An exploratory study among intellectual disability physicians on the care and coercion act and the use of psychotropic drugs for challenging behaviour

Autor: Janouk C. bij de Weg, Marieke Teeuw, Aline K. Honingh, Paula Sterkenburg

Publikováno v: International Journal of Environmental Research and Public Health
International Journal of Environmental Research and Public Health, Vol 18, Iss 10240, p 10240 (2021)
International Journal of Environmental Research and Public Health, 18(19):10240, 1-12. Multidisciplinary Digital Publishing Institute (MDPI)
bij de Weg, J C, Honingh, A K, Teeuw, M & Sterkenburg, P S 2021, ' An exploratory study among intellectual disability physicians on the care and coercion act and the use of psychotropic drugs for challenging behaviour ', International Journal of Environmental Research and Public Health, vol. 18, no. 19, 10240, pp. 1-12 . https://doi.org/10.3390/ijerph181910240
Volume 18
Issue 19

The new Dutch Care and Coercion Act aims to better regulate the use of psychotropic drugs for challenging behaviour in people with an intellectual disability. This study explores experiences of intellectual disability physicians (IDPs) in prescribing

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1ca6096fcaa620c4148d9971616ad1c
https://doi.org/10.3390/ijerph181910240

First steps in exploring prospective exome sequencing of consanguineous couples

Autor: Martina C. Cornel, Quinten Waisfisz, Petra J.G. Zwijnenburg, Marjan M. Weiss, Leo P. ten Kate, Marieke Teeuw, Erik A. Sistermans, Hanne Meijers-Heijboer, Lidewij Henneman

Publikováno v: Teeuw, M E, Waisfisz, Q, Zwijnenburg, P J G, Sistermans, E A, Weiss, M M, Henneman, L, ten Kate, L P, Cornel, M C & Meijers-Heijboer, H 2014, ' First steps in exploring prospective exome sequencing of consanguineous couples ', European Journal of Medical Genetics, vol. 57, no. 11-12, pp. 613-616 . https://doi.org/10.1016/j.ejmg.2014.09.003
European journal of medical genetics, 57(11-12), 613-616. Elsevier Masson SAS
European Journal of Medical Genetics, 57(11-12), 613-616. Elsevier Masson SAS

Consanguinity is one of the most frequent risk factors for congenital disorders. In theory, prospective exome sequencing of consanguineous couples could identify couples who both are carriers of autosomal recessive diseases, and empower such couples

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f90c933ad21b21b10a2db64d21ef2c98
https://doi.org/10.1016/j.ejmg.2014.09.003

Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcome

Autor: Peter Heutink, Fowzan S. Alkuraya, Eamonn Sheridan, Lidewij Henneman, Martina C. Cornel, Piet J. Kostense, A. van Haeringen, Patrizia Rizzu, Wided Kelmemi, Jan-Maarten Cobben, Amira Masri, M. Hashem, Hülya Kayserili, Zoltán Bochdanovits, Charlotte J. Dommering, Sander Ouburg, Marieke Teeuw, Marianne A. Jonker, L. P. ten Kate, H. Bouhamed-Chaabouni

Publikováno v: Kelmemi, W, Teeuw, M E, Bochdanovits, Z, Ouburg, S, Jonker, M A, Alkuraya, F, Hashem, M, Kayserili, H, van Haeringen, A, Sheridan, E, Masri, A, Cobben, J M, Rizzu, P, Kostense, P J, Dommering, C J, Henneman, L, Bouhamed-Chaabouni, H, Heutink, P, ten Kate, L P & Cornel, M C 2015, ' Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcome ', BMC Medical Genetics, vol. 16, 50 . https://doi.org/10.1186/s12881-015-0191-0
BMC Medical Genetics, 16:50. BioMed Central
BMC medical genetics 16(1), 50 (2015). doi:10.1186/s12881-015-0191-0
BMC medical genetics, 16(1). BioMed Central
BMC Medical Genetics
BMC Medical Genetics, 16

