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ROSS MORELL, D.O.
D.O.
Family Medicine Physician
NPI: 1245281633IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
RM008704(MI)
Education
MICHIGAN STATE UNIVERSITY COLLEGE OF OSTEOPATHIC MEDICINE
Class of 1980
Research & Publications (20)
DFNB79: reincarnation of a nonsyndromic deafness locus on chromosome 9q34.3.
PMID 19603065·Eur J Hum Genet·2010
8-other
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
PMID 19576567·Am J Hum Genet·2009
7-preclinical
Mutations of LRTOMT, a fusion gene with alternative reading frames, cause nonsyndromic deafness in humans.
PMID 18953341·Nat Genet·2008
7-preclinical
A locus for autosomal dominant progressive non-syndromic hearing loss, DFNA27, is on chromosome 4q12-13.1.
PMID 18279434·Clin Genet·2008
8-other
Mutational spectrum of MYO15A: the large N-terminal extension of myosin XVA is required for hearing.
PMID 17546645·Hum Mutat·2007
8-other
A twin study of auditory processing indicates that dichotic listening ability is a strongly heritable trait.
PMID 17533509·Hum Genet·2007
4-observational
Signatures from tissue-specific MPSS libraries identify transcripts preferentially expressed in the mouse inner ear.
PMID 17049805·Genomics·2007
7-preclinical
Safety of adenosine stress magnetic resonance imaging using a mobile cardiac magnetic resonance system.
PMID 16755834·J Cardiovasc Magn Reson·2006
8-other
Mutations in TRIOBP, which encodes a putative cytoskeletal-organizing protein, are associated with nonsyndromic recessive deafness.
PMID 16385457·Am J Hum Genet·2006
4-observational
Spatiotemporal pattern and isoforms of cadherin 23 in wild type and waltzer mice during inner ear hair cell development.
PMID 15882574·Dev Biol·2005
7-preclinical
Modification of human hearing loss by plasma-membrane calcium pump PMCA2.
PMID 15829536·N Engl J Med·2005
5-case
Impact of extracorporeal circuit prime volume reduction on whole blood sequestration during acute normovolemic hemodilution for adult cardiac surgery patients.
PMID 15679273·J Extra Corpor Technol·2004
8-other
Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan.
PMID 15447792·BMC Med Genet·2004
8-other
Novel association of hypertrophic cardiomyopathy, sensorineural deafness, and a mutation in unconventional myosin VI (MYO6).
PMID 15060111·J Med Genet·2004
8-other
Men are more susceptible than women to direct pressure on unmyelinated ulnar nerve fibers.
PMID 14500179·Anesth Analg·2003
3-trial
Mutations in the gamma-actin gene (ACTG1) are associated with dominant progressive deafness (DFNA20/26).
PMID 13680526·Am J Hum Genet·2003
8-other
Mutations of MYO6 are associated with recessive deafness, DFNB37.
PMID 12687499·Am J Hum Genet·2003
8-other
Clinical presentation of DFNB12 and Usher syndrome type 1D.
PMID 12408077·Adv Otorhinolaryngol·2002
8-other
Mutation of a transcription factor, TFCP2L3, causes progressive autosomal dominant hearing loss, DFNA28.
PMID 12393799·Hum Mol Genet·2002
7-preclinical
Ulnar nerve injury and perioperative arm positioning.
PMID 12298308·Anesthesiol Clin North Am·2002
6-review
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 5865 WHITMORE LAKE RD, SUITE 1
BRIGHTON, MI 48116 - Phone
- (810) 227-1200
Quick Facts
- NPI
- 1245281633
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 46
- Publications
- 20
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