Medical Genetics244

Pub YearTitleAJOU Author(s)
2013Association between the SPRY1 gene polymorphism and obesity-related traits and osteoporosis in Korean women.김보영, 정선용, 정윤석, 진현석
2011Association of 20 potential ATP2B1-interacting genes with blood pressure in Koreans.진현석
2015Association of the I264T variant in the sulfide quinone reductase-like (SQRDL) gene with osteoporosis in Korean postmenopausal women.김범택, 김정현, 박은국, 정선용
2020Ataxia Associated with CADASIL: a Pathology-Confirmed Case Report and Literature Review박동규, 손성향, 손영배, 윤정한
2012Auditory characteristics and therapeutic effects of enzyme replacement in mouse model of the mucopolysaccharidosis (MPS) II손영배
2024Biomarkers of Glycosaminoglycans (GAG) accumulation in patients with mucopolysaccharidosis type VI—LeukoGAG, Corneal Opacification (COM) and Carotid Intima Media Thickening (CIMT)손영배
1996Buschke-Ollendorff Syndrome(A Case Report)김병석, 김현주, 원예연, 이은소, 주희재, 한경진
2016Caloric restriction improves diabetes-induced cognitive deficits by attenuating neurogranin-associated calcium signaling in high-fat diet-fed mice김정현, 정선용
2016Caloric restriction of db/db mice reverts hepatic steatosis and body weight with divergent hepatic metabolism김정현, 정선용
2015Case of mild Schmid-type metaphyseal chondrodysplasia with novel sequence variation involving an unusual mutational site of the COL10A1 gene.손영배
2016Cerebellar vermis hypoplasia in CHARGE syndrome: clinical and molecular characterization of 18 unrelated Korean patients손영배
2015Cerebral ischemia-induced mitochondrial changes in a global ischemic rat model by AFM.박은국
2008Challenge of Personalized Medicine in the Genomic Era김현주
2013Characterization of functional variants in 33 blood pressure loci using 1000 genomes project data.진현석
2012Characterization of the ATP2B gene family in blood pressure진현석
2005Childhood X-linked adrenoleukodystrophy: clinical-pathologic overview and MR imaging manifestations at initial evaluation and follow-up.김현주
2019Cirsium japonicum var. maackii and apigenin block Hif-2alpha-induced osteoarthritic cartilage destruction강이중, 박은국, 양시영, 정선용
1999Clinical Analysis of 1,068 Cases of Mid-trimester Genetic Amniocentesis김행수, 김현주, 양정인, 오기석
2013Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization.김성환, 박문성, 손영배, 이장훈
2013Clinical and cytogenetic features of a Potocki-Lupski syndrome with the shortest 0.25Mb microduplication in 17p11.2 including RAI1.손영배, 임신영
2011Clinical and genetic characteristics of Korean patients with Gaucher disease.김현주, 정선용
2013Clinical and genetic spectrum of 18 unrelated Korean patients with Sotos syndrome: frequent 5q35 microdeletion and identification of four novel NSD1 mutations.손영배, 정선용, 진현석
2003Clinical and neuroradiological features of patients with spinocerebellar ataxias from Korean kindreds.김현주, 방오영, 이필휴, 허균
2017Clinical characteristics and mutation spectrum of GLA in Korean patients with Fabry disease by a nationwide survey: Underdiagnosis of late-onset phenotype손영배
2010Clinical characterization and analysis of the SRD5A2 gene in six Korean patients with 5alpha-reductase type 2 deficiency.고정민
2013Clinical characterization and molecular classification of 12 Korean patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism.손영배
2010Clinical features and outcomes of holoprosencephaly in Korea.고정민, 김성환
2017Clinical, biochemical and molecular characterization of Korean patients with mucolipidosis II/III and successful prenatal diagnosis손영배
2012Clinical, biochemical, and genetic analysis of two korean patients with trichorhinophalangeal syndrome type I and growth hormone deficiency김옥화, 손영배
2012Clinical, radiologic, and genetic features of Korean patients with Mucopolysaccharidosis IVA손영배
2010Cognitive Profile of Children with Williams Syndrome: Comparison with Children with Prader-Willi Syndrome and Down Syndrome김현주, 임신영
2018Concurrent TSHR mutations and DIO2 T92A polymorphism result in abnormal thyroid hormone metabolism김정현, 박은국, 정선용
2012Continuous renal replacement therapy in neonates weighing less than 3 kg손영배
2007Controversial issues in the legal restriction for Prenatal genetic testing in Korea김현주, 정선용
2019Correction to: Neuronopathic Gaucher disease presenting with microcytic hypochromic anemia손영배
2012Correlation Between Unidentified Bright Objects on Brain Magnetic Resonance Imaging (MRI) and Cerebral Glucose Metabolism in Patients with Neurofibromatosis Type 1김현주, 손영배, 안영실, 이수진, 정선용, 최진욱
2010De novo pericentric inversion of chromosome 9 in congenital anomaly.정선용
2019Deletion of exons 16-17b of CFTR is frequently identified in Korean patients with cystic fibrosis손영배, 장주영
2016Determination of Autosomal Dominant or Recessive Methionine Adenosyltransferase I/III Deficiencies Based on Clinical and Molecular Studies손영배
2007Development of medical genetics training program and certification process for medical geneticist as a specialist in Korea김현주
2012Diagnosis and constitutional and laboratory features of Korean girls referred for precocious puberty손영배
2001Diagnostic patterns of very-long-chain fatty acids in plasma of patients with X-linked adrenoleukodystrophy.김현주
2015Disease-specific growth charts for Korean infants with Prader-Willi syndrome.손영배
2015Disease-specific Growth Charts of Marfan Syndrome Patients in Korea.손영배
2019Drp1 Phosphorylation Is Indispensable for Steroidogenesis in Leydig Cells정선용
2010Early Diagnosis of Fabry Disease in a Patient with Toe Tip Pain고정민, 김찬, 한경림
2015Effect of systemic high dose enzyme replacement therapy on the improvement of CNS defects in a mouse model of mucopolysaccharidosis type II.손영배
2016Effects of Dihydrophaseic Acid 3'-O-beta-d-Glucopyranoside Isolated from Lycii radicis Cortex on Osteoblast Differentiation김정현, 박은국, 정선용
2022Effects of Loganin on Bone Formation and Resorption In Vitro and In Vivo김정현, 박은국, 정선용
2004Effects of Pamidronate Treatment on Osteogenesis Imperfecta김대중, 김현주, 이관우, 정윤석
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