A citation-based method for searching scientific literature

Chih-Ping Chen, Tung-Yao Chang, Wan-Yuo Guo, Pei-Chen Wu, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Yu-Ting Chen, Li-Feng Chen, Wayseen Wang. Gene 2013
Times Cited: 14







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



Times Cited
  Times     Co-cited
Similarity


Refinement of a 400-kb critical region allows genotypic differentiation between isolated lissencephaly, Miller-Dieker syndrome, and other phenotypes secondary to deletions of 17p13.3.
Carlos Cardoso, Richard J Leventer, Heather L Ward, Kazuhito Toyo-Oka, June Chung, Alyssa Gross, Christa L Martin, Judith Allanson, Daniela T Pilz, Ann H Olney,[...]. Am J Hum Genet 2003
157
35

Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypes.
Damien L Bruno, Britt-Marie Anderlid, Anna Lindstrand, Conny van Ravenswaaij-Arts, Devika Ganesamoorthy, Johanna Lundin, Christa Lese Martin, Jessica Douglas, Catherine Nowak, Margaret P Adam,[...]. J Med Genet 2010
105
35

Further delineation of the 17p13.3 microdeletion involving YWHAE but distal to PAFAH1B1: four additional patients.
Manuel Schiff, Andrée Delahaye, Joris Andrieux, Damien Sanlaville, Catherine Vincent-Delorme, Azzedine Aboura, Brigitte Benzacken, Sonia Bouquillon, Monique Elmaleh-Berges, Audrey Labalme,[...]. Eur J Med Genet 2010
29
28

Prenatal diagnosis of monosomy 17p (17p13.3-->pter) associated with polyhydramnios, intrauterine growth restriction, ventriculomegaly, and Miller-Dieker lissencephaly syndrome in a fetus.
Chin-Yi Lin, Chih-Ping Chen, Chiung-Ling Liau, Pen-Hua Su, Teng-Fu Tsao, Tung-Yao Chang, Wayseen Wang. Taiwan J Obstet Gynecol 2009
8
50

Further delineation of 17p13.3 microdeletion involving CRK. The effect of growth hormone treatment.
John R Østergaard, Jesper Graakjær, Carsten Brandt, Niels H Birkebæk. Eur J Med Genet 2012
12
25

Deletion of YWHAE in a patient with periventricular heterotopias and pronounced corpus callosum hypoplasia.
Cécile Mignon-Ravix, Pierre Cacciagli, Bilal El-Waly, Anne Moncla, Mathieu Milh, Nadine Girard, Brigitte Chabrol, Nicole Philip, Laurent Villard. J Med Genet 2010
30
21

Clinical and molecular diagnosis of Miller-Dieker syndrome.
W B Dobyns, C J Curry, H E Hoyme, L Turlington, D H Ledbetter. Am J Hum Genet 1991
174
21


17p13.3 Microdeletion: Insights on Genotype-Phenotype Correlation.
Marshall I Barros Fontes, Ana P Dos Santos, Fábio Rossi Torres, Iscia Lopes-Cendes, Fernando Cendes, Simone Appenzeller, Tânia Kawasaki de Araujo, Isabella Lopes Monlleó, Vera L Gil-da-Silva-Lopes. Mol Syndromol 2017
8
37

22q11 deletion syndrome: current perspective.
Bülent Hacıhamdioğlu, Duygu Hacıhamdioğlu, Kenan Delil. Appl Clin Genet 2015
40
14

Prenatal and postnatal diagnosis of 22q11.2 deletion syndrome.
Florence Bretelle, Laura Beyer, Marie Christine Pellissier, Chantal Missirian, Sabine Sigaudy, Marc Gamerre, Claude D'Ercole, Nicole Philip. Eur J Med Genet 2010
31
14

Conotruncal anomalies in fetal life: accuracy of diagnosis, associated defects and outcome.
A Galindo, A Mendoza, J Arbues, A Grañeras, D Escribano, O Nieto. Eur J Obstet Gynecol Reprod Biol 2009
37
14


Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats.
O Reiner, R Carrozzo, Y Shen, M Wehnert, F Faustinella, W B Dobyns, C T Caskey, D H Ledbetter. Nature 1993
837
14

Miller-Dieker syndrome: lissencephaly and monosomy 17p.
W B Dobyns, R F Stratton, J T Parke, F Greenberg, R L Nussbaum, D H Ledbetter. J Pediatr 1983
139
14

