Temporal Change of Soil Carbon on a Long-Term Experimental Site with Variable Crop Rotations and Tillage Systems by Ahmed Laamrani, Paul R. Voroney, Aaron A. Berg, Adam W. Gillespie, Michael March, Bill Deen, Ralph C. Martin

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P286: Single vs dual disease causing variant load in a pediatric cohort with congenital anomalies and cancer by Amir Hossein Saeidian, Deborah Watson, Xiang Wang, Margaret Harr, Shannon Terek, Michael March, Haijun Qiu, Isabella Barcelos, Patrick Sleiman, Joseph Glessner, Hakon Hakonarson

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Single Cell Transcriptome Analysis of Peripheral Blood Mononuclear Cells in Freshly Isolated versus Stored Blood Samples by Hui-Qi Qu, Charlly Kao, James Garifallou, Fengxiang Wang, James Snyder, Diana J. Slater, Cuiping Hou, Michael March, John J. Connolly, Joseph T. Glessner, Hakon Hakonarson

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Insights into non-autoimmune type 1 diabetes with 13 novel loci in low polygenic risk score patients by Jingchun Qu, Hui-Qi Qu, Jonathan P. Bradfield, Joseph T. Glessner, Xiao Chang, Lifeng Tian, Michael March, John J. Connolly, Jeffrey D. Roizen, Patrick M. A. Sleiman, Hakon Hakonarson

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Genetic architecture of type 1 diabetes with low genetic risk score informed by 41 unreported loci by Hui-Qi Qu, Jingchun Qu, Jonathan Bradfield, Luc Marchand, Joseph Glessner, Xiao Chang, Michael March, Jin Li, John J. Connolly, Jeffrey D. Roizen, Patrick Sleiman, Constantin Polychronakos, Hakon Hakonarson

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Application of Whole Exome Sequencing in Six Families with an Initial Diagnosis of Autosomal Dominant Retinitis Pigmentosa: Lessons Learned. by Berta Almoguera, Jiankang Li, Patricia Fernandez-San Jose, Yichuan Liu, Michael March, Renata Pellegrino, Ryan Golhar, Marta Corton, Fiona Blanco-Kelly, Maria Isabel López-Molina, Blanca García-Sandoval, Yiran Guo, Lifeng Tian, Xuanzhu Liu, Liping Guan, Jianguo Zhang, Brendan Keating, Xun Xu, Hakon Hakonarson, Carmen Ayuso

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O27: Utility of cfDNA in comprehensive genomic profiling of complex vascular anomalies: Informing decision making in medical therapy by Dong Li, Sarah Sheppard, Michael March, Mark Battig, Lea Surrey, Abhay Srinivasan, Alexandra Borst, Fengxiang Wang, Tamjeed Sikder, Nora O’Connor, Alexandria Thomas, Erin Pinto, Allison Britt, Joseph Napoli, David Low, Seth Vatsky, James Treat, Janet Reid, Christopher Smith, Kristen Snyder, Anne Marie Cahill, Yoav Dori, Denise Adams, Hakon Hakonarson

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Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations by Yun Rose Li, Joseph T. Glessner, Bradley P. Coe, Jin Li, Maede Mohebnasab, Xiao Chang, John Connolly, Charlly Kao, Zhi Wei, Jonathan Bradfield, Cecilia Kim, Cuiping Hou, Munir Khan, Frank Mentch, Haijun Qiu, Marina Bakay, Christopher Cardinale, Maria Lemma, Debra Abrams, Andrew Bridglall-Jhingoor, Meckenzie Behr, Shanell Harrison, George Otieno, Alexandria Thomas, Fengxiang Wang, Rosetta Chiavacci, Lawrence Wu, Dexter Hadley, Elizabeth Goldmuntz, Josephine Elia, John Maris, Robert Grundmeier, Marcella Devoto, Brendan Keating, Michael March, Renata Pellagrino, Struan F. A. Grant, Patrick M. A. Sleiman, Mingyao Li, Evan E. Eichler, Hakon Hakonarson

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