Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Noah A Kallsen"'
Autor:
Pagna Sok, Philip J Lupo, Melissa A Richard, Karen R Rabin, Erik A Ehli, Noah A Kallsen, Gareth E Davies, Michael E Scheurer, Austin L Brown
Publikováno v:
PLoS ONE, Vol 15, Iss 2, p e0229352 (2020)
IntroductionHeel pricks are performed on newborns for diagnostic screenings of various pre-symptomatic metabolic and genetic diseases. Excess blood is spotted on Guthrie cards and archived by many states in biobanks for follow-up diagnoses and public
Externí odkaz:
https://doaj.org/article/238552a88e6e4f40a56f366c60ab8be2
Publikováno v:
Brain Sciences, Vol 13, Iss 12, p 1689 (2023)
Oxytocin is well known for its role in relationships and social cognition and has more recently been implicated in pain relief and pain perception. Connections between prosocial feelings and pain relief are also well documented; however, the effects
Externí odkaz:
https://doaj.org/article/e722138977294149ad06947cbf1e6f3a
Autor:
Jamie L. Scholl, Zach R. King, Kami Pearson, Noah A. Kallsen, Erik A. Ehli, Kelene A. Fercho, Kathleen A. Brown-Rice, Gina L. Forster, Lee A. Baugh
Publikováno v:
Brain, Behavior, & Immunity - Health, Vol 25, Iss , Pp 100505- (2022)
Many Americans are adult children of an alcoholic parent (ACoA), which can confer an increased risk of trauma and hazardous alcohol use, as well as heritable and environmental genetic influence. Psychological health and related neural activity can be
Externí odkaz:
https://doaj.org/article/fede53d9c79c4dcd8e0de0cd8fb906cf
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:
Veronika V. Odintsova, Fiona A. Hagenbeek, Matthew Suderman, Doretta Caramaschi, Catharina E. M. van Beijsterveldt, Noah A. Kallsen, Erik A. Ehli, Gareth E. Davies, Gennady T. Sukhikh, Vassilios Fanos, Caroline Relton, Meike Bartels, Dorret I. Boomsma, Jenny van Dongen
Publikováno v:
Nutrients, Vol 11, Iss 11, p 2804 (2019)
Breastfeeding has long-term benefits for children that may be mediated via the epigenome. This pathway has been hypothesized, but the number of empirical studies in humans is small and mostly done by using peripheral blood as the DNA source. We perfo
Externí odkaz:
https://doaj.org/article/058f2769d0c54f629732106d69e996b8
Autor:
Catharina E. M. van Beijsterveldt, Noah A. Kallsen, Jenny van Dongen, Erik A. Ehli, Dorret I. Boomsma, Meike Bartels, Vassilios Fanos, Matthew Suderman, Caroline L Relton, Gareth E. Davies, Doretta Caramaschi, Fiona A. Hagenbeek, Veronika V. Odintsova, Gennady T. Sukhikh
Publikováno v:
Nutrients, 11(11):2804, 1-26. Multidisciplinary Digital Publishing Institute (MDPI)
Nutrients, Vol 11, Iss 11, p 2804 (2019)
Nutrients
Volume 11
Issue 11
Odintsova, V, Hagenbeek, F A, Suderman, M, Caramaschi, D, Beijsterveldt, C E M V, Kallsen, N A, Ehli, E A, Davies, G E, Sukhikh, G T, Fanos, V, Relton, C, Bartels, M, Boomsma, D I & van Dongen, J 2019, ' DNA Methylation Signatures of Breastfeeding in Buccal Cells Collected in Mid-Childhood ', Nutrients, vol. 11, no. 11, 2804 . https://doi.org/10.3390/nu11112804
Odintsova, V V, Hagenbeek, F A, Suderman, M, Caramaschi, D, van Beijsterveldt, C E M, Kallsen, N A, Ehli, E A, Davies, G E, Sukhikh, G T, Fanos, V, Relton, C, Bartels, M, Boomsma, D I & van Dongen, J 2019, ' DNA methylation signatures of breastfeeding in buccal cells collected in mid-childhood ', Nutrients, vol. 11, no. 11, 2804, pp. 1-26 . https://doi.org/10.3390/nu11112804
Nutrients, Vol 11, Iss 11, p 2804 (2019)
Nutrients
Volume 11
Issue 11
Odintsova, V, Hagenbeek, F A, Suderman, M, Caramaschi, D, Beijsterveldt, C E M V, Kallsen, N A, Ehli, E A, Davies, G E, Sukhikh, G T, Fanos, V, Relton, C, Bartels, M, Boomsma, D I & van Dongen, J 2019, ' DNA Methylation Signatures of Breastfeeding in Buccal Cells Collected in Mid-Childhood ', Nutrients, vol. 11, no. 11, 2804 . https://doi.org/10.3390/nu11112804
Odintsova, V V, Hagenbeek, F A, Suderman, M, Caramaschi, D, van Beijsterveldt, C E M, Kallsen, N A, Ehli, E A, Davies, G E, Sukhikh, G T, Fanos, V, Relton, C, Bartels, M, Boomsma, D I & van Dongen, J 2019, ' DNA methylation signatures of breastfeeding in buccal cells collected in mid-childhood ', Nutrients, vol. 11, no. 11, 2804, pp. 1-26 . https://doi.org/10.3390/nu11112804
Breastfeeding has long-term benefits for children that may be mediated via the epigenome. This pathway has been hypothesized, but the number of empirical studies in humans is small and mostly done by using peripheral blood as the DNA source. We perfo
Autor:
Tammy Jung, Erik A. Ehli, J. Kittelsrud, Noah A. Kallsen, Patricia E. Huizenga, Vikki Petersen, Brittany Holm, Jeffrey J. Beck, Gareth E. Davies
Publikováno v:
Kittelsrud, J M, Ehli, E A, Petersen, V, Jung, T, Beck, J J, Kallsen, N, Huizenga, P, Holm, B & Davies, G E 2019, ' Avera Twin Register Growing Through Online Consenting and Survey Collection ', Twin Research and Human Genetics, vol. 22, no. 6, pp. 686-690 . https://doi.org/10.1017/thg.2019.73
Twin Research and Human Genetics, 22(6), 686-690. Australian Academic Press
Twin Research and Human Genetics, 22(6), 686-690. Australian Academic Press
The aim of the Avera Twin Register (ATR) is to establish a prospective longitudinal repository of twins, multiples, siblings and family members’ biological samples to study environmental and genetic influences on health and disease. Also, it is our
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