Výsledky vyhledávání - "Sasja N. Duijff"

Akademický článek

Implementing 'Online Communities' for pregnant women in times of COVID-19 for the promotion of maternal well-being and mother-to-infant bonding: a pretest–posttest study

Autor: Eva S. Potharst, Mirla A. Schaeffer, Cecile Gunning, Merith Cohen de Lara, Myrthe G. B. M. Boekhorst, Lianne P. Hulsbosch, Victor J. M. Pop, Sasja N. Duijff

Publikováno v: BMC Pregnancy and Childbirth, Vol 22, Iss 1, Pp 1-12 (2022)

Abstract Background The Coronavirus Disease 2019 (COVID-19) pandemic elevated the risk for mental health problems in pregnant women, thereby increasing the risk for long-term negative consequences for mother and child well-being. There was an immedia

Externí odkaz: https://doaj.org/article/71ea86f279904e0e9b2ea81507ee70b2

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Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion

Autor: Richard Duncan, Tao Wang, Carrie E. Bearden, David J. Cutler, Stephen T. Warren, Maria Pontillo, Robert Sean Gallagher, Elemi J. Breetvelt, Tingwei Guo, Nancy J. Butcher, Jennifer G. Mulle, Claudia Ornstein, Claudia Vingerhoets, Clodagh M. Murphy, Ehud Mekori-Domachevsky, Wendy R. Kates, Jacob A. S. Vorstman, Tracy Heung, Joris Vermeesch, Maria Gudbrandsen, Ann Swillen, H. Richard Johnston, Oanh Tran, Marco Armando, Joseph F. Cubells, Raoul Belzeaux, Jeroen Breckpot, Bruno Marino, Tony J. Simon, Harold I. Salmons, Maria Jalbrzikowski, Wanda Fremont, Anna J. Voss, Worrawat Engchuan, Opal Y. Ousley, Stefano Vicari, Jordi Rosell, Sixto García-Miñaur, Declan G. Murphy, Alexander Diacou, Ania Fiksinski, Abraham Weizman, Edward Moss, Stephan Eliez, Miri Carmel, Vandana Shashi, Anne S. Bassett, Ronnie Weinberger, Hayley Moss, Marianne Bernadette van den Bree, Kelly Schoch, Maude Schneider, Linda E. Campbell, Sasja N. Duijff, Eileen Daly, Annick Vogels, Stephen R. Hooper, David Fraguas, Sarah E. Prasad, Chelsea Lowther, Michael John Owen, Frédérique Béna, Gabriela M. Repetto, Eva W.C. Chow, Bernice E. Morrow, Robert J. Sharkus, Celso Arango, Christian R. Marshall, Jasna Raventos-Simic, Jaume Morey-Canyelles, Tiffany Busa, Andrea Jin, James T.R. Walters, Leila Kushan, Wolfram Demaerel, Monica E. Calkins, Jhih Rong Lin, Elaine H. Zackai, Esther D.A. van Duin, Antonio Buzzanca, Corrado Sandini, Kieran C. Murphy, Beverly S. Emanuel, Erik Boot, Maria Niarchou, Nigel Williams, Elfi Vergaelen, Maria Cristina Digilio, Daniele Merico, Karlene Coleman, Gregory A. Costain, Matthew S. Hestand, Peter Holmans, Michael E. Zwick, Michael P. Epstein, Damià H. Suñer, Yingjie Zhao, Marta Unolt, Kathryn McCabe, Aaron M. Holleman, Zhengdong Zhang, Rosemarie Fritsch, Alex V. Kotlar, Elena Michaelovsky, T. Blaine Crowley, Brenna Lilley, Sunny X. Tang, Rens Evers, Ruben C. Gur, Isabelle Cleynen, Flora Tassone, Nicole Philip, Kevin M. Antshel, Koen Devriendt, Antonio F. Pardiñas, Pankaj Chopra, Thomas Monfeuga, Fabio Di Fabio, Therese van Amelsvoort, Aaron Golden, Doron Gothelf, Donna M. McDonald-McGinn, Raquel E. Gur, Daniel E. McGinn

Publikováno v: Molecular Psychiatry
Molecular Psychiatry, Nature Publishing Group, 2020, ⟨10.1038/s41380-020-0654-3⟩
Molecular Psychiatry, 2020, ⟨10.1038/s41380-020-0654-3⟩
Molecular Psychiatry (2020)
Molecular psychiatry
Molecular Psychiatry, 26(8), 4496-4510. Nature Publishing Group

Schizophrenia occurs in about one in four individuals with 22q11.2 deletion syndrome (22q11.2DS). The aim of this International Brain and Behavior 22q11.2DS Consortium (IBBC) study was to identify genetic factors that contribute to schizophrenia, in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4c91788310dcf6c66ef3ac3973170b9
http://hdl.handle.net/20.500.12278/33344

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Variance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects

Publikováno v: American Journal of Medical Genetics. A, Vol. 176, No 10 (2018) pp. 2172-2181
American Journal of Medical Genetics Part A, 176(10), 2172-2181. Wiley
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
American journal of medical genetics. Part A, vol 176, iss 10

The 22q11.2 deletion syndrome is caused by non-allelic homologous recombination events during meiosis between low copy repeats (LCR22) termed A, B, C, and D. Most patients have a typical LCR22A-D (AD) deletion of 3 million base pairs (Mb). In this re

