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 現在位置:   現在位置: 略過巡覽連結首頁 > 教學研究 > 期刊論文 網站更新日期: 2022/11/11

 
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(A) SCI published papers
  
1Ma 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. Am J Med Genet A. (in press). SCI (IF=2.404)
2Yu 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 pentadactyla) and its phylogenetic implications for Pholidota in extant mammals. Theriogenology; 2011; 75: 55-64. SCI (IF=2.073)
3Chen 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. Taiwan J Obstet Gynecol; 2010; 49: 500-505. SCIE
4Chen 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. Taiwan J Obstet Gynecol; 2010; 49: 320-326. SCIE
5Lee 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. Am J Med Genet A; 2010: 152A:2327-2334. SCI (IF=2.404)
6Kuo 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; 2010; 201: 94-101. SCI (IF=1.537)
7Chen 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 Obstet Gynecol; 2010; 36: 255-258. SCI (IF=3.154)
8Ma 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. Am J Med Genet A; 2010; 152A: 784-788. SCI (IF=2.404)
9Lee 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. Cardiovasc Pathol; doi:10.1016/j.carpath.2010.01.006. SCI (IF=1.626)
10You 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. Anim Genet; 2010; 41: 365-376. SCI (IF=2.292)
11Wu 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; 38(6):1932-49. SCI (IF=7.479)
12Ma GC, Ke YY, Lee ML, Tsao LY, Lee DJ, Yang CW, Kuo SJ, Chiu HY, Chen M*. De novo triple aneuploid of 1p, 1q, 4q in a girl with hypertrophic cardiomyopathy, muscle hypotonia, and multiple congenital anomalies. Am J Med Genet A; 2010; 152A(3):784-8. SCI (IF=2.404)
13Chen 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; 42(3):134-8. SCI (IF=0.875)
14Lee 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. Prenat Diagn; 2009; 29(11):1058-60. SCI (IF=1.707)
15Chen CH#, Chen TH#, Kuo SJ, Chen CD, Yang YS, Chen M. Late termination of pregnancy: experience from an Oriental population and report of a novel technique for feticide. J Med Ultrasound; 2009; 17:193-9.
16Chen 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. Am J Med Genet; 2009; 149A: 1550-4. SCI (IF=2.404)
17Lin CJ, Chang SP, Ke YY, Chiu HY, Tsao LY, Chen M*.Phenotype and Genotype of Two Taiwanese Cystic Fibrosis Siblings and a Survey of Delta F508 in East Asians. Pediatr Neonatol; 2008; 49(6):240-4.
18Chen TH, Chen CH, Hong YC, Chen M*. Puerperal pelvic hematoma successfully treated by primary transcatheteral arterial embolization. Taiwan J Obstet Gynecol; 2009; 48(2): 200-2. SCIE
19Chen CH, Hsieh HC, Ysai HD, Chen TH, Chen M*. Cardiac tamponade-a new alternative procedure for late feticide: a case report and literature review. Taiwan J Obstet Gynecol. 2009; 48(2): 159-62. SCIE
20Lee 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. Int J Cardiol; 2010; 141: e47-50. SCI (IF=3.121)
21Lee 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; 50(1):95-104. SCI (IF=0.772)
22Chen 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. Taiwan J Obstet Gynecol; 2009; 48(2): 98-107. SCIE
23Huang CC, Chen TH, Ho SY, Chen M*. Antenatally ultrasound-impressed placenta percreta complicatedwith massive hemorrhage despite a combinational arterial embolization and two-stage surgery. J Med Ultrasound; 2008; 16: 296-300.
24Ho WK, Wang YF, Wu HH, Tsai HD, Chen TH, Chen M*. Ruptured corpus luteum with hemoperitoneum: case characteristics and demographic changes over time. Taiwan J Obstet Gynecol. 2009; 48(2): 108-112. SCIE
25Ma 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. Prenat Diagn; 2008; 28(11):1057-63. SCI (IF=1.707)
26Ma 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. SCI (IF=2.505)
27Ma 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. Fertil Steril; 2008; 90: 1279-1282. SCI (IF=3.970)
28Lee 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. Int J Cardiol; 2007; 114:e27-30. SCI (IF=3.469)
