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Chen-Chi Lee

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Physiology

Disorders

Procedures

Concepts & Ideas

Second Pregnancy Trimester

Anatomy

Chromosomes, Human, Pair 18

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Network (preview)

Co-Publications
Name
51
Chen, Chih-Ping
42
Wang, Wayseen
36
Chern, Schu-Rern
14
Chen, Wen-Lin
14
Lin, Shuan-Pei
12
Tzen, Chin-Yuan
11
Chang, Tung-Yao
10
Town, Dai-Dyi
9
Lin, Chyi-Chyang
9
Chen, Li-Feng
8
Li, Yueh-Chun
7
Hsieh, Lie-Jiau
6
Pan, Chen-Wen
4
Tsai, Fuu-Jen
4
Wang, Tzu-Hao

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Publications

TOP 3
Chen Chih-Ping; Chen Yann-Jang; Chern Schu-Rern; Tsai Fuu-Jen; Lin Hung-Hung; Lee Chen-Chi; Wang Wayseen
Prenatal diagnosis of mosaic 1q31.3q32.1 trisomy associated with occipital encephalocele.
Chen Chih-Ping; Lin Shuan-Pei; Tsai Fuu-Jen; Chern Schu-Rern; Lee Chen-Chi; Wang Wayseen
A 5.6-Mb deletion in 15q14 in a boy with speech and language disorder, cleft palate, epilepsy, a ventricular septal defect, mental retardation and developmental delay.
Chen Chih-Ping; Chen Yann-Jang; Chern Schu-Rern; Tsai Fuu-Jen; Chang Tung-Yao; Lee Chen-Chi; Town Dai-Dyi; Lee Meng-Shan; Wang Wayseen
Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand-foot malformation associated with partial monosomy 4p (4p16.1-->pter) and partial trisomy 10q (10q25.1-->qter).

