المؤلفون: Wang, Yuejun Jessie, Zhang, Xicheng, Lam, Chi Keung, Guo, Hongchao, Wang, Cheng, Zhang, Sai, Wu, Joseph C, Snyder, Michael, Li, Jingjing

المصدر: Cell Systems. 13(11)

مصطلحات موضوعية: Biochemistry and Cell Biology, Biological Sciences, Cardiovascular, Infant Mortality, Perinatal Period - Conditions Originating in Perinatal Period, Heart Disease, Pediatric Research Initiative, Pediatric, Congenital Structural Anomalies, Genetics, Good Health and Well Being, Humans, Hypoplastic Left Heart Syndrome, Endothelial Cells, Heart Defects, Congenital, Mutation, Systems Analysis, biological networks, congenital heart diseases, hypoplastic heart, personal genomes, single cell, systems biology, Biochemistry and cell biology

URL الوصول: https://escholarship.org/uc/item/2sk9c797

المؤلفون: Lasse Folkersen, Oliver Pain, Andrés Ingason, Thomas Werge, Cathryn M. Lewis, Jehannine Austin

المصدر: Frontiers in Genetics, Vol 11 (2020)

مصطلحات موضوعية: genetics, polygenic risk scores, direct-to-consumer, personal genomes, risk prediction, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/article/10.3389/fgene.2020.00578/full; https://doaj.org/toc/1664-8021

URL الوصول: https://doaj.org/article/97a57f4460604774bfc4c2617af37a37

المؤلفون: Saito, Taro L.^Aff17

المساهمون: Hutchison, David, Series editor^Aff1, Kanade, Takeo, Series editor^Aff2, Kittler, Josef, Series editor^Aff3, Kleinberg, Jon M., Series editor^Aff4, Mattern, Friedemann, Series editor^Aff5, Mitchell, John C., Series editor^Aff6, Naor, Moni, Series editor^Aff7, Nierstrasz, Oscar, Series editor^Aff8, Pandu Rangan, C., Series editor^Aff9, Steffen, Bernhard, Series editor^Aff10, Sudan, Madhu, Series editor^Aff11, Terzopoulos, Demetri, Series editor^Aff12, Tygar, Doug, Series editor^Aff13, Vardi, Moshe Y., Series editor^Aff14, Weikum, Gerhard, Series editor^Aff15, Kikuchi, Shinji, editor^Aff16, Madaan, Aastha, editor^Aff16, Sachdeva, Shelly, editor^Aff16, Bhalla, Subhash, editor^Aff16

المصدر: Databases in Networked Information Systems : 7th International Workshop, DNIS 2011, Aizu-Wakamatsu, Japan, December 12-14, 2011. Proceedings. 7108:78-88

المؤلفون: Yuejun Jessie Wang, Xicheng Zhang, Chi Keung Lam, Hongchao Guo, Cheng Wang, Sai Zhang, Joseph C. Wu, Michael Snyder, Jingjing Li

المصدر: Cell systems, vol 13, iss 11

مصطلحات موضوعية: Heart Defects, Congenital, Pediatric Research Initiative, Histology, Systems Analysis, Cardiovascular, Pathology and Forensic Medicine, Congenital, Infant Mortality, Hypoplastic Left Heart Syndrome, Genetics, Humans, Heart Defects, Pediatric, Endothelial Cells, systems biology, Cell Biology, Perinatal Period - Conditions Originating in Perinatal Period, hypoplastic heart, single cell, congenital heart diseases, biological networks, Heart Disease, Good Health and Well Being, Mutation, Congenital Structural Anomalies, Biochemistry and Cell Biology, personal genomes

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::903c4edb57a1a93cccef9013eefd12aa
https://pubmed.ncbi.nlm.nih.gov/36167075

المؤلفون: Choi, Murim, Scholl, Ute I., Ji, Weizhen, Liu, Tiewen, Tikhonova, Irina R., Zumbo, Paul, Nayir, Ahmet, Bakkaloğlu, Ayşin, Özen, Seza, Sanjad, Sami, Nelson-Williams, Carol, Farhi, Anita, Mane, Shrikant, Lifton, Richard P.

المصدر: Proceedings of the National Academy of Sciences of the United States of America, 2009 Nov 01. 106(45), 19096-19101.

URL الوصول: https://www.jstor.org/stable/25593149

المؤلفون: Hasija, Yasha, Khan, Jameel Ahmad, Scaria, Vinod

المصدر: Current Genetic Medicine Reports. September 2014 2(3):182-189

المؤلفون: Manuel Corpas, Stephan Beck, Gustavo Glusman, Mahsa Shabani

المصدر: Frontiers in Genetics, Vol 12 (2021)
Re-Unir. Archivo Institucional de la Universidad Internacional de La Rioja
Universitat Rovira i virgili (URV)

مصطلحات موضوعية: WOS(2), data sharing, Interpretation (philosophy), direct-to-consumer genetic testing, Scopus(2), Genomics, QH426-470, Genome, Data science, personal genomics, Data sharing, ethical, ComputingMethodologies_PATTERNRECOGNITION, citizen science, Genetics, Citizen science, Molecular Medicine, Sociology, personal genomes, Genetics (clinical), legal, Personal genomics

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54b5fcc67a622b7f9fb82eb7f8797d28
https://doi.org/10.3389/fgene.2021.687584

المؤلفون: Ozge Ozalp Yuregir, Xiaofei Song, Jennifer E. Posey, Vahid Bahrambeigi, Yavuz Bayram, Zeynep Coban Akdemir, Davut Pehlivan, Donna M. Muzny, Sedat Isikay, Tamar Harel, Ender Karaca, Sevcan Tug Bozdogan, James R. Lupski, Shalini N. Jhangiani, Richard A. Gibbs, Gozde Yesil

المساهمون: HKÜ, Sağlık Bilimleri Fakültesi, Fizyoterapi ve Rehabilitasyon Bölümü, YEŞİL, Gözde, Çukurova Üniversitesi

المصدر: Genetics in medicine : official journal of the American College of Medical Genetics

مصطلحات موضوعية: Male, 0301 basic medicine, Heterozygote, Genotype, Sequencing data, Locus (genetics), Disease, Biology, Article, 03 medical and health sciences, Exome Sequencing, Humans, Exome, Pathology, Molecular, multilocus variation, Genetic Association Studies, Genetics (clinical), Genetics, Disease gene, Karaca E., Posey J. E. , Akdemir Z. C. , Pehlivan D., Harel T., Jhangiani S. N. , Bayram Y., Song X., Bahrambeigi V., Yuregir O. O. , et al., -Phenotypic expansion illuminates multilocus pathogenic variation-, GENETICS IN MEDICINE, cilt.20, ss.1528-1537, 2018, Affected sibling, Genetic Diseases, Inborn, Infant, Newborn, distinct/overlapping blended phenotypes, neurodevelopmental disorder, personal genomes, phenotypic expansion of Mendelizing disease traits, Genetic Variation, High-Throughput Nucleotide Sequencing, Infant, Variant call file, Phenotype, Pedigree, 3. Good health, 030104 developmental biology, Child, Preschool, Mutation, Female

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::179f58391e08db28dbb6e01869919795
https://doi.org/10.1038/gim.2018.33

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