論文發表

• PUBLICATION

1. Prenatal Ultrasound Imaging of Orofacial Clefts: A Pictorial Essay. 

Yang TY, Chang TY. Journal of Medical Ultrasound 32(1):p 8-13, Jan–Mar 2024. 

2. A practical method for prenatal diagnosis of anal atresia by second trimester ultrasound screening - A retrospective study. 

Ko H, Chou YC, Olisova K, Chang TY. Taiwanese Journal of Obstetrics and Gynecology. 2023;62: 884–890.

3. Ultrasonographic cervical length screening at 20–24 weeks of gestation in twin pregnancies for prediction of spontaneous preterm birth: A 10-year Taiwanese cohort. 

Olisova K, Sao CH, Lussier EC, Sung CY, Wang PH, Yeh CC, et al. PLOS ONE 18(10): e0292533. 5 Oct 2023.

4. High-type anal atresia presenting as a pseudo “target sign” on prenatal ultrasound. 

Ko H, Chou YC, Olisova K, Chang TY. Taiwanese Journal of Obstetrics and Gynecology. 2023;62: 742–744.

5. Associated factors with parental pregnancy decision-making and use of consultation after a prenatal congenital heart disease diagnosis. 

Chih WL, Tung YH, Lussier EC, Sung CY, Huang YL, Hung WL, et al. Pediatrics & Neonatology. 2023;64: 371–380.

6. Ultrasound Assessment of the Fetal Optic Chiasm. 

Wang JT, Chang TY. Journal of Medical Ultrasound. 2023;31: 195. 

7. Fetal arrhythmias case series: Experiences from a fetal screening center in Taiwan. 

Chih WL, Olisova K, Tung YH, Huang YL, Chang TY. Taiwanese Journal of Obstetrics and Gynecology. 2023;62: 480–484. 

8. Novel approach to distinguish submucous cleft palate from isolated cleft palate by ultrasound visualization of fetal swallowing. 

Yang TY, Li WC, Chen PKT, Olisova K, Ko H, Chang TY. Ultrasound in Obstetrics & Gynecology. 2023;62: 603–605. 

9. Congenital radioulnar synostosis: is prenatal diagnosis possible? - A case report. 

Li YY, Olisova K, Chen YN, Chang CH, Chang TY. Taiwanese Journal of Obstetrics and Gynecology. 2023;62: 334–335. 

10. A call for a standardized placenta accreta spectrum screening in Taiwan. 

Wu PC, Olisova K, Ko H, Chang TY. Taiwanese Journal of Obstetrics and Gynecology. 2023;62: 191–192. 

11. Risk factors for anxiety and depression among pregnant women during the COVID-19 pandemic: Results of a web-based multinational cross-sectional study. 

Kajdy A, Sys D, Pokropek A, Shaw SW, Chang TY, Calda P, et al. Int J Gynaecol Obstet. 2023;160: 167–186. 

12. Physiological QT Interval Changes in Early Infancy Using Post-Menstrual and Post-Natal Age Calculation for Electrocardiogram Long QT Interval Screening in Taiwan. 

Chih WL, Lussier EC, Chen JA, Yeh SJ, Lin SM, Chang TY, et al. Acta Cardiol Sin. 2022;38: 73–83. 

13. Revisions to mid-pregnancy cervical length reference range for preterm birth screening among singleton pregnancies in Taiwan – 10 years’ experiences. 

Olisova K, Sung CY, Lussier EC, Chang TY. Taiwanese Journal of Obstetrics and Gynecology. 2021;60: 836–839. 

14. Age-specific effect of fresh versus frozen embryo transfer on fetal anomalies or intrauterine growth restriction rate. 

Chou YC, Lussier EC, Olisova K, Chang TY. Taiwanese Journal of Obstetrics and Gynecology. 2021;60: 831–835. 

15. Prenatal ultrasound diagnosis of neural tube defects in the era of intrauterine repair – Eleven years’ experiences. 

Huang YS, Lussier EC, Olisova K, Chang YC, Ko H, Chang TY. Taiwanese Journal of Obstetrics and Gynecology. 2021;60: 281–289. 

16. 運用跨專科團隊於產前診斷胎兒心臟異常孕婦及家庭之照顧模式. 

