المؤلفون: Chang, H, Hoshina, N, Zhang, C, Ma, Y, Cao, H, Wang, Y, Wu, DD, Bergen, SE, Landén, M, Hultman, CM, Preisig, M, Kutalik, Z, Castelao, E, Grigoroiu-Serbanescu, M, Forstner, AJ, Strohmaier, J, Hecker, J, Schulze, TG, Müller-Myhsok, B, Reif, A, Mitchell, PB, Martin, NG, Schofield, PR, Cichon, S, Nöthen, MM, Walter, H, Erk, S, Heinz, A, Amin, N, Van Duijn, CM, Meyer-Lindenberg, A, Tost, H, Xiao, X, Yamamoto, T, Rietschel, M, Li, M, Backlund, L, Frisén, L, Lavebratt, C, Schalling, M, Ösby, U, Mühleisen, TW, Leber, M, Degenhardt, F, Treutlein, J, Mattheisen, M, Maaser, A, Meier, S, Herms, S, Hoffmann, P, Lacour, A, Witt, SH, Streit, F, Lucae, S, Maier, W, Schwarz, M, Vedder, H, Kammerer-Ciernioch, J, Pfennig, A, Bauer, M, Hautzinger, M, Wright, A, Fullerton, JM, Montgomery, GW, Medland, SE, Gordon, SD, Becker, T, Schumacher, J, Propping, P

المصدر: urn:ISSN:1359-4184 ; urn:ISSN:1476-5578 ; Molecular Psychiatry, 23, 2, 400-412

مصطلحات موضوعية: Clinical Research, Genetics, Behavioral and Social Science, Depression, Neurosciences, Serious Mental Illness, Brain Disorders, Mental Health, 2 Aetiology, 1.1 Normal biological development and functioning, 2.1 Biological and endogenous factors, 1 Underpinning research, Neurological, Adult, Amygdala, Bipolar Disorder, Brain, Cadherins, Cognition, Dendrites, Dendritic Spines, Depressive Disorder, Major, Female, Genetic Predisposition to Disease, Genotype, Humans, Male, Middle Aged, Mood Disorders

وصف الملف: application/pdf

العلاقة: http://hdl.handle.net/1959.4/unsworks_56621Test; https://unsworks.unsw.edu.au/bitstreams/8dfeba0c-83a8-422b-b5ea-9b0be2bd5508/downloadTest; https://doi.org/10.1038/mp.2016.231Test

الإتاحة: https://doi.org/10.1038/mp.2016.231Test
http://hdl.handle.net/1959.4/unsworks_56621Test
https://unsworks.unsw.edu.au/bitstreams/8dfeba0c-83a8-422b-b5ea-9b0be2bd5508/downloadTest

المؤلفون: Mühleisen, TW, Leber, M, Schulze, TG, Strohmaier, J, Degenhardt, F, Treutlein, J, Mattheisen, M, Forstner, AJ, Schumacher, J, Breuer, R, Meier, S, Herms, S, Hoffmann, P, Lacour, A, Witt, SH, Reif, A, Müller-Myhsok, B, Lucae, S, Maier, W, Schwarz, M, Vedder, H, Kammerer-Ciernioch, J, Pfennig, A, Bauer, M, Hautzinger, M, Moebus, S, Priebe, L, Czerski, PM, Hauser, J, Lissowska, J, Szeszenia-Dabrowska, N, Brennan, P, McKay, JD, Wright, A, Mitchell, PB, Fullerton, JM, Schofield, PR, Montgomery, GW, Medland, SE, Gordon, SD, Martin, NG, Krasnow, V, Chuchalin, A, Babadjanova, G, Pantelejeva, G, Abramova, LI, Tiganov, AS, Polonikov, A, Khusnutdinova, E, Alda, M, Grof, P, Rouleau, GA, Turecki, G, Laprise, C, Rivas, F, Mayoral, F, Kogevinas, M, Grigoroiu-Serbanescu, M, Propping, P, Becker, T, Rietschel, M, Nöthen, MM, Cichon, S, Schofield, Peter

