CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

Autor: Lot Snijders Blok, Justine Rousseau, Joanna Twist, Sophie Ehresmann, Motoki Takaku, Hanka Venselaar, Lance H. Rodan, Catherine B. Nowak, Jessica Douglas, Kathryn J. Swoboda, Marcie A. Steeves, Inderneel Sahai, Connie T. R. M. Stumpel, Alexander P. A. Stegmann, Patricia Wheeler, Marcia Willing, Elise Fiala, Aaina Kochhar, William T. Gibson, Ana S. A. Cohen, Ruky Agbahovbe, A. Micheil Innes, P. Y. Billie Au, Julia Rankin, Ilse J. Anderson, Steven A. Skinner, Raymond J. Louie, Hannah E. Warren, Alexandra Afenjar, Boris Keren, Caroline Nava, Julien Buratti, Arnaud Isapof, Diana Rodriguez, Raymond Lewandowski, Jennifer Propst, Ton van Essen, Murim Choi, Sangmoon Lee, Jong H. Chae, Susan Price, Rhonda E. Schnur, Ganka Douglas, Ingrid M. Wentzensen, Christiane Zweier, André Reis, Martin G. Bialer, Christine Moore, Marije Koopmans, Eva H. Brilstra, Glen R. Monroe, Koen L. I. van Gassen, Ellen van Binsbergen, Ruth Newbury-Ecob, Lucy Bownass, Ingrid Bader, Johannes A. Mayr, Saskia B. Wortmann, Kathy J. Jakielski, Edythe A. Strand, Katja Kloth, Tatjana Bierhals, The DDD study, John D. Roberts, Robert M. Petrovich, Shinichi Machida, Hitoshi Kurumizaka, Stefan Lelieveld, Rolph Pfundt, Sandra Jansen, Pelagia Deriziotis, Laurence Faivre, Julien Thevenon, Mirna Assoum, Lawrence Shriberg, Tjitske Kleefstra, Han G. Brunner, Paul A. Wade, Simon E. Fisher, Philippe M. Campeau

Publikováno v: Nature Communications, Vol 9, Iss 1, Pp 1-12 (2018)

Chromodomain Helicase DNA-binding (CHD) proteins have been implicated in neurodevelopmental processes. Here, the authors identify missense variants in CHD3 that disturb its chromatin remodeling activities and cause a neurodevelopmental disorder with

Externí odkaz: https://doaj.org/article/2f149b8196854879821d3ece66218bf2

Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization

Autor: Scott T. Weiss, Marcie A. Steeves, Kurt D. Christensen, Jordan W. Smoller, Kalotina Machini, Lisa Mahanta, Christopher Koch, Nidhi Shah, Nina B. Gold, Robert C. Green, Carrie L. Blout Zawatsky, Hana Zouk, Matthew S. Lebo, Heidi L. Rehm, Janelle Shea, Emma Perez, Natalie T. Boutin, Joel B. Krier, Melissa K Uveges, Elizabeth W. Karlson

Publikováno v: American Journal of Human Genetics

Summary Over 100 million research participants around the world have had research array-based genotyping (GT) or genome sequencing (GS), but only a small fraction of these have been offered return of actionable genomic findings (gRoR). Between 2017 a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0222f0c6a002127be64f3bb169c68424
https://pubmed.ncbi.nlm.nih.gov/34752750

Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor beta Signaling

Autor: Brett V. Johnson, Raman Kumar, Sabrina Oishi, Suzy Alexander, Maria Kasherman, Michelle Sanchez Vega, Atma Ivancevic, Alison Gardner, Deepti Domingo, Mark Corbett, Euan Parnell, Sehyoun Yoon, Tracey Oh, Matthew Lines, Henrietta Lefroy, Usha Kini, Margot Van Allen, Sabine Grønborg, Sandra Mercier, Sébastien Küry, Stéphane Bézieau, Laurent Pasquier, Martine Raynaud, Alexandra Afenjar, Thierry Billette de Villemeur, Boris Keren, Julie Désir, Lionel Van Maldergem, Martina Marangoni, Nicola Dikow, David A. Koolen, Peter M. VanHasselt, Marjan Weiss, Petra Zwijnenburg, Joaquim Sa, Claudia Falcao Reis, Carlos López-Otín, Olaya Santiago-Fernández, Alberto Fernández-Jaén, Anita Rauch, Katharina Steindl, Pascal Joset, Amy Goldstein, Suneeta Madan-Khetarpal, Elena Infante, Elaine Zackai, Carey Mcdougall, Vinodh Narayanan, Keri Ramsey, Saadet Mercimek-Andrews, Loren Pena, Vandana Shashi, Kelly Schoch, Jennifer A. Sullivan, Filippo Pinto e Vairo, Pavel N. Pichurin, Sarah A. Ewing, Sarah S. Barnett, Eric W. Klee, M. Scott Perry, Mary Kay Koenig, Catherine E. Keegan, Jane L. Schuette, Stephanie Asher, Yezmin Perilla-Young, Laurie D. Smith, Jill A. Rosenfeld, Elizabeth Bhoj, Paige Kaplan, Dong Li, Renske Oegema, Ellen van Binsbergen, Bert van der Zwaag, Marie Falkenberg Smeland, Ioana Cutcutache, Matthew Page, Martin Armstrong, Angela E. Lin, Marcie A. Steeves, Nicolette den Hollander, Mariëtte J.V. Hoffer, Margot R.F. Reijnders, Serwet Demirdas, Daniel C. Koboldt, Dennis Bartholomew, Theresa Mihalic Mosher, Scott E. Hickey, Christine Shieh, Pedro A. Sanchez-Lara, John M. Graham, Kamer Tezcan, G.B. Schaefer, Noelle R. Danylchuk, Alexander Asamoah, Kelly E. Jackson, Naomi Yachelevich, Margaret Au, Luis A. Pérez-Jurado, Tjitske Kleefstra, Peter Penzes, Stephen A. Wood, Thomas Burne, Tyler Mark Pierson, Michael Piper, Jozef Gécz, Lachlan A. Jolly, Maria T. Acosta, David R. Adams, Aaron Aday, Mercedes E. Alejandro, Patrick Allard, Euan A. Ashley, Mahshid S. Azamian, Carlos A. Bacino, Guney Bademci, Eva Baker, Ashok Balasubramanyam, Dustin Baldridge, Deborah Barbouth, Gabriel F. Batzli, Alan H. Beggs, Hugo J. Bellen, Jonathan A. Bernstein, Gerard T. Berry, Anna Bican, David P. Bick, Camille L. Birch, Stephanie Bivona, Carsten Bonnenmann, Devon Bonner, Braden E. Boone, Bret L. Bostwick, Lauren C. Briere, Elly Brokamp, Donna M. Brown, Matthew Brush, Elizabeth A. Burke, Lindsay C. Burrage, Manish J. Butte, Olveen Carrasquillo, Ta Chen Peter Chang, Hsiao-Tuan Chao, Gary D. Clark, Terra R. Coakley, Laurel A. Cobban, Joy D. Cogan, F. Sessions Cole, Heather A. Colley, Cynthia M. Cooper, Heidi Cope, William J. Craigen, Precilla D'Souza, Surendra Dasari, Mariska Davids, Jean M. Davidson, Jyoti G. Dayal, Esteban C. Dell'Angelica, Shweta U. Dhar, Naghmeh Dorrani, Daniel C. Dorset, Emilie D. Douine, David D. Draper, Annika M. Dries, Laura Duncan, David J. Eckstein, Lisa T. Emrick, Christine M. Eng, Gregory M. Enns, Cecilia Esteves, Tyra Estwick, Liliana Fernandez, Carlos Ferreira, Elizabeth L. Fieg, Paul G. Fisher, Brent L. Fogel, Irman Forghani, Noah D. Friedman, William A. Gahl, Rena A. Godfrey, Alica M. Goldman, David B. Goldstein, Jean-Philippe F. Gourdine, Alana Grajewski, Catherine A. Groden, Andrea L. Gropman, Melissa Haendel, Rizwan Hamid, Neil A. Hanchard, Frances High, Ingrid A. Holm, Jason Hom, Alden Huang, Yong Huang, Rosario Isasi, Fariha Jamal, Yong-hui Jiang, Jean M. Johnston, Angela L. Jones, Lefkothea Karaviti, Emily G. Kelley, David M. Koeller, Isaac S. Kohane, Jennefer N. Kohler, Deborah Krakow, Donna M. Krasnewich, Susan Korrick, Mary Koziura, Joel B. Krier, Jennifer E. Kyle, Seema R. Lalani, Byron Lam, Brendan C. Lanpher, Ian R. Lanza, C. Christopher Lau, Jozef Lazar, Kimberly LeBlanc, Brendan H. Lee, Hane Lee, Roy Levitt, Shawn E. Levy, Richard A. Lewis, Sharyn A. Lincoln, Pengfei Liu, Xue Zhong Liu, Sandra K. Loo, Joseph Loscalzo, Richard L. Maas, Ellen F. Macnamara, Calum A. MacRae, Valerie V. Maduro, Marta M. Majcherska, May Christine V. Malicdan, Laura A. Mamounas, Teri A. Manolio, Thomas C. Markello, Ronit Marom, Martin G. Martin, Julian A. Martínez-Agosto, Shruti Marwaha, Thomas May, Jacob McCauley, Allyn McConkie-Rosell, Colleen E. McCormack, Alexa T. McCray, Jason D. Merker, Thomas O. Metz, Matthew Might, Eva Morava-Kozicz, Paolo M. Moretti, Marie Morimoto, John J. Mulvihill, David R. Murdock, Avi Nath, Stan F. Nelson, J. Scott Newberry, John H. Newman, Sarah K. Nicholas, Donna Novacic, Devin Oglesbee, James P. Orengo, Stephen Pak, J. Carl Pallais, Christina GS. Palmer, Jeanette C. Papp, Neil H. Parker, John A. Phillips, Jennifer E. Posey, John H. Postlethwait, Lorraine Potocki, Barbara N. Pusey, Genecee Renteri, Chloe M. Reuter, Lynette Rives, Amy K. Robertson, Lance H. Rodan, Robb K. Rowley, Ralph Sacco, Jacinda B. Sampson, Susan L. Samson, Mario Saporta, Judy Schaechter, Timothy Schedl, Daryl A. Scott, Lisa Shakachite, Prashant Sharma, Kathleen Shields, Jimann Shin, Rebecca Signer, Catherine H. Sillari, Edwin K. Silverman, Janet S. Sinsheimer, Kevin S. Smith, Lilianna Solnica-Krezel, Rebecca C. Spillmann, Joan M. Stoler, Nicholas Stong, David A. Sweetser, Cecelia P. Tamburro, Queenie K.-G. Tan, Mustafa Tekin, Fred Telischi, Willa Thorson, Cynthia J. Tifft, Camilo Toro, Alyssa A. Tran, Tiina K. Urv, Tiphanie P. Vogel, Daryl M. Waggott, Colleen E. Wahl, Nicole M. Walley, Chris A. Walsh, Melissa Walker, Jennifer Wambach, Jijun Wan, Lee-kai Wang, Michael F. Wangler, Patricia A. Ward, Katrina M. Waters, Bobbie-Jo M. Webb-Robertson, Daniel Wegner, Monte Westerfield, Matthew T. Wheeler, Anastasia L. Wise, Lynne A. Wolfe, Jeremy D. Woods, Elizabeth A. Worthey, Shinya Yamamoto, John Yang, Amanda J. Yoon, Guoyun Yu, Diane B. Zastrow, Chunli Zhao, Stephan Zuchner, William Gahl

