المؤلفون: Andreas Dahl, Espen M. Eilertsen, Sara F. Rodriguez-Cabello, Linn B. Norbom, Anneli D. Tandberg, Esten Leonardsen, Sang Hong Lee, Eivind Ystrom, Christian K. Tamnes, Dag Alnæs, Lars T. Westlye

المصدر: Developmental Cognitive Neuroscience, Vol 65, Iss , Pp 101339- (2024)

مصطلحات موضوعية: Brain similarity, Morphometricity, Cortical Thickness, ABCD study, SNP heritability, Neurophysiology and neuropsychology, QP351-495

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S1878929323001445; https://doaj.org/toc/1878-9293

URL الوصول: https://doaj.org/article/720f2116ebbf4348a0fcdc6d8c60bee2

المؤلفون: Hon-Cheong So, Xiao Xue, Zhijie Ma, Pak-Chung Sham

المصدر: International Journal of Molecular Sciences, Vol 25, Iss 2, p 1347 (2024)

مصطلحات موضوعية: genome-wide association studies, SNP heritability, genetic epidemiology, bioinformatics, immunogenetics, Biology (General), QH301-705.5, Chemistry, QD1-999

Relation: https://www.mdpi.com/1422-0067/25/2/1347; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067; https://doaj.org/article/5c5bffd00db14839bf27aada6a4cad0f

الاتاحة: https://doi.org/10.3390/ijms25021347
https://doaj.org/article/5c5bffd00db14839bf27aada6a4cad0f

المؤلفون: Ronald De Vlaming, Eric A. W. Slob, Patrick J. F. Groenen, Cornelius A. Rietveld

المصدر: BMC Bioinformatics, Vol 23, Iss 1, Pp 1-11 (2022)

مصطلحات موضوعية: SNP heritability, Genetic correlation, GREML, Genetic factor model, Genomic SEM, Computer applications to medicine. Medical informatics, R858-859.7, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1471-2105

URL الوصول: https://doaj.org/article/4fc565e0deb04703976500ec4dd8d233

المؤلفون: Ni, Guiyan, Moser, Gerhard, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Wray, Naomi R, Lee, S Hong

المصدر: American journal of human genetics. 102(6)

مصطلحات موضوعية: Schizophrenia Working Group of the Psychiatric Genomics Consortium, Humans, Body Height, Likelihood Functions, Regression Analysis, Schizophrenia, Genotype, Haplotypes, Inheritance Patterns, Linkage Disequilibrium, Phenotype, Polymorphism, Single Nucleotide, Genome, Human, Computer Simulation, Databases, Genetic, Adult, SNP heritability, accuracy, biasedness, body mass index, genetic correlation, genome-wide SNPs, genomic restricted maximum likelihood, height, linkage disequilibrium score regression, schizophrenia, Brain Disorders, Human Genome, Genetics, Mental Health, Biological Sciences, Medical and Health Sciences, Genetics & Heredity

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/2w3550cp

المؤلفون: Kemppainen, Petri, Husby, Arild, Associate Senior Lecturer

المصدر: Evolution Letters. 2(6):599-609

مصطلحات موضوعية: Chromosome partitioning, heritability, infinitesimal model, genomic relatedness, GCTA, SNP heritability

وصف الملف: electronic

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-373018
https://doi.org/10.1002/evl3.88
https://uu.diva-portal.org/smash/get/diva2:1277499/FULLTEXT01.pdf

المؤلفون: De Vlaming, Ronald, Slob, Eric AW, Groenen, Patrick JF, Rietveld, Cornelius A

المصدر: essn: 1471-2105 ; nlmid: 100965194

مصطلحات موضوعية: GREML, Genetic correlation, Genetic factor model, Genomic SEM, SNP heritability, Genome, Genome-Wide Association Study, Genomics, Humans, Models, Genetic, Multifactorial Inheritance, Phenotype, Polymorphism, Single Nucleotide

وصف الملف: application/pdf

Relation: https://www.repository.cam.ac.uk/handle/1810/340633

الاتاحة: https://www.repository.cam.ac.uk/handle/1810/340633
https://doi.org/10.17863/CAM.88071

المؤلفون: Huanhuan Zhu, Xiang Zhou

المصدر: Computational and Structural Biotechnology Journal, Vol 18, Iss , Pp 1557-1568 (2020)

