Nik Jorstad, Ph.D.
Nik joined the at the Allen Institute in May 2019 as a Scientist working on the Human Cell Types team. His research is focused on developing analytical tools and drawing biological insight to characterize all the cells that make up the human brain.
Nik received his BA in Biochemistry from the University of Washington in June 2012. After graduating, Nik began his career as a research scientist in the labs of Drs. Thomas Montine and C. Dirk Keene at the University of Washington studying Alzheimer’s, Parkinson’s, and other neurodegenerative disorders. During these 3 years, Nik developed skills in automated image analyses, electrophysiology, surgical techniques, and various molecular biological assays, as well as microscopy expertise. He was also an autopsy technician for 5 years and performed over 100 human brain removals and dissections in support of the ADRC, ACT, and PANUC studies, among others.
Following his research scientist position, Nik joined the Molecular Medicine and Mechanisms of Disease PhD program in the Department of Pathology at the University of Washington. His dissertation work was performed in the lab of Dr. Thomas Reh studying mammalian retinal regeneration. During his PhD, Nik gained expertise in various molecular biological techniques, including epigenetic assays, single-cell RNA-sequencing, and advanced confocal and electron microscopy. He earned his PhD in May 2019 and was the first to show that adult mice can regenerate functional retinal neurons from Muller glial cells.
I am particularly interested in characterizing the healthy brain to better understand what goes wrong during disease. The Institute is currently undertaking the monumental task of characterizing every cell type in the human brain using single-cell genomics, electrophysiology, and morphology. By building a reference of the healthy human brain, future research efforts might be able to pin disease-related genes/variants to a specific cell type and open the door to targeted treatments of brain disease. On a more technical level, I am keenly interested in why similar broad classes of brain cells have different transcriptomic profiles and how these divergent features might inform the functional roles of these cells in circuits and the workings of the brain.
- Human Cell Types
Annals of Medicine and Surgery
March 28, 2019
Bingham JR, Kniery KR, Jorstad NL, Horkayne-Szakaly I, Hoffer ZS, Salgar SK
November 9, 2017
Miller JA, Guillozet-Bongaarts A, Gibbons LE, Postupna N, Renz A, E Beller AE, Sunkin SM, Ng L, Rose SE, Smith KA, Szafer A, Barber C, Bertagnolli D, Bickley K, Brouner K, Caldejon S, Chapin M, Chua ML, Coleman NM, Cudaback E, Cuhaciyan C, Dalley RA, Dee N, Desta T, Dolbeare TA, Dotson NI, Fisher M, Gaudreault N, Gee G, Gilbert TL, Goldy J, Griffin F, Habel C, Haradon Z, Hejazinia N, Hellstern LL, Horvath S, Howard K, Howard R, Johal J, L Jorstad NL, Josephsen SR, Kuan CL, Lai F, Lee E, Lee F, Lemon T, Li X, Marshall DA, Melchor J, Mukherjee S, Nyhus J, Pendergraft J, Potekhina L, Rha EY, Rice S, Rosen D, Sapru A, Schantz A, Shen E, Sherfield E, Shi S, Sodt AJ, Thatra N, Tieu M, Wilson AM, Montine TJ, Larson EB, Bernard A, Crane PK, Ellenbogen RG, Keene CD, Lein E
November 17, 2017
Wohl SG, Jorstad NL, Levine EM, Reh TA