Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Sanja Franić"'
Autor:
Meike Bartels, Sanja Franić, Dorret I. Boomsma, Catherina E. M. van Beijsterveldt, Hilleke E. Hulshoff Pol, Conor V. Dolan
Publikováno v:
Franic, S F, Dolan, C V, van Beijsterveldt, C E M, Hulshoff Pol, H E, Bartels, M & Boomsma, D I 2014, ' Genetic and Environmental Stability of Intelligence in Childhood and Adolescence ', Twin Research and Human Genetics, vol. 17, no. 3, pp. 151-163 . https://doi.org/10.1017/thg.2014.26
Twin Research and Human Genetics
Twin Research and Human Genetics, 17(3), 151-163. Australian Academic Press
Twin Research and Human Genetics
Twin Research and Human Genetics, 17(3), 151-163. Australian Academic Press
The present study examined the genetic and environmental contributions to the temporal stability of verbal, non-verbal and general intelligence across a developmental period spanning childhood and adolescence (5-18 years). Longitudinal twin data coll
Publikováno v:
Behavior genetics, 44(6), 591-604. Springer New York
Franic, S, Borsboom, D, Dolan, C V & Boomsma, D I 2014, ' The Big Five Personality Traits: Psychological Entities or Statistical Constructs? ', Behavior Genetics, vol. 44, no. 6, pp. 591-604 . https://doi.org/10.1007/s10519-013-9625-7
Behavior Genetics, 44(6), 591-604. Springer
Behavior Genetics
Franic, S, Borsboom, D, Dolan, C V & Boomsma, D I 2014, ' The Big Five Personality Traits: Psychological Entities or Statistical Constructs? ', Behavior Genetics, vol. 44, no. 6, pp. 591-604 . https://doi.org/10.1007/s10519-013-9625-7
Behavior Genetics, 44(6), 591-604. Springer
Behavior Genetics
The present study employed multivariate genetic item-level analyses to examine the ontology and the genetic and environmental etiology of the Big Five personality dimensions, as measured by the NEO Five Factor Inventory (NEO-FFI) [Costa and McCrae, R
Autor:
Dorret I. Boomsma, Erik A. Ehli, Xiangjun Xiao, James J. Hudziak, Meike Bartels, Catharina E. M. van Beijsterveldt, Eco J. C. de Geus, Maria M. Groen-Blokhuis, Gareth E. Davies, Robert R. Althoff, Christel M. Middeldorp, Paul Scheet, Sanja Franić
Publikováno v:
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 162(5), 457-465. Wiley-Liss Inc.
American journal of medical genetics. Part B, Neuropsychiatric genetics, 162(5), 457-465. Wiley-Liss Inc.
Groen-Blokhuis, M M, Franic, S, van Beijsterveldt, C E M, de Geus, E J C, Bartels, M, Davies, G E, Ehli, E A, Xiao, X, Scheet, P, Althoff, R R, Hudziak, J J, Middeldorp, C M & Boomsma, D I 2013, ' A prospective study of the effects of breastfeeding and FADS2 polymorphisms on cognition and hyperactivity/attention problems ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 162, no. 5, pp. 457-465 . https://doi.org/10.1002/ajmg.b.32175
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
American journal of medical genetics. Part B, Neuropsychiatric genetics, 162(5), 457-465. Wiley-Liss Inc.