مصطلحات موضوعية: SNP heritability, Linear mixed model, REML, Method of moments, Summary statistics, Biotechnology, TP248.13-248.65

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2001037020303007; https://doaj.org/toc/2001-0370

URL الوصول: https://doaj.org/article/28c43cad5034421cb8980b0cd3dfa54f

المؤلفون: Jungsoo Gim, Jaehoon An, Joohon Sung, Edwin K. Silverman, Michael H. Cho, Sungho Won

المصدر: Frontiers in Genetics, Vol 11 (2020)

مصطلحات موضوعية: COPD, ethnicity-specific, SNP heritability, susceptible loci, BLUP-filtered SNP, genetic prediction, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/article/10.3389/fgene.2020.00329/full; https://doaj.org/toc/1664-8021

URL الوصول: https://doaj.org/article/0bfac44868e24aa49c293e16d38d2a19

المؤلفون: Qiao, Zhen, Zheng, Jie, Helgeland, Øyvind, Vaudel, Marc, Johansson, Stefan, Njølstad, Pål R., Smith, George Davey, Warrington, Nicole M., Evans, David M.

المصدر: Qiao , Z , Zheng , J , Helgeland , Ø , Vaudel , M , Johansson , S , Njølstad , P R , Smith , G D , Warrington , N M & Evans , D M 2020 , ' Introducing M-GCTA a Software Package to Estimate Maternal (or Paternal) Genetic Effects on Offspring Phenotypes ' , Behavior Genetics , vol. 50 , pp. 51-66 . https://doi.org/10.1007/s10519-019-09969-4

مصطلحات موضوعية: SNP heritability, Heritability, G-REML, Paternal effects, Maternal effects, M-GCTA

وصف الملف: application/pdf

Relation: https://research-information.bris.ac.uk/en/publications/8d649575-20f6-4267-8ad4-13ae1ac078bc

الاتاحة: https://hdl.handle.net/1983/8d649575-20f6-4267-8ad4-13ae1ac078bc
https://research-information.bris.ac.uk/en/publications/8d649575-20f6-4267-8ad4-13ae1ac078bc
https://doi.org/10.1007/s10519-019-09969-4
https://research-information.bris.ac.uk/ws/files/207903720/M_GCTA_R1.pdf
https://research-information.bris.ac.uk/ws/files/207903721/M_GCTA_Supplementary_Materials_R1.pdf
http://www.scopus.com/inward/record.url?scp=85073965845&partnerID=8YFLogxK

