A citation-based method for searching scientific literature

E S Saunders, D Shortland, P M Dunn. J Med Genet 1984
Times Cited: 37







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



Times Cited
  Times     Co-cited
Similarity




Alobar holoprosencephaly: ultrasonographic prenatal diagnosis.
R A Filly, D H Chinn, P W Callen. Radiology 1984
67
35

Diagnosis and management of fetal holoprosencephaly.
F A Chervenak, G Isaacson, J C Hobbins, U Chitkara, M Tortora, R L Berkowitz. Obstet Gynecol 1985
52
32

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
32




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
27

Holoprosencephaly in the west of Scotland 1975-1994.
M L Whiteford, J L Tolmie. J Med Genet 1996
39
21

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
27


The obstetric significance of holoprosencephaly.
F A Chervenak, G Isaacson, M J Mahoney, M Tortora, T Mesologites, J C Hobbins. Obstet Gynecol 1984
42
18

Single central incisor in familial holoprosencephaly.
S A Berry, M E Pierpont, R J Gorlin. J Pediatr 1984
57
18

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
26


Familial holoprosencephaly with endocrine dysgenesis.
R L Hintz, M Menking, J F Sotos. J Pediatr 1968
92
18



Holoprosencephaly and related entities.
C R Fitz. Neuroradiology 1983
62
16


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

Holoprosencephaly and agenesis of the corpus callosum: frequency of associated malformations.
K Jellinger, H Gross, E Kaltenbäck, W Grisold. Acta Neuropathol 1981
93
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.
Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Catherine Henry, Sylvie Odent, Véronique David. Orphanet J Rare Dis 2007
223
16

Single central maxillary incisor and holoprosencephaly.
H Hattori, T Okuno, T Momoi, K Kataoka, H Mikawa, K Shiota. Am J Med Genet 1987
37
16

Reliable criteria for the prenatal sonographic diagnosis of alobar holoprosencephaly.
M F Greene, B R Benacerraf, F D Frigoletto. Am J Obstet Gynecol 1987
30
16

Familial agnathia-holoprosencephaly.
R M Pauli, J C Pettersen, S Arya, E F Gilbert. Am J Med Genet 1983
75
13

Genetic heterogeneity of cebocephaly.
L B Holmes, S Driscoll, L Atkins. J Med Genet 1974
33
15


Genetics of the Meckel syndrome (dysencephalia splanchnocystica).
Y E Hsia, M Bratu, A Herbordt. Pediatrics 1971
119
13


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

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
50





Prenatal diagnosis of semilobar holoprosencephaly.
P D Cayea, I Balcar, O Alberti, T B Jones. AJR Am J Roentgenol 1984
14
35

Holoprosencephaly and endocrine dysgenesis in brothers.
M L Begleiter, D J Harris. Am J Med Genet 1980
24
20

Early diagnosis of holoprosencephaly.
L H Nelson, M King. J Ultrasound Med 1992
24
16



The spectrum of the DiGeorge syndrome.
M E Conley, J B Beckwith, J F Mancer, L Tenckhoff. J Pediatr 1979
326
10

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

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

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
21


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
23

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


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.