Professor, Psychiatry, University of Miami School of Medicine
Psychiatry
Dr. Susan E. Folstein, MD
|
|
Give Review
Susan Folstein is an expert in the field of Psychiatry. He graduated from Weill Cornell Medical College of Cornell University. Weill Cornell Medical College of Cornell University is ranked 18/49 in Research/PrimaryCare. Susan Folstein is a published doctor as well. He has 101 publications published. The latest was: Early detection of social interaction problems: development of a social interaction instrument in young children. Susan Folstein accepts Medicare.
Publications
- Convergence of genes and cellular pathways dysregulated in autism spectrum Disorders.
- A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum Disorder.
- Language and reading abilities of children with autism spectrum Disorders and specific language impairment and their first-degree relatives.
- Overlap between Autism and specific language impairment: comparison of Autism Diagnostic Interview and Autism Diagnostic Observation Schedule scores.
- Overrepresentation of mood and anxiety Disorders in adults with autism and their first-degree relatives: what does it mean?
- Etiologies of Autism in a case-series from Tanzania.
- Comorbid psychiatric Disorders in children with autism: interview development and rates of Disorders.
- Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to Autism and rigid-compulsive behaviors.
- A linkage disequilibrium map of the 1-Mb 15q12 GABA(A) receptor subunit cluster and association to Autism.
- A principal components analysis of the Autism Diagnostic Interview-Revised.
- Exploratory subsetting of Autism families based on savant skills improves evidence of genetic linkage to 15q11-q13.
- Autism-related language, personality, and cognition in people with absolute pitch: results of a preliminary study.
- Diagnostic reliability of bipolar II Disorder.
- Evaluation of FOXP2 as an Autism susceptibility gene.
- Genome-wide and Ordered-Subset linkage analyses provide support for Autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates.
- Atypical behaviors in children with Autism and children with a history of language impairment.
- Functional impact of global rare copy number variation in autism spectrum Disorders.
- A genome-wide scan for common alleles affecting risk for Autism.
- Invited reply to ''The death knoll for the MMSE: has it outlived its purpose?''.
- Functional expressions of the aging brain.
- Head circumference and height in Autism: a study by the Collaborative Program of Excellence in Autism.
- Communicative competence in parents of children with Autism and parents of children with specific language impairment.
- Mapping Autism risk loci using genetic linkage and chromosomal rearrangements.
- Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as Autism candidate genes.
- Incorporating language phenotypes strengthens evidence of linkage to Autism.
- How might genetic mechanisms operate in Autism?
- Diagnosing Autism: analyses of data from the Autism Diagnostic Interview.
- Early detection of social interaction problems: development of a social interaction instrument in young children.
- Full-genome scan for linkage in 50 families segregating the bipolar affective disease phenotype.
- Selective serotonin reuptake inhibitor-induced mydriasis.
- Current directions in research on Autism.
- Protecting the privacy of family members in research.
- Personality characteristics of the parents of autistic individuals.
- The etiology of Autism: pre-, peri- and neonatal factors.
- Unimpaired verbal memory and oculomotor control in asymptomatic adults with the genetic marker for Huntington's disease.
- Trinucleotide repeat length instability and age of onset in Huntington's disease.
- Evidence for linkage of bipolar Disorder to chromosome 18 with a parent-of-origin effect.
- A phenocopy of Huntington's disease: lacunar infarcts of the corpus striatum.
- Twin and adoption studies in child and adolescent psychiatric Disorders.
- Genetic influences and infantile Autism.
- Infantile Autism: a genetic study of 21 twin pairs.
- Psychiatric Disorders in the parents of autistic individuals.
- The prevalence of fragile X in a sample of autistic individuals diagnosed using a standardized interview.
- Nigral dopamine type-1 receptors are reduced in Huntington's disease: a postmortem autoradiographic study using [3H]SCH 23390 and correlation with [3H]forskolin binding.
- Magnetic resonance imaging evidence for a defect of cerebral cortical development in Autism.
- Clinical assessment of irritability, aggression, and apathy in Huntington and Alzheimer disease.
- The new genetics of bipolar affective Disorder: clinical implications.
- Depression and neurological Disorders. New treatment opportunities for elderly depressed patients.
- Recognition and expression of emotional cues by autistic and normal adults.
- Positron emission tomography imaging of dopamine and serotonin receptors in Huntington's chorea.
- Neuropsychological and neuroradiological correlates in Huntington''s disease.
- Neurotransmitter receptor alterations in Huntington's disease: autoradiographic and homogenate studies with special reference to benzodiazepine receptor complexes.
- Clinical predictors of improvement after electroconvulsive therapy of patients with schizophrenia, neurotic reactions, and affective Disorders.
- The association of affective Disorder with Huntington''s disease in a case series and in families.
- Diagnosis and treatment of Huntington's disease.
- Development and maturation of postural reflexes in normal kittens.
- Selective loss of [3H]kainic acid and [3H]AMPA binding in layer VI of frontal cortex in Huntington's disease.
- Affective Disorders in people with autism: a review of published cases.