المؤلفون: Nievergelt, Caroline M., Maihofer, Adam X., Klengel, Torsten, Atkinson, Elizabeth G., Chen, Chia-Yen, Choi, Karmel W., Coleman, Jonathan R., Dalvie, Shareefa, Duncan, Laramie E., Gelernter, Joel, Levey, Daniel F., Logue, Mark W., Polimanti, Renato, Provost, Allison C., Ratanatharathorn, Andrew, Stein, Murray B., Torres, Katy, Aiello, Allison E., Almli, Lynn M., Amstadter, Ananda B., Andersen, Sren B., Andreassen, Ole A., Arbisi, Paul A., Ashley-Koch, Allison E., Austin, S. Bryn, Avdibegovic, Esmina, Babic, Dragan, Baekvad-Hansen, Marie, Baker, Dewleen G., Beckham, Jean C., Bierut, Laura J., Bisson, Jonathan, Boks, Marco P., Bolger, Elizabeth A., Brglum, Anders D., Bradley, Bekh, Brashear, Megan, Breen, Gerome, Bryant, Richard A., Bustamante, Angela C., Bybjerg-Grauholm, Jonas, Calabrese, Joseph R., Caldas-de-Almeida, Jose M., Dale, Anders M., Daly, Mark J., Daskalakis, Nikolaos P., Deckert, Juergen, Delahanty, Douglas L., Dennis, Michelle F., Disner, Seth G., Domschke, Katharina, Dzubur-Kulenovic, Alma, Erbes, Christopher R., Evans, Alexandra, Farrer, Lindsay A., Feeny, Norah C., Flory, Janine D., Forbes, David, Franz, Carol E., Galea, Sandro, Garrett, Melanie E., Gelaye, Bizu, Geuze, Elbert, Gillespie, Charles, Uka, Aferdita Goci, Gordon, Scott D., Guffanti, Guia, Hammamieh, Rasha, Harnal, Supriya, Hauser, Michael A., Heath, Andrew C., Hemmings, Sian M. J., Hougaard, David Michael, Jakovljevic, Miro, Jett, Marti, Johnson, Eric Otto, Jones, Ian, Jovanovic, Tanja, Qin, Xue-Jun, Junglen, Angela G., Karstoft, Karen-Inge, Kaufman, Milissa L., Kessler, Ronald C., Khan, Alaptagin, Kimbrel, Nathan A., King, Anthony P., Koen, Nastassja, Kranzler, Henry R., Kremen, William S., Lawford, Bruce R., Lebois, Lauren A. M., Lewis, Catrin E., Linnstaedt, Sarah D., Lori, Adriana, Lugonja, Bozo, Luykx, Jurjen J., Lyons, Michael J., Maples-Keller, Jessica, Marmar, Charles, Martin, Alicia R., Martin, Nicholas G., Maurer, Douglas, Mavissakalian, Matig R., McFarlane, Alexander, McGlinchey, Regina E., McLaughlin, Katie A., McLean, Samuel A., McLeay, Sarah, Mehta, Divya, Milberg, William P., Miller, Mark W., Morey, Rajendra A., Morris, Charles Phillip, Mors, Ole, Mortensen, Preben B., Neale, Benjamin M., Nelson, Elliot C., Nordentoft, Merete, Norman, Sonya B., O'Donnell, Meaghan, Orcutt, Holly K., Panizzon, Matthew S., Peters, Edward S., Peterson, Alan L., Peverill, Matthew, Pietrzak, Robert H., Polusny, Melissa A., Rice, John P., Ripke, Stephan, Risbrough, Victoria B., Roberts, Andrea L., Rothbaum, Alex O., Rothbaum, Barbara O., Roy-Byrne, Peter, Ruggiero, Ken, Rung, Ariane, Rutten, Bart P. F., Saccone, Nancy L., Sanchez, Sixto E., Schijven, Dick, Seedat, Soraya, Seligowski, Antonia, Seng, Julia S., Sheerin, Christina M., Silove, Derrick, Smith, Alicia K., Smoller, Jordan W., Sponheim, Scott R., Stein, Dan J., Stevens, Jennifer S., Sumner, Jennifer A., Teicher, Martin H., Thompson, Wesley K., Trapido, Edward, Uddin, Monica, Ursano, Robert J., van den Heuvel, Leigh Luella, Van Hooff, Miranda, Vermetten, Eric, Vinkers, Christiaan H., Voisey, Joanne, Wang, Yunpeng, Wang, Zhewu, Werge, Thomas, Williams, Michelle A., Williamson, Douglas E., Winternitz, Sherry, Wolf, Christiane, Wolf, Erika J., Wolff, Jonathan D., Yehuda, Rachel, Young, Ross McD, Young, Keith A., Zhao, Hongyu, Zoellner, Lori A., Liberzon, Israel, Ressler, Kerry J., Haas, Magali, Koenen, Karestan C.

المصدر: Nievergelt , C M , Maihofer , A X , Klengel , T , Atkinson , E G , Chen , C-Y , Choi , K W , Coleman , J R , Dalvie , S , Duncan , L E , Gelernter , J , Levey , D F , Logue , M W , Polimanti , R , Provost , A C , Ratanatharathorn , A , Stein , M B , Torres , K , Aiello , A E , Almli , L M , Amstadter , A B , Andersen , S B , Andreassen ....