Genomic copy number variations at 17p13.3 and epileptogenesis.
Keiko Shimojima, Chitose Sugiura, Hiroka Takahashi, Mariko Ikegami, Yukitoshi Takahashi, Kousaku Ohno, Mari Matsuo, Kayoko Saito, Toshiyuki Yamamoto. Epilepsy Res 2010
28
14


Expression analysis of a 17p terminal deletion, including YWHAE, but not PAFAH1B1, associated with normal brain structure on MRI in a young girl.
Keisuke Enomoto, Yasuhiro Kishitani, Makiko Tominaga, Aki Ishikawa, Noritaka Furuya, Noriko Aida, Mitsuo Masuno, Ken-Ichiro Yamada, Kenji Kurosawa. Am J Med Genet A 2012
4
50

Microdeletions including YWHAE in the Miller-Dieker syndrome region on chromosome 17p13.3 result in facial dysmorphisms, growth restriction, and cognitive impairment.
S C Sreenath Nagamani, F Zhang, O A Shchelochkov, W Bi, Z Ou, F Scaglia, F J Probst, M Shinawi, C Eng, J V Hunter,[...]. J Med Genet 2009
75
14

14-3-3epsilon is important for neuronal migration by binding to NUDEL: a molecular explanation for Miller-Dieker syndrome.
Kazuhito Toyo-oka, Aki Shionoya, Michael J Gambello, Carlos Cardoso, Richard Leventer, Heather L Ward, Ramses Ayala, Li-Huei Tsai, William Dobyns, David Ledbetter,[...]. Nat Genet 2003
293
14

LISSENCEPHALY IN 2 SIBLINGS.
J Q MILLER. Neurology 1963
137
14

Ventriculomegaly, intrauterine growth restriction, and congenital heart defects as salient prenatal sonographic findings of Miller-Dieker lissencephaly syndrome associated with monosomy 17p (17p13.2 --> pter) in a fetus.
Chih-Ping Chen, Yu-Peng Liu, Shaun-Pei Lin, Ming Chen, Fuu-Jen Tsai, Yu-Ting Chen, Li-Feng Chen, Jonathan Kwei Hwang, Wayseen Wang. Taiwan J Obstet Gynecol 2010
9
22


Chromosomal microarray versus karyotyping for prenatal diagnosis.
Ronald J Wapner, Christa Lese Martin, Brynn Levy, Blake C Ballif, Christine M Eng, Julia M Zachary, Melissa Savage, Lawrence D Platt, Daniel Saltzman, William A Grobman,[...]. N Engl J Med 2012
643
14

Association of copy number variants with specific ultrasonographically detected fetal anomalies.
Jennifer C Donnelly, Lawrence D Platt, Andrei Rebarber, Julia Zachary, William A Grobman, Ronald J Wapner. Obstet Gynecol 2014
81
14

Increased LIS1 expression affects human and mouse brain development.
Weimin Bi, Tamar Sapir, Oleg A Shchelochkov, Feng Zhang, Marjorie A Withers, Jill V Hunter, Talia Levy, Vera Shinder, Daniel A Peiffer, Kevin L Gunderson,[...]. Nat Genet 2009
166
14

Microdeletions/duplications involving TBX1 gene in fetuses with conotruncal heart defects which are negative for 22q11.2 deletion on fluorescence in-situ hybridization.
M Chen, Y-S Yang, J-C Shih, W-H Lin, D-J Lee, Y-S Lin, C-H Chou, A D Cameron, N A Ginsberg, C-A Chen,[...]. Ultrasound Obstet Gynecol 2014
17
14

Identification of a new BRCA2 large genomic deletion associated with high risk male breast cancer.
Ana Rafaela de Souza Timoteo, Betina Menezes Albuquerque, Patricia Cristina Pascoto Moura, Carlos Cesar de Oliveira Ramos, Lucymara Fassarela Agnez-Lima, Tom Walsh, Mary-Claire King, Tirzah Braz Petta Lajus. Hered Cancer Clin Pract 2015
13
7

A pattern-based method for the identification of MicroRNA binding sites and their corresponding heteroduplexes.
Kevin C Miranda, Tien Huynh, Yvonne Tay, Yen-Sin Ang, Wai-Leong Tam, Andrew M Thomson, Bing Lim, Isidore Rigoutsos. Cell 2006
7

