نتائج البحث - "Martin Woods"

المساهمون: Tourette International Collaborative Genetics Study (TIC Genetics), Tourette Syndrome Genetics Southern and Eastern Europe Initiative (TSGENESEE), Tourette Association of America International Consortium for Genetics (TAAICG), Abdulkadir, M., Arbelaez, J., Bodmer, B., Bromberg, Y., Brown, L.W., Cheon, K.A., Coffey, B.J., Deng, L., Dietrich, A., Dong, S., Duhn, C., Elzerman, L., Fernandez, T.V., Fremer, C., Garcia-Delgar, B., Gilbert, D.L., Grice, D.E., Hagstrøm, J., Hedderly, T., Heiman, G.A., Heyman, I., Hoekstra, P.J., Hong, H.J., Huyser, C., Kim, E.J., Kim, Y.K., Kim, Y.S., King, R.A., Koh, Y.J., Kook, S., Kuperman, S., Leventhal, B.L., Ludolph, A.G., Madruga-Garrido, M., Mandell, J.D., Maras, A., Mir, P., Morer, A., Morris, M.T., Müller-Vahl, K., Münchau, A., Murphy, T.L., Nasello, C., Plessen, K.J., Poisner, H., Roessner, V., Sanders, S.J., Shin, E.Y., Song, D.H., Song, J., State, M.W., Sun, N., Thackray, J.K., Tischfield, J.A., Tübing, J., Visscher, F., Wanderer, S., Wang, S., Willsey, A.J., Woods, M., Xing, J., Zhang, Y., Zhao, X., Zinner, S.H., Androutsos, C., Barta, C., Farkas, L., Fichna, J., Georgitsi, M., Janik, P., Karagiannidis, I., Koumoula, A., Nagy, P., Paschou, P., Puchala, J., Rizzo, R., Szejko, N., Szymanska, U., Tarnok, Z., Tsironi, V., Wolanczyk, T., Zekanowski, C., Barr, C.L., Batterson, J.R., Berlin, C., Bruun, R.D., Budman, C.L., Cath, D.C., Chouinard, S., Coppola, G., Cox, N.J., Darrow, S., Davis, L.K., Dion, Y., Freimer, N.B., Grados, M.A., Hirschtritt, M.E., Huang, A.Y., Illmann, C., Kurlan, R., Leckman, J.F., Lyon, G.J., Malaty, I.A., Mathews, C.A., MacMahon, W.M., Neale, B.M., Okun, M.S., Osiecki, L., Pauls, D.L., Posthuma, D., Ramensky, V., Robertson, M.M., Rouleau, G.A., Sandor, P., Scharf, J.M., Singer, H.S., Smit, J., Sul, J.H., Yu, D.

المصدر: Cell Reports, Vol 24, Iss 13, Pp 3441-3454.e12 (2018)
Cell reports, vol. 24, no. 13, pp. 3441-3454.e12
Cell reports
Cell reports, 24(13), 3441-3454.e12. CELL PRESS

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, medicine.medical_specialty, DNA Copy Number Variations, Receptors, Cell Surface, Biology, Genome, Article, General Biochemistry, Genetics and Molecular Biology, 03 medical and health sciences, 0302 clinical medicine, RARE, SCHIZOPHRENIA, medicine, Humans, Copy-number variation, Child, NEURODEVELOPMENTAL DISORDERS, Gene, lcsh:QH301-705.5, Exome sequencing, 030304 developmental biology, Medicinsk genetik, Sequence (medicine), Genetics, 0303 health sciences, SEVERE INTELLECTUAL DISABILITY, Cadherin, MUTATIONS, AUTISM SPECTRUM DISORDER, Cell Polarity, OBSESSIVE-COMPULSIVE DISORDER, Cadherins, medicine.disease, Pedigree, PREVALENCE, CONGENITAL HEART-DISEASE, GENOME, 030104 developmental biology, lcsh:Biology (General), Schizophrenia, Medical genetics, Female, Cadherins/genetics, Receptors, Cell Surface/genetics, Tourette Syndrome/genetics, Tourette Syndrome/pathology, TIC Genetics, Tourette disorder, cell polarity, copy number variants, de novo variants, gene discovery, microarray genotyping, multiplex, simplex, whole exome sequencing, Medical Genetics, 030217 neurology & neurosurgery, Tourette Syndrome

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e531960f737482f236b0bf416aab09c3Test
http://www.sciencedirect.com/science/article/pii/S221112471831386XTest

8

‘Every Woman Wants to Know What Came out of Her Body’: Grief Experiences of Women After Stillbirth in Nigeria

