Shiing-Shen Chern - Publications

Affiliations: 
Mathematics University of California, Berkeley, Berkeley, CA 

171 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Chuang TY, Wang W. Detection of a familial 21q22.3 microduplication in a fetus associated with congenital heart defects. Taiwanese Journal of Obstetrics & Gynecology. 58: 869-871. PMID 31759545 DOI: 10.1016/j.tjog.2019.09.024  0.32
2019 Chen CP, Ko TM, Chen CY, Chern SR, Wu PS, Chen SW, Wu FT, Pan CW, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 3. Taiwanese Journal of Obstetrics & Gynecology. 58: 864-868. PMID 31759544 DOI: 10.1016/j.tjog.2019.09.023  0.32
2019 Chen CP, Huang JP, Chen YY, Chern SR, Wu PS, Chen SW, Wang W, Lee CC. Detection of a familial 1q21.1 microdeletion and concomitant CHD1L mutation in a fetus with oligohydramnios and bilateral renal dysplasia on prenatal ultrasound. Taiwanese Journal of Obstetrics & Gynecology. 58: 859-863. PMID 31759543 DOI: 10.1016/j.tjog.2019.07.031  0.32
2019 Chen CP, Chern SR, Wu PS, Chen SW, Wu FT, Town DD, Wang W. Mosaic isochromosome 20q at amniocentesis: Prenatal diagnosis, genetic counseling and literature review. Taiwanese Journal of Obstetrics & Gynecology. 58: 855-858. PMID 31759542 DOI: 10.1016/j.tjog.2019.08.002  0.32
2019 Chen CP, Hung FY, Chern SR, Chen SW, Wu FT, Town DD, Wang W. Prenatal diagnosis of mosaicism for trisomy 7 in a single colony at amniocentesis in a pregnancy with a favorable outcome. Taiwanese Journal of Obstetrics & Gynecology. 58: 852-854. PMID 31759541 DOI: 10.1016/j.tjog.2019.09.022  0.32
2019 Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Wu FT, Chen LF, Wang W. Detection of de novo del(18)(q22.2) and a familial of 15q13.2-q13.3 microduplication in a fetus with congenital heart defects. Taiwanese Journal of Obstetrics & Gynecology. 58: 704-708. PMID 31542097 DOI: 10.1016/j.tjog.2019.07.022  0.32
2019 Chen CP, Ko TM, Wang LK, Chern SR, Wu PS, Chen SW, Wu FT, Chen LF, Wang W. Inv dup del(10p): Prenatal diagnosis and molecular cytogenetic characterization. Taiwanese Journal of Obstetrics & Gynecology. 58: 698-703. PMID 31542096 DOI: 10.1016/j.tjog.2019.07.021  0.32
2019 Chen CP, Huang MC, Chern SR, Wu PS, Chen SW, Chuang TY, Town DD, Wang W. Mosaic trisomy 22 at amniocentesis: Prenatal diagnosis and literature review. Taiwanese Journal of Obstetrics & Gynecology. 58: 692-697. PMID 31542095 DOI: 10.1016/j.tjog.2019.07.020  0.32
2018 Chuang TY, Chang SY, Chen CP, Lin MH, Chen CY, Chen SW, Chern SR, Lee CC, Town DD, Wang W. Digynic triploidy in a fetus presenting with semilobar holoprosencephaly. Taiwanese Journal of Obstetrics & Gynecology. 57: 881-884. PMID 30545546 DOI: 10.1016/j.tjog.2018.11.001  0.32
2018 Chen CP, Chang SY, Huang MC, Chern SR, Chen SW, Lai ST, Chuang TY, Wang W. Detection of hypomethylation of H19 in a pregnancy with limb-body wall complex. Taiwanese Journal of Obstetrics & Gynecology. 57: 769-771. PMID 30342671 DOI: 10.1016/j.tjog.2018.08.032  0.32
2018 Chen CP, Chang SY, Lin SP, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Chen WL, Wang W. Array comparative genomic hybridization characterization of a 3.3-Mb 17p13.3-p13.2 deletion encompassing YWHAE, CRK, HIC1 and PAFAH1B1 in an 8-year-old girl with Miller-Dieker lissencephaly syndrome, congenital heart defects, growth restriction and developmental delay. Taiwanese Journal of Obstetrics & Gynecology. 57: 765-768. PMID 30342670 DOI: 10.1016/j.tjog.2018.08.031  0.32
2018 Chen CP, Chang SY, Chen YN, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Chen LF, Wang W. Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound. Taiwanese Journal of Obstetrics & Gynecology. 57: 739-744. PMID 30342663 DOI: 10.1016/j.tjog.2018.08.024  0.32
2018 Chen CP, Chang SY, Lin CJ, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Chen WL, Yang CW, Wang W. Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound. Taiwanese Journal of Obstetrics & Gynecology. 57: 734-738. PMID 30342662 DOI: 10.1016/j.tjog.2018.08.023  0.32
2018 Chen CP, Chang SY, Wang LK, Chang TY, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Town DD, Chen LF, Wang W. Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound. Taiwanese Journal of Obstetrics & Gynecology. 57: 730-733. PMID 30342661 DOI: 10.1016/j.tjog.2018.08.022  0.32
2018 Chen CP, Lin SP, Chern SR, Chen SW, Lai ST, Chuang TY, Chen LF, Wang W. A 17-year-old boy with Klinefelter syndrome presenting Marfan syndrome-like clinical features of tall stature, scoliosis, arachnodactyly and subluxation of bilateral elbow joints. Taiwanese Journal of Obstetrics & Gynecology. 57: 608-610. PMID 30122589 DOI: 10.1016/j.tjog.2018.06.025  0.32
2018 Chen CP, Lin SP, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Chen WL, Wang W. A 13-year-old girl with 18p deletion syndrome presenting Turner syndrome-like clinical features of short stature, short webbed neck, low posterior hair line, puffy eyelids and increased carrying angle of the elbows. Taiwanese Journal of Obstetrics & Gynecology. 57: 583-587. PMID 30122583 DOI: 10.1016/j.tjog.2018.06.019  0.32
2018 Chen CP, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Chen WL, Yang CW, Wang W. Prenatal diagnosis of a 3.2-Mb 2p16.1-p15 duplication associated with familial intellectual disability. Taiwanese Journal of Obstetrics & Gynecology. 57: 578-582. PMID 30122582 DOI: 10.1016/j.tjog.2018.06.018  0.32
2018 Chen CP, Ko TM, Wang LK, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Lee CC, Wang W. Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities. Taiwanese Journal of Obstetrics & Gynecology. 57: 128-132. PMID 29458882 DOI: 10.1016/j.tjog.2017.12.022  0.32
2018 Chen CP, Ko TM, Chang TY, Chern SR, Chen SW, Lai ST, Chuang TY, Wang W. Prenatal diagnosis of short-rib polydactyly syndrome type III or short-rib thoracic dysplasia 3 with or without polydactyly (SRTD3) associated with compound heterozygous mutations in DYNC2H1 in a fetus. Taiwanese Journal of Obstetrics & Gynecology. 57: 123-127. PMID 29458881 DOI: 10.1016/j.tjog.2017.12.021  0.32
