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1دورية أكاديمية
المؤلفون: Basilio Noris, Jacqueline Nadel, Mandy Barker, Nouchine Hadjikhani, Aude Billard
المصدر: PLoS ONE, Vol 7, Iss 9, p e44144 (2012)
وصف الملف: electronic resource
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المؤلفون: Peter Hindley, Mandy Barker, Andy Holwell, Maria Gascon-Ramos, Kate Moore, Valerie Leach, Sara Rhys-Jones, Barry Wright, Nicoletta Gentili, Rob Walker
المصدر: Advances in Mental Health. 11:95-105
مصطلحات موضوعية: Service (business), Psychiatry and Mental health, Nursing, business.industry, Publishing, Project commissioning, Psychological intervention, Medicine, business, Mental health, Social policy, Unit (housing), Mental health service
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المؤلفون: Laurent Pasquier, Anne V. Snow, David T. Miller, Louise Harewood, Christina Triantafallou, Timothy P.L. Roberts, Leighton B. Hinkley, Zili Chu, Louis Vallée, Alyss Lian Cavanagh, Evica Rajcan-Separovic, Patricia Blanchet, Fiona Miller, Robin P. Goin-Kochel, Beau Reilly, Bettina Cerban, Vanessa Siffredi, Bridget A. Fernandez, Roger Vaughan, Brianna M. Paul, Fanny Morice-Picard, Elisabeth Flori, Dominique Campion, Gérard Didelot, Anne Philippe, Christa Lese Martin, Srikantan S. Nagarajan, Joris Andrieux, Jacques Puechberty, Marie Pierre Cordier, Jill V. Hunter, Ellen van Binsbergen, Catherine Vincent-Delorme, Vivek Swarnakar, Jean Marie Cuisset, Monica Proud, Patrick Callier, Bert B.A. de Vries, Jeffrey I. Berman, Sarah J. Spence, Alexandra Bowe, Wendy K. Chung, Katy Ankenman, Katherine Hines, Sarah E. Gobuty, Philippe Jonveaux, Lisa Blaskey, Alice Goldenberg, Sylvie Jaillard, Alessandra Renieri, Anne M. Maillard, Tracy Luks, Lee Anne Green Snyder, Elliott H. Sherr, Sarah Y. Khan, Fabienne Prieur, Simon A. Zwolinski, Andres Metspalu, Ghislaine Plessis, Jean Chiesa, Rita J. Jeremy, Valérie Malan, Michèle Mathieu-Dramard, Loyse Hippolyte, Bethanny Smith-Packard, Andrea M. Paal, Bénédicte Duban Bedu, Claudine Rieubland, Jordan Burko, Sylvie Joriot, Philippe Conus, Dominique Bonneau, Benoit Arveiler, Nicole de Leeuw, Allison G. Dempsey, John E. Spiro, Julia Wenegrat, Bertrand Isidor, Cédric Le Caignec, Kyle J. Steinman, Bruno Delobel, Ashlie Llorens, Jacques S. Beckmann, Kelly Johnson, Sean Ackerman, Polina Bukshpun, Silvia Garza, Alexandre Reymond, Damien Sanlaville, Ellen Hanson, Martine Doco-Fenzy, Jacques Thonney, Mari Wakahiro, Juliane Hoyer, Jacqueline Vigneron, Katrin Õunap, Arthur L. Beaudet, Mandy Barker, Nicole Visyak, Sonia Bouquillon, W. Andrew Faucett, Raphael Bernier, Sudha Kilaru Kessler, Audrey Lynn Bibb, Dennis Shaw, R. Frank Kooy, Suzanne M E Lewis, Anna L. Laakman, Nicholas J. Pojman, Hubert Journel, Laura Bernardini, Arianne Stevens, Julia P. Owen, Rebecca Mc Nally Keehn, Stéphanie Selmoni, Sébastien Lebon, Aurélien Macé, Bruno Leheup, Saba Qasmieh, Zoltán Kutalik, Anita Rauch, Yiping Shen, Elysa J. Marco, Nathalie Van der Aa, Carina Ferrari, Noam D. Beckmann, Delphine Héron, Jennifer Tjernage, Benjamin Aaronson, Albert David, Marie Pierre Lemaitre, Muriel Holder, Eve Õiglane-Shlik, Anneke T. Vulto-van Silfhout, Flore Zufferey, Constance Atwell, Marta Benedetti, Ellen Grant, Jenna Elgin, Patricia Z. Page, Caroline Rooryck, Randy L. Buckner, Qixuan Chen, Laurence Faivre, Sébastien Jacquemont, Kerri P. Nowell, Florence Fellmann, Disciglio Vittoria, Katharina Magdalena Rötzer, Hana Lee, Alastair J. Martin, Marion Greenup, David H. Ledbetter, Katrin Männik, Morgan W. Lasala, Jennifer Gerdts, Hanalore Alupay, Florence Petit, Elizabeth Aylward, Gerald D. Fischbach, Mafalda Mucciolo, Maxwell Cheong, Gabriela Marzano, Frédérique Béna, Danielle Martinet, Timothy J. Moss, Odile Boute, Jennifer Olson, Marco Belfiore, Christina Fagerberg, Corby L. Dale, Robert M. Witwicki, Yolanda L. Evans, Melissa B. Ramocki, Marie-Claude Addor, Christèle Dubourg, Mariken Ruiter, Tuhin K. Sinha, Mieke M. van Haelst, Alan Packer, Kathleen E. McGovern, Christie M. Brewton, Stephen M. Kanne, Richard I. Fisher, Tracey Ward, Sophie Dupuis-Girod, Pratik Mukherjee
