Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Shanna A. Peyton"'
Autor:
Jenny van Dongen, Erik A. Ehli, Rick Jansen, Catharina E. M. van Beijsterveldt, Gonneke Willemsen, Jouke J. Hottenga, Noah A. Kallsen, Shanna A. Peyton, Charles E. Breeze, Cornelis Kluft, Bastiaan T. Heijmans, Meike Bartels, Gareth E. Davies, Dorret I. Boomsma
Publikováno v:
Epigenetics & Chromatin, Vol 11, Iss 1, Pp 1-14 (2018)
Abstract Background DNA methylation arrays are widely used in epigenome-wide association studies and methylation quantitative trait locus (mQTL) studies. Here, we performed the first genome-wide analysis of monozygotic (MZ) twin correlations and mQTL
Externí odkaz:
https://doaj.org/article/5ee79e6350ae48e68e870e924ea93735
Autor:
Noah A. Kallsen, Charles G. Mullighan, Jun J. Yang, Karen R. Rabin, Jasmine Healy, Catherine Metayer, Michael E. Scheurer, Andrew J. Carroll, Jonathan M. Chernus, Nyla A. Heerema, Logan G. Spector, Andrew T. DeWan, Gareth E. Davies, Mignon L. Loh, Shanna A. Peyton, Eleanor Feingold, Philip J. Lupo, Naomi J. Winick, Daniel Sinnett, William L. Carroll, Lisa F. Barcellos, Stephen P. Hunger, Austin L. Brown, Stephanie L. Sherman, Libby M. Morimoto, Mary V. Relling, Maria S. Pombo-de-Oliveira, Erik A. Ehli, Beth A. Mueller, Xiaomei Ma, Ivan Smirnov, Ching-Hon Pui, Vincent U. Gant, Brent L. Wood, Helen M. Hansen, Elizabeth A. Raetz, Pamela D. Thompson, Jillian M. Birch, Alice Y. Kang, Kyle M. Walsh, Adam J. de Smith, Wenjian Yang, Meenakshi Devidas, Joseph L. Wiemels, Jeffrey W. Taub, Caroline Laverdière, Michael J. Borowitz, Michael E. Zwick
Publikováno v:
Blood. 134:1227-1237
Children with Down syndrome (DS) have a 20-fold increased risk of acute lymphoblastic leukemia (ALL) and distinct somatic features, including CRLF2 rearrangement in ∼50% of cases; however, the role of inherited genetic variation in DS-ALL susceptib
Autor:
Suzan L. Carmichael, Ismael Zamilpa, Philip J. Lupo, Shanna A. Peyton, Noah A. Kallsen, Austin L. Brown, Richard A. Wyatt, Stephen Canon, Erik A. Ehli, Pagna Sok, Erin C. Peckham-Gregory, Ashay Patel, Charlotte A. Hobbs, Michael E. Scheurer, Gareth E. Davies, Wendy N. Nembhard, Melissa A. Richard
Publikováno v:
Birth Defects Res
BACKGROUND: Recent genome-wide association studies of hypospadias have implicated the role of genetic variants in or near the diacylglycerol kinase kappa (DGKK) gene. However, these variants are largely identified among samples of mild and moderate h
Genomic landscape of allelic imbalance in premalignant atypical adenomatous hyperplasias of the lung
Autor:
Noah A. Kallsen, Yasushi Yatabe, Humam Kadara, Junya Fukuoka, Junya Fujimoto, Shanna A. Peyton, Erik A. Ehli, F. Anthony San Lucas, P. Andrew Futreal, Gareth E. Davies, Ignacio I. Wistuba, Paul Scheet, Smruthy Sivakumar, Ernest T. Hawk, Yasminka A. Jakubek, Tina McDowell, Jianjun Zhang, Wenhua Lang, Jerry Fowler
Publikováno v:
EBioMedicine. 42:296-303
Background Genomic investigation of atypical adenomatous hyperplasia (AAH), the only known precursor lesion to lung adenocarcinomas (LUAD), presents challenges due to the low mutant cell fractions. This necessitates sensitive methods for detection of
Autor:
Ashay Patel, Minh Ton, Erin C. Peckham-Gregory, Shanna A. Peyton, Gareth E. Davies, Ismael Zamilpa, Austin L. Brown, Erik A. Ehli, Philip J. Lupo, Michael E. Scheurer, Charlotte A. Hobbs, Pagna Sok, Noah A. Kallsen, Wendy N. Nembhard, Melissa A. Richard, Stephen Canon
Publikováno v:
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)
Hypospadias is a common birth defect where the urethral opening forms on the ventral side of the penis. We performed integrative methylomic, genomic, and transcriptomic analyses to characterize sites of DNA methylation that influence genital developm
