Kathryn McCabe

Oldham Council — United Kingdom

Biochemistry, Genetics and Molecular Biology · Life Sciences

23h-index1.9kcitations56works3.02yr avg
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Research Topics

Congenital heart defects research(22), Coronary Artery Anomalies(11), Congenital Heart Disease Studies(8), Autism Spectrum Disorder Research(6), Genetics and Neurodevelopmental Disorders(6)

Publications55 total

Archival Data Reveals Human Impacts on Blanding's Turtle Population Persistence
SSRN Electronic Journal·2025Open Access
Source‐based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome
Human Brain Mapping·2024· 6 citedOpen Access
Segmental growth relationships between fetal and postnatal measures in the Manchester BabyGRO Study
Endocrine Abstracts·2023
Comparison of Automatic Speech Recognition Systems
Lecture notes in electrical engineering·2022· 1 cited
The Importance of Understanding Individual Differences of Emotion Regulation Abilities in 22q11.2 Deletion Syndrome
Journal of Autism and Developmental Disorders·2021· 4 cited
Prioritizing Genetic Contributors to Cortical Alterations in 22q11.2 Deletion Syndrome Using Imaging Transcriptomics
Cerebral Cortex·2021· 13 citedOpen Access
Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness
American Journal of Psychiatry·2020· 84 citedOpen Access
Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects
The American Journal of Human Genetics·2019· 72 citedOpen Access
Quantifying the resolution of spatial and temporal representation in children with 22q11.2 deletion syndrome
Journal of Neurodevelopmental Disorders·2019· 5 citedOpen Access
Interrelationship Between Cognitive Control, Anxiety, and Restricted and Repetitive Behaviors in Children with 22q11.2 Deletion Syndrome
Autism Research·2019· 13 citedOpen Access
Altered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study
Molecular Psychiatry·2019· 75 citedOpen Access
190. Novel Diffusion MRI Measures in 22q Deletion Syndrome: Large-Scale International Studies by the ENIGMA-22q Consortium
Biological Psychiatry·2019
A Comparison of Online Automatic Speech Recognition Systems and the Nonverbal Responses to Unintelligible Speech
arXiv (Cornell University)·2019· 17 citedOpen Access
A Comparison of Online Automatic Speech Recognition Systems and the\n Nonverbal Responses to Unintelligible Speech
arXiv (Cornell University)·2019· 23 citedOpen Access
Alternative diffusion anisotropy measures for the investigation of white matter alterations in 22q11.2 deletion syndrome
2018· 5 cited
Improving Moderator Responsiveness in Online Peer Support Through Automated Triage
Journal of Medical Internet Research·2018· 29 citedOpen Access
Retraction Notice to: Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements
The American Journal of Human Genetics·2018· 2 citedOpen Access
Improving Moderator Responsiveness in Online Peer Support Through Automated Triage (Preprint)
2018Open Access
Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size
Molecular Psychiatry·2018· 192 citedOpen Access
A Comparative Test of Creative Thinking in Dolphins (Tursiops Truncaus) and Preschool Children
2018
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Frequent Co-authors

Linda Campbell(17), Carmel M. Loughland(15), Donna M. McDonald‐McGinn(13), Beverly S. Emanuel(13), Ulrich Schall(13), Declan Murphy(12), Leila Kushan(11), Thérèse van Amelsvoort(11), Wendy R. Kates(11), Raquel E. Gur(11), Kieran C. Murphy(11), Carrie E. Bearden(11), Wanda Fremont(10), Marianne van den Bree(10), Kevin M. Antshel(9), Clodagh M. Murphy(9), Jacob Vorstman(9), Michael J. Owen(9), Vaughan J. Carr(9), Tony J. Simon(8)