Professor of Clinical Genetics, University Alabama
Medical Genetics
Dr. Bruce R. Korf, MD
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Bruce R. Korf, MD is an expert in the field of Medical Genetics. He graduated from Weill Cornell Medical College of Cornell University. Weill Cornell Medical College of Cornell University is ranked 18/49 in Research/PrimaryCare. He has 10 awards "America's Top Doctors", "Award for Excellence in Human Genetics Education", "Honoree", "Courtmanche Award", "President's Award", "Von Recklinghausen Award", "Von Meyer Traveling Fellowship", "PhiBetaKappaandPhiKappaPhi", "BodmanScholarandCornellNationalScholar" and "Fellow (FAAP)". Bruce Korf is also a published doctor. He has 53 paper published. The most recent paper is: High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype-Phen... Bruce Korf is registered with Medicare and accepts Medicare payments.
Publications
- High Incidence of Noonan Syndrome Features Including Short Stature and Pulmonic Stenosis in Patients carrying NF1 Missense Mutations Affecting p.Arg1809: Genotype-Phen...
- Clinical response to bevacizumab in schwannomatosis.
- Sirolimus for progressive neurofibromatosis type 1-associated plexiform neurofibromas: a Neurofibromatosis Clinical Trials Consortium phase II study.
- Framework for development of physician competencies in genomic medicine: report of the Competencies Working Group of the Inter-Society Coordinating Committee for Physi...
- CTF meeting 2012: Translation of the basic understanding of the biology and genetics of NF1, NF2, and schwannomatosis toward the development of effective therapies.
- Phase 2 randomized, flexible crossover, double-blinded, placebo-controlled trial of the farnesyltransferase inhibitor tipifarnib in children and young adults with neur...
- Prenatal whole-genome sequencing--is the quest to know a fetus's future ethical?
- Germline loss-of-function mutations in LZTR1 predispose to an inherited disorder of multiple schwannomas.
- Integration of genomics into medical practice.
- Response to townsend et Al.
- Genomic medicine: educational challenges.
- ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
- Genomic Privacy in the Information Age.
- New approaches to molecular diagnosis.
- Optimizing biologically targeted clinical trials for neurofibromatosis.
- Update from the 2011 International Schwannomatosis Workshop: From genetics to diagnostic criteria.
- Implementing genomic medicine in the clinic: the future is here.
- Overview of molecular genetic diagnosis.
- Consensus recommendations for current treatments and accelerating clinical trials for patients with neurofibromatosis type 2.
- Competencies for the physician medical geneticist in the 21st century.
- Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or...
- Genetics and genomics education: the next generation.
- Back to the future: proceedings from the 2010 NF Conference.
- Phenotypic variability among café-au-lait macules in neurofibromatosis type 1.
- Proceedings from the 2009 genetic syndromes of the Ras/MAPK pathway: From bedside to bench and back.
- AsktheGeneticist: five years of online experience.
- Neurofibromatosis type 1 revisited.
- Report of the Banbury Summit Meeting on the evolving role of the medical geneticist, February 12-14, 2006.
- Developing a national collaborative study system for rare genetic diseases.
- Characterization of apparently balanced chromosomal rearrangements from the developmental genome anatomy project.
- Genetic testing in cardiovascular disease.
- Disruption of diacylglycerol kinase delta (DGKD) associated with seizures in humans and mice.
- Impact of neurofibromatosis 1 on Quality of Life: a cross-sectional study of 176 American cases.
- Genetics training in the genomic era.
- Psychiatric genetics: a survey of psychiatrists' knowledge, opinions, and practice patterns.
- Report of Banbury Summit meeting on training of physicians in medical genetics, October 20-22, 2004.
- Genetics in medical practice: the need for ultimate makeover.
- Case records of the Massachusetts General Hospital. Case 13-2005. A 48-year-old man with weakness of the limbs and multiple tumors of spinal Nerves.
- Outline of a medical genetics curriculum for internal medicine residency training programs.
- Basic genetics.
- Deletion of the SLUG (SNAI2) gene results in human piebaldism.
- Rib defects in patterns of multiple malformations: a retrospective review and phenotypic analysis of 47 cases.
- Early childhood hearing loss: clinical and molecular genetics. An educational slide set of the American College of Medical Genetics.
- Human chromosome 7: DNA sequence and biology.
- Genetics and medical practice: new approaches to "old" disorders.
- Integration of genetics into clinical teaching in medical school education.
- Genetics in medical practice.
- Clinical features and pathobiology of neurofibromatosis 1.
- Determination of end points for treatment of neurofibromatosis 1.
- Cardiovascular disease in neurofibromatosis 1: report of the NF1 Cardiovascular Task Force.
- Case vignette: genetic secrets.
- Neurofibromatosis.
Schools
Joan Sanford I Weill Medical College Of Cornell University
Children39s Hospital
Conditions Treated
- Nerve Sheath Tumors
- Tuberous Sclerosis
Doctors Specialties
- Clinical Cytogenetics
- Clinical Genetics
- Clinical Molecular Genetics
- Pediatric Neurology
- Pediatrics
- Medical Genetics
Accepted Insurances
- Choice Plus POS II
- Blue Card PPO
- Dental Blue 100/200/300
- Cigna HMO
- Cigna PPO
- Great West Healthcare-Cigna PPO
- Open Access Plus
- Commercial Insurance Company
- First Health (Coventry Health Care) PPO
- Medicare MCR
- MultiPlan PPO
- Choice Plus POS
- Navigate POS
- Options PPO
- United Healthcare
Awards
- America's Top Doctors
- Award for Excellence in Human Genetics Education
- Honoree
- Courtmanche Award
- President's Award
- Von Recklinghausen Award
- Von Meyer Traveling Fellowship
- Phi Beta Kappa and Phi Kappa Phi
- Bodman Scholar and Cornell National Scholar
- Fellow (FAAP)
Education
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Boston Children's Hospital -
Weill Cornell Medical College of Cornell University
Hospital
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University of Alabama Hospital
Drug Facts
| NPI NUMBER | 1306874409 | |
| NPPES Provider LastName | KORF | |
| NPPES Provider FirstName | BRUCE | |
| NPPES Provider ZIPCode | 352332032 | |
| NPPES Provider State | AL | |
| Specialty Description | Pediatric Medicine | |
| Total Claim Count | 13.0 | |
| Distinct Opioid Count | 0.0 | |
| Opioid Claim Count | 0.0 | |
| Percent Opioid Claims | 0.0 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1306874409 |
| Last Name Of The Provider | KORF |
| First Name Of The Provider | BRUCE |
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