29Wu 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. SCI (IF=0.860)
30Chen 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. Prenat Diagn; 2007; 27: 435-441. SCI (IF=1.707)
31Lee ML*, Chen M. Tibial Agenesis-Ectrodactyly Syndrome Associated with Novel Cardiovascular and Bronchopulmonary Malformations. Clinical Dysmorphology; 2007; 16: 47-49. SCI (IF=0.468)
32Ke 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. J Formos Med Assoc; 2007; 106: 582-588. SCI (IF=0.661)
33Wu 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. J Formos Med Assoc; 2007; 106: 402-409. SCI (IF=0.661)
34Kuo 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. Taiwan J Obstet Gynecol; 2007; 46: 146-151. SCIE
35Wong 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: 686-7. SCI (IF=0.707)
36Yang 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. SCI (IF=1.861)
37Chen M, Hwu WL, Kuo SJ, Yin PL, Chang SP, Lee DJ, Chen TH, Wang BT, Lin CC*. Screening of subtelomere rearrangements and 22q11.2 deletion syndrome in fetuses affected with intrauterine growth restriction plus structural anomaly but with normal or balanced G-banded karyotype. Ultrasound Obstet Gynecol; 2006: 28: 939-43. SCI (IF=3.154)
38Chen 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. Prenat Diagn; 2006: 26: 226-30. SCI (IF=1.707)
39Chen 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. Prenat Diagn; 2006: 26: 383-7. SCI (IF=1.707)
40Chen 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. Prenat Diagn; 2006; 26: 86-89. SCI (IF=1.707)
41Lee ML*, Chen HN, Chen M, Tsao LY, Wang BT, Lee MH, Chiu IS. Persistent fifth aortic arch associated with 22q11.2 deletion syndrome. J Formos Med Assoc; 2006; 105: 284-9. SCI (IF=0.661)
42Chen 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. Prenat Diagn; 2006; 26: 725-9. SCI (IF=1.707)
43Chen M*, Chen CP, Shih JC, Chou HC, Yu CL, Wang BT, Hsieh CY. Antenatal management of cystic hygroma and chylothorax with OK432 in non-immune hydrops fetalis. Fetal Diagnosis and Therapy; 2005; 20(4): 309-15. SCI (IF=0.911)
44Chen M*, Shih JC, Wang BT, Chen CP, Yu CL. Fetal OK-432 pleurodesis: complete or incomplete? Ultrasound Obstet Gynecol; 2005; 26: 791-3. SCI (IF=3.154)
45Chen M*, Hsieh CY, Cameron AD, Shih JC, Lee CN, Ho HN, Chen TH. , Chen CP. Management of oligohydramnios with amnioinfusion,amniopatch,and cerclage. Taiwan J Obstet Gynecol; 2005; 44:347-52. SCIE
46Chen M*, Chen CP. Invasive fetal therapy: its global status and local development. Taiwanese J Obstet Gynecol; 2004; 20(4): 309-15. SCIE
47Wu 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 J Obstet Gynecol; 2004; 43(4): 222-225. SCIE
48Chen FY*, Chen M, Shih JC, Tsao PN, Lee CN, Hsieh FJ. Meconium peritonitis presenting as a massive fetal ascites. Prenatal Diagnosis; 2004; 24(11): 930-1. SCI (IF=1.707)
49Hsieh 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): 356-60. SCI (IF=0.911)
50Chang 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 Obstet Gynecol Scand; 2004; 83(7): 661-6. SCI (IF=1.618)
51Wang 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): 107-9. SCI (IF=0.468)
52Chen 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): 137-43. SCI (IF=1.707)
53 Chen M*, Shih JC, Wang BT. Trisomy 13 manifested as hypoplastic left heart and other structural abnormalities. Prenatal Diagnosis; 2003; 23(13): 1102-3. SCI (IF=1.707)
54 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 Obstet Gynecol Scand; 2003; 82(6): 585-6. SCI (IF=1.618)
55Chang 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): 172-8. SCI (IF=3.082)
56 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: 227-37. SCI (IF=2.093)
57 Chen M, Chow SN. Additive effect of alfacalcidol on bone mineral density of the lumbar spine in Taiwanese in Taiwanese postmenopausal women treated with hormone replacement therapy and calcium supplementation: a randomized 2-year study. Clin Endocrinol; 2001; 55: 253-258. SCI (IF=3.201)


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