CPT2 Deficiency Modeled in Zebrafish: Abnormal Neural Development, Electrical Activity, Behavior, and Schizophrenia-Related Gene Expression
Baker, Carly E, Marta, Aaron G, Zimmerman, Nathan D, Korade, Zeljka, Mathy, Nicholas W, Wilton, Delaney, Simeone, Timothy, Kochvar, Andrew, Kramer, Kenneth L, Stessman, Holly A. F, Shibata, Annemarie
Published in Biomolecules (Basel, Switzerland) (01.08.2024)
Published in Biomolecules (Basel, Switzerland) (01.08.2024)
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Journal Article
Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity
Coe, Bradley P, Stessman, Holly A F, Sulovari, Arvis, Geisheker, Madeleine R, Bakken, Trygve E, Lake, Allison M, Dougherty, Joseph D, Lein, Ed S, Hormozdiari, Fereydoun, Bernier, Raphael A, Eichler, Evan E
Published in Nature genetics (01.01.2019)
Published in Nature genetics (01.01.2019)
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Journal Article
Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibility
Nuttle, Xander, Giannuzzi, Giuliana, Duyzend, Michael H, Schraiber, Joshua G, Narvaiza, Iñigo, Sudmant, Peter H, Penn, Osnat, Chiatante, Giorgia, Malig, Maika, Huddleston, John, Benner, Chris, Camponeschi, Francesca, Ciofi-Baffoni, Simone, Stessman, Holly A F, Marchetto, Maria C N, Denman, Laura, Harshman, Lana, Baker, Carl, Raja, Archana, Penewit, Kelsi, Janke, Nicolette, Tang, W Joyce, Ventura, Mario, Banci, Lucia, Antonacci, Francesca, Akey, Joshua M, Amemiya, Chris T, Gage, Fred H, Reymond, Alexandre, Eichler, Evan E
Published in Nature (London) (11.08.2016)
Published in Nature (London) (11.08.2016)
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Journal Article
KMT5B is required for early motor development
Hulen, Jason, Kenny, Dorothy, Black, Rebecca, Hallgren, Jodi, Hammond, Kelley G, Bredahl, Eric C, Wickramasekara, Rochelle N, Abel, Peter W, Stessman, Holly A F
Published in Frontiers in genetics (12.08.2022)
Published in Frontiers in genetics (12.08.2022)
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The evolution and population diversity of human-specific segmental duplications
Dennis, Megan Y, Harshman, Lana, Nelson, Bradley J, Penn, Osnat, Cantsilieris, Stuart, Huddleston, John, Antonacci, Francesca, Penewit, Kelsi, Denman, Laura, Raja, Archana, Baker, Carl, Mark, Kenneth, Malig, Maika, Janke, Nicolette, Espinoza, Claudia, Stessman, Holly A F, Nuttle, Xander, Hoekzema, Kendra, Lindsay-Graves, Tina A, Wilson, Richard K, Eichler, Evan E
Published in Nature ecology & evolution (01.01.2017)
Published in Nature ecology & evolution (01.01.2017)
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Epidemiologic and Genomic Analysis of the Severe Acute Respiratory Syndrome Coronavirus 2 Epidemic in the Nebraska Region of the United States, March 2020-2021
Siedlik, Jacob A, Watson, Cynthia J, Raine, Morgan A, Cheng, Anne V, Goering, Richard V, Stessman, Holly A F, Belshan, Michael
Published in Frontiers in microbiology (18.05.2022)
Published in Frontiers in microbiology (18.05.2022)
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Journal Article
Histone 4 Lysine 20 Methylation: A Case for Neurodevelopmental Disease
Wickramasekara, Rochelle N, Stessman, Holly A F
Published in Biology (Basel, Switzerland) (03.03.2019)
Published in Biology (Basel, Switzerland) (03.03.2019)
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Journal Article
Associations between Familial Rates of Psychiatric Disorders and De Novo Genetic Mutations in Autism
Bernier, Raphael, Stessman, Holly A. F., Gerdts, Jennifer, Hudac, Caitlin M., Ward, Tracey, Luhrs, Kyleen, Eichler, Evan E.
