1 Chang SP， Ma GC， Chen M*， Wu SH*. Species and sex comparisons of karyotype and genome size in two Kurixalus tree frogs (Anura， Rhacophoridae). ACTA HERPETOLOGICA. 2017-09(Accepted). (Original Article， SCI， IF=0.654， Zoology: 127/163) Co-corresponding author.
2 Chen HF， Chen SU， Ma GC， Hsieh ST， Tsai HD， Yang YS， Chen M. Preimplantation Genetic Diagnosis and Screening: Current Status and Future Challenges. JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION. 2017-09. (In press). (Review， SCI， IF=1.969， Medicine， General & Internal: 46/154) doi: 10.1016/j.jfma.2017.08.006.
3 Chen CP， Chen M， Chern SR， Chang SP， Chen SW， Lai ST， Chen WL， Lee MS， Wang W. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2017-08. 56(4):566-8. (Case Report， SCI)
4 Chen CP， Chen M， Wu CH， Lin CJ， Chern SR， Wu PS， Chen YN， Chen SW， Chang SP， Chen LF， Wang W. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2017-08. 56(4):554-7. (Case Report， SCI)
5 Chen CP， Chen M， Wang LK， Chern SR， Wu PS， Chen SW， Lai ST， Chang SP， Yang CW， Pan CW， Wang W. Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2017-08. 6(4):527-33. (Short Communication， SCI)
6 Chen CP， Chen M， Hwu YM， Chang SP， Chen SW， Lai ST， Lee CC， Wang W. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 7 in the male partner of a phenotypically normal couple with repeated spontaneous abortions. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2017-06. 56(3):410-1. (Research Letter， SCI)
7 Chen CP， Chen M， Wang PT， Chern SR， Chen SW， Lai ST， Wu PS， Chang SP， Pan CW， Wang W. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2017-06. 56(3):394-7. (Case Report， SCI)
8 Ma GC， Wu WJ， Lee MH， Lin YS， Chen M. Normal prenatal ultrasound findings reflect outcome in case of trisomy 14 confined placental mosaicism developing after preimplantation genetic diagnosis. ULTRASOUND IN OBSTETRICS & GYNECOLOGY. 2017-07. 50(1):128-130. (Letter to the Editor， SCI， IF=4.71， Obstetrics & Gynecology: 6/80; Acoustics: 1/32; Radiology， Nuclear Medicine & Medical Imaging: 11/126)
9 Wu WJ， Shih JC， Sago H， Chen M. Complete resolution of hydrops by placement of double basket catheter in a case of macrocystic type multilocular pulmonary sequestration. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2017-06. 56(3):402-5. (Case Report， SCI)
10 Chen CP， Chen M， Chang SP， Hung FY， Lee MJ， Chern SR， Wu PS， Chen YN， Chen SW， Lee CC， Town DD， Chen WL， Wang W. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 2. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2017-04. 56(2):234-7. (Case Report， SCI)
11 Wu WJ， Ma GC， Lee MH， Chen YC， Chen M. The use of low molecular weight heparin reduced the fetal fraction and rendered the cell-free DNA testing for trisomy 21 false negative. ULTRASOUND IN OBSTETRICS & GYNECOLOGY. 2017-03. doi: 10.1002/uog.17473 (in press) (Letter to the Editor， SCI， IF=4.71， Obstetrics & Gynecology: 6/80; Acoustics: 1/32; Radiology， Nuclear Medicine & Medical Imaging: 11/126)
12 Lin PH， Li HY， Fan SC， Yuan TH， Chen M， Hsu YH， Yang YH， Li LY， Yeh SP， Bai LY， Liao Y， Lin CY， Hsieh CY， Lin CC， Lin CH， Lien MY， Chen TT， Ni YH， Chiu CF. A targeted next-generation sequencing in the molecular risk stratification of adult acute myeloid leukemia: implications for clinical practice. CANCER MEDICINE. 2017-01. doi: 10.1002/cam4.969. (Original Research， SCI， IF= 3.362， Onology: 90/217)
13 Wu WJ， Ma GC， Lin YS， Yeang CH， Ni YH， Li WC， Tsai HD， Gau SS， Chen M*. Detection of 22q11.2 microduplication by cell-free DNA screening and chromosomal microarray in fetus with multiple anomalies. ULTRASOUND IN OBSTETRICS & GYNECOLOGY. 2016-10. 48(4):530-532. (Letter to the Editor， SCI， IF=4.71， Obstetrics & Gynecology: 6/80; Acoustics: 1/32; Radiology， Nuclear Medicine & Medical Imaging: 11/126)
14 Shen MC， Chen M， Ma GC， Chang SP， Lin CY， Lin BD， Hsieh HN. De novo mutation and somatic mosaicism of gene mutation in type 2A， 2B and 2M VWD. THROMBOSIS JOURNAL. 2016-10. 14(Suppl 1):36. (Research， Peer reviewed article)
15 Chen M， Chang SP， Ma GC， Lin WH， Chen HF， Chen SU， Tsai HD， Tsai FP， Shen MC. Preimplantation genetic diagnosis of hemophilia A. THROMBOSIS JOURNAL. 2016-10. 14(Suppl 1): 33. (Review， Peer reviewed article)
