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TRanscriptome ANalysis of StratifiEd CohorTs (TRANSECT) enables automated assessment of global gene regulation linked to disparate expression in user defined genes and gene sets 分层队列的转录组分析 (TRANSECT) 可以自动评估与用户定义基因和基因集的不同表达相关的全局基因调控 Toubia, John; Kusay, Yasir; Maqsood, Muneeza; Warnock, Nicholas, I; Lawrence, David M.; Bracken, Cameron P.; Gregory, Philip A.; Kan, Winnie L.; Selth, Luke A.; Conn, Simon J.; Lopez, Angel F.; Branford, Susan; Scott, Hamish S.; Kok, Chung Hoow; Goodall, Gregory J.; Schreiber, Andreas W. 分享 收藏
Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41 Homan, Claire C.; Drazer, Michael W.; Yu, Kai; Lawrence, David M.; Feng, Jinghua; Arriola-Martinez, Luis; Pozsgai, Matthew J.; Mcneely, Kelsey E.; Ha, Thuong; Venugopal, Parvathy; Arts, Peer; King-Smith, Sarah L.; Cheah, Jesse; Armstrong, Mark; Wang, Paul; Bodor, Csaba; Cantor, Alan B.; Cazzola, Mario; Degelman, Erin; Dinardo, Courtney D.; Duployez, Nicolas; Favier, Remi; Froehling, Stefan; Rio-Machin, Ana; Klco, Jeffery M.; Kraemer, Alwin; Kurokawa, Mineo; Lee, Joanne; Malcovati, Luca; Morgan, Neil, V; Natsoulis, Georges; Owen, Carolyn; Patel, Keyur P.; Preudhomme, Claude; Raslova, Hana; Rienhoff, Hugh; Ripperger, Tim; Schulte, Rachael; Tawana, Kiran; Velloso, Elvira; Yan, Benedict; Kim, Erika; NISC Comparative Sequencing Program, Amy P.; Hsu, Amy P.; Holland, Steven M.; Phillips, Kerry; Poplawski, Nicola K.; Babic, Milena; Wei, Andrew H.; Forsyth, Cecily; Fan, Helen Mar; Lewis, Ian D.; Cooney, Julian; Susman, Rachel; Fox, Lucy C.; Blombery, Piers; Singhal, Deepak; Hiwase, Devendra; Phipson, Belinda; Schreiber, Andreas W.; Hahn, Christopher N.; Scott, Hamish S.; Liu, Paul; Godley, Lucy A.; Brown, Anna L. 分享 收藏
Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death ( jan, pg - 180 ,2023) Byrne, Alicia B.; Arts, Peer; Ha, Thuong T.; Kassahn, Karin S.; Paris, Lynn S.; O'Donnell-Luria, Anne; Babic, Milena; Frank, Mahalia S. B.; Feng, Jinghua; Wang, Paul; Lawrence, David M.; Eshraghi, Leila; Arriola, Luis; Toubia, John; Nguyen, Hung; McGillivray, George; Pinner, Jason; McKenzie, Fiona; Morrow, Rebecca; Lipsett, Jill; Manton, Nick; Khong, T. Yee; Moore, Lynette; Liebelt, Jan E.; Schreiber, Andreas W.; King-Smith, Sarah L.; Hardy, Tristan S. E.; Jackson, Matilda R.; Barnett, Christopher P.; Scott, Hamish S. 分享 收藏
Reference isotherms for water vapor sorption on nanoporous carbon: results of an interlaboratory study Nguyen, Huong Giang T.; Toman, Blaza; van Zee, Roger D. D.; Prinz, Carsten; Thommes, Matthias; Ahmad, Riaz; Kiska, David; Salinger, Jamie; Walton, Ian M. M.; Walton, Krista S. S.; Broom, Darren P. P.; Benham, Michael J. J.; Ansari, Humera; Pini, Ronny; Petit, Camille; Adolphs, Juergen; Schreiber, Andreas; Shigeoka, Toshihiro; Konishi, Yuko; Nakai, Kazuyuki; Henninger, Matthias; Petrzik, Thomas; Kececi, Can; Martis, Vladimir; Paschke, Thomas; Mangano, Enzo; Brandani, Stefano 分享 收藏
