Dr. Ellis has over 25 years experience in the patent industry, she focuses her practice on patent prosecution and litigation with a particular emphasis in the chemical and life science fields. Dr. Ellis represents clients in post-grant proceedings and ex parte appeals before the USPTO Patent Trial and Appeal Board as well as patent infringement litigations at the Court of Appeals for the Federal Circuit and the International Trade Commission. She regularly serves as an expert witness in district court litigations involving inventorship, inequitable conduct, derivation, double-patenting, and priority disputes as well as USPTO procedure. She also conducts arbitration proceedings involving a wide variety of contractual and patent disputes.
Dr. Ellis has a strong life sciences background and over 20 years experience as a patent examiner and an Administrative Patent Judge at the U.S. Patent and Trademark Office. As a judge, Dr. Ellis authored over 250 ex parte and 50 inter partes decisions. Prior to becoming a lawyer, she was a Damon Runyon fellow at the Rockefeller University where she conducted research involving genetic material. Her experimental areas included molecular biology, particularly as it relates to the study of human malarial genes and immunology. She holds a patent directed to an antigenic malaria surface protein.
Dr. Ellis also serves as a panelist for the American Arbitration Association and is an Officer of the Board of the Giles S. Rich American Inn of Court.
In addition, Dr. Ellis has represented political asylum applicants and veterans pro bono before the Department of Homeland Security and the United States Court of Appeals for Veterans Claims and the Board of Veteran’s Appeals, respectively.
Inside The Minds, “The Changing Litigation Landscape From IPRs to Landmark Supreme Court Decision“ (2016).
Speaker, “Prosecution Tips to Strengthen a Case for Ex Parte Appeal,” AIPLA/USPTO Bench and Bar Conference, Alexandria, VA, June 15, 2016.
“Does Patent Protection for Personalized Medicine Still Exist in the USA?” Pharmaceutical Patent Analyst, Vol. 5, No. 2, February 2016.
“The Impact of Recent IPR Decisions and Events on the Biotech Industry,” Biotechnology Law Report, Vol. 34, No. 5, October 2015.
Speaker, "Personalized Medicine and Companion Diagnostics", Pharma Leaders IP Conference 2015, London, September 2015.
“Patent Protection on Biotechnology Inventions after Myriad,” J. Ellis, Ph.D. Genetic Engineering and Biotechnology News, April 2015.
Speaker, “Life Science Focus: Hatch-Waxman Litigation and Patentability Matters,” US Patent Forum 2015, Washington DC, March 18, 2015.
"Did Teva Alter the Standard for Invalidating a Patent for Indefiniteness?," J. Ellis, Ph.D. Dickinson Wright's Intellectual Property Legal News, Vol. 2, No. 1, March 2015.
“Arbitration: A Cost-Effective Alternative for Litigating Patent Disputes,” J. Ellis, Ph.D., Biotechnology Law Report, Vol. 32, No. 5, October 2013.
"The Supreme Court Holds Human Genes Are Unpatentable," J. Ellis, Ph.D. Dickinson Wright's Intellectual Property Legal News, Vol. 1, No. 4, July 25, 2013, also published In Dickinson Wright's Healthcare Legal News Vol. 3, No.4, August 7, 2013.
"On Patenting Genes," J. Ellis, Ph.D., The Scientist, Vol. 27, No.7, July 2013.
"Are Human Genes Patentable," J. Ellis, Ph.D., Dickinson Wright's Intellectual Property Legal News, Vol. 1, No. 2, March 22, 2013.
May 17, 2011, National Institutes of Health, lecture on Prometheus v. Mayo (Fed. Cir. 2010).
"Reexamination Strategy," J. Ellis, Ph.D. IPO Inter Partes Committee meeting, November 9, 2010.
"New USPTO Rules for Claim Examination and Continuing Applications," J. Ellis, PhD., Venable's IP Law Alert, September, 2007.
"USPTO Proposes New Rules of Ex Parte practice Before the Board of Appeals and Interferences," J. Ellis, Ph.D., Venable's IP Law Alert, August 2007.
"The Year in Review 2006, Pharmaceutical Biotech/Chemical Patent Law," Ludwig, Ellis and Gollln, Venable LLP publication.