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All papers authored by Holly Stessman

This paper is made freely available by the publisher.

2023 Sarah E. Sheppard

ORCID

ORCID

, Rochelle N. Wickramasekara

ORCID

, Courtney Vaccaro, Brynn Robertson, Jodi Hallgren

ORCID

, Jason Hulen, Cynthia J. Watson, Victor Faundes

ORCID

, Yannis Duffourd, Pearl Lee

ORCID

, M. Celeste Simon

ORCID

, Xavier de la Cruz

ORCID

, Natália Padilla

ORCID

, Marco Flores-Mendez

ORCID

and 105 other authors

Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice

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2020 Rochelle N. Wickramasekara

ORCID

, Pashayar P. Lookian, Jeannie Ngo, Annemarie Shibata, Holly A. F. Stessman

ORCID

Schizophrenic Psychosis Symptoms in a Background of Mild-to-Moderate Carnitine Palmitoyltransferase II Deficiency: A Case Report

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Ravyn M. Duncan

ORCID

, Leticia Reyes, Katelyn Moats

ORCID

, Reeder M. Robinson, Sara A. Murphy, Balveen Kaur

ORCID

, Holly A. F. Stessman

ORCID

, Nathan G. Dolloff

ATF3 Coordinates Antitumor Synergy between Epigenetic Drugs and Protein Disulfide Isomerase Inhibitors

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2019 Rochelle Wickramasekara, Holly Stessman

ORCID

Histone 4 Lysine 20 Methylation: A Case for Neurodevelopmental Disease

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2017 Holly A. F. Stessman

ORCID

, Arie van Haeringen, Stessman Ha, Bradley P. Coe, Bo Xiong, Tianyun Wang, Coe Bp, Kendra Hoekzema, Tychele N. Turner, Michaela Fenckova, Claudia Ruivenkamp, Malin Kvarnung, Marjolein Kriek, A. Van Haeringen, Jennifer Gerdts and 43 other authors

Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases

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My Dennis, Ml Dougherty, Lana Harshman, Bj Nelson, Osnat Penn, Stuart Cantsilieris, John Huddleston, Francesca Antonacci

ORCID

, Kelsi Penewit, F. Penewit, Laura Denman, Archana Raja, Carl Baker, Kenneth Mark, Maika Malig

ORCID

and 9 other authors

The evolution and population diversity of human-specific segmental duplications

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2015 Niklas Krumm, Tychele N. Turner, Carl Baker, Laura Vives, Kiana Mohajeri, Kali Witherspoon, Archana Raja, Bradley P. Coe, Holly A. Stessman

ORCID

, Zong-Xiao He, Suzanne M. Leal, Raphael Bernier, Evan E. Eichler

Excess of rare, inherited truncating mutations in autism

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2014 B. J. O'Roak, H. A. Stessman

ORCID

, E. A. Boyle, K. T. Witherspoon, B. Martin, C. Lee, L. Vives, C. Baker, J. B. Hiatt, D. A. Nickerson, R. Bernier, J. Shendure

ORCID

, E. E. Eichler

Recurrent de novo mutations implicate novel genes underlying simplex autism risk

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Ivan Iossifov, Brian J. O'Roak, Stephan J. Sanders

ORCID

, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A. Stessman

ORCID

, Kali T. Witherspoon, Laura Vives, Karynne E. Patterson, Joshua D. Smith, Bryan Paeper, Deborah A. Nickerson, Jeanselle Dea, Shan Dong and 35 other authors

The contribution of de novo coding mutations to autism spectrum disorder

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H. A. F. Stessman

ORCID

, A. Lulla, T. Xia, A. Mitra

ORCID

, T. Harding, A. Mansoor, C. L. Myers, B. G. Van Ness, N. G. Dolloff

High-throughput drug screening identifies compounds and molecular strategies for targeting proteasome inhibitor-resistant multiple myeloma

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Raphael Bernier, Christelle Golzio, Bo Xiong, Holly A. Stessman

ORCID

, Bradley P. Coe, Osnat Penn, Kali Witherspoon, Jennifer Gerdts, Carl Baker, A. T. Van Silfhout, Anneke T. Vulto-Van Silfhout, Janneke H. M. Schuurs-Hoeijmakers, Marco Fichera, Paolo Bosco, Serafino Buono and 22 other authors

Disruptive CHD8 mutations define a subtype of autism early in development

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Holly A. Stessman

ORCID

, Raphael Bernier, Evan E. Eichler

A Genotype-First Approach to Defining the Subtypes of a Complex Disease

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Deanna J. Fall, Holly Stessman

ORCID

, Sagar S. Patel, Zohar Sachs, Brian G. Van Ness, Linda B. Baughn, Michael A. Linden

Utilization of Translational Bioinformatics to Identify Novel Biomarkers of Bortezomib Resistance in Multiple Myeloma

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2013 Holly A. F. Stessman

ORCID

, Aatif Mansoor, Fenghuang Zhan, Michael A. Linden, Brian Van Ness, Linda B. Baughn

Bortezomib Resistance Can Be Reversed by Induced Expression of Plasma Cell Maturation Markers in a Mouse In Vitro Model of Multiple Myeloma

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Holly A. F. Stessman

ORCID

, Aatif Mansoor, Michael A. Linden, Brian Van Ness, Linda B. Baughn

Stabilization of activation induced cytidine deaminase by bortezomib does not confer increased drug target mutation frequency

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Haf A. F. Stessman

ORCID

, A. Mansoor, F. Zhan, S. Janz, M. A. Linden, Lb B. Baughn, B. Van Ness

Reduced CXCR4 expression is associated with extramedullary disease in a mouse model of myeloma and predicts poor survival in multiple myeloma patients treated with bortezomib

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Holly A. F. Stessman

ORCID

, Linda B. Baughn, Aaron Sarver, Tian Xia, Raamesh Deshpande, Aatif Mansoor, Susan A. Walsh, John J. Sunderland, Nathan G. Dolloff, Michael A. Linden, Fenghuang Zhan, Siegfried Janz, Chad L. Myers, Brian G. Van Ness

Profiling Bortezomib Resistance Identifies Secondary Therapies in a Mouse Myeloma Model

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