المؤلفون: Kelsey E Grinde, Brian L Browning, Alexander P Reiner, Timothy A Thornton, Sharon R Browning

المصدر: PLoS Genetics, Vol 20, Iss 12, p e1011242 (2024)

مصطلحات موضوعية: Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1553-7390; https://doaj.org/toc/1553-7404

URL الوصول: https://doaj.org/article/843f85a9885c41e6ba6b099974e20531

المؤلفون: Sharon R Browning, Brian L Browning, Martha L Daviglus, Ramon A Durazo-Arvizu, Neil Schneiderman, Robert C Kaplan, Cathy C Laurie

المصدر: PLoS Genetics, Vol 14, Iss 5, p e1007385 (2018)

مصطلحات موضوعية: Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://europepmc.org/articles/PMC5967706?pdf=render; https://doaj.org/toc/1553-7390; https://doaj.org/toc/1553-7404

URL الوصول: https://doaj.org/article/5cd6805c4d604ce2bba0951b3590e68e

المؤلفون: Chani J Hodonsky, Deepti Jain, Ursula M Schick, Jean V Morrison, Lisa Brown, Caitlin P McHugh, Claudia Schurmann, Diane D Chen, Yong Mei Liu, Paul L Auer, Cecilia A Laurie, Kent D Taylor, Brian L Browning, Yun Li, George Papanicolaou, Jerome I Rotter, Ryo Kurita, Yukio Nakamura, Sharon R Browning, Ruth J F Loos, Kari E North, Cathy C Laurie, Timothy A Thornton, Nathan Pankratz, Daniel E Bauer, Tamar Sofer, Alex P Reiner

المصدر: PLoS Genetics, Vol 13, Iss 4, p e1006760 (2017)

مصطلحات موضوعية: Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://europepmc.org/articles/PMC5428979?pdf=render; https://doaj.org/toc/1553-7390; https://doaj.org/toc/1553-7404

URL الوصول: https://doaj.org/article/d79b27a0384a489caf7bdbe0fd8fe84d

المؤلفون: Rozenn N Lemaitre, Toshiko Tanaka, Weihong Tang, Ani Manichaikul, Millennia Foy, Edmond K Kabagambe, Jennifer A Nettleton, Irena B King, Lu-Chen Weng, Sayanti Bhattacharya, Stefania Bandinelli, Joshua C Bis, Stephen S Rich, David R Jacobs, Antonio Cherubini, Barbara McKnight, Shuang Liang, Xiangjun Gu, Kenneth Rice, Cathy C Laurie, Thomas Lumley, Brian L Browning, Bruce M Psaty, Yii-Der I Chen, Yechiel Friedlander, Luc Djousse, Jason H Y Wu, David S Siscovick, André G Uitterlinden, Donna K Arnett, Luigi Ferrucci, Myriam Fornage, Michael Y Tsai, Dariush Mozaffarian, Lyn M Steffen

المصدر: PLoS Genetics, Vol 7, Iss 7, p e1002193 (2011)

مصطلحات موضوعية: Genetics, QH426-470

وصف الملف: electronic resource

Relation: http://europepmc.org/articles/PMC3145614?pdf=render; https://doaj.org/toc/1553-7390; https://doaj.org/toc/1553-7404

URL الوصول: https://doaj.org/article/f6f6354b54a24b3b90a488ba87a15695

المؤلفون: Li Li, Yun Li, Sharon R Browning, Brian L Browning, Andrew J Slater, Xiangyang Kong, Jennifer L Aponte, Vincent E Mooser, Stephanie L Chissoe, John C Whittaker, Matthew R Nelson, Margaret Gelder Ehm

المصدر: PLoS ONE, Vol 6, Iss 9, p e24945 (2011)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

Relation: http://europepmc.org/articles/PMC3176314?pdf=render; https://doaj.org/toc/1932-6203