المساهمون: Simons VIP Consortium, 16p11.2 European Consortium, Addor, MC., Arveiler, B., Belfiore, M., Bena, F., Bernardini, L., Blanchet, P., Bonneau, D., Boute, O., Callier, P., Campion, D., Chiesa, J., Cordier, MP., Cuisset, JM., David, A., de Leeuw, N., de Vries, B., Didelot, G., Doco-Fenzy, M., Bedu, BD., Dubourg, C., Dupuis-Girod, S., Fagerberg, CR., Faivre, L., Fellmann, F., Fernandez, BA., Fisher, R., Flori, E., Goldenberg, A., Heron, D., Holder, M., Hoyer, J., Isidor, B., Jaillard, S., Jonveaux, P., Joriot, S., Journel, H., Kooy, F., le Caignec, C., Leheup, B., Lemaitre, MP., Lewis, S., Malan, V., Mathieu-Dramard, M., Metspalu, A., Morice-Picard, F., Mucciolo, M., Oiglane-Shlik, E., Ounap, K., Pasquier, L., Petit, F., Philippe, A., Plessis, G., Prieur, F., Puechberty, J., Rajcan-Separovic, E., Rauch, A., Renieri, A., Rieubland, C., Rooryck, C., Rötzer, KM., Ruiter, M., Sanlaville, D., Selmoni, S., Shen, Y., Siffredi, V., Thonney, J., Vallée, L., van Binsbergen, E., Van der Aa, N., van Haelst MM., Vigneron, J., Vincent-Delorme, C., Vittoria, D., Vulto-van Silfhout AT., Witwicki, RM., Zwolinski, SA., Bowe, A., Beaudet, AL., Brewton, CM., Chu, Z., Dempsey, AG., Evans, YL., Garza, S., Kanne, SM., Laakman, AL., Lasala, MW., Llorens, AV., Marzano, G., Moss, TJ., Nowell, KP., Proud, MB., Chen, Q., Vaughan, R., Berman, J., Blaskey, L., Hines, K., Kessler, S., Khan, SY., Qasmieh, S., Bibb, AL., Paal, AM., Page, PZ., Smith-Packard, B., Buckner, R., Burko, J., Cavanagh, AL., Cerban, B., Snow, AV., Snyder, LG., Keehn, RM., Miller, DT., Miller, FK., Olson, JE., Triantafallou, C., Visyak, N., Atwell, C., Benedetti, M., Fischbach, GD., Greenup, M., Packer, A., Bukshpun, P., Cheong, M., Dale, C., Gobuty, SE., Hinkley, L., Jeremy, RJ., Lee, H., Luks, TL., Marco, EJ., Martin, AJ., McGovern, KE., Nagarajan, SS., Owen, J., Paul, BM., Pojman, NJ., Sinha, T., Swarnakar, V., Wakahiro, M., Alupay, H., Aaronson, B., Ackerman, S., Ankenman, K., Elgin, J., Gerdts, J., Johnson, K., Reilly, B., Shaw, D., Stevens, A., Ward, T., Wenegrat, J., Other departments, Service de génétique médicale, Centre Hospitalier Universitaire Vaudois [Lausanne] (CHUV), CHU Pontchaillou [Rennes], Department of Medical Genetics, Université de Lausanne (UNIL), Centre de Génétique Chromosomique, Hôpital Saint Vincent de Paul-GHICL, Department of Molecular and Human Genetics, Baylor College of Medicine (BCM), Baylor University-Baylor University, Texas Children's Hospital [Houston, USA], Department of pediatrics, Primary palliative Care Research Group, Community Health Sciences, General Practice Section, University of Edinburgh, Center for Integrative Genomics - Institute of Bioinformatics, Génopode (CIG), Swiss Institute of Bioinformatics [Lausanne] (SIB), Université de Lausanne (UNIL)-Université de Lausanne (UNIL), Physiopathologie et neuroprotection des atteintes du cerveau en développement, Université Paris Diderot - Paris 7 (UPD7)-Institut National de la Santé et de la Recherche Médicale (INSERM), Developmental Brain and Behaviour Unit, University of Southampton, Institute of Molecular and Cell Biology, University of Tartu, Department of Human Genetics, UCLA, University of California [Los Angeles] (UCLA), University of California-University of California-Semel Institute, Institut de Génétique et Développement de Rennes (IGDR), Université de Rennes 1 (UR1), Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Centre