Groen-Blokhuis, M M, Franic, S, van Beijsterveldt, C E M, de Geus, E J C, Bartels, M, Davies, G E, Ehli, E A, Xiao, X, Scheet, P, Althoff, R R, Hudziak, J J, Middeldorp, C M & Boomsma, D I 2013, ' A prospective study of the effects of breastfeeding and FADS2 polymorphisms on cognition and hyperactivity/attention problems ', American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, vol. 162, no. 5, pp. 457-465 . https://doi.org/10.1002/ajmg.b.32175
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
Breastfeeding has been associated with improved cognitive functioning. There is a beneficial effect on IQ, and possibly on associated phenotypes such as attention problems. It has been suggested that the effect on IQ is moderated by polymorphisms in
Autor:
Diane J. Lamb, Catharina E. M. van Beijsterveldt, Dorret I. Boomsma, Paul Scheet, James J. Hudziak, Eco J. C. de Geus, Jacob F. Orlebeke, Nienke M. Schutte, Michel G. Nivard, Cyrina Brouwer, Erik A. Ehli, T.J. Glasner, T.M. Stroet, Suzanne C. Swagerman, Conor V. Dolan, Dustin Nowotny, Kees-Jan Kan, Sanja Franić, Dirk J.A. Smit, Gareth E. Davies, Eveline L. de Zeeuw, Meike Bartels, Charlotte Huppertz, Christel M. Middeldorp, Jouke-Jan Hottenga, Maria M. Groen-Blokhuis, Michelle Van Fulpen
Publikováno v:
Twin Research and Human Genetics, 16(1), 252-267. Australian Academic Press
Twin Research and Human Genetics
van Beijsterveldt, C E M, Groen-Blokhuis, M M, Franic, S, Hudziak, J J, Lamb, D J, Huppertz, C, de Zeeuw, E L, Nivard, M G, Schutte, N M, Swagerman, S C, Glasner, T J, van Fulpen, M J, Brouwer, C D, Stroet, T M, Nowotny, D, Ehli, E A, Davies, G E, Scheet, P, Orlebeke, J F, Kan, K J, Smit, D J A, Dolan, C V, Middeldorp, C M, de Geus, E J C, Bartels, M & Boomsma, D I 2013, ' The Young Netherlands Twin Register (YNTR): Longitudinal Twin and Family Studies in Over 70,000 Children ', Twin Research and Human Genetics, vol. 16, no. 1, pp. 252-267 . https://doi.org/10.1017/thg.2012.118
Twin Research and Human Genetics
van Beijsterveldt, C E M, Groen-Blokhuis, M M, Franic, S, Hudziak, J J, Lamb, D J, Huppertz, C, de Zeeuw, E L, Nivard, M G, Schutte, N M, Swagerman, S C, Glasner, T J, van Fulpen, M J, Brouwer, C D, Stroet, T M, Nowotny, D, Ehli, E A, Davies, G E, Scheet, P, Orlebeke, J F, Kan, K J, Smit, D J A, Dolan, C V, Middeldorp, C M, de Geus, E J C, Bartels, M & Boomsma, D I 2013, ' The Young Netherlands Twin Register (YNTR): Longitudinal Twin and Family Studies in Over 70,000 Children ', Twin Research and Human Genetics, vol. 16, no. 1, pp. 252-267 . https://doi.org/10.1017/thg.2012.118
The Netherlands Twin Register (NTR) began in 1987 with data collection in twins and their families, including families with newborn twins and triplets. Twenty-five years later, the NTR has collected at least one survey for 70,784 children, born after
Autor:
Thomas Espeseth, Hilleke E. Hulshoff Pol, David Shum, Narelle K. Hansell, Andrea Christoforou, Glenda Andrews, Nicholas G. Martin, Jodie N. Painter, Brendan P. Zietsch, Gail Davies, Grant W. Montgomery, Erik A. Ehli, Ian J. Deary, Sanja Franić, Graeme S. Halford, Stephanie Le Hellard, John M. Starr, Sarah E. Medland, Dorret I. Boomsma, Gareth E. Davies, Vidar M. Steen, Astri J. Lundervold, Ivar Reinvang, Margaret J. Wright, Sarah E. Harris
Publikováno v:
Hansell, N K, Halford, G S, Andrews, G, Shum, D H K, Harris, S E, Davies, G, Franic, S, Christoforou, A, Zietsch, B, Painter, J, Medland, S E, Ehli, E A, Davies, G E, Steen, V M, Lundervold, A J, Reinvang, I, Montgomery, G W, Espeseth, T, Hulshoff Pol, H E, Starr, J M, Martin, N G, Le Hellard, S, Boomsma, D I, Deary, I J & Wright, M J 2015, ' Genetic basis of a cognitive complexity metric ', PLoS ONE, vol. 10, no. 4, pp. e0123886 . https://doi.org/10.1371/journal.pone.0123886
