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M

Mary J. Emond

University of Washington

49H指数
172论文数
1.4W被引数
收录论文 66
发表时间
An exome-wide study of renal operational tolerance
err2023-05-17
err2
errOAAI
errMassart, Annick; Danger, Richard; Olsen, Catharina J.; Emond, Mary; Viklicky, Ondrej; Jacquemin, Valerie; Soblet, Julie; Duerinckx, Sarah; Croes, Didier; Perazzolo, Camille; Hruba, Petra; Daneels, Dorien; Caljon, Ben; Sever, Mehmet Sukru; Pascual, Julio; Miglinas, Marius; Pirson, Isabelle; Ghisdal, Lidia; Smits, Guillaume; Giral, Magali; Abramowicz, Daniel; Abramowicz, Marc; Brouard, Sophie
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Homologous recombination resolution defect in Werner syndrome
err2023-03-28
err236
errOAAI
errSaintigny, Y; Makienko, K; Swanson, C; Emond, MJ; Monnat, RJ
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Genome Capture Sequencing Selectively Enriches Bacterial DNA and Enables Genome-Wide Measurement of Intrastrain Genetic Diversity in Human Infections
errMBIO
IF4.7
err2022-10-26
err5
errOAAI
errHayden, Hillary S.; Joshi, Snehal; Radey, Mathew C.; Vo, Anh T.; Forsberg, Cara; Morgan, Sarah J.; Waalkes, Adam; Holmes, Elizabeth A.; Klee, Sara M.; Emond, Mary J.; Singh, Pradeep K.; Salipante, Stephen J.
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Club cell secretory protein and lung function in children with cystic fibrosis
err2022-09-01
err12
errOAAI
errZhai, Jing; Emond, Mary J.; Spangenberg, Amber; Stern, Debra A.; Vasquez, Monica M.; Blue, Elizabeth E.; Buckingham, Kati J.; Sherrill, Duane L.; Halonen, Marilyn; Gibson, Ronald L.; Rosenfeld, Margaret; Sagel, Scott D.; Bamshad, Michael J.; Morgan, Wayne J.; Guerra, Stefano
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Inflammasome Genetic Variants, Macrophage Function, and Clinical Outcomes in Cystic Fibrosis
err2021-08-01
err12
errOAAI
errGraustein, Andrew D.; Berrington, William R.; Buckingham, Kati J.; Nguyen, Felicia K.; Joudeh, Lara L.; Rosenfeld, Margaret; Bamshad, Michael J.; Gibson, Ronald L.; Hawn, Thomas R.; Emond, Mary J.
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Ultra-Sensitive TP53 Sequencing for Cancer Detection Reveals Progressive Clonal Selection in Normal Tissue over a Century of Human Lifespan用于癌症检测的超灵敏TP53测序揭示了人类寿命一个世纪以来正常组织中的渐进克隆选择
err2019-07-01
err79
errOAAI
errSalk, Jesse J.; Loubet-Senear, Kaitlyn; Maritschnegg, Elisabeth; Valentine, Charles C.; Williams, Lindsey N.; Higgins, Jacob E.; Horvat, Reinhard; Vanderstichele, Adriaan; Nachmanson, Daniela; Baker, Kathryn T.; Emond, Mary J.; Loter, Emily; Tretiakova, Maria; Soussi, Thierry; Loeb, Lawrence A.; Zeillinger, Robert; Speiser, Paul; Risques, Rosa Ana
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Exonic sequencing identifies TLR1 genetic variation associated with mortality in Thais with melioidosis外显子测序鉴定与类鼻疽病泰国人死亡率相关的TLR1遗传变异
err2019-02-19
err4
errOAAI
errWright, Shelton W.; Emond, Mary J.; Lovelace-Macon, Lara; Ducken, Deirdre; Kashima, James; Hantrakun, Viriya; Chierakul, Wirongrong; Teparrukkul, Prapit; Chantratita, Narisara; Limmathurotsakul, Direk; West, T. Eoin
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Whole genome sequencing of extreme phenotypes identifies variants in CD101 and UBE2V1 associated with increased risk of sexually acquired HIV-1 (vol 13, e1006703, 2017)
err2019-02-11
err0
errOAAI
errMackelprang, Romel D.; Bamshad, Michael J.; Chong, Jessica X.; Hou, Xuanlin; Buckingham, Kati J.; Shively, Kathryn; deBruyn, Guy; Mugo, Nelly R.; Mullins, James I.; McElrath, M. Juliana; Baeten, Jared M.; Celum, Connie; Emond, Mary J.; Lingappa, Jairam R.
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Mitochondrial DNA Mutations are Associated with Ulcerative Colitis Preneoplasia but Tend to be Negatively Selected in Cancer
err2019-02-01
err29
errOAAI
errBaker, Kathryn T.; Nachmanson, Daniela; Kumar, Shilpa; Emond, Mary J.; Ussakli, Cigdem; Brentnall, Teresa A.; Kennedy, Scott R.; Risques, Rosa Ana
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Cirrhosis in Hemochromatosis: Independent Risk Factors in 368 HFE p.C282Y Homozygotes
err2018-09-01
err29
errOAAI
errBarton, James C.; McLaren, Christine E.; Chen, Wen-pin; Ramm, Grant A.; Anderson, Gregory J.; Powell, Lawrie W.; Subramaniam, V. Nathan; Adams, Paul C.; Phatak, Pradyumna D.; Gurrin, Lyle C.; Phillips, John D.; Parker, Charles J.; Emond, Mary J.; McLaren, Gordon D.