2018 Chen CP, Chang TY, Lin TW, Chern SR, Chen SW, Lai ST, Chuang TY, Wang W. Prenatal diagnosis of hydrancephaly and enlarged cerebellum and cisterna magna in a fetus with thanatophoric dysplasia type II and a review of prenatal diagnosis of brain anomalies associated with thanatophoric dysplasia. Taiwanese Journal of Obstetrics & Gynecology. 57: 119-122. PMID 29458880 DOI: 10.1016/j.tjog.2017.12.020  0.32
2017 Chen CP, Hsieh CH, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Lee CC, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA, CELF4 and SETBP1. Taiwanese Journal of Obstetrics & Gynecology. 56: 847-851. PMID 29241933 DOI: 10.1016/j.tjog.2017.10.027  0.32
2017 Chen CP, Chang TY, Hung FY, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Lee CC, Wang W. Prenatal diagnosis of an 8q22.2-q23.3 deletion associated with bilateral cleft lip and palate and intrauterine growth restriction on fetal ultrasound. Taiwanese Journal of Obstetrics & Gynecology. 56: 843-846. PMID 29241932 DOI: 10.1016/j.tjog.2017.10.026  0.32
2017 Chen CP, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Lee CC, Wang W. Prenatal diagnosis of low-level mosaicism for trisomy 13 at amniocentesis associated with a favorable outcome. Taiwanese Journal of Obstetrics & Gynecology. 56: 840-842. PMID 29241931 DOI: 10.1016/j.tjog.2017.10.025  0.32
2017 Chen CP, Ko TM, Chen YY, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Pan CW, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome. Taiwanese Journal of Obstetrics & Gynecology. 56: 836-839. PMID 29241930 DOI: 10.1016/j.tjog.2017.10.024  0.32
2017 Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Lai ST, Chuang TY, Yang CW, Chen LF, Wang W. Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bones. Taiwanese Journal of Obstetrics & Gynecology. 56: 821-826. PMID 29241927 DOI: 10.1016/j.tjog.2017.10.021  0.32
2017 Chen CP, Tsai C, Lin MH, Chern SR, Chen SW, Lai ST, Chen WL, Pan CW, Wang W. Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism. Taiwanese Journal of Obstetrics & Gynecology. 56: 691-693. PMID 29037560 DOI: 10.1016/j.tjog.2017.09.001  0.32
2017 Chen CP, Huang JP, Chern SR, Chen SW, Lai ST, Wu PS, Lee CC, Yang CW, Wang W. Prenatal diagnosis of mosaicism for trisomy 2 in a single colony at amniocentesis in a pregnancy with a favorable outcome. Taiwanese Journal of Obstetrics & Gynecology. 56: 569-570. PMID 28805623 DOI: 10.1016/j.tjog.2017.05.007  0.32
2017 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. 56: 566-568. PMID 28805622 DOI: 10.1016/j.tjog.2017.05.006  0.32
2017 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. 56: 554-557. PMID 28805618 DOI: 10.1016/j.tjog.2017.06.004  0.32
2017 Chen CP, Chen CY, Chern SR, Wu PS, Chen SW, Lai ST, Lee CC, Yang CW, Wang W. Molecular cytogenetic characterization of a duplication of 15q24.2-q26.2 associated with anencephaly and neural tube defect. Taiwanese Journal of Obstetrics & Gynecology. 56: 550-553. PMID 28805617 DOI: 10.1016/j.tjog.2017.06.003  0.32
2017 Chen CP, Ko TM, Chern SR, Wu PS, Chen SW, Lai ST, Yang CW, Pan CW, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16. Taiwanese Journal of Obstetrics & Gynecology. 56: 545-549. PMID 28805616 DOI: 10.1016/j.tjog.2017.05.004  0.32
2017 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. 56: 527-533. PMID 28805612 DOI: 10.1016/j.tjog.2017.06.002  0.32
2017 Chen CP, Lin SP, Liu YP, Chern SR, Chen SW, Lai ST, Wang W. Pfeiffer syndrome with FGFR2 C342R mutation presenting extreme proptosis, craniosynostosis, hearing loss, ventriculomegaly, broad great toes and thumbs, maxillary hypoplasia, and laryngomalacia. Taiwanese Journal of Obstetrics & Gynecology. 56: 412-414. PMID 28600064 DOI: 10.1016/j.tjog.2017.04.030  0.32
2017 Chen CP, Lin CJ, Chen YN, Chern SR, Chen SW, Lai ST, Wu PS, Chen LF, Wang W. Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency. Taiwanese Journal of Obstetrics & Gynecology. 56: 398-401. PMID 28600059 DOI: 10.1016/j.tjog.2017.04.026  0.32
2017 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. 56: 394-397. PMID 28600058 DOI: 10.1016/j.tjog.2017.04.025  0.32
2017 Chen CP, Yin CS, Wang LK, Chern SR, Chen SW, Lai ST, Wu PS, Chen WL, Wang W. Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 20p (20p12-p13) encompassing JAG1 and a literature review of prenatal diagnosis of Alagille syndrome. Taiwanese Journal of Obstetrics & Gynecology. 56: 390-393. PMID 28600057 DOI: 10.1016/j.tjog.2017.04.024  0.32
2017 Chen CP, Yip HK, Wang LK, Chern SR, Chen SW, Lai ST, Wu PS, Wang W. Molecular genetic characterization of a prenatally detected 1.484-Mb Xq13.3-q21.1 duplication encompassing ATRX and a literature review of syndromic intellectual disability and congenital abnormalities in males with a duplication at Xq13.3-q21.1. Taiwanese Journal of Obstetrics & Gynecology. 56: 385-389. PMID 28600056 DOI: 10.1016/j.tjog.2017.04.023  0.32
2017 Chen CP, Hung FY, Chern SR, Wu PS, Chen YN, Chen SW, Yang CW, Chen WL, Wang W. Prenatal diagnosis of mosaicism for trisomy 15 in a single colony at amniocentesis with a favorable fetal outcome. Taiwanese Journal of Obstetrics & Gynecology. 56: 268-269. PMID 28420524 DOI: 10.1016/j.tjog.2017.01.007  0.32
2017 Chen CP, Ko TM, Wang LK, Lin SP, Chern SR, Wu PS, Chen YN, Chen SW, Yang CW, Town DD, Lee MS, Wang W. Molecular cytogenetic characterization and prenatal diagnosis of familial Xp22.33 microdeletion encompassing short stature homeobox gene in a male fetus with a favorable outcome. Taiwanese Journal of Obstetrics & Gynecology. 56: 264-267. PMID 28420523 DOI: 10.1016/j.tjog.2017.01.006  0.32
2017 Chen CP, Lin CJ, Chern SR, Wu PS, Chen YN, Chen SW, Pan CW, Yang CW, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome. Taiwanese Journal of Obstetrics & Gynecology. 56: 238-242. PMID 28420516 DOI: 10.1016/j.tjog.2017.01.005  0.32
2017 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. 56: 234-237. PMID 28420515 DOI: 10.1016/j.tjog.2017.01.004  0.32
2017 Chen CP, Wang KG, Huang HK, Peng CR, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Wang W. Detection of mosaic 15q11.1-q11.2 deletion encompassing NBEAP1 and POTEB in a fetus with diffuse lymphangiomatosis. Taiwanese Journal of Obstetrics & Gynecology. 56: 230-233. PMID 28420514 DOI: 10.1016/j.tjog.2017.01.003  0.32
