A citation-based method for searching scientific literature

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
Times Cited: 167







List of co-cited articles
1156 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
843
40

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
32

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
631
31

Mutations in the human sterol delta7-reductase gene at 11q12-13 cause Smith-Lemli-Opitz syndrome.
C A Wassif, C Maslen, S Kachilele-Linjewile, D Lin, L M Linck, W E Connor, R D Steiner, F D Porter. Am J Hum Genet 1998
305
28

The Smith-Lemli-Opitz syndrome.
R I Kelley, R C Hennekam. J Med Genet 2000
332
27

A NEWLY RECOGNIZED SYNDROME OF MULTIPLE CONGENITAL ANOMALIES.
D W SMITH, L LEMLI, J M OPITZ. J Pediatr 1964
544
25

A defective response to Hedgehog signaling in disorders of cholesterol biosynthesis.
Michael K Cooper, Christopher A Wassif, Patrycja A Krakowiak, Jussi Taipale, Ruoyu Gong, Richard I Kelley, Forbes D Porter, Philip A Beachy. Nat Genet 2003
276
25

Teratogen-mediated inhibition of target tissue response to Shh signaling.
M K Cooper, J A Porter, K E Young, P A Beachy. Science 1998
698
24

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
487
24

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
22

Defective cholesterol biosynthesis in Smith-Lemli-Opitz syndrome.
M Irons, E R Elias, G Salen, G S Tint, A K Batta. Lancet 1993
297
22

Mutations in the Delta7-sterol reductase gene in patients with the Smith-Lemli-Opitz syndrome.
B U Fitzky, M Witsch-Baumgartner, M Erdel, J N Lee, Y K Paik, H Glossmann, G Utermann, F F Moebius. Proc Natl Acad Sci U S A 1998
296
20


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
20

Smith-Lemli-Opitz syndrome is caused by mutations in the 7-dehydrocholesterol reductase gene.
H R Waterham, F A Wijburg, R C Hennekam, P Vreken, B T Poll-The, L Dorland, M Duran, P E Jira, J A Smeitink, R A Wevers,[...]. Am J Hum Genet 1998
219
19



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
19


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
18

Smith-Lemli-Opitz syndrome: a variable clinical and biochemical phenotype.
A K Ryan, K Bartlett, P Clayton, S Eaton, L Mills, D Donnai, R M Winter, J Burn. J Med Genet 1998
174
18

Identification of a palmitic acid-modified form of human Sonic hedgehog.
R B Pepinsky, C Zeng, D Wen, P Rayhorn, D P Baker, K P Williams, S A Bixler, C M Ambrose, E A Garber, K Miatkowski,[...]. J Biol Chem 1998
527
18


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
18

Mutational spectrum in the Delta7-sterol reductase gene and genotype-phenotype correlation in 84 patients with Smith-Lemli-Opitz syndrome.
M Witsch-Baumgartner, B U Fitzky, M Ogorelkova, H G Kraft, F F Moebius, H Glossmann, U Seedorf, G Gillessen-Kaesbach, G F Hoffmann, P Clayton,[...]. Am J Hum Genet 2000
145
17

Teratogenesis of holoprosencephaly.
M Michael Cohen, Kohei Shiota. Am J Med Genet 2002
131
17

Defective forebrain development in mice lacking gp330/megalin.
T E Willnow, J Hilpert, S A Armstrong, A Rohlmann, R E Hammer, D K Burns, J Herz. Proc Natl Acad Sci U S A 1996
397
15



Holoprosencephaly: from Homer to Hedgehog.
J E Ming, M Muenke. Clin Genet 1998
98
15

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
15

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
15


7-Dehydrocholesterol-dependent proteolysis of HMG-CoA reductase suppresses sterol biosynthesis in a mouse model of Smith-Lemli-Opitz/RSH syndrome.
B U Fitzky, F F Moebius, H Asaoka, H Waage-Baudet, L Xu, G Xu, N Maeda, K Kluckman, S Hiller, H Yu,[...]. J Clin Invest 2001
124
14

Altered neural cell fates and medulloblastoma in mouse patched mutants.
L V Goodrich, L Milenković, K M Higgins, M P Scott. Science 1997
14




Inhibition of Hedgehog signaling by direct binding of cyclopamine to Smoothened.
James K Chen, Jussi Taipale, Michael K Cooper, Philip A Beachy. Genes Dev 2002
14

Behavior phenotype in the RSH/Smith-Lemli-Opitz syndrome.
E Tierney, N A Nwokoro, F D Porter, L S Freund, J K Ghuman, R I Kelley. Am J Med Genet 2001
120
13

A loss-of-function mutation in the CFC domain of TDGF1 is associated with human forebrain defects.
June M de la Cruz, Richard N Bamford, Rebecca D Burdine, Erich Roessler, A James Barkovich, Dian Donnai, Alexander F Schier, Maximilian Muenke. Hum Genet 2002
80
16


A freely diffusible form of Sonic hedgehog mediates long-range signalling.
X Zeng, J A Goetz, L M Suber, W J Scott, C M Schreiner, D J Robbins. Nature 2001
337
13


Repression of smoothened by patched-dependent (pro-)vitamin D3 secretion.
Maarten F Bijlsma, C Arnold Spek, Danica Zivkovic, Sandra van de Water, Farhad Rezaee, Maikel P Peppelenbosch. PLoS Biol 2006
226
13


Molecular cloning and expression of the human delta7-sterol reductase.
F F Moebius, B U Fitzky, J N Lee, Y K Paik, H Glossmann. Proc Natl Acad Sci U S A 1998
167
12

Inborn errors of sterol biosynthesis.
R I Kelley, G E Herman. Annu Rev Genomics Hum Genet 2001
155
12

Mutations affecting segment number and polarity in Drosophila.
C Nüsslein-Volhard, E Wieschaus. Nature 1980
12


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.