مصطلحات موضوعية: POSTTRAUMATIC-STRESS-DISORDER, HUMAN DEMOGRAPHIC HISTORY, LD SCORE REGRESSION, PARKINSON DISEASE, SNP HERITABILITY, TRAUMA, EFFICIENT, PREVENTION, PROFILES, SYMPTOMS

الاتاحة: https://cris.maastrichtuniversity.nl/en/publications/cb1c480f-bb38-4c34-812a-9afbd42ef111
https://doi.org/10.1038/s41467-019-12576-w

المؤلفون: Psychiat Genomics Consortium, Lönnqvist, Jouko, Paunio, Tiina

المساهمون: Clinicum, Department of Psychiatry, HUS Psychiatry

مصطلحات موضوعية: COMPLEX HUMAN TRAITS, BODY-MASS INDEX, WIDE ASSOCIATION, PARTITIONING HERITABILITY, SUSCEPTIBILITY LOCI, SNP HERITABILITY, HUMAN HEIGHT, SCHIZOPHRENIA, INFORMATION, STATISTICS, Biomedicine, Neurology and psychiatry

وصف الملف: application/pdf

Relation: This research is supported by the Australian National Health and Medical Research Council (1080157, 1087889) and the Australian Research Council (DP160102126, FT160100229). This research has been conducted using the UK Biobank Resource. UK Biobank Research Ethics Committee (REC) approval number is 11/NW/0382. Our reference number approved by UK Biobank is 14575. GERA data came from a grant, the Resource for Genetic Epidemiology Research in Adult Health and Aging (RC2 AG033067; Schaefer and Risch, PIs) awarded to the Kaiser Permanente Research Program on Genes, Environment, and Health (RPGEH) and the UCSF Institute for Human Genetics. The RPGEH was supported by grants from the Robert Wood Johnson Foundation, the Wayne and Gladys Valley Foundation, the Ellison Medical Foundation, Kaiser Permanente Northern California, and the Kaiser Permanente National and Northern California Community Benefit Programs. The RPGEH and the Resource for Genetic Epidemiology Research in Adult Health and Aging are described in the GERA website (see Web Resources). This study makes use of data generated by the Wellcome Trust Case-Control Consortium. A full list of the investigators who contributed to the generation of the WTCCC data is available online. Funding for the WTCCC project was provided by the Wellcome Trust under awards 076113, 085475, and 090355.; Psychiat Genomics Consortium , Lönnqvist , J & Paunio , T 2018 , ' Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood ' , American Journal of Human Genetics , vol. 102 , no. 6 , pp. 1185-1194 . https://doi.org/10.1016/j.ajhg.2018.03.021; http://hdl.handle.net/10138/305741; 254082cb-f767-4dfd-a219-0cfeb172a567; 85046126170; 000434946200014

الاتاحة: http://hdl.handle.net/10138/305741

المؤلفون: Kemppainen, Petri, Husby, Arild

المساهمون: External Funding, Ecological Genetics Research Unit

مصطلحات موضوعية: Chromosome partitioning, heritability, infinitesimal model, genomic relatedness, GCTA, SNP heritability, GENOME-WIDE ASSOCIATION, GENETIC ARCHITECTURE, MISSING HERITABILITY, QUANTITATIVE TRAITS, COMMON SNPS, CHALLENGES, SCHIZOPHRENIA, PROPORTION, DISSECTION, SIZE, Environmental biotechnology

وصف الملف: application/pdf

Relation: We would like to thank Christopher Knight and Doug Speed for useful discussions and Hans Ellegren and an anonymous reviewer for comments and suggestions. We would also especially like to acknowledge Anna Santure for very helpful comments and suggestions that greatly improved the manuscript. We acknowledge computing resource support from CSC - the Finnish IT Center for Science Ltd. administered by the Ministry of Education and Culture, Finland and funding from the University of Helsinki to A.H.; Kemppainen , P & Husby , A 2018 , ' Accounting for heteroscedasticity and censoring in chromosome partitioning analyses ' , Evolution Letters , vol. 2 , no. 6 , pp. 599-609 . https://doi.org/10.1002/evl3.88; ORCID: /0000-0003-1911-8351/work/54791796; http://hdl.handle.net/10138/299699; 01fded7c-91c1-4c2a-9924-caa64035eacf; 000452990000006

الاتاحة: http://hdl.handle.net/10138/299699

المؤلفون: Int League Against Epilepsy Conso, Abou-Khalil, Bassel, Eriksson, Johan G., Lehesjoki, Anna-Elina, Palotie, Aarno

المساهمون: Johan Eriksson / Principal Investigator, Department of General Practice and Primary Health Care, Clinicum, Department of Medical and Clinical Genetics, Medicum, Centre of Excellence in Complex Disease Genetics, Aarno Palotie / Principal Investigator, Institute for Molecular Medicine Finland, Genomics of Neurological and Neuropsychiatric Disorders