2017 Chen CP, Chern SR, Chen YN, Chen SW, Wu PS, Yang CW, Lee CC, Lee MS, Pan CW, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1-q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality. Taiwanese Journal of Obstetrics & Gynecology. 56: 217-223. PMID 28420511 DOI: 10.1016/j.tjog.2017.01.002  0.32
2017 Chen CP, Lin SP, Lee CL, Chern SR, Wu PS, Chen YN, Chen SW, Wang W. Recurrent 2q13 microduplication encompassing MALL, NPHP1, RGPD6, and BUB1 associated with autism spectrum disorder, intellectual disability, and liver disorder. Taiwanese Journal of Obstetrics & Gynecology. 56: 98-101. PMID 28254236 DOI: 10.1016/j.tjog.2016.12.003  0.32
2017 Chen CP, Lin SP, Lee CL, Chern SR, Wu PS, Chen YN, Chen SW, Wang W. Familial transmission of recurrent 15q11.2 (BP1-BP2) microdeletion encompassing NIPA1, NIPA2, CYFIP1, and TUBGCP5 associated with phenotypic variability in developmental, speech, and motor delay. Taiwanese Journal of Obstetrics & Gynecology. 56: 93-97. PMID 28254235 DOI: 10.1016/j.tjog.2016.12.002  0.32
2017 Chen SW, Chen CP, Wang LK, Chern SR, Wu PC, Chen YN, Lin CJ, Chen WL, Wang W. Perinatal imaging findings and molecular genetic analysis of thanatophoric dysplasia type 1 in a fetus with a c.2419T>G (p.Ter807Gly) (X807G) mutation in FGFR3. Taiwanese Journal of Obstetrics & Gynecology. 56: 87-92. PMID 28254233 DOI: 10.1016/j.tjog.2016.12.013  0.32
2017 Chen CP, Wang LK, Wu PC, Chang TY, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Yang CW, Wang W. 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. Taiwanese Journal of Obstetrics & Gynecology. 56: 102-105. PMID 28254208 DOI: 10.1016/j.tjog.2016.12.004  0.32
2016 Chen CP, Hung FY, Chern SR, Wu PS, Chen YN, Chen SW, Lee MS, Yang CW, Wang W. Prenatal diagnosis of low-level mosaicism for trisomy 18 associated with a favorable fetal outcome. Taiwanese Journal of Obstetrics & Gynecology. 55: 902-903. PMID 28040147 DOI: 10.1016/j.tjog.2016.10.001  0.32
2016 Chen CP, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Yang CW, Wang W. Prenatal diagnosis of low-level mosaicism for trisomy 12 associated with a favorable pregnancy outcome. Taiwanese Journal of Obstetrics & Gynecology. 55: 900-901. PMID 28040146 DOI: 10.1016/j.tjog.2016.08.006  0.32
2016 Chen CP, Chern SR, Chiu NC, Liu YP, Chen YN, Chen SW, Wang W. Detection of a novel c.7106_7110delinsT heterozygous mutation in the FLNA gene in an asymptomatic mother with periventricular nodular heterotopia during prenatal genetic counseling. Taiwanese Journal of Obstetrics & Gynecology. 55: 897-899. PMID 28040145 DOI: 10.1016/j.tjog.2016.08.005  0.32
2016 Chen CP, Fu CH, Lin YH, Chern SR, Wu PS, Chen YN, Chen SW, Wang W. Prenatal diagnosis of familial transmission of 17q12 microduplication associated with no apparent phenotypic abnormality. Taiwanese Journal of Obstetrics & Gynecology. 55: 871-873. PMID 28040137 DOI: 10.1016/j.tjog.2016.08.004  0.32
2016 Chen CP, Lin SP, Chern SR, Wu PS, Chen YN, Chen SW, Yang CW, Lee MS, Wang W. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22→q11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder, and intellectual disability. Taiwanese Journal of Obstetrics & Gynecology. 55: 856-860. PMID 28040133 DOI: 10.1016/j.tjog.2016.08.003  0.32
2016 Chen CP, Lin SP, Lin YH, Chern SR, Wu PS, Chen YN, Chen SW, Yang CW, Chen WL, Wang W. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities. Taiwanese Journal of Obstetrics & Gynecology. 55: 852-855. PMID 28040132 DOI: 10.1016/j.tjog.2016.08.002  0.32
2016 Chen CP, Ko TM, Su YN, Wang LK, Chern SR, Wu PS, Chen YN, Chen SW, Ko K, Lee CC, Chen LF, Yang CW, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentric inversion. Taiwanese Journal of Obstetrics & Gynecology. 55: 733-737. PMID 27751426 DOI: 10.1016/j.tjog.2016.07.007  0.32
2016 Chen CP, Lin SP, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Town DD, Yang CW, Wang W. Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome. Taiwanese Journal of Obstetrics & Gynecology. 55: 728-732. PMID 27751425 DOI: 10.1016/j.tjog.2016.06.017  0.32
2016 Chen CP, Wang LK, Chern SR, Chen YN, Chen SW, Wu PS, Town DD, Pan CW, Yang CW, Wang W. Mosaic trisomy 17 at amniocentesis: Prenatal diagnosis, molecular genetic analysis, and literature review. Taiwanese Journal of Obstetrics & Gynecology. 55: 712-717. PMID 27751421 DOI: 10.1016/j.tjog.2016.07.006  0.32
2016 Chen CP, Chen CY, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Town DD, Lee MS, Yang CW, Wang W. Molecular cytogenetic characterization of Xp22.32→pter deletion and Xq26.3→qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq) inv(X)(p22.3q26.3), a hypoplastic left heart, short stature, and maternal X chromosome pericentric inversion. Taiwanese Journal of Obstetrics & Gynecology. 55: 705-711. PMID 27751420 DOI: 10.1016/j.tjog.2016.05.009  0.32
2016 Chen CP, Chang SJ, Chern SR, Wu PS, Chen YN, Chen SW, Yang CW, Pan CW, Wang W. Rapid diagnosis of pseudomosaicism in a case of Level II mosaicism for trisomy 5 in a single colony from an in situ culture of amniocytes and a review of mosaic trisomy 5 at amniocentesis. Taiwanese Journal of Obstetrics & Gynecology. 55: 602-3. PMID 27590391 DOI: 10.1016/j.tjog.2016.05.005  0.32
2016 Chen CP, Lin CJ, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Chen LF, Yang CW, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication. Taiwanese Journal of Obstetrics & Gynecology. 55: 596-601. PMID 27590390 DOI: 10.1016/j.tjog.2016.06.008  0.32
2016 Chen CP, Wang LK, Chern SR, Wu PS, Ko K, Chen YN, Chen SW, Lee MS, Wang W. Prenatal diagnosis of partial monosomy 5p (5p15.1→pter) and partial trisomy 7p (7p15.2→pter) associated with cystic hygroma, abnormal skull development, and ventriculomegaly. Taiwanese Journal of Obstetrics & Gynecology. 55: 591-5. PMID 27590389 DOI: 10.1016/j.tjog.2016.06.014  0.32
2016 Chen CP, Chang TY, Wang LK, Chern SR, Wu PS, Chen YN, Chen SW, Chen WL, Wang W. 22q13 deletion syndrome in a fetus associated with microtia, hemivertebrae, and congenital heart defects on prenatal ultrasound. Taiwanese Journal of Obstetrics & Gynecology. 55: 455-6. PMID 27343339 DOI: 10.1016/j.tjog.2016.05.003  0.32
