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1دورية أكاديمية
المؤلفون: Vysotskiy, Mikhail, Zhong, Xue, Miller-Fleming, Tyne W, Zhou, Dan, Cox, Nancy J, Weiss, Lauren A
المصدر: Genome Medicine. 13(1)
مصطلحات موضوعية: Biological Sciences, Genetics, Human Genome, Brain Disorders, Intellectual and Developmental Disabilities (IDD), Mental Health, Genetic Testing, Schizophrenia, Autism, Biotechnology, Clinical Research, 2.1 Biological and endogenous factors, Aetiology, Mental health, Good Health and Well Being, Autism Spectrum Disorder, Autistic Disorder, Chromosome Deletion, Chromosome Disorders, Chromosomes, Human, Pair 16, DNA Copy Number Variations, DiGeorge Syndrome, Genotype, Humans, Intellectual Disability, Phenotype, Psychotic Disorders, Scavenger Receptors, Class F, Transcriptome, Tumor Suppressor Proteins, Copy number variants, Transcriptome imputation, Electronic health records, Psychiatric traits, Phenome-wide association studies, Autism Working Group of the Psychiatric Genomics Consortium^, Bipolar Disorder Working Group of the Psychiatric Genomics Consortium^, Schizophrenia Working Group of the Psychiatric Genomics Consortium^, Clinical Sciences
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/2ft6z860Test
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2دورية أكاديمية
المؤلفون: Hu, Yao, Stilp, Adrienne M, McHugh, Caitlin P, Rao, Shuquan, Jain, Deepti, Zheng, Xiuwen, Lane, John, de Bellefon, Sébastian Méric, Raffield, Laura M, Chen, Ming-Huei, Yanek, Lisa R, Wheeler, Marsha, Yao, Yao, Ren, Chunyan, Broome, Jai, Moon, Jee-Young, de Vries, Paul S, Hobbs, Brian D, Sun, Quan, Surendran, Praveen, Brody, Jennifer A, Blackwell, Thomas W, Choquet, Hélène, Ryan, Kathleen, Duggirala, Ravindranath, Heard-Costa, Nancy, Wang, Zhe, Chami, Nathalie, Preuss, Michael H, Min, Nancy, Ekunwe, Lynette, Lange, Leslie A, Cushman, Mary, Faraday, Nauder, Curran, Joanne E, Almasy, Laura, Kundu, Kousik, Smith, Albert V, Gabriel, Stacey, Rotter, Jerome I, Fornage, Myriam, Lloyd-Jones, Donald M, Vasan, Ramachandran S, Smith, Nicholas L, North, Kari E, Boerwinkle, Eric, Becker, Lewis C, Lewis, Joshua P, Abecasis, Goncalo R, Hou, Lifang, O’Connell, Jeffrey R, Morrison, Alanna C, Beaty, Terri H, Kaplan, Robert, Correa, Adolfo, Blangero, John, Jorgenson, Eric, Psaty, Bruce M, Kooperberg, Charles, Walton, Russell T, Kleinstiver, Benjamin P, Tang, Hua, Loos, Ruth JF, Soranzo, Nicole, Butterworth, Adam S, Nickerson, Debbie, Rich, Stephen S, Mitchell, Braxton D, Johnson, Andrew D, Auer, Paul L, Li, Yun, Mathias, Rasika A, Lettre, Guillaume, Pankratz, Nathan, Laurie, Cathy C, Laurie, Cecelia A, Bauer, Daniel E, Conomos, Matthew P, Reiner, Alexander P, Consortium, NHLBI Trans-Omics for Precision Medicine
المصدر: American Journal of Human Genetics. 108(5)
مصطلحات موضوعية: Epidemiology, Biological Sciences, Health Sciences, Genetics, Biotechnology, Clinical Research, Hematology, Human Genome, Aetiology, 2.1 Biological and endogenous factors, Good Health and Well Being, Adult, Aged, Chromosomes, Human, Pair 16, Datasets as Topic, Erythrocytes, Female, Gene Editing, Genetic Variation, Genome-Wide Association Study, HEK293 Cells, Humans, Male, Middle Aged, National Heart, Lung, and Blood Institute (U.S.), Phenotype, Quality Control, Reproducibility of Results, United States, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, base editing, red blood cell traits, whole-genome sequencing, Medical and Health Sciences, Genetics & Heredity, Biological sciences, Biomedical and clinical sciences, Health sciences