- Early loss of neostriatal striosome neurons in Huntington's disease.
- The measurement of abnormal movement: methods developed for Huntington's disease.
- Psychiatric features of Huntington''s disease: recent approaches and findings.
- Clinical correlates of dementia and disability in Huntington''s disease.
- Phenotypic heterogeneity in Huntington disease.
- Conduct Disorder and affective Disorder among the offspring of patients with Huntington''s disease.
- The nucleus basalis in Huntington's disease.
- Abnormal ocular motor control in Huntington's disease.
- Autism: familial aggregation and genetic implications.
- Psychiatric manifestations of homocystinuria due to cystathionine beta-synthase deficiency: prevalence, natural history, and relationship to neurologic impairment and ...
- Genetic aspects of infantile Autism.
- Huntington's disease: two families with differing clinical features show linkage to the G8 probe.
- Differential cognitive impairment in Alzheimer's disease and Huntington's disease.
- Voluntary movement dysfunction in Huntington''s disease and tardive dyskinesia.
- Localization of the Huntington's disease gene to a small segment of chromosome 4 flanked by D4S10 and the telomere.
- Corticotropin-releasing hormone (CRH) is decreased in the basal ganglia in Huntington''s disease.
- Brainstem findings in Huntington''s disease. Possible mechanisms for slow vertical saccades.
- Covariate-dependent genetic counseling in Huntington''s disease.
- The diagnosis of Huntington's disease.
- Saccades in Huntington's disease: initiation defects and distractibility.
- Genetic analysis workshop IV: Huntington disease linkage analysis, data description.
- The decision to be tested for Huntington's disease.
- Huntington disease in Maryland: clinical aspects of racial variation.
- Use of the G8 probe in predicting risk of Huntington disease.
- Olfactory recognition: differential impairments in early and late Huntington''s and Alzheimer''s diseases.
- Saccades in Huntington's disease: slowing and dysmetria.
- Huntington disease: no evidence for locus heterogeneity.
- Comprehension of prosody in Huntington''s disease.
- Presymptomatic diagnosis of delayed-onset disease with linked DNA markers. The experience in Huntington's disease.
- Brain atrophy in Huntington''s disease. A CT-scan study.
- Linkage to the Huntington's disease locus in a family with unusual clinical and pathological features.
- Knowledge, attitude, and the decision to be tested for Huntington''s disease.
- Presymptomatic DNA testing for Huntington's disease.
- Bipolar II Disorder in six sisters.
- Huntington's disease as a model for mood Disorders. Clues from neuropathology and neurochemistry.
- A family history study of neuropsychiatric Disorders in the adult siblings of autistic individuals.
- Genetic linkage studies of bipolar affective Disorder.
- D2 receptors in Huntington's disease: positron emission tomography findings and clinical correlates.
- Platelet serotonin, a possible marker for familial Autism.
- Postural control in Huntington''s disease (HD).
- Neuronal loss in layers V and VI of cerebral cortex in Huntington''s disease.
- The split-brain neonate: a surgical method for corpus callosum section in newborn kittens.
Schools
Weill Cornell Medical College
Procedures Preformed
- Group Psychotherapy
- Psychiatric Evaluation
- Psychotherapy and Psychophysiological Therapy (incl. Biofeedback)
Conditions Treated
- Adjustment Disorder
- Autism
- Phobia
Doctors Specialties
- Psychiatry
Accepted Insurances
- Amerigroup (Wellpoint)
- AvMed
- Blue Cross Blue Shield
- Cigna HMO
- Cigna PPO
- Great West Healthcare-Cigna PPO
- LocalPlus
- Open Access Plus
- Commercial Insurance Company
- Choice Care PPO
- Preferred PPO
- Medicaid
- Medicare MCR
Education
-
Johns Hopkins University -
Albert Einstein College of Medicine at Jacobi Medical Center -
Weill Cornell Medical College of Cornell University
Drug Facts
| NPI NUMBER | 1205868734 | |
| NPPES Provider LastName | FOLSTEIN | |
| NPPES Provider FirstName | SUSAN | |
| NPPES Provider ZIPCode | 331361409 | |
| NPPES Provider State | FL | |
| Specialty Description | Psychiatry | |
| Total Claim Count | 244.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1205868734 |
| Last Name Of The Provider | FOLSTEIN |
| First Name Of The Provider | SUSAN |
| View All |
Similar Doctors
|
|
Dr. Ginger E. Shupe, MD
 This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Alberto A. Penalver, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Karen U. Breakstone, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Vivian D. Cuevas, MD |
|
|
Dr. Lester P. Hartswick, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Lydia M. Usategui, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Rigoberto J. Rodriguez, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Barry R. Kaplowitz, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Anna R. Rzadkowolsky, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Jahanbakhsh Nasserzare, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Aaron Short, MD |
|
|
Dr. Luis M. Carcache, MD
This Doctor is OpenDoctor Recommended.
|
|
|
Dr. Zaida T. Cruzet, MD |
|
|
Dr. Fernando R. Salvato, MD
This Doctor is OpenDoctor Recommended.
|