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1
المؤلفون: Lucia Sobrin, Janine Y. Yang
المصدر: JAMA Ophthalmology. 140:260
مصطلحات موضوعية: Macular Degeneration, Ophthalmology, Chromosomes, Human, Pair 1, Chromosomes, Human, Pair 10, Humans, Proteins, High-Temperature Requirement A Serine Peptidase 1, Alleles
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0760a6590dd0bcfd1cb8465e5100130Test
https://doi.org/10.1001/jamaophthalmol.2021.6069Test -
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المؤلفون: Steffen Schmitz-Valckenberg, Monika Fleckenstein, Moussa A. Zouache, Maximilian Pfau, Christian Pappas, Jill L. Hageman, Elvira Agrón, Claire Malley, Tiarnan D. L. Keenan, Emily Y. Chew, Gregory S. Hageman
المصدر: JAMA Ophthalmology. 140:252
مصطلحات موضوعية: Male, Macular Degeneration, Ophthalmology, Chromosomes, Human, Pair 1, Chromosomes, Human, Pair 10, Risk Factors, Complement Factor H, Humans, Proteins, Female, High-Temperature Requirement A Serine Peptidase 1, Polymorphism, Single Nucleotide, Alleles
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::37d784f4b86d973949d4f47d398667daTest
https://doi.org/10.1001/jamaophthalmol.2021.6072Test -
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المؤلفون: David E Pleasure, Phillip F. Chance
المصدر: Archives of Neurology. 50:1180-1184
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, X Chromosome, Unequal crossing over, Genetic Linkage, Biology, Mice, Arts and Humanities (miscellaneous), Charcot-Marie-Tooth Disease, Genetic linkage, Gene duplication, Animals, Humans, Missense mutation, Crossing Over, Genetic, X chromosome, Repetitive Sequences, Nucleic Acid, Genetics, Autosome, Chromosome Mapping, Peripheral Nervous System Diseases, Karyotype, Chromosome Banding, Chromosome 17 (human), Meiosis, Chromosomes, Human, Pair 1, Mutation, Neurology (clinical), Gene Deletion, Myelin Proteins, Chromosomes, Human, Pair 17
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec979e7b1d0172a35cb2630019794114Test
https://doi.org/10.1001/archneur.1993.00540110060006Test -
4
المصدر: Archives of Dermatology. 139
مصطلحات موضوعية: Nevus, Pigmented, Pathology, medicine.medical_specialty, Skin Neoplasms, business.industry, Dermatology, General Medicine, medicine.disease, Chromosomes, Human, Pair 1, medicine, Dysplastic nevus, Humans, Identification (biology), Chromosome Deletion, Chromosomes, Human, Pair 9, business, Dysplastic Nevus Syndrome, Melanoma
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5418da020dc884dd0d3d1bb0c32485c2Test
https://doi.org/10.1001/archderm.139.6.816Test -
5
المؤلفون: Weidong Ji, Jie Liu, Qian Zhao, Zhiwei Hu, Guoquan Zhou, Guoyin Feng, Zhen Zeng, Junyan Li, Yang Wang, Lin He, Tao Li, Ti Wang, Yifeng Shen, Linqing Zheng, Yongyong Shi, You Li, Peng Chen
المصدر: Archives of General Psychiatry. 68:232
مصطلحات موضوعية: Adult, Male, Oncology, Psychosis, medicine.medical_specialty, Candidate gene, Bipolar Disorder, DNA Copy Number Variations, Genotype, Single-nucleotide polymorphism, Context (language use), Polymorphism, Single Nucleotide, Asian People, Arts and Humanities (miscellaneous), Internal medicine, medicine, Humans, Genetic Predisposition to Disease, Bipolar disorder, Risk factor, Psychiatry, Alleles, Genetic Association Studies, Depressive Disorder, Major, Genetic Variation, Middle Aged, medicine.disease, Neoplasm Proteins, Psychiatry and Mental health, Chromosomes, Human, Pair 1, Schizophrenia, Major depressive disorder, Female, Chromosome Deletion, Psychology, Genome-Wide Association Study, Transcription Factors
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dca18914514fa26fd0573849737aba66Test
https://doi.org/10.1001/archgenpsychiatry.2011Test.1 -
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المؤلفون: Duncan McLean, Elizabeth G. Holliday, Dale R. Nyholt, Bryan J. Mowry
المصدر: Archives of General Psychiatry. 66:1058
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Linkage disequilibrium, Genotype, Genetic Linkage, Schizophrenia (object-oriented programming), Taiwan, Context (language use), Genome-wide association study, behavioral disciplines and activities, Genetic Heterogeneity, Arts and Humanities (miscellaneous), Genetic linkage, mental disorders, medicine, Humans, Genetic Predisposition to Disease, Psychiatry, Genetic association, Psychiatric Status Rating Scales, Genetics, Models, Statistical, Genome, Human, Genetic heterogeneity, Chromosome Mapping, Latent class model, Diagnostic and Statistical Manual of Mental Disorders, Psychiatry and Mental health, Phenotype, Chromosomes, Human, Pair 1, Multivariate Analysis, Schizophrenia, Female, Psychology, Genome-Wide Association Study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c8be7c6cbcca925d58c0728e7bd604eTest
https://doi.org/10.1001/archgenpsychiatry.2009.136Test -
7
المؤلفون: Nicholas G. Martin, Scott F. Saccone, Anjali K. Henders, Michele L. Pergadia, Richard D. Todd, Robertino Garcia, Arpana Agrawal, Jen C. Wang, Grant W. Montgomery, Pamela A. F. Madden, Andrew C. Heath, Alison Goate, Dixie J. Statham, Michael T. Lynskey, John P. Rice, Jaakko Kaprio, Ulla Broms, Megan Campbell
المصدر: University of Helsinki
مصطلحات موضوعية: Adult, Genetic Markers, Male, Marijuana Abuse, Cell Adhesion Molecules, Neuronal, Receptors, Cell Surface, Context (language use), Receptors, G-Protein-Coupled, Arts and Humanities (miscellaneous), Genetic linkage, Diseases in Twins, medicine, Humans, Genetic Predisposition to Disease, Cannabis Dependence, Genetic association, Chromosome Aberrations, Genetics, biology, Neuropeptides, Australia, Chromosome Mapping, Tobacco Use Disorder, Middle Aged, Receptors, GABA-A, biology.organism_classification, medicine.disease, Protocadherins, Substance abuse, Psychiatry and Mental health, Phenotype, Chromosome 4, Chromosome 3, Chromosomes, Human, Pair 1, Chromosomes, Human, Pair 6, Female, Cannabis, Chromosomes, Human, Pair 4, Lod Score, Psychology
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84f6c7072ebb2069afe4a7d147cd0541Test
https://doi.org/10.1001/archpsyc.65.6.713Test -
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المؤلفون: Janey L. Wiggs, Douglas Vollrath
المصدر: Archives of Ophthalmology. 119:1674
مصطلحات موضوعية: Adult, genetic structures, DNA Mutational Analysis, Nonsense mutation, Mutation, Missense, Glaucoma, medicine.disease_cause, Bioinformatics, medicine, Humans, Missense mutation, Eye Proteins, Gene, Intraocular Pressure, Glycoproteins, Genetics, Mutation, business.industry, Chromosome, medicine.disease, eye diseases, Pedigree, Cytoskeletal Proteins, Ophthalmology, Chromosomes, Human, Pair 1, Genetic marker, Female, Chromosome Deletion, Haploinsufficiency, business, Glaucoma, Open-Angle, Microsatellite Repeats
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51704d319578cb4edfc4195f17be2e55Test
https://doi.org/10.1001/archopht.119.11.1674Test