2016 Chen CP, Chiang S, Wang KL, Cho FN, Chen M, Chern SR, Wu PS, Chen YN, Chen SW, Chang SP, Chen WL, Wang W. Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay, and speech delay. Taiwanese Journal of Obstetrics & Gynecology. 55: 419-22. PMID 27343327 DOI: 10.1016/j.tjog.2016.05.002  0.32
2016 Chen CP, Ko TM, Huang WC, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Pan CW, Yang CW, Wang W. Molecular cytogenetic characterization of inv dup del(8p) in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction. Taiwanese Journal of Obstetrics & Gynecology. 55: 415-8. PMID 27343326 DOI: 10.1016/j.tjog.2016.05.001  0.32
2016 Chen CP, Ko TM, Chern SR, Wu PS, Chen YN, Chen SW, Chen LF, Yang CW, Wang W. Prenatal diagnosis of low-level mosaicism for trisomy 2 associated with a favorable pregnancy outcome. Taiwanese Journal of Obstetrics & Gynecology. 55: 303-4. PMID 27125422 DOI: 10.1016/j.tjog.2016.03.001  0.32
2016 Chen CP, Hung FY, Chern SR, Wu PS, Chen YN, Chen SW, Lee CC, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter). Taiwanese Journal of Obstetrics & Gynecology. 55: 288-92. PMID 27125417 DOI: 10.1016/j.tjog.2016.02.015  0.32
2016 Chen CP, Wang YL, Chern SR, Wu PS, Chen YN, Chen SW, Chen LF, Lee MS, Yang CW, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes. Taiwanese Journal of Obstetrics & Gynecology. 55: 285-7. PMID 27125416 DOI: 10.1016/j.tjog.2016.02.014  0.32
2016 Chen CP, Chen CY, Chern SR, Wu PS, Chen YN, Chen SW, Chen LF, Yang CW, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetralogy of Fallot. Taiwanese Journal of Obstetrics & Gynecology. 55: 270-4. PMID 27125413 DOI: 10.1016/j.tjog.2016.02.013  0.32
2015 Chen CP, Lin MH, Chen YY, Chern SR, Chen YN, Wu PS, Pan CW, Lee MS, Wang W. Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3-q24.11 and 8q24.13 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT1. Taiwanese Journal of Obstetrics & Gynecology. 54: 592-6. PMID 26522117 DOI: 10.1016/j.tjog.2015.08.013  0.32
2015 Chen CP, Chern SR, Chen YN, Wu PS, Yang CW, Chen LF, Wang W. Mosaic trisomy 15 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review. Taiwanese Journal of Obstetrics & Gynecology. 54: 426-31. PMID 26384064 DOI: 10.1016/j.tjog.2015.06.002  0.32
2015 Chen YH, Chang CY, Chang CF, Chen PC, Lee YT, Chern CY, Tsai JN. Pro-Angiogenic Effects of Chalcone Derivatives in Zebrafish Embryos in Vivo. Molecules (Basel, Switzerland). 20: 12512-24. PMID 26184137 DOI: 10.3390/molecules200712512  0.32
2015 Chen CP, Huang MC, Chern SR, Kuo YL, Chen YN, Wu PS, Chen LF, Pan CW, Wang W. Distal 3p duplication and terminal 7q deletion associated with nuchal edema and cyclopia in a fetus and a review of the literature. Taiwanese Journal of Obstetrics & Gynecology. 54: 297-302. PMID 26166345 DOI: 10.1016/j.tjog.2015.04.001  0.32
2015 Li W, Liu Y, Wang J, He M, Zhou X, Yang C, Yuan C, Wang J, Chern M, Yin J, Chen W, Ma B, Wang Y, Qin P, Li S, et al. The durably resistant rice cultivar Digu activates defence gene expression before the full maturation of Magnaporthe oryzae appressorium. Molecular Plant Pathology. PMID 26095454 DOI: 10.1111/mpp.12286  0.32
2015 Chen CP, Wang LK, Chern SR, Kuo YL, Chen YN, Pan CW, Wang W. First-trimester diagnosis of recurrent omphalocele associated with fetal trisomy 18 but without parental mosaicism. Taiwanese Journal of Obstetrics & Gynecology. 54: 194-5. PMID 25951728 DOI: 10.1016/j.tjog.2015.01.001  0.32
2015 Chen CP, Ko TM, Huang MC, Chern SR, Lin TW, Chang TY, Kuo YL, Chen WL, Wang W. Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma. Taiwanese Journal of Obstetrics & Gynecology. 54: 78-80. PMID 25675926 DOI: 10.1016/j.tjog.2014.12.003  0.32
2015 Chen CP, Wang YL, Chern SR, Liu YP, Peng CR, Kuo YL, Wu PS, Chen WL, Wang W. Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diaphragmatic hernia. Taiwanese Journal of Obstetrics & Gynecology. 54: 66-70. PMID 25675923 DOI: 10.1016/j.tjog.2014.12.001  0.32
2015 Chen CP, Su JW, Chern SR, Kuo YL, Wu PS, Lee MS, Yang CW, Wang W. Detection of no isochromosome 20q by interphase fluorescent in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis. Taiwanese Journal of Obstetrics & Gynecology. 54: 58-61. PMID 25675921 DOI: 10.1016/j.tjog.2014.12.002  0.32
2014 Chen CP, Lin CJ, Chern SR, Liu YP, Kuo YL, Chen YN, Wu PS, Town DD, Chen LF, Yang CW, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2-q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome. Taiwanese Journal of Obstetrics & Gynecology. 53: 583-7. PMID 25510705 DOI: 10.1016/j.tjog.2014.10.002  0.32
2014 Chen CP, Ko TM, Chen CY, Wang TY, Chern SR, Kuo YL, Wang W. First-trimester molecular diagnosis of complete hydatidiform mole associated with dizygotic twin pregnancy conceived by intrauterine insemination. Taiwanese Journal of Obstetrics & Gynecology. 53: 572-8. PMID 25510703 DOI: 10.1016/j.tjog.2014.10.001  0.32
2014 Chen CP, Peng CR, Chern SR, Kuo YL, Wu PS, Town DD, Pan CW, Yang CW, Wang W. Interphase fluorescence in situ hybridization characterization of mosaicism using uncultured amniocytes and cultured stimulated cord blood lymphocytes in prenatally detected Pallister-Killian syndrome. Taiwanese Journal of Obstetrics & Gynecology. 53: 566-71. PMID 25510702 DOI: 10.1016/j.tjog.2014.09.004  0.32
2014 Chen JF, Lee CF, Chern Y. Adenosine receptor neurobiology: overview. International Review of Neurobiology. 119: 1-49. PMID 25175959 DOI: 10.1016/B978-0-12-801022-8.00001-5  0.36
2014 Sun CS, Wang CY, Chen BP, He RY, Liu GC, Wang CH, Chen W, Chern Y, Huang JJ. The influence of pathological mutations and proline substitutions in TDP-43 glycine-rich peptides on its amyloid properties and cellular toxicity. Plos One. 9: e103644. PMID 25090004 DOI: 10.1371/journal.pone.0103644  0.52
2014 Kuo YL, Chen CP, Wang LK, Ko TM, Chang TY, Chern SR, Wu PS, Chen YT, Chang SY. Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects. Taiwanese Journal of Obstetrics & Gynecology. 53: 248-51. PMID 25017279 DOI: 10.1016/j.tjog.2014.04.021  0.32
2014 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. 53: 129-32. PMID 24767667 DOI: 10.1016/j.tjog.2013.12.004  0.32
2014 Chen CP, Lin CL, Ko TM, Chern SR, Chen YT, Wu PS, Kuo YL, Lee MS, Wang W. Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid confirmation of low-level mosaicism for tetrasomy 18p. Taiwanese Journal of Obstetrics & Gynecology. 53: 126-8. PMID 24767666 DOI: 10.1016/j.tjog.2013.11.003  0.32
