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1دورية أكاديمية
المؤلفون: Hongjian Qi, Lan Yu, Xueya Zhou, Julia Wynn, Haoquan Zhao, Yicheng Guo, Na Zhu, Alexander Kitaygorodsky, Rebecca Hernan, Gudrun Aspelund, Foong-Yen Lim, Timothy Crombleholme, Robert Cusick, Kenneth Azarow, Melissa E Danko, Dai Chung, Brad W Warner, George B Mychaliska, Douglas Potoka, Amy J Wagner, Mahmoud ElFiky, Jay M Wilson, Debbie Nickerson, Michael Bamshad, Frances A High, Mauro Longoni, Patricia K Donahoe, Wendy K Chung, Yufeng Shen
المصدر: PLoS Genetics, Vol 14, Iss 12, p e1007822 (2018)
وصف الملف: electronic resource
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المؤلفون: Sarah U. Morton, Alexandre C. Pereira, Daniel Quiat, Felix Richter, Alexander Kitaygorodsky, Jacob Hagen, Daniel Bernstein, Martina Brueckner, Elizabeth Goldmuntz, Richard W. Kim, Richard P. Lifton, George A. Porter, Martin Tristani-Firouzi, Wendy K. Chung, Amy Roberts, Bruce D. Gelb, Yufeng Shen, Jane W. Newburger, J.G. Seidman, Christine E. Seidman
المصدر: Circ Genom Precis Med
مصطلحات موضوعية: Heart Defects, Congenital, Infant, Newborn, Infant, Mothers, General Medicine, Article, Body Mass Index, Pregnancy, Diabetes Mellitus, Humans, Female, Gene Regulatory Networks, Obesity, Child
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1983bb17d64aef92743f2c49e544baaa
https://doi.org/10.1161/circgen.121.003500 -
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المؤلفون: Daniel Bernstein, Martin Tristani-Firouzi, Jane W. Newburger, Sarah U. Morton, Diane E. Dickel, Lauren K. Wasson, Seong Won Kim, Jonathan G. Seidman, Martina Brueckner, Hongjian Qi, Elizabeth Goldmuntz, George A. Porter, Eric E. Schadt, Olga G. Troyanskaya, Kathryn B. Manheimer, Jian Zhou, Jason Homsy, Michael Parfenov, Steven R. DePalma, Bruce D. Gelb, Andrew Farrell, Alexander Kitaygorodsky, Matt Velinder, Gabor T. Marth, Richard B. Kim, Nihir Patel, Jonathan R. Kaltman, Felix Richter, Deepak Srivastava, Kathleen M. Chen, Yufeng Shen, Joshua M. Gorham, Christine E. Seidman, Alessandro Giardini, Wendy K. Chung
المصدر: Nature Genetics. 52:769-777
مصطلحات موضوعية: Proband, Genetics, 0303 health sciences, Heart disease, Genomics, Odds ratio, Biology, medicine.disease, Genome, 03 medical and health sciences, 0302 clinical medicine, medicine, Young adult, Enhancer, Gene, 030217 neurology & neurosurgery, 030304 developmental biology
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المؤلفون: Jin E, Yufeng Shen, Alexander Kitaygorodsky
مصطلحات موضوعية: genetic structures, Immunoprecipitation, Genetic variation, RNA-binding protein, Functional impact, Computational biology, Biology, ENCODE, Genome, Convolutional neural network, psychological phenomena and processes, Backpropagation
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::b400125da70124486f58ccfd09c18d16
https://doi.org/10.1101/2021.06.02.446817 -
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المؤلفون: Michael J. Bamshad, Timothy M. Crombleholme, Yufeng Shen, Dai H. Chung, Douglas A. Potoka, Alexander Kitaygorodsky, Julia Wynn, Frances A. High, Patricia K. Donahoe, Foong-Yen Lim, Na Zhu, Deborah A. Nickerson, Gudrun Aspelund, Amy J. Wagner, Lan Yu, Hongjian Qi, Melissa E. Danko, Mahmoud Elfiky, Wendy K. Chung, Yicheng Guo, Mauro Longoni, Xueya Zhou, Haoquan Zhao, George B. Mychaliska, Robert A. Cusick, Rebecca Hernan, Brad W. Warner, Jay M. Wilson, Kenneth S. Azarow
المصدر: PLoS Genetics
PLoS Genetics, Vol 14, Iss 12, p e1007822 (2018)مصطلحات موضوعية: 0301 basic medicine, Male, Cancer Research, Cytoskeleton organization, Developmental Disabilities, Respiratory System, Gene Expression, QH426-470, Biochemistry, Transcriptome, 0302 clinical medicine, Thoracic Diaphragm, Medicine and Health Sciences, Missense mutation, Longitudinal Studies, Genetics (clinical), Exome sequencing, Genetics, education.field_of_study, Heart, Syndrome, Congenital Anomalies, 3. Good health, Phenotype, Child, Preschool, Medical genetics, Female, Anatomy, Research Article, Heart Defects, Congenital, medicine.medical_specialty, DNA Copy Number Variations, Population, Mutation, Missense, Biology, 03 medical and health sciences, DNA-binding proteins, Exome Sequencing, medicine, Congenital Disorders, Humans, Gene Regulation, education, Molecular Biology, Ecology, Evolution, Behavior and Systematics, Clinical Genetics, Whole Genome Sequencing, Sequence Analysis, RNA, Infant, Newborn, Congenital diaphragmatic hernia, Biology and Life Sciences, Proteins, Genetic Variation, Membrane Proteins, Human Genetics, medicine.disease, Human genetics, Regulatory Proteins, 030104 developmental biology, Genetics of Disease, Mutation, Cardiovascular Anatomy, Hernias, Diaphragmatic, Congenital, 030217 neurology & neurosurgery, Transcription Factors
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المؤلفون: Timothy M. Crombleholme, George B. Mychaliska, Deborah A. Nickerson, Dai H. Chung, Brad W. Warner, Yufeng Shen, Douglas A. Potoka, Alexander Kitaygorodsky, Lexiang Yu, Robert A. Cusick, Kenneth S. Azarow, Gudrun Aspelund, Patricia K. Donahoe, Mahmoud Elfiky, Melissa E. Danko, Amy J. Wagner, Xueya Zhou, Wendy K. Chung, Jay M. Wilson, Foong-Yen Lim, Frances A. High, Na Zhu, Mauro Longoni, Michael J. Bamshad, Julia Wynn, Hongjian Qi
مصطلحات موضوعية: Genetics, 0303 health sciences, Candidate gene, 030305 genetics & heredity, Congenital diaphragmatic hernia, Genomics, Biology, medicine.disease, Genetic analysis, 03 medical and health sciences, medicine, Missense mutation, Gene, Exome, Exome sequencing, 030304 developmental biology
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3487c74886c38be9bbe76a4cb0295616
https://doi.org/10.1101/206037