Autor:
Meike Bartels, Rick Jansen, Charles E. Breeze, Catharina E.M. van Beijsterveldt, Jouke J. Hottenga, Erik A. Ehli, Bastiaan T. Heijmans, Jenny van Dongen, Noah A. Kallsen, Gonneke Willemsen, Gareth E. Davies, Dorret I. Boomsma, Cornelis Kluft, Shanna A. Peyton
Publikováno v:
Epigenetics and Chromatin
Epigenetics and Chromatin, 11
Van Dongen, J, Ehli, E A, Jansen, R, Van Beijsterveldt, C E M, Willemsen, G, Hottenga, J J, Kallsen, N A, Peyton, S A, Breeze, C E, Kluft, C, Heijmans, B T, Bartels, M, Davies, G E & Boomsma, D I 2018, ' Genome-wide analysis of DNA methylation in buccal cells : A study of monozygotic twins and mQTLs ', Epigenetics and Chromatin, vol. 11, no. 1, 54 . https://doi.org/10.1186/s13072-018-0225-x
Epigenetics & Chromatin, Vol 11, Iss 1, Pp 1-14 (2018)
Van Dongen, J, Ehli, E A, Jansen, R, Van Beijsterveldt, C E M, Willemsen, G, Hottenga, J J, Kallsen, N A, Peyton, S A, Breeze, C E, Kluft, C, Heijmans, B T, Bartels, M, Davies, G E & Boomsma, D I 2018, ' Genome-wide analysis of DNA methylation in buccal cells : A study of monozygotic twins and mQTLs ', Epigenetics and Chromatin, vol. 11, 54, pp. 1-14 . https://doi.org/10.1186/s13072-018-0225-x
Epigenetics and Chromatin, 11(1):54. BioMed Central
Epigenetics and Chromatin, 11:54, 1-14. BioMed Central
Epigenetics and Chromatin, 11
Van Dongen, J, Ehli, E A, Jansen, R, Van Beijsterveldt, C E M, Willemsen, G, Hottenga, J J, Kallsen, N A, Peyton, S A, Breeze, C E, Kluft, C, Heijmans, B T, Bartels, M, Davies, G E & Boomsma, D I 2018, ' Genome-wide analysis of DNA methylation in buccal cells : A study of monozygotic twins and mQTLs ', Epigenetics and Chromatin, vol. 11, no. 1, 54 . https://doi.org/10.1186/s13072-018-0225-x
Epigenetics & Chromatin, Vol 11, Iss 1, Pp 1-14 (2018)
Van Dongen, J, Ehli, E A, Jansen, R, Van Beijsterveldt, C E M, Willemsen, G, Hottenga, J J, Kallsen, N A, Peyton, S A, Breeze, C E, Kluft, C, Heijmans, B T, Bartels, M, Davies, G E & Boomsma, D I 2018, ' Genome-wide analysis of DNA methylation in buccal cells : A study of monozygotic twins and mQTLs ', Epigenetics and Chromatin, vol. 11, 54, pp. 1-14 . https://doi.org/10.1186/s13072-018-0225-x
Epigenetics and Chromatin, 11(1):54. BioMed Central
Epigenetics and Chromatin, 11:54, 1-14. BioMed Central
Background: DNA methylation arrays are widely used in epigenome-wide association studies and methylation quantitative trait locus (mQTL) studies. Here, we performed the first genome-wide analysis of monozygotic (MZ) twin correlations and mQTLs on dat
Autor:
Reuven J. Schore, Maria S. Pombo-de-Oliveira, Helen M. Hansen, Beth A. Mueller, Ching-Hon Pui, Elizabeth A. Raetz, Austin L. Brown, Erik A. Ehli, Jillian M. Birch, Michael E. Zwick, Brent L. Wood, Xiaomei Ma, Mignon L. Loh, Shanna A. Peyton, Elanor Feingold, Jeffrey W. Taub, Meenakshi Devidas, Catherine Metayer, Stephanie L. Sherman, Naomi J. Winick, Jun J. Yang, Kyle M. Walsh, Daniel Sinnett, Jasmine Healy, Michael E. Scheurer, William L. Carroll, Michael J. Borowitz, Stephen P. Hunger, Noah A. Kallsen, Karen R. Rabin, Andrew J. Carroll, Philip J. Lupo, Gareth E. Davies, Lisa F. Barcellos, Kelly W. Maloney, Charles G. Mullighan, Ivan Smirnov, Mary V. Relling, Michael M. Burke, Nyla A. Heerema, Wanda L. Salzer, Joseph L. Wiemels, Anne L. Angiolillo, Adam J. de Smith, Wenjian Yang, Andrew T. DeWan
Publikováno v:
Cancer Research. 78:222-222
Purpose: Children with Down syndrome (DS) have a 20-fold increased risk of acute lymphoblastic leukemia (ALL) compared to children without DS. While genome-wide association studies (GWAS) have identified several susceptibility loci in childhood ALL,