未登录 Current and Future Utilization of Optical Genome Mapping Insights From the 2024 College of American Pathologists Supplemental Questionnaire 2024年美国病理学家学会补充问卷中光学基因组图谱的当前与未来应用 Gardner, Juli-Anne; Nusapan, Rangsinee; Tan, Julian; Levy, Brynn; Tang, Guilin; Fang, Min; Velagaleti, Gopalrao V.; Cao, Yang; Astbury, Caroline; Mixon, James Christopher; Souers, Rhona J.; Peterson, Jess F.; Zou, Ying S. 分享 收藏
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Integration of Optical Genome Mapping in the Cytogenomic and Molecular Work-Up of Hematological Malignancies: Expert Recommendations From the International Consortium for Optical Genome Mapping 在血液系统恶性肿瘤的细胞基因组学和分子研究中整合光学基因组图谱: 国际光学基因组图谱协会的专家建议 Kanagal-Shamanna, R; Puiggros, A; Granada, I; Raca, G; Rack, K; Mallo, M; Dewaele, B; Smith, AC; Akkari, Y; Levy, B; Hasserjian, RP; Cisneros, A; Salido, M; Garcia-Manero, G; Yang, H; Iqbal, MA; Kolhe, R; Solé, F; Espinet, B 分享 收藏
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Multisite Evaluation and Validation of Optical Genome Mapping for Prenatal Genetic Testing Levy, Brynn; Liu, Jie; Iqbal, M. Anwar; DuPont, Barbara; Sahajpal, Nikhil; Ho, Monique; Yu, Jingwei; Brody, Sam J.; Ganapathi, Mythily; Rajkovic, Aleksandar; Smolarek, Teresa A.; Boyar, Fatih; Bui, Peter; Dubuc, Adrian M.; Kolhe, Ravindra; Stevenson, Roger E. 分享 收藏
Conventional Cytogenetic Analysis of Constitutional Abnormalities Boles, Brittney; Gardner, Juli-Anne; Rehder, Catherine W.; Levy, Brynn; Velagaleti, Gopalrao V.; Toydemir, Reha M.; Sukov, William R.; Larson, Daniel P.; Cao, Yang; Mixon, Christopher; Vanderscheldon, Rachel K.; Zou, Ying S.; Astbury, Caroline; Tsuchiya, Karen D.; Peterson, Jess F. 分享 收藏
Detection of Constitutional Structural Variants by Optical Genome Mapping A Multisite Study of Postnatal Samples Broeckel, Ulrich; Iqbal, M. Anwar; Levy, Brynn; Sahajpal, Nikhil; Nagy, Peter L.; Scharer, Gunter; Rodriguez, Vanessa; Bossler, Aaron; Stence, Aaron; Skinner, Cindy; Skinner, Steven A.; Kolhe, Ravindra; Stevenson, Roger 分享 收藏
A framework for the clinical implementation of optical genome mapping in hematologic malignancies 在血液系统恶性肿瘤中进行光学基因组定位的临床实施框架 Levy, Brynn; Kanagal-Shamanna, Rashmi; Sahajpal, Nikhil S.; Neveling, Kornelia; Rack, Katrina; Dewaele, Barbara; Weghuis, Daniel Olde; Stevens-Kroef, Marian; Puiggros, Anna; Mallo, Mar; Clifford, Benjamin; Mantere, Tuomo; Hoischen, Alexander; Espinet, Blanca; Kolhe, Ravindra; Sole, Francesc; Raca, Gordana; Smith, Adam C. 分享 收藏
Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies Lowther, Chelsea; Valkanas, Elise; Giordano, Jessica L.; Wang, Harold Z.; Currall, Benjamin B.; O'Keefe, Kathryn; Pierce-Hoffman, Emma; Kurtas, Nehir E.; Whelan, Christopher W.; Hao, Stephanie P.; Weisburd, Ben; Jalili, Vahid; Fu, Jack; Wong, Isaac; Collins, Ryan L.; Zhao, Xuefang; Austin-Tse, Christina A.; Evangelista, Emily; Lemire, Gabrielle; Aggarwal, Vimla S.; Lucente, Diane; Gauthier, Laura D.; Tolonen, Charlotte; Sahakian, Nareh; Stevens, Christine; An, Joon-Yong; Dong, Shan; Norton, Mary E.; Mackenzie, Tippi C.; Devlin, Bernie; Gilmore, Kelly; Powell, Bradford C.; Brandt, Alicia; Vetrini, Francesco; Divito, Michelle; Sanders, Stephan J.; Macarthur, Daniel G.; Hodge, Jennelle C.; O'Donnell-Luria, Anne; Rehm, Heidi L.; Vora, Neeta L.; Levy, Brynn; Brand, Harrison; Wapner, Ronald J.; Talkowski, Michael E. 分享 收藏
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Optical genome mapping in acute myeloid leukemia: a multicenter evaluation Levy, Brynn; Baughn, Linda B.; Akkari, Yassmine; Chartrand, Scott; LaBarge, Brandon; Claxton, David; Lennon, P. Alan; Cujar, Claudia; Kolhe, Ravindra; Kroeger, Kate; Pitel, Beth; Sahajpal, Nikhil; Sathanoori, Malini; Vlad, George; Zhang, Lijun; Fang, Min; Kanagal-Shamanna, Rashmi; Broach, James R. 分享 收藏
Multisite Assessment of Optical Genome Mapping for Analysis of Structural Variants in Constitutional Postnatal Cases Iqbal, M. Anwar; Broeckel, Ulrich; Levy, Brynn; Skinner, Steven; Sahajpal, Nikhil S.; Rodriguez, Vanessa; Stence, Aaron; Awayda, Kamel; Scharer, Gunter; Skinner, Cindy; Stevenson, Roger; Bossler, Aaron; Nagy, Peter L.; Kolhe, Ravindra 分享 收藏
Rapid Nanopore Sequencing-Based Screen for Aneuploidy in Reproductive Care Wei, Shan; Djandji, Alexandre; Lattin, Miriam T.; Nahum, Odelia; Hoffman, Nataly; Cujar, Claudia; Kayali, Refik; Cinnioglu, Cengiz; Wapner, Ronald; D'Alton, Mary; Levy, Brynn; Williams, Zev 分享 收藏
Whole-genome risk prediction of common diseases in human preimplantation embryos Kumar, Akash; Im, Kate; Banjevic, Milena; Ng, Pauline C.; Tunstall, Tate; Garcia, Geronimo; Galhardo, Luisa; Sun, Jiayi; Schaedel, Oren N.; Levy, Brynn; Hongo, Donna; Kijacic, Dusan; Kiehl, Michelle; Tran, Nam D.; Klatsky, Peter C.; Rabinowitz, Matthew 分享 收藏
Optical genome mapping for constitutional postnatal SV, CNV, and repeat array sizing: A multi-site clinical study Sahajpal, Nikhil; Rodriguez, Vanessa; Kanyo, Luca; Stence, Aaron; Skinner, Steven; Iqbal, Anwar; Awayda, Kamel; Levy, Brynn; Broeckel, Ulrich; Scharer, Gunter; Hackman, Jason; Mondal, Ashis; Bossler, Aaron; Nagy, Peter; Kolhe, Ravindra 分享 收藏
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Validation Studies for Single Circulating Trophoblast Genetic Testing as a Form of Noninvasive Prenatal Diagnosis Vossaert, Liesbeth; Wang, Qun; Salman, Roseen; McCombs, Anne K.; Patel, Vipulkumar; Qu, Chunjing; Mancini, Michael A.; Edwards, Dean P.; Malovannaya, Anna; Liu, Pengfei; Shaw, Chad A.; Levy, Brynn; Wapner, Ronald J.; Bi, Weimin; Breman, Amy M.; Van den Veyver, Ignatia B.; Beaudet, Arthur L. 分享 收藏