Hansell, N K, Halford, G S, Andrews, G, Shum, D H K, Harris, S E, Davies, G, Franic, S, Christoforou, A, Zietsch, B, Painter, J, Medland, S E, Ehli, E A, Davies, G E, Steen, V M, Lundervold, A J, Reinvang, I, Montgomery, G W, Espeseth, T, Hulshoff Pol, H E, Starr, J M, Martin, N G, Le Hellard, S, Boomsma, D I, Deary, I J & Wright, M J 2015, ' Genetic Basis of a Cognitive Complexity Metric ', PLoS ONE, vol. 10, no. 4, e0123886, pp. e0123886 . https://doi.org/10.1371/journal.pone.0123886
PLoS ONE, Vol 10, Iss 4, p e0123886 (2015)
PLoS ONE [E], 10(4). Public Library of Science
PLoS ONE, 10(4):e0123886. Public Library of Science
PLoS ONE
Hansell, N K, Halford, G S, Andrews, G, Shum, D H K, Harris, S E, Davies, G, Franic, S, Christoforou, A, Zietsch, B, Painter, J, Medland, S E, Ehli, E A, Davies, G E, Steen, V M, Lundervold, A J, Reinvang, I, Montgomery, G W, Espeseth, T, Hulshoff Pol, H E, Starr, J M, Martin, N G, Le Hellard, S, Boomsma, D I, Deary, I J & Wright, M J 2015, ' Genetic Basis of a Cognitive Complexity Metric ', PLoS ONE, vol. 10, no. 4, e0123886, pp. e0123886 . https://doi.org/10.1371/journal.pone.0123886
PLoS ONE, Vol 10, Iss 4, p e0123886 (2015)
PLoS ONE [E], 10(4). Public Library of Science
PLoS ONE, 10(4):e0123886. Public Library of Science
PLoS ONE
Relational complexity (RC) is a metric reflecting capacity limitation in relational processing. It plays a crucial role in higher cognitive processes and is an endophenotype for several disorders. However, the genetic underpinnings of complex relatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1ba46198180218768e32a11af5287b4
https://dspace.library.uu.nl/handle/1874/350385
https://dspace.library.uu.nl/handle/1874/350385
Autor:
Dorret I. Boomsma, Tomasz Zemojtel, Erik A. Ehli, John Broxholme, Sanja Franić, René Pool, Conor V. Dolan, Hao Hu, Garreth E. Davies, Jouke-Jan Hottenga, Hans-Hilger Ropers, Kelly A. Nelson
Publikováno v:
Intelligence, 49, 10-22. Elsevier Limited
Intelligence
Franic, S, Dolan, C V, Broxholme, J, Hu, H, Zemojtel, T, Davies, G E, Nelson, K A, Ehli, E A, Pool, R, Hottenga, J J, Ropers, H-H & Boomsma, D I 2015, ' Mendelian and polygenic inheritance of intelligence: A common set of causal genes? Using next-generation sequencing to examine the effects of 168 intellectual disability genes on normal-range intelligence ', Intelligence, vol. 49, pp. 10-22 . https://doi.org/10.1016/j.intell.2014.12.001
Intelligence
Franic, S, Dolan, C V, Broxholme, J, Hu, H, Zemojtel, T, Davies, G E, Nelson, K A, Ehli, E A, Pool, R, Hottenga, J J, Ropers, H-H & Boomsma, D I 2015, ' Mendelian and polygenic inheritance of intelligence: A common set of causal genes? Using next-generation sequencing to examine the effects of 168 intellectual disability genes on normal-range intelligence ', Intelligence, vol. 49, pp. 10-22 . https://doi.org/10.1016/j.intell.2014.12.001
Despite twin and family studies having demonstrated a substantial heritability of individual differences in intelligence, no genetic variants have been robustly associated with normal-range intelligence to date. This is largely ascribed to the high p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50771ee79890ccad703c3a3d9bf9e0b7
https://research.vu.nl/en/publications/e75db7be-98c1-4884-adca-9375de47e3ce
https://research.vu.nl/en/publications/e75db7be-98c1-4884-adca-9375de47e3ce
Autor:
