المؤلفون: Nicholas L. Smith, Alan M. Kwong, Gonçalo R. Abecasis, Jennifer A. Smith, Celeste Eng, Charles Kooperberg, John Barnard, L. Adrienne Cupples, Ani Manichaikul, Wonji Kim, Dan M. Roden, Nicholette D. Palmer, M. Benjamin Shoemaker, Eric Boerwinkle, Michael Boehnke, John Blangero, Marguerite R. Irvin, Hemant K. Tiwari, Albert V. Smith, Alexander P. Reiner, Daniel E. Weeks, Tanika N. Kelly, Mariza de Andrade, Steven A. Lubitz, Laura J. Scott, Kathleen C. Barnes, Esteban G. Burchard, Han Chen, Scott T. Weiss, May E. Montasser, Yan Gao, Angel C.Y. Mak, Brian E. Cade, Thomas W. Blackwell, Courtney G. Montgomery, Solomon K. Musani, Xiuqing Guo, Daniel I. Chasman, Gina M. Peloso, Jessica Su, Hyun Min Kang, Dandi Qiao, Matthew P. Conomos, Patrick T. Ellinor, Jonathon LeFaive, Rasika A. Mathias

المصدر: Genetics

مصطلحات موضوعية: Genotype, Population structure, Biology, Linkage Disequilibrium, Statistical power, 03 medical and health sciences, 0302 clinical medicine, Gene Frequency, Statistics, Genetics, False positive paradox, Humans, Alleles, 030304 developmental biology, Investigation, 0303 health sciences, Models, Statistical, Models, Genetic, Hardy–Weinberg principle, Exact test, Genetics, Population, Phenotype, Data quality, Metric (mathematics), Scalability, Software, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44e0a8adfa5ceb89422a4f2b3c3eaed9Test
https://doi.org/10.1093/genetics/iyab044Test

المؤلفون: Laura M. Raffield, Alex P. Reiner, Andrew D. Johnson, Eric Boerwinkle, Juan M. Peralta, Michael H. Cho, Jiang He, Amanda L. Tapia, Jessica Lasky-Su, Scott T. Weiss, Edwin K. Silverman, Mary Cushman, L. Adrienne Cupples, Robert C. Kaplan, Yue Shan, Lisa R. Yanek, Marguerite R. Irvin, Paul L. Auer, Tanika N. Kelly, Hélène Choquet, Stacey Gabriel, Yun Li, Deepti Jain, Steve Buyske, Sebastian Zöllner, Nicholette D. Palmer, Caitlin P. McHugh, Michelle Daya, Jee-Young Moon, Patricia A. Peyser, Patrick T. Ellinor, Paul S. de Vries, Ruth J. F. Loos, Steven A. Lubitz, Timothy A. Thornton, Donald W. Bowden, Christy L. Avery, Courtney G. Montgomery, Misa Graff, Jonathan D. Rosen, Seung Hoan Choi, Kent D. Taylor, Kathleen C. Barnes, Rasika A. Mathias, George Papanicolaou, Santhi K. Ganesh, Alanna C. Morrison, Maria Argos, Nicholas L. Smith, Stephen S. Rich, Donna K. Arnett, Myriam Fornage, Namrata Gupta, Lewis C. Becker, Madeline H. Kowalski, Jennifer A. Smith, Lu-Chen Weng, Eric Jorgenson, Chani J. Hodonsky, Joshua C. Bis, Kari E. North, Jianwen Cai, Ziyi Hou, Jerome I. Rotter, Susan R. Heckbert, Stephanie A. Bien, John Blangero, Sharon L.R. Kardia, Kerri L. Wiggins, Russell P. Tracy, James G. Wilson, Nathan Pankratz, Huijun Qian, Nauder Faraday, Tao Wang, Bertha Hidalgo, Charles Kooperberg, Hemant K. Tiwari

المصدر: PLoS Genetics
PLoS Genetics, Vol 15, Iss 12, p e1008500 (2019)