16 Shen MC， Wu WJ， Cheng PJ， Ma GC， Li WC， Liou JD， Chang CS， Lin WH， Chen M. Low-molecular-weight-heparin can benefit women with recurrent pregnancy loss and sole protein S deficiency: a historical control cohort study from Taiwan. THROMBOSIS JOURNAL. 2016-10. 28;14:44. (Research， Peer reviewed article)
17 Huang KY， Kuo KT， Li YP， Chen M， Yu CU， Shih JC. Urorectal septum malformation sequence-Fetal series with the description of a new "intermediate" variant. Time to refine the terminology? AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2016-09. 170(9):2479-82. (Research Letter， SCI， IF=2.259， Genetics & Heredity: 99/166)
18 Cheng HH#， Ma GC#， Tsai CC#， Wu WJ， Lan KC， Hsu TY， Yang CW， Chen M*. Confined placental mosaicism of double trisomies 9 and 21: discrepancy among noninvasive prenatal testing， chorionic villus sampling， and postnatal confirmation. ULTRASOUND IN OBSTETRICS & GYNECOLOGY. 2016-08. 48(2):251-3. (Letter to the Editor， SCI， IF=4.71， Obstetrics & Gynecology: 6/80; Acoustics: 1/32; Radiology， Nuclear Medicine & Medical Imaging: 11/126)
19 Ma GC， Chen HF， Yang YS， Lin WH， Tsai FP， Lin CF， Chiu C， Chen M*. A pilot proof-of-principle study to compare fresh and vitrified cycle preimplantation genetic screening by chromosome microarray and next generation sequencing. MOLECULAR CYTOGENETICS. 2016-03. 21;9:25. (Research， SCI， IF=1.455， Genetics & Heredity: 131/166)
20 Yang YS#， Chang SP#， Chen HF#， Ma GC#， Lin WH， Lin CF， Tsai FP， Wu CH， Tsai HD， Lee TH ，Chen M*. Preimplantation genetic screening of blastocysts by multiplex qPCR followed by fresh embryo transfer: validation and verification. MOLECULAR CYTOGENETICS. 2015-07. 8:49. (Research， SCI， IF=1.455， Genetics & Heredity: 131/166)
21 Leung KY， Poon CF， Teotico AR， Hata T， Won HS， Chen M， Chittacharoen A， Malhotra J， Shah PK， Salim A; Ultrasound Committee， Asia and Oceania Federation of Obstetrics & Gynaecology. Recommendations on routine mid-trimester anomaly scan. JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH. 2015-05. 41(5):653-61. (AOFOG Committee Report， SCI)
22 Wu WJ#， Ma GC#， Wu PC， Huang KS， Liu YL， Chang SP， Ginsberg NA， Chen M*. 2015. Lessons learned from two missed prenatal cases of hemoglobin Bart’s hydrops fetalis until second trimester despite a nationwide screening program. Hereditary Genet S7: 003. (Peer reviewed article)
23 Tsai MC， Cheng HY， Su MT， Chen M， Kuo PL. Partial trisomy 8 mosaicism not detected by cultured amniotic-fluid cells. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2014-12. 53(4):598-601. (Case Report， SCI)
24 Chen HF， Chang SP， Wu SH， Lin WH， Lee YC， Ni YH， Chen CA， Ma GC， Ginsberg NA， You EM， Tsai FP， Chen M*. Validating a rapid， real-time， PCR-based direct mutation detection assay for preimplantation genetic diagnosis. GENE. 2014-09. 5;548(2):299-305. (Methods Paper， SCI ， IF=2.415， Genetics & Heredity: 89/166)
25 Yeang CH， Ma GC， Hsu HW， Lin YS， Chang SM， Cheng PJ， Chen CA， Ni YH， Chen M*. Genome-wide normalized score: a novel counting algorithm to detect fetal trisomy 21 in non-invasive prenatal testing. ULTRASOUND IN OBSTETRICS & GYNECOLOGY. 2014-07. 44(1):25-30. (Original Paper， SCI ， IF=4.71， Obstetrics & Gynecology: 6/80; Acoustics: 1/32; Radiology， Nuclear Medicine & Medical Imaging: 11/126)
26 Chen M#， Yang YS#， Shih JC， Lin WH， Lee DJ， Lin YS， Chou CH， Cameron AD， Ginsberg NA， Chen CA， Lee ML， Ma GC. Microdeletions/duplications involving TBX1 gene in fetuses with conotruncal heart defects which are negative for 22q11.2 deletion on fluorescence in-situ hybridization. ULTRASOUND IN OBSTETRICS & GYNECOLOGY. 2014-04. 43(4):396-403. (Original Paper， SCI ， IF=4.71， Obstetrics & Gynecology: 6/80; Acoustics: 1/32; Radiology， Nuclear Medicine & Medical Imaging: 11/126)
27 Jhang KM， Chang TM， Chen M， Liu CS. Generalized epilepsy in a patient with mosaic Turner syndrome: a case report. JOURNAL OF MEDICAL CASE REPORTS. 2014-04. 2;8:109. (Case Report， Peer reviewed article)
28 Chen CP， Chen M， Su YN， Chern SR， Wu PS， Chang SP， Kuo YL， Chen WL， Wang W. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2014-03. 53(1):129-32. (Research Letter， SCI)
