NicholasTylerGordenMD

Oncology • Boise, ID

Physician

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Office
500 W Fort St
Boise, ID 83702
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Education & Training

University of ColoradoFellowship, Hematology and Medical Oncology, 2016 - 2019
University of ColoradoResidency, Internal Medicine, 2013 - 2016
University of Washington School of MedicineClass of 2013

Certifications & Licensure

OR State Medical License 2019 - 2025
ID State Medical License 2019 - 2024
CO State Medical License 2013 - 2019
American Board of Internal Medicine Internal Medicine
American Board of Internal Medicine Hematology
American Board of Internal Medicine Medical Oncology

Publications & Presentations

PubMed

17 citations
Pre-Treatment Mutational and Transcriptomic Landscape of Responding Metastatic Melanoma Patients to Anti-PD1 Immunotherapy
Carol M. Amato, Jennifer D. Hintzsche, Keith Wells, Allison Applegate, Nicholas T. Gorden, Victoria M. Vorwald, Richard P Tobin, Kelsey W. Nassar, Yiqun G. Shellman, J...> ;Cancers. 2020 Jul 17
92 citations
Whole-exome sequencing identifies recurrent SF3B1 R625 mutation and comutation of NF1 and KIT in mucosal melanoma.
Jennifer D. Hintzsche, Nicholas T. Gorden, Carol M. Amato, Jihye Kim, Kelsey E. Wuensch, Steven E. Robinson, Allison J. Applegate, Kasey L. Couts, Theresa Medina, Keit...> ;Melanoma Research. 2017 Jun 1
190 citations
Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity.
Ruxandra Bachmann-Gagescu, Jennifer C. Dempsey, Ian G. Phelps, Brian J. O'Roak, Dana M. Knutzen, Tessa Rue, Gisele E. Ishak, Christine R. Isabella, Nicholas T. Gorden,...> ;Journal of Medical Genetics. 2015 Jun 19
108 citations
Mutations in 3 genes (MKS3, CC2D2A and RPGRIP1L) cause COACH syndrome (Joubert syndrome with congenital hepatic fibrosis)
, , , , , , , , , , , , , , , , , , , , , > ;Journal of Medical Genetics. 2010 Jan 1
149 citations
OFD1 is mutated in X-linked Joubert syndrome and interacts with LCA5-encoded lebercilin.
Karlien L.M. Coene, Ronald Roepman, Dan Doherty, Bushra Afroze, Hester Y. Kroes, Stef J.F. Letteboer, Lock Hock Ngu, Bartłomiej Budny, Erwin van Wijk, Nicholas T. Gord...> ;American Journal of Human Genetics. 2009 Oct 9
174 citations
CC2D2A Is Mutated in Joubert Syndrome and Interacts with the Ciliopathy-Associated Basal Body Protein CEP290
, , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , > ;American Journal of Human Genetics. 2008 Nov 17
8 citations
Transferrin fails to provide protection against Fas-induced hepatic injury in mice with deletion of functional transferrin-receptor type 2.
Vladimir Lesnikov, Nicholas T. Gorden, Nelson Fausto, Emily Spaulding, Jean S. Campbell, Howard M. Shulman, Robert E. Fleming, H. Joachim Deeg> ;Apoptosis. 2008 Jun 17
250 citations
Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome
Heleen H. Arts, Dan Doherty, Sylvia E. C. van Beersum, Melissa A. Parisi, Stef J.F. Letteboer, Nicholas T. Gorden, Theo A. Peters, Tina Märker, Krysta Voesenek, Aileen...> ;Nature Genetics. 2007 Jun 10
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