Author

Newaz I. Ahmed

The University of Texas Southwestern Medical CenterORCID 0000-0002-8932-5877Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Newaz I. Ahmed1 paper · Icahn School of Medicine at Mount Sinai

Biology Disciplines

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Neuroscience· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:mouse· 3 Approach:experimental assay· 1 Approach:statistical model· 1

Frequent Co-Authors

Ashwinikumar KulkarniiD· 2 shared Geneviève KonopkaiD· 2 shared Jay R. GibsoniD· 2 shared Nitin KhandelwaliD· 2 shared Ashley G. AndersoniD· 1 shared Carlos M. CastorenaiD· 1 shared Emily OhiD· 1 shared Jennifer A. MohawkiD· 1 shared

Activity by Year

2017-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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2 shared papersNeuroscience

Ashwinikumar KulkarniORCID

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3 papers

Recent·Most cited

FOXP1 regulates the development of excitatory synaptic inputs onto striatal neurons and induces phenotypic reversal with reinstatement

Nitin Khandelwal, Ashwinikumar Kulkarni, Newaz I. Ahmed, Matthew J. Harper, Geneviève Konopka, Jay R. Gibson

This study shows FOXP1 regulates glutamatergic input development in striatal neurons, with potential therapeutic implications for FOXP1 syndrome.

Science Advances · May 3, 2024Peer-reviewedNeuroscience

Compensation between FOXP transcription factors maintains proper striatal function

Newaz I. Ahmed, Nitin Khandelwal, Ashley G. Anderson, Emily Oh, Rachael M. Vollmer, Ashwinikumar Kulkarni, Jay R. Gibson, Geneviève Konopka

The paper shows that Foxp1 and Foxp2 compensate for each other in D1-SPNs, and their loss causes motor and social deficits, which can be reversed by re-expressing Foxp1.

Cell Reports · May 1, 2024Peer-reviewedNeuroscience

Asleep at the Wheel: Forward Genetic ENU Mutagenesis Screen for Mouse Models of Chronic Fatigue Identifies a Mutation in Slc2a4 (GLUT4)

Marleen H. M. de Groot, Carlos M. Castorena, Vivek Kumar, Jennifer A. Mohawk, Newaz I. Ahmed, Joseph S. Takahashi

The paper identifies a mutation in Slc2a4 (GLUT4) in mice that causes chronic fatigue-like behaviors through a forward genetic screen.

bioRxiv · Aug 7, 2017 · PreprintGenetics