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RUTH MICHAELIS, MD
MD
Family Medicine Physician
NPI: 1982698320IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
MD00040067(WA)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
SOUTHERN ILLINOIS UNIVERSITY SCHOOL OF MEDICINE
Class of 1999
Research & Publications (20)
A DRD1 haplotype is associated with risk for autism spectrum disorders in male-only affected sib-pair families.
PMID 18205172·Am J Med Genet B Neuropsychiatr Genet·2008
4-observational
Ribavirin inhibits angiogenesis by tetrahydrobiopterin depletion.
PMID 17135367·FASEB J·2007
7-preclinical
SALL1 mutation analysis in Townes-Brocks syndrome: twelve novel mutations and expansion of the phenotype.
PMID 16088922·Hum Mutat·2005
8-other
Familial pericentric inversion of chromosome 18: behavioral abnormalities in patients heterozygous for either the dup(18p)/del(18q) or dup(18q)/del(18p) recombinant chromosome.
PMID 15470365·Eur J Hum Genet·2005
5-case
A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A.
PMID 15389703·Am J Med Genet A·2004
8-other
High incidence of the R276X SALL1 mutation in sporadic but not familial Townes-Brocks syndrome and report of the first familial case.
PMID 14627694·J Med Genet·2003
4-observational
[Mandatory reporting according to the infection control regulation and biosubstance law].
PMID 12940265·Urologe A·2003
8-other
The HOXA1 A218G polymorphism and autism: lack of association in white and black patients from the South Carolina Autism Project.
PMID 12908836·J Autism Dev Disord·2003
8-other
[European Association of Urology guidelines on urinary and male genital tract infections].
PMID 12577160·Urologe A·2003
6-review
Absence of MeCP2 mutations in patients from the South Carolina autism project.
PMID 12555243·Am J Med Genet B Neuropsychiatr Genet·2003
8-other
Molecular cytogenetic characterization of a de novo unbalanced translocation leading to trisomy 17q25-->qter and monosomy 18p11.3-->pter in a girl with dysmorphic features.
PMID 12514362·Clin Dysmorphol·2003
5-case
Hydrocephalus and intestinal aganglionosis: is L1CAM a modifier gene in Hirschsprung disease?
PMID 11857550·Am J Med Genet·2002
8-other
Scanning for telomeric deletions and duplications and uniparental disomy using genetic markers in 120 children with malformations.
PMID 11702212·Hum Genet·2001
8-other
Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families.
PMID 11543639·Genomics·2001
8-other
Microsatellite analysis reveals a high incidence of maternal cell contamination in 46,XX products of conception consisting of villi or a combination of villi and membranous material.
PMID 11483928·Am J Obstet Gynecol·2001
8-other
Lack of association of the (AAAT)6 allele of the GXAlu tetranucleotide repeat in intron 27b of the NF1 gene with autism.
PMID 11449390·Am J Med Genet·2001
8-other
Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15 in a boy with a balanced 3;21 translocation.
PMID 11337756·Am J Med Genet·2001
5-case
A novel intronic polymorphism (intron 2 +130 (CT)n) in the human homeobox gene HOXB3.
PMID 11180611·Hum Mutat·2001
8-other
Usefulness and limitations of FISH to characterize partially cryptic complex chromosome rearrangements.
PMID 11074491·Am J Med Genet·2000
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
- 403 E MEEKER ST
KENT, WA 98030 - Phone
- (253) 852-2866
Quick Facts
- NPI
- 1982698320
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 27
- Publications
- 20
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