URL الوصول: https://doaj.org/article/1d7226c76e3d4abaa5db8e155cd10b8e

المؤلفون: Anna Marie De Asis Tuazon, Paul Lott, Mabel Bohórquez, Jennyfer Benavides, Carolina Ramirez, Angel Criollo, Ana Estrada-Florez, Gilbert Mateus, Alejandro Velez, Jenny Carmona, Justo Olaya, Elisha Garcia, Guadalupe Polanco-Echeverry, Jacob Stultz, Carolina Alvarez, Teresa Tapia, Patricia Ashton-Prolla, Brazilian Familial Cancer Network, Ana Vega, Conxi Lazaro, Eva Tornero, Cristina Martinez-Bouzas, Mar Infante, Miguel De La Hoya, Orland Diez, Brian L. Browning, COLUMBUS Consortium, Bruce Rannala, Manuel R. Teixeira, Pilar Carvallo, Magdalena Echeverry, Luis G. Carvajal-Carmona

المصدر: Breast Cancer Research, Vol 22, Iss 1, Pp 1-10 (2020)

مصطلحات موضوعية: Breast cancer, Haplotype, BRCA1 c.3331_3334delCAAG, Founder mutation, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

Relation: http://link.springer.com/article/10.1186/s13058-020-01341-3; https://doaj.org/toc/1465-542X; https://doaj.org/article/228752d7de16406a9de9be2986016bb9

الاتاحة: https://doi.org/10.1186/s13058-020-01341-3
https://doaj.org/article/228752d7de16406a9de9be2986016bb9

المؤلفون: Brian L. Browning, Sharon R. Browning

المصدر: Am J Hum Genet

مصطلحات موضوعية: Report, Genetics, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a4e0621b0cd6819aaf723c26dd274f9
https://pubmed.ncbi.nlm.nih.gov/36450278

المؤلفون: Ruoyi Cai, Brian L. Browning, Sharon R. Browning

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::0faad2f719041c6d49b8798a9bafd002
https://doi.org/10.1101/2022.07.06.499007

المؤلفون: Nancy L. Heard-Costa, Lucas Barwick, Clary B. Clish, Celeste Eng, Joanne M. Murabito, Esteban G. Burchard, Yii-Der Ida Chen, Daniel I. Chasman, Robert C. Kaplan, James B. Meigs, Deborah A. Nickerson, Cashell E. Jaquish, Eric Boerwinkle, Jennifer A. Brody, Charles Kooperberg, Mark T. Gladwin, Sebastian Schoenherr, Keng-Han Lin, John Barnard, Ryan D. Hernandez, Andrew D. Johnson, Edwin K. Silverman, Mollie A. Minear, Michelle Daya, Barbara A. Konkle, Sharon R. Browning, Daniel E. Weeks, Wendy S. Post, Alexander P. Reiner, Kathryn L. Lunetta, Gina M. Peloso, David Van Den Berg, Dan E. Arking, Seung-been Lee, Leslie A. Lange, Cristen J. Willer, Zachary A. Szpiech, Tasha E. Fingerlin, Wayne E. Clarke, Xutong Zhao, Stephen S. Rich, Nora Franceschini, Sudha Seshadri, Chloé Sarnowski, Hyun Min Kang, Sayantan Das, Michael C. Zody, Stephanie M. Fullerton, Dean Bobo, Alanna C. Morrison, Brian Custer, Nona Sotoodehnia, Shannon Kelly, Thomas W. Blackwell, Bruce M. Psaty, Yingze Zhang, Susan R. Heckbert, Robert E. Gerszten, M. Benjamin Shoemaker, Daniel Taliun, Leslie S. Emery, André Corvelo, Michael H. Cho, Braxton D. Mitchell, Xiaoming Liu, Stella Aslibekyan, Paul L. Auer, Brandon Chalazan, Sarah C. Nelson, Seung Hoan Choi, Jeong-Sun Seo, Matthew P. Conomos, Anne-Katrin Emde, Lawrence F. Bielak, Alisa K. Manning, Allison E. Ashley-Koch, Diane Fatkin, Xiaowen Tian, Emelia J. Benjamin, D. C. Rao, Mina K. Chung, Myriam Fornage, Daniel Levy, Michael D. Kessler, Weihong Tang, Daniel J. Gottlieb, Pradeep Natarajan, Jessica Lasky-Su, Amol C. Shetty, Cathy C. Laurie, Dan M. Roden, Timothy D. O’Connor, Jedidiah Carlson, Lewis C. Becker, Achilleas N. Pitsillides, Karine A. Viaud-Martinez, Raul Torres, Adolfo Correa, Christian Fuchsberger, Deborah A. Meyers, Alvaro Alonso, Sanghamitra Mohanty, Jonathon LeFaive, Soren Germer, Julie L. Mikulla, François Aguet, Susan K. Dutcher, Sarah A Gagliano Taliun, Ani Manichaikul, Lori Garman, Xiuqing Guo, Timothy A. Thornton, David D. McManus, Albert V. Smith, Kristin G. Ardlie, Anna Köttgen, Sharon L.R. Kardia, Quenna Wong, Jill M. Johnsen, Andrea Natale, Richard A. Gibbs, Douglas P. Kiel, Ingo Ruczinski, Susan Redline, Lukas Forer, Scott I. Vrieze, May E. Montasser, Rasika A. Mathias, Jerome I. Rotter, Jacob Pleiness, Chunyu Liu, Brian L. Browning, James G. Wilson, Weiniu Gan, Christine M. Albert, Marilyn J. Telen, Courtney G. Montgomery, Steven A. Lubitz, Robert Klemmer, Ramachandran S. Vasan, Nathan Pankratz, Mariza de Andrade, Vivien A. Sheehan, Kenneth Rice, Xihong Lin, Eimear E. Kenny, Stephanie M. Gogarten, John Blangero, Donna K. Arnett, Jiang He, Pankaj Qasba, James F. Casella, Patrick T. Ellinor, Nicholette D. Palmer, R. Graham Barr, Scott T. Weiss, Joanne E. Curran, Bruce S. Weir, Kari E. North, L. Adrienne Cupples, Dawn L. DeMeo, Tanika N. Kelly, Angel C.Y. Mak, Russell P. Tracy, David A. Schwartz, Kent D. Taylor, Rebecca L. Beer, Daniel N. Harris, George J. Papanicolaou, Marguerite R. Irvin, Stephen T. McGarvey, Sebastian Zöllner, Patricia A. Peyser, Brian E. Cade, Ruth J. F. Loos, Douglas Loesch, Nicholas L. Smith, Gonçalo R. Abecasis, Jennifer A. Smith, Michael E. Hall, Lu-Chen Weng, Jeffrey R. O'Connell, Adrienne M. Stilp, Donald W. Bowden, Kathleen C. Barnes, Stacey Gabriel, Michael Boehnke, Wayne Huey-Herng Sheu, Dawood Darbar