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/24j6v92rTest
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3دورية أكاديمية
المؤلفون: Mostovoy, Yulia, Yilmaz, Feyza, Chow, Stephen K, Chu, Catherine, Lin, Chin, Geiger, Elizabeth A, Meeks, Naomi JL, Chatfield, Kathryn C, Coughlin, Curtis R, Surti, Urvashi, Kwok, Pui-Yan, Shaikh, Tamim H
المصدر: Genetics. 217(2)
مصطلحات موضوعية: Biological Sciences, Genetics, Human Genome, 2.1 Biological and endogenous factors, Aetiology, Chromosome Breakpoints, Chromosome Deletion, Chromosome Disorders, Chromosomes, Human, Pair 15, Chromosomes, Human, Pair 16, Craniofacial Abnormalities, Developmental Disabilities, Genomic Structural Variation, Heart Defects, Congenital, Humans, Intellectual Disability, Mental Disorders, Segmental Duplications, Genomic, Seizures, Williams Syndrome, segmental duplications, genome mapping, structural variation, genomic disorders, Developmental Biology, Biochemistry and cell biology
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/15562671Test
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4دورية أكاديمية
المؤلفون: Zhang, Lianjun, Nguyen, Le Xuan Truong, Chen, Ying-Chieh, Wu, Dijiong, Cook, Guerry J, Hoang, Dinh Hoa, Brewer, Casey J, He, Xin, Dong, Haojie, Li, Shu, Li, Man, Zhao, Dandan, Qi, Jing, Hua, Wei-Kai, Cai, Qi, Carnahan, Emily, Chen, Wei, Wu, Xiwei, Swiderski, Piotr, Rockne, Russell C, Kortylewski, Marcin, Li, Ling, Zhang, Bin, Marcucci, Guido, Kuo, Ya-Huei
المصدر: Nature Communications. 12(1)
مصطلحات موضوعية: Medicinal and Biomolecular Chemistry, Chemical Sciences, Pediatric, Pediatric Cancer, Rare Diseases, Cancer, Biotechnology, Childhood Leukemia, Stem Cell Research, Hematology, Pediatric Research Initiative, Genetics, 2.1 Biological and endogenous factors, Aetiology, Animals, Antineoplastic Agents, Calcium-Binding Proteins, Cell Cycle Proteins, Cell Survival, Chromosome Inversion, Chromosomes, Human, Pair 16, EGF Family of Proteins, GATA2 Transcription Factor, Guanine Nucleotide Exchange Factors, Histone Deacetylases, Humans, Karyopherins, Leukemia, Myeloid, Acute, Mice, MicroRNAs, Molecular Targeted Therapy, Myeloid Progenitor Cells, Neoplastic Stem Cells, Nuclear Proteins, Oncogene Proteins, Fusion, Repressor Proteins, Xenograft Model Antitumor Assays, ran GTP-Binding Protein
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/4xm3c5w5Test
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5دورية أكاديمية
المؤلفون: Kim, So Hyun, Green‐Snyder, LeeAnne, Lord, Catherine, Bishop, Somer, Steinman, Kyle J, Bernier, Raphael, Hanson, Ellen, Goin‐Kochel, Robin P, Chung, Wendy K
المصدر: American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 183(6)
مصطلحات موضوعية: Biological Sciences, Biomedical and Clinical Sciences, Genetics, Clinical Sciences, Neurosciences, Clinical Research, Behavioral and Social Science, Autism, Intellectual and Developmental Disabilities (IDD), Mental Health, Brain Disorders, Pediatric, 2.1 Biological and endogenous factors, Aetiology, Mental health, Adolescent, Adult, Autism Spectrum Disorder, Autistic Disorder, Child, Child, Preschool, Chromosome Deletion, Chromosome Disorders, Chromosome Duplication, Chromosomes, Human, Pair 16, Cognitive Dysfunction, DNA Copy Number Variations, Family, Female, Heterozygote, Humans, Intellectual Disability, Language, Male, Middle Aged, Siblings, Speech, Verbal Behavior, Young Adult, 16p11, deletion, duplication, autism, genetics, language profiles, 16p11.2 deletion, 16p11.2 duplication, Clinical sciences
