A citation-based method for searching scientific literature

M Urioste, E Valcarcel, M A Gomez, I Pinel, R Garcia de León, A Diaz de Bustamante, R Tebar, M L Martinez-Frias. Am J Med Genet 1988
Times Cited: 29







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



Times Cited
  Times     Co-cited
Similarity


CNS dysplasia in dysencephalia splanchnocystica (Gruber's syndrome). A case report.
A Hori, H Orthner, A Kohlschütter, K M Schott, K Hirabayashi, K Shimokawa. Acta Neuropathol 1980
19
5



The epidemiology of diabetes and pregnancy in the U.S., 1988.
M M Engelgau, W H Herman, P J Smith, R R German, R E Aubert. Diabetes Care 1995
148
3



Niemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasis.
E D Carstea, J A Morris, K G Coleman, S K Loftus, D Zhang, C Cummings, J Gu, M A Rosenfeld, W J Pavan, D B Krizman,[...]. Science 1997
3



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
150
3

Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene.
J W Foster, M A Dominguez-Steglich, S Guioli, C Kwok, P A Weller, M Stevanović, J Weissenbach, S Mansour, I D Young, P N Goodfellow. Nature 1994
3





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
743
3

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
109
3



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
3


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
131
3

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
89
3

Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family.
Q Y Li, R A Newbury-Ecob, J A Terrett, D I Wilson, A R Curtis, C H Yi, T Gebuhr, P J Bullen, S C Robson, T Strachan,[...]. Nat Genet 1997
649
3


Pseudo-trisomy 13 syndrome with upper limb shortness and radial hypoplasia.
R G Boles, A S Teebi, K A Neilson, M S Meyn. Am J Med Genet 1992
10
10

Hedgehog patterning activity: role of a lipophilic modification mediated by the carboxy-terminal autoprocessing domain.
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
397
3


Aniridia-associated cytogenetic rearrangements suggest that a position effect may cause the mutant phenotype.
J Fantes, B Redeker, M Breen, S Boyle, J Brown, J Fletcher, S Jones, W Bickmore, Y Fukushima, M Mannens. Hum Mol Genet 1995
167
3


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.