نتایج جستجو برای: broad autism phenotype questionnaire bapq

تعداد نتایج: 527153  

2010
Michael SL Ching Yiping Shen Wen-Hann Tan Shafali S Jeste Eric M Morrow Xiaoli Chen Nahit M Mukaddes Seung-Yun Yoo Ellen Hanson Rachel Hundley Christina Austin Ronald E Becker Gerard T Berry Katherine Driscoll Elizabeth C Engle Sandra Friedman James F Gusella Fuki M Hisama Mira B Irons Tina Lafiosca Elaine LeClair David T Miller Michael Neessen Jonathan D Picker Leonard Rappaport Cynthia M Rooney Dean P Sarco Joan M Stoler Christopher A Walsh Robert R Wolff Ting Zhang Ramzi H Nasir Bai-Lin Wu

Research has implicated mutations in the gene for neurexin-1 (NRXN1) in a variety of conditions including autism, schizophrenia, and nicotine dependence. To our knowledge, there have been no published reports describing the breadth of the phenotype associated with mutations in NRXN1. We present a medical record review of subjects with deletions involving exonic sequences of NRXN1. We ascertaine...

Journal: :Journal of autism and developmental disorders 2012
Yonit K Stoch Cori J Williams Joanna Granich Anna M Hunt Lou I Landau John P Newnham Andrew J O Whitehouse

An existing randomised controlled trial was used to investigate whether multiple ultrasound scans may be associated with the autism phenotype. From 2,834 single pregnancies, 1,415 were selected at random to receive ultrasound imaging and continuous wave Doppler flow studies at five points throughout pregnancy (Intensive) and 1,419 to receive a single imaging scan at 18 weeks (Regular), with fur...

Journal: :The Journal of biological chemistry 2006
Igor Splawski Dana S Yoo Stephanie C Stotz Allison Cherry David E Clapham Mark T Keating

Autism spectrum disorders (ASD) are neurodevelopmental conditions characterized by impaired social interaction, communication skills, and restricted and repetitive behavior. The genetic causes for autism are largely unknown. Previous studies implicate CACNA1C (L-type Ca(V)1.2) calcium channel mutations in a disorder associated with autism (Timothy syndrome). Here, we identify missense mutations...

Journal: :International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience 2002
Heather Cody Kevin Pelphrey Joseph Piven

Magnetic resonance imaging (MRI) of brain structures and function is uniquely suited to characterize the range of neuroanatomical and physiological changes that characterize the autism phenotype as it develops over time. In this review, we examine the scientific literature in MRI as applied to autism and related areas, over approximately the last decade, discussing findings which have emerged, ...

Journal: :Journal of autism and developmental disorders 2012
Diana E Schendel Carolyn Diguiseppi Lisa A Croen M Daniele Fallin Philip L Reed Laura A Schieve Lisa D Wiggins Julie Daniels Judith Grether Susan E Levy Lisa Miller Craig Newschaffer Jennifer Pinto-Martin Cordelia Robinson Gayle C Windham Aimee Alexander Arthur S Aylsworth Pilar Bernal Joseph D Bonner Lisa Blaskey Chyrise Bradley Jack Collins Casara J Ferretti Homayoon Farzadegan Ellen Giarelli Marques Harvey Susan Hepburn Matthew Herr Kristina Kaparich Rebecca Landa Li-Ching Lee Brooke Levenseller Stacey Meyerer Mohammad H Rahbar Andria Ratchford Ann Reynolds Steven Rosenberg Julie Rusyniak Stuart K Shapira Karen Smith Margaret Souders Patrick Aaron Thompson Lisa Young Marshalyn Yeargin-Allsopp

The Study to Explore Early Development (SEED), a multisite investigation addressing knowledge gaps in autism phenotype and etiology, aims to: (1) characterize the autism behavioral phenotype and associated developmental, medical, and behavioral conditions and (2) investigate genetic and environmental risks with emphasis on immunologic, hormonal, gastrointestinal, and sociodemographic characteri...

Journal: :Developmental Neuropsychology 2009

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید