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Times Cited: 83
Times Cited: 83
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
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40
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
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
31
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
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
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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
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Perspectives on holoprosencephaly: Part III. Spectra, distinctions, continuities, and discontinuities.
M M Cohen. Am J Med Genet 1989
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Perspectives on holoprosencephaly: Part I. Epidemiology, genetics, and syndromology.
M M Cohen. Teratology 1989
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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
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
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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
C Chiang, Y Litingtung, E Lee, K E Young, J L Corden, H Westphal, P A Beachy. Nature 1996
22
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
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
21
Molecular characterization of breakpoints in patients with holoprosencephaly and definition of the HPE2 critical region 2p21.
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Physical mapping of the holoprosencephaly critical region in 21q22.3, exclusion of SIM2 as a candidate gene for holoprosencephaly, and mapping of SIM2 to a region of chromosome 21 important for Down syndrome.
M Muenke, L J Bone, H F Mitchell, I Hart, K Walton, K Hall-Johnson, E F Ippel, J Dietz-Band, K Kvaløy, C M Fan. Am J Hum Genet 1995
M Muenke, L J Bone, H F Mitchell, I Hart, K Walton, K Hall-Johnson, E F Ippel, J Dietz-Band, K Kvaløy, C M Fan. Am J Hum Genet 1995
21
Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephaly.
E Roessler, D E Ward, K Gaudenz, E Belloni, S W Scherer, D Donnai, J Siegel-Bartelt, L C Tsui, M Muenke. Hum Genet 1997
E Roessler, D E Ward, K Gaudenz, E Belloni, S W Scherer, D Donnai, J Siegel-Bartelt, L C Tsui, M Muenke. Hum Genet 1997
20
Perspectives on holoprosencephaly: Part II. Central nervous system, craniofacial anatomy, syndrome commentary, diagnostic approach, and experimental studies.
M M Cohen, K K Sulik. J Craniofac Genet Dev Biol 1992
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Holoprosencephaly in human embryos: epidemiologic studies of 150 cases.
E Matsunaga, K Shiota. Teratology 1977
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Holoprosencephaly: a paradigm for the complex genetics of brain development.
E Roessler, M Muenke. J Inherit Metab Dis 1998
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A gene for autosomal dominant sacral agenesis maps to the holoprosencephaly region at 7q36.
S A Lynch, P M Bond, A J Copp, W O Kirwan, S Nour, R Balling, E Mariman, J Burn, T Strachan. Nat Genet 1995
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Clinical, cytogenetic, and molecular approaches to the genetic heterogeneity of holoprosencephaly.
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Teratogenicity of low doses of all-trans retinoic acid in presomite mouse embryos.
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Mutations affecting segment number and polarity in Drosophila.
C Nüsslein-Volhard, E Wieschaus. Nature 1980
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Sonic hedgehog, a member of a family of putative signaling molecules, is implicated in the regulation of CNS polarity.
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Y Echelard, D J Epstein, B St-Jacques, L Shen, J Mohler, J A McMahon, A P McMahon. Cell 1993
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Holoprosencephaly: epidemiologic and clinical characteristics of a California population.
L A Croen, G M Shaw, E J Lammer. Am J Med Genet 1996
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14
Cloning, expression, and chromosomal location of SHH and IHH: two human homologues of the Drosophila segment polarity gene hedgehog.
V Marigo, D J Roberts, S M Lee, O Tsukurov, T Levi, J M Gastier, D J Epstein, D J Gilbert, N G Copeland, C E Seidman. Genomics 1995
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14
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
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14
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
E Roessler, E Belloni, K Gaudenz, F Vargas, S W Scherer, L C Tsui, M Muenke. Hum Mol Genet 1997
13
A novel homeobox protein which recognizes a TGT core and functionally interferes with a retinoid-responsive motif.
