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NEIL ROSENBERG, MD
MD
Neurocritical Care Physician
NPI: 1285896845IndividualAccepts Medicare
Specialties, Licenses & Credentials
Neurocritical Care PhysicianPrimary
Psychiatry & Neurology — Neurocritical Care
Code: 2084A2900X
8743839-1205(UT)
Neurology Physician
Psychiatry & Neurology — Neurology
Code: 2084N0400X
125.050947(IL)
CMS Specialties
PrimaryNEUROLOGY
Education
OTHER
Class of 2006
Research & Publications (20)
Replication of genetic associations as pseudoreplication due to shared genealogy.
PMID 19191270·Genet Epidemiol·2009
8-other
The relationship between homozygosity and the frequency of the most frequent allele.
PMID 18689892·Genetics·2008
8-other
Trp207Gly in platelet glycoprotein Ibalpha is a novel mutation that disrupts the connection between the leucine-rich repeat domain and the disulfide loop structure and causes Bernard-Soulier syndrome.
PMID 17083647·J Thromb Haemost·2007
5-case
Statistical tests for taxonomic distinctiveness from observations of monophyly.
PMID 17348942·Evolution·2007
8-other
Standardized subsets of the HGDP-CEPH Human Genome Diversity Cell Line Panel, accounting for atypical and duplicated samples and pairs of close relatives.
PMID 17044859·Ann Hum Genet·2006
8-other
Low levels of genetic divergence across geographically and linguistically diverse populations from India.
PMID 17194221·PLoS Genet·2006
4-observational
Shoulder impairment following treatment of diaphysial fractures of humerus by functional brace.
PMID 16810551·Arch Orthop Trauma Surg·2006
8-other
A general population-genetic model for the production by population structure of spurious genotype-phenotype associations in discrete, admixed or spatially distributed populations.
PMID 16582435·Genetics·2006
8-other
A 13-bp deletion in alpha(IIb) gene is a founder mutation that predominates in Palestinian-Arab patients with Glanzmann thrombasthenia.
PMID 16359514·J Thromb Haemost·2005
7-preclinical
Clines, clusters, and the effect of study design on the inference of human population structure.
PMID 16355252·PLoS Genet·2005
8-other
Algorithms for selecting informative marker panels for population assignment.
PMID 16305328·J Comput Biol·2005
4-observational
Polyploid and multilocus extensions of the Wahlund inequality.
PMID 15560915·Theor Popul Biol·2004
8-other
A novel Phe171Cys mutation in integrin alpha causes Glanzmann thrombasthenia by abrogating alphabeta complex formation.
PMID 15219201·J Thromb Haemost·2004
8-other
Comparison of two methods for the evaluation of treatment in medial epicondylitis: pain estimation vs grip strength measurements.
PMID 15108009·Arch Orthop Trauma Surg·2004
4-observational
Informativeness of genetic markers for inference of ancestry.
PMID 14631557·Am J Hum Genet·2003
8-other
The shapes of neutral gene genealogies in two species: probabilities of monophyly, paraphyly, and polyphyly in a coalescent model.
PMID 12940352·Evolution·2003
8-other
On the use of star-shaped genealogies in inference of coalescence times.
PMID 12930771·Genetics·2003
8-other
Estimating change rates of genetic markers using serial samples: applications to the transposon IS6110 in Mycobacterium tuberculosis.
PMID 12742178·Theor Popul Biol·2003
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
- 750 W 800 N
OREM, UT 84057 - Phone
- (801) 714-6235
Quick Facts
- NPI
- 1285896845
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 20
- Publications
- 20
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