A citation-based method for searching scientific literature

Chih-Ping Chen, Ming Chen, Yi-Ning Su, Fuu-Jen Tsai, Schu-Rern Chern, Pei-Chen Wu, Wen-Lin Chen, Li-Feng Chen, Chen-Wen Pan, Wayseen Wang. Taiwan J Obstet Gynecol 2011
Times Cited: 8







List of co-cited articles
15 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity




Handling small supernumerary marker chromosomes in prenatal diagnostics.
Thomas Liehr, Elisabeth Ewers, Nadezda Kosyakova, Vivian Klaschka, Franziska Rietz, Rebecca Wagner, Anja Weise. Expert Rev Mol Diagn 2009
40
50

Small supernumerary marker chromosomes (sSMC) in humans.
T Liehr, U Claussen, H Starke. Cytogenet Genome Res 2004
205
50

Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2.
Chih-Ping Chen, Ming Chen, Schu-Rern Chern, Peih-Shan Wu, Shun-Ping Chang, Dong-Jay Lee, Yu-Ting Chen, Li-Feng Chen, Jun-Wei Su, Alan Hwa-Ruey Hsieh,[...]. Taiwan J Obstet Gynecol 2012
8
50

Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8.
Chih-Ping Chen, Ming Chen, Tsang-Ming Ko, Gwo-Chin Ma, Fuu-Jen Tsai, Ming-Song Tsai, Pei-Chen Wu, Chen-Chi Lee, Li-Feng Chen, Wayseen Wang. Taiwan J Obstet Gynecol 2010
13
37

Small supernumerary marker chromosomes--progress towards a genotype-phenotype correlation.
T Liehr, K Mrasek, A Weise, A Dufke, L Rodríguez, N Martínez Guardia, A Sanchís, J R Vermeesch, C Ramel, A Polityko,[...]. Cytogenet Genome Res 2006
142
37

Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 22.
Chih-Ping Chen, Chyi-Chyang Lin, Yi-Ning Su, Fuu-Jen Tsai, Schu-Rern Chern, Chen-Chi Lee, Wen-Ling Chen, Li-Feng Chen, Pei-Chen Wu, Wayseen Wang. Taiwan J Obstet Gynecol 2010
7
42


Delineation of supernumerary marker chromosomes in 38 patients.
R Viersbach, H Engels, U Gamerdinger, M Hansmann. Am J Med Genet 1998
61
25

Supernumerary marker chromosomes management in prenatal diagnosis.
Nicolas Gruchy, Marine Lebrun, Michel Herlicoviez, Jacques Alliet, Dominique Gourdier, Marie-Laure Kottler, Hervé Mittre, Nathalie Leporrier. Am J Med Genet A 2008
11
25

Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18.
Chih-Ping Chen, Chyi-Chyang Lin, Yi-Ning Su, Fuu-Jen Tsai, Ju-Ting Chen, Schu-Rern Chern, Chen-Chi Lee, Dai-Dyi Town, Li-Feng Chen, Pei-Chen Wu,[...]. Taiwan J Obstet Gynecol 2010
9
25

Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 21.
Chih-Ping Chen, Chyi-Chyang Lin, Tsang-Ming Ko, Fuu-Jen Tsai, Schu-Rern Chern, Chen-Chi Lee, Yu-Ting Chen, Pei-Chen Wu, Wayseen Wang. Taiwan J Obstet Gynecol 2010
7
28

Supernumerary marker chromosomes in man: parental origin, mosaicism and maternal age revisited.
John A Crolla, Sheila A Youings, Sarah Ennis, Patricia A Jacobs. Eur J Hum Genet 2005
71
25

Molecular characterization of 39 de novo sSMC: contribution to prognosis and genetic counselling, a prospective study.
N Marle, D Martinet, A Aboura, G Joly-Helas, J Andrieux, E Flori, J Puechberty, F Vialard, D Sanlaville, S Fert Ferrer,[...]. Clin Genet 2014
21
25