Hilleke E. Hulshoff Pol, Eco J. C. de Geus, Nicholas G. Martin, Gareth E. Davies, Abdel Abdellaoui, Sanja Franić, Conor V. Dolan, James J. Hudziak, Xiangjun Xiao, Jouke-Jan Hottenga, Erik A. Ehli, Paul Scheet, Maria M. Groen-Blokhuis, Suzanne C. Swagerman, Catherina E. M. van Beijsterveldt, Mathijs Kattenberg, Sophie van der Sluis, René Pool, Hans-Hilger Ropers, Meike Bartels, Narelle K. Hansell, Dorret I. Boomsma
Publikováno v:
Franic, S, Blokhuis, M M, Dolan, C V, Kattenberg, V M, Pool, R, Xiao, X, Scheet, P, Ehli, E A, Davies, G E, van der Sluis, S, Abdellaoui, A, Hansell, N K, Martin, N G, Hudziak, J J, van Beijsterveldt, C E M, Swagerman, S C, Hulshoff Pol, H E, de Geus, E J C, Bartels, M, Ropers, H-H, Hottenga, J J & Boomsma, D I 2015, ' Intelligence: shared genetic basis between Mendelian disorders and a polygenic trait ', European Journal of Human Genetics, vol. 23, no. 10, pp. 1378-1383 . https://doi.org/10.1038/ejhg.2015.3
European Journal of Human Genetics, 23(10), 1378-1383. Nature Publishing Group
European journal of human genetics
European Journal of Human Genetics, 23(10), 1378. Nature Publishing Group
European Journal of Human Genetics, 23(10), 1378-1383. Nature Publishing Group
European journal of human genetics
European Journal of Human Genetics, 23(10), 1378. Nature Publishing Group
Multiple inquiries into the genetic etiology of human traits indicated an overlap between genes underlying monogenic disorders (eg, skeletal growth defects) and those affecting continuous variability of related quantitative traits (eg, height). Exten
Autor:
Danielle Posthuma, Claire M. A. Haworth, Peter M. Visscher, Nicholas J. Timpson, Robert Plomin, Beate St Pourcain, Robert M. Kirkpatrick, Oliver S. P. Davis, Beben Benyamin, Dorret I. Boomsma, Rolieke A. M. Cents, Susan M. Ring, M-Ja Brion, Lyle J. Palmer, John M. Starr, Nicholas G. Martin, Henning Tiemeier, Emma L. Meaburn, S. E. Medland, David M. Evans, Grant W. Montgomery, Sarah E. Harris, Gary Davies, E.J.C. de Geus, Matt McGue, Xiangjun Xiao, G Davey Smith, Wendy L. McArdle, Craig E. Pennell, Narelle K. Hansell, Thomas S. Price, Vincent W. V. Jaddoe, John P. Kemp, P Scheet, William G. Iacono, Ian J. Deary, Jian Yang, Sanja Franić, Margaret J. Wright, James J. Hudziak, Frank C. Verhulst, Michael B. Miller, D C Liewald
Publikováno v:
Molecular Psychiatry, 19(2), 253-258. Nature Publishing Group
Molecular Psychiatry
Benyamin, B, St Pourcain, B, Davis, O S, Davies, G, Hansell, N K, Brion, M J A, Kirkpatrick, R M, Cents, R A M, Franic, S, Miller, M B, Haworth, C M A, Meaburn, E, Price, T S, Evans, D M, Timpson, N, Kemp, J, Ring, S, McArdle, W, Medland, S E, Yang, J, Harris, S E, Liewald, D C, Scheet, P, Xiao, X, Hudziak, J J, de Geus, E J C, Jaddoe, V W V, Starr, J M, Verhulst, F C, Pennell, C, Tiemeier, H, Iacono, W G, Palmer, L J, Montgomery, G W, Martin, N G, Boomsma, D I, Posthuma, D, McGue, M, Wright, M J, Smith, G D, Deary, I J, Plomin, R & Visscher, P M 2014, ' Childhood intelligence is heritable, highly polygenic and associated with FNBP1L ', Molecular Psychiatry, vol. 19, no. 2, pp. 253-258 . https://doi.org/10.1038/mp.2012.184
Benyamin, B, Pourcain, B, Davis, O S, Davies, G, Hansell, N K, Brion, M J, Kirkpatrick, R M, Cents, R A, Franić, S, Miller, M B, Haworth, C M, Meaburn, E, Price, T S, Evans, D M, Timpson, N, Kemp, J, Ring, S, McArdle, W, Medland, S E, Yang, J, Harris, S E, Liewald, D C, Scheet, P, Xiao, X, Hudziak, J J, de Geus, E J C, Jaddoe, V W, Star, J M, Verhulst, F C, Pennell, C, Tiemeier, H, Iacono, W G, Palmer, L J, Montgomery, G W, Martin, N G, Boomsma, D I, Posthuma, D, McGue, M, Wright, M J, Davey Smith, G, Deary, I J, Plomin, R & Visscher, P M 2014, ' Childhood intelligence is heritable, highly polygenic and associated with FNBP1L ', Molecular Psychiatry, vol. 19, no. 2, pp. 253-258 . https://doi.org/10.1038/mp.2012.184
