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1. Full Text META-ANALYSIS OF MULTI-ANCESTRY CASE-CONTROL SAMPLES IN THE BIPOLAR SEQUENCING CONSORTIUM
by Stahl, Eli and Case-Control group Bipolar Sequencing Consortium
European neuropsychopharmacology, ISSN 0924-977X, 2019, Volume 29, pp. S1058 - S1058
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2. Full Text Progress and promise of genome-wide association studies for human complex trait genetics
by Stranger, Barbara E and Stahl, Eli A and Raj, Towfique
Genetics (Austin), ISSN 0016-6731, 02/2011, Volume 187, Issue 2, pp. 367 - 383
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Multifactorial Inheritance - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Animals | Humans | Chromosome Mapping | Models, Genetic | Polymorphism, Single Nucleotide | Quantitative Trait Loci | Genome-wide association studies | Heritability | Research | Human genetics | Multifactorial traits | Studies | Quantitative genetics | Genomics | Rheumatoid arthritis | Principal components analysis | Standard deviation | Statistical methods | Index Medicus | Review
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3. Full Text Partitioning heritability by functional annotation using genome-wide association summary statistics
by Finucane, Hilary K and Bulik-Sullivan, Brendan and Gusev, Alexander and Trynka, Gosia and Reshef, Yakir and Loh, Po-Ru and Anttila, Verneri and Xu, Han and Zang, Chongzhi and Farh, Kyle and Ripke, Stephan and Day, Felix R and Purcell, Shaun and Stahl, Eli and Lindstrom, Sara and Perry, John R.B and Okada, Yukinori and Raychaudhuri, Soumya and Daly, Mark J and Patterson, Nick and Neale, Benjamin M and Price, Alkes L and RACI Consortium and Psychiat Genomics Consortium and ReproGen Consortium and The RACI Consortium and Schizophrenia Working Group of the Psychiatric Genomics Consortium
Nature genetics, ISSN 1061-4036, 11/2015, Volume 47, Issue 11, pp. 1228 - 1235
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genome-wide association studies | Genetic research | Heritability | Genetic aspects | Research | Population genetics | Methods | Studies | Economic models | Statistics | Index Medicus
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4. Full Text A Role for Noncoding Variation in Schizophrenia
by Roussos, Panos and Mitchell, Amanda C and Voloudakis, Georgios and Fullard, John F and Pothula, Venu M and Tsang, Jonathan and Stahl, Eli A and Georgakopoulos, Anastasios and Ruderfer, Douglas M and Charney, Alexander and Okada, Yukinori and Siminovitch, Katherine A and Worthington, Jane and Padyukov, Leonid and Klareskog, Lars and Gregersen, Peter K and Plenge, Robert M and Raychaudhuri, Soumya and Fromer, Menachem and Purcell, Shaun M and Brennand, Kristen J and Robakis, Nikolaos K and Schadt, Eric E and Akbarian, Schahram and Sklar, Pamela
Cell reports (Cambridge), ISSN 2211-1247, 11/2014, Volume 9, Issue 4, pp. 1417 - 1429
Life Sciences & Biomedicine | Science & Technology | Cell Biology | Promoter Regions, Genetic | Genetic Predisposition to Disease | Genome-Wide Association Study | Protein Binding - genetics | Humans | Molecular Sequence Annotation | Risk Factors | Gene Expression Regulation | Databases, Genetic | Genetic Loci | DNA, Intergenic - genetics | Organ Specificity - genetics | Arthritis, Rheumatoid - genetics | Calcium Channels, L-Type - genetics | Schizophrenia - genetics | Polymorphism, Single Nucleotide - genetics | Enhancer Elements, Genetic - genetics | Index Medicus | Medicin och hälsovetenskap
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5. Full Text Genetic identification of a common collagen disease in puerto ricans via identity-by-descent mapping in a health system