Prenatal diagnosis of mosaic trisomy 9.
Chih-Ping Chen, Fang-Yu Hung, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Chen-Chi Lee, Yu-Ting Chen, Wen-Lin Chen, Wayseen Wang. Taiwan J Obstet Gynecol 2011
8
12


Characterization of a small supernumerary ring marker derived from chromosome 2 by forward and reverse chromosome painting.
N V Ostroverkhova, S A Nazarenko, N B Rubtsov, L P Nazarenko, E N Bunina. Am J Med Genet 1999
17
12

Prenatal diagnosis of mosaic trisomy 8: clinical report and literature review.
Chih-Ping Chen, Ming Chen, Yi-Ju Pan, Yi-Ning Su, Schu-Rern Chern, Fuu-Jen Tsai, Yu-Ting Chen, Wayseen Wang. Taiwan J Obstet Gynecol 2011
22
12

Trisomy 7 mosaicism at amniocentesis: interphase FISH, QF-PCR, and aCGH analyses on uncultured amniocytes for rapid distinguishing of true mosaicism from pseudomosaicism.
Chih-Ping Chen, Hsu-Kuang Huang, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Chen-Chi Lee, Dai-Dyi Town, Wen-Lin Chen, Yu-Ting Chen, Wayseen Wang. Taiwan J Obstet Gynecol 2012
9
12

Duplication 2 (q11.2-q21): a previously unreported abnormality.
L B Cooke, H Richards, P W Lunt, L Burvill-Holmes, R T Howell, A McDermott. J Med Genet 1995
7
14


Trisomy 2q11.2-->q21.1 resulting from an unbalanced insertion in two generations.
I A Glass, P Stormer, P T Oei, E Hacking, P D Cotter. J Med Genet 1998
28
12



Intrachromosomal triplication of 2q11.2-q21 in a severely malformed infant: case report and review of triplications and their possible mechanism.
J Wang, K S Reddy, E Wang, L Halderman, B L Morgan, R S Lachman, H J Lin, M E Cornford. Am J Med Genet 1999
33
12

Small familial supernumerary ring chromosome 2: FISH characterization and genotype-phenotype correlation.
Daniela Giardino, Palma Finelli, Silvia Russo, Giulietta Gottardi, Ornella Rodeschini, Maria Gabriella Atza, Federica Natacci, Lidia Larizza. Am J Med Genet 2002
11
12

Prenatal diagnosis of a small chromosome 2-derived supernumerary marker, and review of the reported cases.
Daniela Giardino, Emanuele Valtorta, Gabriella De Canal, Cecilia Corti, Chiara Valtorta, Palma Finelli, Concetta Vardè, Maria Iandolo, Cristiana Marchese, Lidia Larizza. Am J Med Genet A 2007
2
50

Identification of a small supernumerary marker chromosome, r(2)(p10q11.2), and the problem of determining prognosis.
N Villa, P Riva, D Colombo, E Sala, S Mariani, C Zorloni, F Crosti, L Dalprà. Prenat Diagn 2001
13
12


Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses.
Chih-Ping Chen, Hsien-Ming Lin, Yi-Ning Su, Schu-Rern Chern, Fuu-Jen Tsai, Pei-Chen Wu, Chen-Chi Lee, Yu-Ting Chen, Meng-Shan Lee, Chen-Wen Pan,[...]. Taiwan J Obstet Gynecol 2010
16
12

A novel case of infantile sacral teratoma and a constitutional t(12;15)(q13;q25) pat.
Imke Veltman, Martien van Asseldonk, Marga Schepens, Hans Stoop, Leendert Looijenga, Cokkie Wouters, Lutgarde Govaerts, Ron Suijkerbuijk, Ad van Kessel. Cancer Genet Cytogenet 2002
11
12

Origin of adult male mediastinal germ-cell tumours.
R S Chaganti, E Rodriguez, S Mathew. Lancet 1994
84
12

Molecular cytogenetics of human germ cell tumours: i(12p) and related chromosomal anomalies.
A Geurts van Kessel, R F Suijkerbuijk, R J Sinke, L Looijenga, J W Oosterhuis, B de Jong. Eur Urol 1993
25
12



