A citation-based method for searching scientific literature

P Volpe, G Campobasso, V De Robertis, G Rembouskos. Prenat Diagn 2009
Times Cited: 49







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



Times Cited
  Times     Co-cited
Similarity


Neuroimaging advances in holoprosencephaly: Refining the spectrum of the midline malformation.
Jin S Hahn, Patrick D Barnes. Am J Med Genet C Semin Med Genet 2010
93
24

Characteristics, associations and outcome of partial agenesis of the corpus callosum in the fetus.
P Volpe, D Paladini, M Resta, A Stanziano, M Salvatore, M Quarantelli, V De Robertis, A L Buonadonna, G Caruso, M Gentile. Ultrasound Obstet Gynecol 2006
83
22


Agenesis of corpus callosum: prenatal diagnosis and prognosis.
Marie-Laure Moutard, Virginie Kieffer, Josué Feingold, François Kieffer, Fanny Lewin, Catherine Adamsbaum, Antoinette Gélot, Jaume Campistol I Plana, Patrick van Bogaert, Monique André,[...]. Childs Nerv Syst 2003
86
18

Holoprosencephaly.
Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Catherine Henry, Sylvie Odent, Véronique David. Orphanet J Rare Dis 2007
221
18

Prenatal diagnosis and outcome of partial agenesis and hypoplasia of the corpus callosum.
T Ghi, A Carletti, E Contro, E Cera, P Falco, G Tagliavini, L Michelacci, G Tani, A Youssef, P Bonasoni,[...]. Ultrasound Obstet Gynecol 2010
51
18

Diagnosis of midline anomalies of the fetal brain with the three-dimensional median view.
G Pilu, M Segata, T Ghi, A Carletti, A Perolo, D Santini, P Bonasoni, G Tani, N Rizzo. Ultrasound Obstet Gynecol 2006
78
16

Differential diagnosis in fetuses with absent septum pellucidum.
G Malinger, D Lev, D Kidron, F Heredia, R Hershkovitz, T Lerman-Sagie. Ultrasound Obstet Gynecol 2005
63
16

Holoprosencephaly: a survey of the entity, with embryology and fetal imaging.
Thomas C Winter, Anne M Kennedy, Paula J Woodward. Radiographics 2015
43
18

Sonoembryology and early prenatal diagnosis of neural anomalies.
H-G K Blaas, S H Eik-Nes. Prenat Diagn 2009
62
14

Sonography of fetal agenesis of the corpus callosum: a survey of 35 cases.
G Pilu, F Sandri, A Perolo, M C Pittalis, G Grisolia, G Cocchi, M P Foschini, G P Salvioli, L Bovicelli. Ultrasound Obstet Gynecol 1993
103
14


Outcome of prenatally diagnosed agenesis of the corpus callosum.
N Fratelli, A T Papageorghiou, F Prefumo, S Bakalis, T Homfray, B Thilaganathan. Prenat Diagn 2007
52
14

Holoprosencephaly: clinical, anatomic, and molecular dimensions.
M Michael Cohen. Birth Defects Res A Clin Mol Teratol 2006
138
14

The significance of fetal ventriculomegaly: etiology, short- and long-term outcomes.
Pietro Gaglioti, Manuela Oberto, Tullia Todros. Prenat Diagn 2009
84
12

Neurodevelopmental outcome in prenatally diagnosed isolated agenesis of the corpus callosum.
A Chadie, S Radi, L Trestard, A Charollais, D Eurin, E Verspyck, S Marret. Acta Paediatr 2008
28
21

Outcome in prenatally diagnosed fetal agenesis of the corpus callosum.
P W Goodyear, C M Bannister, S Russell, S Rimmer. Fetal Diagn Ther 2001
64
12


Agenesis of the corpus callosum in California 1983-2003: a population-based study.
Hannah C Glass, Gary M Shaw, Chen Ma, Elliott H Sherr. Am J Med Genet A 2008
122
12

Agenesis of the corpus callosum: an MR imaging analysis of associated abnormalities in the fetus.
P H Tang, A I Bartha, M E Norton, A J Barkovich, E H Sherr, O A Glenn. AJNR Am J Neuroradiol 2009
77
12

Agenesis of the corpus callosum: genetic, developmental and functional aspects of connectivity.
Lynn K Paul, Warren S Brown, Ralph Adolphs, J Michael Tyszka, Linda J Richards, Pratik Mukherjee, Elliott H Sherr. Nat Rev Neurosci 2007
463
12

The molecular genetics of holoprosencephaly.
Erich Roessler, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
155
12