Offspring of consanguineous couples are at increased risk of congenital disorders. The risk increases as parents are more closely related. Individuals that have the same degree of relatedness according to their pedigree, show variable genomic kinship

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7be1eec32d5a333f92bac57d08e74873
https://research.vu.nl/en/publications/a11d44ba-b8ef-426c-bbb5-d951bf8d5b1a

Comment on Gialluisi et al

Autor: Leo P. ten Kate, Lidewij Henneman, Martina C. Cornel, Marieke Teeuw

Publikováno v: ten Kate, L P, Teeuw, M E, Henneman, L & Cornel, M C 2014, ' Comment on Gialluisi et al ', European Journal of Human Genetics, vol. 22, no. 2, pp. 157-157 . https://doi.org/10.1038/ejhg.2013.152
European Journal of Human Genetics, 22(2), 157-157. Nature Publishing Group

As authors of the first paper describing the methodology used by Gialluisi et al in their paper on the high allele frequency for Wilson disease in the Sardinian population, we want to congratulate them with their result.1, 2 The paper clearly shows t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::396a4f06c4c755e72b88d018c304f424
https://europepmc.org/articles/PMC3895651/

Consanguineous marriages, pearls and perils: Geneva International Consanguinity Workshop Report

Autor: Mona Aglan, Cornelia M. van Duijn, Emmanuelle Ranza-Boscardin, Leo P. ten Kate, Luigi Luca Cavalli-Sforza, Eric Engel, Samia A. Temtamy, Joël Zlotogora, Mubasshir Ajaz, André Mégarbané, Steve Arsenault, Siv Fokstuen, Lorraine Gwanmesia, Mohamed K. Alwasiyah, Saghira Malik Sharif, Rawan Awwad, Melissa Bonnefin, Heli Bathija, Tommaso Pippucci, Michael A. Morris, Marieke Teeuw, Stylianos E. Antonarakis, Sophie Dahoun, M.D. Peter Corry, Gulshan A. Karbani, Maryam Mostafavi, Giovanni Romeo, Alison Shaw, Bruno Reversade, Alan H. Bittles, Emmanouil T. Dermitzakis, Hanan Hamamy, Nawfal Anwer, Robin L. Bennett, Dhekra AlNaqeb, Ayad Alkalamchi, Armand Bottani

Publikováno v: Genetics in Medicine, Vol. 13, No 9 (2011) pp. 841-7
Hamamy, H, Antonarakis, S E, Cavalli-Sforza, L L, Temtamy, S, Romeo, G, ten Kate, L P, Bennett, R L, Shaw, A, Megarbane, A, van Duijn, C, Bathija, H, Fokstuen, S, Engel, E, Zlotogora, J, Dermitzakis, E, Bottani, A, Dahoun, S, Morris, M A, Arsenault, S, Aglan, M S, Ajaz, M, Alkalamchi, A, Alnaqeb, D, Alwasiyah, M K, Anwer, N, Awwad, R, Bonnefin, M, Corry, P, Gwanmesia, L, Karbani, G A, Mostafavi, M, Pippucci, T, Ranza-Boscardin, E, Reversade, B, Sharif, S M, Teeuw, M E & Bittles, A H 2011, ' Consanguineous marriages, pearls and perils: Geneva international consanguinity workshop report ', Genetics in Medicine, vol. 13, no. 9, pp. 841-847 . https://doi.org/10.1097/GIM.0b013e318217477f
Genetics in Medicine, 13(9), 841-847. Lippincott Williams & Wilkins
Genetics in Medicine, 13(9), 841-847. Lippincott Williams and Wilkins
Genetics in medicine, 13(9), 841-847. Lippincott Williams and Wilkins

Approximately 1.1 billion people currently live in countries where consanguineous marriages are customary, and among them one in every three marriages is between cousins. Opinions diverge between those warning of the possible health risks to offsprin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::236d2d9b51fc34ea8f246bb4d6814166
https://archive-ouverte.unige.ch/unige:32205