Near-haploidy in a malignant sacrococcygeal teratoma.
R Noguera, S Navarro, C Carda, A Peydró-Olaya, A Llombart-Bosch. Cancer Genet Cytogenet 1999
13
12

Chromosomal translocation, t(1;11)(q12;p15), in an extragonadal immature teratoma.
T Houri, N Hashimoto, N Ibayashi, T Mori, M Fujimoto, S Ueda, T Abe, J Inazawa. Cancer Genet Cytogenet 1997
5
20

Direct prenatal chromosome diagnosis of a malignancy.
F Hecht, A Grix, B K Hecht, C Berger, H Bixenman, S Szucs, D O'Keeffe, H J Finberg. Cancer Genet Cytogenet 1984
37
12

Development of a high-density pericentromeric region BAC clone set for the detection and characterization of small supernumerary marker chromosomes by array CGH.
Blake C Ballif, Sara A Hornor, Scott G Sulpizio, Richard M Lloyd, Sara L Minier, Emily A Rorem, Aaron Theisen, Bassem A Bejjani, Lisa G Shaffer. Genet Med 2007
43
12

Second-trimester evaluation of fetal sacrococcygeal teratoma using three-dimensional color Doppler ultrasound and magnetic resonance imaging.
Chih-Ping Chen, Jin-Chung Shih, Jon-Kway Huang, Wayseen Wang, Chin-Yuan Tzen. Prenat Diagn 2003
8
12

Detection of low-level mosaicism by array CGH in routine diagnostic specimens.
Blake C Ballif, Emily A Rorem, Kyle Sundin, Matt Lincicum, Shannon Gaskin, Justine Coppinger, Catherine D Kashork, Lisa G Shaffer, Bassem A Bejjani. Am J Med Genet A 2006
207
12

Prenatally diagnosed sacrococcygeal teratoma: a unique expression of trisomy 1q.
J R Wax, P Benn, J D Steinfeld, C J Ingardia. Cancer Genet Cytogenet 2000
32
12

Mechanisms of ring chromosome formation in 11 cases of human ring chromosome 21.
M J McGinniss, H H Kazazian, G Stetten, M B Petersen, H Boman, E Engel, F Greenberg, J M Hertz, A Johnson, Z Laca. Am J Hum Genet 1992
86
12

Amplification of chromosome subregion 12p11.2-p12.1 in a metastasis of an i(12p)-negative seminoma: relationship to tumor progression?
R F Suijkerbuijk, R J Sinke, D E Weghuis, L Roque, A Forus, F Stellink, A Siepman, C van de Kaa, J Soares, A Geurts van Kessel. Cancer Genet Cytogenet 1994
71
12

Fusion of the SUMO/Sentrin-specific protease 1 gene SENP1 and the embryonic polarity-related mesoderm development gene MESDC2 in a patient with an infantile teratoma and a constitutional t(12;15)(q13;q25).
Imke M Veltman, Lilian A Vreede, Jinke Cheng, Leendert H J Looijenga, Bert Janssen, Eric F P M Schoenmakers, Edward T H Yeh, Ad Geurts van Kessel. Hum Mol Genet 2005
21
12


Origin of male mediastinal germ-cell tumours.
H Hasle, B B Jacobsen. Lancet 1995
9
12

A fetus with ring chromosome 21 characterized by aCGH shows no clinical findings after birth.
Ioannis Papoulidis, Emmanouil Manolakos, Elisavet Siomou, Kostantinos Kefalas, Loretta Thomaidis, Thomas Liehr, Annalisa Vetro, Apostolos Athanasiadis, Orsetta Zuffardi, Michael B Petersen. Prenat Diagn 2010
5
20

Malignant transformation of an untreated congenital sacrococcygeal teratoma: a amplification at 8q and 12p detected by comparative genomic hybridization.
Mariola Monika Golas, Bastian Gunawan, Björn-Werner Raab, László Füzesi, Bettina Lange. Cancer Genet Cytogenet 2010
12
12


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.