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SAMUEL FRIEDEL, M.D.
M.D.
Ophthalmology Physician
NPI: 1417973785IndividualAccepts Medicare
Specialties, Licenses & Credentials
Ophthalmology PhysicianPrimary
Ophthalmology
Code: 207W00000X
D0020950(MD)
CMS Specialties
PrimaryOPHTHALMOLOGY
Education
UNIVERSITY OF MARYLAND SCHOOL OF MEDICINE
Class of 1977
Research & Publications (20)
Familiality and molecular genetics of attention networks in ADHD.
PMID 19418498·Am J Med Genet B Neuropsychiatr Genet·2010
8-other
Non-replication of an association of CTNNBL1 polymorphisms and obesity in a population of Central European ancestry.
PMID 19228371·BMC Med Genet·2009
8-other
Serotonin transporter gene polymorphism (5-HTTLPR), environmental conditions, and developing negative emotionality and fear in early childhood.
PMID 19137235·J Neural Transm (Vienna)·2009
8-other
Lifestyle intervention in obese children with variations in the melanocortin 4 receptor gene.
PMID 18997677·Obesity (Silver Spring)·2009
4-observational
Genetic aspects in attention-deficit/hyperactivity disorder.
PMID 18200432·J Neural Transm (Vienna)·2008
6-review
Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder.
PMID 18988193·Am J Med Genet B Neuropsychiatr Genet·2008
1-meta
Evidence for an influence of TCF7L2 polymorphism rs7903146 on insulin resistance and sensitivity indices in overweight children and adolescents during a lifestyle intervention.
PMID 18762805·Int J Obes (Lond)·2008
3-trial
Genome wide association (GWA) study for early onset extreme obesity supports the role of fat mass and obesity associated gene (FTO) variants.
PMID 18159244·PLoS One·2007
8-other
Gender-specific association of a functional coding polymorphism in the Neuropeptide S receptor gene with panic disorder but not with schizophrenia or attention-deficit/hyperactivity disorder.
PMID 17669576·Prog Neuropsychopharmacol Biol Psychiatry·2007
8-other
Association and linkage of allelic variants of the dopamine transporter gene in ADHD.
PMID 17579611·Mol Psychiatry·2007
8-other
Mutation screen and association studies in the diacylglycerol O-acyltransferase homolog 2 gene (DGAT2), a positional candidate gene for early onset obesity on chromosome 11q13.
PMID 17477860·BMC Genet·2007
8-other
No evidence for an involvement of variants in the cannabinoid receptor gene (CNR1) in obesity in German children and adolescents.
PMID 17292652·Mol Genet Metab·2007
8-other
No evidence for preferential transmission of common valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor gene (BDNF) in ADHD.
PMID 17219016·J Neural Transm (Vienna)·2007
8-other
Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sample.
PMID 17093889·J Neural Transm (Vienna)·2007
4-observational
[Genetic findings in Attention-Deficit and Hyperactivity Disorder (ADHD)].
PMID 17094061·Z Kinder Jugendpsychiatr Psychother·2006
6-review
Evidence for involvement of the vitamin D receptor gene in idiopathic short stature via a genome-wide linkage study and subsequent association studies.
PMID 16905557·Hum Mol Genet·2006
8-other
Twin study on heritability of activity, attention, and impulsivity as assessed by objective measures.
PMID 16648224·J Atten Disord·2006
4-observational
Case-control and combined family trios analysis of three polymorphisms in the ghrelin gene in European patients with anorexia and bulimia nervosa.
PMID 16538179·Psychiatr Genet·2006
4-observational
A genome-wide scan for attention-deficit/hyperactivity disorder in 155 German sib-pairs.
PMID 16222334·Mol Psychiatry·2006
3-trial
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 827 LINDEN AVE
BALTIMORE, MD 21201 - Phone
- (410) 225-8077
Quick Facts
- NPI
- 1417973785
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 49
- Publications
- 20
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