National de la Recherche Scientifique (CNRS)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique ), Service de Cytogénétique et de Biologie Cellulaire, Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Hôpital Pontchaillou-CHU Pontchaillou [Rennes], Université de Lausanne = University of Lausanne (UNIL), Hôpital Saint Vincent de Paul-Groupement des Hôpitaux de l'Institut Catholique de Lille (GHICL), Université catholique de Lille (UCL)-Université catholique de Lille (UCL), Université de Lausanne = University of Lausanne (UNIL)-Université de Lausanne = University of Lausanne (UNIL), University of California (UC)-University of California (UC)-Semel Institute, Université de Rennes (UR)-Centre National de la Recherche Scientifique (CNRS)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique ), Université de Rennes (UR)-Hôpital Pontchaillou-CHU Pontchaillou [Rennes], Kooy, Frank
المصدر: Journal of Medical Genetics
Journal of Medical Genetics, vol. 49, no. 10, pp. 660-668
Journal of medical genetics, 49(10), 660-668. BMJ Publishing Group
Journal of Medical Genetics, BMJ Publishing Group, 2012, 49 (10), pp.660-8. ⟨10.1136/jmedgenet-2012-101203⟩
Journal of Medical Genetics, 2012, 49 (10), pp.660-8. ⟨10.1136/jmedgenet-2012-101203⟩
Journal of medical genetics
JOURNAL OF MEDICAL GENETICSمصطلحات موضوعية: Adult, Male, Pediatrics, medicine.medical_specialty, Heterozygote, Adolescent, [SDV]Life Sciences [q-bio], Developmental Disabilities, Biology, Body Mass Index, 03 medical and health sciences, Young Adult, 0302 clinical medicine, Gene Order, Genetics, medicine, Humans, Copy-number variation, Clinical genetics, Obesity, Young adult, Child, Genetics (clinical), 030304 developmental biology, Child Development Disorders, Pervasive/diagnosis, Child Development Disorders, Pervasive/genetics, Chromosome Deletion, Chromosomes, Human, Pair 16, Developmental Disabilities/diagnosis, Developmental Disabilities/genetics, Female, Intelligence Tests, Phenotype, Syndrome, 2. Zero hunger, Psychiatry, 0303 health sciences, Intelligence quotient, Neuropsychology, Complex traits, medicine.disease, Comorbidity, 3. Good health, Autism spectrum disorder, Child Development Disorders, Pervasive, Autism, Medical genetics, Human medicine, Copy-Number Variation, 030217 neurology & neurosurgery
وصف الملف: application/pdf; pdf
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المؤلفون: Gordon Jackson, Mandy Barker, Stella Cosgrove, Nigel Howorth, Jacqueline McMahon, Lewis Blacow
المصدر: British journal of nursing (Mark Allen Publishing). 20(19)
مصطلحات موضوعية: Clinical placement, business.industry, Hospitals, Public, education, Mentors, Sign (semiotics), Pilot Projects, Nursing Staff, Hospital, State Medicine, United Kingdom, Practice education, Mentorship, Nursing, Nursing Evaluation Research, Medicine, Humans, Student nurse, Nurse education, Staff Development, business, General Nursing, Education, Professional, Retraining
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6cf20d602459f989675494ea196b6460
https://pubmed.ncbi.nlm.nih.gov/22067838 -
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المؤلفون: Jacqueline Nadel, Aude Billard, Basilio Noris, Francois Hentsch, Mandy Barker, François Ansermet
المصدر: EMBC
Conference proceedings : IEEE Engineering in Medicine and Biology Society, Vol. 2011 (2011) pp. 5356-9مصطلحات موضوعية: Male, media_common.quotation_subject, Monitoring, Ambulatory, Fixation, Ocular, Child Development Disorders, Pervasive/diagnosis/physiopathology, Developmental psychology, ddc:616.89, Typically developing, Monitoring, Ambulatory/instrumentation, Perception, medicine, Humans, Attention, Interpersonal Relations, Child, media_common, Stimuli, Lateral field, Social communication, Equipment Design, medicine.disease, Gaze, Equipment Failure Analysis, Child Development Disorders, Pervasive, Autism spectrum disorder, Child, Preschool, Dyadic interaction, Autism, Female, Psychology