Holoprosencephaly due to numeric chromosome abnormalities.
Benjamin D Solomon, Kenneth N Rosenbaum, Jeanne M Meck, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
40
15


Transfrontal three-dimensional visualization of midline cerebral structures.
F Viñals, M Muñoz, R Naveas, A Giuliano. Ultrasound Obstet Gynecol 2007
43
11


Management of children with holoprosencephaly.
Eric B Levey, Elaine Stashinko, Nancy J Clegg, Mauricio R Delgado. Am J Med Genet C Semin Med Genet 2010
49
10


Septo-optic dysplasia.
Emma A Webb, Mehul T Dattani. Eur J Hum Genet 2010
113
10

Holoprosencephaly in infants of diabetic mothers.
M Barr, J W Hanson, K Currey, S Sharp, H Toriello, R D Schmickel, G N Wilson. J Pediatr 1983
158
10


Frequency of holoprosencephaly in the International Clearinghouse Birth Defects Surveillance Systems: searching for population variations.
Emanuele Leoncini, Giovanni Baranello, Iêda M Orioli, Göran Annerén, Marian Bakker, Fabrizio Bianchi, Carol Bower, Mark A Canfield, Eduardo E Castilla, Guido Cocchi,[...]. Birth Defects Res A Clin Mol Teratol 2008
64
10

First-trimester sonographic diagnosis of holoprosencephaly: value of the "butterfly" sign.
Waldo Sepulveda, Victor Dezerega, Cecilia Be. J Ultrasound Med 2004
45
11

Genetic counseling and "molecular" prenatal diagnosis of holoprosencephaly (HPE).
Sandra Mercier, Christèle Dubourg, Marion Belleguic, Laurent Pasquier, Philippe Loget, Josette Lucas, Claude Bendavid, Sylvie Odent. Am J Med Genet C Semin Med Genet 2010
28
17

A randomized trial of prenatal versus postnatal repair of myelomeningocele.
N Scott Adzick, Elizabeth A Thom, Catherine Y Spong, John W Brock, Pamela K Burrows, Mark P Johnson, Lori J Howell, Jody A Farrell, Mary E Dabrowiak, Leslie N Sutton,[...]. N Engl J Med 2011
900
10

Neurodevelopmental outcome following prenatal diagnosis of an isolated anomaly of the corpus callosum.
R Mangione, N Fries, P Godard, C Capron, V Mirlesse, D Lacombe, M Duyme. Ultrasound Obstet Gynecol 2011
36
13

Biometry of the fetal corpus callosum by three-dimensional ultrasound.
S Pashaj, E Merz, S Wellek. Ultrasound Obstet Gynecol 2013
31
16

Neuropathology of holoprosencephaly.
Pascale Marcorelles, Annie Laquerriere. Am J Med Genet C Semin Med Genet 2010
34
14

Non-genetic risk factors for holoprosencephaly.
Candice Y Johnson, Sonja A Rasmussen. Am J Med Genet C Semin Med Genet 2010
45
11



Prenatal screening and diagnosis of neural tube defects.
Martin Cameron, Paul Moran. Prenat Diagn 2009
91
8

The fetal cerebellum. Pitfalls in diagnosis and management.
Gustavo Malinger, Dorit Lev, Tally Lerman-Sagie. Prenat Diagn 2009
62
8

Fetal magnetic resonance imaging in the evaluation of fetuses referred for sonographically suspected abnormalities of the corpus callosum.
Orit A Glenn, Ruth B Goldstein, Katy C Li, Sun J Young, Mary E Norton, Reed F Busse, James D Goldberg, A James Barkovich. J Ultrasound Med 2005
79
8



Septo-optic dysplasia: MR imaging.
A J Barkovich, E K Fram, D Norman. Radiology 1989
125
8

Phenotypic variability in human embryonic holoprosencephaly in the Kyoto Collection.
Shigehito Yamada, Chigako Uwabe, Shingo Fujii, Kohei Shiota. Birth Defects Res A Clin Mol Teratol 2004
63
8

Neuroanatomy of holoprosencephaly as predictor of function: beyond the face predicting the brain.
L L Plawner, M R Delgado, V S Miller, E B Levey, S L Kinsman, A J Barkovich, E M Simon, N J Clegg, V T Sweet, E E Stashinko,[...]. Neurology 2002
63
8

A retrospective survey of perinatal risk factors of 104 living children with holoprosencephaly.
Elaine E Stashinko, Nancy J Clegg, Heather A Kammann, Vicki T Sweet, Mauricio R Delgado, Jin S Hahn, Eric B Levey. Am J Med Genet A 2004
37
10


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.