A citation-based method for searching scientific literature

Thomas C Winter, Anne M Kennedy, Paula J Woodward. Radiographics 2015
Times Cited: 42







List of co-cited articles
177 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
92
38


Holoprosencephaly.
Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Catherine Henry, Sylvie Odent, Véronique David. Orphanet J Rare Dis 2007
221
26

Neuropathology of holoprosencephaly.
Pascale Marcorelles, Annie Laquerriere. Am J Med Genet C Semin Med Genet 2010
34
29

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
23

Epidemiology of holoprosencephaly: Prevalence and risk factors.
Iêda M Orioli, Eduardo E Castilla. Am J Med Genet C Semin Med Genet 2010
62
23

The middle interhemispheric variant of holoprosencephaly.
Erin M Simon, Robert F Hevner, Joseph D Pinter, Nancy J Clegg, Mauricio Delgado, Stephen L Kinsman, Jin S Hahn, A James Barkovich. AJNR Am J Neuroradiol 2002
96
21


Disorders of prosencephalic development.
P Volpe, G Campobasso, V De Robertis, G Rembouskos. Prenat Diagn 2009
49
19

Septo-optic dysplasia.
Emma A Webb, Mehul T Dattani. Eur J Hum Genet 2010
111
16

Non-genetic risk factors for holoprosencephaly.
Candice Y Johnson, Sonja A Rasmussen. Am J Med Genet C Semin Med Genet 2010
45
16

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
17

Middle interhemispheric fusion: an unusual variant of holoprosencephaly.
A J Barkovich, D J Quint. AJNR Am J Neuroradiol 1993
110
14


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
14

Middle interhemispheric variant of holoprosencephaly: a distinct cliniconeuroradiologic subtype.
A J Lewis, E M Simon, A J Barkovich, N J Clegg, M R Delgado, E Levey, J S Hahn. Neurology 2002
64
11


Septopreoptic holoprosencephaly: a mild subtype associated with midline craniofacial anomalies.
J S Hahn, P D Barnes, N J Clegg, E E Stashinko. AJNR Am J Neuroradiol 2010
33
15

Clinical epidemiologic study of holoprosencephaly in South America.
Iêda M Orioli, Eduardo E Castilla. Am J Med Genet A 2007
36
13

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



Prenatal diagnosis of holoprosencephaly.
Youssef A Kousa, Adré J du Plessis, Gilbert Vezina. Am J Med Genet C Semin Med Genet 2018
6
83

Holoprosencephaly: new concepts.
E M Simon, A J Barkovich. Magn Reson Imaging Clin N Am 2001
24
16

Prenatal MR findings of the middle interhemispheric variant of holoprosencephaly.
Steven B Pulitzer, Erin M Simon, Timothy M Crombleholme, Jeffrey A Golden. AJNR Am J Neuroradiol 2004
25
16


Holoprosencephaly: clinical, anatomic, and molecular dimensions.
M Michael Cohen. Birth Defects Res A Clin Mol Teratol 2006
138
9

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
9

An epidemiological study of holoprosencephaly from a regional congenital anomaly register: 1995-2004.
S Ong, A Tonks, E R Woodward, M P Wyldes, M D Kilby. Prenat Diagn 2007
30
13


Brains and faces in holoprosencephaly: pre- and postnatal description of 30 cases.
H G K Blaas, A G Eriksson, K A Salvesen, C V Isaksen, B Christensen, G Møllerløkken, S H Eik-Nes. Ultrasound Obstet Gynecol 2002
63
9

Syndromes associated with holoprosencephaly.
Paul Kruszka, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2018
23
17

Analysis of genotype-phenotype correlations in human holoprosencephaly.
Benjamin D Solomon, Sandra Mercier, Jorge I Vélez, Daniel E Pineda-Alvarez, Adrian Wyllie, Nan Zhou, Christèle Dubourg, Veronique David, Sylvie Odent, Erich Roessler,[...]. Am J Med Genet C Semin Med Genet 2010
107
9

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
9


New findings for phenotype-genotype correlations in a large European series of holoprosencephaly cases.
Sandra Mercier, Christèle Dubourg, Nicolas Garcelon, Boris Campillo-Gimenez, Isabelle Gicquel, Marion Belleguic, Leslie Ratié, Laurent Pasquier, Philippe Loget, Claude Bendavid,[...]. J Med Genet 2011
76
9

Septo-optic dysplasia: MR imaging.
A J Barkovich, E K Fram, D Norman. Radiology 1989
125
7


Genetics of septo-optic dysplasia.
Daniel Kelberman, Mehul Tulsidas Dattani. Pituitary 2007
53
7


Assessment of the deep gray nuclei in holoprosencephaly.
E M Simon, R Hevner, J D Pinter, N J Clegg, V S Miller, S L Kinsman, J S Hahn, A J Barkovich. AJNR Am J Neuroradiol 2000
66
7

Disorders of cortical formation: MR imaging features.
A A K Abdel Razek, A Y Kandell, L G Elsorogy, A Elmongy, A A Basett. AJNR Am J Neuroradiol 2009
62
7

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
8


Fetal holoprosencephaly: associated malformations and chromosomal defects.
S M Berry, C Gosden, R J Snijders, K H Nicolaides. Fetal Diagn Ther 1990
32
9

Evaluation and management of children with holoprosencephaly.
Jin S Hahn, Lauren L Plawner. Pediatr Neurol 2004
47
7

Holoprosencephaly at prenatal diagnosis: analysis of 28 cases regarding etiopathogenic diagnoses.
F Petracchi, L Crespo, C Michia, L Igarzabal, E Gadow. Prenat Diagn 2011
11
27

Holoprosencephaly in RSH/Smith-Lemli-Opitz syndrome: does abnormal cholesterol metabolism affect the function of Sonic Hedgehog?
R L Kelley, E Roessler, R C Hennekam, G L Feldman, K Kosaki, M C Jones, J C Palumbos, M Muenke. Am J Med Genet 1996
166
7

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
10

The molecular genetics of holoprosencephaly.
Erich Roessler, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
155
7


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.