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec4840498a1e52ca84a24195f68b91a8
https://doi.org/10.1109/iembs.2011.6091325
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المؤلفون: Bruno Pardo, Jamel Chelly, Bernard Conrad, Lucia Bartoloni, Stylianos E. Antonarakis, Armand Bottani, Mandy Barker, Arjan P.M. de Brouwer, Valeria Capra
المصدر: American Journal of Medical Genetics. Part A, 143, 888-90
American Journal of Medical Genetics. A, Vol. 143A, No 8 (2007) pp. 888-890
American Journal of Medical Genetics. Part A, 143, 8, pp. 888-90مصطلحات موضوعية: ddc:616, Male, Mental Retardation, X-Linked/etiology/ genetics, Base Sequence, media_common.quotation_subject, Conserved Sequence/ genetics, Genetic Variation, Art, University hospital, Genomic disorders and inherited multi-system disorders [IGMD 3], Genetic defects of metabolism [UMCN 5.1], Gene Frequency, Genetics, Mental Retardation, X-Linked, Humans, University medical, Female, Sequence variation, Humanities, Functional Neurogenomics [DCN 2], Genetics (clinical), Conserved Sequence, media_common
وصف الملف: application/pdf
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المؤلفون: Jacques S. Beckmann, Martine Doco-Fenzy, Mandy Barker, Alexandre Reymond, Borja Rodriguez-Herreros, Raphael Bernier, Katrin Männik, Andres Metspalu, Loyse Hippolyte, Marion Gérard, Anne M. Maillard, Bogdan Draganski, Anu Reigo, Laurent Mottron, Laurence Schneider, Philippe Conus, Cédric Le Caignec, Sandra Martin-Brevet, Carina Ferrari, Anneli Kolk, Aurélie Pain, Robin P. Goin-Kochel, Nouchine Hadjikhani, Boris Keren, Ellen Hanson, Cyril Mignot, Franck Ramus, Lee Anne Green Snyder, Sébastien Jacquemont, Aurélien Macé, Albert David, Bertrand Isidor
المساهمون: 16p11.2 European Consortium, Simons Variation in Individuals Project Consortium, 16p11.2 European Consortium, Simons Variation in Individuals Project Consortium
المصدر: Biological psychiatry, vol. 80, no. 2, pp. 129-139
Biological Psychiatry
Biological psychiatryمصطلحات موضوعية: Adult, Male, 0301 basic medicine, Heterozygote, Adolescent, DNA Copy Number Variations, Intelligence, Chromosome Disorders, Locus (genetics), ASD, Executive Function, Young Adult, 03 medical and health sciences, 0302 clinical medicine, Memory, Intellectual Disability, Chromosome Duplication, mental disorders, medicine, Humans, Cognitive Dysfunction, Copy-number variation, Autistic Disorder, Child, Biological Psychiatry, Inhibition, Language, Genetics, Working memory, Copy number variation, Neuropsychology, Cognition, Middle Aged, medicine.disease, 16p11.2, Pedigree, Autistic Disorder/diagnostic imaging, Autistic Disorder/genetics, Autistic Disorder/physiopathology, Child, Preschool, Chromosome Deletion, Chromosome Disorders/diagnostic imaging, Chromosome Disorders/genetics, Chromosome Disorders/physiopathology, Chromosome Duplication/genetics, Chromosomes, Human, Pair 16/genetics, Cognitive Dysfunction/diagnostic imaging, Cognitive Dysfunction/genetics, Cognitive Dysfunction/physiopathology, DNA Copy Number Variations/genetics, Executive Function/physiology, Female, Intellectual Disability/diagnostic imaging, Intellectual Disability/genetics, Intellectual Disability/physiopathology, Intelligence/genetics, Memory/physiology, Motor Skills/physiology, 030104 developmental biology, Motor Skills, Autism spectrum disorder, Autism, Verbal memory, Psychology, Chromosomes, Human, Pair 16, 030217 neurology & neurosurgery
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::178ed1b8601c25473c2a6e5fb24bcc3c
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