Mutations of the HIPK2 gene in acute myeloid leukemia and myelodysplastic syndrome impair AML1- and p53-mediated transcription.
X-L Li, Y Arai, H Harada, Y Shima, H Yoshida, S Rokudai, Y Aikawa, A Kimura, I Kitabayashi. Oncogene 2007
55
7

The emerging landscape of circular RNA ciRS-7 in cancer (Review).
Li Peng, Xiao Qing Yuan, Guan Cheng Li. Oncol Rep 2015
128
7


Genomic deletion of MAP3K7 at 6q12-22 is associated with early PSA recurrence in prostate cancer and absence of TMPRSS2:ERG fusions.
Martina Kluth, Jana Hesse, Anna Heinl, Antje Krohn, Stefan Steurer, Hüseyin Sirma, Ronald Simon, Pascale-Sophia Mayer, Udo Schumacher, Katharina Grupp,[...]. Mod Pathol 2013
117
7

Pseudogenes: a novel source of trans-acting antisense RNAs.
Per Johnsson, Kevin V Morris, Dan Grandér. Methods Mol Biol 2014
20
7


Recent Advances in the 5q- Syndrome.
Andrea Pellagatti, Jacqueline Boultwood. Mediterr J Hematol Infect Dis 2015
21
7

Characterization of a large genomic deletion in four Irish families with C7 deficiency.
A D Thomas, A Orren, J Connaughton, C Feighery, B P Morgan, A G Roberts. Mol Immunol 2012
2
50

Deletion 5q MDS: molecular and therapeutic implications.
Rami S Komrokji, Eric Padron, Benjamin L Ebert, Alan F List. Best Pract Res Clin Haematol 2013
31
7

A ceRNA analysis on LMNA gene focusing on the Hutchinson-Gilford progeria syndrome.
Walter Arancio, Carla Giordano, Giuseppe Pizzolanti. J Clin Bioinforma 2013
13
7

Molecular characterization of a patient with 3p deletion syndrome and a review of the literature.
Thomas V Fernandez, I J García-González, Christopher E Mason, G Hernández-Zaragoza, V C Ledezma-Rodríguez, V M Anguiano-Alvarez, R E'Vega, M Gutiérrez-Angulo, M L Maya, H E García-Bejarano,[...]. Am J Med Genet A 2008
32
7

Human MicroRNA targets.
Bino John, Anton J Enright, Alexei Aravin, Thomas Tuschl, Chris Sander, Debora S Marks. PLoS Biol 2004
7

Pseudogenes as regulators of biological function.
Ryan C Pink, David R F Carter. Essays Biochem 2013
24
7

SPARC is dispensable for murine hematopoiesis, despite its suspected pathophysiological role in 5q-myelodysplastic syndrome.
K Siva, P Jaako, K Miharada, E Rörby, M Ehinger, G Karlsson, S Karlsson. Leukemia 2012
12
8

A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia.
Maria Chiara Di Bernardo, Dalemari Crowther-Swanepoel, Peter Broderick, Emily Webb, Gabrielle Sellick, Ruth Wild, Kate Sullivan, Jayaram Vijayakrishnan, Yufei Wang, Alan M Pittman,[...]. Nat Genet 2008
258
7

Molecular heterogeneity of multiple myeloma: pathogenesis, prognosis, and therapeutic implications.
Avet-Loiseau Hervé, Magrangeas Florence, Moreau Philippe, Attal Michel, Facon Thierry, Anderson Kenneth, Harousseau Jean-Luc, Munshi Nikhil, Minvielle Stéphane. J Clin Oncol 2011
49
7



The multilayered complexity of ceRNA crosstalk and competition.
Yvonne Tay, John Rinn, Pier Paolo Pandolfi. Nature 2014
7

Competing endogenous RNA and interactome bioinformatic analyses on human telomerase.
Walter Arancio, Giuseppe Pizzolanti, Swonild Ilenia Genovese, Concetta Baiamonte, Carla Giordano. Rejuvenation Res 2014
21
7

Jumping translocations, a novel finding in chronic lymphocytic leukaemia.
Cecelia R Miller, Deborah Stephens, Amy S Ruppert, Frederick Racke, Andrew McFaddin, Heather Breidenbach, Huey-Jen Lin, Kathy Waller, Tammy Bannerman, Jeffrey A Jones,[...]. Br J Haematol 2015
4
25


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.