Molecular Psychiatry
Benyamin, B, St Pourcain, B, Davis, O S, Davies, G, Hansell, N K, Brion, M J A, Kirkpatrick, R M, Cents, R A M, Franic, S, Miller, M B, Haworth, C M A, Meaburn, E, Price, T S, Evans, D M, Timpson, N, Kemp, J, Ring, S, McArdle, W, Medland, S E, Yang, J, Harris, S E, Liewald, D C, Scheet, P, Xiao, X, Hudziak, J J, de Geus, E J C, Jaddoe, V W V, Starr, J M, Verhulst, F C, Pennell, C, Tiemeier, H, Iacono, W G, Palmer, L J, Montgomery, G W, Martin, N G, Boomsma, D I, Posthuma, D, McGue, M, Wright, M J, Smith, G D, Deary, I J, Plomin, R & Visscher, P M 2014, ' Childhood intelligence is heritable, highly polygenic and associated with FNBP1L ', Molecular Psychiatry, vol. 19, no. 2, pp. 253-258 . https://doi.org/10.1038/mp.2012.184
Benyamin, B, Pourcain, B, Davis, O S, Davies, G, Hansell, N K, Brion, M J, Kirkpatrick, R M, Cents, R A, Franić, S, Miller, M B, Haworth, C M, Meaburn, E, Price, T S, Evans, D M, Timpson, N, Kemp, J, Ring, S, McArdle, W, Medland, S E, Yang, J, Harris, S E, Liewald, D C, Scheet, P, Xiao, X, Hudziak, J J, de Geus, E J C, Jaddoe, V W, Star, J M, Verhulst, F C, Pennell, C, Tiemeier, H, Iacono, W G, Palmer, L J, Montgomery, G W, Martin, N G, Boomsma, D I, Posthuma, D, McGue, M, Wright, M J, Davey Smith, G, Deary, I J, Plomin, R & Visscher, P M 2014, ' Childhood intelligence is heritable, highly polygenic and associated with FNBP1L ', Molecular Psychiatry, vol. 19, no. 2, pp. 253-258 . https://doi.org/10.1038/mp.2012.184
Intelligence in childhood, as measured by psychometric cognitive tests, is a strong predictor of many important life outcomes, including educational attainment, income, health and lifespan. Results from twin, family and adoption studies are consisten
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8d7b73e5955071ebd9aa5b4b7843c8d
https://research.vu.nl/en/publications/aff752e7-2d3a-4631-9a3d-cdbc3130fc9a
https://research.vu.nl/en/publications/aff752e7-2d3a-4631-9a3d-cdbc3130fc9a
Autor:
Denny Borsboom, Catherina E. M. van Beijsterveldt, Sanja Franić, Conor V. Dolan, Dorret I. Boomsma
Publikováno v:
Behavior Genetics, 44(3), 254-268. Springer
Franic, S F, Dolan, C V, Borsboom, D, van Beijsterveldt, C E M & Boomsma, D I 2014, ' Three-and-a-Half-Factor Model? The Genetic and Environmental Structure of the CBCL/6–18 Internalizing Grouping ', Behavior Genetics, vol. 44, no. 3, pp. 254-268 . https://doi.org/10.1007/s10519-013-9628-4
Behavior genetics, 44(3), 254-268. Springer New York
Franic, S F, Dolan, C V, Borsboom, D, van Beijsterveldt, C E M & Boomsma, D I 2014, ' Three-and-a-Half-Factor Model? The Genetic and Environmental Structure of the CBCL/6–18 Internalizing Grouping ', Behavior Genetics, vol. 44, no. 3, pp. 254-268 . https://doi.org/10.1007/s10519-013-9628-4
Behavior genetics, 44(3), 254-268. Springer New York
In the present article, multivariate genetic item analyses were employed to address questions regarding the ontology and the genetic and environmental etiology of the Anxious/Depressed, Withdrawn, and Somatic Complaints syndrome dimensions of the Int
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb86e4e2e2cb86599e6609ef3e50e9f1
https://research.vu.nl/en/publications/f3995b3f-51de-432e-ada4-b4e36071915b
https://research.vu.nl/en/publications/f3995b3f-51de-432e-ada4-b4e36071915b
Autor:
Sanja Franić, Conor V. Dolan, Denny Borsboom, Catherina E. M. van Beijsterveldt, Dorret I. Boomsma
Publikováno v:
Behavior Genetics.