董于瑄, 池宛玲, 張重義, 徐綱宏, 洪偉力, 張東曜, et al. 醫療品質雜誌. 2021;15: 40–44.

17. Multidisciplinary team approach to the prenatal management of orofacial clefts: a single center cohort study in Taiwan. 

Ko H, Chang TY, Lussier EC, Olisova K, Sung CY, Chen PKT, et al. Sci Rep. 2020;10: 13916. 

18. Newborn Hip Screenings at 4 to 8 Weeks Are Optimal in Predicting Referral and Treatment Outcomes: A Retrospective Review. 

Lussier EC, Lei WT, Sun YT, Chen HW, Chang TY, Chang CH. Open Journal of Pediatrics. 2020;10: 332. 

19. Reference ranges and Z-scores for fetal cardiac measurements from two-dimensional echocardiography in Asian population. 

Lussier EC, Yeh SJ, Chih WL, Lin SM, Chou C, Huang SP, et al. PLOS ONE. 2020;15: e0233179.

20. One size fits all? A call to establish Taiwanese fetal growth standards. 

Olisova K, Sung CY, Li YY, Hsia CC, Chang TY. Taiwanese Journal of Obstetrics and Gynecology. 2020;59: 468.

21. Ultrasound screening for developmental dysplasia of the hip after 4 weeks increases exam accuracy and decreases follow-up visits. 

Lussier EC, Sun YT, Chen HW, Chang TY, Chang CH. Pediatrics & Neonatology. 2019;60: 270–277. 

22. Prenatal diagnosis of coarctation of the aorta with ventricular septal defect: A case report. Huang YL, Hsu KH, Chuluunbaatar E, Wen TM, Li YY, Chen MR, et al. Taiwanese Journal of Obstetrics and Gynecology. 2018;57: 885–889. 

23. Flow mediated dilatation of Taiwanese women with normal singleton pregnancies. 

Hou WC, Chen JY, Huang HY, Sun YT, Su HY, Chang TY. Taiwanese Journal of Obstetrics and Gynecology. 2018;57: 683–687. 

24. Antiepileptic drug use among women from the Taiwanese Registry of Epilepsy and Pregnancy: Obstetric complications and fetal malformation outcomes. 

Yeh CC, Lussier EC, Sun YT, Lan TY, Yu HY, Chang TY. PLOS ONE. 2017;12: e0189497. 

25. Prenatal Diagnosis of Persistent Left Superior Vena Cava is Associated with Coarctation of the Aorta – A Case Report. 

Wen TM, Huang YL, Wu PC, Li YY, Chen MR, Chang TY. Journal of Medical Ultrasound. 2017;25: 244–247. 

26. Prenatal Diagnosis of Anal Atresia – A Case Report. 

Chou YC, Chang WT. Journal of Medical Ultrasound. 2017;25: 180–183. 

27. Prenatal Diagnosis of Hypospadias – A Case Report. 

Lin TW, Wang JT. J Med Ultrasound. 2017;25: 115–117. 

28. Molecular cytogenetic characterization of Jacobsen syndrome (11q23.3-q25 deletion) in a fetus associated with double outlet right ventricle, hypoplastic left heart syndrome and ductus venosus agenesis on prenatal ultrasound. 

Chen CP, Wang LK, Wu PC, Chang TY, Chern SR, Wu PS, et al. Taiwanese Journal of Obstetrics and Gynecology. 2017;56: 102–105.

29. Prenatal imaging findings of a rapidly involuting congenital hemangioma (RICH) over right flank in a fetus with a favorable outcome. 

Chen CP, Chen CY, Chang TY, Yang HY, Chen YN, Chen SW, et al. Taiwanese Journal of Obstetrics and Gynecology. 2016;55: 745–747.

30. 22q13 deletion syndrome in a fetus associated with microtia, hemivertebrae, andcongenital heart defects on prenatal ultrasound. 

Chen CP, Chang TY, Wang LK, Chern SR, Wu PS, Chen YN, et al. Taiwanese Journal of Obstetrics and Gynecology. 2016;55: 455–456. 

31. Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion. 

Chen YN, Chen CP, Ko TM, Wang LK, Wu PC, Chang TY, et al. Taiwanese Journal of Obstetrics and Gynecology. 2016;55: 117–120. 