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c08da23afa70859c4fc6d6aa3b110d39
https://doi.org/10.1002/ajmg.a.40359

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White matter abnormalities in 22q11.2 deletion syndrome patients showing cognitive decline

Autor: Elemi J. Breetvelt, Iris E. C. Sommer, Marc M. Bohlken, Jasper O. Nuninga, Sanne Koops, Jacob A. S. Vorstman, René C.W. Mandl, Sasja N. Duijff, Ania Fiksinski, René S. Kahn

Publikováno v: Psychological Medicine. 48:1655-1663

BackgroundDecline in cognitive functioning precedes the first psychotic episode in the course of schizophrenia and is considered a hallmark symptom of the disorder. Given the low incidence of schizophrenia, it remains a challenge to investigate wheth

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4f0baca463ded89f1b9307a18253c40
https://doi.org/10.1017/s0033291717003142

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Autism Spectrum and psychosis risk in the 22q11.2 deletion syndrome. Findings from a prospective longitudinal study

Autor: Jacob A. S. Vorstman, René S. Kahn, Ania Fiksinski, Anne S. Bassett, Sasja N. Duijff, Elemi J. Breetvelt

Publikováno v: Schizophrenia Research. 188:59-62

Background Individuals with 22q11.2 deletion syndrome (22q11DS) have a 25% risk for schizophrenia and related psychotic disorders. Some have hypothesized that Autism Spectrum Disorders (ASDs) diagnosed in children with 22q11DS may actually represent

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b5a8a369708e81a46bfaf19aa2fcd1f
https://doi.org/10.1016/j.schres.2017.01.032

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Explaining the variable penetrance of CNVs: Parental intelligence modulates expression of intellectual impairment caused by the 22q11.2 deletion

Autor: Henriette F. N. Swanenburg de Veye, Renske Schappin, Gerben Sinnema, Frits A. Beemer, Sasja N. Duijff, Jacob A. S. Vorstman, Elemi J. Breetvelt, Petra W.J. Klaassen

Publikováno v: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 171:790-796

The role of rare genetic variants, in particular copy number variants (CNVs), in the etiology of neurodevelopmental disorders is becoming increasingly clear. While the list of these disorder-related CNVs continues to lengthen, it has also become clea

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::97d7661cc78ed4e5fff358498951475a
https://doi.org/10.1002/ajmg.b.32441

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Cognitive and behavioral trajectories in 22q11DS from childhood into adolescence: A prospective 6-year follow-up study

Autor: Jacob A. S. Vorstman, Henriette F. N. Swanenburg de Veye, Petra W.J. Klaassen, Gerben Sinnema, Frits A. Beemer, Sasja N. Duijff

Publikováno v: Research in Developmental Disabilities. 34:2937-2945

Patients with 22q11DS are at risk of behavioral problems and cognitive impairment. Recent studies suggest a possible intellectual decline in 22q11DS children. To date it is unknown if cognitive development is related to the behavioral problems in 22q

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::faf3e3dc4047ed6b95c3e5133e030dc0
https://doi.org/10.1016/j.ridd.2013.06.001

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Early interventions in risk groups for schizophrenia : what are we waiting for?

Autor: Christiaan H. Vinkers, Covadonga M. Díaz-Caneja, Raquel E. Gur, Carrie E. Bearden, Celso Arango, Jacob A. S. Vorstman, Sasja N. Duijff, Kim Maijer, Therese van Amelsvoort, Lieuwe de Haan, Edwin van Dellen, Elemi J. Breetvelt, Iris E. C. Sommer

Publikováno v: Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
NPJ Schizophrenia
Sommer, I E, Bearden, C E, van Dellen, E, Breetvelt, E J, Duijff, S N, Maijer, K, van Amelsvoort, T, de Haan, L, Gur, R E, Arango, C, Díaz-Caneja, C M, Vinkers, C H & Vorstman, J A 2016, ' Early interventions in risk groups for schizophrenia : what are we waiting for? ', Schizophrenia Research, vol. 2, pp. 16003 . https://doi.org/10.1038/npjschz.2016.3
NPJ schizophrenia, vol 2, iss 1
NPJ schizophrenia, 2. Nature Publishing Group
npj Schizophrenia, 2. Nature Publishing Group

Intervention strategies in adolescents at ultra high-risk (UHR) for psychosis are promising for reducing conversion to overt illness, but have only limited impact on functional outcome. Recent studies suggest that cognition does not further decline d

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c21c5770cfbe36db971f7d75c0fbf13
https://dspace.library.uu.nl/handle/1874/342739

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Behavioral phenotype in children with 22q11Ds : Agreement between parents and teachers

Autor: Jacob A. S. Vorstman, Henriette F. N. Swanenburg de Veye, Gerben Sinnema, Frits A. Beemer, Sasja N. Duijff, Petra W.J. Klaassen

Publikováno v: Psychological Assessment, 27(1), 272. American Psychological Association Inc.

Patients with the 22q11-deletion syndrome (22q11DS) are at an increased risk of developing schizophrenia. Besides the effects of genetic variation, environmental factors could also be important in modifying the risk of schizophrenia in 22q11DS patien

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bedf438a5c620e9d03b2805776be1022
https://dspace.library.uu.nl/handle/1874/331598

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