Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Shareef A. Nahas"'
Autor:
Mallory J. Owen, Sebastien Lefebvre, Christian Hansen, Chris M. Kunard, David P. Dimmock, Laurie D. Smith, Gunter Scharer, Rebecca Mardach, Mary J. Willis, Annette Feigenbaum, Anna-Kaisa Niemi, Yan Ding, Luca Van Der Kraan, Katarzyna Ellsworth, Lucia Guidugli, Bryan R. Lajoie, Timothy K. McPhail, Shyamal S. Mehtalia, Kevin K. Chau, Yong H. Kwon, Zhanyang Zhu, Sergey Batalov, Shimul Chowdhury, Seema Rego, James Perry, Mark Speziale, Mark Nespeca, Meredith S. Wright, Martin G. Reese, Francisco M. De La Vega, Joe Azure, Erwin Frise, Charlene Son Rigby, Sandy White, Charlotte A. Hobbs, Sheldon Gilmer, Gail Knight, Albert Oriol, Jerica Lenberg, Shareef A. Nahas, Kate Perofsky, Kyu Kim, Jeanne Carroll, Nicole G. Coufal, Erica Sanford, Kristen Wigby, Jacqueline Weir, Vicki S. Thomson, Louise Fraser, Seka S. Lazare, Yoon H. Shin, Haiying Grunenwald, Richard Lee, David Jones, Duke Tran, Andrew Gross, Patrick Daigle, Anne Case, Marisa Lue, James A. Richardson, John Reynders, Thomas Defay, Kevin P. Hall, Narayanan Veeraraghavan, Stephen F. Kingsmore
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-14 (2022)
Rapid diagnosis and implementation of treatments is crucial in many genetic conditions. Here the authors describe Genome-to-Treatment, a virtual disease management system that can achieve a rapid diagnosis by expedited whole genome sequencing in 13.5
Externí odkaz:
https://doaj.org/article/c8a8f4d045b24f4586c6fb67d44e877e
Autor:
Chirayu Goswami, Michael Sheldon, Christian Bixby, Mehdi Keddache, Alexander Bogdanowicz, Yihe Wang, Jonathan Schultz, Jessica McDevitt, James LaPorta, Elaine Kwon, Steven Buyske, Dana Garbolino, Glenys Biloholowski, Alex Pastuszak, Mary Storella, Amit Bhalla, Florence Charlier-Rodriguez, Russ Hager, Robin Grimwood, Shareef A. Nahas
Publikováno v:
BMC Infectious Diseases, Vol 22, Iss 1, Pp 1-12 (2022)
Abstract Background The Centers for Disease Control and Prevention contracted with laboratories to sequence the SARS-CoV-2 genome from positive samples across the United States to enable public health officials to investigate the impact of variants o
Externí odkaz:
https://doaj.org/article/e8bee7780dda4d538db015dfa1fe10c0
Autor:
Nathaly M. Sweeney, Shareef A. Nahas, Sh. Chowdhury, Sergey Batalov, Michelle Clark, Sara Caylor, Julie Cakici, John J. Nigro, Yan Ding, Narayanan Veeraraghavan, Charlotte Hobbs, David Dimmock, Stephen F. Kingsmore
Publikováno v:
npj Genomic Medicine, Vol 6, Iss 1, Pp 1-10 (2021)
Abstract Congenital heart disease (CHD) is the most common congenital anomaly and a major cause of infant morbidity and mortality. While morbidity and mortality are highest in infants with underlying genetic conditions, molecular diagnoses are ascert
Externí odkaz:
https://doaj.org/article/9e711bd54acf4e9aa9ebc1d277aeea67
Autor:
Jennifer Friedman, Lynne M. Bird, Richard Haas, Shira L. Robbins, Shareef A. Nahas, David P. Dimmock, Matthew J. Yousefzadeh, Mariah A. Witt, Laura J. Niedernhofer, Shimul Chowdhury
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 7, Pp n/a-n/a (2021)
ABSTRACT Background Cockayne syndrome (CS) is a rare autosomal recessive disorder characterized by growth failure and multisystemic degeneration. Excision repair cross‐complementation group 6 (ERCC6 OMIM: *609413) is the gene most frequently mutate
Externí odkaz:
https://doaj.org/article/8adc526922e441619f5e782f3745aa77
Autor:
Nathaly M. Sweeney, Shareef A. Nahas, Shimul Chowdhury, Sergey Batalov, Michelle Clark, Sara Caylor, Julie Cakici, John J. Nigro, Yan Ding, Narayanan Veeraraghavan, Charlotte Hobbs, David Dimmock, Stephen F. Kingsmore
Publikováno v:
npj Genomic Medicine, Vol 6, Iss 1, Pp 1-1 (2021)
Externí odkaz:
https://doaj.org/article/609e8d7e94744aeeb47768b2e021dd86
Autor:
Nathaly M. Sweeney, Shareef A. Nahas, Shimul Chowdhury, Sergey Batalov, Michelle Clark, Sara Caylor, Julie Cakici, John J. Nigro, Yan Ding, Narayanan Veeraraghavan, Charlotte Hobbs, David Dimmock, Stephen F. Kingsmore
Publikováno v:
