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1دورية أكاديمية
المؤلفون: Xianyong Yin, Lap Sum Chan, Debraj Bose, Anne U. Jackson, Peter VandeHaar, Adam E. Locke, Christian Fuchsberger, Heather M. Stringham, Ryan Welch, Ketian Yu, Lilian Fernandes Silva, Susan K. Service, Daiwei Zhang, Emily C. Hector, Erica Young, Liron Ganel, Indraniel Das, Haley Abel, Michael R. Erdos, Lori L. Bonnycastle, Johanna Kuusisto, Nathan O. Stitziel, Ira M. Hall, Gregory R. Wagner, FinnGen, Jian Kang, Jean Morrison, Charles F. Burant, Francis S. Collins, Samuli Ripatti, Aarno Palotie, Nelson B. Freimer, Karen L. Mohlke, Laura J. Scott, Xiaoquan Wen, Eric B. Fauman, Markku Laakso, Michael Boehnke
المصدر: Nature Communications, Vol 13, Iss 1, Pp 1-14 (2022)
مصطلحات موضوعية: Science
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2041-1723
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2دورية أكاديمية
المؤلفون: Liron Ganel, Lei Chen, Ryan Christ, Jagadish Vangipurapu, Erica Young, Indraniel Das, Krishna Kanchi, David Larson, Allison Regier, Haley Abel, Chul Joo Kang, Alexandra Scott, Aki Havulinna, Charleston W. K. Chiang, Susan Service, Nelson Freimer, Aarno Palotie, Samuli Ripatti, Johanna Kuusisto, Michael Boehnke, Markku Laakso, Adam Locke, Nathan O. Stitziel, Ira M. Hall
المصدر: Human Genomics, Vol 15, Iss 1, Pp 1-17 (2021)
مصطلحات موضوعية: Metabolic syndrome, Mitochondrial content, Human genetics, Human genome sequencing, Genome-wide association studies, Mendelian randomization, Medicine, Genetics, QH426-470
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1479-7364
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المؤلفون: Peter VandeHaar, Eric B. Fauman, Samuli Ripatti, Nelson B. Freimer, Michael R. Erdos, Debraj Bose, Heather M. Stringham, Xianyong Yin, Nathan O. Stitziel, Ketian Yu, Johanna Kuusisto, Xiaoquan Wen, Anne U. Jackson, Jean Morrison, Aarno Palotie, FinnGen, Lori L. Bonnycastle, Markku Laakso, Christian Fuchsberger, Liron Ganel, Laura J. Scott, Lilian Fernandes Silva, Ira M. Hall, Daiwei Zhang, Erica Young, Gregory R. Wagner, Indraniel Das, Michael Boehnke, Adam E. Locke, Francis S. Collins, Lap Sum Chan, Haley J. Abel, Charles F. Burant, Karen L. Mohlke, Jian Kang, Emily C. Hector
مصطلحات موضوعية: Genetics, Minor allele frequency, Genome-wide association study, Biology
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::2bb90e151daa4b96aa4cd4b48897c8b3
https://doi.org/10.1101/2021.10.19.21265094 -
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المؤلفون: Xianyong, Yin, Lap Sum, Chan, Debraj, Bose, Anne U, Jackson, Peter, VandeHaar, Adam E, Locke, Christian, Fuchsberger, Heather M, Stringham, Ryan, Welch, Ketian, Yu, Lilian, Fernandes Silva, Susan K, Service, Daiwei, Zhang, Emily C, Hector, Erica, Young, Liron, Ganel, Indraniel, Das, Haley, Abel, Michael R, Erdos, Lori L, Bonnycastle, Johanna, Kuusisto, Nathan O, Stitziel, Ira M, Hall, Gregory R, Wagner, Jian, Kang, Jean, Morrison, Charles F, Burant, Francis S, Collins, Samuli, Ripatti, Aarno, Palotie, Nelson B, Freimer, Karen L, Mohlke, Laura J, Scott, Xiaoquan, Wen, Eric B, Fauman, Markku, Laakso
المصدر: Nature communications. 13(1)
مصطلحات موضوعية: Male, Phenotype, Gene Frequency, Humans, Genetic Predisposition to Disease, Polymorphism, Single Nucleotide, Alleles, Finland, Genome-Wide Association Study
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المؤلفون: Charleston W. K. Chiang, Ira M. Hall, Nelson B. Freimer, Aarno Palotie, Michael Boehnke, David E. Larson, Alexandra J. Scott, Krishna L. Kanchi, Allison A. Regier, Lei Chen, Erica Young, Johanna Kuusisto, Samuli Ripatti, Chul Joo Kang, Nathan O. Stitziel, Ryan Christ, Haley J. Abel, Indraniel Das, Adam E. Locke, Markku Laakso, Jagadish Vangipurapu, Aki S. Havulinna, Liron Ganel