by Belbin, Gillian Morven and Odgis, Jacqueline and Sorokin, Elena P and Yee, Muh-Ching and Kohli, Sumita and Glicksberg, Benjamin S and Gignoux, Christopher R and Wojcik, Genevieve L and Van Vleck, Tielman and Jeff, Janina M and Linderman, Michael and Schurmann, Claudia and Ruderfer, Douglas and Cai, Xiaoqiang and Merkelson, Amanda and Justice, Anne E and Young, Kristin L and Graff, Misa and North, Kari E and Peters, Ulrike and James, Regina and Hindorff, Lucia and Kornreich, Ruth and Edelmann, Lisa and Gottesman, Omri and Stahl, Eli E. A and Cho, Judy H and Loos, Ruth J. F and Bottinger, Erwin P and Nadkarni, Girish N and Abul-Husn, Noura S and Kenny, Eimear E
eLife, ISSN 2050-084X, 09/2017, Volume 6
Biology | Life Sciences & Biomedicine - Other Topics | Life Sciences & Biomedicine | Science & Technology | Multigene Family | Fibrillar Collagens - genetics | Humans | Middle Aged | Hispanic Americans | Genotype | Male | Collagen Diseases - genetics | Musculoskeletal Diseases - genetics | Whole Genome Sequencing | Young Adult | Homozygote | Molecular Epidemiology | Musculoskeletal Diseases - epidemiology | New York City - ethnology | Pedigree | Adolescent | Adult | Female | Heterozygote | New York City - epidemiology | Aged | Collagen Diseases - epidemiology | Child | Haplotypes | Medical research | Genetic disorders | Disease | Statistical genetics | Ecosystems | Genomics | Heterozygotes | Medical records | Genomes | Patients | Epidemiology | Medicine | Homozygotes | Collagen | Genetics | Software | Gene mapping | Public health | Index Medicus
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6. Full Text Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia
by Genovese, Giulio and Fromer, Menachem and Stahl, Eli A and Ruderfer, Douglas M and Chambert, Kimberly and Landén, Mikael and Moran, Jennifer L and Purcell, Shaun M and Sklar, Pamela and Sullivan, Patrick F and Hultman, Christina M and McCarroll, Steven A and Sahlgrenska akademin and Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi and Göteborgs universitet and Gothenburg University and Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry and Sahlgrenska Academy
Nature neuroscience, ISSN 1097-6256, 10/2016, Volume 19, Issue 11, pp. 1433 - 1441
Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Exome - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Sweden | Schizophrenia - genetics | Humans | Female | Male | Risk | Mutation - genetics | Nerve Tissue Proteins - genetics | Schizophrenia | Physiological aspects | Development and progression | Genetic aspects | Research | Genetic variation | Index Medicus | translocation | genes | association | heritability | de-novo | bipolar disorder | brain-development | mutations | autism spectrum disorders | Neurovetenskaper | of-function variants | Medicin och hälsovetenskap
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7. Full Text Integrating Autoimmune Risk Loci with Gene-Expression Data Identifies Specific Pathogenic Immune Cell Subsets
by Hu, Xinli and Kim, Hyun and Stahl, Eli and Plenge, Robert and Daly, Mark and Raychaudhuri, Soumya
American journal of human genetics, ISSN 0002-9297, 2011, Volume 89, Issue 4, pp. 496 - 506
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | General aspects. Genetic counseling | Medical genetics | Biological and medical sciences | Molecular and cellular biology | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Genetic Predisposition to Disease | Genome-Wide Association Study | CD4-Positive T-Lymphocytes - cytology | Humans | Gene Expression Regulation | Risk | Gene Expression Profiling | Models, Statistical | Autoimmune Diseases - genetics | Arthritis, Rheumatoid - genetics | Animals | Immune System | Alleles | Mice | Polymorphism, Single Nucleotide | Bacteria, Pathogenic | Causes of | Physiological aspects | Genetic aspects | Cellular immunity | Research | Autoimmune diseases | Gene expression | T cells | Genomes | T cell receptors | Gene loci | Index Medicus
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