المصدر: Nature

مصطلحات موضوعية: Quality Control, Heterozygote, Genomics, Computational biology, Biology, Polymorphism, Single Nucleotide, Genome, Article, DNA sequencing, INDEL Mutation, Loss of Function Mutation, Genetics research, Genetic variation, Humans, Precision Medicine, Genetic association, Population Density, Multidisciplinary, Whole Genome Sequencing, Genome, Human, Genetic Variation, Rare variants, United States, Genetic architecture, Phenotype, Cytochrome P-450 CYP2D6, Haplotypes, Mutagenesis, Sample Size, Next-generation sequencing, National Heart, Lung, and Blood Institute (U.S.), Imputation (genetics), Reference genome

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3466ed35ebc952114103dd5987431af
https://doi.org/10.1038/s41586-021-03205-y

المؤلفون: Brian L. Browning, Sharon R. Browning, Ying Zhou

المصدر: Am J Hum Genet

مصطلحات موضوعية: Linkage disequilibrium, Population, Recombination rate, Biology, Polymorphism, Single Nucleotide, Identity by descent, Linkage Disequilibrium, White People, Article, symbols.namesake, 03 medical and health sciences, 0302 clinical medicine, Data sequences, Population specific, Statistics, Genetics, Humans, International HapMap Project, 1000 Genomes Project, education, Genetics (clinical), 030304 developmental biology, Recombination, Genetic, 0303 health sciences, education.field_of_study, Genotype imputation, Genome, Human, Haplotype, Pearson product-moment correlation coefficient, Black or African American, Genetics, Population, Haplotypes, symbols, Cartography, 030217 neurology & neurosurgery, Recombination

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19dd15d611d9e69eb79954a9b8cb7931
https://doi.org/10.1016/j.ajhg.2020.05.016