المصدر: urn:ISSN:2041-1723 ; Nature Communications, 5, 1, 3339

مصطلحات موضوعية: Mental Health, Serious Mental Illness, Prevention, Brain Disorders, Human Genome, Genetics, Bipolar Disorder, 2 Aetiology, 2.1 Biological and endogenous factors, 3 Good Health and Well Being, Adenylyl Cyclases, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Male, Polymorphism, Single Nucleotide

وصف الملف: application/pdf

العلاقة: http://purl.org/au-research/grants/nhmrc/APP1037196Test; http://hdl.handle.net/1959.4/unsworks_13067Test; https://unsworks.unsw.edu.au/bitstreams/0e4f4bc2-b7a9-4d60-b695-f272b9b97eab/downloadTest; https://doi.org/10.1038/ncomms4339Test

الإتاحة: https://doi.org/10.1038/ncomms4339Test
http://hdl.handle.net/1959.4/unsworks_13067Test
https://unsworks.unsw.edu.au/bitstreams/0e4f4bc2-b7a9-4d60-b695-f272b9b97eab/downloadTest

المؤلفون: O'Donovan, MC, Norton, N, Williams, H, Peirce, T, Moskvina, V, Nikolov, I, Hamshere, M, Carroll, L, Georgieva, L, Dwyer, S, Holmans, P, Marchini, JL, Spencer, CCA, Howie, B, Leung, H-T, Giegling, I, Hartmann, AM, Möller, H-J, Morris, DW, Shi, Y, Feng, G, Hoffmann, P, Propping, P, Vasilescu, C, Maier, W, Rietschel, M, Zammit, S, Schumacher, J, Quinn, EM, Schulze, TG, Iwata, N, Ikeda, M, Darvasi, A, Shifman, S, He, L, Duan, J, Sanders, AR, Levinson, DF, Adolfsson, R, Ösby, U, Terenius, L, Jönsson, EG, Cichon, S, Nöthen, MM, Gill, M, Corvin, AP, Rujescu, D, Gejman, PV, Kirov, G, Craddock, N, Williams, NM, Owen, MJ, Buccola, NG, Mowry, BJ, Freedman, R, Amin, F, Black, DW, Silverman, JM, Byerley, WJ, Cloninger, CR

مصطلحات موضوعية: Adult, Male, Linkage disequilibrium, Genotype, Genome-wide association study, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Linkage Disequilibrium, Article, Cellular and Molecular Neuroscience, Young Adult, Gene Frequency, Meta-Analysis as Topic, Polymorphism (computer science), SNP, Humans, Genetic Predisposition to Disease, Allele, Receptor, Fibroblast Growth Factor, Type 2, Molecular Biology, Allele frequency, Aged, Genetics, Aged, 80 and over, Fibroblast growth factor receptor 2, Chromosomes, Human, Pair 10, Middle Aged, Psychiatry and Mental health, Schizophrenia, Female, Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd3a9dda9388dc75c45476f00e4f2727Test
https://doi.org/10.1038/mp.2008.108Test

المؤلفون: Leon, C.A., Schumacher, J., Kluck, N., Herold, C., Schulze, T.G., Propping, P., Rietschel, M, Cichon, S., Nöthen, M.M., Abou Jamra, R.

المصدر: Psychiatric genetics 21, 114 (2011). doi:10.1097/YPG.0b013e328341a334

مصطلحات موضوعية: info:eu-repo/classification/ddc/610, Adaptor Proteins, Vesicular Transport: genetics, Adult, Case-Control Studies, Female, Genetic Predisposition to Disease, Germany, Haplotypes: genetics, Humans, Male, Middle Aged, Polymorphism, Single Nucleotide: genetics, Receptors, AMPA: genetics, Schizophrenia: genetics, Vesicular Transport, ENTH protein, human, AMPA, glutamate receptor ionotropic, AMPA 1