مصطلحات موضوعية: Male, Cancer Research, Linkage disequilibrium, Heredity, Genotyping Techniques, Social Sciences, Genome-wide association study, beta-Globins, QH426-470, Biochemistry, Linkage Disequilibrium, 0302 clinical medicine, Gene Frequency, Sociology, Consortia, Databases, Genetic, Genotype, Medicine and Health Sciences, Precision Medicine, Genetics (clinical), Aged, 80 and over, Genetics, education.field_of_study, 0303 health sciences, 030305 genetics & heredity, Hispanic or Latino, Hematology, Genomics, Middle Aged, 3. Good health, Genetic Mapping, Female, Research Article, Adult, Genotyping, Population, Variant Genotypes, Biology, Research and Analysis Methods, 03 medical and health sciences, Genome-Wide Association Studies, Humans, Genetic Predisposition to Disease, Hemoglobin, 1000 Genomes Project, Molecular Biology Techniques, education, Molecular Biology, Allele frequency, Alleles, Ecology, Evolution, Behavior and Systematics, Aged, 030304 developmental biology, Genetic association, Whole Genome Sequencing, Haplotype, Computational Biology, Biology and Life Sciences, Proteins, Human Genetics, Genome Analysis, United States, Black or African American, Minor allele frequency, Genetics, Population, Haplotypes, Genetic Loci, 030217 neurology & neurosurgery, Imputation (genetics), Genome-Wide Association Study

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0704998c62e9584f7c2aae45f775edb3Test
https://doi.org/10.1101/683201Test

المؤلفون: Jose M. Ordovas, Ingrid B. Borecki, Edmond K. Kabagambe, Hemant K. Tiwari, Alexis C. Frazier-Wood, Donna K. Arnett

المصدر: PLoS ONE
PLoS ONE, Vol 7, Iss 2, p e30732 (2012)

مصطلحات موضوعية: Apolipoprotein E, Male, Heredity, Epidemiology, lcsh:Medicine, 030204 cardiovascular system & hematology, Biochemistry, Body Mass Index, 0302 clinical medicine, Genotype, lcsh:Science, 2. Zero hunger, Genetics, 0303 health sciences, Multidisciplinary, Middle Aged, 3. Good health, Medicine, lipids (amino acids, peptides, and proteins), Female, Low Density Lipoprotein Receptor-Related Protein-1, Research Article, Adult, Lipoproteins, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, Chylomicron remnant, Apolipoproteins E, medicine, Humans, Allele, Triglycerides, 030304 developmental biology, Aged, Nutrition, Population Biology, lcsh:R, Proteins, Computational Biology, medicine.disease, Lipid Metabolism, Obesity, Minor allele frequency, lcsh:Q, Body mass index, Population Genetics

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fca8172881f1a9d991412937b14f6cdeTest
https://pubmed.ncbi.nlm.nih.gov/22347399Test

المؤلفون: Nathan E. Wineinger, Nicholas M. Pajewski, Hemant K. Tiwari

المصدر: Frontiers in Genetics, Vol 2 (2011)
Frontiers in Genetics

مصطلحات موضوعية: Genetics, 0303 health sciences, Linkage disequilibrium, lcsh:QH426-470, 030305 genetics & heredity, copy number variation, Single-nucleotide polymorphism, Tag SNP, Biology, 03 medical and health sciences, lcsh:Genetics, Genotype, CNV–SNP haplotype, Molecular Medicine, SNP, Copy-number variation, Genetic variability, Allele frequency, Genetics (clinical), CNV-SNP haplotype, linkage disequilibrium, 030304 developmental biology, Original Research

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da96e94b17380c338304e66315200eb2Test

