Psychosocial adversity and socioeconomic position during childhood and epigenetic age: analysis of two prospective cohort studies (English)
- New search for: Lawn, Rebecca B
- New search for: Anderson, Emma L
- New search for: Suderman, Matthew
- New search for: Simpkin, Andrew J
- New search for: Gaunt, Tom R
- New search for: Teschendorff, Andrew E
- New search for: Widschwendter, Martin
- New search for: Hardy, Rebecca
- New search for: Kuh, Diana
- New search for: Relton, Caroline L
- New search for: Howe, Laura D
- New search for: Lawn, Rebecca B
- New search for: Anderson, Emma L
- New search for: Suderman, Matthew
- New search for: Simpkin, Andrew J
- New search for: Gaunt, Tom R
- New search for: Teschendorff, Andrew E
- New search for: Widschwendter, Martin
- New search for: Hardy, Rebecca
- New search for: Kuh, Diana
- New search for: Relton, Caroline L
- New search for: Howe, Laura D
In:
Human molecular genetics
;
27
, 7
;
1301-1308
;
2018
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ISSN:
- Article (Journal) / Print
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Title:Psychosocial adversity and socioeconomic position during childhood and epigenetic age: analysis of two prospective cohort studies
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Contributors:Lawn, Rebecca B ( author ) / Anderson, Emma L ( author ) / Suderman, Matthew ( author ) / Simpkin, Andrew J ( author ) / Gaunt, Tom R ( author ) / Teschendorff, Andrew E ( author ) / Widschwendter, Martin ( author ) / Hardy, Rebecca ( author ) / Kuh, Diana ( author ) / Relton, Caroline L ( author )
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Published in:Human molecular genetics ; 27, 7 ; 1301-1308
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Publisher:
- New search for: Oxford University Press
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Publication date:2018-01-01
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Size:8 pages
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ISSN:
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Type of media:Article (Journal)
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Type of material:Print
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Language:English
- New search for: 572.8
- Further information on Dewey Decimal Classification
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Classification:
DDC: 572.8 -
Source:
© Metadata Copyright the British Library Board and other contributors. All rights reserved.
Table of contents – Volume 27, Issue 7
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 1123
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Testicular MTHFR deficiency may explain sperm DNA hypomethylation associated with high dose folic acid supplementationAarabi, Mahmoud / Christensen, Karen E / Chan, Donovan / Leclerc, Daniel / Landry, Mylène / Ly, Lundi / Rozen, Rima / Trasler, Jacquetta et al. | 2018
- 1136
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CHEK1 coordinates DNA damage signaling and meiotic progression in the male germline of miceAbe, H. / Alavattam, K. G. / Kato, Y. / Castrillon, D. H. / Pang, Q. / Andreassen, P. R. / Namekawa, S. H. et al. | 2018
- 1150
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Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2Guo, Tingwei / Diacou, Alexander / Nomaru, Hiroko / McDonald-McGinn, Donna M / Hestand, Matthew / Demaerel, Wolfram / Zhang, Liangtian / Zhao, Yingjie / Ujueta, Francisco / Shan, Jidong et al. | 2018
- 1164
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From a dominant to an oligogenic model of inheritance with environmental modifiers in acute intermittent porphyriaLenglet, H. / Schmitt, C. / Grange, T. / Manceau, H. / Karboul, N. / Bouchet-Crivat, F. / Robreau, A. M. / Nicolas, G. / Lamoril, J. m. / Simonin, S. et al. | 2018
- 1174