جغرافية الموضوع: DE

العلاقة: info:eu-repo/semantics/altIdentifier/issn/0955-8829; info:eu-repo/semantics/altIdentifier/wos/WOS:000287841700009; info:eu-repo/semantics/altIdentifier/pmid/pmid:21116212; https://juser.fz-juelich.de/record/17369Test; https://juser.fz-juelich.de/searchTest?p=id:%22PreJuSER-17369%22

الإتاحة: https://doi.org/10.1097/YPG.0b013e328341a334Test
https://juser.fz-juelich.de/record/17369Test
https://juser.fz-juelich.de/searchTest?p=id:%22PreJuSER-17369%22

المؤلفون: Abou Jamra, R., Schulze, T.G., Georgi, A., Craddock, N., Propping, P., Rietschel, M., Nöthen, M.M., Cichon, S., Schumacher, J., Becker, T., Brockschmidt, F.F., Green, E., Alblas, M.A., Wendland, J.R., Adli, M., Grozeva, D., Strohmeier, J.

المصدر: American journal of medical genetics / B 9999B, 878 - 884 (2010). doi:10.1002/ajmg.b.31051

مصطلحات موضوعية: info:eu-repo/classification/ddc/570, Adult, Affective Disorders, Psychotic: genetics, Bipolar Disorder: genetics, Case-Control Studies, Chromosomes, European Continental Ancestry Group: genetics, Female, Genotype, Haplotypes, Humans, Male, Middle Aged, Polymorphism, Single Nucleotide, Risk Factors, BPAD, GPR145, LD, genotype-phenotype analysis, MCHR2, psy, socio

جغرافية الموضوع: DE

العلاقة: https://juser.fz-juelich.de/record/10095Test

الإتاحة: https://doi.org/10.1002/ajmg.b.31051Test
https://juser.fz-juelich.de/record/10095Test

المؤلفون: Suliman, H., Schumacher, J., Becker, T., Cichon, S., Schulze, T.G., Propping, P., Rietschel, M., Nöthen, M.M., Abou Jamra, R.

المصدر: Psychiatric genetics 20, 2 82 - 83 (2010). doi:10.1097/YPG.0b013e3283351244

مصطلحات موضوعية: info:eu-repo/classification/ddc/610, Base Sequence, D-Amino-Acid Oxidase: genetics, DNA Primers, Female, Genetic Variation, Humans, Male, Schizophrenia: enzymology, Schizophrenia: genetics, D-Amino-Acid Oxidase

جغرافية الموضوع: DE

العلاقة: info:eu-repo/semantics/altIdentifier/issn/0955-8829; info:eu-repo/semantics/altIdentifier/pmid/pmid:20145586; info:eu-repo/semantics/altIdentifier/wos/WOS:000275867300005; https://juser.fz-juelich.de/record/10084Test; https://juser.fz-juelich.de/searchTest?p=id:%22PreJuSER-10084%22

الإتاحة: https://doi.org/10.1097/YPG.0b013e3283351244Test
https://juser.fz-juelich.de/record/10084Test
https://juser.fz-juelich.de/searchTest?p=id:%22PreJuSER-10084%22

المؤلفون: Aretz, S, Stienen, D, Uhlhaas, S, Stolte, M, Entius, M M, Loff, S, Back, W, Kaufmann, A, Keller, K-M, Blaas, S H, Siebert, R, Vogt, S, Spranger, S, Holinski-Feder, E, Sunde, L, Propping, P, Friedl, W

المصدر: Aretz , S , Stienen , D , Uhlhaas , S , Stolte , M , Entius , M M , Loff , S , Back , W , Kaufmann , A , Keller , K-M , Blaas , S H , Siebert , R , Vogt , S , Spranger , S , Holinski-Feder , E , Sunde , L , Propping , P & Friedl , W 2007 , ' High proportion of large genomic deletions and a genotype phenotype update in 80 unrelated families with juvenile polyposis syndrome. ' , Journal of Medical Genetics , vol. ....

