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JUDITH HARDY, PHD
PHD
Psychologist
NPI: 1235379116Individual
Specialties, Licenses & Credentials
PsychologistPrimary
Psychologist
Code: 103T00000X
010476(NY)
Research & Publications (20)
Functional characterization of three single-nucleotide polymorphisms present in the human APOE promoter sequence: Differential effects in neuronal cells and on DNA-protein interactions.
PMID 19504470·Am J Med Genet B Neuropsychiatr Genet·2010
7-preclinical
Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP.
PMID 18667258·Neurobiol Aging·2010
8-other
Acute and chronic toxicity of atrazine and its metabolites deethylatrazine and deisopropylatrazine on aquatic organisms.
PMID 19533344·Ecotoxicology·2009
4-observational
The genetics of Parkinson's syndromes: a critical review.
PMID 19419854·Curr Opin Genet Dev·2009
6-review
SNCA variants are associated with increased risk for multiple system atrophy.
PMID 19475667·Ann Neurol·2009
8-other
Robust production of a peptide library using methodological synchronization.
PMID 19457455·Protein Expr Purif·2009
8-other
The amyloid hypothesis for Alzheimer's disease: a critical reappraisal.
PMID 19457065·J Neurochem·2009
6-review
The T cell STAT signaling network is reprogrammed within hours of bacteremia via secondary signals.
PMID 19494279·J Immunol·2009
7-preclinical
Modified Folts models in the rabbit: variations on a well worn theme.
PMID 19401666·Eur J Anaesthesiol·2009
7-preclinical
A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial disease.
PMID 19375058·Am J Hum Genet·2009
8-other
Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Greece.
PMID 19383421·Neurosci Lett·2009
8-other
Prioritising drugs for single patient (n-of-1) trials in palliative care.
PMID 19605605·Palliat Med·2009
8-other
Genetic control of human brain transcript expression in Alzheimer disease.
PMID 19361613·Am J Hum Genet·2009
8-other
Glucocerebrosidase mutations in 108 neuropathologically confirmed cases of multiple system atrophy.
PMID 19332698·Neurology·2009
5-case
Dissecting an allosteric switch in caspase-7 using chemical and mutational probes.
PMID 19581639·J Biol Chem·2009
8-other
GLUT1 gene mutations cause sporadic paroxysmal exercise-induced dyskinesias.
PMID 19630075·Mov Disord·2009
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 48 BURD ST, SUITE 303
NYACK, NY 10960 - Phone
- (845) 353-6879
Quick Facts
- NPI
- 1235379116
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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