29 Shaw SW， Hsiao CH， Chen CY， Ren Y， Tian F， Tsai C， Chen M， Cheng PJ. Noninvasive prenatal testing for whole fetal chromosomal aneuploidies: a multicenter prospective cohort trial in Taiwan. FETAL DIAGNOSIS AND THERAPY. 2014-02. 35(1):13-7. (Original Paper， SCI ， IF=2.323， Obstetrics & Gynecology= 23/80)
30 Hsu HK， Su MT， Chen M， Yen P， Kuo PL. Two Y chromosomes with duplication of the distal long arm including the entire AZFc region. GENE. 2014-02. 25;536(2):444-8. (Short Communication， SCI ， IF=2.415， Genetics & Heredity: 89/166)
31 Chen CP， Chen M， Chen CY， Chern SR， Wu PS， Chang SP， Kuo YL， Chen WL， Pan CW， Wang W. Prenatal diagnosis and molecular cytogenetic characterization of de novo pure partial trisomy 6p associated with microcephaly， craniosynostosis and abnormal maternal serum biochemistry. GENE. 2014-02. 25;536(2):425-9. (Short Communication， SCI ， IF=2.415， Genetics & Heredity: 89/166)
32 Kuan LC， Su MT， Chen M， Kuo PL， Kuo TC. A non-mosaic isodicentric Y chromosome resulting from breakage and fusion at the Yq pseudo-autosomal region in a fetus. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS. 2013-12. 30(12):1559-62. (Genetics， SCI ， IF=2.163， Obstetrics & Gynecology: 38/80; Genetics & heredity: 106/166)
33 Shaw SSW， Hsiao CH， Chen CY， Ren Y， Tian F， Tsai C， Chen M， Cheng PJ. Noninvasive Prenatal Testing for Whole Fetal Chromosomal Aneuploidies: A Multicenter Prospective Cohort Trial in Taiwan. FETAL DIAGNOSIS & THERAPY. 2013-11. 35(1):13-7. (Original Paper， SCI ， IF=2.699， Obstetrics & Gynecology: 23/80)
34 Lin LK， Ma GC， Chen TH， Lin WH， Lee DJ， Wen PY， Wu SH， Chen M*. Genomic analyses of the Formosan harvest mouse (Micromys minutus) and comparisons to the brown Norway rat (Rattus norvegicus) and the house mouse (Mus musculus). ZOOLOGY. 2013-10. 116(5):307-15. (Original Paper， SCI ， IF=1.51， Zoology: 46/162)
Chen CP， Chen M， Su YN， Huang JP， Chern SR， Wu PS， Su JW， Chang SP， Chen YT， Lee CC， Chen LF， Pan CW， Wang W. Mosaic small supernumerary marker chromosome 1 at amniocentesis: Prenatal diagnosis， molecular genetic analysis and literature review. GENE. 2013-10. 529(1):169-75. (Short Communication， SCI ， IF=2.415， Genetics & Heredity: 89/166)
35 Kuan LC， Su MT， Chen M， Kuo PL， Kuo TC. A dicentric Y chromosome resulting from pericentric inversion between the centromere and Yq heterochromatin. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2013-09. 52(3):443-5. (Research Letter， SCI)
36 Lin CJ， Wang SC， Ku CL， Kao JK， Chen M， Liu CS. Successful Unrelated Cord Blood Stem Cell Transplantation in an X-linked Chronic Granulomatous Disease Patient with Disseminated BCG-induced Infection. PEDIATRICS AND NEONATOLOGY. 2013-03. S1875-9572(13)00070-3. (Case report， SCI ， IF=1.287， Pediatrics: 78/121)
37 Chen CP， Chen M， Ma GC， Su YN， Ko TM， Lin YH， Wang W. Array comparative genomic hybridization characterization of prenatally detected de novo apparently balanced reciprocal translocations with or without genomic imbalance in other chromosomes. JOURNAL OF THE CHINESE MEDICAL ASSOCIATION. 2013-01. 76(1):53-6. (Case report， SCI ， IF=1.252， Medicine， General & Internal: 82/154)
38 Su SL， Wang WF， Wu SL， Wu HM， Chang JC， Huang CS， Cheng WL， Soong BW， Lee YC， Li JY， Kuo SJ， Chen M， Huang CN， Liu CS. FGF21 in ataxia patients with spinocerebellar atrophy and mitochondrial disease. CLINICA CHIMICA ACTA. 2012-09. 414:225–227. (Original Research， SCI ， IF= 2.873， Medical Laboratory Technology: 8/30)
39 Chen CP， Chen M， Su YN， Huang JP， Ma GC， Chang SP， Chern SR， Chen YT， Su JW， Lee CC， Town DD， Wang W. Inv dup del(10q): Identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2012-06. 51(2): 245-252. (Short Communication， SCI)
40 Chen CP， Chang SD， Su YN， Chen M， Chern SR， Su JW， Chen YT， Chen WL， Pan CW， Lee MS， Wang W. Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase fluorescence in situ hybridization， quantitative fluorescent polymerase chain reaction， and array comparative genomic hybridization on uncultured amniocytes in a pregnancy with fetal pyelectasis. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2012-06. 51(3):405-410. (Short Communication， SCI)
