المؤلفون: D StClair, Marcella Rietschel, Rosie M. Walker, Markus M. Nöthen, Kevin A. McGhee, Andrea Christoforou, David J. Porteous, Walter J. Muir, Kathryn L. Evans, Thomas W. Mühleisen, Pippa A. Thomson, Sven Cichon, Douglas Blackwood, Omer Jilani, Alan Maclean, Jana Strohmaier, S. W. Morris, Vanessa Nieratschker

المصدر: Walker, R, Christoforou, A, Thomson, P, McGhee, K, Maclean, A, Muhleisen, T W, Strohmaier, J, Nieratschker, V, Nothen, M M, Rietschel, M, Cichon, S, Morris, S W, Jilani, O, Stclair, D, Blackwood, D, Muir, W, Porteous, D J & Evans, K L 2010, ' Association analysis of Neuregulin 1 candidate regions in schizophrenia and bipolar disorder ', Neuroscience Letters, vol. 478, no. 1, pp. 9-13 . https://doi.org/10.1016/j.neulet.2010.04.056

مصطلحات موضوعية: Candidate gene, Bipolar Disorder, 5' Flanking Region, Neuroscience(all), Neuregulin-1, Population, Single-nucleotide polymorphism, Genome-wide association study, Polymorphism, Single Nucleotide, behavioral disciplines and activities, Germany, mental disorders, medicine, Humans, Genetic Predisposition to Disease, 3' Flanking Region, Bipolar disorder, education, Genetic association, Genetics, education.field_of_study, General Neuroscience, Haplotype, medicine.disease, Haplotypes, Scotland, Schizophrenia, Case-Control Studies, Psychology, Genome-Wide Association Study

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a38f0342799e39f258f07d76c6bf441e
https://doi.org/10.1016/j.neulet.2010.04.056

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المؤلفون: John Coates, Alistair Cumming, Jean-Charles Lambert, D StClair, David G. Mann, Corinne Lendon, Judith Harris, Helen Lemmon

المصدر: Neuroscience Letters. 306:193-197

مصطلحات موضوعية: Male, Apolipoprotein E, medicine.medical_specialty, medicine.drug_class, Estrogen receptor, Disease, Biology, Cohort Studies, Degenerative disease, Alzheimer Disease, Polymorphism (computer science), Internal medicine, medicine, Estrogen Receptor beta, Humans, Cognitive decline, Aged, Polymorphism, Genetic, General Neuroscience, Estrogen Receptor alpha, Middle Aged, medicine.disease, Endocrinology, Haplotypes, Receptors, Estrogen, Estrogen, Female, Alzheimer's disease

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3d24205adff9113c3e5ca695729c1dc
https://doi.org/10.1016/s0304-3940(01)01806-7

المؤلفون: Douglas Blackwood, Walter J. Muir, Kathryn L. Evans, Helen S. Torrance, D StClair, Andrea Christoforou, David J. Porteous, Alan W. McLean, S Le Hellard, Stewart W. Morris, Kevin A. McGhee, Benjamin S. Pickard, P. A. Thomson, Susan Anderson

المصدر: Molecular Psychiatry. 16:240-242

مصطلحات موضوعية: medicine.medical_specialty, Psychosis, Bipolar Disorder, endocrine system diseases, Genetic Linkage, Receptors, Cell Surface, Genome-wide association study, Polymorphism, Single Nucleotide, behavioral disciplines and activities, Cellular and Molecular Neuroscience, Genetic linkage, mental disorders, medicine, Humans, Bipolar disorder, Psychiatry, Molecular Biology, Linkage (software), Genetics, Chromosome Mapping, Chromosome, medicine.disease, Psychiatry and Mental health, Phenotype, Schizophrenia, Behavioral medicine, Chromosomes, Human, Pair 4, Psychology, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bac27427036d7d72792e37302b13d3c
https://doi.org/10.1038/mp.2010.25

المؤلفون: Derek J. Nancarrow, G Kalsi, Dermot Walsh, Hugh Gurling, J Brynjolfsson, Hannes Petursson, Jeremy M. Silverman, Kenneth S. Kendler, Robin M. Murray, T. d'Amato, Lynn R. Goldin, Hiroshi Kunugi, Robert B. Freedman, M. Jay, T. Sigmundson, W. Muri, Wolfgang Maier, William Byerley, J. Mallet, L. Yang, A. E. Pulver, C J MacLean, P. C. Sham, L. He, Raymond R. Crowe, R. E. Straub, Margot Albus, Dominique Campion, Michael John Owen, Richard P. Ebstein, Elliot S. Gershon, H. Donis-Keller, Hans W. Moises, Gerald Nestadt, D. H. R. Blackwood, Haig H. Kazazian, D. StClair, Claudine Laurent, Joachim Hallmayer, Claudia Wiese, D. B. Wildenauer, Stylianos E. Antonarakis, Bryan J. Mowry, Michael Gill, Homero Vallada, David E. Housman, H. Kristbjarnarson, R. Lofthouse, C. M. Read, Shinichiro Nanko, Mihael H. Polymeropoulos, P. McGuffin, Nicholas K. Hayward, H-G Hwu, S. Bodeau-Pean, Manfred Ackenheil, B. Lerer, David A. Collier, Douglas F. Levinson, Hilary Coon, Lynn E. DeLisi, J. H. Zhao, David Curtis, S. Maguire