Publikováno v: Biological Psychiatry, 87, 100-112
Biological Psychiatry, 87, 2, pp. 100-112
Johnson, B V, Kumar, R, Oishi, S, Alexander, S, Kasherman, M, Vega, M S, Ivancevic, A, Gardner, A, Domingo, D, Corbett, M, Parnell, E, Yoon, S, Oh, T, Lines, M, Lefroy, H, Kini, U, van Allen, M, Grønborg, S, Mercier, S, Küry, S B, Bézieau, S, Pasquier, L, Raynaud, M, Afenjar, A, Billette de Villemeur, T, Keren, B, Désir, J, van Maldergem, L, Marangoni, M, Dikow, N, Koolen, D A, VanHasselt, P M, Weiss, M, Zwijnenburg, P, Sa, J, Reis, C F, López-Otín, C, Santiago-Fernández, O, Fernández-Jaén, A, Rauch, A, Steindl, K, Joset, P, Goldstein, A, Madan-Khetarpal, S, Infante, E, Zackai, E, Mcdougall, C, Narayanan, V, Ramsey, K, Undiagnosed Diseases Network, Davids, M, Sullivan, J A, Au, M, Pérez-Jurado, L A, Kleefstra, T, Penzes, P, Wood, S A, Burne, T, Pierson, T, Piper, M, Gecz, J & Jolly, L A 2020, ' Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling ', Biological Psychiatry, vol. 87, no. 2, pp. 100-112 . https://doi.org/10.1016/j.biopsych.2019.05.028
Biol Psychiatry
Biological Psychiatry, 87(2), 100-112. ELSEVIER SCIENCE INC
Biological Psychiatry, 87(2), 100-112. Elsevier Inc.
Biological Psychiatry, 87(2), 100-112. Elsevier USA
Biological Psychiatry, 87(2), 100-112. Elsevier Science