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/6h67t169Test
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6دورية أكاديمية
المؤلفون: Oz-Levi, Danit, Olender, Tsviya, Bar-Joseph, Ifat, Zhu, Yiwen, Marek-Yagel, Dina, Barozzi, Iros, Osterwalder, Marco, Alkelai, Anna, Ruzzo, Elizabeth K, Han, Yujun, Vos, Erica SM, Reznik-Wolf, Haike, Hartman, Corina, Shamir, Raanan, Weiss, Batia, Shapiro, Rivka, Pode-Shakked, Ben, Tatarskyy, Pavlo, Milgrom, Roni, Schvimer, Michael, Barshack, Iris, Imai, Denise M, Coleman-Derr, Devin, Dickel, Diane E, Nord, Alex S, Afzal, Veena, van Bueren, Kelly Lammerts, Barnes, Ralston M, Black, Brian L, Mayhew, Christopher N, Kuhar, Matthew F, Pitstick, Amy, Tekman, Mehmet, Stanescu, Horia C, Wells, James M, Kleta, Robert, de Laat, Wouter, Goldstein, David B, Pras, Elon, Visel, Axel, Lancet, Doron, Anikster, Yair, Pennacchio, Len A
المصدر: Nature. 571(7763)
مصطلحات موضوعية: Intestines, Chromosomes, Human, Pair 16, Animals, Mice, Transgenic, Mice, Knockout, Humans, Mice, Disease Models, Animal, Diarrhea, Pedigree, Gene Expression Regulation, Developmental, Sequence Deletion, Phenotype, Genes, Genes, Reporter, Transgenes, Female, Male, Enhancer Elements, Genetic, Transcriptional Activation, Genetic Loci, Transcriptome, Chromosomes, Human, Pair 16, Transgenic, Knockout, Disease Models, Animal, Gene Expression Regulation, Developmental, Reporter, Enhancer Elements, Genetic, Genetics, Human Genome, Biotechnology, Digestive Diseases, 2.1 Biological and endogenous factors, Oral and Gastrointestinal, General Science & Technology
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/6dn666prTest
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7دورية أكاديمية
المؤلفون: Xian, Rena R, Xie, Yi, Haley, Lisa M, Yonescu, Raluca, Pallavajjala, Aparna, Pittaluga, Stefania, Jaffe, Elaine S, Duffield, Amy S, McCall, Chad M, Gheith, Shereen MF, Gocke, Christopher D
المصدر: Blood Cancer Journal. 10(6)
مصطلحات موضوعية: Biomedical and Clinical Sciences, Cardiovascular Medicine and Haematology, Oncology and Carcinogenesis, Human Genome, Rare Diseases, Genetics, Hematology, Clinical Research, Cancer, Biotechnology, Lymphoma, 2.1 Biological and endogenous factors, Aetiology, Adult, Aged, CREB-Binding Protein, Chromosome Deletion, Chromosomes, Human, Pair 1, Chromosomes, Human, Pair 16, Female, Humans, Lymphoma, Follicular, Male, Middle Aged, Mutation, Polymorphism, Single Nucleotide, STAT6 Transcription Factor, Translocation, Genetic, Cardiorespiratory Medicine and Haematology, Cardiovascular medicine and haematology, Oncology and carcinogenesis
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/39n9r2kjTest
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8دورية أكاديمية
المؤلفون: Hinkley, Leighton BN, Dale, Corby L, Luks, Tracy L, Findlay, Anne M, Bukshpun, Polina, Pojman, Nick, Thieu, Tony, Chung, Wendy K, Berman, Jeffrey, Roberts, Timothy PL, Mukherjee, Pratik, Sherr, Elliott H, Nagarajan, Srikantan S
المصدر: Journal of Neuroscience. 39(37)
