Jeremy W Prokop (Jeremy Prokop)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 10

Top Venues

eLife

American journal of medical genetics. Part A

The Journal of biological chemistry

Journal of proteome research

Michigan State University

The University of Akron (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Michigan State University Feb 01 2018

United States

Assistant Professor :: Pediatrics and Human Development

Education History

The University of Akron

United States

PHD :: Integrated Biosciences

Publications

Tariq Zaman, Daniel Vogt, Jeremy W Prokop, Qusai Abdulkhaliq Alsabia, Gabriel Simms, April Stafford, Bryan W Luikart, Michael R Williams
Kit Ligand and Kit receptor tyrosine kinase sustain synaptic inhibition of Purkinje cells. eLife 12 (2024)
Tariq Zaman, Daniel Vogt, Jeremy W Prokop, Qusai Abdulkhaliq Alsabia, Gabriel Simms, April Stafford, Bryan W Luikart, Michael R Williams
Kit Ligand and Kit receptor tyrosine kinase sustain synaptic inhibition of Purkinje cells. eLife 12 (2024)
Tariq Zaman, Daniel Vogt, Jeremy W Prokop, Qusai Abdulkhaliq Alsabia, Gabriel Simms, April Stafford, Bryan W Luikart, Michael R Williams
Kit Ligand and Kit receptor tyrosine kinase sustain synaptic inhibition of Purkinje cells. eLife 12 (2024)
Ruchir Gupta, Mara L Leimanis, Marie Adams, André S Bachmann, Katie L Uhl, Caleb P Bupp, Nicholas L Hartog, Eric J Kort, Rosemary Olivero, Sarah S Comstock, Dominic J Sanfilippo, Sophia Y Lunt, Jeremy W Prokop, Surender Rajasekaran
Balancing precision versus cohort transcriptomic analysis of acute and recovery phase of viral bronchiolitis. American journal of physiology. Lung cellular and molecular physiology 320 (6) (2021)
Elizabeth A VanSickle, Julianne Michael, André S Bachmann, Surender Rajasekaran, Jeremy W Prokop, Ruben Kuzniecky, Floris C Hofstede, Katharina Steindl, Anita Rauch, Mark H Lipson, Caleb P Bupp
Expanding the phenotype: Four new cases and hope for treatment in Bachmann-Bupp syndrome. American journal of medical genetics. Part A 185 (11) (2021)
Jacob G Charron, Angel Hernandez, Stephanie M Bilinovich, Daniel L Vogt, Laura A Bedinger, Laurie H Seaver, Michael Williams, Seth Devries, Daniel B Campbell, Caleb P Bupp, Jeremy W Prokop
N-methyl-d-aspartate (NMDA) receptor genetics: The power of paralog homology and protein dynamics in defining dominant genetic variants. American journal of medical genetics. Part A (2021)
Olivia Sirpilla, Jacob Bauss, Ruchir Gupta, Adam Underwood, Dinah Qutob, Tom Freeland, Caleb Bupp, Joseph Carcillo, Nicholas Hartog, Surender Rajasekaran, Jeremy W Prokop
SARS-CoV-2-Encoded Proteome and Human Genetics: From Interaction-Based to Ribosomal Biology Impact on Disease and Risk Processes. Journal of proteome research 19 (11) (2020)
Ruchir Gupta, Jacob Charron, Cynthia L Stenger, Jared Painter, Hunter Steward, Taylor W Cook, William Faber, Austin Frisch, Eric Lind, Jacob Bauss, Xiaopeng Li, Olivia Sirpilla, Xavier Soehnlen, Adam Underwood, David Hinds, Michele Morris, Neil Lamb, Joseph A Carcillo, Caleb Bupp, Bruce D Uhal, Surender Rajasekaran, Jeremy W Prokop
SARS-CoV-2 (COVID-19) structural and evolutionary dynamicome: Insights into functional evolution and human genomics. The Journal of biological chemistry 295 (33) (2020)
J Nicholas Cochran, Emily Carol McKinley, Meagan Cochran, Michelle D Amaral, Bryan A Moyers, Brittany N Lasseigne, David E Gray, James M J Lawlor, Jeremy W Prokop, Ethan G Geier, James M Holt, Michelle L Thompson, J Scott Newberry, Jennifer S Yokoyama, Elizabeth A Worthey, David S Geldmacher, Marissa Natelson Love, Gregory M Cooper, Richard M Myers, Erik D Roberson
Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles. Cold Spring Harbor molecular case studies 5 (6) (2019)
Susan M Hiatt, Matthew B Neu, Ryne C Ramaker, Andrew A Hardigan, Jeremy W Prokop, Miroslava Hancarova, Darina Prchalova, Marketa Havlovicova, Jan Prchal, Viktor Stránecký, Dwight K C Yim, Zöe Powis, Boris Keren, Caroline Nava, Mignot Cyril, Marlène Rio, Anya Revah-Politi, Parisa Hemati, Nicholas Stong, Alejandro D Iglesias, Sharon F Suchy, Rebecca Willaert, Ingrid M Wentzensen, Patricia G Wheeler, Lauren Brick, Mariya Kozenko, Anna C E Hurst, James W Wheless, Yves Lacassie, Richard M Myers, Gregory S Barsh, Zdenek Sedlacek, Gregory M Cooper
De novo mutations in the GTP/GDP-binding region of RALA, a RAS-like small GTPase, cause intellectual disability and developmental delay. PLoS genetics 14 (11) (2018)

Jeremy W Prokop.css-eqlu8i{font-size:small;padding-left:4px;} (Jeremy Prokop)

Publication Activity (10 Years)

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Jeremy W Prokop (Jeremy Prokop)