Prof. Paul G Rothberg PH.D.
Geneticist | Clinical Molecular Genetics
601 Elmwood Ave University Of Roches Rochester NY, 14642About
Dr. Paul Rothberg practices Genetic Medicine in Rochester, NY. As a geneticist, Dr. Rothberg performs experiments and analyzes data to interpret the inheritance of different traits in patients. A geneticist evaluates, diagnoses, and manages patients? with hereditary conditions or congenital malformations, genetic risk calculations, and mutation analysis. Dr. Rothberg carries out studies, tests, and counsels patients with genetic diseases.
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Cytokine-mediated stimulation of laminin expression and cell-growth arrest in a human submandibular gland duct-cell line (HSG).
- Simultaneous detection of five mutations in the steroid 21-hydroxylase gene using nested allele-specific amplification.
- Processed pseudogene from the von Hippel-Lindau disease gene is located on human chromosome 1.
- Two distinct phenotypes caused by two different missense mutations in the same codon of the VHL gene.
- Diminished energy metabolism and enhanced apoptosis in livers of B6C3F1 mice treated with the antihepatocarcinogen rotenone.
- Diagnostic dilemma caused by overlapping features of Prader-Willi syndrome and trisomy 18 during infancy.
- Metabolic pathway for leucovorin.
- Gene symbol: VHL. Disease: pancreatic cancer.
- Gene symbol: VHL. Disease: Von-Hippel-Lindau syndrome.
- Imatinib: resisting the resistance.
- Extended electrophoresis resolves the dystrophin gene 5.2-kbp cDMD4-5a/HindIII fragment into two bands.
- Homogeneous polymerase chain reaction nucleobase quenching assay to detect the 1-kbp deletion in CLN3 that causes Batten disease.
- Liver transplantation for type 1 primary hyperoxaluria as a cure for combined thrombophilia.
- Autoimmunity to glutamic acid decarboxylase in the neurodegenerative disorder Batten disease.
- Gene symbol: CLN3. Disease: juvenile neuronal ceroid lipofuscinosis (Batten disease).
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