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PAUL ROTHBERG, PH.D.
PH.D.
Clinical Molecular Genetics Physician
NPI: 1932110780Individual
Specialties, Licenses & Credentials
Clinical Molecular Genetics PhysicianPrimary
Medical Genetics — Clinical Molecular Genetics
Code: 207SG0203X
CQP26695 ROTHP1(NY)
Research & Publications (20)
Laboratory practice guidelines for detecting and reporting BCR-ABL drug resistance mutations in chronic myelogenous leukemia and acute lymphoblastic leukemia: a report of the Association for Molecular Pathology.
PMID 19095773·J Mol Diagn·2009
6-review
Homogeneous polymerase chain reaction nucleobase quenching assay to detect the 1-kbp deletion in CLN3 that causes Batten disease.
PMID 15269304·J Mol Diagn·2004
8-other
Phase II study of a TLR-9 agonist (1018 ISS) with rituximab in patients with relapsed or refractory follicular lymphoma.
PMID 19519691·Br J Haematol·2009
3-trial
Mixed chimerism in SCT: conflict or peaceful coexistence?
PMID 18660844·Bone Marrow Transplant·2008
6-review
A 46 XY phenotypic female adolescent with bilateral gonadal tumors consisting of five different components.
PMID 18580319·Int J Gynecol Pathol·2008
5-case
Rapid method for detection of mutations in the nucleophosmin gene in acute myeloid leukemia.
PMID 18556765·J Mol Diagn·2008
8-other
Detection of clonality in lymphoproliferations using PCR of the antigen receptor genes: does size matter?
PMID 17588658·Leuk Res·2008
5-case
A case of JAK2 positive essential thrombocythemia 16.5 years after autologous marrow transplantation for AML.
PMID 17401398·Bone Marrow Transplant·2007
5-case
Homogeneous PCR nucleobase quenching assays to detect four mutations that cause neuronal ceroid lipofuscinosis: T75P and R151X in CLN1, and IVS5-1G>C and R208X in CLN2.
PMID 16720047·J Neurosci Methods·2006
4-observational
Standardized assessment of behavior and adaptive living skills in juvenile neuronal ceroid lipofuscinosis.
PMID 16542512·Dev Med Child Neurol·2006
8-other
Is there an association between ocular adnexal lymphoma and infection with Chlamydia psittaci? The University of Rochester experience.
PMID 16246419·Leuk Res·2006
8-other
Sequence diversity in the glycoprotein B gene complicates real-time PCR assays for detection and quantification of cytomegalovirus.
PMID 16207949·J Clin Microbiol·2005
8-other
Novel CLN3 mutation predicted to cause complete loss of protein function does not modify the classical JNCL phenotype.
PMID 16087292·Neurosci Lett·2005
8-other
A clinical rating scale for Batten disease: reliable and relevant for clinical trials.
PMID 16043799·Neurology·2005
8-other
Re: Prognostic significance of a short sequence insertion in the MCL-1 promoter in chronic lymphocytic leukemia.
PMID 16030309·J Natl Cancer Inst·2005
8-other
Gene symbol: CLN3. Disease: Juvenile neuronal ceroid lipofuscinosis (Batten disease).
PMID 15991331·Hum Genet·2005
8-other
Homogeneous amplification nucleobase quenching assay to detect the E474Q LCHAD deficiency mutation.
PMID 15857179·Genet Test·2005
8-other
Gene symbol: CLN3. Disease: juvenile neuronal ceroid lipofuscinosis (Batten disease).
PMID 15818814·Hum Genet·2005
8-other
Autoimmunity to glutamic acid decarboxylase in the neurodegenerative disorder Batten disease.
PMID 15728308·Neurology·2005
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 601 ELMWOOD AVE, UNIVERSITY OF ROCHESTER MEDICAL CENTER
ROCHESTER, NY 14642 - Phone
- (585) 273-2229
Quick Facts
- NPI
- 1932110780
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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