Author

Kristi Niblo

Icahn School of Medicine at Mount Sinai

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

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Neuroscience· 3

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:rat· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Organism:mouse· 1 Approach:statistical model· 1

Frequent Co-Authors

Hala Harony‐NicolasiD· 2 shared Joseph D. BuxbaumiD· 2 shared Silvia De RubeisiD· 2 shared Andrea BoitnottiD· 1 shared Andrew Browne· 1 shared Arthur LefèvreiD· 1 shared Carla E. M. GoldeniD· 1 shared Daniele Di MarinoiD· 1 shared

Activity by Year

2019-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersNeuroscience

Hala Harony‐NicolasORCID

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3 papers

Recent·Most cited

Oxytocin activity in the Paraventricular and Supramammillary Nuclei of the Hypothalamus is Essential for Social Recognition Memory in Rats

Keerthi Thirtamara Rajamani, Marie Barbier, Arthur Lefèvre, Kristi Niblo, Nicholas Cordero, Shai Netser, Valery Grinevich, Shlomo Wagner, Hala Harony‐Nicolas

This study identifies the supramammillary nucleus as a target of PVH oxytocin neurons and shows its necessity for social recognition memory in rats.

bioRxiv · May 23, 2022 · PreprintNeuroscience

Developmental and behavioral phenotypes in a new mouse model of DDX3X syndrome

Andrea Boitnott, Marta García-Forn, Dévina C. Ung, Kristi Niblo, Danielle Mendonca, Yeaji Park, Michael Flores, Sylvia Maxwell, Jacob Ellegood, Lily R. Qiu, Dorothy E. Grice, Jason P. Lerch, Mladen‐Roko Rašin, Joseph D. Buxbaum, Elodie Drapeau, Silvia De Rubeis

This study develops a Ddx3x haploinsufficient mouse model to investigate DDX3X syndrome, finding developmental and behavioral abnormalities linked to brain structural changes.

Biological Psychiatry · Jun 7, 2021Peer-reviewedNeuroscience

Disruption of the KH1 domain of Fmr1 leads to transcriptional alterations and attentional deficits in rats

Carla E. M. Golden, Michael S. Breen, Lacin Koro, Sankalp Sonar, Kristi Niblo, Andrew Browne, Natalie Burlant, Daniele Di Marino, Silvia De Rubeis, Mark G. Baxter, Joseph D. Buxbaum, Hala Harony‐Nicolas

This study shows that deleting the KH1 domain of Fmr1 in rats causes attention deficits and transcriptional changes in the medial prefrontal cortex, similar to FXS, and identifies potential therapeutic targets.

Cerebral Cortex · Feb 6, 2019Peer-reviewedNeuroscience