Leila Kushan

University of California, Los Angeles — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

24h-index2.3kcitations119works2.42yr avg
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Research Topics

Congenital heart defects research(88), Congenital Heart Disease Studies(34), Coronary Artery Anomalies(33), Autism Spectrum Disorder Research(23), Genomic variations and chromosomal abnormalities(19)

Publications118 total

Multicenter retrospective study on effectiveness, reported side effects, and cognitive outcomes of SSRIs in 22q11.2 deletion syndrome
2025Open Access
Neurobehavioral risk factors influence prevalence and severity of hazardous substance use in youth at genetic and clinical high risk for psychosis
UNC Libraries·2025Open Access
Convergent and Divergent Cerebellar Alterations in 22q11.2 Copy Number Variants
2025Open Access
THE IMPACT OF RARE GENETIC VARIANTS ON BRAIN STRUCTURE AND RISK FOR NEUROPSYCHIATRIC DISORDERS
European Neuropsychopharmacology·2025
Gene dosage effects of 22q11.2 copy number variants on in-vivo measures of white matter axonal density and dispersion
2025Open Access
0308 Associations Between Actigraph-Derived Sleep Measures and Psychosis-Risk Symptoms in 22q11.2 Deletion Syndrome
SLEEP·2025Open Access
0130 Frontal Sleep Spindles, IQ, and Sleep Dependent Memory Consolidation in 22q11.2 Deletion Carriers
SLEEP·2025Open Access
Cortical differences across psychiatric disorders and associated common and rare genetic variants
2025· 1 citedOpen Access
5. Discordant Cortical Patterns Between Psychiatric Disorders and Corresponding Common and Rare Genetic Risks
Biological Psychiatry·2025
Synaptic-dependent developmental dysconnectivity in 22q11.2 deletion syndrome
Science Advances·2025· 9 citedOpen Access
Comparison of autism domains across thirty rare variant genotypes
EBioMedicine·2025· 4 citedOpen Access
Lifespan Normative Modeling of Brain Microstructure
2024· 4 citedOpen Access
Unique Functional Neuroimaging Signatures of Genetic Versus Clinical High Risk for Psychosis
Biological Psychiatry·2024· 5 citedOpen Access
Neurocognitive profiles of 22q11.2 and 16p11.2 deletions and duplications
Molecular Psychiatry·2024· 14 citedOpen Access
Differential inflammatory profiles in carriers of reciprocal 22q11.2 copy number variants
Psychoneuroendocrinology·2024· 2 citedOpen Access
494. Reciprocal 22q10.2 CNV Carriers Exhibit Distinct Autism Symptom Profiles
Biological Psychiatry·2024
9. Normative Modeling of Diffusion Tensor Imaging Metrics of White Matter Microstructure in 52,719 Subjects
Biological Psychiatry·2024
403. Disrupted NREM Sleep Physiology Linked to 22q10.2 Deletion Syndrome
Biological Psychiatry·2024
36. Unique Functional Neuroimaging Signatures of Genetic Versus Clinical High Risk for Psychosis
Biological Psychiatry·2024
0284 Disrupted NREM Sleep Physiology Linked to 22q11.2 Deletion Syndrome
SLEEP·2024
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Frequent Co-authors

Carrie E. Bearden(48), Amy Lin(19), Marianne van den Bree(19), Donna M. McDonald‐McGinn(19), Raquel E. Gur(18), Wendy R. Kates(17), Maria Jalbrzikowski(15), Declan Murphy(15), Beverly S. Emanuel(15), Jacob Vorstman(14), Michael J. Owen(14), Ariana Vajdi(13), Christopher R. K. Ching(12), Eileen Daly(12), Maria Gudbrandsen(12), Clodagh M. Murphy(12), Paul M. Thompson(12), Elaine H. Zackai(12), Thérèse van Amelsvoort(11), Michael Craig(11)