A. M. Higgins

发表

Neuroanatomic Predictors to Prodromal Psychosis in Velocardiofacial Syndrome (22q11.2 Deletion Syndrome): A Longitudinal Study

R. Shprintzen, S. Faraone, W. Kates, 2011, Biological Psychiatry.

The Effects of Gender and Catechol O-Methyltransferase ( COMT ) Val 108 / 158 Met Polymorphism on Emotion Regulation in Velo-Cardio-Facial Syndrome ( 22 q 11 . 2 Deletion Syndrome ) : An f MRI Study

Matthew H. Gnirke, R. Shprintzen, F. Middleton, 2016 .

Association between autism spectrum disorder in individuals with velocardiofacial (22q11.2 deletion) syndrome and PRODH and COMT genotypes

R. Shprintzen, F. Middleton, B. Morrow, 2014, Psychiatric genetics.

Cleft palate, retrognathia and congenital heart disease in velo-cardio-facial syndrome: a phenotype correlation study.

R. Shprintzen, B. Morrow, W. Kates, 2011, International journal of pediatric otorhinolaryngology.

Overt cleft palate phenotype and TBX1 genotype correlations in velo‐cardio‐facial/DiGeorge/22q11.2 deletion syndrome patients

Mark J. Bowser, Jonathan H. Chung, E. Zackai, 2012, American journal of medical genetics. Part A.

Mapping cortical morphology in youth with velocardiofacial (22q11.2 deletion) syndrome.

B. Peterson, R. Shprintzen, Jun Liu, 2011, Journal of the American Academy of Child and Adolescent Psychiatry.

Cortical gyrification in velo-cardio-facial (22q11.2 deletion) syndrome: A longitudinal study

R. Shprintzen, W. Kates, K. Antshel, 2012, Schizophrenia Research.

Detecting the Hidden Properties of Immunological Data and Predicting the Mortality Risks of Infectious Syndromes

T. Buranda, G. Tegos, A. Rivas, 2016, Front. Immunol..

Rhinovirus infection associated with serious illness among pediatric patients.

L. Weiner, A. M. Higgins, J. Mcmillan, 1993, The Pediatric infectious disease journal.

22q11.2DS Deletion Syndrome: Developmental Milestones in Infants and Toddlers

Nuria Y. AbdulSabur, R. Shprintzen, W. Kates, 2007, Journal of developmental and behavioral pediatrics : JDBP.

Pharyngitis associated with herpes simplex virus in college students.

L. Weiner, A. M. Higgins, J. Mcmillan, 1993, The Pediatric infectious disease journal.

Associations Between Performance on the Rey-Osterrieth Complex Figure and Regional Brain Volumes in Children with and without Velocardiofacial Syndrome

Wendy R. Kates, Kevin M. Antshel, Nuria AbdulSabur, 2008, Developmental neuropsychology.

Enhanced maternal origin of the 22q11.2 deletion in velocardiofacial and DiGeorge syndromes.

A. Auton, T. Werge, E. Zackai, 2013, American journal of human genetics.

Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo‐cardio‐facial/digeorge/22q11.2 deletion syndrome patients

Mark J. Bowser, Jonathan H. Chung, E. Zackai, 2011, Human mutation.

Velo-cardio-facial syndrome

Wanda Fremont, Anne Marie Higgins, R. Shprintzen, 2005, Journal of mental health research in intellectual disabilities.

Velo-cardio-facial syndrome

Wanda Fremont, Anne Marie Higgins, R. Shprintzen, 2005, Current opinion in pediatrics.

Temperament in velocardiofacial syndrome.

Nuria Y. AbdulSabur, A M Higgins, R. Shprintzen, 2007, Journal of intellectual disability research : JIDR.

Catatonia in an adolescent with velo‐cardio‐facial syndrome

R. Shprintzen, A. M. Higgins, G. Faedda, 2015, American journal of medical genetics. Part A.

Digitalcommons@shu Speech-language Pathology Faculty Publications Speech-language Pathology Manic Symptoms and Behavioral Dysregulation in Youth with Velocardiofacial Syndrome (22q11.2 Deletion Syndrome). Manic Symptoms and Behavioral Dysregulation in Youth with Velocardiofacial Syndrome (22q11.2 De

Nuria Y. AbdulSabur, R. Shprintzen, S. Faraone, 2022 .

Cognitive and psychiatric predictors to psychosis in velocardiofacial syndrome: a 3-year follow-up study.

R. Shprintzen, S. Faraone, W. Kates, 2010, Journal of the American Academy of Child and Adolescent Psychiatry.

The effects of gender and catechol O-methyltransferase (COMT) Val108/158Met polymorphism on emotion regulation in velo-cardio-facial syndrome (22q11.2 deletion syndrome): An fMRI study

Ioana L. Coman, Wendy R. Kates, Kevin M. Antshel, 2010, NeuroImage.

Comparing phenotypes in patients with idiopathic autism to patients with velocardiofacial syndrome (22q11 DS) with and without autism

Anne Marie Higgins, R. Shprintzen, W. Kates, 2007, American journal of medical genetics. Part A.

Autistic Spectrum Disorders in Velo-cardio Facial Syndrome (22q11.2 Deletion)

Nuria Y. AbdulSabur, R. Shprintzen, W. Kates, 2007, Journal of autism and developmental disorders.

ADHD, major depressive disorder, and simple phobias are prevalent psychiatric conditions in youth with velocardiofacial syndrome.

Wanda Fremont, Anne Marie Higgins, R. Shprintzen, 2006, Journal of the American Academy of Child and Adolescent Psychiatry.

A gender‐moderated effect of a functional COMT polymorphism on prefrontal brain morphology and function in velo‐cardio‐facial syndrome (22q11.2 deletion syndrome)

Birgit Funke, Wanda Fremont, Nuria Y. AbdulSabur, 2006, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

The longitudinal course of attention deficit/hyperactivity disorder in velo-cardio-facial syndrome.

R. Shprintzen, S. Faraone, W. Kates, 2013, The Journal of pediatrics.

The neural correlates of non-spatial working memory in velocardiofacial syndrome (22q11.2 deletion syndrome)

Wendy R. Kates, Kevin M. Antshel, Nuria Y. AbdulSabur, 2007, Neuropsychologia.

Immunoblot analysis of anti-Ureaplasma urealyticum antibody in pregnant women and newborn infants

L. Weiner, C. Bonville, C. Cunningham, 1996, Clinical and diagnostic laboratory immunology.

22q11.2 deletion syndrome: are motor deficits more than expected for IQ level?

R. Shprintzen, W. Kates, K. Antshel, 2010, The Journal of pediatrics.

Digitalcommons@shu Speech-language Pathology Faculty Publications Speech-language Pathology 22q11.2 Deletion Syndrome: Are Motor Deficits More than Expected for Iq Level? Recommended Citation 22q11.2 Deletion Syndrome: Are Motor Deficits More than Expected for Iq Level? Nih Public Access Author Manu

R. Shprintzen, W. Kates, K. Antshel, 2022 .

A gender‐moderated effect of a functional COMT polymorphism on prefrontal brain morphology and function in velo‐cardio‐facial syndrome (22q11.2 deletion syndrome)

Nuria Y. AbdulSabur, R. Kucherlapati, R. Shprintzen, 2006, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Speech-Language Pathology 8-2008 Associations Between Performance on the Rey-Osterrieth Complex Figure and Regional Brain Volumes in Children with and without Velocardiofacial Syndrome

Nuria Y. AbdulSabur, R. Shprintzen, W. Kates, 2016 .