مصطلحات موضوعية: LD SCORE REGRESSION, SUSCEPTIBILITY LOCI, GENETIC ARCHITECTURE, SNP HERITABILITY, ILAE COMMISSION, FRONTAL-LOBE, ASSOCIATION, METAANALYSIS, EXPRESSION, ABSENCE, Biomedicine

وصف الملف: application/pdf

Relation: We are grateful to the patients and volunteers who participated in this research. We thank the following clinicians and research scientists for their contribution through sample collection (cases and controls), data analysis, and project support: Geka Ackerhans, Muna Alwaidh, R E Appleton, Willem Frans Arts, Guiliano Avanzini, Paul Boon, Sarah Borror, Kees Braun, Oebele Brouwer, Hans Carpay, Karen Carter, Peter Cleland, Oliver C Cockerell, Paul Cooper, Celia Cramp, Emily de los Reyes, Chris French, Catharine Freyer, William Gallentine, Michel Georges, Peter Goulding, Micheline Gravel, Rhian Gwilliam, Lori Hamiwka, Steven J Howell, Adrian Hughes, Aatif Husain, Monica Islam, Floor Jansen, Mary Karn, Mark Kellett, Ditte B Kjelgaard, Karl Martin Klein, Donna Kring, Annie WC Kung, Mark Lawden, Jo Ellen Lee, Benjamin Legros, Leanne Lehwald, Edouard Louis, Colin HT Lui, Zelko Matkovic, Jennifer McKinney, Brendan McLean, Mohamad Mikati, Bethanie Morgan-Followell, Wim Van Paesschen, Anup Patel, Manuela Pendziwiat, Marcus Reuber, Richard Roberts, Guy Rouleau, Cathy Schumer, B Sharack, Kevin Shianna, NC Sin, Saurabh Sinha, Laurel Slaughter, Sally Steward, Deborah Terry, Chang-Yong Tsao, TH Tsoi, Patrick Tugendhaft, Jaime-Dawn Twanow, Jorge Vidaurre, Sarah Weckhuysen, Pedro Weisleder, Kathleen White, Virginia Wong, Raju Yerra, Jacqueline Yinger and all contributing clinicians from the Department of Clinical and Experimental Epilepsy at the National Hospital for Neurology and Neurosurgery and UCL Institute of Neurology. Data generated as part of the EPIGEN Consortium was included in this study. We would like to thank Dr. Weihua Meng (University of Dundee), Dr. Mark Adams (University of Edinburgh) and Dr. Ynte Ruigrok (UMC Utrecht), Dr. Bjarke Feenstra (Statens Serum Institut, Denmark), Dr. Risto Kayanne (Institute for Molecular Medicine Finland) and the International Headache Genetics Consortium for providing GWAS summary statistics for their respective cohorts. Ischemic stroke summary statistics were accessed through the ISGC Cerebrovascular Disease Knowledge Portal. We would like to thank Dr. Weihua Meng (University of Dundee), Dr. Mark Adams (University of Edinburgh) and Dr. Ynte Ruigrok (UMC Utrecht), Dr. Bjarke Feenstra (Statens Serum Institut, Denmark), Dr. Risto Kayanne (Institute for Molecular Medicine Finland), and the International Headache Genetics Consortium for providing GWAS summary statistics for their respective cohorts. We would like to thank the Ming Fund for providing funding for Re. St. M.McC. has received funding from the European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No 751761. This work was in part supported by an award by a Translational Research Scholars award from the Health Research Board of Ireland (C.D.W.), by research grants from Science Foundation Ireland (SFI) (16/RC/3948 and X) and co-funded under the European Regional Development Fund and by FutureNeuro industry partners. Further funding sources include: Wellcome Trust (grant 084730); Epilepsy Society, UK, NIHR (08-08-SCC); GIHE: NIH R01-NS-49306-01 (R.J.B.); NIH R01-NS-053998 (D.H.L); GSCFE: NIH R01-NS-064154-01 (R.J.B. and Ha.Ha.); NIH: UL1TR001070, Development Fund from The Children's Hospital of Philadelphia (Ha. Ha.); NHMRC Program Grant ID: 1091593 (S.F.B., I.E.S., K.L.O., and K.E.B.); The Royal Melbourne Hospital Foundation Lottery Grant (S.P.); The RMH Neuroscience Foundation (T.J.O'B.; Int League Against Epilepsy Conso , Abou-Khalil , B , Eriksson , J G , Lehesjoki , A-E & Palotie , A 2018 , ' Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies ' , Nature Communications , vol. 9 , 5269 . https://doi.org/10.1038/s41467-018-07524-z; ORCID: /0000-0002-2527-5874/work/97266470; http://hdl.handle.net/10138/287694; 00856f27-7109-4b84-af35-18f32d7f63ba; 85058169154; 000452633700009

