A citation-based method for searching scientific literature

G Corsello, P Buttitta, M Cammarata, A Lo Presti, E Maresi, L Zumpani, L Giuffrè. Am J Med Genet 1990
Times Cited: 18







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



Times Cited
  Times     Co-cited
Similarity






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
27


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
22

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
16

Sonography of facial features of alobar and semilobar holoprosencephaly.
J P McGahan, D A Nyberg, L A Mack. AJR Am J Roentgenol 1990
32
16

Holoprosencephaly: a developmental field defect.
V P Johnson. Am J Med Genet 1989
36
16

Cyclopia and congenital cytomegalovirus infection.
P J Byrne, M M Silver, J M Gilbert, W Cadera, A K Tanswell. Am J Med Genet 1987
41
16



Holoprosencephaly: a family showing dominant inheritance and variable expression.
A L Collins, P W Lunt, C Garrett, N R Dennis. J Med Genet 1993
25
11


Blastogenesis and the "primary field" in human development.
J M Opitz. Birth Defects Orig Artic Ser 1993
83
11

Cyclopia: craniofacial appearance on MR and three-dimensional CT.
D P Liu, D M Burrowes, M N Qureshi. AJNR Am J Neuroradiol 1997
6
33

An anatomic comparison of cebocephaly and ethmocephaly.
J P Souza, J R Siebert, J B Beckwith. Teratology 1990
14
14

The midline craniofacial skeleton in holoprosencephalic fetuses.
I Kjaer, J W Keeling, N Graem. J Med Genet 1991
45
11


Otx2 and HNF3beta genetically interact in anterior patterning.
O Jin, K Harpal, S L Ang, J Rossant. Int J Dev Biol 2001
30
11


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
11

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
11

Mutations in holoprosencephaly.
D Wallis, M Muenke. Hum Mutat 2000
137
11

Segregation analysis in nonsyndromic holoprosencephaly.
S Odent, B Le Marec, A Munnich, M Le Merrer, C Bonaïti-Pellié. Am J Med Genet 1998
43
11

Holoprosencephaly and trisomy 21 in a child born to a nondiabetic mother.
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
29
11


A case of holoprosencephaly and cebocephaly associated to torch infection.
Nizamettin Kilic, Zeynep Yazici. Int J Pediatr Otorhinolaryngol 2005
7
28

Teratogenesis of holoprosencephaly.
M Michael Cohen, Kohei Shiota. Am J Med Genet 2002
131
11

Current recommendations for the molecular evaluation of newly diagnosed holoprosencephaly patients.
Daniel E Pineda-Alvarez, Christèle Dubourg, Véronique David, Erich Roessler, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
46
11



Holoprosencephaly.
Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Catherine Henry, Sylvie Odent, Véronique David. Orphanet J Rare Dis 2007
223
11


What is the incidence of holoprosencephaly?
E S Saunders, D Shortland, P M Dunn. J Med Genet 1984
37
11


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


Clinical spectrum of SIX3-associated mutations in holoprosencephaly: correlation between genotype, phenotype and function.
F Lacbawan, B D Solomon, E Roessler, K El-Jaick, S Domené, J I Vélez, N Zhou, D Hadley, J Z Balog, R Long,[...]. J Med Genet 2009
65
11

Pallister-Hall syndrome associated with an unbalanced chromosome translocation.
J A Kuller, V A Cox, S A Schonberg, M Golabi. Am J Med Genet 1992
31
11


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
11


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
11

Clinical aspects of the MASA syndrome in a large family, including expressing females.
L Kaepernick, E Legius, J Higgins, S Kapur. Clin Genet 1994
37
5

VATER and hydrocephalus: distinct syndrome?
A K Iafolla, A McConkie-Rosell, Y T Chen. Am J Med Genet 1991
43
5

Spectrum of X-linked hydrocephalus (HSAS), MASA syndrome, and complicated spastic paraplegia (SPG1): Clinical review with six additional families.
C Schrander-Stumpel, C Höweler, M Jones, A Sommer, C Stevens, S Tinschert, J Israel, J P Fryns. Am J Med Genet 1995
41
5

The clinical spectrum of mutations in L1, a neuronal cell adhesion molecule.
E Fransen, L Vits, G Van Camp, P J Willems. Am J Med Genet 1996
52
5



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.