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All Publications

2008: Chen Chih-Ping; Chen Yann-Jang; Chern Schu-Rern; Tsai Fuu-Jen; Lin Hung-Hung; Lee Chen-Chi; Wang Wayseen
Prenatal diagnosis of mosaic 1q31.3q32.1 trisomy associated with occipital encephalocele.
Prenatal diagnosis 2008;28(9):865-7.
2008: Chen Chih-Ping; Lin Shuan-Pei; Tsai Fuu-Jen; Chern Schu-Rern; Lee Chen-Chi; Wang Wayseen
A 5.6-Mb deletion in 15q14 in a boy with speech and language disorder, cleft palate, epilepsy, a ventricular septal defect, mental retardation and developmental delay.
European journal of medical genetics 2008;51(4):368-72.
2008: Chen Chih-Ping; Chen Yann-Jang; Chern Schu-Rern; Tsai Fuu-Jen; Chang Tung-Yao; Lee Chen-Chi; Town Dai-Dyi; Lee Meng-Shan; Wang Wayseen
Prenatal diagnosis of concomitant Wolf-Hirschhorn syndrome and split hand-foot malformation associated with partial monosomy 4p (4p16.1-->pter) and partial trisomy 10q (10q25.1-->qter).
Prenatal diagnosis 2008;28(5):450-3.
2007: Chen Chih-Ping; Tsai Fuu-Jen; Chern Schu-Rern; Lee Chen-Chi; Town Dai-Dyi; Wang Wayseen
Cytogenetic variability in the proportion of abnormal cells between the various tissues in prenatally detected mosaic tetrasomy 12p.
Prenatal diagnosis 2007;27(12):1170-3.
2006: Chen Chih-Ping; Lin Chyi-Chyang; Li Yueh-Chun; Hsieh Lie-Jiau; Lee Chen-Chi; Wang Wayseen
Primary ovarian failure in a mentally retarded woman with a de novo unbalanced X;autosome translocation.
Fertility and sterility 2006;86(5):1514.e1-2.
2006: Chen C-P; Wang T-H; Lin S-P; Chern S-R; Chen M-R; Lee C-C; Chen Y-J; Wang W
24 Mb deletion of 6q22.1-->q23.2 in an infant with pulmonary atresia, ventricular septal defect, microcephaly, developmental delay and facial dysmorphism.
European journal of medical genetics 2006;49(6):516-9.
2006: Chen Chih-Ping; Lin Shuan-Pei; Lin Chyi-Chyang; Chen Yann-Jang; Chern Schu-Rern; Li Yueh-Chun; Hsieh Lie-Jiau; Lee Chen-Chi; Pan Chen-Wen; Wang Wayseen
Molecular cytogenetic analysis of de novo dup(5)(q35.2q35.3) and review of the literature of pure partial trisomy 5q.
American journal of medical genetics. Part A 2006;140(14):1594-600.
2006: Chen Chih-Ping; Chern Schu-Rern; Lin Chyi-Chyang; Wang Tzu-Hao; Li Yueh-Chun; Hsieh Lie-Jiau; Lee Chen-Chi; Hua Hui-Min; Wang Wayseen
Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
Prenatal diagnosis 2006;26(4):313-20.
2006: Chen Chih-Ping; Chern Schu-Rern; Lee Chen-Chi; Lin Chyi-Chyang; Li Yueh-Chun; Hsieh Lie-Jiau; Chen Wen-Lin; Wang Wayseen
Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
Prenatal diagnosis 2006;26(2):138-46.
2006: Chen C P; Lin S P; Lee C C; Town D D; Wang W
Partial trisomy 1p (1p36.22-->pter) and partial monosomy 9p (9p22.2-->pter) associated with achalasia, flexion deformity of the fingers and epilepsy in a girl.
Genetic counseling (Geneva, Switzerland) 2006;17(3):301-6.
2006: Chen C P; Lin S P; Chern S R; Lee C C; Huang J K; Wang W
Direct transmission of the 18q- syndrome from mother to daughter.
Genetic counseling (Geneva, Switzerland) 2006;17(2):185-9.
2006: Chen C P; Lee C C; Town D D; Chen W L; Chen L F; Lee M S; Pan C W; Wang W
Detection of euchromatic variants and unusual C band heterochromatin variants at genetic amniocentesis.
Genetic counseling (Geneva, Switzerland) 2006;17(1):91-5.
2006: Chen C P; Lin S P; Lin C C; Li Y C; Hsieh L J; Huang J K; Lee C C; Wang W
Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
Genetic counseling (Geneva, Switzerland) 2006;17(1):57-63.
2005: Chen Chih-Ping; Chern Schu-Rern; Lin Shuan-Pei; Lin Chyi-Chyang; Li Yueh-Chun; Wang Tzu-Hao; Lee Chen-Chi; Pan Chen-Wen; Hsieh Lie-Jiau; Wang Wayseen
A paternally derived inverted duplication of distal 14q with a terminal 14q deletion.
American journal of medical genetics. Part A 2005;139A(2):146-50.
2005: Chen Chih-Ping; Chern Schu-Rern; Sheu Jin-Chern; Lin Shuan-Pei; Hsu Chin-Yuan; Chang Tung-Yao; Lee Chen-Chi; Wang Wayseen; Chen Hsiao-En Cindy
Prenatal diagnosis, sonographic findings and molecular genetic analysis of a 46,XX/46,XY true hermaphrodite chimera.
Prenatal diagnosis 2005;25(6):502-6.
2005: Chen Chih-Ping; Chern Schu-Rern; Wang Tzu-Hao; Hsueh Ding-Wei; Lee Chen-Chi; Town Dai-Dyi; Wang Wayseen; Ko Tsang-Ming
Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
Prenatal diagnosis 2005;25(6):492-6.
2005: Chen Chih-Ping; Chang Tung-Yao; Tzen Chin-Yuan; Wang Wayseen; Lee Chen-Chi
Recurrent fetal pyelectasis in a family with fetuses associated with partial trisomy 10q (10q24.1-->qter).
Prenatal diagnosis 2005;25(3):263-4.
2005: Chen Chih-Ping; Lin Shuan-Pei; Lin Chyi-Chyang; Li Yueh-Chun; Chern Schu-Rern; Chen Wei-Min; Lee Chen-Chi; Hsieh Lie-Jiau; Wang Wayseen
Perinatal findings and molecular cytogenetic analysis of de novo partial trisomy 16q (16q22.1-->qter) and partial monosomy 20q (20q13.3-->qter).
Prenatal diagnosis 2005;25(2):112-8.
2005: Chen C P; Chern S R; Lin C J; Lee C C; Wang W; Tzen C Y
A comparison of maternal age, sex ratio and associated anomalies among numerically aneuploid, structurally aneuploid and euploid holoprosencephaly.
Genetic counseling (Geneva, Switzerland) 2005;16(1):49-57.
2004: Chen Chih-Ping; Lin Chyi-Chyang; Li Yueh-Chun; Chern Schu-Rern; Lee Chen-Chi; Chen Wen-Lin; Lee Men-Shan; Wang Wayseen; Tzen Chin-Yuan
Clinical, cytogenetic, and molecular analyses of prenatally diagnosed mosaic tetrasomy for distal chromosome 15q and review of the literature.
Prenatal diagnosis 2004;24(10):767-73.
2004: Chen Chih-Ping; Chern Schu-Rern; Cheng Sho-Jen; Chang Tung-Yao; Yeh Li-Fan; Lee Chen-Chi; Pan Chen-Wen; Wang Wayseen; Tzen Chin-Yuan
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 2004;24(6):455-62.
2004: Chen Chih-Ping; Chern Schu-Rern; Lee Chen-Chi; Chen Wen-Lin; Wang Wayseen
Prenatal diagnosis of interstitially satellited 6p.
Prenatal diagnosis 2004;24(6):430-3.
2004: Chen Chih-Ping; Chern Schu-Rern; Chang Tung-Yao; Tzen Chin-Yuan; Lee Chen-Chi; Chen Wen-Lin; Chen Li-Feng; Wang Wayseen
Prenatal diagnosis of the distal 11q deletion and review of the literature.
Prenatal diagnosis 2004;24(2):130-6.
2004: Chen Chih-Ping; Shih Jin-Chung; Chern Schu-Rern; Lee Chen-Chi; Wang Wayseen
Prenatal diagnosis of mosaic trisomy 16 associated with congenital diaphragmatic hernia and elevated maternal serum alpha-fetoprotein and human chorionic gonadotrophin.
Prenatal diagnosis 2004;24(1):63-6.
2004: Chen Chih-Ping; Lee Chen-Chi; Chang Tung-Yao; Town Dai-Dyi; Wang Wayseen
Prenatal diagnosis of mosaic distal 5p deletion and review of the literature.
Prenatal diagnosis 2004;24(1):50-7.
2004: Chen Chih-Ping; Chern Schu-Rern; Lee Chen-Chi; Chang Tung-Yao; Wang Wayseen; Tzen Chin-Yuan
Clinical, cytogenetic, and molecular findings of prenatally diagnosed mosaic trisomy 4.
Prenatal diagnosis 2004;24(1):38-44.
2004: Chen Chih-Ping; Lee Chen-Chi; Chen Wen-Lin; Wang Wayseen; Tzen Chin-Yuan
Prenatal diagnosis of premature centromere division-related mosaic variegated aneuploidy.
Prenatal diagnosis 2004;24(1):19-25.
2004: Chen C P; Lee C C; Town D D; Lee M S; Wang W
Discrepancy between the fetus and extra-embryonic tissues in prenatally detected mosaic distal 5p deletion.
Genetic counseling (Geneva, Switzerland) 2004;15(4):473-6.
2004: Chen C P; Lin S P; Chern S R; Lee C C; Huang J K; Wang W; Liao Y W
De novo satellited 21q associated with corpus callosum dysgenesis, colpocephaly, a concealed penis, congenital heart defects, and developmental delay.
Genetic counseling (Geneva, Switzerland) 2004;15(4):437-42.
2003: Chen Chih-Ping; Chern Schu-Rern; Lee Chen-Chi; Chen Li-Feng; Chin Daniel T H; Tzen Chin-Yuan; Wang Wayseen
Prenatal diagnosis of trisomy 18p and distal 21q22.3 deletion.
Prenatal diagnosis 2003;23(9):758-61.
2003: Chen Chih-Ping; Lin Shuan-Pei; Chern Schu-Rern; Shih Shin-Lin; Lee Chen-Chi; Wang Wayseen; Liao You-Wei
Perinatal findings and molecular cytogenetic analysis of trisomy 16q and 22q13.3 deletion.
Prenatal diagnosis 2003;23(6):504-8.
2003: Chen Chih-Ping; Chern Schu-Rern; Chang Tung-Yao; Tzen Chin-Yuan; Lee Chen-Chi; Chen Wen-Lin; Lee Meng-Shan; Wang Wayseen
Prenatal diagnosis of de novo terminal deletion of chromosome 7q.
Prenatal diagnosis 2003;23(5):375-9.
2003: Chen Chih-Ping; Hwu Yuh-Ming; Yeh Li-Fan; Chern Schu-Rern; Lee Chen-Chi; Wang Wayseen
Successful triplet pregnancy and delivery after oocyte donation in an infertile female with chromosome mosaicism for monosomy X, partial trisomy X, and terminal Xp deletion.