المساهمون: Medicum, Institute for Molecular Medicine Finland, Complex Disease Genetics, Helsinki Institute of Life Science HiLIFE, University of Helsinki, Centre of Excellence in Complex Disease Genetics, Aarno Palotie / Principal Investigator, Genomics of Neurological and Neuropsychiatric Disorders, Department of Public Health, Samuli Olli Ripatti / Principal Investigator, Biostatistics Helsinki, Department of Biochemistry and Developmental Biology
المصدر: Human Genomics
Human Genomics, Vol 15, Iss 1, Pp 1-17 (2021)
Human genomics, vol 15, iss 1مصطلحات موضوعية: Male, Genome-wide association study, QH426-470, Genome, Genome-wide association studies, 0302 clinical medicine, Human genetics, GENETIC-VARIANTS, Drug Discovery, Genotype, 2.1 Biological and endogenous factors, Aetiology, Exome sequencing, Genetics & Heredity, Genetics, 0303 health sciences, INSULIN SENSITIVITY, HERITABILITY, FETAL-HEMOGLOBIN, 1184 Genetics, developmental biology, physiology, Single Nucleotide, Middle Aged, Metabolic syndrome, INTERGENIC VARIANTS, Mitochondrial, Phenotype, HBS1L-MYB, OBESITY, Medicine, Molecular Medicine, Female, Primary Research, Sequence Analysis, Adult, Mitochondrial DNA, DNA Copy Number Variations, Locus (genetics), PHENOTYPES, Biology, DNA, Mitochondrial, Polymorphism, Single Nucleotide, DNA sequencing, 03 medical and health sciences, Proto-Oncogene Proteins c-myb, Human genome sequencing, GTP-Binding Proteins, Exome Sequencing, Mendelian randomization, Humans, Cell Lineage, Genetic Predisposition to Disease, Polymorphism, Mitochondrial content, Molecular Biology, Gene, Metabolic and endocrine, 030304 developmental biology, Aged, FATTY LIVER-DISEASE, Human Genome, Membrane Proteins, DNA, Sequence Analysis, DNA, Mendelian Randomization Analysis, FINNISH FAMILIES, Genome, Mitochondrial, 3111 Biomedicine, Apoptosis Regulatory Proteins, 030217 neurology & neurosurgery, Genome-Wide Association Study
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3571fd60bd62350794f27d98e14101eb
http://hdl.handle.net/10138/333048 -
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المؤلفون: Nathan O. Stitziel, Alexandra J. Scott, Allison A. Regier, Chul Joo Kang, Aki S. Havulinna, Lei Chen, Colby Chiang, Charleston W. K. Chiang, Liron Ganel, Aarno Palotie, Shuangjia Lu, Nelson B. Freimer, Erica P. Young, Ryan Christ, Johanna Kuusisto, Ira M. Hall, Xinxin Wang, Adam E. Locke, Indraniel Das, David E. Larson, Krishna L. Kanchi, Samuli Ripatti, Haley J. Abel, Michael Boehnke, Markku Laakso
المصدر: American journal of human genetics, vol 108, iss 4
Am J Hum Genetمصطلحات موضوعية: Male, Genome-wide association study, Medical and Health Sciences, 0302 clinical medicine, Genotype, Pyruvic Acid, 2.1 Biological and endogenous factors, Copy-number variation, Aetiology, Promoter Regions, Genetic, Genetics (clinical), Exome sequencing, Finland, Genetics, Genetics & Heredity, 0303 health sciences, Genome, High-Throughput Nucleotide Sequencing, Biological Sciences, Finnish population, Phenotype, Cholesterol, Cardiovascular Diseases, Female, cardiometabolic traits, Human, DNA Copy Number Variations, Serum Albumin, Human, Biology, Quantitative trait locus, Article, Structural variation, Mitochondrial Proteins, Promoter Regions, 03 medical and health sciences, Genetic, Humans, Alleles, Serum Albumin, 030304 developmental biology, Genetic association, genome-wide association study, Genome, Human, Human Genome, structural variation, Pyruvate Dehydrogenase (Lipoamide)-Phosphatase, Genomic Structural Variation, 030217 neurology & neurosurgery
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c832a8ee03956867402e4f3cdc4da0f6
https://escholarship.org/uc/item/9wd603z3 -
