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


Otocephaly-midline malformation association.
J H Hersh, R H McChane, E M Rosenberg, W H Powers, C Corrigan, L Pancratz. Am J Med Genet 1989
24
12


Monozygotic twin aborted fetuses discordant for holoprosencephaly/synotia.
G A Machin, G H Sperber, J Wootliffe. Teratology 1985
16
18


[Two cases of cyclopia].
Y Castel, D Riviere, L Toudic, Y Nouaille, J L'Henoret, H Duparcmeur, J P Leroy, G Balouet. Ann Pediatr (Paris) 1976
6
50


Cyclopia with trisomy D.
E Z Zimmer, M Y Divon, M Halperin, B A Peretz. Eur J Obstet Gynecol Reprod Biol 1982
6
50

Holoprosencephaly: An update on cytogenetic abnormalities.
Claude Bendavid, Valérie Dupé, Lucie Rochard, Isabelle Gicquel, Christèle Dubourg, Véronique David. Am J Med Genet C Semin Med Genet 2010
36
8


Clinical epidemiologic study of holoprosencephaly in South America.
Iêda M Orioli, Eduardo E Castilla. Am J Med Genet A 2007
36
8


A case of holoprosencephaly and cebocephaly associated to torch infection.
Nizamettin Kilic, Zeynep Yazici. Int J Pediatr Otorhinolaryngol 2005
7
42





Ultrasonic findings with holoprosencephaly.
L M Hill, R Breckle, C R Bonebrake. J Reprod Med 1982
18
16

Synophthalmia and cyclopia: a histopathologic, radiographic, and organogenetic analysis.
E Torczynski, F A Jacobiec, M C Johnston, R L Font, J A Madewell. Doc Ophthalmol 1977
43
6

Cyclopia as a result of an unbalanced familial translocation, rcp(7;18)(q34;q21)
R D Smart, J Ross, G Amann, M M Nelson. Am J Med Genet 1986
18
16

An autosomal dominant midline cleft syndrome resembling familial holoprosencephaly.
A O Martin, J C Perrin, W A Muir, E Ruch, I A Schafer. Clin Genet 1977
19
15



The spectrum of the DiGeorge syndrome.
M E Conley, J B Beckwith, J F Mancer, L Tenckhoff. J Pediatr 1979
329
6


Descriptive neuropathology of chromosomal disorders in man.
F Gullotta, H Rehder, A Gropp. Hum Genet 1981
42
7

Microcephaly in familial holoprosencephaly.
H H Ardinger, J A Bartley. J Craniofac Genet Dev Biol 1988
18
16

Letter: Holoprosencephaly.
R B Lowry. Am J Dis Child 1974
28
10


Cebocephaly in an infant with trisomy 18.
A G Hunter, M Ray, C Langston. J Med Genet 1977
13
23

Campomelic dysplasia. Further elucidation of a distinct entity.
B D Hall, J W Spranger. Am J Dis Child 1980
71
6

Brief clinical reports: aprosencephaly-atelencephaly and the aprosencephaly (XK) syndrome.
I W Lurie, M K Nedzved, G I Lazjuk, I A Kirillova, E D Cherstvoy. Am J Med Genet 1979
36
8

The syndrome associated with the partial D-monosomy. Case report and review.
D J Orbeli, I W Lurie, J L Goroshenko. Humangenetik 1971
35
8

Letter: Holoprosencephaly revisited.
M M Cohen. Am J Dis Child 1974
18
16

Are 1q plus chromosomes harmless?
R J Gardner, H R McCreanor, M I Parslow, A M Veale. Clin Genet 1974
37
8


Absent left hemidiaphragm, arhinencephaly, and cardiac malformations.
N Fitch, H Srolovitz, Y Robitaille, F Guttman. J Med Genet 1978
48
6



Detecting and treating retinopathy in patients with type I diabetes mellitus. A health policy model.
J C Javitt, J K Canner, R G Frank, D M Steinwachs, A Sommer. Ophthalmology 1990
100
6

Effects on the fetal rat eye of maternal benomyl exposure and protein malnutrition.
E R Hoogenboom, J F Ransdell, W G Ellis, R J Kavlock, F J Zeman. Curr Eye Res 1991
23
13

Automatic detection of diabetic retinopathy using an artificial neural network: a screening tool.
G G Gardner, D Keating, T H Williamson, A T Elliott. Br J Ophthalmol 1996
145
6


Cost-effectiveness of alternative methods for diabetic retinopathy screening.
D R Lairson, J A Pugh, A S Kapadia, R J Lorimor, J Jacobson, R Velez. Diabetes Care 1992
60
6


Neural network feature detector for real-time video signal processing.
D Naylor, S Jones, D Myers, J Vincent. Int J Neural Syst 1993
3
100

A relative cost-effectiveness analysis of different methods of screening for diabetic retinopathy.
M J Sculpher, M J Buxton, B A Ferguson, J E Humphreys, J F Altman, D J Spiegelhalter, A J Kirby, J S Jacob, H Bacon, S B Dudbridge. Diabet Med 1991
42
7

Sonographic findings in otocephaly (synotia).
P D Cayea, F R Bieber, M J Ross, A Davidoff, R Osathanondh, T B Jones. J Ultrasound Med 1985
10
20

Cyclopia.
J M Opitz. Clin Genet 1980
8
25

Birth defects monitoring in California: a resource for epidemiological research.
L A Croen, G M Shaw, N G Jensvold, J A Harris. Paediatr Perinat Epidemiol 1991
143
4

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
286
4


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.