A citation-based method for searching scientific literature

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
Times Cited: 96







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



Times Cited
  Times     Co-cited
Similarity


Middle interhemispheric fusion: an unusual variant of holoprosencephaly.
A J Barkovich, D J Quint. AJNR Am J Neuroradiol 1993
110
45

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
57


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
42

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
42

Holoprosencephaly.
Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Catherine Henry, Sylvie Odent, Véronique David. Orphanet J Rare Dis 2007
223
28

The mutational spectrum of the sonic hedgehog gene in holoprosencephaly: SHH mutations cause a significant proportion of autosomal dominant holoprosencephaly.
L Nanni, J E Ming, M Bocian, K Steinhaus, D W Bianchi, C Die-Smulders, A Giannotti, K Imaizumi, K L Jones, M D Campo,[...]. Hum Mol Genet 1999
259
23


Holoprosencephaly due to mutations in ZIC2: alanine tract expansion mutations may be caused by parental somatic recombination.
L Y Brown, S Odent, V David, M Blayau, C Dubourg, C Apacik, M A Delgado, B D Hall, J F Reynolds, A Sommer,[...]. Hum Mol Genet 2001
138
20


Mutations in the human Sonic Hedgehog gene cause holoprosencephaly.
E Roessler, E Belloni, K Gaudenz, P Jay, P Berta, S W Scherer, L C Tsui, M Muenke. Nat Genet 1996
843
18

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
19

Analysis of the cerebral cortex in holoprosencephaly with attention to the sylvian fissures.
A James Barkovich, Erin M Simon, Nancy J Clegg, Steven L Kinsman, Jin S Hahn. AJNR Am J Neuroradiol 2002
34
50



Holoprosencephaly: clinical, anatomic, and molecular dimensions.
M Michael Cohen. Birth Defects Res A Clin Mol Teratol 2006
139
17

Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired.
S A Brown, D Warburton, L Y Brown, C Y Yu, E R Roeder, S Stengel-Rutkowski, R C Hennekam, M Muenke. Nat Genet 1998
365
16



Neuropathologic research strategies in holoprosencephaly.
H B Sarnat, L Flores-Sarnat. J Child Neurol 2001
60
25


Zic2 regulates the kinetics of neurulation.
T Nagai, J Aruga, O Minowa, T Sugimoto, Y Ohno, T Noda, K Mikoshiba. Proc Natl Acad Sci U S A 2000
179
15

Cyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function.
C Chiang, Y Litingtung, E Lee, K E Young, J L Corden, H Westphal, P A Beachy. Nature 1996
15

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
60

The dorsal cyst in holoprosencephaly and the role of the thalamus in its formation.
E M Simon, R F Hevner, J Pinter, N J Clegg, M Delgado, S L Kinsman, J S Hahn, A J Barkovich. Neuroradiology 2001
26
53


Holoprosencephaly survival and performance.
M Barr, M M Cohen. Am J Med Genet 1999
62
22

Evaluation and management of children with holoprosencephaly.
Jin S Hahn, Lauren L Plawner. Pediatr Neurol 2004
47
29


Unusual variant of holoprosencephaly in monosomy 13q.
Pascale Marcorelles, Philippe Loget, Catherine Fallet-Bianco, Joëlle Roume, Ferechte Encha-Razavi, Anne-Lise Delezoide. Pediatr Dev Pathol 2002
22
59

Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly.
Jeffrey E Ming, Michelle E Kaupas, Erich Roessler, Han G Brunner, Mahin Golabi, Mustafa Tekin, Robert F Stratton, Eva Sujansky, Sherri J Bale, Maximilian Muenke. Hum Genet 2002
159
13

Teratogenesis of holoprosencephaly.
M Michael Cohen, Kohei Shiota. Am J Med Genet 2002
131
12

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
159
12


Neuropathology of holoprosencephaly.
Pascale Marcorelles, Annie Laquerriere. Am J Med Genet C Semin Med Genet 2010
34
35

The molecular genetics of holoprosencephaly.
Erich Roessler, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
157
12

Holoprosencephaly: new concepts.
E M Simon, A J Barkovich. Magn Reson Imaging Clin N Am 2001
24
45


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
29

Dose-dependent functions of Fgf8 in regulating telencephalic patterning centers.
Elaine E Storm, Sonia Garel, Ugo Borello, Jean M Hebert, Salvador Martinez, Susan K McConnell, Gail R Martin, John L R Rubenstein. Development 2006
264
11

Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination.
K W Gripp, D Wotton, M C Edwards, E Roessler, L Ades, P Meinecke, A Richieri-Costa, E H Zackai, J Massagué, M Muenke,[...]. Nat Genet 2000
301
10

Genetics of ventral forebrain development and holoprosencephaly.
M Muenke, P A Beachy. Curr Opin Genet Dev 2000
199
10

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
15

Phenotypic and molecular variability of the holoprosencephalic spectrum.
Leila Lazaro, Christéle Dubourg, Laurent Pasquier, Franck Le Duff, Martine Blayau, Marie-Renée Durou, Armelle Thomas de la Pintière, Céline Aguilella, Véronique David, Sylvie Odent. Am J Med Genet A 2004
55
18

Central roles of the roof plate in telencephalic development and holoprosencephaly.
Xun Cheng, Ching-mei Hsu, D Spencer Currle, Jia Sheng Hu, A James Barkovich, Edwin S Monuki. J Neurosci 2006
80
12

FGF signalling generates ventral telencephalic cells independently of SHH.
Grigoriy Gutin, Marie Fernandes, Laura Palazzolo, Hunki Paek, Kai Yu, David M Ornitz, Susan K McConnell, Jean M Hébert. Development 2006
110
10

Holoprosencephaly: from Homer to Hedgehog.
J E Ming, M Muenke. Clin Genet 1998
98
9

Mutations in holoprosencephaly.
D Wallis, M Muenke. Hum Mutat 2000
137
9


Mouse models of holoprosencephaly.
Monica Hayhurst, Susan K McConnell. Curr Opin Neurol 2003
48
18


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.