T. Koomar

发表

Exome sequencing of 457 autism families recruited online provides evidence for novel ASD genes

Richard A Marini, Simon X. Xu, Nicole M. Russo-Ponsaran, 2019 .

Genetic and morphological estimates of androgen exposure predict social deficits in multiple neurodevelopmental disorder cohorts

J. Michaelson, L. Brueggeman, E. Bahl, 2020, Molecular Autism.

Genetic Intersections of Language and Neuropsychiatric Conditions

J. Michaelson, T. Koomar, 2020, Current Psychiatry Reports.

Clinical autism subscales have common genetic liabilities that are heritable, pleiotropic, and generalizable to the general population

J. Michaelson, T. Koomar, T. Thomas, 2022, Translational Psychiatry.

Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

Chin Yang Shapland, Timothy C. Bates, Till F. M. Andlauer, 2022, Proceedings of the National Academy of Sciences of the United States of America.

Integrating de novo and inherited variants in over 42,607 autism cases 1 identifies mutations in new moderate risk genes 2

Nicole M. Russo-Ponsaran, M. Dennis, T. Shaikh, 2021 .

Psychiatric and Medical Profiles of Autistic Adults in the SPARK Cohort

Richard A Marini, Simon X. Xu, Nicole M. Russo-Ponsaran, 2020, Journal of Autism and Developmental Disorders.

Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities

Timothy C. Bates, Till F. M. Andlauer, C. Francks, 2022, Translational Psychiatry.

Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

Richard A Marini, W. T. Harvey, Bradley P. Coe, 2020, Nature Communications.

Integrating de novo and inherited variants in over 42,607 autism cases identifies mutations in new moderate risk genes

William T. Harvey, Richard A Marini, Simon X. Xu, 2021, medRxiv.

Author Correction: Forecasting risk gene discovery in autism with machine learning and genome-scale data

J. Michaelson, T. Koomar, Leo Brueggeman, 2020, Scientific Reports.

Forecasting risk gene discovery in autism with machine learning and genome-scale data

J. Michaelson, T. Koomar, Leo Brueggeman, 2020, Scientific Reports.

Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes

Richard A Marini, Simon X. Xu, Nicole M. Russo-Ponsaran, 2019, npj Genomic Medicine.

Estimating the Prevalence and Genetic Risk Mechanisms of ARFID in a Large Autism Cohort

M. Lutter, J. Michaelson, T. Koomar, 2021, Frontiers in Psychiatry.

Whole-genome sequencing in a family with twin boys with autism and intellectual disability suggests multimodal polygenic risk

J. Michaelson, T. Koomar, Brooke G. McKenna, 2018, Cold Spring Harbor molecular case studies.

Forecasting autism gene discovery with machine learning and genome-scale data

Leo Brueggeman, Tanner Koomar, J. Michaelson, 2018, bioRxiv.

Genome-wide association analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

Chin Yang Shapland, Timothy C. Bates, Till F. M. Andlauer, 2021 .

cerebroViz: an R package for anatomical visualization of spatiotemporal brain data

Tanner Koomar, Ethan Bahl, Jacob J. Michaelson, 2016, Bioinform..

Whole Genome Sequencing Illuminates the Developmental Signatures of Human Language Ability

J. Michaelson, J. Tomblin, T. Koomar, 2021, medRxiv.

Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

Richard A Marini, W. T. Harvey, B. Coe, 2020, Nature Communications.

Clinical autism subscales have common genetic liability that is heritable, pleiotropic, and generalizable to the general population

J. Michaelson, T. Koomar, T. Thomas, 2021, medRxiv.

Language and reading impairments are associated with increased prevalence of non‐right‐handedness

J. Talcott, D. Boomsma, J. Michaelson, 2023, Child development.

Sex Differences in the Brain: Divergent Results from Traditional Machine Learning and Convolutional Networks

Leo Brueggeman, Brady Hoskins, Jacob J. Michaelson, 2020, 2020 IEEE 17th International Symposium on Biomedical Imaging (ISBI).

Beliefs in vaccine as causes of autism among SPARK cohort caregivers.

Richard A Marini, Simon X. Xu, Jacob B. Hall, 2020, Vaccine.

Exome sequencing of 457 autism families recruited online provides evidence for autism risk genes

Richard A Marini, Simon X. Xu, Deana D. Li, 2019, npj Genomic Medicine.

Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes

Richard A Marini, Deana D. Li, B. O’Roak, 2022, Nature Genetics.

Integrating de novo and inherited variants in over 42,607 autism cases 1 identifies mutations in new moderate risk genes 2

B. O’Roak, M. Dennis, L. Soorya, 2021 .

Integrating de novo and inherited variants in over 42,607 autism cases 1 identifies mutations in new moderate risk genes 2

M. Dennis, L. Soorya, S. Hepburn, 2021 .

Integrating de novo and inherited variants in over 42,607 autism cases 1 identifies mutations in new moderate risk genes 2

M. Dennis, L. Soorya, S. Hepburn, 2021 .

Integrating de novo and inherited variants in over 42,607 autism cases 1 identifies mutations in new moderate risk genes 2

M. Dennis, L. Soorya, S. Hepburn, 2021 .

Integrating de novo and inherited variants in over 42,607 autism cases 1 identifies mutations in new moderate risk genes 2

M. Dennis, L. Soorya, S. Hepburn, 2021 .

Clinical autism subscales have common genetic liabilities that are heritable, pleiotropic, and generalizable to the general population

T. Koomar, T. Thomas, L. Casten, 2022, Translational Psychiatry.

Ensemble Modeling of Neurocognitive Performance Using MRI-Derived Brain Structure Volumes

Yongchao Huang, Hans J. Johnson, Leo Brueggeman, 2019, ABCD-NP@MICCAI.