41 Yu HT#， Ma GC#， Lee DJ， Chin SC， Chen TL， Tsao HS， Lin WH， Wu SH， Lin CC， Chen M*. Use of a cytogenetic whole-genome comparison to resolve phylogenetic relationship among three species: implications for mammalian systematics and conservation biology. THERIOGENOLOGY. 2012-05. 77(8): 1615-1623. (Research Article， SCI ， IF= 1.986， Veterinary Science: 15/136; Reproductive Biology: 20/29)
42 Yeang CH#， Ma GC#， Shih JC， Yang YS， Chen CP， Chang SP， Wu SH， Liu CS， Kuo SJ， Chou HC， Hwu WL， Cameron AD， Ginsberg NA， Lin YS， Chen M*. Genome-wide gene expression analysis implicates the immune response and lymphangiogenesis in the pathogenesis of fetal chylothorax. PLoS ONE. 2012-03. 7(4): e34901. (Research Article， SCI ， IF= 2.806， Multidisciplinary Sciences: 15/64)
43 Chen CP， Su YN， Chen M， Tsai FJ， Chen YY， Ma GC， Chang SP， Su JW， Chen YT， Chen WL， Chen LF， Wang W. Unexplained shortening of the long bones in the third trimester as the only prenatal feature in a male fetus with 45，X/46，X，r(Y) mosaicism. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2012-03. 51(1): 134-138. (Research Letter， SCI)
44 Yang YS#， Ma GC#， Shih JC， Chen CP， Chou CH， Yeh KT， Kuo SJ， Chen TH， Hwu WL， Lee TH， Chen M*. Experimental treatment of bilateral fetal chylothorax using in utero pleurodesis. ULTRASOUND IN OBSTETRICS & GYNECOLOGY. 2012-01. 39(1):56-62. (Original Paper， SCI ， IF=4.71， Obstetrics & Gynecology: 6/80; Acoustics: 1/32; Radiology， Nuclear Medicine & Medical Imaging: 11/126)
45 Kuo SJ#， Ma GC#， Chang SP#， Wu HH， Chen CP， Chang TM， Lin WH， Wu SH， Lee MH， Hwu WL， Chen M*. Preimplantation and prenatal genetic diagnosis of aromatic L-amino acid decarboxylase deficiency with an amplification refractory mutation system-quantitative polymerase chain reaction. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2011-12. 50(4): 468-73. (Original Article， SCI)
46 Chen CP#*， Huang HK#， Ling PY， Su YN， Chen M， Tsai FJ， Wu PC， Chern SR， Chen YT， Lee CC， Wang W. A de novo duplication of chromosome 21q22.11/qter associated with Down syndrome: Prenatal diagnosis， molecular cytogenetic characterization and fetal ultrasound findings. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2011-12. 50(4): 492-98. (Short Communication， SCI)
47 Chen CP*， Su YN， Chen M， Huang JP， Tsai FJ， Wu PC， Chen WL， Wang W. Prenatal diagnosis and molecular cytogenetic characterization of a mosaic derivative Y chromosome derived from a de novo unbalanced reciprocal Yq;13q translocation. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2011-9. 50(3): 394-8. (Research Letter， SCI)
48 Chen CP#*， Chen M#， Pan YJ， Su YN， Chern SR， Tsai FJ， Chen YT， Wang W. Prenatal diagnosis of mosaic trisomy 8: Clinical report and literature review. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2011-9. 50(3): 331-8. (Short Communication， SCI)
49 Kuan LC， Su MT， Wu CM， Chen M， Kuo PL， Kuo TC*. A family with Xq22.3q25 interstitial deletion and normal ovarian function. FERTILITY AND STERILITY. 2011-7. 96(1):e29-34. (Original Article， SCI， IF=4.373， Obstetrics & Gynecology: 8/80; Reproductive Biology: 3/29)
50 Chen CP*， Lin SP， Chen M， Su YN， Chern SR， Wang TY， Liu YP， Tsai FJ， Lee CC， Chen YJ， Wang W. Mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy facial asymmetry psychomotor retardation kyphoscoliosis dermatofibrosarcoma and multiple exostoses. GENETIC COUNSELING. 2011-7. 22(3): 273-80. (Case report， SCI)
51 Yu HT#， Ma GC#， Lee DJ#， Chin SC， Tsao HS， Wu SH， Shin SY， Chen M*. Molecular delineation of the Y-borne Sry gene in the Formosan pangolin (Manis pentadactyla) and its phylogenetic implications for Pholidota in extant mammals. THERIOGENOLOGY. 2011-6. 75(1): 55-64. (Research Article， SCI， IF= 1.986). Veterinary Science: 15/136; Reproductive Biology: 20/29)
52 Chen CP*， Chen M， Ma GC， Chang SP， Chen YY， Wu PC， Chen LF， Wang W. Prenatal diagnosis and molecular cytogenetic characterization of a small marker chromosome derived from Y chromosome. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2011-6. 50(2): 253-7. (Case Report， SCI)
53 Chen CP*， Chen M， Su YN， Tsai FJ， Chern SR， Wu PC， Chen WL， Chen LF， Pan CW， Wang W. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2011-6. 50(2): 188-95. (Short Communication， SCI)
