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收藏Characterization of monoclonal gammopathy of undetermined significance progression to multiple myeloma through meta-analysis of GEO data
Aljabban, Jihad; Syed, Sharjeel; Syed, Saad; Rohr, Michael; Mukhtar, Mohamed; Aljabban, Hisham; Cottini, Francesca; Mohammed, Mohammed; Hughes, Tiffany; Gonzalez, Taylor; Panahiazr, Maryam; Hadley, Dexter; Benson, Don 分享 收藏 分享 收藏 分享 收藏 分享 收藏 分享 收藏 Metaanalysis Reveals Genetic Correlates of Osteoporosis PathogenesisHasan, Laith K.; Aljabban, Jihad; Rohr, Michael; Mukhtar, Mohamed; Adapa, Nikhil; Salim, Rahaf; Aljabban, Nabeal; Syed, Saad; Syed, Sharjeel; Panahiazar, Maryam; Hadley, Dexter; Jarjour, Wael 分享 收藏 Investigating genetic drivers of dermatomyositis pathogenesis using meta-analysisAljabban, Jihad; Syed, Saad; Syed, Sharjeel; Rohr, Michael; Weisleder, Noah; McElhanon, Kevin E.; Hasan, Laith; Safeer, Laraib; Hoffman, Kalyn; Aljabban, Nabeal; Mukhtar, Mohamed; Adapa, Nikhil; Allarakhia, Zahir; Panahiazar, Maryam; Neuhaus, Isaac; Kim, Susan; Hadley, Dexter; Jarjour, Wael 分享 收藏 Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associationsLi, Yun Rose; Glessner, Joseph T.; Coe, Bradley P.; Li, Jian-jun; Mohebnasab, Maede; Chang, Xiao; Connolly, John; Kao, Charlly; Wei, Zhi; Bradfield, Jonathan; Kim, Cecilia; Hou, Cuiping; Khan, Munir; Mentch, Frank; Qiu, Haijun; Bakay, Marina; Cardinale, Christopher; Lemma, Maria; Abrams, Debra; Bridglall-Jhingoor, Andrew; Behr, Meckenzie; Harrison, Shanell; Otieno, George; Thomas, Alexandria; Wang, Fengxiang; Chiavacci, Rosetta; Wu, Lawrence; Hadley, Dexter; Goldmuntz, Elizabeth; Elia, Josephine; Maris, John; Grundmeier, Robert; Devoto, Marcella; Keating, Brendan; March, Michael; Pellagrino, Renata; Grant, Struan F. A.; Sleiman, Patrick M. A.; Li, Mingyao; Eichler, Evan E.; Hakonarson, Hakon 分享 收藏 分享 收藏 Meta-analysis Illustrates the Genetic Signature Underlying Allergic Rhinitis Pathophysiology and Potential Therapeutic TargetsAljabban, Jihad; McDermott, Sean; Wanner, Ross A.; Salhi, Hussam; Aljabban, Nabeal; Mukhtar, Mohamad; Mohammed, Zhraa; Aljabban, Hisham; Panahiazar, Maryam; Hadley, Dexter 分享 收藏 A Deep Learning Model to Predict a Diagnosis of Alzheimer Disease by Using 18F-FDG PET of the BrainDing, Yuming; Sohn, Jae Ho; Kawczynski, Michael G.; Trivedi, Hari; Harnish, Roy; Jenkins, Nathaniel W.; Lituiev, Dmytro; Copeland, Timothy P.; Aboian, Mariam S.; Aparici, Carina Mari; Behr, Spencer C.; Flavell, Robert R.; Huang, Shih-Ying; Zalocusky, Kelly A.; Nardo, Lorenzo; Seo, Youngho; Hawkins, Randall A.; Pampaloni, Miguel Hernandez; Hadley, Dexter; Franc, Benjamin L. 