High-resolution genomic alterations in Barrett's metaplasia of patients who progress to esophageal dysplasia and adenocarcinoma 进展为食管异型增生和腺癌的患者的Barrett化生的高分辨率基因组改变 Sepulveda, Jorge L.; Komissarova, Elena, V; Kongkarnka, Sarawut; Friedman, Richard A.; Davison, Jon M.; Levy, Brynn; Bryk, Diana; Jobanputra, Vaidehi; Del Portillo, Armando; Falk, Gary W.; Sonett, Joshua R.; Lightdale, Charles J.; Abrams, Julian A.; Wang, Timothy C.; Sepulveda, Antonia R. 分享 收藏
The copy number variation landscape of congenital anomalies of the kidney and urinary tract (vol 51, pg 117, 2018) Verbitsky, Miguel; Westland, Rik; Perez, Alejandra; Kiryluk, Krzysztof; Liu, Qingxue; Krithivasan, Priya; Mitrotti, Adele; Fasel, David A.; Batourina, Ekaterina; Sampson, Matthew G.; Bodria, Monica; Werth, Max; Kao, Charlly; Martino, Jeremiah; Capone, Valentina P.; Vivante, Asaf; Shril, Shirlee; Kil, Byum Hee; Marasa, Maddalena; Zhang, Jun Y.; Na, Young-Ji; Lim, Tze Y.; Ahram, Dina; Weng, Patricia L.; Heinzen, Erin L.; Carrea, Alba; Piaggio, Giorgio; Gesualdo, Loreto; Manca, Valeria; Masnata, Giuseppe; Gigante, Maddalena; Cusi, Daniele; Izzi, Claudia; Scolari, Francesco; van Wijk, Joanna A. E.; Saraga, Marijan; Santoro, Domenico; Conti, Giovanni; Zamboli, Pasquale; White, Hope; Drozdz, Dorota; Zachwieja, Katarzyna; Miklaszewska, Monika; Tkaczyk, Marcin; Tomczyk, Daria; Krakowska, Anna; Sikora, Przemyslaw; Jarmolinski, Tomasz; Borszewska-Kornacka, Maria K.; Pawluch, Robert; Szczepanska, Maria; Adamczyk, Piotr; Mizerska-Wasiak, Malgorzata; Krzemien, Grazyna; Szmigielska, Agnieszka; Zaniew, Marcin; Dobson, Mark G.; Darlow, John M.; Puri, Prem; Barton, David E.; Furth, Susan L.; Warady, Bradley A.; Gucev, Zoran; Lozanovski, Vladimir J.; Tasic, Velibor; Pisani, Isabella; Allegri, Landino; Rodas, Lida M.; Campistol, Josep M.; Jeanpierre, Cecile; Alam, Shumyle; Casale, Pasquale; Wong, Craig S.; Lin, Fangming; Miranda, Debora M.; Oliveira, Eduardo A.; Simoes-e-Silva, Ana Cristina; Barasch, Jonathan M.; Levy, Brynn; Wu, Nan; Hildebrandt, Friedhelm; Ghiggeri, Gian Marco; Latos-Bielenska, Anna; Materna-Kiryluk, Anna; Zhang, Feng; Hakonarson, Hakon; Papaioannou, Virginia E.; Mendelsohn, Cathy L.; Gharavi, Ali G.; Sanna-Cherchi, Simone 分享 收藏
Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study Petrovski, Slave; Aggarwal, Vimla; Giordano, Jessica L.; Stosic, Melissa; Wou, Karen; Bier, Louise; Spiegel, Erica; Brennan, Kelly; Stong, Nicholas; Jobanputra, Vaidehi; Ren, Zhong; Zhu, Xiaolin; Mebane, Caroline; Nahum, Odelia; Wang, Quanli; Kamalakaran, Sitharthan; Malone, Colin; Anyane-Yeboa, Kwame; Miller, Russell; Levy, Brynn; Goldstein, David B.; Wapner, Ronald J. 分享 收藏
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