2014 Chen CP, Lin MH, Chern SR, Chen YT, Wu PS, Kuo YL, Lee MS, Wang W. Directly transmitted 4.5-Mb triplication of 4q12-q13.1: prenatal diagnosis and molecular cytogenetic characterization. Taiwanese Journal of Obstetrics & Gynecology. 53: 123-5. PMID 24767665 DOI: 10.1016/j.tjog.2013.11.002  0.32
2014 Chen CP, Wang PT, Lin SP, Chern SR, Chen YT, Wu PS, Kuo YL, Chen WL, Wang W. Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid diagnosis of true mosaicism in a case of level II mosaicism involving trisomy 21 in a single colony from an in situ culture of amniocytes. Taiwanese Journal of Obstetrics & Gynecology. 53: 120-2. PMID 24767664 DOI: 10.1016/j.tjog.2013.11.001  0.32
2014 Chen CP, Su YN, Chen SU, Chang TY, Wu PC, Chern SR, Wu PS, Kuo YL, Wang W. 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. Taiwanese Journal of Obstetrics & Gynecology. 53: 90-4. PMID 24767654 DOI: 10.1016/j.tjog.2013.12.003  0.32
2014 Chen CP, Wang LK, Chern SR, Wu PS, Chen YT, Kuo YL, Chen WL, Lee MS, Wang W. Mosaic tetrasomy 9p at amniocentesis: prenatal diagnosis, molecular cytogenetic characterization, and literature review. Taiwanese Journal of Obstetrics & Gynecology. 53: 79-85. PMID 24767652 DOI: 10.1016/j.tjog.2013.12.002  0.32
2014 Chen CP, Lin SP, Chern SR, Wu PS, Su JW, Lee CC, Wang W. A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation. Taiwanese Journal of Obstetrics & Gynecology. 53: 74-8. PMID 24767651 DOI: 10.1016/j.tjog.2013.10.037  0.32
2014 Chen CP, Su YN, Lin MH, Wang TY, Chern SR, Kuo YL, Chen YT, Wang W. Detection of altered methylation status at 11p15.5 and 7q32 in placental mesenchymal dysplasia. Taiwanese Journal of Obstetrics & Gynecology. 53: 68-73. PMID 24767650 DOI: 10.1016/j.tjog.2013.10.036  0.32
2014 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. 536: 425-9. PMID 24374139 DOI: 10.1016/j.gene.2013.12.036  0.32
2014 Chen CP, Lin SP, Chern SR, Kuo YL, Wu PS, Chen YT, Lee MS, Wang W. Array CGH characterization of an unbalanced X-autosome translocation associated with Xq27.2-qter deletion, 11q24.3-qter duplication and Xq22.3-q27.1 duplication in a girl with primary amenorrhea and mental retardation. Gene. 535: 88-92. PMID 24279999 DOI: 10.1016/j.gene.2013.11.026  0.32
2014 Chern SJ, Sun CH. Linearly constrained RLS algorithm with variable forgetting factor for DS-CDMA system 2014 International Symposium On Intelligent Signal Processing and Communication Systems, Ispacs 2014. 261-264. DOI: 10.1109/ISPACS.2014.7024464  0.88
2013 Chen CP, Chen YY, Chern SR, Kuo YL, Lee CC, Wang W. First-trimester sonographic demonstration of digynic triploidy. Taiwanese Journal of Obstetrics & Gynecology. 52: 613-5. PMID 24411058 DOI: 10.1016/j.tjog.2013.10.033  0.32
2013 Chen CP, Hwu YM, Chen CY, Su YN, Lin TH, Kuo YL, Chern SR, Wang W. Concordant myelomeningocele in dizygotic twins conceived by intracytoplasmic sperm injection, in vitro fertilization, and embryo transfer Taiwanese Journal of Obstetrics and Gynecology. 52: 611-612. PMID 24411057 DOI: 10.1016/j.tjog.2013.10.032  0.32
2013 Chen CP, Huang HK, Liu YP, Chern SR, Su JW, Wang W. Pfeiffer syndrome with FGFR2 W290C mutation perinatally presenting extreme proptosis Taiwanese Journal of Obstetrics and Gynecology. 52: 607-610. PMID 24411056 DOI: 10.1016/j.tjog.2013.10.031  0.32
2013 Sung PL, Cheng EE, Chen YJ, Chern SR, Shih CY, Chang CM, Wang PH, Yen MS, Huang CY, Chen CP. Prenatal diagnosis of de novo monosomy 7q33-qter associated with hydrops fetalis, semilobar holoprosencephaly, and premaxillary dysgenesis. Taiwanese Journal of Obstetrics & Gynecology. 52: 602-6. PMID 24411055 DOI: 10.1016/j.tjog.2013.10.030  0.32
2013 Chen CP, Chang TY, Chen YY, Chern SR, Su JW, Wang W. VACTERL association with hydrocephalus in a fetus conceived by in vitro fertilization and embryo transfer. Taiwanese Journal of Obstetrics & Gynecology. 52: 575-9. PMID 24411047 DOI: 10.1016/j.tjog.2013.10.022  0.32
2013 Chen CP, Chang SD, Wang TH, Wang LK, Tsai JD, Liu YP, Chern SR, Wu PS, Su JW, Chen YT, Wang W. Detection of recurrent transmission of 17q12 microdeletion by array comparative genomic hybridization in a fetus with prenatally diagnosed hydronephrosis, hydroureter, and multicystic kidney, and variable clinical spectrum in the family. Taiwanese Journal of Obstetrics & Gynecology. 52: 551-7. PMID 24411042 DOI: 10.1016/j.tjog.2013.10.017  0.32
2013 Chen CP, Chern SR, Wu PS, Su JW, Chen YT, Chen LF, Pan CW, Wang W. Application of interphase fluorescence in situ hybridization to uncultured amniocytes for differential diagnosis of pseudomosaicism from true mosaicism in mosaic isochromosome 20q detected at amniocentesis. Taiwanese Journal of Obstetrics & Gynecology. 52: 450-3. PMID 24075394 DOI: 10.1016/j.tjog.2013.06.007  0.32
2013 Chen CP, Wang KG, Ko TM, Chern SR, Su JW, Town DD, Wang W. Mosaic trisomy 14 at amniocentesis: prenatal diagnosis and literature review. Taiwanese Journal of Obstetrics & Gynecology. 52: 446-9. PMID 24075393 DOI: 10.1016/j.tjog.2013.07.001  0.32
2013 Chen CP, Chang TY, Lin MH, Chern SR, Su JW, Wang W. 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 Taiwanese Journal of Obstetrics and Gynecology. 52: 420-425. PMID 24075385 DOI: 10.1016/j.tjog.2013.05.003  0.32
2013 Chen CP, Chang TY, Guo WY, Su YN, Chen YY, Chern SR, Su JW, Wang W. 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. Taiwanese Journal of Obstetrics & Gynecology. 52: 415-9. PMID 24075384 DOI: 10.1016/j.tjog.2013.05.002  0.32
2013 Chen CP, Fu CH, Chern SR, Wu PS, Su JW, Lee CC, Lee MS, Wang W. De novo unbalanced translocation resulting in monosomy for distal 5p (5p14.1 → pter) and 14q (14q32.31 → qter) associated with fetal nuchal edema, microcephaly, intrauterine growth restriction, and single umbilical artery: prenatal diagnosis and molecular cytogenetic characterization. Taiwanese Journal of Obstetrics & Gynecology. 52: 401-6. PMID 24075381 DOI: 10.1016/j.tjog.2013.06.005  0.32
2013 Chen CP, Chen YY, Chern SR, Wu PS, Su JW, Chen YT, Lee CC, Chen LF, Wang W. Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly, and facial dysmorphism. Taiwanese Journal of Obstetrics & Gynecology. 52: 395-400. PMID 24075380 DOI: 10.1016/j.tjog.2013.06.004  0.32
