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WILLIAM SIEGFRIED, M.D.
M.D.
Psychiatry Physician
NPI: 1821162041Individual
Specialties, Licenses & Credentials
Psychiatry PhysicianPrimary
Psychiatry & Neurology — Psychiatry
Code: 2084P0800X
G40134(CA)
Research & Publications (17)
Analysis of sequence variations in the suppressor of cytokine signaling (SOCS)-3 gene in extremely obese children and adolescents.
PMID 17445271·BMC Med Genet·2007
8-other
[Long-term inpatient treatment of extreme juvenile obesity: an 18-month catamnestic study].
PMID 16995363·MMW Fortschr Med·2006
4-observational
Mutation analysis of the MCHR1 gene in human obesity.
PMID 15941924·Eur J Endocrinol·2005
7-preclinical
Human galanin (GAL) and galanin 1 receptor (GALR1) variations are not involved in fat intake and early onset obesity.
PMID 15930442·J Nutr·2005
8-other
Mutation screen of the brain derived neurotrophic factor gene (BDNF): identification of several genetic variants and association studies in patients with obesity, eating disorders, and attention-deficit/hyperactivity disorder.
PMID 15457498·Am J Med Genet B Neuropsychiatr Genet·2005
4-observational
Medical care of obese children and adolescents. APV: a standardised multicentre documentation derived to study initial presentation and cardiovascular risk factors in patients transferred to specialised treatment institutions.
PMID 15346912·Eur J Pediatr·2004
8-other
Melanocortin-4 receptor gene: case-control study and transmission disequilibrium test confirm that functionally relevant mutations are compatible with a major gene effect for extreme obesity.
PMID 12970296·J Clin Endocrinol Metab·2003
3-trial
No evidence for involvement of the promoter polymorphism -866 G/A of the UCP2 gene in childhood-onset obesity in humans.
PMID 12746756·Exp Clin Endocrinol Diabetes·2003
8-other
Genome scan for childhood and adolescent obesity in German families.
PMID 12563058·Pediatrics·2003
4-observational
No evidence for involvement of the calpain-10 gene 'high-risk' haplotype combination for non-insulin-dependent diabetes mellitus in early onset obesity.
PMID 12083814·Mol Genet Metab·2002
8-other
Ghrelin gene: identification of missense variants and a frameshift mutation in extremely obese children and adolescents and healthy normal weight students.
PMID 12050239·J Clin Endocrinol Metab·2002
8-other
No evidence for involvement of alleles of the 825-C/T polymorphism of the G-protein subunit beta 3 in body weight regulation.
PMID 11748488·Exp Clin Endocrinol Diabetes·2001
8-other
Systematic screening for mutations in the human necdin gene (NDN): identification of two naturally occurring polymorphisms and association analysis in body weight regulation.
PMID 11439287·Int J Obes Relat Metab Disord·2001
8-other
Identification of a deletion variant in the gene encoding the human alpha(2A)-adrenergic receptor.
PMID 11248750·Eur J Endocrinol·2001
8-other
Significant association between a silent polymorphism in the neuromedin B gene and body weight in German children and adolescents.
PMID 11194934·Acta Diabetol·2000
8-other
Rates of psychiatric disorders in a clinical study group of adolescents with extreme obesity and in obese adolescents ascertained via a population based study.
PMID 11126229·Int J Obes Relat Metab Disord·2000
8-other
Independent confirmation of a major locus for obesity on chromosome 10.
PMID 10946912·J Clin Endocrinol Metab·2000
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
- 5151 N PALM AVE, SUITE 800
FRESNO, CA 93704 - Phone
- (559) 499-1233
Quick Facts
- NPI
- 1821162041
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 17
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