algorithms to Detect and Quantify Cracks on Concrete Surfaces from UAV Videos.Sensors (Basel)2020
33318169Deep learning extended depth-of-field microscope for fast and slide-free histology.Proc Natl Acad Sci U S A2020
33018201PPG3D: Does 3D head tracking improve camera-based PPG estimation?Annu Int Conf IEEE Eng Med Biol Soc2020
32179806PulseCam: a camera-based, motion-robust and highly sensitive blood perfusion imaging modality.Sci Rep2020
31069074WISH: wavefront imaging sensor with high resolution.Light Sci Appl2019
31412054Bioluminescent flashes drive nighttime schooling behavior and synchronized swimming dynamics in flashlight fish.PLoS One2019
31564432A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants.Am J Hum Genet2019
31019026Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation.Sci Transl Med2019
29644095Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization.NPJ Genom Med2018
30281456Zero-Shot Learning via Category-Specific Visual-Semantic Mapping and Label Refinement.IEEE Trans Image Process2018
30469803Integrated light-sheet illumination using metallic slit microlenses.Opt Express2018
29449963The NSIGHT1-randomized controlled trial: rapid whole-genome sequencing for accelerated etiologic diagnosis in critically ill infants.NPJ Genom Med2018
28880960Correction: Correction: A Novel Rhabdovirus Associated with Acute Hemorrhagic Fever in Central Africa.PLoS Pathog2017
28439550SAVI: Synthetic apertures for long-range, subdiffraction-limited visible imaging using Fourier ptychography.Sci Adv2017
28300864Whole exome sequencing in the Framingham Heart Study identifies rare variation in HYAL2 that influences platelet aggregation.Thromb Haemost2017
28151979Whole genome sequencing of an African American family highlights toll like receptor 6 variants in Kawasaki disease susceptibility.PLoS One2017
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Collaborators

Rady Children's Institute for Genomic Medicine
Co-authored papers 15
Baylor College of Medicine
Co-authored papers 12
Baylor College of Medicine
Co-authored papers 12
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Co-authored papers 11
Co-authored papers 11
Baylor College of Medicine
Co-authored papers 11
School of Public Health, San Diego State University
Co-authored papers 8
Rady Children's Institute for Genomic Medicine, Rady Children's Hospital
Co-authored papers 7
Co-authored papers 6
Co-authored papers 5
Fabric Genomics Inc.
Co-authored papers 5
University of California-San Francisco
Co-authored papers 5
Co-authored papers 4
Baylor College of Medicine
Co-authored papers 4
Institute of Social and Preventive Medicine (I.S.P.M.), University of Bern
Co-authored papers 4
Fabric Genomics Inc.
Co-authored papers 4
Harvard T.H. Chan School of Public Health
Co-authored papers 4
University of California san francisco
Co-authored papers 4
Beth Israel Deaconess Medical Center
Co-authored papers 3
Google LLC
Co-authored papers 3
Co-authored papers 3
Rady Children's Hospital and The University of California
Co-authored papers 3
School of Public Health, Imperial College London
Co-authored papers 3
National Institute of Biomedical Research (INRB)
Co-authored papers 3
East China University of Science and Technology
Co-authored papers 3
Brigham and Women's Hospital, Broad Institute Ariadne Labs and Harvard Medical School
Co-authored papers 3
University of Toledo
Co-authored papers 3
Co-authored papers 3
Co-authored papers 3
University of North Carolina
Co-authored papers 3