Impact of additional genetic abnormalities at diagnosis of chronic myeloid leukemia for first-line imatinib-treated patients receiving proactive treatment intervention Shanmuganathan, Naranie; Wadham, Carol; Shahrin, NurHezrin; Feng, Jinghua; Thomson, Daniel; Wang, Paul; Saunders, Verity; Kok, Chung Hoow; King, Rob M.; Kenyon, Rosalie R.; Lin, Ming; Pagani, Ilaria S.; Ross, David M.; Yong, Agnes S. M.; Grigg, Andrew P.; Mills, Anthony K.; Schwarer, Anthony P.; Braley, Jodi; Altamura, Haley; Yeung, David T.; Scott, Hamish S.; Schreiber, Andreas W.; Hughes, Timothy P.; Branford, Susan 分享 收藏
Novel modes of MPL activation in triple-negative myeloproliferative neoplasms Samaraweera, Saumya E.; Geukens, Tatjana; Casolari, Debora A.; Nguyen, Tran; Sun, Caitlyn; Bailey, Sheree; Moore, Sarah; Feng, Jinghua; Schreiber, Andreas W.; Parker, Wend T.; Brown, Anna L.; Butcher, Carolyn; Bardy, Peter G.; Osborn, Michael; Scott, Hamish S.; Talaulikar, Dipti; Grove, Carolyn S.; Hahn, Christopher N.; D'andrea, Richard J.; Ross, David M. 分享 收藏
Genomic autopsy to identify underlying causes of pregnancy loss and perinatal death 基因组尸检以确定妊娠丢失和围产儿死亡的根本原因 Byrne, Alicia B.; Arts, Peer; Ha, Thuong T.; Kassahn, Karin S.; Pais, Lynn S.; O'Donnell-Luria, Anne; Babic, Milena; Frank, Mahalia S. B.; Feng, Jinghua; Wang, Paul; Lawrence, David M.; Eshraghi, Leila; Arriola, Luis; Toubia, John; Nguyen, Hung; McGillivray, George; Pinner, Jason; McKenzie, Fiona; Morrow, Rebecca; Lipsett, Jill; Manton, Nick; Khong, T. Yee; Moore, Lynette; Liebelt, Jan E.; Schreiber, Andreas W.; King-Smith, Sarah L.; Hardy, Tristan S. E.; Jackson, Matilda R.; Barnett, Christopher P.; Scott, Hamish S.; Aguet, Francois; Arachchi, Harindra M.; Austin-Tse, Christina A.; Babb, Larry; Baxter, Samantha M.; Brand, Harrison; Byrne, Alicia B.; Chang, Jaime; Chao, Katherine R.; Collins, Ryan L.; Cummings, Beryl; Delano, Kayla; DiTroia, Stephanie P.; England, Eleina; Evangelista, Emily; Everett, Selin; Francioli, Laurent C.; Fu, Jack; Ganesh, Vijay S.; Garimella, Kiran, V; Gauthier, Laura D.; Goodrich, Julia K.; Gudmundsson, Sanna; Hall, Stacey J.; Huang, Yongqing; Jahl, Steve; Laricchia, Kristen M.; Larkin, Kathryn E.; Lek, Monkol; Lemire, Gabrielle; Lipson, Rachel B.; Lovgren, Alysia Kern; MacArthur, Daniel G.; Mangilog, Brian E.; Mano, Stacy; Marshall, Jamie L.; Mullen, Thomas E.; Nguyen, Kevin K.; O'Heir, Emily; O'Leary, Melanie C.; Osei-Owusu, Ikeoluwa A.; Pais, Lynn S.; Chavez, Jorge Perez de Acha; Pierce-Hoffman, Emma; Rehm, Heidi L.; Serrano, Milan; Singer-Berk, Moriel; Snow, Hana; Solomonson, Matthew; Son, Rachel