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MICHELLE BOBROW, MD
MD
Neurology Physician
NPI: 1861923385IndividualAccepts Medicare
Specialties, Licenses & Credentials
Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology
Code: 2084N0400X
310860(NY)
CMS Specialties
PrimaryNEUROLOGY
Education
OTHER
Class of 2017
Research & Publications (20)
A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation.
PMID 19377476·Nat Genet·2009
8-other
Mutations in CUL4B, which encodes a ubiquitin E3 ligase subunit, cause an X-linked mental retardation syndrome associated with aggressive outbursts, seizures, relative macrocephaly, central obesity, hypogonadism, pes cavus, and tremor.
PMID 17236139·Am J Hum Genet·2007
8-other
Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation.
PMID 17704778·Nat Genet·2007
8-other
The GRAIDS Trial: a cluster randomised controlled trial of computer decision support for the management of familial cancer risk in primary care.
PMID 17700548·Br J Cancer·2007
4-observational
Mutations in the BRWD3 gene cause X-linked mental retardation associated with macrocephaly.
PMID 17668385·Am J Hum Genet·2007
5-case
Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a Marfanoid habitus.
PMID 17436253·Am J Hum Genet·2007
5-case
Mutations in the gene encoding the Sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardation.
PMID 17186471·Am J Hum Genet·2006
5-case
Prenatal detection of unbalanced chromosomal rearrangements by array CGH.
PMID 16199537·J Med Genet·2006
4-observational
Re: Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1 (Messiaen and Wimmer).
PMID 15994866·J Med Genet·2005
8-other
Re: Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1 (Messiaen and Wimmer).
PMID 15937073·J Med Genet·2005
8-other
Automated comparative sequence analysis identifies mutations in 89% of NF1 patients and confirms a mutation cluster in exons 11-17 distinct from the GAP related domain.
PMID 15060124·J Med Genet·2004
4-observational
Psychological impact of genetic testing for familial hypercholesterolemia within a previously aware population: a randomized controlled trial.
PMID 15216550·Am J Med Genet A·2004
3-trial
Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation.
PMID 15185169·Am J Hum Genet·2004
8-other
Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features.
PMID 15060094·J Med Genet·2004
4-observational
High-content proteomics: fluorescence multiplexing using an integrated, high-sensitivity, multiwavelength charge-coupled device imaging system.
PMID 12872212·Proteomics·2003
6-review
Genetic information and testing in insurance and employment: technical, social and ethical issues.
PMID 14718940·Eur J Hum Genet·2003
6-review
Polygenic susceptibility to breast cancer and implications for prevention.
PMID 11984562·Nat Genet·2002
8-other
Outcomes of pregnancies diagnosed with Klinefelter syndrome: the possible influence of health professionals.
PMID 12124688·Prenat Diagn·2002
4-observational
An assessment of screening strategies for fragile X syndrome in the UK.
PMID 11262423·Health Technol Assess·2001
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
- NORTH SHORE UNIVERSITY HOSPITAL NEUROLOGY, 300 COMMUNITY DRIVE, 9 TOWER
MANHASSET, NY 11030 - Phone
- (516) 562-3029
Quick Facts
- NPI
- 1861923385
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 9
- Publications
- 20
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