A citation-based method for searching scientific literature

S Ong, A Tonks, E R Woodward, M P Wyldes, M D Kilby. Prenat Diagn 2007
Times Cited: 30







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



Times Cited
  Times     Co-cited
Similarity





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
36

Holoprosencephaly in the west of Scotland 1975-1994.
M L Whiteford, J L Tolmie. J Med Genet 1996
39
36

Holoprosencephaly.
Christèle Dubourg, Claude Bendavid, Laurent Pasquier, Catherine Henry, Sylvie Odent, Véronique David. Orphanet J Rare Dis 2007
221
36


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


Descriptive epidemiology of holoprosencephaly and arhinencephaly in metropolitan Atlanta, 1968-1992.
S A Rasmussen, C A Moore, M J Khoury, J F Cordero. Am J Med Genet 1996
41
30


A retrospective survey of perinatal risk factors of 104 living children with holoprosencephaly.
Elaine E Stashinko, Nancy J Clegg, Heather A Kammann, Vicki T Sweet, Mauricio R Delgado, Jin S Hahn, Eric B Levey. Am J Med Genet A 2004
37
23


Holoprosencephaly: clinical, anatomic, and molecular dimensions.
M Michael Cohen. Birth Defects Res A Clin Mol Teratol 2006
138
23

Frequency of holoprosencephaly in the International Clearinghouse Birth Defects Surveillance Systems: searching for population variations.
Emanuele Leoncini, Giovanni Baranello, Iêda M Orioli, Göran Annerén, Marian Bakker, Fabrizio Bianchi, Carol Bower, Mark A Canfield, Eduardo E Castilla, Guido Cocchi,[...]. Birth Defects Res A Clin Mol Teratol 2008
64
23

Epidemiology of holoprosencephaly: Prevalence and risk factors.
Iêda M Orioli, Eduardo E Castilla. Am J Med Genet C Semin Med Genet 2010
62
23

Holoprosencephaly survival and performance.
M Barr, M M Cohen. Am J Med Genet 1999
62
20

Epidemiology of holoprosencephaly in Hawaii, 1986-97.
M B Forrester, R D Merz. Paediatr Perinat Epidemiol 2000
17
35

Risk factors for non-syndromic holoprosencephaly in the National Birth Defects Prevention Study.
Eric A Miller, Sonja A Rasmussen, Anna Maria Siega-Riz, Jaime L Frías, Margaret A Honein. Am J Med Genet C Semin Med Genet 2010
43
20

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
20

Holoprosencephaly due to numeric chromosome abnormalities.
Benjamin D Solomon, Kenneth N Rosenbaum, Jeanne M Meck, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
40
20



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
17

Brains and faces in holoprosencephaly: pre- and postnatal description of 30 cases.
H G K Blaas, A G Eriksson, K A Salvesen, C V Isaksen, B Christensen, G Møllerløkken, S H Eik-Nes. Ultrasound Obstet Gynecol 2002
63
16

The molecular genetics of holoprosencephaly.
Erich Roessler, Maximilian Muenke. Am J Med Genet C Semin Med Genet 2010
155
16

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
16

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
300
16

Neuroanatomy of holoprosencephaly as predictor of function: beyond the face predicting the brain.
L L Plawner, M R Delgado, V S Miller, E B Levey, S L Kinsman, A J Barkovich, E M Simon, N J Clegg, V T Sweet, E E Stashinko,[...]. Neurology 2002
63
13

Molecular screening of SHH, ZIC2, SIX3, and TGIF genes in patients with features of holoprosencephaly spectrum: Mutation review and genotype-phenotype correlations.
Christèle Dubourg, Leïla Lazaro, Laurent Pasquier, Claude Bendavid, Martine Blayau, Franck Le Duff, Marie-Renée Durou, Sylvie Odent, Véronique David. Hum Mutat 2004
115
13

Teratogenesis of holoprosencephaly.
M Michael Cohen, Kohei Shiota. Am J Med Genet 2002
130
13

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
13



Analysis of genotype-phenotype correlations in human holoprosencephaly.
Benjamin D Solomon, Sandra Mercier, Jorge I Vélez, Daniel E Pineda-Alvarez, Adrian Wyllie, Nan Zhou, Christèle Dubourg, Veronique David, Sylvie Odent, Erich Roessler,[...]. Am J Med Genet C Semin Med Genet 2010
107
13

Array-CGH analysis indicates a high prevalence of genomic rearrangements in holoprosencephaly: an updated map of candidate loci.
Claude Bendavid, Lucie Rochard, Christèle Dubourg, Jonathan Seguin, Isabelle Gicquel, Laurent Pasquier, Jaqueline Vigneron, Annie Laquerrière, Pascale Marcorelles, Corinne Jeanne-Pasquier,[...]. Hum Mutat 2009
35
13

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
35
13

Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly.
Jeffrey E Ming, Michelle E Kaupas, Erich Roessler, Han G Brunner, Mahin Golabi, Mustafa Tekin, Robert F Stratton, Eva Sujansky, Sherri J Bale, Maximilian Muenke. Hum Genet 2002
158
13

Evaluating the incidence and likelihood ratios for chromosomal abnormalities in fetuses with common central nervous system malformations.
Katherine R Goetzinger, David M Stamilio, Jeffrey M Dicke, George A Macones, Anthony O Odibo. Am J Obstet Gynecol 2008
36
13

First-trimester sonographic diagnosis of holoprosencephaly: value of the "butterfly" sign.
Waldo Sepulveda, Victor Dezerega, Cecilia Be. J Ultrasound Med 2004
45
13

Holoprosencephaly: a survey of the entity, with embryology and fetal imaging.
Thomas C Winter, Anne M Kennedy, Paula J Woodward. Radiographics 2015
42
13


What is the incidence of holoprosencephaly?
E S Saunders, D Shortland, P M Dunn. J Med Genet 1984
37
10

Prenatal diagnosis of alobar holoprosencephaly at 10 weeks of gestation.
C D Turner, S Silva, P Jeanty. Ultrasound Obstet Gynecol 1999
18
16

Alobar holoprosencephaly at 9 weeks gestational age visualized by two- and three-dimensional ultrasound.
H G Blaas, S H Eik-Nes, T Vainio, C V Isaksen. Ultrasound Obstet Gynecol 2000
45
10

A case of suspected teratogenic holoprosencephaly.
M Stabile, A Bianco, S Iannuzzi, M C Buonocore, V Ventruto. J Med Genet 1985
11
27

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
10

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
10

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



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.