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المؤلفون: David E. Larson, Allison A. Regier, Aarno Palotie, Shuangjia Lu, Nelson B. Freimer, Colby Chiang, Aki S. Havulinna, Markku Laakso, Xinxin Wang, Lei Chen, Erica P. Young, Adam E. Locke, Ryan Christ, Samuli Ripatti, Charleston W. K. Chiang, Nathan O. Stitziel, Liron Ganel, Johanna Kuusisto, Indraniel Das, Alexandra J. Scott, Ira M. Hall, Michael Boehnke, Chul Joo Kang, Krishna L. Kanchi, Haley J. Abel
مصطلحات موضوعية: Whole genome sequencing, Genetics, 0303 health sciences, Biology, Quantitative trait locus, Phenotype, Structural variation, 03 medical and health sciences, 0302 clinical medicine, Genotype, Copy-number variation, 030217 neurology & neurosurgery, Exome sequencing, 030304 developmental biology, Genetic association
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::9654cb6887480e67513f056a2fa53428
https://doi.org/10.1101/2020.12.13.422502 -
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المؤلفون: Nelson B. Freimer, Chul Joo Kang, Aki S. Havulinna, Aarno Palotie, Samuli Ripatti, Michael Boehnke, Nathan O. Stitziel, Charleston W. K. Chiang, Adam E. Locke, Ira M. Hall, Lei Chen, David E. Larson, Ryan Christ, Indraniel Das, Johanna Kuusisto, Markku Laakso, Allison A. Regier, Erica Young, Liron Ganel, Jagadish Vangipurapu, Krishna L. Kanchi, Haley J. Abel
مصطلحات موضوعية: Genetics, 0303 health sciences, education.field_of_study, Mitochondrial DNA, Population, Locus (genetics), Biology, medicine.disease, Genome, 3. Good health, 03 medical and health sciences, 0302 clinical medicine, Mendelian randomization, medicine, Metabolic syndrome, education, Gene, 030217 neurology & neurosurgery, Exome sequencing, 030304 developmental biology
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::da8b7116ec7420b3a070080afe24e283
https://doi.org/10.1101/2020.10.23.20218586 -
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المؤلفون: Haley J. Abel, Ira M. Hall, Liron Ganel
المصدر: Bioinformatics
مصطلحات موضوعية: 0301 basic medicine, Statistics and Probability, In silico, Population, Single-nucleotide polymorphism, Computational biology, Biology, Polymorphism, Single Nucleotide, Biochemistry, Structural variation, 03 medical and health sciences, Negative selection, 0302 clinical medicine, Gene Frequency, Humans, SNP, education, Molecular Biology, Allele frequency, Selection (genetic algorithm), Sequence Deletion, 030304 developmental biology, Genetics, Whole genome sequencing, education.field_of_study, 0303 health sciences, Breakpoint, Genomics, Genome Analysis, Applications Notes, Computer Science Applications, Computational Mathematics, 030104 developmental biology, Computational Theory and Mathematics, Genomic Structural Variation, Human genome, Software, 030217 neurology & neurosurgery
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::928baa8ceee24f366c0a8c1066fe328e
https://doi.org/10.1101/073833 -
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المؤلفون: Donald F. Conrad, Xin Li, Farhan N. Damani, Liron Ganel, Tarik Hadzic, Emily K. Tsang, Joe R. Davis, Yungil Kim, Alexandra J. Scott, Colby Chiang, Alexis Battle, Stephen B. Montgomery, Ira M. Hall
المصدر: Nature genetics
مصطلحات موضوعية: 0301 basic medicine, Quantitative Trait Loci, Biology, Genome, Polymorphism, Single Nucleotide, Article, Structural variation, 03 medical and health sciences, 0302 clinical medicine, INDEL Mutation, Genetic variation, Genetics, Humans, Indel, Gene, Genetic association, Regulation of gene expression, Genome, Human, Chromosome Mapping, Genetic Variation, Sequence Analysis, DNA, 030104 developmental biology, Gene Expression Regulation, Expression quantitative trait loci, Linear Models, 030217 neurology & neurosurgery, Algorithms, Genome-Wide Association Study