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ROBERT DELORME, MD
MD
Family Medicine Physician
NPI: 1912908005IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
134470(NY)
Geriatric Medicine (Family Medicine) Physician
Family Medicine — Geriatric Medicine
Code: 207QG0300X
134470(NY)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
OTHER
Class of 1974
Research & Publications (20)
Reduced 3-O-methyl-dopa levels in OCD patients and their unaffected parents is associated with the low activity M158 COMT allele.
PMID 19676096·Am J Med Genet B Neuropsychiatr Genet·2010
8-other
Psychiatric and psychosocial problems in adults with normal-intelligence autism spectrum disorders.
PMID 19515234·BMC Psychiatry·2009
8-other
Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.
PMID 19278672·Biol Psychiatry·2009
8-other
An investigation of ribosomal protein L10 gene in autism spectrum disorders.
PMID 19166581·BMC Med Genet·2009
8-other
Four-factor structure of obsessive-compulsive disorder symptoms in children, adolescents, and adults.
PMID 18520961·J Am Acad Child Adolesc Psychiatry·2008
8-other
Analysis of X chromosome inactivation in autism spectrum disorders.
PMID 18361425·Am J Med Genet B Neuropsychiatr Genet·2008
8-other
Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.
PMID 17173049·Nat Genet·2007
8-other
Mutation analysis of the NSD1 gene in patients with autism spectrum disorders and macrocephaly.
PMID 18001468·BMC Med Genet·2007
8-other
Association of the SLC1A1 glutamate transporter gene and obsessive-compulsive disorder.
PMID 17894418·Am J Med Genet B Neuropsychiatr Genet·2007
4-observational
A genetic family-based association study of OLIG2 in obsessive-compulsive disorder.
PMID 17283288·Arch Gen Psychiatry·2007
4-observational
Shared executive dysfunctions in unaffected relatives of patients with autism and obsessive-compulsive disorder.
PMID 17127035·Eur Psychiatry·2007
8-other
No human tryptophan hydroxylase-2 gene R441H mutation in a large cohort of psychiatric patients and control subjects.
PMID 16581035·Biol Psychiatry·2006
8-other
[School phobia or school refusal: controversial concepts].
PMID 17650748·Bull Acad Natl Med·2006
6-review
Exploratory analysis of obsessive compulsive symptom dimensions in children and adolescents: a prospective follow-up study.
PMID 16396684·BMC Psychiatry·2006
4-observational
Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disorders.
PMID 16331680·Am J Med Genet B Neuropsychiatr Genet·2006
4-observational
A genetic analysis of mancozeb resistance in Typhlodromus pyri (Acari: Phytoseiidae).
PMID 16180074·Exp Appl Acarol·2005
7-preclinical
Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder.
PMID 16088327·Mol Psychiatry·2005
3-trial
Early-onset obsessive-compulsive disorder: a subgroup with a specific clinical and familial pattern?
PMID 16033636·J Child Psychol Psychiatry·2005
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 164 BROAD ST
HAMILTON, NY 13346 - Phone
- (315) 824-4600
Quick Facts
- NPI
- 1912908005
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 52
- Publications
- 20
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