A citation-based method for searching scientific literature

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
Times Cited: 29







List of co-cited articles
265 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
158
48

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
31

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
31

Epidemiology of holoprosencephaly and phenotypic characteristics of affected children: New York State, 1984-1989.
C L Olsen, J P Hughes, L G Youngblood, M Sharpe-Stimac. Am J Med Genet 1997
97
27

What is the incidence of holoprosencephaly?
E S Saunders, D Shortland, P M Dunn. J Med Genet 1984
37
27

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
105
27




Cyclopia and other anomalies following maternal ingestion of salicylates.
R Benawra, H H Mangurten, D R Duffell. J Pediatr 1980
47
24

Prenatal diagnosis of a new syndrome: holoprosencephaly with hypokinesia.
R P Morse, E Rawnsley, S K Sargent, J M Graham. Prenat Diagn 1987
25
24

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




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


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
20

Single central incisor in familial holoprosencephaly.
S A Berry, M E Pierpont, R J Gorlin. J Pediatr 1984
57
17


Alobar holoprosencephaly: ultrasonographic prenatal diagnosis.
R A Filly, D H Chinn, P W Callen. Radiology 1984
66
17



Ultrasonic findings with holoprosencephaly.
L M Hill, R Breckle, C R Bonebrake. J Reprod Med 1982
18
27

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
20

Holoprosencephaly.
Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Catherine Henry, Sylvie Odent, Véronique David. Orphanet J Rare Dis 2007
219
17

The cyclops and the mermaid: an epidemiological study of two types of rare malformation.
B Källén, E E Castilla, P A Lancaster, O Mutchinick, L B Knudsen, M L Martínez-Frías, P Mastroiacovo, E Robert. J Med Genet 1992
63
17

An epidemiological study of holoprosencephaly from a regional congenital anomaly register: 1995-2004.
S Ong, A Tonks, E R Woodward, M P Wyldes, M D Kilby. Prenat Diagn 2007
30
17

Holoprosencephaly in the west of Scotland 1975-1994.
M L Whiteford, J L Tolmie. J Med Genet 1996
37
17

Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination.
K W Gripp, D Wotton, M C Edwards, E Roessler, L Ades, P Meinecke, A Richieri-Costa, E H Zackai, J Massagué, M Muenke,[...]. Nat Genet 2000
299
13

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
839
13

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

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
236
13

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
16


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
28

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

Genetics of the Meckel syndrome (dysencephalia splanchnocystica).
Y E Hsia, M Bratu, A Herbordt. Pediatrics 1971
120
13

Holoprosencephaly as a possible embryonic alcohol effect.
G M Ronen, W L Andrews. Am J Med Genet 1991
60
13




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.