Professor of Pediatrics, UC Irvine
Medical Genetics
Dr. Suzanne B. Cassidy, MD
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Suzanne Cassidy works in the field of Medical Genetics. He researched medicine at Vanderbilt University School of Medicine. He received 1 awards: "Whos Who in Medicine and Healthcare". Suzanne B. Cassidy, MD is also a published physician. He has 76 publication published. The most recent publication is: Molecular mechanism of angelman syndrome in two large families involves an imprinting mutation.
Publications
- Frequency of Prader-Willi syndrome in births conceived via assisted reproductive technology.
- In memoriam: Eric Engel, M.D., an innovator, mentor, and humanist.
- Elements of morphology: standard terminology for the periorbital region.
- Gastric rupture and necrosis in Prader-Willi syndrome.
- Clinical consult: developmental delay/fragile X syndrome.
- Terminal 22q deletion syndrome: a newly recognized cause of speech and language disability in the autism spectrum.
- Detection of deletions in de novo "balanced" chromosome rearrangements: further evidence for their role in phenotypic abnormalities.
- Prader-Willi syndrome: causes of death in an international series of 27 cases.
- The burden of genetic disease on inpatient care in a children's hospital.
- Myeloid leukemia in Prader-Willi syndrome.
- Behavioral phenotypes in genetic syndromes: genetic clues to human behavior.
- Trigonocephaly and the 11q- syndrome.
- Is tuberous sclerosis a cause of autism?
- Connatal Pelizaeus-Merzbacher disease: an autosomal recessive form.
- New syndrome: mother and son with hypertelorism, downslanting palpebral fissures, malar hypoplasia, and apparently low-set ears associated with joint and scrotal anoma...
- Is there an embryo-fetal exogenous sex steroid exposure syndrome (EFESSES)?
- Arteriohepatic dysplasia (Alagille syndrome): extreme variability among affected family members.
- Methylphenidate therapy for aggression in a man with ring 22 chromosome. Report and literature review.
- Ehlers-Danlos syndrome type IV: cosegregation of the phenotype to a COL3A1 allele of type III procollagen.
- Trisomy 8 syndrome.
- [Prenatal diagnosis. Review, personal and prospective studies].
- 7p deletion syndrome: an adult with mild manifestations.
- American College of Medical Genetics statement of diagnostic testing for uniparental disomy.
- Family studies in tuberous sclerosis. evaluation of apparently unaffected parents.
- Uniparental disomy and genomic imprinting as causes of human genetic disease.
- Jarcho-Levin syndrome: unusual survival in a classical case.
- Photographic documentation of syndrome diagnosis.
- Hydrolethalus syndrome: report of an apparent mild case, literature review, and differential diagnosis.
- Pulmonary atresia associated with maternal 22q11.2 deletion: possible parent of origin effect in the conotruncal anomaly face syndrome.
- Chromosome 11 long arm partial deletion: a new syndrome.
- New syndrome of macrocephaly, hypertelorism, short limbs, hearing loss, and developmental delay.
- The chromosome 2 distal short arm trisomy syndrome.
- Prader-Willi and Angelman syndromes: sister imprinted disorders.
- Recurrence risk in Prader-Willi syndrome.
- Respiratory sinus arrhythmia in patients with Prader-Willi syndrome.
- Deletion of chromosome 15 (q11-13) in a Prader-Labhart-Willi syndrome clinic population.
- Comparison of high resolution chromosome banding and fluorescence in situ hybridization (FISH) for the laboratory evaluation of Prader-Willi syndrome and Angelman synd...
- Prader-Willi syndrome in a brother and sister without cytogenetic or detectable molecular genetic abnormality at chromosome 15q11q13.
- Cephalometric analysis of the Prader-Willi syndrome.
- Prader-Willi syndrome. Characteristics, management, and etiology.
- Correlates of maladaptive behavior in children and adults with Prader-Willi syndrome.
- The need for anonymous genetic counseling and testing.
- Evaluation of mental retardation: recommendations of a Consensus Conference: American College of Medical Genetics.
- Chromosome 7p--syndrome: craniosynostosis with preservation of region 7p2.
- Clinical correlates of chromosome 15 deletions and maternal disomy in Prader-Willi syndrome.
- Obsessions and compulsions in Prader-Willi syndrome.
- Maladaptive behavior differences in Prader-Willi syndrome due to paternal deletion versus maternal uniparental disomy.
- Genetics of childhood disorders: XII. Genomic imprinting: breaking the rules.
- Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy.
- Nutrient intake and body composition variables in Prader-Willi syndrome--effect of growth hormone supplementation and genetic subtype.
- An evaluation of autonomic nervous system function in patients with Prader-Willi syndrome.
- Pulmonary function abnormalities in Prader-Willi syndrome.
- Prader-Willi and other syndromes associated with obesity and mental retardation.
- Molecular refinement of karyotype: beyond the cytogenetic band.
- Hand and foot length in Prader-Willi syndrome.
- Klinefelter and trisomy X syndromes in patients with Prader-Willi syndrome and uniparental maternal disomy of chromosome 15--a coincidence?
- Photoanthropometric study of craniofacial traits of individuals with Prader-Willi syndrome.
- Molecular cytogenetics of a de novo interstitial deletion of chromosome arm 6q in a developmentally normal girl.
- Scanning for telomeric deletions and duplications and uniparental disomy using genetic markers in 120 children with malformations.
- A blind prometaphase study of Prader-Willi syndrome: frequency and consistency in interpretation of del 15q.
- Physical features of Prader-Willi syndrome in neonates.
- Deletion 10q23.2-q23.33 in a patient with gastrointestinal juvenile polyposis and other features of a Cowden-like syndrome.
- Molecular mechanism of angelman syndrome in two large families involves an imprinting mutation.
- Occupational hydrocarbon exposure among fathers of Prader-Willi syndrome patients with and without deletions of 15q.
- Prader-Willi syndrome: consensus diagnostic criteria.
- Prader-Willi and Angelman syndromes. Disorders of genomic imprinting.
- Delayed diagnosis in patients with Prader-Willi syndrome due to maternal uniparental disomy 15.
- Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15.
- Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation.
- The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria.
- Balanced translocation 46,XY,t(2;15)(q37.2;q11.2) associated with atypical Prader-Willi syndrome.
- Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints.
- Molecular characterization and delineation of subtle deletions in de novo "balanced" chromosomal rearrangements.
- Phenotypic differerencss in African Americans with Prader-Willi syndrome.
- Delineation of complex chromosomal rearrangements: evidence for increased complexity.
Schools
Vanderbilt University
Doctors Specialties
- Clinical Genetics
- Pediatrics
- Medical Genetics
Accepted Insurances
- Choice Plus POS II
- Blue Card PPO
- Delta Health System
- Blue & Gold HMO
- Covered California - Bronze PPO
- Employer Group HMO
- Health Net PPO
- Individual and Family PPO
- WholeCare Network HMO
- Medicare MCR
- Heritage Signature
- Choice Plus POS
- Navigate HMO
- Navigate POS
- Options PPO
Awards
- Whos Who in Medicine and Healthcare
Education
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University of Washington -
Vanderbilt University School of Medicine
Hospital
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UCSF Medical Center