مصطلحات موضوعية: Biomedical and Clinical Sciences, Neurosciences, Clinical Research, Basic Behavioral and Social Science, Genetics, Brain Disorders, Behavioral and Social Science, Mental Health, Autism, Genetic Testing, Intellectual and Developmental Disabilities (IDD), 2.1 Biological and endogenous factors, Aetiology, Neurological, Mental health, Adolescent, Adult, Anticipation, Psychological, Autistic Disorder, Child, Chromosome Deletion, Chromosome Disorders, Chromosomes, Human, Pair 16, Female, Gene Deletion, Heterozygote, Humans, Intellectual Disability, Magnetoencephalography, Male, Middle Aged, Sensorimotor Cortex, 16p11.2, autism, beta rhythm, magnetoencephalography, manual, speech, Medical and Health Sciences, Psychology and Cognitive Sciences, Neurology & Neurosurgery
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/6w91v9h9Test
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9دورية أكاديمية
المؤلفون: Qiu, Yuqi, Arbogast, Thomas, Lorenzo, Sandra Martin, Li, Hongying, Tang, Shih C, Richardson, Ellen, Hong, Oanh, Cho, Shawn, Shanta, Omar, Pang, Timothy, Corsello, Christina, Deutsch, Curtis K, Chevalier, Claire, Davis, Erica E, Iakoucheva, Lilia M, Herault, Yann, Katsanis, Nicholas, Messer, Karen, Sebat, Jonathan
المصدر: Cell Reports. 28(13)
مصطلحات موضوعية: Clinical Research, Mental Health, Dental/Oral and Craniofacial Disease, Genetics, Pediatric, Human Genome, Congenital Structural Anomalies, Brain Disorders, Biotechnology, Aetiology, 2.1 Biological and endogenous factors, Autistic Disorder, Chromosome Deletion, Chromosome Disorders, Chromosomes, Human, Pair 16, Craniofacial Abnormalities, DNA Copy Number Variations, Female, Humans, Intellectual Disability, Male, Biochemistry and Cell Biology, Medical Physiology
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/9sd773z9Test
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10دورية أكاديمية
المؤلفون: He, Karen Y, Li, Xiaoyin, Kelly, Tanika N, Liang, Jingjing, Cade, Brian E, Assimes, Themistocles L, Becker, Lewis C, Beitelshees, Amber L, Bress, Adam P, Chang, Yen-Pei Christy, Chen, Yii-Der Ida, de Vries, Paul S, Fox, Ervin R, Franceschini, Nora, Furniss, Anna, Gao, Yan, Guo, Xiuqing, Haessler, Jeffrey, Hwang, Shih-Jen, Irvin, Marguerite Ryan, Kalyani, Rita R, Liu, Ching-Ti, Liu, Chunyu, Martin, Lisa Warsinger, Montasser, May E, Muntner, Paul M, Mwasongwe, Stanford, Palmas, Walter, Reiner, Alex P, Shimbo, Daichi, Smith, Jennifer A, Snively, Beverly M, Yanek, Lisa R, Boerwinkle, Eric, Correa, Adolfo, Cupples, L Adrienne, He, Jiang, Kardia, Sharon LR, Kooperberg, Charles, Mathias, Rasika A, Mitchell, Braxton D, Psaty, Bruce M, Vasan, Ramachandran S, Rao, DC, Rich, Stephen S, Rotter, Jerome I, Wilson, James G, Chakravarti, Aravinda, Morrison, Alanna C, Levy, Daniel, Arnett, Donna K, Redline, Susan, Zhu, Xiaofeng
المصدر: Human Genetics. 138(2)
مصطلحات موضوعية: Biological Sciences, Genetics, Biotechnology, Heart Disease, Human Genome, Cardiovascular, Aetiology, 2.1 Biological and endogenous factors, Good Health and Well Being, Alternative Splicing, Blood Pressure, Chromosomes, Human, Pair 16, Exome, Female, Follow-Up Studies, Genetic Linkage, Genetic Variation, Genome, Human, Genome-Wide Association Study, High-Throughput Nucleotide Sequencing, Humans, Male, RNA Splicing Factors, Recombinases, NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, TOPMed Blood Pressure Working Group, Complementary and Alternative Medicine, Paediatrics and Reproductive Medicine, Genetics & Heredity, Reproductive medicine
وصف الملف: application/pdf
الوصول الحر: https://escholarship.org/uc/item/2g02g3gsTest