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1. Full Text Single-Cell RNA Sequencing Resolves Molecular Relationships Among Individual Plant Cells1[OPEN]
by Ryu, Kook Hui and Huang, Ling and Kang, Hyun Min and Schiefelbein, John
Plant Physiology, ISSN 0032-0889, 4/2019, Volume 179, Issue 4, pp. 1444 - 1456
High-throughput single-cell RNA sequencing of Arabidopsis root protoplasts demonstrates the feasibility and utility of individual cell transcriptomic analyses... 
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2. Full Text Unified representation of genetic variants
by Tan, Adrian and Abecasis, Gonçalo R and Kang, Hyun Min
Bioinformatics, ISSN 1367-4803, 07/2015, Volume 31, Issue 13, pp. 2202 - 2204
A genetic variant can be represented in the Variant Call Format (VCF) in multiple different ways. Inconsistent representation of variants between variant... 
BIOTECHNOLOGY & APPLIED MICROBIOLOGY | BIOCHEMICAL RESEARCH METHODS | MATHEMATICAL & COMPUTATIONAL BIOLOGY | Programming Languages | Genetic Variation - genetics | Software | Algorithms | Genome, Human | Humans | Reproduction | Filtering | Tools | Genetics | Representations | Source code | Bioinformatics | Applications Notes
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3. Full Text Variance component model to account for sample structure in genome-wide association studies
by Kang, Hyun Min and Sul, Jae Hoon and Service, Susan K and Zaitlen, Noah A and Kong, Sit-Yee and Freimer, Nelson B and Sabatti, Chiara and Eskin, Eleazar
Nature Genetics, ISSN 1061-4036, 04/2010, Volume 42, Issue 4, pp. 348 - 354
Although genome-wide association studies (GWASs) have identified numerous loci associated with complex traits, imprecise modeling of the genetic relatedness... 
PAIRWISE RELATEDNESS | INDIVIDUALS | TESTS | FOUNDER POPULATION | QUANTITATIVE TRAITS | GENETICS & HEREDITY | POPULATION-STRUCTURE | MISSING HERITABILITY | COMPLEX DISEASES | CANCER SUSCEPTIBILITY LOCI | STRATIFICATION | Genome-Wide Association Study | Humans | Population Groups - genetics | Models, Genetic | Polymorphism, Single Nucleotide | Software | Models, Statistical | Quantitative Trait Loci | Principal Component Analysis | Quantitative trait loci | Physiological aspects | Usage | Research | Identification and classification | Genomics | Studies | Genotype & phenotype | Genetics | Methods
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4. Full Text Low-coverage sequencing: Implications for design of complex trait association studies
by Li, Yun and Sidore, Carlo and Kang, Hyun Min and Boehnke, Michael and Abecasis, Gonçalo R
Genome Research, ISSN 1088-9051, 06/2011, Volume 21, Issue 6, pp. 940 - 951
New sequencing technologies allow genomic variation to be surveyed in much greater detail than previously possible. While detailed analysis of a single... 
IMPUTATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | LOCI | GENOTYPES | DISEASES | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | SNPS | MISSING HERITABILITY | HAPLOTYPE | EFFICIENT | MAP | GENOME-WIDE ASSOCIATION | Genetic Variation | Computational Biology - methods | Likelihood Functions | Markov Chains | Polymorphism, Single Nucleotide - genetics | Genome-Wide Association Study - methods | Sequence Analysis, DNA - methods | Usage | Genetic variation | Analysis | Genotype | Nucleotide sequencing | Research | Methods | Resource
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5. Full Text Efficient Control of Population Structure in Model Organism Association Mapping
by Kang, Hyun Min and Zaitlen, Noah A and Wade, Claire M and Kirby, Andrew and Heckerman, David and Daly, Mark J and Eskin, Eleazar
Genetics, ISSN 0016-6731, 03/2008, Volume 178, Issue 3, pp. 1709 - 1723
Genomewide association mapping in model organisms such as inbred mouse strains is a promising approach for the identification of risk factors related to human... 
