A citation-based method for searching scientific literature

J A Golden. J Neuropathol Exp Neurol 1998
Times Cited: 67







List of co-cited articles
1122 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
856
38

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
37

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
263
34

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
369
28




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
285
23



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
303
23

Patterning of the embryonic forebrain.
J L Rubenstein, P A Beachy. Curr Opin Neurobiol 1998
160
22


A Smad transcriptional corepressor.
D Wotton, R S Lo, S Lee, J Massagué. Cell 1999
451
20

Genetics of ventral forebrain development and holoprosencephaly.
M Muenke, P A Beachy. Curr Opin Genet Dev 2000
201
20


Holoprosencephaly: from Homer to Hedgehog.
J E Ming, M Muenke. Clin Genet 1998
99
17

Molecular mechanisms of holoprosencephaly.
D E Wallis, M Muenke. Mol Genet Metab 1999
99
17


Identification of Sonic hedgehog as a candidate gene responsible for holoprosencephaly.
E Belloni, M Muenke, E Roessler, G Traverso, J Siegel-Bartelt, A Frumkin, H F Mitchell, H Donis-Keller, C Helms, A V Hing,[...]. Nat Genet 1996
492
16

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
167
14

Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity.
M Muenke, F Gurrieri, C Bay, D H Yi, A L Collins, V P Johnson, R C Hennekam, G B Schaefer, L Weik, M S Lubinsky. Proc Natl Acad Sci U S A 1994
107
14


Ectopic bone morphogenetic proteins 5 and 4 in the chicken forebrain lead to cyclopia and holoprosencephaly.
J A Golden, A Bracilovic, K A McFadden, J S Beesley, J L Rubenstein, J B Grinspan. Proc Natl Acad Sci U S A 1999
125
14



Teratogenicity of low doses of all-trans retinoic acid in presomite mouse embryos.
K K Sulik, D B Dehart, J M Rogers, N Chernoff. Teratology 1995
110
13

Retinoic acid embryopathy.
E J Lammer, D T Chen, R M Hoar, N D Agnish, P J Benke, J T Braun, C J Curry, P M Fernhoff, A W Grix, I T Lott. N Engl J Med 1985
13


Mutations in the C-terminal domain of Sonic Hedgehog cause holoprosencephaly.
E Roessler, E Belloni, K Gaudenz, F Vargas, S W Scherer, L C Tsui, M Muenke. Hum Mol Genet 1997
132
13

Teratogen-mediated inhibition of target tissue response to Shh signaling.
M K Cooper, J A Porter, K E Young, P A Beachy. Science 1998
703
13




Zebrafish organizer development and germ-layer formation require nodal-related signals.
B Feldman, M A Gates, E S Egan, S T Dougan, G Rennebeck, H I Sirotkin, A F Schier, W S Talbot. Nature 1998
529
11

Human developmental disorders and the Sonic hedgehog pathway.
J E Ming, E Roessler, M Muenke. Mol Med Today 1998
125
11


Middle interhemispheric fusion: an unusual variant of holoprosencephaly.
A J Barkovich, D J Quint. AJNR Am J Neuroradiol 1993
111
11

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
12

Teratogenesis of holoprosencephaly.
M Michael Cohen, Kohei Shiota. Am J Med Genet 2002
132
11


Induction of the zebrafish ventral brain and floorplate requires cyclops/nodal signalling.
K Sampath, A L Rubinstein, A M Cheng, J O Liang, K Fekany, L Solnica-Krezel, V Korzh, M E Halpern, C V Wright. Nature 1998
394
10



The expression of the mouse Zic1, Zic2, and Zic3 gene suggests an essential role for Zic genes in body pattern formation.
T Nagai, J Aruga, S Takada, T Günther, R Spörle, K Schughart, K Mikoshiba. Dev Biol 1997
268
10

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
107
10

Physical mapping of the holoprosencephaly critical region in 18p11.3.
J Overhauser, H F Mitchell, E H Zackai, D B Tick, K Rojas, M Muenke. Am J Hum Genet 1995
93
10



Physical mapping of the holoprosencephaly critical region on chromosome 7q36.
F Gurrieri, B J Trask, G van den Engh, C M Krauss, A Schinzel, M J Pettenati, D Schindler, J Dietz-Band, G Vergnaud, S W Scherer. Nat Genet 1993
83
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.