G.; Sveden, Abigail; Talkowski, Michael; Tiao, Grace; Udler, Miriam S.; Valivullah, Zaheer; Valkanas, Elise; VanNoy, Grace E.; Wang, Qingbo S.; Watts, Nicholas A.; Weisburd, Ben; Williamson, Clara E.; Wilson, Michael W.; Witzgall, Lauren; Wojcik, Monica H.; Wong, Isaac; Wood, Jordan C.; Zhang, Shifa; Abeysuriya, Disna; Ades, Lesley C.; Amor, David J.; Arbuckle, Susan; Bakshi, Madhura; Barnete, Christopher P.; Berry, Bligh; Boughtwood, Tiffany; Bournazos, Adam; Bray, Alessandra; Chan, Fiona; Chan, Yuen; Chung, Clara; Clark, Jonathan; Collett, Jackie; Colley, Alison; Collins, Felicity; Cooper, Sandra; Corbett, Mark A.; Dahlstrom, Jane E.; Dargaville, Peter; Davies, Janene; Davis, Tenielle; Dearman, Jarrad; Dissanayake, Jayanthi; Dobbins, Julia; Doyle, Helen; Dubowsky, Andrew; Edwards, Matt; Ewans, Lisa J.; Fadia, Mitali; Fennell, Andrew; Finlay, Ken; French, Andrew; Friend, Kathryn; Gardner, Alison E.; Gecz, Jozef; Graf, Nicole; Haan, Eric A.; Hollingsworth, Georgina; Horton, Ari E.; Howting, Denise; Hunter, Matthew F.; Jevon, Gareth; Kamien, Benjamin; Kennedy, Debra; Khong, T. Yee; Krivanek, Michael; Kroes, Thessa; Krzesinski, Emma, I; Kwan, Edward; Lau, Stephanie; LeBlanc, Shannon; Liebelt, Jan; Lindsey-Temple, Suzanna; Lipsett, Jill; Loo, Christine K. C.; Low, Julia; Mallawaarachchi, Amali; Manton, Nick; Matsika, Admire; Mattiske, Tessa; McGaughran, Julie; McGillivray, George; McGregor, Lesley; McKenzie, Fiona; Mittal, Namita; Moghimi, Ali; Moore, Lynette; Albayrak, Hatice Mutlu; Ng, Jessica; Nicholl, Jillian; Pachter, Nicholas; Papadimitriou, John; Parker, Renae; Parsons, Sarah; Patel, Chirag; Pawlowski, Rhonda; Perez-Jurado, Luis A.; Pinner, Jason R.; Politis, Katerina; Poulton, Cathryn; Power, Theresa; Quinn, Michael; Rajagopalan, Sulekha; Regan, Matthew; Rodgers, Jonathan; Rorke, Steuart; Sachdev, Rani; Sallevelt, Suzanne; Sandaradura, Sarah A.; Shamassi, Maryam; Shamon, Roshan; Sherburn, Isabella; Slee, Ennie; Solinas, Annalisa; Sugo, Ella; Thompson, Elizabeth; Tripathy, Sagarika; Vasudevan, Anand; Vazquez, Melisa; Verma, Kunal; Viki, Mthulisi; Wallis, Mathew; Webber, Dani L.; Weber, Martin; Whale, Karen; Wilson, Meredith; Worgan, Lisa; Yu, Sui 分享 收藏
Clonal hematopoiesis in patients with ANKRD26 or ETV6 germline mutations Drazer, Michael W.; Homan, Claire C.; Yu, Kai; de Andrade Silva, Marcela Cavalcante; McNeely, Kelsey E.; Pozsgai, Matthew J.; Acevedo-Mendez, Maria G.; Segal, Jeremy P.; Wang, Peng; Feng, Jinghua; King-Smith, Sarah L.; Kim, Erika; Korotev, Sophia; Lawrence, David M.; Schreiber, Andreas W.; Hahn, Christopher N.; Scott, Hamish S.; Sood, Raman; Velloso, Elvira D. R. P.; Brown, Anna L.; Liu, Paul P.; Godley, Lucy A. 分享 收藏