2013 Chen CP, Chang TY, Guo WY, Wu PC, Wang LK, Chern SR, Wu PS, Su JW, Chen YT, Chen LF, Wang W. Chromosome 17p13.3 deletion syndrome: aCGH characterization, prenatal findings and diagnosis, and literature review. Gene. 532: 152-9. PMID 24055730 DOI: 10.1016/j.gene.2013.09.044  0.32
2013 Chen CP, Lin CJ, Chen YY, Wang LK, Chern SR, Wu PS, Su JW, Chen LF, Town DD, Pan CW, Wang W. 3q26.31-q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: prenatal diagnosis and aCGH characterization. Gene. 532: 80-6. PMID 24055486 DOI: 10.1016/j.gene.2013.09.025  0.32
2013 Chen CP, Huang MC, Chen YY, Chern SR, Wu PS, Chen YT, Su JW, Wang W. Prenatal diagnosis of de novo interstitial deletions involving 5q23.1-q23.3 and 18q12.1-q12.3 by array CGH using uncultured amniocytes in a pregnancy with fetal interrupted aortic arch and atrial septal defect. Gene. 531: 496-501. PMID 24036431 DOI: 10.1016/j.gene.2013.09.010  0.32
2013 Chen CP, Lin SP, Chern SR, Wu PS, Su JW, Wang W. A boy with cleft palate, hearing impairment, microcephaly, micrognathia and psychomotor retardation and a microdeletion in 6p25.3 involving the DUSP22 gene. Genetic Counseling (Geneva, Switzerland). 24: 243-6. PMID 24032297  0.32
2013 Chen CP, Su YN, Chen CY, Chern SR, Wu PS, Su JW, Lee CC, Chen LF, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of a de novo pure distal 9p deletion and literature review. Genomics. 102: 265-9. PMID 23981964 DOI: 10.1016/j.ygeno.2013.08.003  0.32
2013 Chen CP, Lee MJ, Chern SR, Wu PS, Su JW, Chen YT, Lee MS, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of a de novo proximal interstitial deletion of chromosome 4p (4p15.2→p14). Gene. 529: 351-6. PMID 23948085 DOI: 10.1016/j.gene.2013.07.063  0.32
2013 Chen CP, Tsai CH, Chern SR, Wu PS, Su JW, Lee CC, Chen YT, Chen WL, Chen LF, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13. Gene. 529: 163-8. PMID 23933417 DOI: 10.1016/j.gene.2013.07.050  0.32
2013 Chen CP, Lin SP, Liu YP, Chern SR, Wu PS, Su JW, Chen YT, Lee CC, Wang W. An interstitial deletion of 8q23.3-q24.22 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and epilepsy. Gene. 529: 176-80. PMID 23933416 DOI: 10.1016/j.gene.2013.07.045  0.32
2013 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. 529: 169-75. PMID 23933412 DOI: 10.1016/j.gene.2013.07.048  0.32
2013 Chen CP, Lin CJ, Chen CY, Chern SR, Wu PS, Su JW, Wang W. Maternal transmission of interstitial microdeletion in 5q13.2 detected during prenatal diagnosis of coarctation of the aorta. Taiwanese Journal of Obstetrics & Gynecology. 52: 303-5. PMID 23915873 DOI: 10.1016/j.tjog.2013.04.032  0.32
2013 Chen CP, Hung FY, Chern SR, Wu PS, Su JW, Wang W. Application of interphase FISH to uncultured amniocytes for rapid confirmation of true trisomy 2 mosaicism in the case of suspected amniocyte mosaicism involving trisomy 2 in a single colony. Taiwanese Journal of Obstetrics & Gynecology. 52: 300-2. PMID 23915872 DOI: 10.1016/j.tjog.2013.04.031  0.32
2013 Chen CP, Huang MC, Chern SR, Wu PS, Su JW, Wang W. Discordant anencephaly and Cantrell syndrome in monozygotic twins conceived by ICSI and IVF-ET. Taiwanese Journal of Obstetrics & Gynecology. 52: 297-9. PMID 23915871 DOI: 10.1016/j.tjog.2013.04.029  0.32
2013 Chen CP, Chen YY, Chern SR, Wu PS, Su JW, Chen WL, Wang W. Prenatal diagnosis of a distal 3p deletion associated with fetoplacental chromosomal discrepancy and confined placental mosaicism detected by array comparative genomic hybridization. Taiwanese Journal of Obstetrics & Gynecology. 52: 278-84. PMID 23915866 DOI: 10.1016/j.tjog.2013.04.023  0.32
2013 Chen CP, Su YN, Chang TY, Chern SR, Chen CY, Su JW, Wang W. 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. Taiwanese Journal of Obstetrics & Gynecology. 52: 273-7. PMID 23915865 DOI: 10.1016/j.tjog.2013.04.022  0.32
2013 Chen CP, Huang JP, Chen YY, Chern SR, Wu PS, Su JW, Pan CW, Wang W. Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: prenatal diagnosis and aCGH characterization using uncultured amniocytes. Gene. 527: 636-41. PMID 23850725 DOI: 10.1016/j.gene.2013.06.081  0.32
2013 Chen CP, Huang JP, Chen YY, Chern SR, Wu PS, Su JW, Chen YT, Chen WL, Wang W. Chromosome 22q11.2 deletion syndrome: prenatal diagnosis, array comparative genomic hybridization characterization using uncultured amniocytes and literature review. Gene. 527: 405-9. PMID 23791650 DOI: 10.1016/j.gene.2013.06.009  0.32
2013 Chen CP, Lin SP, Liu YP, Chern SR, Wu PS, Chen YT, Su JW, Lee CC, Wang W. 6p21.2-p12.3 deletion detected by aCGH in an 8-year-old girl with cleidocranial dysplasia and developmental delay. Gene. 523: 99-102. PMID 23578800 DOI: 10.1016/j.gene.2013.03.121  0.32
2013 Chen CP, Hsu CY, Su YN, Wang TY, Chern SR, Su JW, Wang W. Placental mesenchymal dysplasia associated with antepartum hemorrhage, subchorionic hematoma, and intrauterine growth restriction. Taiwanese Journal of Obstetrics & Gynecology. 52: 154-6. PMID 23548244 DOI: 10.1016/j.tjog.2013.01.023  0.32
2013 Chen CP, Lin SP, Su YN, Chern SR, Su JW, Wang W. Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome. Taiwanese Journal of Obstetrics & Gynecology. 52: 152-3. PMID 23548243 DOI: 10.1016/j.tjog.2013.01.022  0.32
2013 Chen CP, Chang SD, Chueh HY, Su YN, Chern SR, Su JW, Chen YT, Chen WL, Lee MS, Wang W. Discrepancy in the trisomy mosaicism level between cultured amniocytes and uncultured amniocytes in prenatally detected mosaic trisomy 20. Taiwanese Journal of Obstetrics & Gynecology. 52: 145-6. PMID 23548241 DOI: 10.1016/j.tjog.2013.01.021  0.32
2013 Chen CP, Hwang KS, Su HY, Lin SP, Su YN, Chern SR, Su JW, Chen YT, Chen WL, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 14q (14q31.3→q32.12) associated with abnormal maternal serum biochemistry. Taiwanese Journal of Obstetrics & Gynecology. 52: 125-8. PMID 23548233 DOI: 10.1016/j.tjog.2012.08.002  0.32
2013 Chen CP, Su YN, Lin SP, Chern SR, Su JW, Chen YT, Lee MS, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3→q23.3) associated with abnormal maternal serum biochemistry. Taiwanese Journal of Obstetrics & Gynecology. 52: 120-4. PMID 23548232 DOI: 10.1016/j.tjog.2013.01.015  0.32