54 Lee IW， Chou YY， Hsu KF， Chou PY， Chen M， Kuo PL， Lin SJ*. Complex Chromosome Rearrangement 46，XY，der(9)t(Y;9)(q12;p23) in a Girl With Sex Reversal and Mental Retardation. UROLOGY. 2011-5. 77(5): 1213-6. (Pediatric Case Report， SCI ， IF= 2.309， Urology & Nephrology: 30/76)
55 Huang SW， Lin YY， You EM， Liu TT， Shu HY， Wu KM， Tsai SF， Lo CF， Kou GH， Ma GC， Chen M， Wu D， Aoki T， Hirono I ，Yu HT. Fosmid library end sequencing reveals a rarely known genome structure of marine shrimp Penaeus monodon. BMC GENOMICS. 2011-5. 12: 242. (Research Article， SCI ， IF= 3.729， Biotechology & Applied Microbiology: 33/158; Genetics & Heredity: 50/166)
56 Ma GC， Ke YY， Chang SP， Lee DJ， Chen YC， Chen M*. A compound heterozygous GNPTAB mutation causes mucolipidosis II with marked hair color change in a Han Chinese baby. AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2011-3. 155(4): 931-4. (Research Letter， SCI ， IF=2.259， Genetics & Heredity: 99/166)
57 Lee ML， Chen M， Tsao LY， Chiu HY， Chiu IS， Yang AD， Tsai PL. Congenital stridor and wheezing as harbingers of the del22q11.2 syndrome presenting cardiovascular malformations of right aortic arch， aberrant left subclavian artery， Kommerell's diverticulum， and left ligamentum arteriosum. CARDIOVASCULAR PATHOLOGY. 2011-3. 20(2): 124-9. (Case Report， SCI ， IF= 2.359， Cardiac & Cardiovascular Systems: 62/126; Pathology: 30/79)
58 Chen ZH， Chen M， Tsai HD， Wu CH* Intrapartum uterine rupture associated with a scarred cervix because of a previous rupture of cystic cervical endometriosis. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2011-3. 50(1): 95-7. (Research Letter， SCI)
59 Chen CP， Chen M， Ko TM， Ma GC， Tsai FJ， Tsai MS， Wu PC， Lee CC， Chen LF， Wang W. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2010-12. 49(4): 500-5. (Case Report， SCI)
60 Lee NC， Chen M， Ma GC， Lee DJ， Wand TJ， Ke YY， Chien YH， Hwu WL. Complex rearrangements between chromosomes 6， 10 and 11 with multiple deletions at breakpoints. AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2010-9. 152A(9): 2327-34. (Clinical Report， SCI， IF=2.259， Genetics & Heredity: 99/166)
61 Kuo SJ#， Chen M#， Ma GC#， Chen ST， Chang SP， Lin W-Y， Chen YC， Lee TH， Lin TT， Liu CS. Number of somatic mutations in the mitochondrial D-loop region indicates poor prognosis in breast cancer， independent of TP53 mutation. CANCER GENETICS AND CYTOGENETICS (CANCER GENETICS). 2010-9. 201(2): 94-101. (Original Article， SCI ， IF= 1.930， Onology: 161/217; Genetics & Heredity: 108/166)
62 Chen CP， Chen M， Su YN， Tsai FJ， Chern SR， Hsu CY， Wu PC， Town DD， Lee DJ， Ma GC， Wang W. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3→pter) and partial monosomy 13q (13q33.3→qter) associated with dandy-walker malformation， abnormal skull develipment and microcephaly. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2010-9. 49(3): 320-6. (Short Communication， SCI)
63 You EM， Liu KF， Huang SW， Chen M， Groumellec ML， Fann SJ， Yu HT. Construction of integrated genetic linkage maps of the tiger shrimp (Penaeus monodon) using microsatellite and AFLP markers. ANIMAL GENETICS. 2010-8. 41(4): 365-76. (Original Article， SCI ， IF= 1.815. Agriculture， Dairy & Animal Science: 3/55; Genetics & Heredity: 90/158)
64 Lee ML*， Chen M， Yang AD， Chiu IS. Mirror-image type D interrupted aortic arch: A novel cardiac phenotype providing some perspective in the del22q11.2 syndrome. INTERNATIONAL JOURNAL OF CARDIOLOGY. 2010-6. 141(3): e47-50. (Letter to the Editor， SCI ， IF= 6.189， Cardiac & Cardiovascular Systems: 16/126)
65 Wu CC， Liu MT， Chang YT， Fang CY， Chou SP， Liao HW， Kuo KL， Hsu SL， Chen YR， Wang PW， Chen YL， Chuang HY， Lee CH， Chen M， Wayne Chang WS， Chen JY. Epstein-Barr Virus DNase (BGLF5) induces genomic instability in human epithelial cells. NUCLEIC ACIDS RESEARCH. 2010-4. 38(6): 1932-49. (Original Article， SCI ， IF= 10.162). Biochemistry & Molocular Biology: 14/286)
66 Chen M， Ke YY， Chang SP， Lee DJ， Chen CH， Ma GC*. Prenatal transient alveolomaxillary defect in a case of Mucolipidosis II (I-cell disease). ULTRASOUND IN OBSTETRICS & GYNECOLOGY. 2010-3. 36(2): 255-8. (Letter to the Editor， SCI ， IF=4.71， Obstetrics & Gynecology: 6/80; Acoustics: 1/32; Radiology， Nuclear Medicine & Medical Imaging: 11/126)
