Beth A Kozel, MD

Dr. Kozel focuses her practice on genetics. She sees children with inherited medical conditions and multiple congenital anomalies. She has a clinical and research interest in the genetics of Williams Syndrome, familial supravalvular aortic stenosis and cutis laxa.

Practice Name: Genetics And Genomic Medicine

Age: 39

Gender: Female

In Area Since: 2009

In Practice Since: 2009

Specialties:

Genetics-Pediatric - certified
*Pediatrics - certified

Hospitals:

Barnes-Jewish Hospital
St. Louis Children's Hospital

Academic Profile:

Washington University School of Medicine

For Patients:
To request an appointment, call 800.678.KIDS (5437) or fill out our online form.

For Referring Physicians:
To refer a patient, call Children's Direct at 800.678.HELP (4357).

Public transportation available | Handicap accessible

One Children's Place
Suite 2D
Saint Louis, MO 63110
314.454.6093

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Education

Medical School: Washington University School of Medicine St. Louis
Internship: St. Louis Children's Hospital
Residency: St. Louis Children's Hospital
Fellowship: Washington University School of Medicine St. Louis

Health Plans Accepted

Aetna Elect Choice EPO	Aetna HealthFund
Aetna HMO/Open Access	Aetna Managed Choice POS
Aetna Medicare HMO	Aetna Medicare Open Access (HMO/POS
Aetna Medicare PPO	Aetna Open Access Elect Choice EPO
Aetna POS/PPO/Choice	Aetna PPO
Aetna Quality Point of Service	Aetna USAccess
Baxter Regional PHO	BCBS of IL PPO
BCBS/Anthem(Blue Access Choice PPO	BCBS/Anthem(Blue Access PPO)
Beech Street/Capp Care PPO	Best Doctors Inc
Capital Regional Medical Center PP	Cigna Open Access HMO/POS
Cigna PPO	CMR (Care Management Resources)
Community Care Network PPO	Community Partners Health Plan/PPO
CorVel PPO	Coventry Advantra HMO (formerlyGHP
Coventry HMO/POS (formerly GHP)	Coventry PPO (formerly GHP)
Decatur Memorial Tertiary/Quarterna	First Health
Great-West HMO/POS	Great-West Open Access
Great-West PPO	Hannibal Health Network Tertiary
Health Alliance HMO & PPO	Healthlink Open Access/HMO/POS
Healthlink PPO	HFN Inc. PPO
Home State-MC+	Humana Gold Choice PFFS Medicare
Humana PPO/ChoiceCare Network	HumanaChoice PPO-Medicare
IPA Secondary to Medicare	Mail Handlers/CNA PPO
Medicare	Mercy Health Plan HMO/POS
Mercy Health Plan PPO	MO Medicaid Secondary to Medicare
MultiPlan PPO	Personal Care Health Mgmt HMO
Personal Care Health Mgmt PPO/POS	PPO Next/HealthStar
Primrose Tertiary/Quarternary	Private Health Care Systems PPO
Providers Network of America	Quincy Health Care Management
St. John's Health System Tertiary	Tricare/Triwest Prime HMO/POS
Tricare/Triwest Extra PPO	Union Pacific RR Emp. Health System
United Healthcare Choice/Choice+	United Healthcare PPO/ Options
United Healthcare Select/Select+POS	USA Managed Care Org
Wellborn HMO

Genetic modifiers of the cardiovascular phenotype caused by elastin haploinsufficiency act by extrinsic Noncomplementation.Kozel BA, Knutsen RH, Ye L, Ciliberto CH, Broekelmann TJ, Mecham RP.J Biol Chem. 2011 Nov 2. [Epub ahead of print]

PMID:: 22049077; [PubMed - as supplied by publisher]

Free Article Related citations BMP4 loss-of-function mutations in developmental eye disorders including SHORT syndrome.Reis LM, Tyler RC, Schilter KF, Abdul-Rahman O, Innis JW, Kozel BA, Schneider AS, Bardakjian TM, Lose EJ, Martin DM, Broeckel U, Semina EV.Hum Genet. 2011 Oct;130(4):495-504. Epub 2011 Feb 22.

PMID:: 21340693; [PubMed - indexed for MEDLINE]

Free PMC Article Related citations Distinct clinical and histopathological presentations of Danon cardiomyopathy in young women.Toib A, Grange DK, Kozel BA, Ewald GA, White FV, Canter CE.J Am Coll Cardiol. 2010 Jan 26;55(4):408-10. No abstract available.

PMID:: 20117447; [PubMed - indexed for MEDLINE]

Related citations Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size.Shinawi M, Liu P, Kang SH, Shen J, Belmont JW, Scott DA, Probst FJ, Craigen WJ, Graham BH, Pursley A, Clark G, Lee J, Proud M, Stocco A, Rodriguez DL, Kozel BA, Sparagana S, Roeder ER, McGrew SG, Kurczynski TW, Allison LJ, Amato S, Savage S, Patel A, Stankiewicz P, Beaudet AL, Cheung SW, Lupski JR.J Med Genet. 2010 May;47(5):332-41. Epub 2009 Nov 12.