INBRED MOUSE STRAINS | PAIRWISE RELATEDNESS | QUANTITATIVE TRAIT LOCI | VARIANCE-COMPONENTS | MOLECULAR MARKERS | LINEAR MIXED MODELS | RATIO TESTS | AVERAGE INFORMATION | GENETICS & HEREDITY | ANIMAL-MODELS | RESTRICTED MAXIMUM-LIKELIHOOD | Zea mays - genetics | Quantitative Trait, Heritable | Genome - genetics | Mice, Inbred Strains | Body Weight - genetics | Arabidopsis - genetics | Phenotype | Animals | Models, Biological | Chromosome Mapping - methods | Organ Size - genetics | Polymorphism, Single Nucleotide - genetics | Inbreeding | Mice | Models, Genetic | Software | Saccharin - metabolism | Flowers - genetics | Population Dynamics | Chromosome mapping | Genes | Research | Gene expression | Population genetics | Identification and classification | Methods | Studies | Human subjects | Genotype & phenotype | Matrix | Principal components analysis | Organisms | Investigations
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6. Performance improvement of gas turbine combined cycle power plant by dual cooling of the inlet air and turbine coolant using an absorption chiller
by Hyun Min Kwon and Tong Seop Kim and Jeong Lak Sohn and Do Won Kang
Energy, ISSN 0360-5442, 11/2018, Volume 163, p. 1050
A critical issue concerning the gas turbine is that its power decreases considerably with increasing ambient temperature. Recently, it was proposed to maximize... 
Economic analysis | Cooling | Refrigerators | Feasibility studies | Gas turbine engines | Combined cycle power generation | Electric power generation | Air cooling | Gas turbines | Absorption | Ambient temperature | Feasibility | Turbines | Power plants
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7. Full Text Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants
by Fu, Wenqing and O'Connor, Timothy D and Jun, Goo and Kang, Hyun Min and Abecasis, Goncalo and Leal, Suzanne M and Gabriel, Stacey and Altshuler, David and Shendure, Jay and Nickerson, Deborah A and Bamshad, Michael J and Akey, Joshua M and NHLBI Exome Sequencing Project
Nature, ISSN 0028-0836, 01/2013, Volume 493, Issue 7431, pp. 216 - 220
Establishing the age of each mutation segregating in contemporary human populations is important to fully understand our evolutionary history(1,2) and will... 
EXCESS | EVOLUTION | RARE | GENE | MULTIDISCIPLINARY SCIENCES | DISEASE | POPULATION-GROWTH | MUTATIONS | HISTORY | AGE | European Continental Ancestry Group - genetics | United States | Humans | Exons - genetics | Open Reading Frames - genetics | Europe - ethnology | Exome - genetics | Africa - ethnology | Alleles | Polymorphism, Single Nucleotide - genetics | Genetic Variation - genetics | African Continental Ancestry Group - genetics | Evolution, Molecular | Physiological aspects | Research | Gene mutations | Genetic variation | Population genetics | Studies | Proteins | Population growth | Quality control | African Americans | Evolution | Principal components analysis | Evolution & development | Age | Methods
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8. A novel coolant cooling method for enhancing the performance of the gas turbine combined cycle
by Seong Won Moon and Hyun Min Kwon and Tong Seop Kim and Do Won Kang and Jeong Lak Sohn
Energy, ISSN 0360-5442, 10/2018, Volume 160, p. 625
The turbine inlet temperature (TIT) has a significant effect on the performance of gas turbines, and enhanced cooling methods are being applied to the latest... 
Temperature requirements | Temperature | Cooling | Inlet temperature | Gas turbine engines | Cooling effects | Combined cycle power generation | Compressors | Geographical variations | Heat recovery | Heat | Gas turbines | Temperature effects | Heat recovery systems | Air temperature | Steam | Power efficiency | Power plants
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9. Full Text Single-Cell RNA Sequencing Resolves Molecular Relationships Among Individual Plant Cells
by Ryu, KH and Huang, L and Kang, HM and Schiefelbein, J
PLANT PHYSIOLOGY, ISSN 0032-0889, 04/2019, Volume 179, Issue 4, pp. 1444 - 1456
Single-cell RNA sequencing (scRNA-seq) has been used extensively to study cell-specific gene expression in animals, but it has not been widely applied to... 
ORGANIZATION | TRICHOME | DIFFERENTIATION | MAP | GENES | PLANT SCIENCES | Arabidopsis thaliana | RNA sequencing | RNA | Gene mutations | Analysis | Gene expression | Cell differentiation
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10. Full Text Author Correction: Using and producing publicly available genomic data to accelerate discovery in nephrology
by Sampson, Matthew G and Kang, Hyun Min
Nature reviews. Nephrology, ISSN 1759-5061, 07/2019, Volume 15, Issue 9, pp. 590 - 590
An amendment to this paper has been published and can be accessed via a link at the top of the paper. 
