Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Srishti Rau"'
Autor:
Lukas Schaffer, Srishti Rau, Isabella G. Larsen, Liv Clasen, Allysa Warling, Ethan T. Whitman, Ajay Nadig, Cassidy McDermott, Anastasia Xenophontos, Kathleen Wilson, Jonathan Blumenthal, Erin Torres, Armin Raznahan
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 16, Iss 1, Pp 1-17 (2024)
Abstract Background Do different genetic disorders impart different psychiatric risk profiles? This question has major implications for biological and translational aspects of psychiatry, but has been difficult to tackle given limited access to share
Externí odkaz:
https://doaj.org/article/02df7531244f4b338214a53e84e86e15
Autor:
Jacqueline I. Fezza, Srishti Rau, Lauren Clary, Oretha Nimene Johnson, Fiona Fimmel, John Barber, Roopa Kanakatti Shankar
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
IntroductionTurner syndrome (TS) is associated with significant neuropsychological challenges, and screening is recommended at key transition stages. Our goal was to describe the institutional experience of formal neuropsychological assessments in TS
Externí odkaz:
https://doaj.org/article/3bfeb7c234fb4f879155412745b3b85c
Autor:
Armin Raznahan, Srishti Rau, Luke Schaffer, Siyuan Liu, Ari M. Fish, Catherine Mankiw, Anastasia Xenophontos, Liv S. Clasen, Lisa Joseph, Audrey Thurm, Jonathan D. Blumenthal, Dani S. Bassett, Erin N. Torres
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 15, Iss 1, Pp 1-16 (2023)
Abstract Background Recurrent gene dosage disorders impart substantial risk for psychopathology. Yet, understanding that risk is hampered by complex presentations that challenge classical diagnostic systems. Here, we present a suite of generalizable
Externí odkaz:
https://doaj.org/article/5d388d471cf141a6aba375131d9104c0
Autor:
Srishti Rau, Ethan T. Whitman, Kimberly Schauder, Nikhita Gogate, Nancy Raitano Lee, Lauren Kenworthy, Armin Raznahan
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 13, Iss 1, Pp 1-12 (2021)
Abstract Background Sex chromosome aneuploidies (SCAs) are a collectively common family of genetic disorders that increase the risk for neuropsychiatric and cognitive impairment. Beyond being important medical disorders in their own right, SCAs also
Externí odkaz:
https://doaj.org/article/5fbbde878e8f40159fc5f197dec2e69f
Autor:
Ethan T. Whitman, Srishti Rau, Kimberly Schauder, Lauren Kenworthy, Nancy Raitano Lee, Nikhita Gogate, Armin Raznahan
Publikováno v:
Journal of Neurodevelopmental Disorders, Vol 13, Iss 1, Pp 1-12 (2021)
Background Sex chromosome aneuploidies (SCAs) are a collectively common family of genetic disorders that increase the risk for neuropsychiatric and cognitive impairment. Beyond being important medical disorders in their own right, SCAs also offer a u
Autor:
Lukas Schaffer, Srishti Rau, Liv Clasen, Yangfeifei Gao, Rachael Arowolo, Ethan Whitman, Allysa Warling, Kathleen Wilson, Lisa Joseph, Audrey Thurm, Erin Torres, Jonathan Blumenthal, Lauren Kenworthy, Armin Raznahan
Publikováno v:
European Neuropsychopharmacology. 63:e97-e98
Autor:
Bridget W. Mahony, Danni Tu, Srishti Rau, Siyuan Liu, François M. Lalonde, Aaron F. Alexander-Bloch, Theodore D. Satterthwaite, Russell T. Shinohara, Dani S. Bassett, Michael P. Milham, Armin Raznahan
Publikováno v:
Journal of the American Academy of Child and Adolescent Psychiatry.
Correlations between cognitive ability and psychopathology are well recognized, but prior research has been limited by focusing on individuals with intellectual disability, single-diagnosis psychiatric populations, or few measures of psychopathology.
Autor:
Ethan T. Whitman, Armin Raznahan, Cassidy L. McDermott, Marissa Miller, Lauren Kenworthy, Allysa Warling, Jonathan D. Blumenthal, Ajay Nadig, Srishti Rau, Erin Torres, Kathleen Wilson, Liv S. Clasen
Publikováno v:
Biological Psychiatry. 87:S355
Autor:
Mary F. Skapek, Alison Burns, Srishti Rau, Sydney Seese, Kaitlyn Tiplady, Lauren Kenworthy, A. Chelsea Armour
Publikováno v:
Research in Autism Spectrum Disorders. 69:101468
Background There are high rates of comorbidity between ADHD and ASD; however, there has been limited work parsing rates by ADHD presentation. In addition, commonly used questionnaires have demonstrated reduced utility in capturing ADHD symptoms in in
Autor:
Karin S. Walsh, Srishti Rau
Studying Autism Spectrum Disorders (ASD) in genetic syndromes has gained interest in the scientific community as a way to elucidate mechanisms and symptom profiles to understand ASD more broadly. Appropriate and adequate measurement of constructs, sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e05a069d16c889fa97bb79ff4bef9bc
https://doi.org/10.1016/bs.pbr.2018.09.015
https://doi.org/10.1016/bs.pbr.2018.09.015