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Temporal requirement of dystroglycan glycosylation during brain development and rescue of severe cortical dysplasia via gene delivery in the fetal stageSudo, A. / Kanagawa, M. / Kondo, M. / Ito, C. / Kobayashi, K. / Endo, M. / Minami, Y. / Aiba, A. / Toda, T. et al. | 2018
- 1186
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A novel mechanism causing imbalance of mitochondrial fusion and fission in human myopathiesBartsakoulia, M. / Pyle, A. / Troncoso-Chandía, D. / Vial-Brizzi, J. / Paz-Fiblas, M. V. / Duff, J. / Griffin, H. / Boczonadi, V. / Lochmüller, H. / Kleinle, S. et al. | 2018
- 1196
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Homozygous missense mutation L673P in adenylate kinase 7 (AK7) leads to primary male infertility and multiple morphological anomalies of the flagella but not to primary ciliary dyskinesiaLorès, P. / Coutton, C. / El Khouri, E. / Stouvenel, L. / Givelet, M. l. / Thomas, L. / Rode, B. / Schmitt, A. / Louis, B. / Sakheli, Z. et al. | 2018
- 1212
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Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disordersEstruch, S. B. / Graham, S. A. / Quevedo, M. / Vino, A. / Dekkers, D. H. / Deriziotis, P. / Sollis, E. / Demmers, J. / Poot, R. A. / Fisher, S. E. et al. | 2018
- 1228
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Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomaliesPortnoi, Marie-France / Dumargne, Marie-Charlotte / Rojo, Sandra / Witchel, Selma F / Duncan, Andrew J / Eozenou, Caroline / Bignon-Topalovic, Joelle / Yatsenko, Svetlana A / Rajkovic, Aleksandar / Reyes-Mugica, Miguel et al. | 2018
- 1241
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A tri-serine cluster within the topoisomerase IIα-interaction domain of the BLM helicase is required for regulating chromosome breakage in human cellsBehnfeldt, J. H. / Acharya, S. / Tangeman, L. / Gocha, A. S. / Keirsey, J. / Groden, J. et al. | 2018
- 1252
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Human cis-acting elements regulating escape from X-chromosome inactivation function in mousePeeters, S. B. / Korecki, A. J. / Simpson, E. M. / Brown, C. J. et al. | 2018
- 1263
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Differentially expressed microRNAs in the aqueous humor of patients with exfoliation glaucoma or primary open-angle glaucomaDrewry, M. D. / Challa, P. / Kuchtey, J. G. / Navarro, I. / Helwa, I. / Hu, Y. / Mu, H. / Daniel Stamer, W. / Kuchtey, R. W. / Liu, Y. et al. | 2018
- 1276
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Elongator subunit 3 (ELP3) modifies ALS through tRNA modificationBento-Abreu, A. / Jager, G. / Swinnen, B. / Rué, L. / Hendrickx, S. / Jones, A. / Staats, K. A. / Taes, I. / Eykens, C. / Nonneman, A. et al. | 2018
- 1290
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Astrocytes: new players in progressive myoclonus epilepsy of Lafora typeRubio-Villena, C. / Viana, R. / Bonet, J. / Garcia-Gimeno, M. A. / Casado, M. / Heredia, M. / Sanz, P. et al. | 2018
- 1301
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Psychosocial adversity and socioeconomic position during childhood and epigenetic age: analysis of two prospective cohort studiesLawn, R. B. / Anderson, E. L. / Suderman, M. / Simpkin, A. J. / Gaunt, T. R. / Teschendorff, A. E. / Widschwendter, M. / Hardy, R. / Kuh, D. / Relton, C. L. et al. | 2018
- 1309
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The integrity and organization of the human AIPL1 functional domains is critical for its role as a HSP90-dependent co-chaperone for rod PDE6Sacristan-Reviriego, A. / Bellingham, J. / Prodromou, C. / Boehm, A. N. / Aichem, A. / Kumaran, N. / Bainbridge, J. / Michaelides, M. / van der Spuy, J. et al. | 2018
- 1310
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A recurrent de novo missense mutation in UBTF causes developmental neuroregressionToro, Camilo / Hori, Roderick T / Malicdan, May Christine V / Tifft, Cynthia J / Goldstein, Amy / Gahl, William A / Adams, David R / Fauni, Harper B / Wolfe, Lynne A / Xiao, Jianfeng et al. | 2018