E Bertolino, B Reimund, D Wildt-Perinic, R G Clerc. J Biol Chem 1995
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13
Cholesterol modification of hedgehog signaling proteins in animal development.
J A Porter, K E Young, P A Beachy. Science 1996
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13
Familial holoprosencephaly associated with a translocation breakpoint at chromosomal position 7q36.
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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
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
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Alobar holoprosencephaly (arhinencephaly) with median cleft lip and palate: clinical, electroencephalographic and nosologic considerations.
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Holoprosencephaly: birth data, benetic and demographic analyses of 30 families.
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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
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
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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
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9
Hedgehog patterning activity: role of a lipophilic modification mediated by the carboxy-terminal autoprocessing domain.
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J A Porter, S C Ekker, W J Park, D P von Kessler, K E Young, C H Chen, Y Ma, A S Woods, R J Cotter, E V Koonin,[...]. Cell 1996
9
Floor plate and motor neuron induction by vhh-1, a vertebrate homolog of hedgehog expressed by the notochord.
H Roelink, A Augsburger, J Heemskerk, V Korzh, S Norlin, A Ruiz i Altaba, Y Tanabe, M Placzek, T Edlund, T M Jessell. Cell 1994
H Roelink, A Augsburger, J Heemskerk, V Korzh, S Norlin, A Ruiz i Altaba, Y Tanabe, M Placzek, T Edlund, T M Jessell. Cell 1994
9
Floor plate and motor neuron induction by different concentrations of the amino-terminal cleavage product of sonic hedgehog autoproteolysis.
H Roelink, J A Porter, C Chiang, Y Tanabe, D T Chang, P A Beachy, T M Jessell. Cell 1995
H Roelink, J A Porter, C Chiang, Y Tanabe, D T Chang, P A Beachy, T M Jessell. Cell 1995
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Holoprosencephaly and sacral agenesis in a fetus with a terminal deletion 7q36-->7qter.
N Morichon-Delvallez, A L Delezoide, M Vekemans. J Med Genet 1993
N Morichon-Delvallez, A L Delezoide, M Vekemans. J Med Genet 1993
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Defective cholesterol biosynthesis associated with the Smith-Lemli-Opitz syndrome.
G S Tint, M Irons, E R Elias, A K Batta, R Frieden, T S Chen, G Salen. N Engl J Med 1994
G S Tint, M Irons, E R Elias, A K Batta, R Frieden, T S Chen, G Salen. N Engl J Med 1994
9
Ectopic expression of Sonic hedgehog alters dorsal-ventral patterning of somites.
R L Johnson, E Laufer, R D Riddle, C Tabin. Cell 1994
R L Johnson, E Laufer, R D Riddle, C Tabin. Cell 1994
9
Autoproteolysis in hedgehog protein biogenesis.
J J Lee, S C Ekker, D P von Kessler, J A Porter, B I Sun, P A Beachy. Science 1994
J J Lee, S C Ekker, D P von Kessler, J A Porter, B I Sun, P A Beachy. Science 1994
8
10
Sonic hedgehog participates in craniofacial morphogenesis and is down-regulated by teratogenic doses of retinoic acid.
J A Helms, C H Kim, D Hu, R Minkoff, C Thaller, G Eichele. Dev Biol 1997
J A Helms, C H Kim, D Hu, R Minkoff, C Thaller, G Eichele. Dev Biol 1997
8
The product of hedgehog autoproteolytic cleavage active in local and long-range signalling.
J A Porter, D P von Kessler, S C Ekker, K E Young, J J Lee, K Moses, P A Beachy. Nature 1995
J A Porter, D P von Kessler, S C Ekker, K E Young, J J Lee, K Moses, P A Beachy. Nature 1995
8
Genetics of ventral forebrain development and holoprosencephaly.
M Muenke, P A Beachy. Curr Opin Genet Dev 2000
M Muenke, P A Beachy. Curr Opin Genet Dev 2000
8
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
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
8
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.