A citation-based method for searching scientific literature

M M Cohen. J Pediatr 1982
Times Cited: 103







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



Times Cited
  Times     Co-cited
Similarity





The facial features of holoprosencephaly in anencephalic human specimens. II. Craniofacial anatomy.
J R Siebert, V G Kokich, J B Beckwith, M M Cohen, R J Lemire. Teratology 1981
47
36


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
26

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
14

Single central incisor in familial holoprosencephaly.
S A Berry, M E Pierpont, R J Gorlin. J Pediatr 1984
57
22


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
46

Holoprosencephaly and agenesis of the corpus callosum: frequency of associated malformations.
K Jellinger, H Gross, E Kaltenbäck, W Grisold. Acta Neuropathol 1981
93
12



What is the incidence of holoprosencephaly?
E S Saunders, D Shortland, P M Dunn. J Med Genet 1984
37
29

Alobar holoprosencephaly: ultrasonographic prenatal diagnosis.
R A Filly, D H Chinn, P W Callen. Radiology 1984
66
16

Solitary maxillary central incisor and normal stature.
R K Wesley, W H Hoffman, J Perrin, J R Delaney. Oral Surg Oral Med Oral Pathol 1978
34
29

Single central maxillary incisor and holoprosencephaly.
H Hattori, T Okuno, T Momoi, K Kataoka, H Mikawa, K Shiota. Am J Med Genet 1987
37
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
23

Familial holoprosencephaly with endocrine dysgenesis.
R L Hintz, M Menking, J F Sotos. J Pediatr 1968
92
10

Atelencephalic microcephaly.
C A Garcia, C Duncan. Dev Med Child Neurol 1977
42
21


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
841
9

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
25

Syndromes with cephaloceles.
M M Cohen, R J Lemire. Teratology 1982
88
10


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
77
11


Solitary maxillary central incisor and short stature.
E B Rappaport, R A Ulstrom, R J Gorlin, A W Lucky, E Colle, J Miser. J Pediatr 1977
72
11

Holoprosencephaly and related entities.
C R Fitz. Neuroradiology 1983
62
12

Cyclopia: an anatomic and histologic study of two specimens.
V G Kokich, C H Ngim, J R Siebert, S K Clarren, M M Cohen. Teratology 1982
30
26

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
8


Holoprosencephaly: prenatal sonographic diagnosis.
D A Nyberg, L A Mack, A Bronstein, J Hirsch, R A Pagon. AJR Am J Roentgenol 1987
48
14


Genetic heterogeneity of cebocephaly.
L B Holmes, S Driscoll, L Atkins. J Med Genet 1974
33
21

A case of cyclopia. Role of environmental factors.
F Mollica, L Pavone, G Nuciforo, G Sorge. Clin Genet 1979
33
21

Genetics of the Meckel syndrome (dysencephalia splanchnocystica).
Y E Hsia, M Bratu, A Herbordt. Pediatrics 1971
119
7


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

Sporadic case of apparent aprosencephaly.
W N Adkins, E G Kaveggia. Am J Med Genet 1979
23
30


Ultrasonic findings with holoprosencephaly.
L M Hill, R Breckle, C R Bonebrake. J Reprod Med 1982
18
38

Arhinencephaly. The spectrum of associated malformations.
J A Kobori, M K Herrick, H Urich. Brain 1987
38
18

Atelencephaly.
M Iivanainen, M Haltia, K Lydecken. Dev Med Child Neurol 1977
33
18

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

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
6

The spectrum of the DiGeorge syndrome.
M E Conley, J B Beckwith, J F Mancer, L Tenckhoff. J Pediatr 1979
326
6


The XK-aprosencephaly syndrome.
I W Lurie, M K Nedzed, G I Lazjuk, I A Kirillova, E D Cherstvoy, T I Ostrovskaja, I A Shved. Am J Med Genet 1980
21
28



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.