Published in Autism Research and Treatment (01.01.2017)
Published in Autism Research and Treatment (01.01.2017)
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Journal Article
Schizophrenic Psychosis Symptoms in a Background of Mild-To-Moderate Carnitine Palmitoyltransferase II Deficiency: A Case Report
Wickramasekara, Rochelle N., Lookian, Pashayar P., Ngo, Jeannie, Shibata, Annemarie, Stessman, Holly A. F.
Published in Reports (MDPI) (01.12.2020)
Published in Reports (MDPI) (01.12.2020)
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Journal Article
Bortezomib resistance can be reversed by induced expression of plasma cell maturation markers in a mouse in vitro model of multiple myeloma
Stessman, Holly A F, Mansoor, Aatif, Zhan, Fenghuang, Linden, Michael A, Van Ness, Brian, Baughn, Linda B
Published in PloS one (2013)
Published in PloS one (2013)
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Exploring the heterogeneity of neural social indices for genetically distinct etiologies of autism
Hudac, Caitlin M, Stessman, Holly A F, DesChamps, Trent D, Kresse, Anna, Faja, Susan, Neuhaus, Emily, Webb, Sara Jane, Eichler, Evan E, Bernier, Raphael A
Published in Journal of neurodevelopmental disorders (26.05.2017)
Published in Journal of neurodevelopmental disorders (26.05.2017)
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Journal Article
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases
Stessman, Holly A F, Xiong, Bo, Coe, Bradley P, Wang, Tianyun, Hoekzema, Kendra, Fenckova, Michaela, Kvarnung, Malin, Gerdts, Jennifer, Trinh, Sandy, Cosemans, Nele, Vives, Laura, Lin, Janice, Turner, Tychele N, Santen, Gijs, Ruivenkamp, Claudia, Kriek, Marjolein, van Haeringen, Arie, Aten, Emmelien, Friend, Kathryn, Liebelt, Jan, Barnett, Christopher, Haan, Eric, Shaw, Marie, Gecz, Jozef, Anderlid, Britt-Marie, Nordgren, Ann, Lindstrand, Anna, Schwartz, Charles, Kooy, R Frank, Vandeweyer, Geert, Helsmoortel, Celine, Romano, Corrado, Alberti, Antonino, Vinci, Mirella, Avola, Emanuela, Giusto, Stefania, Courchesne, Eric, Pramparo, Tiziano, Pierce, Karen, Nalabolu, Srinivasa, Amaral, David G, Scheffer, Ingrid E, Delatycki, Martin B, Lockhart, Paul J, Hormozdiari, Fereydoun, Harich, Benjamin, Castells-Nobau, Anna, Xia, Kun, Peeters, Hilde, Nordenskjöld, Magnus, Schenck, Annette, Bernier, Raphael A, Eichler, Evan E
Published in Nature genetics (01.04.2017)
Published in Nature genetics (01.04.2017)
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Journal Article
De novo genic mutations among a Chinese autism spectrum disorder cohort
Wang, Tianyun, Guo, Hui, Xiong, Bo, Stessman, Holly A F, Wu, Huidan, Coe, Bradley P, Turner, Tychele N, Liu, Yanling, Zhao, Wenjing, Hoekzema, Kendra, Vives, Laura, Xia, Lu, Tang, Meina, Ou, Jianjun, Chen, Biyuan, Shen, Yidong, Xun, Guanglei, Long, Min, Lin, Janice, Kronenberg, Zev N, Peng, Yu, Bai, Ting, Li, Honghui, Ke, Xiaoyan, Hu, Zhengmao, Zhao, Jingping, Zou, Xiaobing, Xia, Kun, Eichler, Evan E
Published in Nature communications (08.11.2016)
Published in Nature communications (08.11.2016)
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Journal Article
ATF3 Coordinates Antitumor Synergy between Epigenetic Drugs and Protein Disulfide Isomerase Inhibitors
Duncan, Ravyn M, Reyes, Leticia, Moats, Katelyn, Robinson, Reeder M, Murphy, Sara A, Kaur, Balveen, Stessman, Holly A F, Dolloff, Nathan G
Published in Cancer research (Chicago, Ill.) (15.08.2020)
Published in Cancer research (Chicago, Ill.) (15.08.2020)
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Journal Article
GluN2D Subunit in Parvalbumin Interneurons Regulates Prefrontal Cortex Feedforward Inhibitory Circuit and Molecular Networks Relevant to Schizophrenia
Gawande, Dinesh Y., S. Narasimhan, Kishore Kumar, Shelkar, Gajanan P., Pavuluri, Ratnamala, Stessman, Holly A.F., Dravid, Shashank M.