المصدر: Schizophrenia Research. 32:115-121

مصطلحات موضوعية: musculoskeletal diseases, Genetics, Linkage disequilibrium, Pedigree chart, Biology, Psychiatry and Mental health, Genetic linkage, Genotype, Allele, skin and connective tissue diseases, HLA-DRB1, Genotyping, Biological Psychiatry, Genetic association

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::ff34745dccce4cde02a71de82c7cf9e3
https://doi.org/10.1016/s0920-9964(98)00048-6

المؤلفون: D StClair, Douglas Blackwood, Shaun Purcell, Pamela Sklar, Andrew McKechanie, Stuart MacGregor, Naomi R. Wray, Eske M. Derks, Jennifer L. Moran, Allan F. McRae, Alan W Maclean, Peter M. Visscher, Benjamin S. Pickard, Kimberly Chambert, Mandy Johnstone, Muhammad Ayub, Jurgen Del Favero

المساهمون: Amsterdam Neuroscience, Amsterdam Public Health, Adult Psychiatry

المصدر: American journal of medical genetics. Part B, Neuropsychiatric genetics, 162(8), 847-854. Wiley-Liss Inc.
American journal of medical genetics: part B: neuropsychiatric genetics

مصطلحات موضوعية: Male, Psychosis, Pediatrics, medicine.medical_specialty, DNA Copy Number Variations, Cellular and Molecular Neuroscience, Cataracts, Chromosome Segregation, Intellectual Disability, Gene duplication, Intellectual disability, Retinitis pigmentosa, Chromosome Duplication, mental disorders, medicine, Humans, Copy-number variation, Genetics (clinical), Genetics, Gene Rearrangement, Chromosomes, Human, Pair 15, business.industry, medicine.disease, Health Surveys, Pedigree, Psychiatry and Mental health, Scotland, Schizophrenia, Learning disability, Female, Human medicine, medicine.symptom, business, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0046bdbe30986101272f7b0e973002e1
https://pure.amc.nl/en/publications/a-genome-wide-survey-supports-the-involvement-of-large-copy-number-variants-in-schizophrenia-with-and-without-intellectual-disability(091b37a9-9b96-4e81-8a99-671da1a44c34).html

المؤلفون: D StClair

المصدر: Oncology reports. 3(3)

مصطلحات موضوعية: Cancer Research, Antioxidant, Oncogene, Tumor suppressor gene, animal diseases, medicine.medical_treatment, fungi, Cell, General Medicine, Mitochondrion, Biology, medicine.disease_cause, enzymes and coenzymes (carbohydrates), medicine.anatomical_structure, Oncology, Apoptosis, medicine, Cancer research, Carcinogenesis, Oxidative stress

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2994f3eafd1f7d33bec923ac8c55634b
https://pubmed.ncbi.nlm.nih.gov/21594386

المؤلفون: Muneyasu Urano, D StClair, Jun Ichi Asaumi, Y Hiraki, T Akagi, Masahiro Kuroda, K Himei, I Sakuma, I Joja, T. Yoshino

المصدر: Oncology reports. 4(5)

مصطلحات موضوعية: Cancer Research, biology, medicine.diagnostic_test, animal diseases, fungi, CD44, Cell, Transferrin receptor, General Medicine, Transfection, Cell cycle, Molecular biology, Flow cytometry, enzymes and coenzymes (carbohydrates), medicine.anatomical_structure, Oncology, Apoptosis, Cell culture, Cancer research, biology.protein, medicine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30a24520473c4ac91601972fed5aefd4
https://pubmed.ncbi.nlm.nih.gov/21590170

المؤلفون: Derek W. Morris, D StClair, Aiden Corvin, Dobril Ivanov, Shaun Purcell, Michael John Owen, Draga Toncheva, Patrick F. Sullivan, Michael Conlon O'Donovan, Pamela Sklar, Mike L. Smith, Michael Gill, Carlos N. Pato, Naomi R. Wray, Peter Holmans, Christina M. Hultman, Colm O'Dushlaine, Douglas Blackwood, Michele T. Pato, George Kirov, Valentina Moskvina

المصدر: Moskvina, V, Smith, M, Ivanov, D, Blackwood, D, StClair, D, Hultman, C, Toncheva, D, Gill, M, Corvin, A, O'Dushlaine, C, Morris, D W, Wray, N R, Sullivan, P, Pato, C, Pato, M T, Sklar, P, Purcell, S, Holmans, P, O'Donovan, M C, Owen, M J, Kirov, G 2010, ' Genetic Differences between Five European Populations ', Human heredity, vol. 70, no. 2, pp. 141-149 . https://doi.org/10.1159/000313854

مصطلحات موضوعية: Genetics, education.field_of_study, Original Paper, Population, Single-nucleotide polymorphism, Human leukocyte antigen, Biology, Polymorphism, Single Nucleotide, White People, Genetics, Population, SNP, Humans, Genetics(clinical), education, Gene, Allele frequency, TLR10, Genetics (clinical), Genetic association, Lactase

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51eeb06e6735a771af6d82026f6d255a
https://europepmc.org/articles/PMC7077089/

المؤلفون: Rp Brettle, Egan, Gm M. Goodwin, D Stclair, A. Chiswick

المصدر: Aids. 4:1243-1250

مصطلحات موضوعية: Drug, medicine.medical_specialty, Auditory event, business.industry, media_common.quotation_subject, Immunology, Disease, Electrophysiology, Infectious Diseases, Psychiatric history, Internal medicine, Cohort, Immunology and Allergy, Medicine, Latency (engineering), Stage (cooking), business, media_common

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::7dd042d97e466ecdb96a0e92f0e8a53e
https://doi.org/10.1097/00002030-199012000-00010