Contains fulltext : 218305.pdf (Publisher’s version ) (Closed access) BACKGROUND: The X-chromosome gene USP9X encodes a deubiquitylating enzyme that has been associated with neurodevelopmental disorders primarily in female subjects. USP9X escapes X

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c52fb15e212408556ad7f7895a16106b
http://hdl.handle.net/2066/218305

Recognition and management of adults with Turner syndrome:From the transition of adolescence through the senior years

Autor: Shahla Nader-Eftekhari, Marcie A. Steeves, Frances J. Hayes, Mette H Viuff, Mary K. Colvin, Lars Kjærsgaard Hansen, Jeffrey B Kreher, Emma A Snyder, Ana Arenivas, Melissa Crenshaw, Laura M. Prager, Ami B. Bhatt, Angela E. Lin, Melissa B. Aldrich, Claus Højbjerg Gravholt, Michelle Rivera-Davila, Niels Holmark Andersen, Lynne L. Levitsky, Evelyn Lilly, Anne Skakkebæk, Siddharth K. Prakash

Publikováno v: Lin, A E, Prakash, S K, Andersen, N H, Viuff, M H, Levitsky, L L, Rivera-Davila, M, Crenshaw, M L, Hansen, L, Colvin, M K, Hayes, F J, Lilly, E, Snyder, E A, Nader-Eftekhari, S, Aldrich, M B, Bhatt, A B, Prager, L M, Arenivas, A, Skakkebaek, A, Steeves, M A, Kreher, J B & Gravholt, C H 2019, ' Recognition and management of adults with Turner syndrome : From the transition of adolescence through the senior years ', American Journal of Medical Genetics, Part A, vol. 179, no. 10, pp. 1987-2033 . https://doi.org/10.1002/ajmg.a.61310
Lin, A E, Prakash, S K, Viuff, M H, Levitsky, L L, Rivera-Davila, M, Crenshaw, M L, Hansen, L, Colvin, M K, Hayes, F J, Lilly, E, Snyder, E A, Nader-Eftekhari, S, Aldrich, M B, Bhatt, A B, Prager, L M, Arenivas, A, Skakkebaek, A, Steeves, M A, Kreher, J B & Gravholt, C H 2019, ' Recognition and management of adults with Turner syndrome: From the transition of adolescence through the senior years ', American Journal of Medical Genetics. Part A . https://doi.org/10.1002/ajmg.a.61310
Lin, A E, Prakash, S K, Andersen, N H, Viuff, M H, Levitsky, L L, Rivera-Davila, M, Crenshaw, M L, Hansen, L, Colvin, M K, Hayes, F J, Lilly, E, Snyder, E A, Nader-Eftekhari, S, Aldrich, M B, Bhatt, A B, Prager, L M, Arenivas, A, Skakkebaek, A, Steeves, M A, Kreher, J B & Gravholt, C H 2019, ' Recognition and management of adults with Turner syndrome : From the transition of adolescence through the senior years ', American Journal of Medical Genetics. Part A, vol. 179, no. 10, pp. 1987-2033 . https://doi.org/10.1002/ajmg.a.61310

Turner syndrome is recognized now as a syndrome familiar not only to pediatricians and pediatric specialists, medical geneticists, adult endocrinologists, and cardiologists, but also increasingly to primary care providers, internal medicine specialis

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f953ad7327695e5078885a2a23fa4afd
https://pure.au.dk/portal/da/publications/recognition-and-management-of-adults-with-turner-syndrome(2c7785fa-0327-4602-affe-216f15deee8a).html

Genetic counseling for women with 45,X/46,XX mosaicism: Towards more personalized management

Autor: Erin A. McNamara, Raul E. Piña-Aguilar, Frances J. Hayes, Marcie A. Steeves, Lynne L. Levitsky, Emma A Snyder, Angela E. Lin, Adrianna K. San Roman, Irene Souter

Publikováno v: European Journal of Medical Genetics. 64:104140

Despite numerous clinical series, consistent karyotype-phenotype correlations for Turner syndrome have not been established, although a lower level of 45,X is generally thought to be associated with a milder phenotype. This limits personalized counse

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6154941d908c26233c7997d4f4dc8e70
https://doi.org/10.1016/j.ejmg.2021.104140