67 Ma GC， Ke YY， Lee ML， Tsao LY， Lee DJ， Yang CW， Kuo SJ， Chiu HY， Chen M*. De novo triple segmental aneuploid of 1p， 1q and 4q in a girl with hypertrophic cardiomyopathy， muscle hypotonia and multiple congenital anomalies. AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2010-3. 152A(3): 784-8. (Research Letter， SCI， IF=2.259， Genetics & Heredity: 99/166)
68 Chen CH#， Chen TH#， Kuo SJ， Chen CD， Yang YS， Chen M*. Late Termination of Pregnancy: Experience From an East Asian Population and Report of a Novel Technique for Feticide. JOURNAL OF MEDICAL ULTRASOUND. 2009-12. 17(4):193-9. (Original Article， Peer reviewed article)
69 Lee NC， Chang SP， Chang CS， Chen CH， Lee DJ， Lin CC， Hwu WL， Chen M*. Cryptic subtelomeric deletion plus inverted duplication at chromosome 18q in a fetus: molecular delineation by multicolor banding. PRENATAL DIAGNOSIS. 2009-11. 29(11): 1058-60. (Research Letter， SCI ， IF=2.523， Genetics & Heredity: 82/166; Obstetrics & Gynecology: 25/80)
70 Chen CH， Chen TH， Kuo SJ， Chen CP， Lee DJ， Ke YY， Yeh KT， Ma GC， Liu CS， Shih JC， Chen M*. Genetic evaluation and management of fetal chylothorax: review and insights from a case of Noonan syndrome. LYMPHOLOGY. 2009-9. 42(3): 134-8. (Case Report ， SCI ， IF=1.079， Immunology: 139/150; Physiology: 75/84)
71 Chen M， Kuo HH， Huang YC， Ke YY， Chang SP， Chen CP， Lee DJ， Lee ML， Lee MH， Chen TH， Chen CH， LinHM， Liu CS， Ma GC*. A case of restrictive dermopathy with complete chorioamniotic membrane separation caused by a novel homozygous nonsense mutation in the ZMPSTE24 gene. AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2009-7. 149A(7): 1550-4. (Research Letter， SCI， IF=2.259， Genetics & Heredity: 99/166)
72 Chen LY， Chen TH， Wen PY， Ying TH， Chang SP， Chen M*. Differential expression of NUDT9 at different phases of menstrual cycle and different components of normal and neoplastic human endometrium. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2009-6. 48(2): 98-107. (Original Article， SCI)
73 Chen TH， Chen CH， Hong YC， Chen M*. Puerperal pelvic hematoma successfully treated by primary transcatheteral arterial embolization. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2009-6. 48(2): 200-2. (Research Letter， SCI)
74 Chen CH， Hsieh HC， Ysai HD， Chen TH， Chen M*. Cardiac tamponade-a new alternative procedure for late feticide: a case report and literature review. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2009-6. 48(2): 159-62. (Short Communication， SCI)
75 Ho WK， Wang YF， Wu HH， Tsai HD， Chen TH， Chen M*. Ruptured corpus luteum with hemoperitoneum: case characteristics and demographic changes over time. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2009-6. 48(2): 108-12. (Original Article， SCI)
76 Chen LY， Chen TH， Wen PY， Ying TH， Chang SP， Chen M*. Differential expression of NUDT9 at different phases of menstrual cycle and different components of normal and neoplastic human endometrium. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2009-6. 48(2): 98-107. (Original Article， SCI)
77 Lee ML， Tsao LY， Chiu HY， Chen M， Chiu IS. Outcomes in Neonates with Pulmonary Atresia and Intact Ventricular Septum Underwent Pulmonary Valvulotomy and Valvuloplasty Using a Flexible 2-French Radiofrequency Catheter. YONSEI MEDICAL JOURNAL. 2009-4. 50(2): 245-51. (Original Article， SCI， IF=1.287， Medicine， General & Internal: 70/154)
78 Lee ML*， Chen M. Diagnosis and Management of Congenital Coronary Arteriovenous Fistula in Pediatric Patients Presenting Congestive Heart Failure and Myocardial Ischemia. YONSEI MEDICAL JOURNAL. 2009-2. 50(1): 95-104. SCI ， IF=1.537). (Original Article， SCI， IF=1.287， Medicine， General & Internal: 70/154)
79 Ho WK， Wang YF， Wu HH， Tsai HD， Chen TH， Chen M*. Ruptured corpus luteum with hemoperitoneum: case characteristics and demographic changes over time. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2009. 48(2): 108-112. (Original Article， SCI)
80 Ma GC#， Liu CS，#， Chang SP， Yeh KT， Ke YY， Chen TH， Wang BBT， Kuo SJ， Shih JC， Chen M*. A recurrent ITGA9 missense mutation in human fetuses with severe chylothorax: possible correlation with poor response to fetal therapy. PRENATAL DIAGNOSIS. 2008. 28(11):1057-1063. (Original Paper， SCI ， IF=2.523， Genetics & Heredity: 82/166; Obstetrics & Gynecology: 25/80)