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Variation in Cilia Protein Genes and Progression of Lung Disease in Cystic Fibrosis
err2018-04-01
err16
errOAAI
errBlue, Elizabeth; Louie, Tin L.; Chong, Jessica X.; Hebbring, Scott J.; Barnes, Kathleen C.; Rafaels, Nicholas M.; Knowles, Michael R.; Gibson, Ronald L.; Bamshad, Michael J.; Emond, Mary J.
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TLR1 GENETIC VARIATION IS ASSOCIATED WITH INCREASED MORTALITY IN GRAM-NEGATIVE INFECTION
err2018-01-01
err0
PREAI
errWright, Shelton; Emond, Mary; Hantrakun, Viriya; Chierakul, Wirongrong; Chantratita, Narisara; Limmathurotsakul, Direk; West, T.
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The Epithelial Sodium Channel Is a Modifier of the Long-Term Nonprogressive Phenotype Associated with F508del CFTR Mutations
err2017-12-01
err33
errOAAI
errAgrawal, Pankaj B.; Wang, Ruobing; Li, Hongmei Lisa; Schmitz-Abe, Klaus; Simone-Roach, Chantelle; Chen, Jingxin; Shi, Jiahai; Louie, Tin; Sheng, Shaohu; Towne, Meghan C.; Brainson, Christine F.; Matthay, Michael A.; Kim, Carla F.; Bamshad, Michael; Emond, Mary J.; Gerard, Norma P.; Kleyman, Thomas R.; Gerard, Craig
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Whole genome sequencing of extreme phenotypes identifies variants in CD101 and UBE2V1 associated with increased risk of sexually acquired HIV-1
err2017-11-06
err17
errOAAI
errMackelprang, Romel D.; Bamshad, Michael J.; Chong, Jessica X.; Hou, Xuanlin; Buckingham, Kati J.; Shively, Kathryn; deBruyn, Guy; Mugo, Nelly R.; Mullins, James I.; McElrath, M. Juliana; Baeten, Jared M.; Celum, Connie; Emond, Mary J.; Lingappa, Jairam R.
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Homozygosity for the WRN Helicase-Inactivating Variant, R834C, does not confer a Werner syndrome clinical phenotype
err2017-03-09
err14
errOAAI
errKamath-Loeb, Ashwini S.; Zavala-van Rankin, Diego G.; Flores-Morales, Jeny; Emond, Mary J.; Sidorova, Julia M.; Carnevale, Alessandra; del Carmen Cardenas-Cortes, Maria; Norwood, Thomas H.; Monnat, Raymond J.; Loeb, Lawrence A.; Mercado-Celis, Gabriela E.
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GNPAT Polymorphism rs11558492 Is Not Associated With Increased Severity in a Large Cohort of HFE p.Cys282Tyr Homozygous Patients REPLY
err2017-02-03
err1
errOAAI
errMcLaren, Gordon D.; Barton, James C.; Ramm, Grant A.; Emond, Mary J.; Subramaniam, V. Nathan; Phatak, Pradyumna D.; Adams, Paul C.; Powell, Lawrie W.; Gurrin, Lyle C.; Anderson, Gregory J.; McLaren, Christine E.
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TLR4 genetic variation is associated with inflammatory responses in Gram-positive sepsis
err2017-01-01
err34
errOAAI
errChantratita, N.; Tandhavanant, S.; Seal, S.; Wikraiphat, C.; Wongsuvan, G.; Ariyaprasert, P.; Suntornsut, P.; Teerawattanasook, N.; Jutrakul, Y.; Srisurat, N.; Chaimanee, P.; Mahavanakul, W.; Srisamang, P.; Phiphitaporn, S.; Mokchai, M.; Anukunananchai, J.; Wongratanacheewin, S.; Chetchotisakd, P.; Emond, M. J.; Peacock, S. J.; West, T. E.
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Ultra-deep sequencing detects ovarian cancer cells in peritoneal fluid and reveals somatic TP53 mutations in noncancerous tissues
err2016-05-05
err167
errOAAI
errKrimmel, Jeffrey D.; Schmitt, Michael W.; Harrell, Maria I.; Agnew, Kathy J.; Kennedy, Scott R.; Emond, Mary J.; Loeb, Lawrence A.; Swisher, Elizabeth M.; Risques, Rosa Ana
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Mitochondrial-targeted catalase is good for the old mouse proteome, but not for the young: 'reverse' antagonistic pleiotropy?
err2016-04-08
err31
errOAAI
errBasisty, Nathan; Dai, Dao-Fu; Gagnidze, Arni; Gitari, Lemuel; Fredrickson, Jeanne; Maina, Yvonne; Beyer, Richard P.; Emond, Mary J.; Hsieh, Edward J.; MacCoss, Michael J.; Martin, George M.; Rabinovitch, Peter S.
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Identification of Rare Variants in ATP8B4 as a Risk Factor for Systemic Sclerosis by Whole-Exome Sequencing
err2015-12-23
err38
errOAAI
errGao, Li; Emond, Mary J.; Louie, Tin; Cheadle, Chris; Berger, Alan E.; Rafaels, Nicholas; Vergara, Candelaria; Kim, Yoonhee; Taub, Margaret A.; Ruczinski, Ingo; Mathai, Stephen C.; Rich, Stephen S.; Nickerson, Deborah A.; Hummers, Laura K.; Bamshad, Michael J.; Hassoun, Paul M.; Mathias, Rasika A.; Barnes, Kathleen C.
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