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Mustafa Kürşat Şahin

Biographic Data

ID7808792
NAMEMustafa Kürşat Şahin
GIVEN NAMESMustafa Kürşat
FAMILY NAMEŞahin
SIGNATUREŞAHIN M K
AFFILIATIONSHarvard University
ORCID0000-0002-3490-6009
VERIFIEDYes
TOTAL WORKS5
TOTAL CITATIONS0
AUTHOR COUNT5
EDITOR COUNT0
FIRST PUBLICATION YEAR2020
LATEST PUBLICATION YEAR2025
H-INDEX0
  • Mental health of general practitioners and family medicine specialists 2 years into the Covid-19 pandemic

    Open Access•Marija Zafirovska, Jelena Danilenko et al.•ARTICLE•Frontiers in Public Health•2025

    Introduction: The COVID-19 pandemic has significantly impacted general medical practice by altering work structures and increasing teamwork while also adversely affecting the mental health of general practitioners and family medicine specialists. This study assesses depression, anxiety, and fear levels among general practitioners and family medicine specialists in Europe 2 years after the COVID-19 pandemic's onset, and it explores influencing fac…

  • Empowering Families Through Technology

    Open Access•Tosca-Marie Heunis, Stacey Bissell et al.•ARTICLE•Frontiers in Psychiatry•2022

    The TANDem project has the potential to transform the global TSC community by empowering families living with TSC through an easily accessible digital solution to allow them to document their own TAND needs linked to an evidence-informed toolkit to enhance personalised healthcare, and by providing healthcare professionals with consensus clinical recommendations to prevent, identify and manage TAND manifestations

  • P13.11 Deletion Variants Associated With Neuropsychiatric Disorders Cause Morphological and Synaptic Changes in Induced Pluripotent Stem Cell-Derived Neurons

    Open Access•Elizabeth D Buttermore, Nickesha C Anderson et al.•ARTICLE•Frontiers in Psychiatry•2022

    16p13.11 copy number variants (CNVs) have been associated with autism, schizophrenia, psychosis, intellectual disability, and epilepsy. The majority of 16p13.11 deletions or duplications occur within three well-defined intervals, and despite growing knowledge of the functions of individual genes within these intervals, the molecular mechanisms that underlie commonly observed clinical phenotypes remain largely unknown. Patient-derived, induced plu…

  • Psychiatric Characteristics Across Individuals With PTEN Mutations

    Open Access•Morgan Steele, Mirko Uljarevic et al.•ARTICLE•Frontiers in Psychiatry•2021

    Germline heterozygous PTEN mutations have been associated with high prevalence of autism spectrum disorder (ASD) and elevated rates and severity of broadly defined behavioral problems. However, limited progress has been made toward understanding whether PTEN mutation is associated with specific psychiatric co-morbidity profiles when compared to idiopathic ASD. The current study aimed to utilize a cross-measure approach to compare concurrent psych…

  • Prevalence of Depression, Anxiety, Distress and Insomnia and Related Factors in Healthcare Workers During Covid-19 Pandemic in Turkey

    Open Access•Mustafa Kürşat Şahin, Servet Aker et al.•ARTICLE•Journal of Community Health•2020

No prominent works on this page.

  • Prevalence of Depression, Anxiety, Distress and Insomnia and Related Factors in Healthcare Workers During Covid-19 Pandemic in Turkey

    Open Access•Mustafa Kürşat Şahin, Servet Aker et al.•ARTICLE•Journal of Community Health•2020

  • Psychiatric Characteristics Across Individuals With PTEN Mutations

    Open Access•Morgan Steele, Mirko Uljarevic et al.•ARTICLE•Frontiers in Psychiatry•2021

    Germline heterozygous PTEN mutations have been associated with high prevalence of autism spectrum disorder (ASD) and elevated rates and severity of broadly defined behavioral problems. However, limited progress has been made toward understanding whether PTEN mutation is associated with specific psychiatric co-morbidity profiles when compared to idiopathic ASD. The current study aimed to utilize a cross-measure approach to compare concurrent psych…

  • Empowering Families Through Technology

    Open Access•Tosca-Marie Heunis, Stacey Bissell et al.•ARTICLE•Frontiers in Psychiatry•2022

    The TANDem project has the potential to transform the global TSC community by empowering families living with TSC through an easily accessible digital solution to allow them to document their own TAND needs linked to an evidence-informed toolkit to enhance personalised healthcare, and by providing healthcare professionals with consensus clinical recommendations to prevent, identify and manage TAND manifestations

  • P13.11 Deletion Variants Associated With Neuropsychiatric Disorders Cause Morphological and Synaptic Changes in Induced Pluripotent Stem Cell-Derived Neurons

    Open Access•Elizabeth D Buttermore, Nickesha C Anderson et al.•ARTICLE•Frontiers in Psychiatry•2022

    16p13.11 copy number variants (CNVs) have been associated with autism, schizophrenia, psychosis, intellectual disability, and epilepsy. The majority of 16p13.11 deletions or duplications occur within three well-defined intervals, and despite growing knowledge of the functions of individual genes within these intervals, the molecular mechanisms that underlie commonly observed clinical phenotypes remain largely unknown. Patient-derived, induced plu…

  • Mental health of general practitioners and family medicine specialists 2 years into the Covid-19 pandemic

    Open Access•Marija Zafirovska, Jelena Danilenko et al.•ARTICLE•Frontiers in Public Health•2025

    Introduction: The COVID-19 pandemic has significantly impacted general medical practice by altering work structures and increasing teamwork while also adversely affecting the mental health of general practitioners and family medicine specialists. This study assesses depression, anxiety, and fear levels among general practitioners and family medicine specialists in Europe 2 years after the COVID-19 pandemic's onset, and it explores influencing fac…

Medicine (4 works) · Biology (3 works) · Clinical Psychology (3 works) · Psychiatry (3 works) · Psychology (3 works) · Anxiety (2 works) · COVID-19 and Mental Health (2 works) · Disease (2 works) · Genetics (2 works) · Genetics and Neurodevelopmental Disorders (2 works)

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