81 Ma GC#， Chang SP#， Chen M*， Kuo SJ， Chang CS， Shen MC*.The spectrum of the factor8 (F8) defects in Taiwanese patients with hemophilia A. HAEMOPHILIA. 2008. 14: 787-795. (Original Article， SCI ， IF=3.569， Hematology: 22/70)
82 Ma GC， Chang SD， Chang Y， Chang SP， Yang CW， Lee MJ， Lee TH， Chen M*. Rapid prenatal confirmation of LIT1 hypomethylation using a novel quantitative method (E-Q-PCR) in Beckwith-Wiedemann syndrome fetuses impressed with ultrasonography. FERTILITY AND STERILITY. 2008. 90: 1279-1282. (Correspondence， SCI ， IF=4.373， Obstetrics & Gynecology: 8/80; Reproductive Biology: 3/29)
83 Huang CC， Chen TH， Ho SY， Chen M*. Antenatally ultrasound-impressed placenta percreta complicatedwith massive hemorrhage despite a combinational arterial embolization and two-stage surgery. JOURNAL OF MEDICAL ULTRASOUND. 2008. 16: 296-300. (Case Report， Peer reviewed article)
84 Chen M#， Hsieh CY#， Shih JC， Chou CH， Ma GC， Chen TH， Lee TH， Tsai HD， Cameron AD， Chen CP*. Proinflammatory MIF and IL-6 are concentrated in pleural effusion of human fetuses with antenatal chylothorax. PRENATAL DIAGNOSIS. 2007. 27: 435-441. (Original Paper， SCI， IF=2.523， Genetics & Heredity: 82/166; Obstetrics & Gynecology: 25/80)
85 Lee ML*， Chen M， Lee MH. Balloon pulmonary valvuloplasty for valvular pulmonary stenosis in double outlet right ventricle incriminating 46，X，der(X)t(X;3)(q28;q13.2)mat in an infant. INTERNATIONAL JOURNAL OF CARDIOLOGY. 2007. 114:e27-30. (Letter to the Editor， SCI， IF= 6.189， Cardiac & Cardiovascular Systems: 16/126)
86 Ke YY#， Lee DJ#， Ma GC， Wang BT， Chen M*. Interstitial deletion of 13q31 associated with a normal phenotype: insight from studying a reciprocal translocation segregated in a family. JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION. 2007. 106: 582-588. (Case Report， SCI， IF=1.969， Medicine， General & Internal: 46/154)
87 Wu HH， Lee TH， Chen CD， Yu HT， Yeh KT， Chen M* Delineation of an Isodicentric Y Chromosome in a Mosaic 45，/46，Xidic(Y)(Qter-p11.3::P11.3-Qter) Fetus by SRY Sequencing， G-banding， FISH， SKY and Study of Distribution in Different Tissues. JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION. 2007. 106: 402-409. (Case Report， SCI ， IF=1.969， Medicine， General & Internal: 46/154)
88 Yang CS， Jan YJ， Wang J， Shen CC， Chen CC*， Chen M. Spinal atypical teratoid/rhabdoid tumor in a 7-year-old boy. NEUROPATHOLOGY. 2007. 27: 139-44. (Case Report， SCI ， IF=1.784， Clinical Neurology: 135/194; Neurosciences: 201/258; Pathology: 44/79)
89 Wu SH#， Chen M#， Chin SC， Lee DJ， Wen PY， Lee LY， Wang BT， Yu HT*. Cytogenetic analysis of Formosan pangolin， Manis pentadactyla pentadactyla (Pholidota: Mammalia). ZOOLOGICAL STUDIES. 2007. 46: 389-396. (Original Article， SCI)
90 Lee ML*， Chen M. Tibial Agenesis-Ectrodactyly Syndrome Associated with Novel Cardiovascular and Bronchopulmonary Malformations. CLINICAL DYSMORPHOLOGY. 2007. 16: 47-49. (Original Article， SCI)
91 Kuo SJ， Wang BT， Chang CS， Chen TH， Yeh KT， Lee DJ， Yin PL， Chen M*. Comparison of immunohistochemical and fluorescence in situ hybridization assessment for HER-2/neu status in Taiwanese breast cancer patients. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2007. 46: 146-151. (Original Article， SCI)
92 Wong LJ， Lee MH， Chen M， Tsao LY， Ozgul A， Wang BT*. The first prenatal exclusion of CF case in an East Asian population. PEDIATRICS INTERNATIONAL. 2007. 49: 686-687. (Patient Report， SCI)
93 Chen M， Hwu WL， Kuo SJ， Yin PL， Chang SP， Lee DJ， Chen TH， Wang BT， Lin CC*. Subtelomeric rearrangements and 22q11.2 deletion syndrome in anomalous growth-restricted fetuses with normal or balanced G-banded karyotype. ULTRASOUND IN OBSTETRICS & GYNECOLOGY. 2006: 28: 939-943. (Original Paper， SCI， IF=4.71， Obstetrics & Gynecology: 6/80; Acoustics: 1/32; Radiology， Nuclear Medicine & Medical Imaging: 11/126)
94 Chen M*， Kuo SJ， Liu CS， Chen WL， Ko TM， Chang SP， Chang YY， Huang CH， Chen TH， Wang BT. A novel heterozygous missense mutation 377T>C (V126A) in TGIF gene in a family segregated with holoprosencephaly and moyamoya disease. PRENATAL DIAGNOSIS. 2006: 26: 226-230. (Original Paper， SCI ， IF=2.523). Genetics & Heredity: 82/166; Obstetrics & Gynecology: 25/80.
