Prenatal stress unmasks behavioral phenotypes in genetic mouse models of neurodevelopmental disorders

por Harper, Kathryn M., Harp, Samuel J., Moy, Sheryl S.
Publicado 2023

Mouse Models of 22q11.2-Associated Autism Spectrum Disorder

por Hiroi, Noboru, Hiramoto, Takeshi, Harper, Kathryn M., Suzuki, Go, Boku, Shuken
Publicado 2012

Stress and Withdrawal from Chronic Ethanol Induce Selective Changes in Neuroimmune mRNAs in Differing Brain Sites

por Knapp, Darin J., Harper, Kathryn M., Whitman, Buddy A., Zimomra, Zachary, Breese, George R.
Publicado 2016

Hypothesis: genetic and epigenetic risk factors interact to modulate vulnerability and resilience to FASD

por Tunc-Ozcan, Elif, Sittig, Laura J., Harper, Kathryn M., Graf, Evan N., Redei, Eva E.
Publicado 2014

Phenotyping CCL2 Containing Central Amygdala Neurons Controlling Alcohol Withdrawal-Induced Anxiety

por Harper, Kathryn M., Knapp, Darin J., Todd, Caroline A., Balan, Irina, Aurelian, Laure, Criswell, Hugh E., Breese, George R.
Publicado 2020

Early life sleep disruption potentiates lasting sex-specific changes in behavior in genetically vulnerable Shank3 heterozygous autism model mice

por Lord, Julia S., Gay, Sean M., Harper, Kathryn M., Nikolova, Viktoriya D., Smith, Kirsten M., Moy, Sheryl S., Diering, Graham H.
Publicado 2022

Developmental pyrethroid exposure and age influence phenotypes in a Chd8 haploinsufficient autism mouse model

por Jiménez, Jessica A., Simon, Jeremy M., Hu, Wenxin, Moy, Sheryl S., Harper, Kathryn M., Liu, Chih-Wei, Lu, Kun, Zylka, Mark J.
Publicado 2022

Loss of GABA co-transmission from cholinergic neurons impairs behaviors related to hippocampal, striatal, and medial prefrontal cortex functions

por Goral, R. Oliver, Harper, Kathryn M., Bernstein, Briana J., Fry, Sydney A., Lamb, Patricia W., Moy, Sheryl S., Cushman, Jesse D., Yakel, Jerrel L.
Publicado 2022

RNA-binding deficient TDP-43 drives cognitive decline in a mouse model of TDP-43 proteinopathy

por Necarsulmer, Julie C, Simon, Jeremy M, Evangelista, Baggio A, Chen, Youjun, Tian, Xu, Nafees, Sara, Marquez, Ariana B, Jiang, Huijun, Wang, Ping, Ajit, Deepa, Nikolova, Viktoriya D, Harper, Kathryn M, Ezzell, J Ashley, Lin, Feng-Chang, Beltran, Adriana S, Moy, Sheryl S, Cohen, Todd J
Publicado 2023

Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome

por Cousin, Margot A., Creighton, Blake A., Breau, Keith A., Spillmann, Rebecca C., Torti, Erin, Dontu, Sruthi, Tripathi, Swarnendu, Ajit, Deepa, Edwards, Reginald J., Afriyie, Simone, Bay, Julia C., Harper, Kathryn M., Beltran, Alvaro A., Munoz, Lorena J., Rodriguez, Liset Falcon, Stankewich, Michael C., Person, Richard E., Si, Yue, Normand, Elizabeth A., Blevins, Amy, May, Alison S., Bier, Louise, Aggarwal, Vimla, Mancini, Grazia M. S., van Slegtenhorst, Marjon A., Cremer, Kirsten, Becker, Jessica, Engels, Hartmut, Aretz, Stefan, MacKenzie, Jennifer J., Brilstra, Eva, van Gassen, Koen L. I., van Jaarsveld, Richard H., Oegema, Renske, Parsons, Gretchen M., Mark, Paul, Helbig, Ingo, McKeown, Sarah E., Stratton, Robert, Cogne, Benjamin, Isidor, Bertrand, Cacheiro, Pilar, Smedley, Damian, Firth, Helen V., Bierhals, Tatjana, Kloth, Katja, Weiss, Deike, Fairley, Cecilia, Shieh, Joseph T., Kritzer, Amy, Jayakar, Parul, Kurtz-Nelson, Evangeline, Bernier, Raphael A., Wang, Tianyun, Eichler, Evan E., van de Laar, Ingrid M. B. H., McConkie-Rosell, Allyn, McDonald, Marie T., Kemppainen, Jennifer, Lanpher, Brendan C., Schultz-Rogers, Laura E., Gunderson, Lauren B., Pichurin, Pavel N., Yoon, Grace, Zech, Michael, Jech, Robert, Winkelmann, Juliane, Beltran, Adriana S., Zimmermann, Michael T., Temple, Brenda, Moy, Sheryl S., Klee, Eric W., Tan, Queenie K.-G., Lorenzo, Damaris N.
Publicado 2021