الاتاحة: http://hdl.handle.net/10138/287694

المؤلفون: Lai, Dongbing, Zhang, Michael, Li, Rudong, Zhang, Chi, Zhang, Pengyue, Liu, Yunlong, Gao, Sujuan, Foroud, Tatiana

المساهمون: Medical and Molecular Genetics, School of Medicine

المصدر: PMC

مصطلحات موضوعية: Alzheimer’s disease, SNP heritability, Gene co-expression module, Gene-based polygenic risk score, Gene-targeting drugs, Protein-protein interaction network

وصف الملف: application/pdf

Relation: Journal of Alzheimer's Disease; Lai D, Zhang M, Li R, et al. Identifying Genes Associated with Alzheimer's Disease Using Gene-Based Polygenic Risk Score. J Alzheimers Dis. 2023;96(4):1639-1649. doi:10.3233/JAD-230510; https://hdl.handle.net/1805/42927

الاتاحة: https://hdl.handle.net/1805/42927

المؤلفون: Posthuma, Danielle

المصدر: Posthuma , D & Schizophrenia Working Group of the Psychiatric Genomics Consortium 2018 , ' Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood ' , American Journal of Human Genetics , vol. 102 , no. 6 , pp. 1185-1194 . https://doi.org/10.1016/j.ajhg.2018.03.021

مصطلحات موضوعية: Adult, Body Height/genetics, Computer Simulation, Databases, Genetic, Genome, Human, Genotype, Haplotypes/genetics, Humans, Inheritance Patterns/genetics, Likelihood Functions, Linkage Disequilibrium/genetics, Phenotype, Polymorphism, Single Nucleotide/genetics, Regression Analysis, Schizophrenia/genetics, accuracy, schizophrenia, biasedness, genome-wide SNPs, linkage disequilibrium score regression, genetic correlation, height, body mass index, SNP heritability, genomic restricted maximum likelihood

وصف الملف: application/pdf

الاتاحة: https://research.vu.nl/en/publications/41ee56a1-47fc-4e4b-9ee2-d91677643fd8
https://doi.org/10.1016/j.ajhg.2018.03.021
https://hdl.handle.net/1871.1/41ee56a1-47fc-4e4b-9ee2-d91677643fd8
https://research.vu.nl/ws/files/83592932/Estimation_of_Genetic_Correlation_via_Linkage_Disequilibrium_Score_Regression_and_Genomic_Restricted_Maximum_Likelihood.pdf
http://www.scopus.com/inward/record.url?scp=85046126170&partnerID=8YFLogxK
http://www.scopus.com/inward/citedby.url?scp=85046126170&partnerID=8YFLogxK

المؤلفون: Smit, Dirk J.A., Wright, Margaret J., Meyers, Jacquelyn L., Martin, Nicholas G., Ho, Yvonne Y.W., Malone, Stephen M., Zhang, Jian, Burwell, Scott J., Chorlian, David B., de Geus, Eco J.C., Denys, Damiaan, Hansell, Narelle K., Hottenga, Jouke Jan, McGue, Matt, van Beijsterveldt, Catharina E.M., Jahanshad, Neda, Thompson, Paul M., Whelan, Christopher D., Medland, Sarah E., Porjesz, Bernice, Lacono, William G., Boomsma, Dorret I.

المصدر: Smit , D J A , Wright , M J , Meyers , J L , Martin , N G , Ho , Y Y W , Malone , S M , Zhang , J , Burwell , S J , Chorlian , D B , de Geus , E J C , Denys , D , Hansell , N K , Hottenga , J J , McGue , M , van Beijsterveldt , C E M , Jahanshad , N , Thompson , P M , Whelan , C D , Medland , S E , Porjesz , ....