分享 收藏 Translational Radiomics: Defining the Strategy Pipeline and Considerations for Application-Part 1: From Methodology to Clinical ImplementationShaikh, Faiq; Franc, Benjamin; Allen, Erastus; Sala, Evis; Awan, Omer; Hendrata, Kenneth; Halabi, Safwan; Mohiuddin, Sohaib; Malik, Sana; Hadley, Dexter; Shrestha, Rasu 分享 收藏 Translational Radiomics: Defining the Strategy Pipeline and Considerations for Application-Part 2: From Clinical Implementation to EnterpriseShaikh, Faiq; Franc, Benjamin; Allen, Erastus; Sala, Evis; Awan, Omer; Hendrata, Kenneth; Halabi, Safivan; Mohiuddin, Sohaib; Malik, Sana; Hadley, Dexter; Shrestha, Rasu 分享 收藏 A genome-wide association study identifies only two ancestry specific variants associated with spontaneous preterm birthRappoport, Nadav; Toung, Jonathan; Hadley, Dexter; Wong, Ronald J.; Fujioka, Kazumichi; Reuter, Jason; Abbott, Charles W.; Oh, Sam; Hu, Donglei; Eng, Celeste; Huntsman, Scott; Bodian, Dale L.; Niederhuber, John E.; Hong, Xiumei; Zhang, Ge; Sikora-Wohfeld, Weronika; Gignoux, Christopher R.; Wang, Hui; Oehlert, John; Jelliffe-Pawlowski, Laura L.; Gould, Jeffrey B.; Darmstadt, Gary L.; Wang, Xiaobin; Bustamante, Carlos D.; Snyder, Michael P.; Ziv, Elad; Patsopoulos, Nikolaos A.; Muglia, Louis J.; Burchard, Esteban; Shaw, Gary M.; O'Brodovich, Hugh M.; Stevenson, David K.; Butte, Atul J.; Sirota, Marina 分享 收藏 分享 收藏 The impact of the metabotropic glutamate receptor and other gene family interaction networks on autismHadley, Dexter; Wu, Zhi-liang; Kao, Charlly; Kini, Akshata; Mohamed-Hadley, Alisha; Thomas, Kelly; Vazquez, Lyam; Qiu, Haijun; Mentch, Frank; Pellegrino, Renata; Kim, Cecilia; Connolly, John; Glessner, Joseph; Hakonarson, Hakon 分享 收藏 Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control population鉴定高风险自闭症家庭中罕见的DNA序列变异及其在大量病例/对照人群中的患病率Matsunami, Nori; Hensel, Charles H.; Baird, Lisa; Stevens, Jeff; Otterud, Brith; Leppert, Tami; Varvil, Tena; Hadley, Dexter; Glessner, Joseph T.; Pellegrino, Renata; Kim, Cecilia; Thomas, Kelly; Wang, Fengxiang; Otieno, Frederick G.; Ho, Karen; Christensen, Gerald B.; Li, Dongying; Prekeris, Rytis; Lambert, Christophe G.; Hakonarson, Hakon; Leppert, Mark F. 分享 收藏 分享 收藏 Copy-Number Disorders Are a Common Cause of Congenital Kidney MalformationsSanna-Cherchi, Simone; Kiryluk, Krzysztof; Burgess, Katelyn E.; Bodria, Monica; Sampson, Matthew G.; Hadley, Dexter; Nees, Shannon N.; Verbitsky, Miguel; Perry, Brittany J.; Sterken, Roel; Lozanovski, Vladimir J.; Materna-Kiryluk, Anna; Barlassina, Cristina; Kini, Akshata; Corbani, Valentina; Carrea, Alba; Somenzi, Danio; Murtas, Corrado; Ristoska-Bojkovska, Nadica; Izzi, Claudia; Bianco, Beatrice; Zaniew, Marcin; Flogelova, Hana; Weng, Patricia L.; Kacak, Nilgun; Giberti, Stefania; Gigante, Maddalena; Arapovic, Adela; Drnasin, Kristina; Caridi, Gianluca; Curioni, Simona; Allegri, Franca; Ammenti, Anita; Ferrettio, Stefania; Goj, Vinicio; Bernardo, Luca; Jobanputra, Vaidehi; Chung, Wendy K.; Lifton, Richard P.; Sanders, Stephan; State, Matthew; Clark, Lorraine N.; Saraga, Marijan; Padmanabhan, Sandosh; Dominiczak, Anna F.; Foroud, Tatiana; Gesualdo, Loreto; Gucev, Zoran; Allegri, Landino; Latos-Bielenska, Anna; Cusi, Daniele; Scolari, Francesco; Tasic, Velibor; Hakonarson, Hakon; Ghiggeri, Gian Marco; Gharavi, Ali G. 分享 收藏 
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