Published in Biological psychiatry (1969) (15.08.2023)
Published in Biological psychiatry (1969) (15.08.2023)
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Journal Article
Human placental lactogen (human chorionic somatomammotropin) and oxytocin during pregnancy: Individual patterns and associations with maternal-fetal attachment, anxiety, and depression
Coté, John J., Coté, Remington D., Dilsaver, Danielle B., Stessman, Holly A.F., Watson, Cynthia, Handelzalts, Jonathan, Doehrman, Pooja, Walters, Ryan W., Badura-Brack, Amy S.
Published in Hormones and behavior (01.07.2024)
Published in Hormones and behavior (01.07.2024)
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Journal Article
De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder
Küry, Sébastien, Besnard, Thomas, Ebstein, Frédéric, Khan, Tahir N., Gambin, Tomasz, Douglas, Jessica, Bacino, Carlos A., Craigen, William J., Sanders, Stephan J., Lehmann, Andrea, Latypova, Xénia, Khan, Kamal, Pacault, Mathilde, Sacharow, Stephanie, Glaser, Kimberly, Bieth, Eric, Perrin-Sabourin, Laurence, Jacquemont, Marie-Line, Cho, Megan T., Roeder, Elizabeth, Denommé-Pichon, Anne-Sophie, Monaghan, Kristin G., Yuan, Bo, Xia, Fan, Simon, Sylvain, Bonneau, Dominique, Parent, Philippe, Gilbert-Dussardier, Brigitte, Odent, Sylvie, Toutain, Annick, Pasquier, Laurent, Barbouth, Deborah, Shaw, Chad A., Patel, Ankita, Smith, Janice L., Bi, Weimin, Schmitt, Sébastien, Deb, Wallid, Nizon, Mathilde, Mercier, Sandra, Vincent, Marie, Rooryck, Caroline, Malan, Valérie, Briceño, Ignacio, Gómez, Alberto, Nugent, Kimberly M., Gibson, James B., Cogné, Benjamin, Lupski, James R., Stessman, Holly A.F., Eichler, Evan E., Retterer, Kyle, Yang, Yaping, Redon, Richard, Katsanis, Nicholas, Rosenfeld, Jill A., Kloetzel, Peter-Michael, Golzio, Christelle, Bézieau, Stéphane, Stankiewicz, Paweł, Isidor, Bertrand
Published in American journal of human genetics (02.02.2017)
Published in American journal of human genetics (02.02.2017)
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Journal Article
Differential effects by sex with Kmt5b loss
Wickramasekara, Rochelle N, Robertson, Brynn, Hulen, Jason, Hallgren, Jodi, Stessman, Holly A F
Published in Autism research (01.08.2021)
Published in Autism research (01.08.2021)
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Journal Article
Complete sequence of the closed circular extrachromosomal element of Naegleria pringsheimi De Jonckheere (strain Singh)
Nguyen, Brian T, Chapman, Nora M, Johnson, Niklas, Stessman, Holly A F, Tracy, Steven, Drescher, Kristen M
Published in Microbiology resource announcements (11.04.2024)
Published in Microbiology resource announcements (11.04.2024)
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