مصطلحات موضوعية: brain expression pathway, electroencephalography (EEG), endophenotype, genetic correlation, Genome-Wide Association Study (GWAS), SNP heritability, /dk/atira/pure/keywords/cohort_studies/netherlands_twin_register_ntr_, name=Netherlands Twin Register (NTR), /dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being, name=SDG 3 - Good Health and Well-being

الاتاحة: https://research.vu.nl/en/publications/dbf3bc91-3473-472d-8c82-1ff14ab73e4d
https://doi.org/10.1002/hbm.24238
https://hdl.handle.net/1871.1/dbf3bc91-3473-472d-8c82-1ff14ab73e4d
http://www.scopus.com/inward/record.url?scp=85054451120&partnerID=8YFLogxK
http://www.scopus.com/inward/citedby.url?scp=85054451120&partnerID=8YFLogxK

المؤلفون: Minică, Camelia C., Neale, Michael C., Boomsma, Dorret I., van Dongen, Jenny

المساهمون: Li, S., Hopper, J.

المصدر: Minică , C C , Neale , M C , Boomsma , D I & van Dongen , J 2021 , Combining twin-family designs with measured genetic variants to study the causes of epigenetic variation . in S Li & J Hopper (eds) , Twin and Family Studies of Epigenetics . vol. 27 , Translational Epigenetics , vol. 27 , Elsevier , pp. 239-259 . https://doi.org/10.1016/B978-0-12-820951-6.00007-7 , https://doi.org/10.1016/B978-0-12-820951-6.00007-7

مصطلحات موضوعية: Causality, Direction of causation (DOC), DNA methylation, Epigenetics, Genetic relatedness matrix (GRM), Heritability, Mendelian Randomization (MR), Mendelian Randomization-direction of causation model (MR-DoC), Single nucleotide polymorphism (SNP) heritability, Twins

Relation: https://research.vu.nl/en/publications/be4b30fc-1046-4df5-985a-1d10e0e56454; urn:ISBN:9780128209516

الاتاحة: https://research.vu.nl/en/publications/be4b30fc-1046-4df5-985a-1d10e0e56454
https://doi.org/10.1016/B978-0-12-820951-6.00007-7
https://hdl.handle.net/1871.1/be4b30fc-1046-4df5-985a-1d10e0e56454
http://www.scopus.com/inward/record.url?scp=85129020654&partnerID=8YFLogxK
http://www.scopus.com/inward/citedby.url?scp=85129020654&partnerID=8YFLogxK
https://www.elsevier.com/books/twin-and-family-studies-of-epigenetics/li/978-0-12-820951-6

المؤلفون: Marinelli, Marcella, Pappa, Irene, Bustamante, Mariona, Bonilla, Carolina, Suarez, Anna, Tiesler, Carla M, Vilor-Tejedor, Natalia, Zafarmand, Mohammad Hadi, Alvarez-Pedrerol, Mar, Andersson, Sture, Bakermans-Kranenburg, Marian J, Estivill, Xavier, Evans, David M, Flexeder, Claudia, Fons, Joan, Gonzalez, Juan R, Guxens, Monica, Huss, Anke, van IJzendoorn, Marinus H, Jaddoe, Vincent W V, Julvez, Jordi, Lahti, Jari, López-Vicente, Mónica, Lopez-Espinosa, Maria-Jose, Manz, Judith, Mileva-Seitz, Viara R, Perola, Markus, Pesonen, Anu-Katriina, Rivadeneira, Fernando, Salo, Perttu P, Shahand, Shayan, Schulz, Holger, Standl, Marie, Thiering, Elisabeth, Timpson, Nicholas J, Torrent, Maties, Uitterlinden, André G, Smith, George Davey, Estarlich, Marisa, Heinrich, Joachim, Räikkönen, Katri, Vrijkotte, Tanja G M, Tiemeier, Henning, Sunyer, Jordi

المساهمون: LS IRAS EEPI EXAS (Arb.hyg+bl.st.kar.), dIRAS RA-2

مصطلحات موضوعية: SNP heritability, childhood sleep duration, genome-wide association study (GWAS), meta-analysis, pathway analysis, Taverne