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11. Full Text Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes
by Jacob A. Tennessen and Abigail W. Bigham and Timothy D. O'Connor and Wenqing Fu and Eimear E. Kenny and Simon Gravel and Sean McGee and Ron Do and Xiaoming Liu and Goo Jun and Hyun Min Kang and Daniel Jordan and Suzanne M. Leal and Stacey Gabriel and Mark J. Rieder and Goncalo Abecasis and David Altshuler and Deborah A. Nickerson and Eric Boerwinkle and Shamil Sunyaev and Carlos D. Bustamante and Michael J. Bamshad and Joshua M. Akey and NHLBI Exome Sequencing Project and Broad GO and Seattle GO and on behalf of the NHLBI Exome Sequencing Project
Science, ISSN 0036-8075, 7/2012, Volume 337, Issue 6090, pp. 64 - 69
As a first step toward understanding how rare variants contribute to risk for complex diseases, we sequenced 15,585 human protein-coding genes to an average... 
Exome | Population growth | Demography | Sample size | Genetic variation | Proportions | RESEARCH ARTICLES | Humans | Genomes | Sequencing | Human genetics | SPECTRUM | POSITIVE SELECTION | MULTIDISCIPLINARY SCIENCES | DISCOVERY | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease | Disease - genetics | Genetic Association Studies | Population Growth | Gene Frequency | Selection, Genetic | African Americans - genetics | Male | Genetic Variation | Female | High-Throughput Nucleotide Sequencing | Polymorphism, Single Nucleotide | Genome, Human | Evolution, Molecular
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12. Full Text Histone deacetylase inhibition ameliorates hypertension and hyperglycemia in a model of cushing’s syndrome
by Lee, Hae-Ahm and Kang, Seol-Hee and Kim, Mina and Lee, Eunjo and Cho, Hyun-Min and Moon, Eun-Kyung and Kim, Inkyeom
American Journal of Physiology - Endocrinology and Metabolism, ISSN 0193-1849, 01/2018, Volume 314, Issue 1, pp. E39 - E52
Hypertension | Histone deacetylashyperglycemia | Cushing’s syndrome | Glucocorticoid receptor
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13. Full Text In-vehicle network intrusion detection using deep convolutional neural network
by Song, Hyun Min and Woo, Jiyoung and Kim, Huy Kang
Vehicular Communications, ISSN 2214-2096, 10/2019, p. 100198
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14. Full Text A global reference for human genetic variation
by Altshuler, D.M and Albers, C.A and Abecasis, G.R and et al and Genomes Project Consortium and 1000 Genomes Project Consortium and The 1000 Genomes Project Consortium
Nature, ISSN 0028-0836, 2015, Volume 526, Issue 7571, pp. 68 - 74
The 1000 Genomes Project set out to provide a comprehensive description of common human genetic variation by applying whole-genome sequencing to a diverse set... 
BAYES FACTORS | INDIVIDUALS | COMPLEMENT FACTOR-H | POPULATION HISTORY | MULTIDISCIPLINARY SCIENCES | MUTATION | DISEASE | SUSCEPTIBILITY | MACULAR DEGENERATION | VARIANT | GENOME-WIDE ASSOCIATION | Rare Diseases - genetics | Genome-Wide Association Study | Datasets as Topic | Demography | Disease Susceptibility | Physical Chromosome Mapping | Humans | Genetics, Population - standards | Genomics - standards | Genotype | INDEL Mutation - genetics | Sequence Analysis, DNA | Genome, Human - genetics | Haplotypes - genetics | Exome - genetics | Reference Standards | Genetics, Medical | Internationality | Polymorphism, Single Nucleotide - genetics | Genetic Variation - genetics | High-Throughput Nucleotide Sequencing | Quantitative Trait Loci - genetics | Genetic research | Nucleotide sequencing | Observations | Genetic variation | Methods | DNA sequencing | Studies | Haplotypes | Genotype & phenotype | Accuracy | Genealogy | Population | Genomes | Genetic diversity | Mitochondrial DNA | Binding sites
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