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Jeremy Prokop

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Assistant Professor

Michigan State University

United States

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About

Jeremy Prokop is an Assistant Professor at Michigan State University in the United States. His research focuses on expanding the understanding of genetic syndromes, exemplified by his recent work on Bachmann‐Bupp syndrome, which seeks to identify new cases and potential treatments. He is committed to advancing knowledge in the field of genetics through innovative research and collaboration.

Recent Grants

Grant: Close

Integrating response genetics into a clinical implementation model

Open Date: 2023-07-01

Close Date: 2026-06-30

Grant: Close

Using a Sequence-to-Structure-to-Function Approach to Functionally Characterize Protein Coding Missense Mutations in the Human and Rat Genomes

Open Date:

Close Date:

Grant: Close

Computational Expansion for a Protein Sequence-to-Structure-to-Function analysis for the Unknown Proteome and the ENCODE ChIP-Seq datasets

Open Date:

Close Date:

Articles (12)

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2026

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2025

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2025

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2025

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2025

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2025

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2025

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2025

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2025

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2025

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UNITED STATES

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Alison Kriegel

Professor

Augusta University

UNITED STATES

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Maximiliano Tamae Kakazu

Associate Professor

Michigan State University College of Human Medicine

UNITED STATES

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Anita Rauch

University of Zurich

SWITZERLAND

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Mara L Leimanis Laurens

Associate Professor (non-prefix)

Michigan State University

UNITED STATES

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Jeremy Prokop

Research Interests

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About

Recent Grants

Articles (12)

Tricuspid Valve Is Transcriptionally Active During Prolonged Pressure Overload, Right-Sided Heart Failure, and Valve Regurgitation.

Relative Quantitation of EFNA1 Expression in Mouse Heart Tissue Histologic Sections Using MALDI-MSI

Connecting genes to physiology: the first 25 years of Physiological Genomics

Methyl-CpG-binding domain as a protein interaction partner in promoter regulation and neurodevelopment through evolutionary expanded entanglement.

A research roadmap for SCN8A-related disorders: addressing knowledge gaps and aligning research priorities across stakeholders

The molecular architecture of severe pediatric traumatic brain injury: integrated omics reveal therapeutic pathways

Commentary: Childhood chronic neurodevelopmental disorders and the crisis of misaligned research funding

Opportunities for RNA sequencing in physiology: from big data to understanding homeostasis and heterogeneity.

Biological sex: why we should listen to genetics and lessons from race to guide precision medicine

SOX3 protein is associated with epithelial-mesenchymal transition (EMT) changes in human melanoma cell

From castaways to discoveries: unveiling treasures in skin RNAseq using a novel multidimensional data processing workflow including infection-host dynamics

Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome

Collaborators (14)

Stephen Duncan

Lisandra E. de Castro Brás

Daniel Vogt

Daniel Campbell

Daniel Woldring

Michael Garrett

Kimberly Kew

Allen W Cowley

Jitka Virag

Michael F. Hammer

Alison Kriegel

Maximiliano Tamae Kakazu

Anita Rauch

Mara L Leimanis Laurens

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