المؤلفون: Tosin Popoola, Joan Skinner, Martin Woods

المصدر: OMEGA - Journal of Death and Dying. :003022282110518

مصطلحات موضوعية: Health (social science), Life-span and Life-course Studies, Critical Care and Intensive Care Medicine, humanities, female genital diseases and pregnancy complications, reproductive and urinary physiology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::926654519637b746e8f8a016de96661fTest
https://doi.org/10.1177/00302228211051823Test

9

Healing Strategies among Thai Buddhist Widows after Sudden of Loss of Spouse in Terrorist Attacks

المؤلفون: Sujira WICHAIDIT, Praneed SONGWATHANA, Karnsunaphat BALTHIP, Martin WOODS

المصدر: Walailak Journal of Science and Technology (WJST). 16:243-254

مصطلحات موضوعية: Multidisciplinary, social sciences

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::3531a54e5bbc266d914f4c4b460e5ba0Test
https://doi.org/10.48048/wjst.2019.4051Test

10

Investigation of previously implicated genetic variants in chronic tic disorders

المؤلفون: Samuel Kuperman, Frank Visscher, Kirsten R. Müller-Vahl, Eun-Young Shin, Jennifer Tübing, Els van den Ban, Sina Wanderer, Hyun Ju Hong, Yun-Joo Koh, Jungeun Song, Gary A. Heiman, Lonneke Elzerman, Donald L. Gilbert, Derek Gordon, Laura Ibanez-Gomez, Keun-Ah Cheon, Douglas Londono, Young Key Kim, Bennett L. Leventhal, Alexander Münchau, Odette Fründt, Andrea G. Ludolph, Astrid Morer, Sodahm Kook, Thomas V. Fernandez, Lawrence W. Brown, Marcos Madruga-Garrido, Ewgeni Jakubovski, Jay A. Tischfield, Mohamed Abdulkadir, Blanca Garcia-Delgar, Carolin Fremer, Samuel H. Zinner, Pablo Mir, Robert A. King, Martin Woods, Veit Roessner, Young Shin Kim, Isobel Heyman, Tara Murphy, Athanasios Maras, Dong-Ho Song, Pieter J. Hoekstra, Tammy Hedderly, Barbara J. Coffey, Andrea Dietrich, Chaim Huyser, Dorothy E. Grice, Kerstin J. Plessen

المساهمون: Clinical Cognitive Neuropsychiatry Research Program (CCNP), Child Psychiatry, Child and Adolescent Psychiatry / Psychology

المصدر: European Archives of Psychiatry and Clinical Neuroscience, 268(3), 301-316. SPRINGER HEIDELBERG
European archives of psychiatry and clinical neuroscience, 268(3), 301-316. Springer Verlag
European Archives of Psychiatry and Clinical Neuroscience
European Archives of Psychiatry and Clinical Neuroscience, 268(3), 301-316. D. Steinkopff-Verlag
European archives of psychiatry and clinical neuroscience, vol 268, iss 3

مصطلحات موضوعية: 0301 basic medicine, Male, Candidate gene, Genome-wide association study, Tryptophan Hydroxylase, Obsessive–compulsive disorder, Severity of Illness Index, Linkage Disequilibrium, PICALM, 0302 clinical medicine, Candidate gene study, Obsessive-compulsive disorder, Pharmacology (medical), Child, POPULATION, Psychiatry, Genetics, LA-TOURETTE-SYNDROME, education.field_of_study, SLITRK1 GENE, Single Nucleotide, General Medicine, Transmission disequilibrium test, Middle Aged, 3. Good health, Psychiatry and Mental health, COMPREHENSIVE METAANALYSIS, Child, Preschool, HISTIDINE-DECARBOXYLASE, Cognitive Sciences, Female, Microtubule-Associated Proteins, Adult, Adolescent, Genotype, Clinical Sciences, Population, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, Young Adult, SNP, Humans, Polymorphism, GENOME-WIDE ASSOCIATION, AUTISM, Preschool, education, Biological Psychiatry, FAMILY-BASED ASSOCIATION, Genetic association, Family Health, Original Paper, Tourette syndrome, Neurosciences, OBSESSIVE-COMPULSIVE DISORDER, Transmission Disequilibrium Test, CROSS-DISORDER, 030104 developmental biology, Attention-deficit/hyperactivity disorder, Tic Disorders, 030217 neurology & neurosurgery, Genome-Wide Association Study

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c080118db5a7932f73b32854e2647093Test
https://doi.org/10.1007/s00406-017-0808-8Test

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