مصطلحات موضوعية: Adolescent, Adult, Age of Onset, Bone Morphogenetic Protein Receptors, Type I, Cadherins, Child, Preschool, Chromosome Deletion, DNA Mutational Analysis, Female, Gastrointestinal Neoplasms, Genetic Heterogeneity, Genotype, Germany, Humans, Infant, Intestinal Polyposis, Male, Neoplastic Syndromes, Hereditary, Nucleic Acid Amplification Techniques, PTEN Phosphohydrolase, Phenotype, Point Mutation, Smad4 Protein, Telangiectasia, Hereditary Hemorrhagic

الإتاحة: https://doi.org/10.1136/jmg.2007.052506Test
https://pure.au.dk/portal/da/publications/high-proportion-of-large-genomic-deletions-and-a-genotype-phenotype-update-in-80-unrelated-families-with-juvenile-polyposis-syndromeTest(6af89d80-e371-11dc-9afb-000ea68e967b).html

المؤلفون: Mcguffin, P, Lim, LCC, Craddock, N, Owen, M, Sham, P, Nöthen, MM, Körner, J, Rietschel, M, Fimmer, R, Propping, P, Murray, R, Gill, M

مصطلحات موضوعية: Adolescent, Adult, Aged, Bipolar Disorder - Diagnosis - Genetics - Psychology, Chromosome Mapping, Computer Simulation, Female, Gene Frequency - Genetics, Genes, Dominant - Genetics, Genetic Linkage - Genetics, Heterozygote Detection, Humans, Male, Middle Aged, Models, Genetic, Phenotype, Risk

العلاقة: Behavior Genetics; http://www.scopus.com/mlt/select.url?eid=2-s2.0-0030012006&selection=ref&src=s&origin=recordpageTest; Behavior Genetics, 1996, v. 26 n. 2, p. 113-122; 122; WOS:A1996UE22600004; 8639147; eid_2-s2.0-0030012006; 113; http://hdl.handle.net/10722/175755Test; 26

الإتاحة: https://doi.org/10.1007/BF02359889Test
http://hdl.handle.net/10722/175755Test

المؤلفون: Lim, L, Dawson, E, Parfitt, E, Roberts, Q, Daniels, J, Sham, P, Nothen, M, Propping, P, Lanczik, M, Maier, W, Reuner, U, Weissenbach, J, Gill, M, Powell, J, Mcguffin, P, Owen, M, Craddock, N

مصطلحات موضوعية: Genetic Linkage, Phospholipases A2, Phospholipases A - Genetics, Pedigree, Male, Lod Score, Humans, Genotype, Genetic Markers, Genes, Dominant, Female, Darier Disease - Genetics, Chromosomes, Human, Pair 12 - Genetics, Chromosome Mapping, Bipolar Disorder - Enzymology - Genetics, Alleles

العلاقة: American Journal of Medical Genetics - Neuropsychiatric Genetics; American Journal Of Medical Genetics - Neuropsychiatric Genetics, 1995, v. 60 n. 2, p. 94-102; 102; WOS:A1995QT74500002; 7485258; eid_2-s2.0-0028965001; 94; http://hdl.handle.net/10722/175723Test; 60

الإتاحة: https://doi.org/10.1002/ajmg.1320600203Test
http://hdl.handle.net/10722/175723Test

المؤلفون: Steinlein, O., Mulley, J., Propping, P., Wallace, R., Phillips, H., Sutherland, G., Scheffer, I., Berkovic, S.

مصطلحات موضوعية: Frontal Lobe, Chromosomes, Human, Pair 20, Animals, Chickens, Humans, Rats, Epilepsy, Receptors, Nicotinic, DNA Primers, Chromosome Mapping, Polymerase Chain Reaction, Pedigree, Amino Acid Sequence, Base Sequence, Sequence Homology, Amino Acid, Genes, Dominant, Point Mutation, Molecular Sequence Data, Female, Male, Genetic Linkage

العلاقة: Nature Genetics, 1995; 11(2):201-203; http://hdl.handle.net/2440/7738Test

الإتاحة: https://doi.org/10.1038/ng1095-201Test
http://hdl.handle.net/2440/7738Test