المؤلفون: Ying Zhou, Brian L. Browning, Sharon R. Browning

المصدر: Am J Hum Genet

مصطلحات موضوعية: Data Analysis, Genetic Markers, Genotype, Computer science, Polymorphism, Single Nucleotide, digestive system, Identity by descent, Chromosomes, Article, 03 medical and health sciences, Centimorgan, 0302 clinical medicine, Data sequences, stomatognathic system, Simple (abstract algebra), Genetics, Humans, Computer Simulation, Alleles, Genetics (clinical), 030304 developmental biology, 0303 health sciences, Genome, Human, business.industry, Haplotype, Pattern recognition, Sequence Analysis, DNA, Large scale data, digestive system diseases, Genetics, Population, Haplotypes, Feature (computer vision), Artificial intelligence, business, Software, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84dc47cdaf7fc2d942cf57d1f3d2d818
https://doi.org/10.1016/j.ajhg.2020.02.010

المؤلفون: Brian L. Browning, Sharon R. Browning

المصدر: Am J Hum Genet

مصطلحات موضوعية: Heredity, Bias, Genotype, Haplotypes, Genetics, Humans, Polymorphism, Single Nucleotide, Genetics (clinical), Article

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f1ab61bf57522aa19b69a87c18c314f
https://pubmed.ncbi.nlm.nih.gov/35659928

المؤلفون: Sharon R. Browning, Kelsey Grinde, Anna Plantinga, Stephanie M. Gogarten, Adrienne M. Stilp, Robert C. Kaplan, M. Larissa Avilés-Santa, Brian L. Browning, Cathy C. Laurie

المصدر: G3: Genes, Genomes, Genetics, Vol 6, Iss 6, Pp 1525-1534 (2016)

مصطلحات موضوعية: Hispanic/Latino, local ancestry, principal components analysis, Genetics, QH426-470

Relation: https://doaj.org/toc/2160-1836; https://doaj.org/article/a789e6c1539649028c80afd4ef0ecbbc

الاتاحة: https://doi.org/10.1534/g3.116.028779
https://doaj.org/article/a789e6c1539649028c80afd4ef0ecbbc

المؤلفون: Sharon R. Browning, Xiaowen Tian, Brian L. Browning

المصدر: Am J Hum Genet

مصطلحات موضوعية: Mutation rate, Heredity, Genotype, Demographic history, Computational biology, Biology, Polymorphism, Single Nucleotide, Identity by descent, Genome, Article, 03 medical and health sciences, symbols.namesake, 0302 clinical medicine, Mutation Rate, Genetics, Humans, Genetics (clinical), 030304 developmental biology, 0303 health sciences, Genome, Human, Robustness (evolution), Confidence interval, Pedigree, Meiosis, Mutation, Mendelian inheritance, symbols, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1d59929e7cd74fe40dc07c90a4da966
https://doi.org/10.1016/j.ajhg.2019.09.012

المؤلفون: Giustina De Silvestro, Maria C. Renda, Fotis Tsetsos, Iosif Lazaridis, Peristera Paschou, John A. Stamatoyannopoulos, Francisco Pérez-Jiménez, Evangelia Yannaki, Anna Razou, Katerina Kanaki, Petros Drineas, Kenneth K. Kidd, George Stamatoyannopoulos, Brian L. Browning, Manolis Michalodimitrakis, Anna Plantinga

المصدر: Annals of Human Genetics

مصطلحات موضوعية: Genotype, media_common.quotation_subject, Human Migration, Population, Population genetics, crete, medieval history, White People, Scarcity, Medieval history, 03 medical and health sciences, Extant taxon, Databases, Genetic, Genetics, whole‐genome, Ethnicity, Humans, Local population, Middle Ages, education, Genetics (clinical), Historical record, Crosses, Genetic, 030304 developmental biology, media_common, 0303 health sciences, education.field_of_study, historical genetics, Geography, Greece, Genome, Human, 030305 genetics & heredity, population genetics, Genetic Variation, Original Articles, Genomics, History, Medieval, Genetics, Population, Ethnology, Original Article

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca33454659b51c105b7f8af86ae57558
http://europepmc.org/articles/PMC6851683

المؤلفون: Xiaowen Tian, Ying Zhou, Sharon R. Browning, Brian L. Browning

المصدر: Am J Hum Genet

مصطلحات موضوعية: Male, Genotype, Computer science, Computation, Scale (descriptive set theory), Polymorphism, Single Nucleotide, Article, Data sequences, Atrial Fibrillation, Genetics, Humans, Genetics (clinical), Genome, Human, Haplotype, Phaser, Asthma, Haplotypes, Sample size determination, Data Interpretation, Statistical, Female, Stage (hydrology), Algorithm, Algorithms, Software, SNP array, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fe46c7e76e568d55e10c8ffbaefbfe3
https://pubmed.ncbi.nlm.nih.gov/34478634