95 Chen M*， Chang SP， Yin PL， Sapeta M， Barringer S， Kuo SJ， Yu HT， Wang BB. Prenatal identification of multiple small supernumerary marker chromosomes in an infant born with mild congenital anomalies. PRENATAL DIAGNOSIS. 2006: 26: 383-387. (Letter to the Editor， SCI ， IF=2.523， Genetics & Heredity: 82/166; Obstetrics & Gynecology: 25/80)
96 Lee ML*， Chen HN， Chen M， Tsao LY， Wang BT， Lee MH， Chiu IS. Persistent fifth aortic arch associated with 22q11.2 deletion syndrome. JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION. 2006. 105: 284-289. (Original Article， SCI， IF=1.969， Medicine， General & Internal: 46/154)
97 Chen CP*， Lin SP， Wang TH， Chen YJ， Chen M， Wang W. Perinatal findings and molecular cytogenetic analyses of de novo interstitial deletion of 9q (9q22.3 q31.3) associated with Gorlin syndrome. PRENATAL DIAGNOSIS. 2006: 26: 725-729. (Case Report， SCI ， IF=2.523， Genetics & Heredity: 82/166; Obstetrics & Gynecology: 25/80)
98 Chen M*， Ho WK， Hsieh TC， Lee CH， Hsiao CC， Chang SP， Lee DJ， Yang AD. Huge duplication cyst of small intestine: ultrasonographic features and antenatal aspiration. PRENATAL DIAGNOSIS. 2006: 26: 86-89. (Letter to the Editor， SCI ， IF=2.523， Genetics & Heredity: 82/166; Obstetrics & Gynecology: 25/80)
99 Chen M*， Shih JC， Wang BT， Chen CP， Yu CL. Fetal OK-432 pleurodesis: complete or incomplete? ULTRASOUND IN OBSTETRICS & GYNECOLOGY. 2005. 26: 791-793. (Letter to the Editor， SCI， IF=4.71， Obstetrics & Gynecology: 6/80; Acoustics: 1/32; Radiology， Nuclear Medicine & Medical Imaging: 11/126)
100 Chen M*， Hsieh CY， Cameron AD， Shih JC， Lee CN， Ho HN， Chen TH. ， Chen CP. Management of oligohydramnios with amnioinfusion，amniopatch，and cerclage. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2005. 44:347-352. (Original Article， SCI)
101 Chen FY*， Chen M， Shih JC， Tsao PN， Lee CN， Hsieh FJ. Meconium peritonitis presenting as a massive fetal ascites. PRENATAL DIAGNOSIS. 2004. 24(11): 930-931. (Letter to the Editor ， SCI ， IF=2.523， Genetics & Heredity: 82/166; Obstetrics & Gynecology: 25/80)
102 Hsieh LJ， Hsieh TC， Yeh GP， Lin MI， Chen M*， Wang BT. Prenatal diagnosis of a fetus affected with Down syndrome and deletion 1p36 syndrome by FISH and spectral karyotyping. FETAL DIAGNOSIS AND THERAPY. 2004. 19(4): 356-360. (Case Report， SCI ， IF=2.939， Obstetrics & Gynecology: 23/80)
103 Chang TC， Lien YR， Chen M， Cheng SP， Chen RJ， Chow SN*. Effect of conjugated equine estrogen in combination with two different progestogens on the risk factors of coronary heart disease in postmenopausal Chinese women in Taiwan: a randomized one-year study. ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA. 2004. 83(7): 661-666. (Original Article， SCI ， IF=2.480， Obstetrics & Gynecology: 27/80)
104 Chen M， Yeh GP， Shih JC， Wang BT*. Trisomy 13 Mosaicism: study of serial cytogenetic changes in a case from early pregnancy to infancy. PRENATAL DIAGNOSIS. 2004. 24(2): 137-143. (Short Communication， SCI ， IF=2.523， Genetics & Heredity: 82/166; Obstetrics & Gynecology: 25/80)
105 Chen M*， Chen CP. Invasive fetal therapy: its global status and local development. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2004. 20(4): 309-315. (Research Article， SCI)
106 Wu JL， Chen M*， Hsieh TC， Chen TH， Chou PH， Lin KC. Early-onset oligohydramnios complicated with hypertension， hyperthyroidism， and a coexisting elevated urine vanillylmandelic acid of unknown origin mimicking a pheochromocytoma. TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY. 2004. 43(4): 222-225. (Short Communication， SCI)
107 Wang BT， Chen M*. Redundant skin over the nape in a girl having monosomy 1p36 caused by a de novo satellited derivative chromosome-A possible new feature? CLINICAL DYSMORPHOLOGY. 2004. 13(2): 107-109. (Letter to the Editor， SCI)
108 Chen M*， Shih JC， Wang BT. Trisomy 13 manifested as hypoplastic left heart and other structural abnormalities. PRENATAL DIAGNOSIS. 2003. 23(13): 1102-1103. (Letter to the Editor， SCI ， IF=2.523， Genetics & Heredity: 82/166; Obstetrics & Gynecology: 25/80)
109 Chen CA， Chen M*. Simultaneous occurrence of hepatic focal nodular hyperplasia and uterine endometrial stromal nodule in a patient having treated breast infiltrating ductal carcinoma. ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA. 2003. 82(6): 585-586. (Case Report， SCI ， IF=2.480， Obstetrics & Gynecology: 27/80)
110 Chang TC， Chen M， Lien YR， Chen RJ， Chow SN*. Comparison of the difference in histopathology and cell cycle kinetics among the postmenopausal endometrium treated with different progestins in sequential-combined hormone replacement therapy. MENOPAUSE. 2003. 10(2): 172-178. (Original Article， SCI ， IF=2.733， Obstetrics & Gynecology: 21/80)
111 Chow SN， Chen M， Chen PJ， Chen RJ， Chien CH. Cell cycle analysis and detection of proliferative cell nuclear antigen of the endometrium after hormone replacement therapy. MATURITAS. 2001. 39: 227-237. (Original Article， SCI ， IF=3.255， Obstetrics & Gynecology: 11/80; Geriatrics & Gerontology: 13/49)
112 Chen M， Chow SN. Additive effect of alfacalcidol on bone mineral density of the lumbar spine in Taiwanese postmenopausal women treated with hormone replacement therapy and calcium supplementation: a randomized 2-year study. CLINICAL ENDOCRINOLOGY. 2001. 55: 253-258. (Original Article， SCI ， IF=3.457， Endocrinology & Metabolism: 60/138)
113 Chen M， Shih JC， Chiu WT， Hsieh FJ. Separation of cesarean scar during second-trimester intravaginal misoprostol abortion. OBSTETRICS AND GYNECOLOGY. 1999. 95(5): 840. (Case Report， SCI ， IF=5.175， Obstetrics & Gynecology: 3/80)