Prediction of phosphorylation sites using SVMs

Jong Hun Kim, Ju‐Young Lee, Bermseok Oh, +2

Bioinformatics

Microstructural white matter abnormality and frontal cognitive dysfunctions in juvenile myoclonic epilepsy

Ji Hyun Kim, Sang‐il Suh, So Yeon Park, +4

Epilepsia

Pan-genome analysis of Bacillus for microbiome profiling

Yihwan Kim, InSong Koh, Mi Young Lim, +2

Scientific Reports

BiologyMicrobial DiversityMicrobiome ProfilingMicrobial SystematicsGenetics +11

Photosynthetic functions of Synechococcus in the ocean microbiomes of diverse salinity and seasons

Yihwan Kim, Jehyun Jeon, Min Seok Kwak, +3

PLoS ONE

The Effect of Increasing Control-to-case Ratio on Statistical Power in a Simulated Case-control SNP Association Study

Moonsu Kang, Sun-Hee Choi, InSong Koh

Genomics & Informatics

Genome-wide association studies and epistasis analyses of candidate genes related to age at menarche and age at natural menopause in a Korean population

Jung-A. Pyun, Sunshin Kim, Nam H. Cho, +4

Menopause The Journal of The North American Menopause Society

Idiopathic hypereosinophilia is clonal disorder? Clonality identified by targeted sequencing

Jee-Soo Lee, Heewon Seo, Kyongok Im, +14

PLoS ONE

ImmunohematologyGene Rearrangement AssaysGeneticsImmunodeficienciesImmunology +27

Exome sequencing and subsequent association studies identify five amino acid-altering variants influencing human height

Jae-Jung Kim, Young-Mi Park, Kyu-Heum Baik, +14

Human Genetics

Genome-wide Association StudyAllelic VariantGenotype-phenotype AssociationExome SequencingGenetics +6

HapAnalyzer: Minimum Haplotype Analysis System for Association Studies

Ho Youl Jung, Jung Sun Park, Yun Ju Park, +3

Genomics & Informatics

GeneticsGenetic EpidemiologyGenomicsMinimum Analysis MethodsGenome-wide Association Studies +16

Exome sequencing identifies KIAA1377 and C5orf42 as susceptibility genes for monomelic amyotrophy

Young‐Min Lim, InSong Koh, Young-Mi Park, +13

Neuromuscular Disorders

Neurodegenerative DiseasesAmyotrophic Lateral SclerosisMolecular NeuroscienceMendelian DisorderGenetic Disorder +9