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HATEM I EL-SHANTI MD
MD
Clinical Genetics (M.D.) Physician
NPI: 1801881685IndividualAccepts Medicare
Specialties, Licenses & Credentials
Pediatrics Physician
Pediatrics
Code: 208000000X
MD-28647(IA)
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
28647(IA)
Education
OTHER
Class of 1983
Research & Publications (20)
Chronic recurrent multifocal osteomyelitis: a concise review and genetic update.
PMID 17496555·Clin Orthop Relat Res·2007
6-review
A distinct autosomal recessive ataxia maps to chromosome 12 in an inbred family from Jordan.
PMID 16376507·Brain Dev·2006
8-other
Alopecia universalis congenita, XY gonadal dysgenesis and laryngomalacia: a novel malformation syndrome.
PMID 12486505·Eur J Pediatr·2003
5-case
The pattern of peripheral blood chromosomal abnormalities in Northern Jordan.
PMID 12518216·Saudi Med J·2002
8-other
Homozygosity mapping identifies an additional locus for Wolfram syndrome on chromosome 4q.
PMID 10739754·Am J Hum Genet·2000
8-other
An autoinflammatory disease with deficiency of the interleukin-1-receptor antagonist.
PMID 19494218·N Engl J Med·2009
8-other
A homozygous mutation in ADAMTSL4 causes autosomal-recessive isolated ectopia lentis.
PMID 19200529·Am J Hum Genet·2009
8-other
A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome.
PMID 18976727·Am J Hum Genet·2008
8-other
Independent introduction of two lactase-persistence alleles into human populations reflects different history of adaptation to milk culture.
PMID 18179885·Am J Hum Genet·2008
7-preclinical
The infevers autoinflammatory mutation online registry: update with new genes and functions.
PMID 18409191·Hum Mutat·2008
8-other
Neutrophil dysfunction in a family with a SAPHO syndrome-like phenotype.
PMID 18821685·Arthritis Rheum·2008
5-case
Breakpoint localization using array-CGH in three siblings with an unbalanced 4q;16q translocation and childhood apraxia of speech (CAS).
PMID 18671280·Am J Med Genet A·2008
8-other
A splice site mutation confirms the role of LPIN2 in Majeed syndrome.
PMID 17330256·Arthritis Rheum·2007
5-case
A homozygous mutation in a novel zinc-finger protein, ERIS, is responsible for Wolfram syndrome 2.
PMID 17846994·Am J Hum Genet·2007
8-other
A missense mutation in pstpip2 is associated with the murine autoinflammatory disorder chronic multifocal osteomyelitis.
PMID 16122996·Bone·2006
7-preclinical
Novel sequence variants in the TMIE gene in families with autosomal recessive nonsyndromic hearing impairment.
PMID 16389551·J Mol Med (Berl)·2006
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 4 locations total
- Address
- 865 Lincoln Rd Ste 400
Bettendorf, IA 52722 - Phone
- (877) 891-5350
Quick Facts
- NPI
- 1801881685
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 4
- Years in Practice
- 43
- Publications
- 20
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