RNA-Based Targeted Gene Sequencing Improves the Diagnostic Yield of Mutant Detection in Chronic Myeloid Leukemia Shanmuganathan, Naranie; Wadham, Carol; Thomson, Daniel; Shahrin, Nur Hezrin; Vignaud, Chloe; Obourn, Vanessa; Chaturvedi, Shalini; Yang, Feng; Feng, Jinghua; Saunders, Verity; Kok, Chung H.; Yeung, David; King, Rob M.; Kenyon, Rosalie R.; Lin, Ming; Wang, Paul; Scott, Hamish; Hughes, Timothy; Schreiber, Andreas W.; Branford, Susan 分享 收藏
The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy Homan, Claire C.; King-Smith, Sarah L.; Lawrence, David M.; Arts, Peer; Feng, Jinghua; Andrews, James; Armstrong, Mark; Ha, Thuong; Dobbins, Julia; Drazer, Michael W.; Yu, Kai; Bodor, Csaba; Cantor, Alan; Cazzola, Mario; Degelman, Erin; DiNardo, Courtney D.; Duployez, Nicolas; Favier, Remi; Frohling, Stefan; Fitzgibbon, Jude; Klco, Jeffery M.; Kramer, Alwin; Kurokawa, Mineo; Lee, Joanne; Malcovati, Luca; Morgan, Neil V.; Natsoulis, Georges; Owen, Carolyn; Patel, Keyur P.; Preudhomme, Claude; Raslova, Hana; Rienhoff, Hugh; Ripperger, Tim; Schulte, Rachael; Tawana, Kiran; Velloso, Elvira; Yan, Benedict; Liu, Paul; Godley, Lucy A.; Schreiber, Andreas W.; Hahn, Christopher N.; Scott, Hamish S.; Brown, Anna L. 分享 收藏
Targeted gene panels identify a high frequency of pathogenic germline variants in patients diagnosed with a hematological malignancy and at least one other independent cancer Singhal, Deepak; Hahn, Christopher N.; Feurstein, Simone; Wee, Li Yan A.; Moma, Luke; Kutyna, Monika M.; Chhetri, Rakchha; Eshraghi, Leila; Schreiber, Andreas W.; Feng, Jinghua; Wang, Paul P-S; Babic, Milena; Parker, Wendy T.; Gao, Song; Moore, Sarah; Das, Soma; Thomas, David; Pattnaik, Swetansu; Brown, Anna L.; D'Andrea, Richard J.; Poplawski, Nicola K.; Thomas, Daniel; Scott, Hamish S.; Godley, Lucy A.; Hiwase, Devendra K. 分享 收藏
2D and 3D convolutional neural networks for outcome modelling of locally advanced head and neck squamous cell carcinoma Starke, Sebastian; Leger, Stefan; Zwanenburg, Alex; Leger, Karoline; Lohaus, Fabian; Linge, Annett; Schreiber, Andreas; Kalinauskaite, Goda; Tinhofer, Inge; Guberina, Nika; Guberina, Maja; Balermpas, Panagiotis; von der Grun, Jens; Ganswindt, Ute; Belka, Claus; Peeken, Jan C.; Combs, Stephanie E.; Boeke, Simon; Zips, Daniel; Richter, Christian; Troost, Esther G. C.; Krause, Mechthild; Baumann, Michael; Loeck, Steffen 分享 收藏
Gene expression profiling to improve prognostic characterization of olfactory neuroblastoma and to define new targetable pathways Romani, C.; Lorini, L.; Ravaggi, A.; Bignotti, E.; Paderno, A.; Mattavelli, D.; Rampinelli, V.; Schreiber, A.; Ferrari, M.; Nicolai, P.; Deganello, A.; Ravanelli, M.; Ardighieri, L.; Bozzola, A.; Battocchio, S.; Castelnuovo, P.; Calza, S.; Magrini, S. M.; Zanoni, M. Turri; Bossi, P. 分享 收藏