npj Genomic Medicine, Vol 6, Iss 1, Pp 1-1 (2021)
Externí odkaz:
https://doaj.org/article/5c84196fbd2942d9ad984aa6da8cb7f5
Autor:
Ricardo Moreno Traspas, Tze Shin Teoh, Pui-Mun Wong, Michael Maier, Crystal Y. Chia, Kenneth Lay, Nur Ain Ali, Austin Larson, Fuad Al Mutairi, Nouriya Abbas Al-Sannaa, Eissa Ali Faqeih, Majid Alfadhel, Huma Arshad Cheema, Juliette Dupont, Stéphane Bézieau, Bertrand Isidor, Dorrain Yanwen Low, Yulan Wang, Grace Tan, Poh San Lai, Hugues Piloquet, Madeleine Joubert, Hulya Kayserili, Kimberly A. Kripps, Shareef A. Nahas, Eric P. Wartchow, Mikako Warren, Gandham SriLakshmi Bhavani, Majed Dasouki, Renata Sandoval, Elisa Carvalho, Luiza Ramos, Gilda Porta, Bin Wu, Harsha Prasada Lashkari, Badr AlSaleem, Raeda M. BaAbbad, Anabela Natália Abreu Ferrão, Vasiliki Karageorgou, Natalia Ordonez-Herrera, Suliman Khan, Peter Bauer, Benjamin Cogne, Aida M. Bertoli-Avella, Marie Vincent, Katta Mohan Girisha, Bruno Reversade
Publikováno v:
Nature genetics. Nature Publishing Group
Cirrhosis is usually a late-onset and life-threatening disease characterized by fibrotic scarring and inflammation that disrupts liver architecture and function. While it is typically the result of alcoholism or hepatitis viral infection in adults, i
Autor:
Robert J. Wechsler-Reya, Jill P. Mesirov, Marcel Kool, Pablo Tamayo, Stefan M. Pfister, Eliezer M. Van Allen, Michael L. Levy, John R. Crawford, Denise Malicki, Shareef A. Nahas, David P. Dimmock, Terence C. Wong, Matija Snuderl, Iris Reyes, James M. Olson, Xiao-Nan Li, Yoon-Jae Cho, Till Milde, Kristiina Vuori, Michael E. Berens, Jacob J. Henderson, Patricia A. Baxter, Yuchen Du, Mari Kogiso, Lin Qi, Jonas Ecker, Jonathan Serrano, Susanne Gröbner, Brendan Reardon, Huriye Seker-Cin, Darren Finlay, Yoko T. Udaka, Sameerah Wahab, Silvia K. Tacheva-Grigorova, Lianne Q. Chau, Alexandra Garancher, James Jensen, Sebastian Brabetz, Edwin F. Juarez, Jessica M. Rusert
Supplementary Tables 1-11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::08e0acfb93f88ece6d7d741e6519b013
https://doi.org/10.1158/0008-5472.22426581
https://doi.org/10.1158/0008-5472.22426581
Autor:
Robert J. Wechsler-Reya, Jill P. Mesirov, Marcel Kool, Pablo Tamayo, Stefan M. Pfister, Eliezer M. Van Allen, Michael L. Levy, John R. Crawford, Denise Malicki, Shareef A. Nahas, David P. Dimmock, Terence C. Wong, Matija Snuderl, Iris Reyes, James M. Olson, Xiao-Nan Li, Yoon-Jae Cho, Till Milde, Kristiina Vuori, Michael E. Berens, Jacob J. Henderson, Patricia A. Baxter, Yuchen Du, Mari Kogiso, Lin Qi, Jonas Ecker, Jonathan Serrano, Susanne Gröbner, Brendan Reardon, Huriye Seker-Cin, Darren Finlay, Yoko T. Udaka, Sameerah Wahab, Silvia K. Tacheva-Grigorova, Lianne Q. Chau, Alexandra Garancher, James Jensen, Sebastian Brabetz, Edwin F. Juarez, Jessica M. Rusert
Supplementary Figures 1-5
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8d9d86caa17333c401c4162c15420ff
https://doi.org/10.1158/0008-5472.22426584
https://doi.org/10.1158/0008-5472.22426584
Autor:
Robert J. Wechsler-Reya, Jill P. Mesirov, Marcel Kool, Pablo Tamayo, Stefan M. Pfister, Eliezer M. Van Allen, Michael L. Levy, John R. Crawford, Denise Malicki, Shareef A. Nahas, David P. Dimmock, Terence C. Wong, Matija Snuderl, Iris Reyes, James M. Olson, Xiao-Nan Li, Yoon-Jae Cho, Till Milde, Kristiina Vuori, Michael E. Berens, Jacob J. Henderson, Patricia A. Baxter, Yuchen Du, Mari Kogiso, Lin Qi, Jonas Ecker, Jonathan Serrano, Susanne Gröbner, Brendan Reardon, Huriye Seker-Cin, Darren Finlay, Yoko T. Udaka, Sameerah Wahab, Silvia K. Tacheva-Grigorova, Lianne Q. Chau, Alexandra Garancher, James Jensen, Sebastian Brabetz, Edwin F. Juarez, Jessica M. Rusert
Medulloblastoma is among the most common malignant brain tumors in children. Recent studies have identified at least four subgroups of the disease that differ in terms of molecular characteristics and patient outcomes. Despite this heterogeneity, mos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22432e8f22e80af772f660919f855f78
https://doi.org/10.1158/0008-5472.c.6512388
https://doi.org/10.1158/0008-5472.c.6512388