Peter L Nagy
Scientific Tracks Abstracts: Commun Disord Deaf Stud Hearing Aids
Our Laboratory of Personalized Genomic Medicine (LPGM) at Columbia University Medical Center started to offer clinical
whole exome sequencing (WES) in January 2013. We processed and issued reports on over 500 constitutional cases including
approximately 70 cases involving hearing loss. Next-generation sequencing in the clinical practice allows for a critical review of
the literature describing the pathogenicity of specific mutations or the disease relatedness of specific genes and also provides an
important discovery tool for new disease genes and disease causing mutations. Because of the large volume and complex nature of
the data obtained from large panels and whole exome sequencing testing, the management of the data in a transparent, yet powerful
analytical framework is the key to a successful clinical operation. We have provided diagnosis for constitutional patients in about one
third of the cases we analyzed. The full potential for discovery of new disease associated genes and disease causing mutations can only
be realized if there is a tight collaborative effort between the clinicians performing the interpretation and structural biologists and
analytical chemists and cell biologists who can help predict and verify the effects of variants identified.
Peter L Nagy has received his MD degree from the University of Pecs, Hungary in 1989. He has obtained his PhD at Purdue University in Biochemistry under the mentorship
of Dr. Howard Zalkin and his Anatomic and Molecular Genetic Pathology training at Stanford University working on the MLL gene with Michael Cleary and Roger Kornberg.
His research is on neurodegenerative disorders like ALS and young adult onset ataxias (AOA2). He built and overseas the clinical next-generation sequencing facility in the
Laboratory of Personalized Genomic Medicine at Columbia University Medical Center.