وصف الملف: application/pdf

Relation: https://dspace.library.uu.nl/handle/1874/350516

الاتاحة: https://dspace.library.uu.nl/handle/1874/350516

المؤلفون: Middeldorp, C.M. (Christel), Hammerschlag, A.R. (Anke R.), Ouwens, K.G. (Klaasjan), Groen-Blokhuis, M. (Maria), St Pourcain, B. (Beate), Greven, C.U. (Corina U.), Pappa, M. (Magda), Tiesler, C.M.T. (Carla M.T.), Ang, W.Q. (Wei), Nolte, I.M. (Ilja), Vilor-Tejedor, N. (Natàlia), Bacelis, J. (Jonas), Ebejer, J.L. (Jane L.), Zhao, H. (Huiying), Davies, G.E. (Gareth), Ehli, E.A. (Erik), Evans, D.M. (David), Fedko, I.O. (Iryna O.), Guxens Junyent, M. (Mònica), Hottenga, J.J. (Jouke Jan), Hudziak, J.J. (James), Juqessur, A. (Astanand), Kemp, J.P. (John), Krapohl, E. (Eva), Martin, N.G. (Nicholas), Murcia, M. (Mario), Myhre, R. (Ronny), Ormel, J. (Johan), Ring, S.M. (Susan), Standl, E. (Eberhard), Stergiakouli, E. (Evangelia), Stoltenberg, C. (Camilla), Thiering, E. (Elisabeth), Timpson, N.J. (Nicholas), Trzaskowski, M. (Maciej), Most, P.J. (Peter) van der, Wang, C.A. (Carol A.), Nyholt, D.R. (Dale), Medland, S.E. (Sarah), Neale, B.M. (Benjamin), Jacobsson, B. (Bo), Sunyer, J. (Jordi), Hartman, C.A. (C.), Whitehouse, A.J.O. (Andrew), Pennell, C.E. (Craig), Heinrich, J. (Joachim), Plomin, R. (Robert), Smith, A.V. (Davey), Tiemeier, H.W. (Henning), Posthuma, D. (Danielle), Boomsma, D.I. (Dorret)

المصدر: American Academy of Child and Adolescent Psychiatry. Journal vol. 55 no. 10, pp. 896-905.e6

مصطلحات موضوعية: ADHD symptoms, attention problems, GWA, meta-analysis, SNP heritability

Relation: info:eu-repo/grantAgreement/EC/FP7/201413; info:eu-repo/grantAgreement/EC/FP7/282957; http://repub.eur.nl/pub/95994; urn:hdl:1765/95994

الاتاحة: http://repub.eur.nl/pub/95994
https://doi.org/10.1016/j.jaac.2016.05.025

المؤلفون: Yanni, Zeng, Navarro, Pau, Xia, Charley, Amador, Carmen, Fernandez-Pujals, Ana Maria, Thomson, Pippa A., Campbell, Archie, Nagy, Reka, Clarke, Toni-Kim, Hafferty, Jonathan D., Smith, Blair, Hocking, Lynne J., Padmanabhan, Sandosh, Hayward, Caroline, MacIntrye, Donald J., Porteous, David J., Haley, Chris S., McIntosh, Andrew M.

المصدر: Yanni , Z , Navarro , P , Xia , C , Amador , C , Fernandez-Pujals , A M , Thomson , P A , Campbell , A , Nagy , R , Clarke , T-K , Hafferty , J D , Smith , B , Hocking , L J , Padmanabhan , S , Hayward , C , MacIntrye , D J , Porteous , D J , Haley , C S & McIntosh , A M 2016 , ' Shared genetics and couple-associated environment are major contributors to the risk of both clinical and self-declared depression ....

مصطلحات موضوعية: Major Depressive Disorder, Self-declared depression, SNP heritability, couple effect, family environment, linear mixed modeling

وصف الملف: application/pdf

الاتاحة: https://discovery.dundee.ac.uk/en/publications/b013d11c-196c-4afa-985f-008c800180ee
https://doi.org/10.1016/j.ebiom.2016.11.003
https://discovery.dundee.ac.uk/ws/files/11503591/1_s2.0_S2352396416305072_main.pdf