A citation-based method for searching scientific literature

R Benawra, H H Mangurten, D R Duffell. J Pediatr 1980
Times Cited: 47







List of co-cited articles
293 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
38


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
39

A case of cyclopia. Role of environmental factors.
F Mollica, L Pavone, G Nuciforo, G Sorge. Clin Genet 1979
33
39

Cyclopia.
G Khudr, L Olding. Am J Dis Child 1973
26
50

Familial agnathia-holoprosencephaly.
R M Pauli, J C Pettersen, S Arya, E F Gilbert. Am J Med Genet 1983
75
25

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
23



Holoprosencephaly and agenesis of the corpus callosum: frequency of associated malformations.
K Jellinger, H Gross, E Kaltenbäck, W Grisold. Acta Neuropathol 1981
93
19

A case of suspected teratogenic holoprosencephaly.
M Stabile, A Bianco, S Iannuzzi, M C Buonocore, V Ventruto. J Med Genet 1985
11
72


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
24

Agnathia, holoprosencephaly, and situs inversus: report of a case.
R W Leech, L S Bowlby, R A Brumback, G B Schaefer. Am J Med Genet 1988
35
17

Agnathia, situs inversus, and associated malformations.
R M Pauli, J M Graham, M Barr. Teratology 1981
66
12




Cyclopia and maternal ingestion of salicylates.
M Agapitos, M Georgiou-Theodoropoulou, A Koutselinis, N Papacharalampus. Pediatr Pathol 1986
8
75

A case of cyclopia.
J A Batts, H H Punnett, M Valdes-Dapena, J W Coles, W R Green. Am J Obstet Gynecol 1972
20
30



Holoprosencephaly in a Down syndrome child.
S Y Pi, R M Fineman, S D Wing, M Grunnet, G Chan. Am J Med Genet 1980
26
23

Trisomy 18 and cyclopia.
A F Lang, F M Schlager, H A Gardner. Teratology 1976
30
20



Holoprosencephaly as a possible embryonic alcohol effect.
G M Ronen, W L Andrews. Am J Med Genet 1991
60
10

Descriptive epidemiology of holoprosencephaly and arhinencephaly in metropolitan Atlanta, 1968-1992.
S A Rasmussen, C A Moore, M J Khoury, J F Cordero. Am J Med Genet 1996
42
11

9
55



Holoprosencephaly and facial dysmorphia: nosology, etiology and pathogenesis.
M M Cohen, J E Jirásek, R T Guzman, R J Gorlin, M Q Peterson. Birth Defects Orig Artic Ser 1971
78
10

Otocephaly: prenatal diagnosis of a new case and etiopathogenetic considerations.
R M Ibba, M A Zoppi, M Floris, M Putzolu, G Monni, P F Todde, G Sardu. Am J Med Genet 2000
22
22



Aspirin and congenital malformations.
D Slone, V Siskind, O P Heinonen, R R Monson, D W Kaufman, S Shapiro. Lancet 1976
150
10


Cyclopism as a hereditary malformation.
P Pfitzer, H Müntefering. Nature 1968
30
16

Cyclopia-otocephaly association: a new case of the most severe variant of agnathia-holoprosencephaly complex.
D Carles, F Serville, M Mainguené, J P Dubecq. J Craniofac Genet Dev Biol 1987
16
31



Alobar holoprosencephaly: ultrasonographic prenatal diagnosis.
R A Filly, D H Chinn, P W Callen. Radiology 1984
67
10


Congenital hypothalamic hamartoblastoma, hypopituitarism, imperforate anus and postaxial polydactyly--a new syndrome? Part I: clinical, causal, and pathogenetic considerations.
J G Hall, P D Pallister, S K Clarren, J B Beckwith, F W Wiglesworth, F C Fraser, S Cho, P J Benke, S D Reed. Am J Med Genet 1980
242
10

Genetic and developmental studies of a new mouse mutation that produces otocephaly.
D M Juriloff, K K Sulik, T H Roderick, B K Hogan. J Craniofac Genet Dev Biol 1985
36
11


Prenatal diagnosis of a new syndrome: holoprosencephaly with hypokinesia.
R P Morse, E Rawnsley, S K Sargent, J M Graham. Prenat Diagn 1987
25
16

A case of deletion 2q35----qter and a peculiar phenotype.
J M Sánchez, A M Pantano. J Med Genet 1984
35
11

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
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.