المؤلفون: Jeffrey C. Edberg, Hemant K. Tiwari, Andrew O. Westfall, James Michael Kelley, Edwin A. Smith, Richard Brasington, Graciela S. Alarcón, Laura B. Hughes, Monica Crawford, Maria I. Danila, Beth Jonas, Doyt L. Conn, Robert P. Kimberly, Jeffrey D. Faggard, David B. Allison, S. Louis Bridges, Miguel A. Padilla, Yuanqing Edberg, Leigh F. Callahan, Larry W. Moreland

المصدر: PLoS Genetics, Vol 5, Iss 12 (2009)
PLoS Genetics
PLoS Genetics, Vol 5, Iss 3, p e1000424 (2009)

مصطلحات موضوعية: Adult, Male, Cancer Research, lcsh:QH426-470, Population, Black People, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Arthritis, Rheumatoid, 03 medical and health sciences, 0302 clinical medicine, Antigens, CD, Genotype, Prevalence, Genetics, Humans, CTLA-4 Antigen, Allele, education, Rheumatology/Rheumatoid Arthritis, Molecular Biology, Genetics and Genomics/Genetics of Disease, Alleles, Genetics (clinical), Ecology, Evolution, Behavior and Systematics, 030304 developmental biology, 030203 arthritis & rheumatology, 0303 health sciences, education.field_of_study, Haplotype, Case-control study, Odds ratio, Middle Aged, 3. Good health, Retraction, Minor allele frequency, Black or African American, lcsh:Genetics, Haplotypes, Case-Control Studies, Immunology, Genetics and Genomics/Genetics of the Immune System, Female, Research Article

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d66bfcb3c770b1e7c33a705b6852578Test
https://doi.org/10.1371/annotation/80bd7285-9d2d-403a-8e6f-9c375bf977caTest

المؤلفون: Michael J. Crowley, E. Christopher Partridge, Dorret I. Boomsma, Teresita Díaz de Ståhl, Antoinet C.J. Gijsbers, Uwe Menzel, Carl E.G. Bruder, Andrzej Poplawski, Robin Andersson, Gert-Jan B. van Ommen, Karin Wirdefeldt, Stephen W. Erickson, Jan Komorowski, Chiquito J. Crasto, Johan T. den Dunnen, Nancy L. Pedersen, David B. Allison, Johanna Sandgren, Desiree von Tell, Jan P. Dumanski, Hemant K. Tiwari, Arkadiusz Piotrowski

المساهمون: Biological Psychology

المصدر: American Journal of Human Genetics, 82(3), 763-771. Cell Press
Bruder, C E G, Piotrowski, A, Gijsbers, A A C J, Anderson, R, Erickson, S, Diaz de Stahl, T, Menzel, U, Sandgren, J, von Tell, D, Poplawski, A, Crowley, M, Crasto, C, Partridge, E C, Tiwari, H, Allison, D B, Komorowski, J, van Ommen, G J B, Boomsma, D I, Pedersen, N L, den Dunnen, J T, Wirdefeldt, K & Dumanski, J P 2008, ' Phenotypically Concordant and Discordant Monozygotic Twins Display Different DNA Copy-Number-Variation Profiles. ', American Journal of Human Genetics, vol. 82, no. 3, pp. 763-771 . https://doi.org/10.1016/j.ajhg.2007.12.011Test

مصطلحات موضوعية: Male, Netherlands Twin Register (NTR), Concordance, Monozygotic twin, Biology, 03 medical and health sciences, 0302 clinical medicine, Report, Genotype, Genetic variation, Genetics, Chromosomes, Human, Humans, Genetics(clinical), Genetic variability, Genetics (clinical), 030304 developmental biology, Oligonucleotide Array Sequence Analysis, 0303 health sciences, Genetic Variation, Neurodegenerative Diseases, DNA, Twins, Monozygotic, Twin study, Phenotype, Human genetics, Female, 030217 neurology & neurosurgery

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c442e17aab1cb31320e3f2a5ea72df1Test
https://research.vu.nl/en/publications/d32b3502-8c41-49e1-9a20-cea0509d4808Test