A citation-based method for searching scientific literature

C J Epstein, S Seto, M Golabi. Am J Med Genet 1988
Times Cited: 15







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



Times Cited
  Times     Co-cited
Similarity


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
73

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
66

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
158
46



What is the incidence of holoprosencephaly?
E S Saunders, D Shortland, P M Dunn. J Med Genet 1984
37
40


Cyclopia and congenital cytomegalovirus infection.
P J Byrne, M M Silver, J M Gilbert, W Cadera, A K Tanswell. Am J Med Genet 1987
40
40

Ultrasonic findings with holoprosencephaly.
L M Hill, R Breckle, C R Bonebrake. J Reprod Med 1982
18
33

Association of holoprosencephaly and Down syndrome.
M L Martinez-Frías. Am J Med Genet 1989
5
100


Genetics of the Meckel syndrome (dysencephalia splanchnocystica).
Y E Hsia, M Bratu, A Herbordt. Pediatrics 1971
119
26


Prenatal detection of cyclopia associated with interstitial deletion of 2p.
H O Grundy, P Niemeyer, M K Rupani, V F Ward, E R Wassman. Am J Med Genet 1989
17
26

Holoprosencephaly and interstitial deletion of 2(p2101p2109).
W G Wilson, D E Shanks, K W Sudduth, K A Couper, J McIlhenny. Am J Med Genet 1989
15
26

Alobar holoprosencephaly: ultrasonographic prenatal diagnosis.
R A Filly, D H Chinn, P W Callen. Radiology 1984
66
26


A male infant with holoprosencephaly, associated with ring chromosome 21.
D C Aronson, M C Jansweijer, J M Hoovers, P G Barth. Clin Genet 1987
24
26

Holoprosencephaly and agenesis of the corpus callosum: frequency of associated malformations.
K Jellinger, H Gross, E Kaltenbäck, W Grisold. Acta Neuropathol 1981
93
26


Familial agnathia-holoprosencephaly.
R M Pauli, J C Pettersen, S Arya, E F Gilbert. Am J Med Genet 1983
75
20

The spectrum of the DiGeorge syndrome.
M E Conley, J B Beckwith, J F Mancer, L Tenckhoff. J Pediatr 1979
326
20


A lethal presentation of de novo deletion 7q.
L E McMorrow, I R Toth, M M Gluckson, A Leff, S R Wolman. J Med Genet 1987
20
20

47, XY, t(9pplus;11qplus) in a mlae infant with multiple malformations.
N D Dinno, G L Silvey, B Weisskopf. Clin Genet 1974
24
20

A case of cyclopia. Role of environmental factors.
F Mollica, L Pavone, G Nuciforo, G Sorge. Clin Genet 1979
33
20

Prenatal diagnosis of a new syndrome: holoprosencephaly with hypokinesia.
R P Morse, E Rawnsley, S K Sargent, J M Graham. Prenat Diagn 1987
25
20

[Lethal chondrodysplasia with short ribs, Majewski type. Diagnosis in utero].
A Nivelon-Chevallier, D Halfon, J P Mabille. Pediatrie 1982
8
37


An infant with trisomy 6q21 leads to 6qter.
R L Neu, J U Gallien, N Steinberg-Warren, R J Wynn, R M Bannerman. Ann Genet 1981
14
21

Single central incisor in familial holoprosencephaly.
S A Berry, M E Pierpont, R J Gorlin. J Pediatr 1984
57
20

Triploidy in 40 human spontaneous abortuses: assessment of phenotype in embryos.
M J Harris, B J Poland, F J Dill. Obstet Gynecol 1981
20
20

Holoprosencephaly as a possible embryonic alcohol effect.
G M Ronen, W L Andrews. Am J Med Genet 1991
60
20


49,XXXXY syndrome.
P D Pallister. Am J Med Genet 1982
20
20


Pseudo-trisomy 13 syndrome.
M M Cohen, R J Gorlin. Am J Med Genet 1991
32
20

Familial holoprosencephaly.
M Khan, B Rozdilsky, J W Gerrard. Dev Med Child Neurol 1970
22
20


Duplication 3p21----3pter and cyclopia.
D N Kurtzman, D L Van Dyke, C A Rich, L Weiss. Am J Med Genet 1987
25
20

Descriptive neuropathology of chromosomal disorders in man.
F Gullotta, H Rehder, A Gropp. Hum Genet 1981
42
20


Triploidy with cyclopia and identical HLA alleles in the parents.
J C Lambert, P Philip, G Charpentier, M Ferrari, M Donzeau, N Ayraud. J Med Genet 1984
10
30



Velo-cardio-facial syndrome presenting as holoprosencephaly.
J E Wraith, M Super, G H Watson, M Phillips. Clin Genet 1985
40
20

Trisomy 22 with holoprosencephaly: a clinicopathologic study.
N B Isada, J C Bolan, J W Larsen, S G Kent. Teratology 1990
13
23

Single central maxillary incisor and holoprosencephaly.
H Hattori, T Okuno, T Momoi, K Kataoka, H Mikawa, K Shiota. Am J Med Genet 1987
37
20




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.