Search Results - Benjamin Currall

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  1. 1
    Describing Sequencing Results of Structural Chromosome Rearrangements with a Suggested Next-Generation Cytogenetic Nomenclature

    Describing Sequencing Results of Structural Chromosome Rearrangements with a Suggested Next-Generation Cytogenetic Nomenclature by Zehra Ordulu, Kristen E. Wong, Benjamin Currall, Andrew R. Ivanov, Shahrin Pereira, Sara Althari, James F. Gusella, Michael E. Talkowski, Cynthia C. Morton

    Published 2014
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  2. 2
    Kctd13-deficient mice display short-term memory impairment and sex-dependent genetic interactions

    Kctd13-deficient mice display short-term memory impairment and sex-dependent genetic interactions by Thomas Arbogast, Parisa Razaz, Jacob Ellegood, Spencer U. McKinstry, Serkan Erdin, Benjamin Currall, Tatsiana Aneichyk, Jason P. Lerch, Lily R. Qiu, Ramona M. Rodriguiz, R. Mark Henkelman, Michael E. Talkowski, William C. Wetsel, Christelle Golzio, Nicholas Katsanis

    Published 2018
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  3. 3
    Comparison of Electronegative Filtration to Magnetic Bead-Based Concentration and V2G-qPCR to RT-qPCR for Quantifying Viral SARS-CoV-2 RNA from Wastewater

    Comparison of Electronegative Filtration to Magnetic Bead-Based Concentration and V2G-qPCR to RT-qPCR for Quantifying Viral SARS-CoV-2 RNA from Wastewater by Kristina M. Babler, Ayaaz Amirali, Mark Sharkey, Siôn L. Williams, Melinda Minucci Boone, Gabriella A. Cosculluela, Benjamin Currall, George S. Grills, Jennifer Laine, Christopher E. Mason, Brian D. Reding, Stephan C. Schürer, Mario Stevenson, D. Vidović, Helena M. Solo‐Gabriele

    Published 2022
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  4. 4
    High-Resolution and Noninvasive Fetal Exome Screening

    High-Resolution and Noninvasive Fetal Exome Screening by Harrison Brand, Christopher W. Whelan, Michael H. Duyzend, John Lemanski, Monica Salani, Stephanie P. Hao, Isaac Wong, Elise Valkanas, Caroline Cusick, Casie A. Genetti, Lori Dobson, Courtney Studwell, Kathleen Gianforcaro, Louise Wilkins‐Haug, Stephanie Guseh, Benjamin Currall, Kathryn J. Gray, Michael E. Talkowski

    Published 2023
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  5. 5
    ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice

    ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice by Oscar Diaz‐Horta, Clemer Abad, Levent Sennaroğlu, Joseph Foster, Alexandra A. DeSmidt, Güney Bademci, Suna Tokgöz-Yılmaz, Duygu Duman, Filiz Başak Cengiz, M’hamed Grati, Suat Fítöz, Xue Z. Liu, Amjad Farooq, Faiqa Imtiaz, Benjamin Currall, Cynthia C. Morton, Michiru Nishita, Yasuhiro Minami, Zhongmin Lu, Katherina Walz, Mustafa Tekin

    Published 2016
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  6. 6
    Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal models

    Tissue- and cell-type-specific molecular and functional signatures of 16p11.2 reciprocal genomic disorder across mouse brain and human neuronal models by Derek J.C. Tai, Parisa Razaz, Serkan Erdin, Dadi Gao, Jennifer Wang, Xander Nuttle, Celine E. de Esch, Ryan L. Collins, Benjamin Currall, Kathryn O’Keefe, Nicholas D. Burt, Rachita Yadav, Lily Wang, Kiana Mohajeri, Tatsiana Aneichyk, Ashok Ragavendran, Alexei Stortchevoi, Elisabetta Morini, Weiyuan Ma, Diane Lucente, Alex Hastie, Raymond J. Kelleher, Roy H. Perlis, Michael E. Talkowski, James F. Gusella

    Published 2022
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  7. 7
    Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome

    Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid human genome by Ryan L. Collins, Harrison Brand, Claire Redin, Carrie Hanscom, Caroline Antolik, Matthew R. Stone, Joseph Glessner, Tamara Mason, Giulia Pregno, Naghmeh Dorrani, Giorgia Mandrile, Daniela Giachino, Danielle Perrin, Cole Walsh, Michelle Cipicchio, Maura Costello, Alexei Stortchevoi, Joon‐Yong An, Benjamin Currall, Catarina M. Seabra, Ashok Ragavendran, Lauren Margolin, Julián A. Martínez-Agosto, Diane Lucente, Brynn Levy, Stephan Sanders, Ronald J. Wapner, Fabiola Quintero‐Rivera, Wigard P. Kloosterman, Michael E. Talkowski

    Published 2017
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  8. 8
    Wastewater based surveillance can be used to reduce clinical testing intensity on a university campus

    Wastewater based surveillance can be used to reduce clinical testing intensity on a university campus by Ayaaz Amirali, Kristina M. Babler, Mark Sharkey, Cynthia Beaver, Melinda Minucci Boone, Samuel Comerford, Daniel Cooper, Benjamin Currall, Kenneth W. Goodman, George S. Grills, Erin N. Kobetz, Naresh Kumar, Jennifer Laine, Walter E. Lamar, Christopher E. Mason, Brian D. Reding, Matthew A. Roca, Krista Ryon, Stephan C. Schürer, Bhavarth Shukla, Natasha Schaefer Solle, Mario Stevenson, John J. Tallon, D. Vidović, Siôn L. Williams, Xue Yin, Helena M. Solo‐Gabriele

    Published 2024
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  9. 9
    Relationships between SARS-CoV-2 in Wastewater and COVID-19 Clinical Cases and Hospitalizations, with and without Normalization against Indicators of Human Waste

    Relationships between SARS-CoV-2 in Wastewater and COVID-19 Clinical Cases and Hospitalizations, with and without Normalization against Indicators of Human Waste by Qingyu Zhan, Kristina M. Babler, Mark Sharkey, Ayaaz Amirali, Cynthia Beaver, Melinda Minucci Boone, Samuel Comerford, Daniel Cooper, Elena M. Cortizas, Benjamin Currall, Jonathan Foox, George S. Grills, Erin N. Kobetz, Naresh Kumar, Jennifer Laine, Walter E. Lamar, Alejandro Mantero, Christopher E. Mason, Brian D. Reding, Maria Robertson, Matthew A. Roca, Krista Ryon, Stephan C. Schürer, Bhavarth Shukla, Natasha Schaefer Solle, Mario Stevenson, John J. Tallon, Collette Thomas, Tori Thomas, D. Vidović, Siôn L. Williams, Xue Yin, Helena M. Solo‐Gabriele

    Published 2022
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  10. 10
    Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder

    Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder by Joon‐Yong An, Kevin Lin, Lingxue Zhu, Donna M. Werling, Shan Dong, Harrison Brand, Harold Z. Wang, Xuefang Zhao, Grace Schwartz, Ryan L. Collins, Benjamin Currall, Claudia Dastmalchi, Jeanselle Dea, Clif Duhn, Michael C. Gilson, Lambertus Klei, Lindsay Liang, Eirene Markenscoff-Papadimitriou, Sirisha Pochareddy, Nadav Ahituv, Joseph D. Buxbaum, Hilary Coon, Mark J. Daly, Young S. Kim, Gábor Marth, Benjamin M. Neale, Aaron R. Quinlan, John L.R. Rubenstein, Nenad Šestan, Matthew W. State, A. Jeremy Willsey, Michael E. Talkowski, Bernie Devlin, Kathryn Roeder, Stephan Sanders

    Published 2018
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  11. 11
    Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly

    Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly by Tatsiana Aneichyk, William T. Hendriks, Rachita Yadav, David Shin, Dadi Gao, Christine A. Vaine, Ryan L. Collins, Aloysius Domingo, Benjamin Currall, Alexei Stortchevoi, Trisha Multhaupt‐Buell, Ellen B. Penney, Lilian Cruz, Jyotsna Dhakal, Harrison Brand, Carrie Hanscom, Caroline Antolik, Marisela Dy-Hollins, Ashok Ragavendran, Jason G. Underwood, Stuart Cantsilieris, Katherine M. Munson, Evan E. Eichler, Patrick Acuña, Criscely L. Go, Roland Dominic G. Jamora, Raymond L. Rosales, Deanna M. Church, Stephen R. Williams, Sarah Garcia, Christine Klein, Ulrich Müller, Kirk C. Wilhelmsen, H. T. Marc Timmers, Yechiam Sapir, Brian J. Wainger, Daniel A. Henderson, Naoto Ito, Neil Weisenfeld, David M. Jaffe, Nutan Sharma, Xandra O. Breakefield, Laurie J. Ozelius, D. Cristopher Bragg, Michael E. Talkowski

    Published 2018
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  12. 12
    An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder

    An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder by Donna M. Werling, Harrison Brand, Joon‐Yong An, Matthew R. Stone, Lingxue Zhu, Joseph Glessner, Ryan L. Collins, Shan Dong, Ryan M. Layer, Eirene Markenscoff-Papadimitriou, Andrew Farrell, Grace Schwartz, Harold Z. Wang, Benjamin Currall, Xuefang Zhao, Jeanselle Dea, Clif Duhn, Carolyn A. Erdman, Michael C. Gilson, Rachita Yadav, Robert E. Handsaker, Seva Kashin, Lambertus Klei, Jeffrey D. Mandell, Tomasz J. Nowakowski, Yuwen Liu, Sirisha Pochareddy, Louw Smith, Michael F. Walker, Matthew J. Waterman, Xin He, Arnold R. Kriegstein, John L.R. Rubenstein, Nenad Šestan, Steven A. McCarroll, Benjamin M. Neale, Hilary Coon, A. Jeremy Willsey, Joseph D. Buxbaum, Mark J. Daly, Matthew W. State, Aaron R. Quinlan, Gábor Marth, Kathryn Roeder, Bernie Devlin, Michael E. Talkowski, Stephan Sanders

    Published 2018
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  13. 13
    Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies

    Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies by Chelsea Lowther, Elise Valkanas, Jessica L. Giordano, Harold Z. Wang, Benjamin Currall, Kathryn O’Keefe, Emma Pierce‐Hoffman, Nehir Edibe Kurtas, Christopher W. Whelan, Stephanie P. Hao, Ben Weisburd, Vahid Jalili, Jack Fu, Isaac Wong, Ryan L. Collins, Xuefang Zhao, Christina Austin‐Tse, Emily Evangelista, Gabrielle Lemire, Vimla S. Aggarwal, Diane Lucente, Laura D. Gauthier, Charlotte Tolonen, Nareh Sahakian, Christine Stevens, Joon‐Yong An, Shan Dong, Mary E. Norton, Tippi C. MacKenzie, Bernie Devlin, Kelly L. Gilmore, Bradford C. Powell, Alicia Brandt, Francesco Vetrini, Michelle DiVito, Stephan Sanders, Daniel G. MacArthur, Jennelle C. Hodge, Anne O’Donnell‐Luria, Heidi L. Rehm, Neeta L. Vora, Brynn Levy, Harrison Brand, Ronald J. Wapner, Michael E. Talkowski

    Published 2023
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  14. 14
    SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome

    SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome by Natalie D. Shaw, Harrison Brand, Zachary A Kupchinsky, Hemant Bengani, Lacey Plummer, Takako I. Jones, Serkan Erdin, Kathleen A. Williamson, Joe Rainger, Alexei Stortchevoi, Kaitlin E. Samocha, Benjamin Currall, Donncha S. Dunican, Ryan L. Collins, Jason R. Willer, Angela Lek, Monkol Lek, Malik Nassan, Shahrin Pereira, Tammy Kammin, Diane Lucente, Alexandra Silva, Catarina M. Seabra, Colby Chiang, Yu An, Morad Ansari, Jacqueline K. Rainger, Shelagh Joss, Jill Smith, Margaret Lippincott, Sylvia Singh, Nirav Patel, Jenny W Jing, Jennifer Law, Nalton Ferraro, Alain Verloès, Anita Rauch, Katharina Steindl, Markus Zweier, Ianina Scheer, Daisuke Sato, Nobuhiko Okamoto, Christina M. Jacobsen, Jeanie B. Tryggestad, Steven D. Chernausek, Lisa A. Schimmenti, Benjamin Brasseur, Claudia Cesaretti, José Elías García‐Ortíz, Tatiana Pineda Buitrago, Orlando Pérez Silva, Jodi D. Hoffman, W. Mühlbauer, Klaus W. Ruprecht, Bart Loeys, Masato Shino, Angela M. Kaindl, Chie Hee Cho, Cynthia C. Morton, Richard R. Meehan, Veronica van Heyningen, Eric C. Liao, Ravikumar Balasubramanian, Janet E. Hall, Stephanie B. Seminara, Daniel G. MacArthur, Steven A. Moore, Koh-ichiro Yoshiura, James F. Gusella, Joseph A. Marsh, John M. Graham, Angela E. Lin, Nicholas Katsanis, Peter L. Jones, William F. Crowley, Erica E. Davis, David Fitzpatrick, Michael E. Talkowski

    Published 2017
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  15. 15
    The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies

    The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies by Claire Redin, Harrison Brand, Ryan L. Collins, Tammy Kammin, Elyse Mitchell, Jennelle C. Hodge, Carrie Hanscom, Vamsee Pillalamarri, Catarina M. Seabra, Mary‐Alice Abbott, Omar Abdul‐Rahman, Erika Aberg, Rhett Adley, Sofía Lizeth Alcaráz‐Estrada, Fowzan S. Alkuraya, Yu An, MaryAnne Anderson, Caroline Antolik, Kwame Anyane‐Yeboa, Joan Atkin, Tina M. Bartell, Jonathan A. Bernstein, Elizabeth Beyer, Ian Blumenthal, Ernie M.H.F. Bongers, Eva H. Brilstra, Chester Brown, Hennie T. Brüggenwirth, Bert Callewaert, Colby Chiang, Ken Corning, Helen Cox, Edwin Cuppen, Benjamin Currall, Tom Cushing, D. David, Matthew A. Deardorff, Annelies Dheedene, Marc D’Hooghe, Bert B.A. de Vries, Dawn Earl, Heather Ferguson, Heather Fisher, David Fitzpatrick, Pamela Gerrol, Daniela Giachino, Joseph Glessner, Troy J. Gliem, Margo Grady, Brett H. Graham, Cristin Griffis, Karen W. Gripp, Andrea Gropman, Andrea Hanson‐Kahn, David J. Harris, Mark A. Hayden, R. Sean Hill, Ron Hochstenbach, Jodi D. Hoffman, Robert J. Hopkin, Monika Weisz Hubshman, A. Micheil Innes, Mira Irons, Melita Irving, Jessie C. Jacobsen, Sandra Janssens, Tamison Jewett, John P. Johnson, Marjolijn C.J. Jongmans, Stephen G. Kahler, David A. Koolen, Jerome Korzelius, Peter M. Kroisel, Yves Lacassie, William Lawless, Emmanuelle Lemyre, Kathleen A. Leppig, Alex V. Levin, Haibo Li, Hong Li, Eric C. Liao, Cynthia Lim, Edward J. Lose, Diane Lucente, Michael J. Macera, Poornima Manavalan, Giorgia Mandrile, Carlo Marcelis, Lauren Margolin, Tamara Mason, Diane Masser‐Frye, Michael McClellan, Cinthya J. Zepeda Mendoza, Björn Menten, Sjors Middelkamp, Liya Regina Mikami, Emily Moe, Shehla Mohammed, Tarja Mononen, Megan Mortenson

    Published 2016
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