32. Prenatal diagnosis of chromosome 8p23.1 microdeletion by array comparative genomic hybridization using uncultured amniocytes in a pregnancy associated with fetal partial corpus callosum agenesis and schizencephaly. 

Chen CP, Peng CR, Chang TY, Guo WY, Chen YN, Wu PS, et al. Taiwanese Journal of Obstetrics and Gynecology. 2015;54: 797–798.

33. Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma. 

Chen CP, Ko TM, Huang MC, Chern SR, Lin TW, Chang TY, et al. Taiwanese Journal of Obstetrics and Gynecology. 2015;54: 78–80. 

34. Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects. 

Kuo YL, Chen CP, Wang LK, Ko TM, Chang TY, Chern SR, et al. Taiwanese Journal of Obstetrics and Gynecology. 2014;53: 248–251.

35. Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by intracytoplasmic sperm injection and in vitro fertilization and embryo transfer. 

Chen CP, Su YN, Chen SU, Chang TY, Wu PC, Chern SR, et al. Taiwanese Journal of Obstetrics and Gynecology. 2014;53: 90–94. 

36. Chromosome 17p13.3 deletion syndrome: aCGH characterization, prenatal findings and diagnosis, and literature review. 

Chen CP, Chang TY, Guo WY, Wu PC, Wang LK, Chern SR, et al. Gene. Volume 532, Issue 1, 2013;532: 152–159. 

37. Detection of a de novo Y278C mutation in FGFR3 in a pregnancy with severe fetal hypochondroplasia: Prenatal diagnosis and literature review. 

Chen CP, Su YN, Lin TH, Chang TY, Su JW, Wang W. Taiwanese Journal of Obstetrics and Gynecology. 2013;52: 580–585. 

38. VACTERL association with hydrocephalus in a fetus conceived by in vitro fertilization and embryo transfer. 

Chen CP, Chang TY, Chen YY, Chern SR, Su JW, Wang W. Taiwanese Journal of Obstetrics and Gynecology. 2013;52: 575–579. 

39. Rapid detection of K650E mutation in FGFR3 using uncultured amniocytes in a pregnancy affected with fetal cloverleaf skull, occipital pseudoencephalocele, ventriculomegaly, straight short femurs, and thanatophoric dysplasia type II. 

Chen CP, Chang TY, Lin MH, Chern SR, Su JW, Wang W. Taiwanese Journal of Obstetrics and Gynecology. 2013;52: 420–425. 

40. Detection of maternal transmission of a splicing mutation in the TSC2 gene following prenatal diagnosis of fetal cardiac rhabdomyomas mimicking congenital cystic adenomatoid malformation of the lung and cerebral tubers and awareness of a family history of maternal epilepsy. 

Chen CP, Chang TY, Guo WY, Su YN, Chen YY, Chern SR, et al. Taiwanese Journal of Obstetrics and Gynecology. 2013;52: 415–419. 

41. Rapid detection of de novo P253R mutation in FGFR2 using uncultured amniocytes in a pregnancy affected by polyhydramnios, Blake’s pouch cyst, and Apert syndrome. 

Chen CP, Su YN, Chang TY, Chern SR, Chen CY, Su JW, et al. Taiwanese Journal of Obstetrics and Gynecology. 2013;52: 273–277. 

42. Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization. 

Chen CP, Lin CJ, Chang TY, Chern SR, Wu PS, Chen YT, et al. Gene. 2013;519: 164–168. 

43. Osteogenesis imperfecta type I: Second-trimester diagnosis and incidental identification of a dominant COL1A1 deletion mutation in the paucisymptomatic father. 

Chen CP, Su YN, Chang TY, Chern SR, Chen CY, Su JW, et al. Taiwanese Journal of Obstetrics and Gynecology. 2012;51: 276–279. 

44. Identification of a deletion mutation in the short flanking repeat region of exon 44 of the COL1A1 gene in a fetus with osteogenesis imperfecta type II. 

Chen CP, Su YN, Chang TY, Chern SR, Su JW, Wang W. Taiwanese Journal of Obstetrics and Gynecology. 2012;51: 308–311.

45. Prenatal diagnosis and molecular genetic analysis of short rib-polydactyly syndrome type III (Verma-Naumoff) in a second-trimester fetus with a homozygous splice site mutation in intron 4 in the NEK1 gene. 