2013 Chen CP, Lin SP, Su YN, Chern SR, Su JW, Wang W. Prenatal diagnosis of recurrent autosomal dominant osteogenesis imperfecta associated with unaffected parents and paternal gonadal mosaicism. Taiwanese Journal of Obstetrics & Gynecology. 52: 106-9. PMID 23548228 DOI: 10.1016/j.tjog.2013.01.013  0.32
2013 Chen CP, Su YN, Su JW, Chern SR, Chen YT, Chen LF, Wang W. Mosaic trisomy 12 at amniocentesis: prenatal diagnosis and molecular genetic analysis. Taiwanese Journal of Obstetrics & Gynecology. 52: 97-105. PMID 23548227 DOI: 10.1016/j.tjog.2013.01.012  0.32
2013 Chen CP, Cheng PJ, Chang SD, Lee YX, Shih JC, Chern SR, Wu PS, Su JW, Chen YT, Hsieh AH, Chen TH, Chen LF, Wang W. Ring chromosome 21 presenting with sacrococcygeal teratoma: prenatal diagnosis, molecular cytogenetic characterization and literature review. Gene. 522: 111-6. PMID 23545316 DOI: 10.1016/j.gene.2013.03.064  0.32
2013 Chen CP, Chang SJ, Chern SR, Wu PS, Chen YT, Su JW, Chen WL, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial deletion of 7q (7q22.1→q31.1). Gene. 521: 311-5. PMID 23545313 DOI: 10.1016/j.gene.2013.03.100  0.32
2013 Chen CP, Huang MC, Chen YY, Chern SR, Wu PS, Su JW, Town DD, Wang W. Cri-du-chat (5p-) syndrome presenting with cerebellar hypoplasia and hypospadias: prenatal diagnosis and aCGH characterization using uncultured amniocytes. Gene. 524: 407-11. PMID 23500598 DOI: 10.1016/j.gene.2013.03.003  0.32
2013 Chen CP, Lin CJ, Chang TY, Chern SR, Wu PS, Chen YT, Su JW, Lee CC, Chen LF, Wang W. Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization. Gene. 519: 164-8. PMID 23403238 DOI: 10.1016/j.gene.2013.01.055  0.32
2013 Chen CP, Chen YY, Chern SR, Wu PS, Su JW, Chen YT, Chen LF, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21→qter) and partial monosomy 6q (6q27→qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold. Gene. 516: 138-42. PMID 23266815 DOI: 10.1016/j.gene.2012.12.051  0.32
2013 Chen CP, Chang YL, Chern SR, Wu PS, Su JW, Chen WL, Chen LF, Wang W. Prenatal diagnosis of partial trisomy 3q (3q27.3→qter) and partial monosomy 14q (14q31.3→qter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints. Gene. 516: 132-7. PMID 23266805 DOI: 10.1016/j.gene.2012.12.052  0.32
2013 Chen CP, Lai TC, Chern SR, Li SH, Chou HC, Chen YW, Lin ST, Lu YC, Wu CL, Li JM, Chan HL. Proteome differences between male and female fetal cells in amniotic fluid. Omics : a Journal of Integrative Biology. 17: 16-26. PMID 22404150 DOI: 10.1089/omi.2010.0145  0.32
2013 Yang RHH, Lee CK, Chern SJ. Continuous phase modulation (CPM) revisited: Using time-Limited phase shaping pulses Ieice Transactions On Communications. 2828-2839. DOI: 10.1587/transcom.E96.B.2828  0.88
2013 Chern SJ, Huang WC, Yang RHH. Adaptive semi-blind channel estimation for ST-BC MIMO-CDMA systems with hybrid user signature Ispacs 2013 - 2013 International Symposium On Intelligent Signal Processing and Communication Systems. 369-373. DOI: 10.1109/ISPACS.2013.6704578  0.88
2013 Chern SJ, Wu CW, Hsieh CT. Degradation algorithm of compressive sensing for integer DCT with application to H. 264/AVC Ispacs 2013 - 2013 International Symposium On Intelligent Signal Processing and Communication Systems. 42-46. DOI: 10.1109/ISPACS.2013.6704519  0.88
2013 Chen CP, Huang HK, Liu YP, Chern SR, Su JW, Wang W. Pfeiffer syndrome with FGFR2 W290C mutation in perinatal presentation of extreme proptosis Taiwanese Journal of Obstetrics and Gynecology. DOI: 10.1016/j.tjog.2013.04.030  0.32
2013 Chern SJ, Cheng MK, Chao PS. Blind capon-like adaptive ST-BC MIMO-CDMA receiver based on constant modulus criterion Digital Signal Processing: a Review Journal. 23: 1958-1966. DOI: 10.1016/j.dsp.2013.08.003  0.88
2012 Chen CP, Lin SP, Huang YL, Chern SR, Su JW, Lee CC, Chen WL, Wang W. De novo satellited 2q associated with corpus callosum dysgenesis, short stature, mental retardation and developmental delay. Genetic Counseling (Geneva, Switzerland). 23: 497-503. PMID 23431751  0.32
2012 Chen CP, Lin SP, Su YN, Chern SR, Su JW, Lee CC, Wang W. Partial trisomy 1q (1q42.13-->qter) and partial monosomy 6q (6q27-->qter) in a girl with single median maxillary central incisor, corpus callosum dysgenesis and developmental delay. Genetic Counseling (Geneva, Switzerland). 23: 447-55. PMID 23431743  0.32
2012 Chen CP, Su YN, Chern SR, Wu PS, Su JW, Town DD, Wang W. Prenatal diagnosis of an interstitial deletion of 10q (10q11.21 → q21.1): array comparative genomic hybridization characterization and literature review. Taiwanese Journal of Obstetrics & Gynecology. 51: 672-6. PMID 23276582 DOI: 10.1016/j.tjog.2012.09.032  0.32
2012 Chen CP, Su YN, Chern SR, Chen YT, Su JW, Pan CW, Wang W. Prenatal diagnosis of trisomy 8 mosaicism. Taiwanese Journal of Obstetrics & Gynecology. 51: 666-8. PMID 23276580 DOI: 10.1016/j.tjog.2012.09.030  0.32
2012 Chen CP, Chen CY, Chern SR, Su JW, Wang W. First-trimester prenatal diagnosis of Ellis-van Creveld syndrome. Taiwanese Journal of Obstetrics & Gynecology. 51: 643-8. PMID 23276573 DOI: 10.1016/j.tjog.2012.10.001  0.32
2012 Chen CP, Su TH, Chern SR, Su JW, Lee CC, Wang W. Alobar holoprosencephaly, cebocephaly, and micropenis in a Klinefelter fetus of a diabetic mother. Taiwanese Journal of Obstetrics & Gynecology. 51: 630-4. PMID 23276570 DOI: 10.1016/j.tjog.2012.09.021  0.32
2012 Chen CP, Ko TM, Su YN, Chern SR, Su JW, Chen YT, Town DD, Wang W. Prenatal diagnosis of mosaic tetrasomy 18p. Taiwanese Journal of Obstetrics & Gynecology. 51: 625-9. PMID 23276569 DOI: 10.1016/j.tjog.2012.09.020  0.32
2012 Chen CP, Su YN, Chern SR, Chen YT, Wu PS, Su JW, Pan CW, Wang W. Mosaic trisomy 2 at amniocentesis: prenatal diagnosis and molecular genetic analysis. Taiwanese Journal of Obstetrics & Gynecology. 51: 603-11. PMID 23276565 DOI: 10.1016/j.tjog.2012.09.016  0.32
2012 Chen CP, Lin SP, Chen MR, Su YN, Chern SR, Liu YP, Su JW, Lee MS, Wang W. Partial monosomy 3p (3p26.2 --> pter) and partial trisomy 5q (5q34 --> qter) in a girl with coarctation of the aorta, congenital heart defects, short stature, microcephaly and developmental delay. Genetic Counseling (Geneva, Switzerland). 23: 405-13. PMID 23072190  0.32
