A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity



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

Middle interhemispheric fusion: an unusual variant of holoprosencephaly.
A J Barkovich, D J Quint. AJNR Am J Neuroradiol 1993
110
28

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
25

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
31




Neuropathologic research strategies in holoprosencephaly.
H B Sarnat, L Flores-Sarnat. J Child Neurol 2001
60
26

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
25

Holoprosencephaly survival and performance.
M Barr, M M Cohen. Am J Med Genet 1999
62
24







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
14

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
12

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
38

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
29

How to construct a neural tube.
H B Sarnat, J H Menkes. J Child Neurol 2000
25
36

Arhinencephaly. The spectrum of associated malformations.
J A Kobori, M K Herrick, H Urich. Brain 1987
39
23


Holoprosencephaly: birth data, benetic and demographic analyses of 30 families.
E Roach, W Demyer, P M Conneally, C Palmer, A D Merritt. Birth Defects Orig Artic Ser 1975
106
11

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
11

Descriptive epidemiology of holoprosencephaly and arhinencephaly in metropolitan Atlanta, 1968-1992.
S A Rasmussen, C A Moore, M J Khoury, J F Cordero. Am J Med Genet 1996
42
21

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
10

Holoprosencephaly: a defect in brain patterning.
J A Golden. J Neuropathol Exp Neurol 1998
66
12

Holoprosencephaly: new concepts.
E M Simon, A J Barkovich. Magn Reson Imaging Clin N Am 2001
24
33

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
10

Holoprosencephaly: from Homer to Hedgehog.
J E Ming, M Muenke. Clin Genet 1998
98
10

Teratogenesis of holoprosencephaly.
M Michael Cohen, Kohei Shiota. Am J Med Genet 2002
131
10


Holoprosencephaly: molecular study of a California population.
L Nanni, L A Croen, E J Lammer, M Muenke. Am J Med Genet 2000
35
20



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

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
9

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
9


Holoprosencephaly.
Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Catherine Henry, Sylvie Odent, Véronique David. Orphanet J Rare Dis 2007
223
9

Holoprosencephaly and agenesis of the corpus callosum: frequency of associated malformations.
K Jellinger, H Gross, E Kaltenbäck, W Grisold. Acta Neuropathol 1981
93
7

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
7

Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly.
D E Wallis, E Roessler, U Hehr, L Nanni, T Wiltshire, A Richieri-Costa, G Gillessen-Kaesbach, E H Zackai, J Rommens, M Muenke. Nat Genet 1999
283
7

A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome.
V des Portes, J M Pinard, P Billuart, M C Vinet, A Koulakoff, A Carrié, A Gelot, E Dupuis, J Motte, Y Berwald-Netter,[...]. Cell 1998
584
7

Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein.
J G Gleeson, K M Allen, J W Fox, E D Lamperti, S Berkovic, I Scheffer, E C Cooper, W B Dobyns, S R Minnerath, M E Ross,[...]. Cell 1998
791
7

Dorsal third ventricular cyst: an entity distinct from holoprosencephaly.
J N Young, W J Oakes, H P Hatten. J Neurosurg 1992
18
33

Alobar holoprosencephaly, diabetes insipidus and coloboma without craniofacial abnormalities: a case report.
S Van Gool, F de Zegher, L S de Vries, M Vanderschueren-Lodeweyckx, H Devlieger, P Casaer, E Eggermont. Eur J Pediatr 1990
15
40

Alobar holoprosencephaly with diabetes insipidus and neuronal migration disorder.
S Takahashi, A Miyamoto, J Oki, T Saino, F Inyaku. Pediatr Neurol 1995
14
42


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.