Chen CP, Chern SR, Chang TY, Su YN, Chen YY, Su JW, et al. Taiwanese Journal of Obstetrics and Gynecology. 2012;51: 266–270. 

46. Persistent cloaca presenting with a perineal cyst: Prenatal ultrasound and magnetic resonance imaging findings. 

Chen CP, Chang TY, Hsu CY, Liu YP, Tsai FJ, Wu PC, et al. Journal of the Chinese Medical Association. 2012;75: 190–193. 

47. Short rib-polydactyly syndrome type II (Majewski): Prenatal diagnosis, perinatal imaging findings and molecular analysis of the NEK1 gene. 

Chen CP, Chang TY, Chen CY, Wang TY, Tsai FJ, Wu PC, et al. Taiwanese Journal of Obstetrics and Gynecology. 2012;51: 100–105. 

48. The Changing Face of Early-onset Neonatal Sepsis After the Implementation of a Maternal Group B Streptococcus Screening and Intrapartum Prophylaxis Policy—A Study in One Medical Center. 

Lin CY, Hsu CH, Huang FY, Chang JH, Hung HY, Kao HA, et al. Pediatrics & Neonatology. 2011;52: 78–84.

49. Prenatal Diagnosis of Rhabdomyomas and Cerebral Tuberous Sclerosis by Magnetic Resonance Imaging in One Fetus of a Dizygotic Twin Pregnancy Associated With a Frameshift Mutation in the TSC2 Gene. 

Chen CP, Su YN, Chang TY, Liu YP, Tsai FJ, Chen MR, et al. Taiwanese Journal of Obstetrics and Gynecology. 2010;49: 387–389. 

50. Prenatal Diagnosis of Persistent Cloaca With Hydrometrocolpos and Ascites by Magnetic Resonance Imaging in One Fetus of a Dizygotic Twin Pregnancy. 

Chen CP, Liu YP, Chang TY, Tsai FJ, Chen CY, Wu PC, et al. Taiwanese Journal of Obstetrics and Gynecology. 2010;49: 385–386. 

51. Prenatal Diagnosis of Monosomy 17p (17p 13.3 → pter) Associated With Polyhydramnios, Intrauterine Growth Restriction, Ventriculomegaly, and Miller-Dieker Lissencephaly Syndrome in a Fetus. 

Lin CY, Chen CP, Liau CL, Su PH, Tsao TF, Chang TY, et al. Taiwanese Journal of Obstetrics and Gynecology. 2009;48: 408–411. 

52. 22q 11.2 Microdeletion in a Fetus With Double-outlet Right Ventricle, Pulmonary Stenosis and a Ventricular Septal Defect: Prenatal Diagnosis by Array Comparative Genomic Hybridization. 

Chen CP, Su YN, Chang TY, Chern SR, Tsai FJ, Hwang JK, et al. Taiwanese Journal of Obstetrics and Gynecology. 2009;48: 437–440. 

53. Prenatal Magnetic Resonance Imaging, Ultrasound Imaging Findings and Genetic Analysis of Concomitant Rhabdomyomas and Cerebral Tuberous Sclerosis. 

Chen CP, Su YN, Chang TY, Liu YP, Tsai FJ, Hwang JK, et al. Taiwanese Journal of Obstetrics and Gynecology. 2009;48: 327–331.

54. Prenatal Diagnosis of 46,XX,der(13;21)(q10;q10),+21 and Transient Abnormal Myelopoiesis in a Fetus with Hepatosplenomegaly and Spontaneous Resolution of Fetal Ascites. 

Chen CP, Tsai FJ, Chern SR, Chang TY, Hsu CY, Lin HH, et al. Taiwanese Journal of Obstetrics and Gynecology. 2009;48: 84–87. 

55. Prenatal 3-dimensional sonographic and MRI findings in omphalocele–exstrophy–imperforate anus–spinal defects complex. 

Chen CP, Chang TY, Liu YP, Tsai FJ, Chien SC, Tsao CM, et al. J. Clin. Ultrasound, 36: 308-311.

56. Prenatal diagnosis of concomitant Wolf–Hirschhorn syndrome and split hand-foot malformation associated with partial monosomy 4p (4p16.1→qter) and partial trisomy 10q (10q25.1→qter). 