المؤلفون: Sharon R. Browning, Brian L. Browning

المصدر: American Journal of Human Genetics

مصطلحات موضوعية: Male, Computer science, Posterior probability, Inheritance Patterns, Computational biology, recent positive selection, Polymorphism, Single Nucleotide, identity by descent, Identity by state, Identity by descent, Article, DNA sequencing, 03 medical and health sciences, 0302 clinical medicine, Genetics, Humans, Family, Spurious relationship, Gene, Genetics (clinical), Selection (genetic algorithm), 030304 developmental biology, Biological Specimen Banks, 0303 health sciences, Models, Statistical, Natural selection, Genome, Human, business.industry, Uncertainty, Chromosome Mapping, natural selection, Pattern recognition, United Kingdom, digestive system diseases, Pedigree, Probabilistic estimation, Homogeneous, Biometric Identification, Female, Artificial intelligence, business, 030217 neurology & neurosurgery, Software, SNP array, Genome-Wide Association Study

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::145d422a20d4bf67b508e528cc0ad89a
https://doi.org/10.1101/2020.07.15.205179

المؤلفون: Brian L. Browning, Sharon R. Browning, Citing Beagle

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: http://www.biostat.wustl.edu/genetics/geneticssoft/manuals/beagle/beagle_2.1.pdf.

وصف الملف: application/pdf

Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.485.4041; http://www.biostat.wustl.edu/genetics/geneticssoft/manuals/beagle/beagle_2.1.pdf

الاتاحة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.485.4041
http://www.biostat.wustl.edu/genetics/geneticssoft/manuals/beagle/beagle_2.1.pdf

المؤلفون: Isabel Benzel, Aruna Bansal, Brian L Browning, Nicholas W Galwey, Peter R Maycox, Ralph Mcginnis, Devi Smart, David St Clair, Phillip Yates, Ian Purvis

المساهمون: The Pennsylvania State University CiteSeerX Archives

المصدر: ftp://ftp.ncbi.nlm.nih.gov/pub/pmc/ed/d3/Behav_Brain_Funct_2007_Jun_28_3_31.tar.gz

وصف الملف: application/zip

Relation: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.279.6324

الاتاحة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.279.6324

المؤلفون: Charles Kooperberg, Raul Mendez-Giraldez, Stephanie M. Gogarten, Chancellor Hohensee, Henry J. Lin, Nona Sotoodehnia, Zhu Ming Zhang, Ulrike Peters, Cathy C. Laurie, Laura M. Raffield, Yun Li, Matthew P. Conomos, Rebecca D. Jackson, Leslie A. Lange, Brian L. Browning, Timothy A. Thornton, Deepti Jain, Eric A. Whitsel, Xiuqing Guo, Kathleen F. Kerr, Alexander P. Reiner, Jerome I. Rotter, Elsayed Z. Soliman, Qian S. Zhang, Sharon R. Browning, Kent D. Taylor, Tamar Sofer, Susan R. Heckbert, Jie Yao, Marco V Perez, Christy L. Avery, James G. Wilson

المصدر: Heart Rhythm. 14:1675-1684

مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, Genotype, Myocardial Infarction, Action Potentials, Single-nucleotide polymorphism, Genome-wide association study, Autonomic Nervous System, Bioinformatics, Polymorphism, Single Nucleotide, Article, Electrocardiography, 03 medical and health sciences, Heart Rate, Physiology (medical), Epidemiology, Diabetes Mellitus, Humans, Heart rate variability, Medicine, SNP, Chromosome 12, business.industry, Arrhythmias, Cardiac, Hispanic or Latino, United States, Black or African American, Phenotype, 030104 developmental biology, Genetic epidemiology, Cohort, Calcium, Hydroxymethylglutaryl-CoA Reductase Inhibitors, Cardiology and Cardiovascular Medicine, business, Genome-Wide Association Study, Demography

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8700a67cbdd7b08760d4867a320b1977
https://doi.org/10.1016/j.hrthm.2017.06.018