Miri Carmel

Tel Aviv University — Israel

Biochemistry, Genetics and Molecular Biology · Life Sciences

20h-index1.1kcitations36works0.72yr avg
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Research Topics

Congenital heart defects research(16), Child and Adolescent Psychosocial and Emotional Development(7), Genetics and Neurodevelopmental Disorders(7), Congenital Heart Disease Studies(6), Genomic variations and chromosomal abnormalities(6)

Publications36 total

Early developmental milestones associated with tics and psychopathological comorbidity: An EMTICS study
European Child & Adolescent Psychiatry·2025Open Access
Early developmental milestones associated with tics and psychopathological comorbidity : An EMTICS study
2024Open Access
Lymphoblast transcriptome analysis in 22q11.2 deletion syndrome individuals with schizophrenia-spectrum disorder
The World Journal of Biological Psychiatry·2024· 2 cited
Vitamin D levels in children and adolescents with chronic tic disorders: a multicentre study
European Child & Adolescent Psychiatry·2021· 17 citedOpen Access
Differential methylation of imprinting genes and MHC locus in 22q11.2 deletion syndrome-related schizophrenia spectrum disorders
The World Journal of Biological Psychiatry·2020· 17 cited
Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
Molecular Psychiatry·2020· 132 citedOpen Access
Differential methylation of imprinting genes and MHC locus in 22q11.2 deletion syndrome-related schizophrenia spectrum disorders
Figshare·2020Open 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
Exploring the potential association among sleep disturbances, cognitive impairments, and immune activation in 22q11.2 deletion syndrome
American Journal of Medical Genetics Part A·2019· 13 cited
Risk gene-set and pathways in 22q11.2 deletion-related schizophrenia: a genealogical molecular approach
Translational Psychiatry·2019· 13 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
Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the <i>GPR98</i> Locus on 5q14.3
Circulation Cardiovascular Genetics·2017· 24 citedOpen Access
RETRACTED: Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements
The American Journal of Human Genetics·2017· 7 citedOpen Access
Runs of homozygosity, copy number variation, and risk for depression and suicidal behavior in an Arab Bedouin kindred
Psychiatric Genetics·2017· 6 citedOpen Access
Neurocognitive profile in psychotic versus nonpsychotic individuals with 22q11.2 deletion syndrome
European Neuropsychopharmacology·2016· 56 cited
Pharmacogenetics of citalopram-related side effects in children with depression and/or anxiety disorders
Journal of Neural Transmission·2016· 26 cited
The Relationship Between Plasma Cytokine Levels and Response to Selective Serotonin Reuptake Inhibitor Treatment in Children and Adolescents with Depression and/or Anxiety Disorders
Journal of Child and Adolescent Psychopharmacology·2016· 77 cited
Hyperactive auditory processing in Williams syndrome: Evidence from auditory evoked potentials
Psychophysiology·2015· 46 citedOpen Access
Thymic and bone marrow output in individuals with 22q11.2 deletion syndrome
Pediatric Research·2015· 22 citedOpen Access
Association of COMT and PRODH gene variants with intelligence quotient (IQ) and executive functions in 22q11.2DS subjects
Journal of Psychiatric Research·2014· 30 cited
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Frequent Co-authors

Abraham Weizman(29), Elena Michaelovsky(22), Amos Frisch(19), Doron Gothelf(13), Ronnie Weinberger(10), Donna M. McDonald‐McGinn(8), Elaine H. Zackai(8), Alan Apter(8), Doron Gothelf(8), Bernice E. Morrow(7), Ann Swillen(7), Joris Vermeesch(7), Sefi Kronenberg(7), Beverly S. Emanuel(7), Matthew S. Hestand(6), Raquel E. Gur(6), Elfi Vergaelen(6), Omer Zarchi(6), Carrie E. Bearden(5), Tingwei Guo(5)