Chen CP, Chen YJ, Chern SR, Tsai FJ, Chang TY, Lee CC, et al. Prenatal Diagnosis. 2008;28: 450–453.

57. Concomitant Omphalocele and Anencephaly Associated with Trisomy 18 and Arthrogryposis Diagnosed in Early Pregnancy. 

Chen CP, Chang TY, Lin HH, Chern SR, Wang W. Taiwanese Journal of Obstetrics and Gynecology. 2008;47: 93–94. 

58. Prenatal Sonographic and Magnetic Resonance Imaging Demonstration of a Right Midline Arachnoid Cyst Associated with Ventriculomegaly, Colpocephaly, Dilation of the Third Ventricle, Absence of Cavum Septi Pellucidi, Agenesis of the Corpus Callosum and Mega Cisterna Magna. 

Chen CP, Chang TY, Hung JH, Chen CY, Wang W. Taiwanese Journal of Obstetrics and Gynecology. 2008;47: 91–92. 

59. Abnormal prenatal hematological findings in congenital leukemia of Down syndrome with hepatosplenomegaly. 

Chen CP, Lin SP, Chang TY, Ho HT. Prenatal Diagnosis. 2007;27: 1266–1267.

60. Prenatal diagnosis of Fryns syndrome associated with a microdeletion at 8p23.1..

Chen CP, Wang TH, Chen YJ, Chang TY, Liu YP, Tzen CY, et al. Prenatal Diagnosis. 2007;27: 967–969.

61. Prenatal Magnetic Resonance Imaging Evaluation of a Digynic Triploid Fetus. 

Chen CP, Chang TY, Liu YP, Chern SR, Wang W. Taiwanese Journal of Obstetrics and Gynecology. 2007;46: 284–285. 

62. .Third-trimester 3D Ultrasound Evaluation of Thanatophoric Dysplasia Type I. 

Chen CP, Chang TY, Chern SR, Wang W. Taiwanese Journal of Obstetrics and Gynecology. 2007;46: 281–283. 

63. Prenatal sonographic findings of Klippel-Trénaunay-Weber syndrome.
    Chen CP, Lin SP, Chang TY, Lee HC, Hung HY, Lin HY, et al. J. Clin. Ultrasound, 35: 409-412.

64. Prenatal diagnosis of low-level mosaic tetrasomy 9p by amniocentesis.
    Chen C-P, Chang TY, Chern SR, Lee CC, Town DD, Lee MS, et al. Prenatal Diagnosis. 2007;27: 383–385.

65. Preliminary Descriptive Statistics of the Taiwanese Registry of Epilepsy and Pregnancy for the First 2 Years. 

Chang TY, Lai CW, Yu HY, Hsu JJ, Shih YH, Chen CP. Taiwanese Journal of Obstetrics and Gynecology. 2007;46: 47–49. 

66. Prenatal diagnosis of the hypoplastic right heart syndrome with sex chromosome pentasomy (49,XXXXY).

ChenC P, Lin CJ, Chang TY, Chern SR, Tzen CY, Chen WL, et al. Prenatal Diagnosis. 27: 285-286.

67. Prenatal diagnosis of a micropenis in a male fetus with partial trisomy 12q (12q24.32→qter) and partial monosomy 21q (21q22.2→ter→qter). 

Chen CP, Lin CC, Chang TY, Li YC, Hsieh LJ, Lee CC, et al. Prenatal Diagnosis. 2006;26: 757–759.

68. Prenatal diagnosis of pure distal 18q deletion. 

Chen CP, Chern SR, Hung FY, Hsu CY, Chang TY, Lee CC, et al. Prenatal Diagnosis. 2006;26: 184–185.

69. Prenatal diagnosis of partial trisomy 10q (10q25.3→qter) and partial monosomy 18q (18q23→qter). 

Chen CP, Chern SR, Chang TY, Lee CC, Chen WL, Wang W. Prenatal Diagnosis. 2005;25: 1069–1071.

70. Prenatal magnetic resonance imaging demonstration of the systemic feeding artery of a pulmonary sequestration associated with in utero regression. 

Chen CP, Liu YP, Lin SP, Sheu JC, Hsu CY, Chang TY, et al. Prenatal Diagnosis. 2005;25: 721–723.