RUNX1mutations in blast-phase chronic myeloid leukemia associate with distinct phenotypes, transcriptional profiles, and drug responses Awad, Shady Adnan; Dufva, Olli; Ianevski, Aleksandr; Ghimire, Bishwa; Koski, Jan; Maliniemi, Pilvi; Thomson, Daniel; Schreiber, Andreas; Heckman, Caroline A.; Koskenvesa, Perttu; Korhonen, Matti; Porkka, Kimmo; Branford, Susan; Aittokallio, Tero; Kankainen, Matti; Mustjoki, Satu 分享 收藏
Aberrant Splicing of SDHC in Families With Unexplained Succinate Dehydrogenase-Deficient Paragangliomas De Sousa, Sunita M. C.; Toubia, John; Hardy, Tristan S. E.; Feng, Jinghua; Wang, Paul; Schreiber, Andreas W.; Geoghegan, Joel; Hall, Rachel; Rawlings, Lesley; Buckland, Michael; Luxford, Catherine; Novos, Talia; Clifton-Bligh, Roderick J.; Poplawski, Nicola K.; Scott, Hamish S.; Torpy, David J. 分享 收藏
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RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML RUNX1-mutated家族显示出表型异质性和种系易感AML特有的体细胞突变谱 Brown, Anna L.; Arts, Peer; Carmichael, Catherine L.; Babic, Milena; Dobbins, Julia; Chong, Chan-Eng; Schreiber, Andreas W.; Feng, Jinghua; Phillips, Kerry; Wang, Paul P. S.; Thuong Ha; Homan, Claire C.; King-Smith, Sarah L.; Rawlings, Lesley; Vakulin, Cassandra; Dubowsky, Andrew; Burdett, Jessica; Moore, Sarah; McKavanagh, Grace; Henry, Denae; Wells, Amanda; Mercorella, Belinda; Nicola, Mario; Suttle, Jeffrey; Wilkins, Ella; Li, Xiao-Chun; Michaud, Joelle; Brautigan, Peter; Cannon, Ping; Altree, Meryl; Jaensch, Louise; Fine, Miriam; Butcher, Carolyn; D'Andrea, Richard J.; Lewis, Ian D.; Hiwase, Devendra K.; Papaemmanuil, Elli; Horwitz, Marshall S.; Natsoulis, Georges; Rienhoff, Hugh Y., Jr.; Patton, Nigel; Mapp, Sally; Susman, Rachel; Morgan, Susan; Cooney, Julian; Currie, Mark; Popat, Uday; Bochtler, Tilmann; Izraeli, Shai; Bradstock, Kenneth; Godley, Lucy A.; Kraemer, Alwin; Froehling, Stefan; Wei, Andrew H.; Forsyth, Cecily; Fan, Helen Mar; Poplawski, Nicola K.; Hahn, Christopher N.; Scott, Hamish S. 分享 收藏
Aberrant RAG-mediated recombination contributes to multiple structural rearrangements in lymphoid blast crisis of chronic myeloid leukemia Thomson, Daniel W.; Shahrin, Nur Hezrin; Wang, Paul P. S.; Wadham, Carol; Shanmuganathan, Naranie; Scott, Hamish S.; Dinger, Marcel E.; Hughes, Timothy P.; Schreiber, Andreas W.; Branford, Susan 分享 收藏
Pseudodiastrophic dysplasia expands the known phenotypic spectrum of defects in proteoglycan biosynthesis Byrne, Alicia B.; Mizumoto, Shuji; Arts, Peer; Yap, Patrick; Feng, Jinghua; Schreiber, Andreas W.; Babic, Milena; King-Smith, Sarah L.; Barnett, Christopher P.; Moore, Lynette; Sugahara, Kazuyuki; Mutlu-Albayrak, Hatice; Nishimura, Gen; Liebelt, Jan E.; Yamada, Shuhei; Savarirayan, Ravi; Scott, Hamish S. 分享 收藏
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