2012 Chen CP, Lin SP, Suo YN, Chern SR, Su JW, Wang W. Identification of a missense mutation of c.3064G>A, Gly1022Ser in exon 43 of COL1A1 gene in a girl with osteogenesis imperfecta type III. Genetic Counseling (Geneva, Switzerland). 23: 359-65. PMID 23072183  0.32
2012 Chen CP, Su YN, Chern SR, Su JW, Chen YT, Lee CC, Wang W. Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo X;Y translocation Taiwanese Journal of Obstetrics and Gynecology. 51: 485-488. PMID 23040947 DOI: 10.1016/j.tjog.2012.07.037  0.32
2012 Chen CP, Su YN, Weng SL, Tsai FJ, Chen CY, Liu YP, Chern SR, Chen WL, Wu PC, Wang W. Rapid aneuploidy diagnosis of trisomy 18 by array comparative genomic hybridization using uncultured amniocytes in a pregnancy with fetal arachnoid cyst detected in late second trimester. Taiwanese Journal of Obstetrics & Gynecology. 51: 481-4. PMID 23040946 DOI: 10.1016/j.tjog.2012.07.036  0.32
2012 Chen CP, Chang SD, Chueh HY, Su YN, Su JW, Chern SR, Chen YT, Lee CC, Town DD, Chen WL, Chen LF, Lee MS, Pan CW, Wang W. Rapid positive confirmation of trisomy 21 mosaicism at amniocentesis by interphase FISH, QF-PCR and aCGH on uncultured amniocytes. Taiwanese Journal of Obstetrics & Gynecology. 51: 475-80. PMID 23040945 DOI: 10.1016/j.tjog.2012.07.035  0.32
2012 Chen CP, Su YN, Chen YY, Chern SR, Su JW, Chen YT, Town DD, Wang W. Usefulness of interphase FISH on uncultured amniocytes for rapid confirmation of low-level trisomy 7 mosaicism in a pregnancy with fetal intrauterine growth restriction and microcephaly Taiwanese Journal of Obstetrics and Gynecology. 51: 471-474. PMID 23040944 DOI: 10.1016/j.tjog.2012.07.034  0.32
2012 Chen CP, Su YN, Chen CY, Su JW, Chern SR, Town DD, Wang W. Pure partial monosomy 3p (3p25.3 → pter): Prenatal diagnosis and array comparative genomic hybridization characterization Taiwanese Journal of Obstetrics and Gynecology. 51: 435-439. PMID 23040932 DOI: 10.1016/j.tjog.2012.07.022  0.32
2012 Chen CP, Chern SR, Chen YY, Wu PC, Town DD, Chen WL, Wang W. Monozygotic twins with trisomy 18 of paternal origin: prenatal diagnosis and molecular cytogenetic characterization in a pregnancy with one structurally abnormal living fetus and one intrauterine fetal demise. Taiwanese Journal of Obstetrics & Gynecology. 51: 430-4. PMID 23040931 DOI: 10.1016/j.tjog.2012.07.021  0.32
2012 Chen CP, Chen M, Chern SR, Wu PS, Chang SP, Lee DJ, Chen YT, Chen LF, Su JW, Hwa-Ruey Hsieh A, Hwa-Jiun Hsieh A, Wang W. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2. Taiwanese Journal of Obstetrics & Gynecology. 51: 411-7. PMID 23040927 DOI: 10.1016/j.tjog.2012.07.017  0.32
2012 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. 51: 405-10. PMID 23040926 DOI: 10.1016/j.tjog.2012.07.016  0.32
2012 Chen CP, Lin SP, Hsu CH, Chern SR, Su JW, Chen YJ, Pan CW, Wang W. Pure distal 11q deletion without additional genomic imbalances in a female infant with Jacobsen syndrome and a de novo unbalanced reciprocal translocation. Genetic Counseling (Geneva, Switzerland). 23: 223-9. PMID 22876581  0.32
2012 Chen CP, Lin SP, Su YN, Su JW, Chern SR, Town DD, Wang W. Pure distal 9p deletion in a female infant with cerebral palsy. Genetic Counseling (Geneva, Switzerland). 23: 215-21. PMID 22876580  0.32
2012 Chen CP, Lin SP, Chen MR, Su JW, Chern SR, Chen YJ, Lee MS, Wang W. Phenotypic features of pure 9p deletion in a male infant include cryptorchidism, congenital heart defects and postaxial polydactyly. Genetic Counseling (Geneva, Switzerland). 23: 195-200. PMID 22876577  0.32
2012 Chen CP, Lin SP, Chern SR, Wu PS, Chang SD, Ng SH, Liu YP, Su JW, Wang W. A de novo 4.4-Mb microdeletion in 2p24.3 → p24.2 in a girl with bilateral hearing impairment, microcephaly, digit abnormalities and Feingold syndrome. European Journal of Medical Genetics. 55: 666-9. PMID 22842076 DOI: 10.1016/j.ejmg.2012.07.003  0.32
2012 Chen CP, Su YN, Hung FY, Chern SR, Su JW, Wang W. Identification of a COL1A2 mutation with a deletion spanning coding and intronic sequence in exon 19 and intron 19 in a fetus with osteogenesis imperfecta type II Taiwanese Journal of Obstetrics and Gynecology. 51: 312-314. PMID 22795120 DOI: 10.1016/j.tjog.2012.04.031  0.32
2012 Chen CP, Chen YH, Chern SR, Chang SJ, Tsai TL, Li SH, Chou HC, Lo YW, Lyu PC, Chan HL. Placenta proteome analysis from Down syndrome pregnancies for biomarker discovery. Molecular Biosystems. 8: 2360-72. PMID 22777171 DOI: 10.1039/c2mb25081k  0.32
2012 Lei TCW, Chern SJ. Padding block based DVC coding scheme with mutual bi-directional frame coding at decoder Ispacs 2012 - Ieee International Symposium On Intelligent Signal Processing and Communications Systems. 644-648. DOI: 10.1109/ISPACS.2012.6473569  0.88
2012 Chern SJ, Huang YS, Jan YG, Yang RHH. Performance of the MIMO PRCP-OFDM system with orthogonal cyclic-shift sequences Ispacs 2012 - Ieee International Symposium On Intelligent Signal Processing and Communications Systems. 553-558. DOI: 10.1109/ISPACS.2012.6473551  0.88
2012 Chen CP, Chern SR, Wu PS, Su JW, Chen LF, Wang W. Rapid Diagnosis of Trisomy 21 by Array Comparative Genomic Hybridization using Uncultured Amniocytes in a Pregnancy with Isolated Ventriculomegaly in the Fetus Journal of Medical Ultrasound. 20: 244-247. DOI: 10.1016/j.jmu.2012.10.004  0.32
2012 Chen CP, Chen YY, Liou JD, Chern SR, Wu PS, Su JW, Lee MS, Wang W. Rapid Diagnosis of Trisomy 18 Using Uncultured Amniocytes in Late Second Trimester in a Pregnancy with Fetal Congenital Heart Defects, Arthrogryposis, Omphalocele, and Mega Cisterna Magna Journal of Medical Ultrasound. 20: 186-190. DOI: 10.1016/j.jmu.2012.08.001  0.32
2007 Liu CL, Chang YC, Cheng SP, Chern SR, Yang TL, Lee JJ, Guo IC, Chen CP. The roles of serum leptin concentration and polymorphism in leptin receptor gene at codon 109 in breast cancer. Oncology. 72: 75-81. PMID 18004080 DOI: 10.1159/000111097  0.32
2004 Chen CP, Chern SR, Cheng SJ, Chang TY, Yeh LF, Lee CC, Pan CW, Wang W, Tzen CY. Second-trimester diagnosis of complete trisomy 9 associated with abnormal maternal serum screen results, open sacral spina bifida and congenital diaphragmatic hernia, and review of the literature. Prenatal Diagnosis. 24: 455-62. PMID 15229846 DOI: 10.1002/pd.900  0.32
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