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1. Whole Exome Sequencing in Patients with Phenotypically Associated Familial Intracranial Aneurysm [ KOREAN JOURNAL OF RADIOLOGY ] - 2022.01.23
2. 부계 완간역위에서 유래한 11pter 중복과 11qter 결실로 발생한 Beckwith-Wiedemann 증후군과 Jacobsen 증후군 1예 [ Laboratory Medicine Online ] - 2020.07.01
3. First Case of Double T-Cell Receptor Alpha/Delta Rearrangements of t(11;14) and inv(14) and Subsequent JAK2 Rearrangement in a Patient With T-cell Acute Lymphoblastic Leukemia [ ANNALS OF LABORATORY MEDICINE ] - 2020.01.01
4. Clinical and Cytogenetic Profiles of Rhabdomyosarcoma with Bone Marrow Involvement in Korean Children: A 15-Year Single-Institution Experience [ ANNALS OF LABORATORY MEDICINE ] - 2018.03.01
5. Langer?Giedion Syndrome with 8q23.1?q24.13 Deletion by Complex Three-way Translocation [ Laboratory Medicine Online ] - 2018.01.01
6. Clinical Manifestation and PRRT2 Analysis of Korean Patients with Paroxysmal Kinesigenic Dyskinesia [ 대한소아신경학회지 ] - 2017.12.01
7. Prognostic significance of recurrent additional chromosomal abnormalities in adult patients with Philadelphia chromosome-positive acute lymphoblastic leukemia [ CANCER GENETICS ] - 2017.10.01
8. A t(8;9)(p22;p24)/PCM1-JAK2 translocation in a patient with myeloproliferative neoplasm and myeloid Sarcoma: first report in Korea [ Annals of Laboratory Medicine ] - 2016.01.01
9. FISH analysis of MLL gene rearrangements: detection of the concurrent loss or gain of the 3' signal and its prognostic significance. [ International Journal of Laboratory Hematology ] - 2014.10.03
10. A de novo microdeletion of ANKRD11 gene in a Korean patient with KBG syndrome [ Annals of Laboratory Medicine ] - 2014.09.05
11. Cytogenetic classification in Korean multiple myeloma patients: prognostic significance of hyperdiploidy with 47-50 chromosomes and the number of structural abnormalities [ EUROPEAN JOURNAL OF HAEMATOLOGY ] - 2014.04.04
12. RANBP2-ALK fusion combined with monosomy 7 in acute myelomonocytic leukemia [ Cancer Genetics ] - 2014.01.03
13. An illustrative case of t(14;19)/BCL3 rearrangement as a karyotypic evolution of chronic lymphocytic leukemia [ ANNALS OF HEMATOLOGY ] - 2013.12.01
14. Double-hit myeloma with IGH/MYC and IGH/CCND1 translocations [ ANNALS OF HEMATOLOGY ] - 2013.08.15
15. Clinical characterization of DISP1 haploinsuf fi ciency: A case report [ European Journal of Medical Genetics ] - 2013.06.01
16. A Case of Systemic Mastocytosis Associated with Acute Myeloid Leukemia Terminating as Aleukemic Mast Cell Leukemia after Allogeneic Hematopoietic Stem Cell Transplantation [ Annals of Laboratory Medicine ] - 2013.03.01
17. OBFC2A/RARA: a novel fusion gene in variant acute promyelocytic leukemia [ BLOOD ] - 2013.02.21
18. Application of an immune-magnetic cell sorting method for CD138-positive plasma cells in FISH analysis of multiple myeloma [ INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY ] - 2012.10.01
19. Identification of the mechanism underlying a human chimera by SNP array analysis [ AMERICAN JOURNAL OF MEDICAL GENETICS PART A ] - 2012.09.01
20. A rare case of Lennert’s type peripheral T-cell lymphoma with t(14;19)(q11.2;q13.3) [ INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY ] - 2012.06.01
21. 염색체 마이크로어레이를 이용한 표지염색체의 분자세포유전학적 특성 [ 대한의학유전학회 ] - 2011.12.31
22. Molecular cytogenetic and clinical characterization of a patient with a 5.6-Mb deletion in 7p15 including HOXA cluster [ AMERICAN JOURNAL OF MEDICAL GENETICS PART A ] - 2011.03.01
23. 염색체 Microarray 검사의 임상적 적용 [ 대한의학유전학회 ] - 2010.12.31
24. 3q29 미세결손증후군에서 Oligonucleotide Array ComparativeGenomicHybridization에 의한 새로운 결손 부위의 검출 [ KOREAN JOURNAL OF LABORATORY MEDICINE ] - 2010.02.01
25. Prognostic significance of TEL/AMl1 rearrangement and its additional genetic changes in Korean childhood precursor B-acute lymphoblastic leukemia [ KOREAN JOURNAL OF LABORATORY MEDICINE ] - 2010.02.01
26. 3q21q26 증후군의 혈액학적, 임상적 소견: 불량한 예후 및 중추성 요붕증과의 연관성 [ 대한진단검사의학회지 ] - 2007.04.15
27. 한국인 만성골수성백혈병 환자의 Imatinib (STI-571) 내성 및 BCR-ABL 유전자 돌연변이 검출 [ 대한혈액학회지 ] - 2005.06.01

1. 유전체염기서열분석에서 부수적으로 발견(Incidental findings)된 변이에 대한 보고(Reporting) 가이드라인 마련 - 2022.04.05 ~ 2023.04.04
2. 소비자대상 직접(DTC) 유전자검사 서비스 인증제 도입을 위한 3차년도 시범사업 연구 - 2021.04.01 ~ 2021.11.01
3. DTC 유전자 검사 서비스 인증제 도입을 위한 2차년도 시범사업 연구 - 2020.04.09 ~ 2021.01.31
4. DTC 유전자검사 서비스 인증제 도입을 위한 시범사업 - 2019.04.05 ~ 2019.12.10
5. 급성백혈병에서 신규 융합유전자의 발굴과 맞춤진료(3) - 2015.06.01 ~ 2016.05.31
6. 급성백혈병에서 신규 융합유전자의 발굴과 맞춤진료(2) - 2014.06.01 ~ 2015.05.31
7. 급성백혈병에서 신규 융합유전자의 발굴과 맞춤진료 - 2013.06.01 ~ 2014.05.31
8. 희귀 염색체 이상 질환의 분자세포 유전학적 진단 및 관리지침 개발 - 2011.04.01 ~ 2012.03.31
9. 희귀 염색체 이상 질환의 분자세포 유전학적 진단 및 관리지침 개발 - 2010.04.01 ~ 2011.03.31
10. 희귀 염색체이상 질환의 분자세포유전학적 진단 및 관리지침개발 - 2009.08.01 ~ 2010.03.31
11. 희귀 염색체이상 질환의 분자세포유전학적 진단 및 관리지침개발 - 2008.08.01 ~ 2009.03.31

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