Fertility and sterility 2003;79(5):1231-3.
2003: Chen Chih-Ping; Chern Schu-Rern; Chang Tung-Yao; Lee Chen-Chi; Chen Li-Feng; Tzen Chin-Yuan; Wang Wayseen; Lin Chen-Ju; Yang Brian P T; Yang Lawrence S T
Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction.
Prenatal diagnosis 2003;23(1):40-3.
2002: Chen Chih-Ping; Chang Tung-Yao; Shih Jin-Chung; Lin Shuan-Pei; Lin Chen-Ju; Wang Wayseen; Lee Chen-Chi; Town Dai-Dyi; Pan Chen-Wen; Tzen Chin-Yuan
Prenatal diagnosis of the Dandy-Walker malformation and ventriculomegaly associated with partial trisomy 9p and distal 12p deletion.
Prenatal diagnosis 2002;22(12):1063-6.
2001: Chen C P; Chern S R; Wang W; Lee C C; Chen W L; Chen L F; Chang T Y; Tzen C Y
Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
Prenatal diagnosis 2001;21(5):346-50.
2001: Chen C P; Chern S R; Lee C C; Chen W L; Wang W
Prenatal diagnosis of mosaic ring chromosome 13 with anencephaly.
Prenatal diagnosis 2001;21(2):102-5.
2000: Chen C P; Chern S R; Chang C L; Lee C C; Chen W L; Chen L F; Wang W
Prenatal diagnosis and genetic analysis of X chromosome polysomy 49, XXXXY.
Prenatal diagnosis 2000;20(9):754-7.
2000: Chen C P; Devriendt K; Chern S R; Lee C C; Wang W; Lin S P
Prenatal diagnosis of inherited satellited non-acrocentric chromosomes.
Prenatal diagnosis 2000;20(5):384-9.
1999: Chen C P; Devriendt K; Lee C C; Chen W L; Wang W; Wang T Y
Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia.
Prenatal diagnosis 1999;19(10):986-9.
1999: Chen C P; Shih J C; Lee C C; Chen L F; Wang W; Wang T Y
Prenatal diagnosis of a fetus with distal 10q trisomy.
Prenatal diagnosis 1999;19(9):876-8.
1999: Chen C P; Chern S R; Lee C C; Town D D; Chen W L; Wang W
Bilateral renal agenesis and fetal ascites in association with partial trisomy 13 and partial trisomy 16 due to a 3:1 segregation of maternal reciprocal translocation t(13;16)(q12.3; p13.2).
Prenatal diagnosis 1999;19(8):783-6.
1998: Chen C P; Lee C C; Pan C W; Kir T Y; Chen B F
Partial trisomy 8q and partial monosomy 15q associated with congenital hydrocephalus, diaphragmatic hernia, urinary tract anomalies, congenital heart defect and kyphoscoliosis.
Prenatal diagnosis 1998;18(12):1289-93.
1998: Chen C P; Chern S R; Lee C C; Chen W L; Chen M H; Chang K M
De novo unbalanced translocation resulting in monosomy for proximal 14q and distal 4p in a fetus with intrauterine growth retardation, Wolf-Hirschhorn syndrome, hypertrophic cardiomyopathy, and partial hemihypoplasia.
Journal of medical genetics 1998;35(12):1050-3.
1998: Chen C P; Chern S R; Lee C C; Town D D
Isochromosome 18q in a fetus with congenital megacystis, intra-uterine growth retardation and cloacal dysgenesis sequence.
Prenatal diagnosis 1998;18(10):1068-74.
1998: Chen C P; Chern S R; Lee C C; Chen L F; Chuang C Y
Prenatal diagnosis of de novo interstitial 16q deletion in a fetus associated with sonographic findings of prominent coronal sutures, a prominent frontal bone, and shortening of the long bones.
Prenatal diagnosis 1998;18(5):490-5.
1998: Chen C P; Chern S R; Lee C C; Chen L F; Chuang C Y; Chen M H
Prenatal diagnosis of de novo isochromosome 13q associated with microcephaly, alobar holoprosencephaly and cebocephaly in a fetus.
Prenatal diagnosis 1998;18(4):393-8.
1997: Chen C P; Lee C C; Chen L F; Chuang C Y; Jan S W; Chen B F
Prenatal diagnosis of de novo proximal interstitial deletion of 14q associated with cebocephaly.
Journal of medical genetics 1997;34(9):777-8.
1997: Chen C P; Lin C C; Chuang C Y; Lee C C; Chen W L; Jan S W; Lin S P
Prenatal diagnosis of partial trisomy 12 and partial trisomy 21 due to a 3:1 segregation of maternal reciprocal translocation t(12;21) (p13.3;q21).
Prenatal diagnosis 1997;17(7):675-80.
1997: Chen C P; Chern S R; Liu F F; Jan S W; Lee C C; Chang Y C; Yue C T
Prenatal diagnosis of a deletion of 18q in a fetus associated with multiple-marker screen positive results.
Prenatal diagnosis 1997;17(6):571-6.
1997: Chen C P; Lee C C; Liu F F; Jan S W; Lin M H; Chen B F
Prenatal diagnosis of cephalothoracopagus janiceps monosymmetros.
Prenatal diagnosis 1997;17(4):384-8.

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